Tag | Content |
---|
EnhancerAtlas ID | HS108-27489 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:13432810-13435260 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:13432998-13433017 | TGACCACCAGGGGGCGAGG | + | 6.94 | MITF | MA0620.2 | chr3:13432988-13433006 | CATGGTCATGTGACCACC | + | 6.3 | MITF | MA0620.2 | chr3:13432988-13433006 | CATGGTCATGTGACCACC | - | 6.3 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09840 | chr3:13432087-13436853 | CD14 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I013390 | chr3 | 13432088 | 13436853 |
|
Enhancer Sequence | TAAGAGCAGA TGGGAGAGGC AGACAGATAT GGAGTTAATT TCCCAGGGTG GAGGGAGGCG 60 TGATGGGAGC TTCTGCCCCA TGCAGGAACC ACACTCCACA TCACCACCCA CCAGGCAGGT 120 GTCATAAACT GTATGTCAGG AGAGGAAACT GAGGCTGAAA GGAATGAAGA CACTTACTCA 180 TGGTCATGTG ACCACCAGGG GGCGAGGCCA GAATTTGAAC CTAGGGCTGT CCGATGAAAG 240 CTTGTGCTCT TCCTGCTGTG ACTCCCTGCC CTTGACTGCA GGACCAGCTC AGTGCAGTGC 300 ATAACACTGC TGCCCCGCAC GTCTGTGAGC GGTTTACAAT TTAGGAGTCT GCTCGGAAAC 360 CTGGGCCATT CATTCCTGCT CACCACTTCC TGGGAGTAAA CTCCTCTCCC TCCCTGTGCA 420 GGGGAGGGGA CCCAGGGTGG AGGGGCATTA CCCAAACTGT CTAGTGTCAC ATGACTCTTG 480 TCTCTTCACC TTGACTGTGA GACTCCTGAG GTCGTGGGGT AGGTAGGGGG CAAGGAGAGC 540 CAGGCCCAGC CAGCCTTGGC TCTTATGTCC TGGCTTGCTG CCTGGGAGCC TTCTGATCTG 600 TCCTTTCCAA TCAAGAAACA GATGCCACAT GCAAGTCTAG TTCTCACCTC CTCTTGAAAG 660 GATGAAGATC CACCCACCTG GGCCTCATTC CCTCTGAGAG CCAGAAGCTG CTCGCCCTCT 720 CTAGAAGGGG CCATGCCACA CTCCTCACCA GCCCCTGATG TTCCACGCCT GTTCCACATC 780 CCTCATCCAC ACTCCCCTTC TGACCAGCTC CCAGTACAAG GGATCTGGGG GCCAAGAAAA 840 GCTGTTTTCT ACAGTGCAAA GGGCAAGGTA TTTAGAGTCT GACGGGCCTG GGGTCCTGCT 900 TCTCTTCACC CCGATCCCTG GCCCTGCAAG GTCTCAAAGA CTGCATGAAA TAGTGCCTAG 960 CAGAAGCTCC AGAAAACTCT GCTCCTTCGC CTTACTTCTC AGGGCATCTT TAATGAAGAG 1020 AGGCATCTTC TTACAGTTCC CTGGGTGTCT TTCCGTCAAT GTGAGCAACT GATCAGAGGA 1080 AGACAACCCC CATCTATGAT GTACATATAT GCGGGAAGAT TTTTTCTTAG AGGTCCAGAG 1140 CAGGATTTTG AGCAAATGAA AACTCTATGG TTTCCTGAAA ATTAATCTGT CTTCCTAACA 1200 TCCAGGGCAT TAGGTGAGGA TGGTGGATAT GAAAATCCAC ACCAGCGAAG CACATCGGCT 1260 GCAAGACAGG AGTCCTCTAG TCCAACCCTT GGATGCTGCG TCCCCATCAG ATGGGGGCTT 1320 GAGACCCTTC CCGCATACCC CAGGGATGAG GAGCTCATCG CCCAGCACAG CCTATTCCTC 1380 TGTTCAACAG CTCTGACTGT GAGAACCTTC TTCTGCACAC TGAGCTGAAA CAGGGTGCAT 1440 ATGGAGTACT GCTGGCCCCA GTTCCACTGT CCGGGGGCAG AGCCAGCAGG TTGGCTTAGC 1500 AGTGTGCTCA GTGAGGGGAG CCTGGGCTCC AATTCCACCT TCTCGGGGAA GAGCCCAGCA 1560 GGCCGGCTTT GCAGTATGCT CGGTGAGGGG AGCCTGGGCC CAAATTCCTG CCTTCCAGAG 1620 TCAGAGCCCA GCAGGCCAGC TTTACAGTGT GCTCAGTGAG GGGAGCATGG AGTCCCTATA 1680 ATAGTGTGAC CCAGTAACCA GAAACGCAAG ACTGCAGACC ACTAGGCAGG CCACTCCCTT 1740 AACACAAATA CATGCCAACA CCACAAGAGT CCTGAATAGC TACCCTGGGG CTTCCACCCA 1800 GCTCAGCTCC AAGCATGGCT TTTCTCTTCT GTAAAATGGG GATGAAAATA CCAACGCATG 1860 GGGTTGGTGG GAAGATCAAA TTGAGAAAGC ACCCCCATGA CATGTCCAGT GTTCACAACG 1920 GTCCGCTTAT GGACAAGGGG ATGGAGGTGG GGGAGGCCCT GCTAAGGGGC TCTTAGCAAG 1980 GAAAACGGTG GGAGAGAATC ATGCCTGCAG ACACTTCAGG GGCTGCACGT GGAGCTCTGT 2040 TTTTCATCAT CTTTGCTCCC CACAGTCTCT CCTGGAAGTC CACCACGTTC AAATGTGGAA 2100 GAAGAGTTGA ATGTGTGGTA ATTTCAAGGG CAGAAAGTGT CCTTAGGCTT CTGTAAGTTA 2160 CCTGCTCGGG CAGGTGCACA CACAGGACCG AGTGCAGGAT TTGCAGGGCT CCGTGCAGAT 2220 GAGAACACAG GGACCCTCGT TCATGCATGG GCCTGCCAGC TGCTGGCCAC TGGCTTTCTC 2280 TCCCGCCAGC TGCTGGCAAC ATGGCCAGAC CCAGCTGCGT GGGCCCTGGG GATGTCAAGG 2340 CAGGTGTCTG CCTTTCCAGG GCCTGCTGCA GGTGGGCATC CCTAAGGGTG GCAAGGGGGA 2400 AGGGAAAGCT CTCAATAAAT CTGTGCCCAA AGTTTTGCTT TTTCCACTCT 2450
|