Tag | Content |
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EnhancerAtlas ID | HS113-14185 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr16:57867940-57870360 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr16:57869163-57869173 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr16:57869163-57869173 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr16:57869163-57869173 | AATGGAAAAT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr16:57869637-57869652 | GAGGTCAGGAGTTCA | + | 6.22 | POU4F2 | MA0683.1 | chr16:57868312-57868328 | TTCATTAATTATTCAG | - | 7.71 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I057834 | chr16 | 57868740 | 57869594 |
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Enhancer Sequence | TATTTTTAGT AGAGACAGGG TTTCACCGTG TTAGCCAGGA TGGTCTCTAC CTCCTGACCT 60 CATGATCTGC CCGCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CACCGCGCCC 120 CGGGAATGCA TTTATTTTTA AAGTAATATA CATACTATAG CTTAGCAACA CATTATCAAA 180 TAAATTATTT GATGAAAAAT TGCAAAAGTT ACCATCTGTG AAAATAATCT CCCAGTATTG 240 TTTCTTAGTG GACCTCTCCT GGTCTTAACT ATTCTAGGCT GGGAAACATT GGTTTGTCCC 300 TGAGCAAACT GCACTCCCTG ACATTTTTTG AACATTAAAA AAATTATCAC AAAAGTTTTA 360 CACATTATAC AATTCATTAA TTATTCAGTA AACTCTTCAC CTTGATCCTT TTTTCAAAGT 420 GTTAAAATTC TGAAGTCTCT GTAAAATAAA AATACCTTTA AATTTTTATT TATTTATTAT 480 TTTATTATTT TTAGAGACAG GTTCTCGCTC TGTTGCCCAG GCTGCAGTGC AGTGGTACCA 540 TTATGGCTCA CTGTAGCCTC AACCCCCTGG ACTCAAGCAA TCCTCCCACC TCAGCCTCCT 600 GAATAGCTAG GATTATAGGC ACACGTCACA AGTCCAGCTA ATTTTTTTAT TTTTTATTTT 660 TGTAGAGACC GGGTCTCACT ATATTGGCCA GGTTGGTCTT AAACTCCTGA CCTCAAGCAA 720 TCCCCTTGCC TCAGCCTCCC AAAGTGTTGG GATTACAGGC ATGAGCCACT GTGCCCTGCA 780 AAAATACCTT TAGGTGCCAT TTGATTGAGT GTTACCTATT GGTGTCTCTA CTGCATGCAA 840 CTCTGCAGAG GAAGCAATTC ATGAGCTATG CTCAAACCTT TGTCATCACT GCTGCCAATA 900 GCTTTTCCCA AGGAGGTAGA TCTGAGAAAC AGAGGGAGAT CCTTGGACAT GGTGGTAAAA 960 TTCAGGAGGA AAAAAAATGC AACAGAAAAG CTGCTTTCTT GTGCTTTCCT CTTTGCTAAG 1020 ACTGGCTCCC TGCAGGCCCC TCCTTCTGTG AGTAAGAACG GAGGCGGGTT CTCTCTTTTG 1080 TTCTAGGTAC AGTCATGGGA GAGATGCTGC CTCTTCCCCA AAGGCACAAT AGCACCGATA 1140 TTTGAAGAGT CAGTGATAGA CGATTTCATC AGAAGGTTCT GGCAACAGAA ACTACCAAAC 1200 GACTTATTTT AAAAACAAAA CAAAATGGAA AATATTAAAA TCCAATCAGC TCATTGATCA 1260 CCAGGGAGAA AGAAAATGAA CATGTGTCTC TTGTACTCAG CCTGCTCTAA AATATGAAAC 1320 TGGAATGTGT TTCAGAAAGC AACAAAGATG TGAGTATGGA ATATTAAAGC ACTATGATAA 1380 TTTGATAGTA CAATTTTCCT TTGTGGATTT CCTGTAGTGA CCAATATTAA TATAATAGGA 1440 GTGAACATCT ACTGGGTACT TATTACATAT TAGCATTTTC TATGGTATTT TATTAGGTTA 1500 CAGAACAACC CAATGAGGAA AGTACTACTC TTGTCAGCCC TGTTTCATAG ACTAGGAACA 1560 GAGGAACCGT GATTCACCCA AAGTTTTGAG TGATTCACCC AAAGTTTTGT GGCTAATAAA 1620 ACTCCATTCC AGCCCAGGCG CAGTGGCTCA TGCCTGTAAT CCCAACACTT CGGGAGGCCG 1680 AGGCAGGCAG ATCACTTGAG GTCAGGAGTT CAAGACCAGC CTGGCCAACA TGGAGAAACC 1740 CTGTCTCTAC TAAAAACATA AAAATTAGCC AGATATGGTG GCATGTGCCT GTAACCCTAG 1800 CTACTCAGGA GGCTAAGGCG TGAAAATGGC TTGAACCCAG GAGGCAGAGG TTGCAGTAAG 1860 CTGAGATTGT GCCACTGCAC TCTAGCCTAG ATGACAGAGT GAGACTACAT CTCAGAAACA 1920 AAAAACAAAC AAAAACTCCA TTCCAGCCTG GGCGCCTCTC TCCAGGCCCT CACTTCCAAC 1980 CCAGAACACA CTAGATTCCA GAGGGAAACC CAGTCGCCAG CCTGAAGCTG GCATTCAGGT 2040 TGCCCTTCTC AGGGAACTCA AAGGGTGACG CAGGAATTTT CTCTGTTTTG CTTGTTTTGA 2100 GTCAGGGCCT CTGTCGCCCA GGCCAGAATG CAGTAGCAAG ATCATGGGCT CACTGCAGCC 2160 TTGACCTTCC TGGGGTCTAG CGATCCTTCC ACCTCAGGCT CCCAAATAGG TGGGACTACA 2220 GGCATTCCAC TACACCCGGC TAATTTTTGT ATTTTTGGTA GAAACAGGAT TTCACCATGT 2280 TGCCCAGTCT GGTCTTGAAC TCCTGGGCTC AAGAGATCCT CCCACCTCAG CCTCCCACAG 2340 TGCTGGCATT ACAGGTTTGA GCCACTGTGC CTGGCCAGTG CAGGCATTTT CTCCTTGGCC 2400 CTTATCAGCT TGGTGGAGCT 2420
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