ID: 130006138 | ATAC-STARR-seq lymphoblastoid active region 5057 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66745538..66745627) | | |
ID: 130006137 | ATAC-STARR-seq lymphoblastoid silent region 3602 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66745258..66745357) | | |
ID: 130006136 | ATAC-STARR-seq lymphoblastoid active region 5056 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66744988..66745097) | | |
ID: 130006135 | ATAC-STARR-seq lymphoblastoid silent region 3601 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66744458..66744847) | | |
ID: 130006134 | ATAC-STARR-seq lymphoblastoid silent region 3600 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66677810..66678089) | | |
ID: 130006133 | ATAC-STARR-seq lymphoblastoid silent region 3599 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66677500..66677609) | | |
ID: 129390294 | MPRA-validated peak1306 silencer [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66649334..66649534) | | |
ID: 127821572 | H3K4me1 hESC enhancer GRCh37_chr11:66511467-66511967 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66743996..66744496) | | |
ID: 127821571 | H3K4me1 hESC enhancer GRCh37_chr11:66487347-66488304 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66719876..66720833) | | |
ID: 127821570 | H3K27ac hESC enhancer GRCh37_chr11:66462288-66462788 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66694817..66695317) | | |
ID: 127821569 | H3K4me1 hESC enhancer GRCh37_chr11:66453249-66453749 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66685778..66686278) | | |
ID: 127821568 | H3K4me1 hESC enhancer GRCh37_chr11:66410755-66411278 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66643284..66643807) | | |
ID: 127821566 | hESC enhancers GRCh37_chr11:66405625-66406338 and GRCh37_chr11:66406339-66407050 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66638154..66639579) | | |
ID: 127821565 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:66384051-66384984 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66616580..66617513) | | |
ID: 109286555 | fragile site, folic acid type, rare, fra(11)(q13.3) [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66744820..66744845) | | |
ID: 106480926 | RNA, 7SL, cytoplasmic 12, pseudogene [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66712720..66713009, complement) | | |
ID: 100526737 | RBM14-RBM4 readthrough [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66616630..66646468) | COAZ, PSP2, RBM14, SIP | |
ID: 100462788 | ferritin light chain pseudogene 6 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66771449..66771870, complement) | | |
ID: 100422299 | complement C1q binding protein pseudogene 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66761403..66762456, complement) | | |
ID: 83759 | RNA binding motif protein 4B [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66664998..66677887, complement) | RBM30, RBM4L, ZCCHC15, ZCCHC21B, ZCRB3B | |