ID: 127818701 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:88704401-88704974 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86944644..86945217) | | |
ID: 127818700 | H3K4me1 hESC enhancer GRCh37_chr10:88700126-88700626 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86940369..86940869) | | |
ID: 127818699 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:88631460-88632021 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86871703..86872264) | | |
ID: 127818698 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:88627361-88627948 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86867604..86868191) | | |
ID: 127818697 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:88624817-88625468 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86865060..86865711) | | |
ID: 127818696 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:88624164-88624816 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86864407..86865059) | | |
ID: 127818695 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:88615649-88616230 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86855892..86856473) | | |
ID: 127818694 | OCT4-NANOG hESC enhancer GRCh37_chr10:88597221-88597813 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86837464..86838056) | | |
ID: 127818693 | H3K27ac hESC enhancer GRCh37_chr10:88552774-88553500 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86793017..86793743) | | |
ID: 127818691 | hESC enhancers GRCh37_chr10:88470545-88471164 and GRCh37_chr10:88471165-88471784 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86710788..86712027) | | |
ID: 111982877 | Sharpr-MPRA regulatory region 4131 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86939452..86939746) | | |
ID: 100873861 | RNA, U1 small nuclear 19, pseudogene [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86889569..86889733) | | |
ID: 100272220 | RNA polymerase II associated protein 2 pseudogene 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86854693..86856358, complement) | | |
ID: 79812 | multimerin 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86935540..86957615, complement) | EMILIN-3, EMILIN3, ENDOGLYX-1 | 608925 |
ID: 11155 | LIM domain binding 3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86666788..86736072) | CMD1C, CMH24, CMPD3, CYPHERZ1, LDB3Z4, LVNC3, MFM4, ORACLE, PDLIM6, ZASP, LDB3 | 605906 |
ID: 657 | bone morphogenetic protein receptor type 1A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86755763..86932844) | 10q23del, ACVRLK3, ALK-3, ALK3, BMPR-1A, CD292, SKR5 | 601299 |