Tag | Content |
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EnhancerAtlas ID | HS113-07432 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr11:110054590-110056990 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr11:110054741-110054752 | AAATCTCAGCA | + | 6.32 | PAX6 | MA0069.1 | chr11:110056898-110056912 | AATTCACGCGTGAA | - | 6.41 | TP53 | MA0106.3 | chr11:110054758-110054776 | AACATCCCCAGACATGTC | - | 6.05 | TP53 | MA0106.3 | chr11:110054758-110054776 | AACATCCCCAGACATGTC | + | 6.24 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I110182 | chr11 | 110053216 | 110056967 |
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Enhancer Sequence | ATGGCACCCT GGACTACAGG GCTCTGGCCA CGCTGCTATC GATGCTTAGG ACTAGGCCGT 60 GCTTTGTGTT GGGAGGGCTG TCCTGTGCAT TGTAGGATGT TTTCCAGCAT CCCAGGCCTA 120 TCCCTGCTAG ATGTCAGTGC CACACACACC CAAATCTCAG CAATCACAAA CATCCCCAGA 180 CATGTCCCCT GGAAGACCAC CAGTGTGCAA GATACAGATA CTGTAGAATA ACAGGAGGGA 240 GAGGGAGCAC GTGAGAGCCC AAGGGCAGAG GGGATGATAG AACAATCTGG CGCTGGAGAC 300 GGAGCTGATC TGAGCACTGT GGCAGCAACA GGGATGTTCA CCAAATCTTC CCTTTGCTAT 360 CCTGCCTTTC CCATCCCCCT TGTAGCCAAG AGAACTCGCT ATATGACTAG CTCTGACCAT 420 GAAATATTGG CAGAAGAGAC AGGTGTCATT CCCAAGCCCA GGCGGTGAAC AGCCCTGTGG 480 GGTTCTCCAG CCTCTGTCTC CCTGACATGG TGCCTAAGAG GTCATATGTT CCTCCTGGTG 540 TAGGGAAATC CAGGTCCCTG AGGGACTGTG CAGAACAAGA TGCCCCCAAA TGAACAGAGA 600 GCAAGGCACG GGCCTCTAAG GTGTAAGCCT TGCAGGGTGG GTGGTAGAGC CTCACCTGCT 660 CTGACTGATG GAAATCGGCA GAGGGAAGAA GGGAAACCCC TTCTGATGGG GGTGGGAGGC 720 CTGAAGGAAG CCCTGGAGAT GGGAAAGTCC TAGAGGGAAC TGGCTGTACT GGAACAGCCA 780 CACTGTGCCA GGAAGTTGCA AAAACTTGTT GCAGGTGGGA GGCGGGGTGT GCAGCGGGCA 840 GCCCACTCAC AGAGGCTGGA GTGAAGGATG TGTGGTCAAC AACACGGATG ATCAGAGGAG 900 AGACATTTTT AGGAATTCAT TGCGTTTGTG GAGTAAAAGA AAGCAGACAC GACACATAGA 960 ACCTGCTGAA TGATGTCAAT TATATAAAGT GCAAGCCAGA TAAAACATAT CTACCTGTTA 1020 GAGTTTGAGA CGGTGCTGAC CTTGGAGGGG GGGCTAGGGC CTGAGAAAAG CACTAGGGAT 1080 GTCTGCGGGG ACACACTCTG CTCTGGCCTT CTCCTGAATC CACTGGCATT CATCACACGG 1140 TTCCCTAACC CGCAAATGTT TGTACTTTTA CACTTCAATG ACAAGTCATT AAAATCCACT 1200 AGCTCCATCA TTATTAAAAA GTCTTTATTT GTGCACAGTG CTGTACAAGG TTTTATCCAA 1260 GGAGAACTGA GCATGTCTCA AACTCTGTTT TAAAATAGCA ATTTCAGGGC TGATGTACAG 1320 CTGCTGTTGA CTCATCTTGC TTTCTGCATA GAACAGAAAT GAGGATAATC CATAATCATT 1380 TGTTTCTCCC CAAGGCCGTG GGCTAGAAGA GGATATTGAT TTGTAAGAAT TACTCATGCT 1440 GACCGAGGAC TGTTTGCCAG CCCCAGGTTA GCAAAGGAGG CCCAGCTGAC TCAGACAGCC 1500 TTGAGAACAT TGGGTTCTTC TGGAGTTTGA GGGAACAATA ACAGAATGCC TTCTCTTAGC 1560 CAAGTGTTCC TTGGGTCTTC AGTGTGGTCT CCAGTCCAGC AGCCTCAGTT TCACTTGGGA 1620 ACTTGTCTGA AATGCAAATT CTTGGGCCCC ACTGCTGACA TGCTGAATCA GAAACTCTGG 1680 TAGCGGAGCC CAGCATGTGT GTTTTCACAA CTCCTGCAGG CAGTTCTGCT GCACATTCGA 1740 GTGAGAACCA CGGGCTAAAT CCATTGAGAA ACAAAGCAAA AGAATAAGGC CGTGAAGCTG 1800 TCAGACCACC TTCATCCTTG ATAAAGCTAG CACTAGAGAA TGTGGGCTTA TGCCTGTGGC 1860 GACTGGGCTT TCTAATACTG AACCCCAGAC TTGCCCCTCC CAGGTGGGAG CCTGGCCTCT 1920 GTGAAACTAT GGCATGGAAG AGCATACTAT GGCGTGGAGG TGCTTATGCT TCCTGCAGAC 1980 AGCTCATTCC CCAAAGGAAA ATCCGGGAAC AGGACTGGGC TACAAACCTA CCAGTCAAGC 2040 AACTCATCCC ACCTGCCTGG AAGCAAATGA GTGGACCACC AGGGAAAGGG TATGGTGCTG 2100 ACTGATGACT GTTGCATCCA CGCTGGAGGA GGGAAGCCCC CCAAACCAAT GCATTTCCTA 2160 AGTATTAGTG ACTAGCTTCC CCGCTTTGTG TTGCTACACC CATCAGCTTT GGGCTTACAC 2220 AGTTGGGAAT AGAACTTGAC CAGGACTGAC ATCTGATAGT TACAGAAGCA CTCTTCATGG 2280 GTCACTGCCC AGCTTGACGG GTGTGGGCAA TTCACGCGTG AAGAAAAGTG GGTTCTTGTT 2340 CTGAGACTTC AGCTTCCCAT CAGAGCATCC CAATGATAAA CACACACTGC AGTCTTTCTG 2400
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