Tag | Content |
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EnhancerAtlas ID | HS176-31058 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr5:32767790-32769280 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr5:32768173-32768184 | TCTTCCCGCCC | - | 6.14 | Six3 | MA0631.1 | chr5:32767972-32767989 | AAGAGGGTATCATGAAG | + | 6.43 | ZNF263 | MA0528.1 | chr5:32768169-32768190 | CTCCTCTTCCCGCCCTTCTCC | - | 6.06 | ZNF263 | MA0528.1 | chr5:32768059-32768080 | CCCTCCTCTTTCCCTGCCTCC | - | 6.19 | ZNF263 | MA0528.1 | chr5:32768062-32768083 | TCCTCTTTCCCTGCCTCCACC | - | 6.86 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_46523 | chr5:32766014-32770299 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I032766 | chr5 | 32767018 | 32770339 |
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Enhancer Sequence | CCACACCTTG AAATTGCTTA AATAAAAACA GGGAAGTTTC ATTTTAGGGT ATAAAGCAGA 60 AATGAAAAAA AAAAGCCATC CATATAAAAA CCTGTATTTT TGTTCATCTC TTCTTTGTAA 120 ACACATCTCT AGGTGACTCA AAAAGTTCAA GGGAAGCTGT CCGAAGTTCT CAGGACAAGT 180 TTAAGAGGGT ATCATGAAGT CAGAGAAATT AGAATTACAT GCTCCTTCTG ATTTTGGACG 240 ATCAGAAGTA ATGAGGCCAG AAATTGGGCC CCTCCTCTTT CCCTGCCTCC ACCTCCGTTT 300 GACCTGATCA CCCCTCTTCC TGTTTGTATT GCTGCCCGGC ACAGTTGCAG GGTGAGTGGG 360 ATGCCTGCTC CTGATCCTGC TCCTCTTCCC GCCCTTCTCC TGTTGGGTTT TGGTTTATGC 420 CTTTGCCTAC CTCAACTTCG TGCCTTGACA GGACACAGAC CTCAGGGAAG AGAGGCCTGC 480 ATGTGTCCCG AGCAGTCTTG TGGGGGTTGG GTCACCAGCC TTTCAGAGGC ATGTCTGGCT 540 GGCACTGGTG AATCATCAGG GCCTAGGACA AACATCACTC ACTTGGTCAT CTGAAGGCCA 600 GGAACGATTG TGTCATTATG TATGTGCATT TCTCAACTAA GCCTTCAAGA GGGTGATGGG 660 ACGAGAAGCA TCTGTATATG ACGCATGTGT GACACATCCA AAGGGCAAAT ATATCATATG 720 ACCATATTCC CTGCATGAGC CTTGGGAGAA TTTTCAAAAG TCATTCTCAC TTACTTGTGC 780 TCCATACCCA CCAATTCCAA AAACTGATGC CTACAGAGAT CTCCTTGTTG CTTCCCATGA 840 ACAAGACCAG CTTTCCTTGC TGAGGTGTGC TTATGCCTCT GGATTCCGTG TGCCAGCTGT 900 GTGACCCTCT GTTGTCCCTG TCATTACAGG AGGTGAATGA GGGCCCTAAC TCTACCTAAT 960 GATCTTCCTA AGACTGCTTT TGTTTAATGA TCCAGTCTGT TCTAGGTCAT GAGAGAGAAA 1020 ACAGTCTGCA GGCAGCCACA CCTCAGGAAG GTCCAAGTTA ATTTGCCAGC CCAGTGCATT 1080 GCTACCAGTT CAGAGCTGAG TCCACGATGG GGACAGTTAT TTGGAAAACT TAGGTCAGAT 1140 CCCACCCTAA GTAAGTTCTA ACTTCAGTCG GGGGAGCAAG AAGTATGCCA GAGGGTTCAG 1200 AGATGCTTCC ACTATGCACA GAGTTGTAGA TGAAGACCCC AGCTCTCTCC CTGTGGTGCT 1260 TCCTGTCAGT CACCTGCCCT TTGCATTTTC CCAGAGTTCC ACTGGGATAA AGGCGCAGAT 1320 TTTCAGCTTA ACTTTCCTCA AGGCTAAAAT ACGTCATCAA GTGACCAAGT GAGAATTCCA 1380 TGAAGACAGG CCCACTATAG AACAGGAATT GGGGTCTCTG TCAGTAAGAA AGAGACCTCC 1440 CTCTGTTTGG TGCTGAGGAG GCTGTGAGGC TACTTGGTTT ATGGCAGTTG 1490
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