Tag | Content |
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EnhancerAtlas ID | HS113-21413 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr2:217427010-217428720 |
Target genes | Number: 11 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr2:217427382-217427394 | TTCTGTTTACAC | - | 6.22 | FOXP2 | MA0593.1 | chr2:217427431-217427442 | ATGTAAACAAA | + | 6.14 | RREB1 | MA0073.1 | chr2:217428551-217428571 | CGCCTACCCACCCCCCACCC | + | 6.01 | TCF7L2 | MA0523.1 | chr2:217427926-217427940 | AAACATCAAAGGGG | + | 6.54 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01759 | chr2:217427070-217428375 | Aorta |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr2 | 217427253 | 217427397 | chr2 | 217427482 | 217428452 | chr2 | 217427760 | 217428080 | chr2 | 217427495 | 217427642 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I216562 | chr2 | 217427071 | 217428375 |
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Enhancer Sequence | AATTAGCCAG GCATGGTGGC ACATGCCTGT AATCCCACCT ACTTGGGAGG CTGAGGCAGG 60 AGACTCCCTT GAACCCTGGA GGTGGAGGTT GCAGTGAGCC GAGATGGTGC CATTGCACTC 120 CAGCCTGGGC AACAATAGTG AAACTCTGTC TCAAAAGAAA AAGAAGAAGA AGAAAAAAAA 180 GACTTCAATT CTGACACTTT CATTGGAATT GGAATGGGGC TGGGAGTGGG AACCGGGGCC 240 ATCTTGCTGC CCCCAGGGAG AACAGGTCTG AGGTGGAGCC AAGCAGAGTG AGCAGAACTG 300 AGATGAGCAG AGAAAAGCAG GGCCTGGTGA AAGAATGTCG CCGCATCATG CCTCCACTCC 360 ATTCCTAAAG TTTTCTGTTT ACACGCAAGC CAGTATGTTC CCTCTTGTCT TGGATAAATG 420 CATGTAAACA AACAAATGGG TGAACACAAG TATTCATGGA CACAACCCAG GCACCTGCTA 480 AGCAGGCCAC CTCGTGTCTG GTGTCCTGGT GTCCTAAGAA GCACCAGCTT CCTTAATCCC 540 CTTGGAGACC CTGTGAGGGC GGGAGGTAAC GTGATGGTTA ACTGCTGAGA ATTCTTAGCC 600 TGCCTACAAC GGCCCTGAAT CAACAACACA AGAGGCTTCC AGACTAGTGA AAACTTAGAC 660 ATATAGTGGA GTGTGAGCCA AAGGTAAAAG AAAAGGAGAC AAAGAGGCTG CAGAGAGAGA 720 CAGGCAGGAA TGAGACGGTG TGAGGGAGGT GGGAGGTGGG TGCTGTTTCT AGATTCCTGT 780 GCAGGAAAAC TCTGCTGGAA GGCCTGCGAT TACATGGCAC TCAAGCATGT GGGTTGCTGC 840 TGGAACTGGG TGCCCCACAT CACGTAGGCC CTGTGAGCAT TAAAATAACA ATCTCCATCG 900 TGTGGCACCT GCAGAGAAAC ATCAAAGGGG TTGAAGCTGT TCAGGCACGA GAAGGTGAGG 960 CCTCACTGCG AGCCTGAAGC TGTTCCCTGA ATGATGACCT GGCAAGTGAG TGTGAATGCC 1020 TGTCTTCCAG CCTAAACCGT CAGGACGGGG CCCAAGTCCT ACTCATCTCA GTAACCTTCA 1080 GAGGATCTGG CACATAGAAA GAGCTGGAAT CAAACGTGTT TCATAAATAA CAAACTGGAA 1140 GAGTGGGTAA ACTTGGGACC CAGGAGCTGG TTCAAACCCT GGTTTGAAGA AGCGAGGTGG 1200 ATCCTTGGAG AGATATCGGC CTGCTGGACT GTCCCTTCCA CTGAGTAGTG TTGGCAGGGA 1260 ATAGGGGTTG GCTTCCCTGT CATAGGGTCC TCTTGCCATG CTTCACTGTG CTGCAGGGAT 1320 GGAGACACAC CTGCAAGTTA AAGGGCCATG TTTGGAAAGG AAAGATTGTT AGGAGCCTAG 1380 TAGCATCAGA GGCCCAGCTT CCCTGACTTC AAGGACCAAC AACGATGAAC TCTGTCTTGG 1440 AGCTGCTGGG CCCTTTTCAT CGCTGTCCAG ACTACAACAC TTCCAGATGA TTCTCACATT 1500 ACAGCTTCTC AATGTCTGCC CTCGCCCTAA CCTCGCTCCC CCGCCTACCC ACCCCCCACC 1560 CAGTTAGCTA CTGGATAGCA ATTCCAGTGT CTCAGTGGGA TTCAGCGGGG TAAGAAGGAA 1620 TGCATTGCTA TCCCATAACT CGAACCTTCT CTTGGCAAAA AGGAAATTCC ATCTGCTCCC 1680 AAAAGAGTGG GAGAAAAATG ACTGCTGGAA 1710
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