Tag | Content |
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EnhancerAtlas ID | HS113-06335 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr11:34615200-34617530 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr11:34616534-34616545 | TCTGATTGGTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26655 | chr11:34615762-34617315 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I034594 | chr11 | 34615763 | 34617315 |
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Enhancer Sequence | CTAAACTAAT GGTTCAAGGC TTATCAAAGA TAAATCCTCT GTCTTGTTCA TCTCTGTGTC 60 TCTCATGGTA TCTAGCAGAC TTCCACCCAA GATATAAAGA CACTATGACT AAGTGAATGA 120 TTTTAGTCTT ACCTACCTGC CTGTTAACTT ACCTACTTGC ATCTCACTTA TACTTCAACT 180 TTTGGCTTCT TCCTCAACCT CAACTACCCC ATTCTTCCCA TGGCTCACTG TGCTCACTGG 240 CCTCCATACT GTCCCTTAAA TAAGGAAAGC TGCCCTAGCC TCAGGGCCTT TGCACCTGCT 300 CTGCCTGCTG TTTGGAATGC TCTTCTTCCC ATATACCCAT CTGTTTTAAT CCCTCATCTT 360 TTAATCCCTC ATCCCATCTC TTCAAATGTG ATTTCTACAG AGGGTTCTCT GACCACCTTA 420 TCCAATAACC AGCATTCCGT CTCCCCTCTG CCATTCTCCA TCATCTCACC ATGCTTTATA 480 TCACATATCA CTAAGTGACA GTATACTATA AACGTACCCA TTTGTTTACT GTCTGCCTCC 540 CTAACTAATG TATAAGCTCT CTGAGGGCAG GGACTCTGTT TTATTTGTAC ACCACAATTA 600 TCTCCAGTGC CTTGAATAGT GTCTGGCATG TAGAAGGAAT TCAAGAAATA CTTGTCAAGC 660 TAGGTGCTGT GATAACTACT TTATATGAAA TTAAGTATTT CTCCTCCAGC AGCTCTAAAA 720 GTTTAGTATG TTATTATTGT CTCTGTTTTA CTGATGAGTG AACTGAGGTT CAGAGAGGTT 780 ATTTAGCATA CGTATGAAGA CAGAATTAGT GAGTGATTGA CCTGAGATTT GAACTCAACC 840 TGTGCTGTCT AAAGCTAGCC AGGCAGCCTC ACATACATGG CAAATGCCTA CTGAGACATG 900 AACATGCAGG TTGGGATCCC AAACTGTTGG GAAGCATAAA AGAAAAACAC TAAAGATGTG 960 GGGAGTGTAG GACTTTTTTT TTTAATAGGC CAGTGGCCCT CTCTGCAACC CTTTGAATGA 1020 TCAGCTTGAT CAGAGAATCC CCTACCCCTA CCCCTGCCTC AGCCAGTTTC TATCTGGCTG 1080 TGTCATCAGC TGGCTGATCC AAACAGCAAT GTCAACAAAA GAATGGTGAT CAGGCACGTA 1140 AAGCAATGTG TCAGAAAGAA AGAAAAGGCA GCTCAGATGA TGCAAGATCA TCCAGATGTC 1200 AAGCACTGTG TGGTGGCACA CTTGCCCGTT CATGTTGTTG ATTTTTTAAA CATTTGTGAT 1260 AAGAACAAAA ACTTAGTTGC TTCCCTCAGG TCCTCCCTGT ATGGATTAGT GCAGACATCT 1320 GCCGCTTCAG GCTTTCTGAT TGGTTCCCAC TGGTTTGGGG CAAAACCGGA AGCTTCTGAG 1380 CCAAGTGCAG GGGCAGAAGA GCTCCCAAGA GCTCCTGGGA AAACTAGGAA GGACAATCAA 1440 GAAACCACCG GCAGCTCCAT TTGCAGGATC TCATCCCATC AGGGGCTGTC TCAGGAGGGG 1500 GAATTGGAAT ACCATTCACC TGTCCCCTTT GCAGATACAC CAATGTCTCG TTCAAGAACA 1560 AGCAGAAAGG AAACACCAGA TTGCCCAGAG CACAGGATTA GGACACACCA CACAGAGCCA 1620 ACTCAGCGTA TCATTGTTTG CATTGATCAT CTGGGGATGA AGCAGGCTCC GTTCTGGAAG 1680 GGGCAACCTG AATAGAGAAG AGTCTGACAT TGGAGTCAAG CAGAACTTGG TTGGAATTTG 1740 GCTCATTGCT GGGTGATCCA GAGACAGTTA TTTAATCTGA GAATCAGATA TCTTGTCTGT 1800 TAAATGGAAA TTATAGTAGC CACTTCACAG GATTGCTGTA AAGAGTACAT AAAACCAGGT 1860 ACCTGCAATG TATAGTGCTA AGCCTGACAC GTAGCAGGGT GTTAGTAAGT GGTACCTCTG 1920 ACTGGGGATG GAAGCCAGAG GAGCTGGACC TTTATTTGAC TGGCCAGAAG CCAGCTCTCT 1980 AGTCACCTTC CTGATCCTTC CTTCTTCTGT GTGTACACGG ACAATGTTTT TCTACATAAT 2040 GGAACAGTGG CCCTCAAAAC TTGTTTTCAT AAGAATTATC CAGGTTGCTA GTTATTAATA 2100 CTAGTTATCC AGGTTGCTAG TTATTAATAC TAGTTATCTG TGTTGCTAGC TAAAAATACA 2160 CTCAGTTCCC ATCCCCAGAT TTTTCTATTT CAGTAGGTGG TAGTGGGTTC AGGAAATCTG 2220 TGTTTTTACC AAAGTATCCC CTACTATAGA ATTAATTTTT GTGTTCCCCC CTCATTCATA 2280 TGTTGACATT TAAACCTCCA CTGTGATGAT ACCAGGTGGC TTTGGGAGGT 2330
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