ID: 129930750 | ATAC-STARR-seq lymphoblastoid active region 1185 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68496923..68496982) | | |
ID: 129930749 | ATAC-STARR-seq lymphoblastoid active region 1184 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68496763..68496812) | | |
ID: 127269508 | OCT4-NANOG hESC enhancer GRCh37_chr1:68930526-68931161 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68464843..68465478) | | |
ID: 127269507 | H3K4me1 hESC enhancer GRCh37_chr1:68761039-68761917 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68295356..68296234) | | |
ID: 127269506 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:68760160-68761038 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68294477..68295355) | | |
ID: 127269505 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:68759281-68760159 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68293598..68294476) | | |
ID: 126805754 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:68924860-68926059 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68459177..68460376) | | |
ID: 126805753 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:68849743-68850942 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68384060..68385259) | | |
ID: 124904198 | uncharacterized LOC124904198 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68420051..68451523) | | |
ID: 105378782 | uncharacterized LOC105378782 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68293251..68305568) | | |
ID: 101927220 | DEPDC1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68496676..68538627) | | |
ID: 100130626 | elongin C pseudogene 18 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68375322..68375662, complement) | TCEB1P18 | |
ID: 171416 | thioredoxin pseudogene 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68513844..68514743, complement) | | |
ID: 55635 | DEP domain containing 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68474152..68497082, complement) | DEP.8-V2, DEPDC1A, SDP35, DEPDC1 | 612002 |
ID: 6121 | retinoid isomerohydrolase RPE65 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (68428822..68449954, complement) | BCO3, LCA2, RP20, mRPE65, p63, rd12, sRPE65 | 180069 |