Tag | Content |
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EnhancerAtlas ID | HS113-18173 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr19:46255260-46256870 |
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) |
HES2 | MA0616.2 | chr19:46255452-46255462 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr19:46255452-46255462 | GGCACGTGCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26963 | chr19:46256071-46256654 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I045752 | chr19 | 46256021 | 46256150 |
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Enhancer Sequence | GATTACAGCT GTGAGCCCCT GCTCCTAGCC GTTTTTTTTT TTTTTTTTTT TTGAGACAAG 60 GTCTCACTCT GTCACCCAGG CTGGAATGCA GTGGCATGAT CATGGCTCAC TGTAACCTCA 120 AAATCCCAGG ACTCAAAACT CCAGGGGTCA AGCAATCCTC CTGCCGCAGA CTTCTAAGCA 180 GCTTGTACTA CAGGCACGTG CCACCAATAT CCAGATAATT TTCTTTTTTT TGAGATGGAG 240 TTTCTCTCTG TCGCCCAGAC TAGAGTGCAG TGGCGTGATC TCAGCTCACT GCAAGCTCTG 300 CCTCCCAGGT TCAAGCCATT CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA CTACAGGCGC 360 CCGCCACCAC ACCCAGCTAA TTTTTATATT TTTAGTAGAG ACAGGATTTT GCCGTGGTCG 420 CCAAGCTGGT ATCACCTCAA GTGATCCACC CATCTCAGCC TCCTAAAGTG CTGGGATGAC 480 AGATGTGAGC CATCGTGCCT GGCTCTGGCT AATATTTTTG TTTGTTTTTT TGTAGAGACA 540 GAGTCTCACT GTGTTGCCCA AGCTGGTCTT AAACCCCTGG GCTTAAGCAA TTCTCCCGCC 600 TTGGCCTCCC AAAGTGCTGG GATTATAGGA GTGGGCCACC AAGCCTGACT TGTTTCTATG 660 TATTAACTCA CATTTAATCG TCAGGACAAA TACCGAAGGG AAAAGCTAAT GTGGTCCTGT 720 TTTGCAGGTG ATGGAACTGA AGCCCAGAGA GGTTAAGGTC ACAGAGATGA GCCTGAGTCA 780 GGGCCTGGCT CAGAGCCCAC ACACATCATC TCCATGCCAC GCAGACCTCC AATCACACCC 840 AATGACTTGC CTGTCCCCAG ACACCCCGCG CGTGTCTTCT CATGCCTGCA AGCTCTTACT 900 CAGATAGTTT CTTCTTCTTT TTTTTTTTTT TTTTTTCTGA GGCGGAGTCT CGCTCTTTTC 960 GCCCAGGCTG GAGTGAAGTG GCGAAATTTC GGATCACTGC AAGCTCCACC CCCTGGGTTC 1020 AAGCGATTCT CCTGCCTCAG CCTCCCAAGT AACTGGGATT ACAGGCACCC GCCACCACAC 1080 CCAGCTAATT TTTGTCCCTG ACATGTAGTG TTGAGGACTG GTCATGAAGT GAGAGACTGG 1140 AGTCAGGGAG ATGAGGAAAG ACACTGTTCG GAGTGATCTA GACGGGACAA TTAGGCCCAA 1200 GCTAGCGCTG TAGATGAGAA TGTGGATAGA AGTGAGTAAA CCTAGAAGAT GTTAATGAGG 1260 AAGAATCGAG AGGCCAGAGG GAAAGGCCCC AGTGACCTTG AGGGGGTCGG CTAGGAGACC 1320 CTCACTGTGT TGAGGAAGGC GGGAGGAGGT ACTGGTGTGG GCGGGGAGAG GGTGAAGCAT 1380 CCTCAAGGTG CCCAGTCTGG GGAAGTGTTG ATTCCATTCT CCCACTGAGC CAAGGCCCAA 1440 AACAGCCCTG AAGAAACCTG AGTTCTTGCC CTCTACTTTC ACAGTCCTGA CTGAGCGGCC 1500 TTGGATAAGC CCTCAGTTTC CACACTGTAA AGTCAGCCTG GGGGCCCACC CTGACCCGGG 1560 ACTGAGGAGC ATTGTCTGGA AGGCAGGAAC TGCAGTTGGA TGCAGATGGG 1610
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