ID: 130064495 | ATAC-STARR-seq lymphoblastoid active region 14669 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40818514..40818723) | | |
ID: 130064494 | ATAC-STARR-seq lymphoblastoid active region 14668 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40804203..40804382) | | |
ID: 130064493 | ATAC-STARR-seq lymphoblastoid silent region 10650 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40799479..40799528) | | |
ID: 130064492 | ATAC-STARR-seq lymphoblastoid silent region 10649 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40798969..40799328) | | |
ID: 130064491 | ATAC-STARR-seq lymphoblastoid active region 14667 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40778361..40778430) | | |
ID: 130064490 | ATAC-STARR-seq lymphoblastoid silent region 10648 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40778061..40778300) | | |
ID: 130064489 | ATAC-STARR-seq lymphoblastoid silent region 10647 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40777381..40777510) | | |
ID: 127891573 | H3K4me1 hESC enhancer GRCh37_chr19:41332287-41332788 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40826382..40826883) | | |
ID: 127891572 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:41317625-41318515 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40811720..40812610) | | |
ID: 127891571 | H3K4me1 hESC enhancer GRCh37_chr19:41314255-41314754 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40808350..40808849) | | |
ID: 127891570 | H3K4me1 hESC enhancer GRCh37_chr19:41307710-41308450 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40801805..40802545) | | |
ID: 127891569 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:41306857-41307531 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40800952..40801626) | | |
ID: 127891568 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr19:41285223-41285754 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40779318..40779849) | | |
ID: 100529264 | RAB4B-EGLN2 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40778219..40808441) | EGLN2, EIT-6, EIT6, HIF-PH1, HPH-1, HPH-3, PHD1, RERT-lncRNA | |
ID: 100529262 | MIA-RAB4B readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40775537..40796944) | RAB4B | |
ID: 171523 | cytochrome P450 family 2 subfamily T member 1, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40808443..40811100, complement) | CYP2T2P | |
ID: 171427 | cytochrome P450 family 2 subfamily F member 2, pseudogene [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40818477..40826773, complement) | CYP2F1P | |
ID: 112398 | egl-9 family hypoxia inducible factor 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40799191..40808434) | EIT-6, EIT6, HIF-PH1, HIFPH1, HPH-1, HPH-3, PHD1 | 606424 |
ID: 53916 | RAB4B, member RAS oncogene family [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40778247..40796942) | | 612945 |
ID: 8190 | MIA SH3 domain containing [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (40775160..40777490) | CD-RAP1, MIA | 601340 |