ID: 127887660 | H3K4me1 hESC enhancer GRCh37_chr17:64356585-64357085 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66360467..66360967) | | |
ID: 127887659 | H3K4me1 hESC enhancer GRCh37_chr17:64299525-64300026 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66303407..66303908) | | |
ID: 127887658 | OCT4-NANOG hESC enhancer GRCh37_chr17:64205560-64206125 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66209442..66210007) | | |
ID: 127887657 | NANOG hESC enhancer GRCh37_chr17:64106810-64107347 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66110692..66111229) | | |
ID: 127887656 | H3K4me1 hESC enhancer GRCh37_chr17:64010153-64010652 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66014035..66014534) | | |
ID: 127887655 | H3K4me1 hESC enhancer GRCh37_chr17:64009651-64010152 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66013533..66014034) | | |
ID: 126862620 | MED14-independent group 3 enhancer GRCh37_chr17:63996564-63997763 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66000446..66001645) | | |
ID: 125316773 | Sharpr-MPRA regulatory region 14325 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66276531..66276825) | | |
ID: 125316772 | Sharpr-MPRA regulatory region 2592 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66233051..66233345) | | |
ID: 121603770 | Sharpr-MPRA regulatory region 4334 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66345931..66346225) | | |
ID: 116276478 | CRISPRi-validated cis-regulatory element chr17.4440 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66296187..66296627) | | |
ID: 112533659 | Sharpr-MPRA regulatory region 10613 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66348591..66348885) | | |
ID: 107984972 | nuclear transport factor 2-like [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66000372..66001141, complement) | | |
ID: 106480529 | RNA, 7SL, cytoplasmic 735, pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66364029..66364319) | | |
ID: 100873690 | RNA, 5S ribosomal pseudogene 444 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66267743..66267848) | RN5S444 | |
ID: 280637 | proteasome 26S subunit, non-ATPase 7 pseudogene 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66197595..66198707) | MOV34L, PSMD7L | |
ID: 201134 | centrosomal protein 112 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (65635537..66192133, complement) | CCDC46, MACOCO, SPGF44 | 618980 |
ID: 5578 | protein kinase C alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66302613..66810743) | AAG6, PKC-alpha, PKCA, PKCI+/-, PKCalpha, PRKACA | 176960 |
ID: 350 | apolipoprotein H [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66212033..66229415, complement) | B2G1, B2GP1, BG | 138700 |