ID: 127267318 | H3K4me1 hESC enhancer GRCh37_chr1:9048516-9049016 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8988457..8988957) | | |
ID: 127267317 | H3K4me1 hESC enhancer GRCh37_chr1:9046209-9046710 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8986150..8986651) | | |
ID: 127267316 | H3K4me1 hESC enhancer GRCh37_chr1:8968693-8969193 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8908634..8909134) | | |
ID: 127267315 | H3K4me1 hESC enhancer GRCh37_chr1:8968192-8968692 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8908133..8908633) | | |
ID: 127267314 | NANOG-H3K4me1 hESC enhancer GRCh37_chr1:8943543-8944262 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8883484..8884203) | | |
ID: 127267313 | H3K27ac hESC enhancer GRCh37_chr1:8938769-8939360 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8878710..8879409) | | |
ID: 127267312 | H3K27ac hESC enhancer GRCh37_chr1:8938175-8938768 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8878060..8878709) | | |
ID: 127267311 | H3K27ac hESC enhancer GRCh37_chr1:8937582-8938174 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8877523..8878115) | | |
ID: 127267310 | H3K4me1 hESC enhancer GRCh37_chr1:8925615-8926450 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8865556..8866391) | | |
ID: 126805609 | MED14-independent group 3 enhancer GRCh37_chr1:8933339-8934538 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8873100..8874479) | | |
ID: 121677386 | Sharpr-MPRA regulatory region 1652 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8962990..8963284) | | |
ID: 120883620 | Sharpr-MPRA regulatory region 9811 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8862530..8862824) | | |
ID: 112268261 | uncharacterized LOC112268261 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8905216..8926874, complement) | | |
ID: 106481275 | RNA, U6 small nuclear 304, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8883427..8883533, complement) | | |
ID: 106480431 | ENO1 intronic transcript 1 [Homo sapiens (human)] | | | |
ID: 106480377 | RNA, 7SL, cytoplasmic 451, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8979576..8979874, complement) | | |
ID: 102465436 | microRNA 6728 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8866502..8866590, complement) | hsa-mir-6728 | |
ID: 100505975 | ENO1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8878835..8879885) | | |
ID: 100113373 | high mobility group nucleosomal binding domain 2 pseudogene 17 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8893411..8894603) | | |
ID: 155184 | solute carrier family 2 member 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8992534..9026423, complement) | GLUT-7, GLUT7, hGLUT7 | 610371 |