Tag | Content |
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EnhancerAtlas ID | HS052-21077 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr2:109587870-109589320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox6 | MA0515.1 | chr2:109589188-109589198 | AAAACAATGG | - | 6.02 | Stat6 | MA0520.1 | chr2:109588727-109588742 | CTGTTCCACAGAACT | + | 6.08 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26844 | chr2:109586492-109590435 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I108971 | chr2 | 109587479 | 109589380 |
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Enhancer Sequence | AAATCACATT TTCAGATTAT GACTCCAGAA GGAGGACTCT CAACCCTGCC CGCACAGTAG 60 CATCACTAGG GGAGACTTAA AACCAGGCAT CAGTCTTTTT GAAACTCCCC AGGCATTCTA 120 GCAGAGAGCT GAGTAAATGT TTAGTAAATA AATACCCAGA ATGAATGAAG GTGTGAGGGT 180 GTGAGGGCTG AGAGGAAGGG TATTAGAGAT AGGATCAGCT CTCTCATTTT ATGGAAGAAG 240 AAACTGAGGC TGAGAGATTT AGAGCAATTT GCCCAAGGTT ACACAGAAGT TAAAGAGGAG 300 TTGGCATTAG AAGTCAGGTG TTGTGGTTTA TAACACATAC ACAAACTCTT TGATACCACC 360 TTCAAAAGGT GGAGCCTAAT TCCTCTCCCT GTGTGAACGG GCTGGATTTT AGTGACTCGT 420 TTCTAGCCAA CAGAAAAAAG GGCAGAAGAG ACGGTGCAAT TACAGAGACC AGGTCACCAA 480 AGGCACTGAG CTTCCTGCTG TGCCGTGGCT GCTGCTCAGT CACATAGGGG CAACAGAGGA 540 GCAGCCGTGG GGAGCTCCCG TGGCCCGGAG CTGAGGCCTC CTGCCGCAGC CACTTGCGAG 600 GCCTCTGGAT GTGGGTCCTC CAGCCTGGCC TGGCCCGCAG ATGTTGCAGC CCAGCCGACT 660 GCAGCCTCAG GAAGGACACT GAGCCAGAAC CACCCAGCGG AGCCGCTCCC TGATTCCTGA 720 CCCTCAAAAT CTGTGGGATG GTCACATTTG TTGTTTTAAG CAGTTACATT TGGGAGTCAT 780 TTATTACACA GCACAGATGA CTAATACGCC TTCCAGTCCT TTGCTGTTTC AGCCACACCC 840 CTGTAAGAGA CCAACTTCTG TTCCACAGAA CTTCAATAGC CATGCCGGCC CAGTTCTCGA 900 CAAGCTTAGG ATTGAACACA GACAATGATG ACCAAATCAA AACAGGGGCA GGGCACTGCA 960 TGGTGTGGTC TCCACTCCTT CCTCACGGGC CCTGGAGCCC TTGCCCAACC CTCCTGGCTG 1020 GCTTTCATGC CAACGTGCCA GACACTGCCC TTTCCAATCC TGCCCGCTGT GGGAGTGCCG 1080 GGGCAGGGCA AGGTCAGGCT GCAACGGGCC GAGGCAGCCT AGGAAAAAAG AGATTGTAGG 1140 TGACCTGGGT TCAGAAGCTG GTGCCTTGCC CTGCACGCCA AGTGTTGGTA AAACAAGTGT 1200 CTGCACAAGG GTGACGGGTG TCTTCCCCAC TCTGCTTGCC TTGTAGCTAT GGCTGTGATC 1260 AGAGAACTTG ACGTGATCAT TTGAAAAATA AGCAGCCCTC ATCTGATTTG TCAGTCACAA 1320 AACAATGGCT CACAGCCCAT GCAGATGCTG AGACTCAGAA GGGGGTGAGG ACCGGGGGGC 1380 CTCCGGCAGG GGCGTTCACT CTTCCTCCAA CCTCCCCAAC CTTGGCTAGC TGGATTCTCC 1440 TCTTTGCCTT 1450
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