ID: 130062093 | ATAC-STARR-seq lymphoblastoid active region 13032 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2972602..2972751) | | |
ID: 130062092 | ATAC-STARR-seq lymphoblastoid active region 13031 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2960318..2960417) | | |
ID: 130062091 | ATAC-STARR-seq lymphoblastoid active region 13030 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2957974..2958133) | | |
ID: 130062090 | ATAC-STARR-seq lymphoblastoid active region 13029 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2957039..2957098) | | |
ID: 130062089 | ATAC-STARR-seq lymphoblastoid active region 13028 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2907585..2907784) | | |
ID: 130062088 | ATAC-STARR-seq lymphoblastoid silent region 9250 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2906285..2907144) | | |
ID: 130062087 | ATAC-STARR-seq lymphoblastoid silent region 9249 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2847894..2847983) | | |
ID: 130062086 | ATAC-STARR-seq lymphoblastoid silent region 9248 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2847224..2847273) | | |
ID: 127888645 | H3K4me1 hESC enhancer GRCh37_chr18:2974861-2975362 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2974863..2975364) | | |
ID: 127888644 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:2919273-2920004 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2919275..2920006) | | |
ID: 125338465 | Sharpr-MPRA regulatory region 3375 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2842131..2842425) | | |
ID: 124904372 | uncharacterized LOC124904372 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2774846..2774963) | | |
ID: 124904236 | uncharacterized LOC124904236 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2978355..2985410) | | |
ID: 112538445 | Sharpr-MPRA regulatory region 4434 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2854151..2854445) | | |
ID: 105371963 | uncharacterized LOC105371963 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2967000..2970109) | | |
ID: 100310848 | small nuclear ribonucleoprotein polypeptide C pseudogene 4 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2990650..2991310) | | |
ID: 727896 | CHORDC1 pseudogene 4 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2943212..2946623, complement) | | |
ID: 84034 | elastin microfibril interfacer 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2846232..2916003) | EMILIN-2, FOAP-10 | 608928 |
ID: 23347 | structural maintenance of chromosomes flexible hinge domain containing 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2655726..2805017) | BAMS, FSHD2 | 614982 |
ID: 9663 | lipin 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (2916994..3013144, complement) | CRMO1, MJDS | 605519 |