Tag | Content |
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EnhancerAtlas ID | HS053-28984 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr4:1581170-1582590 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr4:1581712-1581723 | AATTTAATTAA | + | 6.32 | PHOX2A | MA0713.1 | chr4:1581711-1581722 | TAATTTAATTA | + | 6.62 | PROP1 | MA0715.1 | chr4:1581711-1581722 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr4:1581711-1581722 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr4:1581711-1581722 | TAATTTAATTA | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACTCGCCCCC TTGTCCCAGC CCCGCGTCCT GGGGAGGAGG CTTGGGCCGC AGCCCAGCAC 60 CCAGAAGTGC AACGCGCACG GGTGGGGCCA GGCTCGAGTC AGCCGGTGAC GCAGCCTCTG 120 TGTGACCAGG GCGGATGGCC CGACCTCTCT GAGCCCCCGT TTCCCCGCCT GTAAAAGGGG 180 GTGGGGCTGC CTCCCAGCGC CGCTGCGAGG CGTGAGTGAG TTACGACTCA GAACGCCCAG 240 GTCCGAGGTG AGCACACGCG ACACCCGCGA GCCACGGCCA CGCGTGTCCC CAGGGCGCCT 300 CCCGCCACGG GCTGGCCAGG AGTGTCCGCG CTGTGGGGAT ACGAAGGGGC GCGGCCCCAG 360 CGCTGCGGGG CCCGCAGGGA GGGCGCAGGG GCCGAGCATC CGCCCCGGGG CATCCACCCA 420 TCAGGCCTCG CCGTAAACTT CCTCCTAACA GCCGCTCCTG CAGCCGGAAG ATATTGACTC 480 GAAGGAGAAA CAATGGCAGG AATAAAATAA AAATAAAAAA GTTAATTATC CTTTGTGTTT 540 GTAATTTAAT TAAAGATGCA GTAAAGTTTT ACTGTTTTTC CAGGTGATGA TGTTTAGAGC 600 CCCGAGAAGC TATTTGTGCT GGTGAGATTA AAGTGCATTT TAAAATGTTC CTCCAGTACT 660 TTCACATTTG TTGATAGATT TTTAAATTAA ACTTTAAATT GTAATCTAAA TTACCTCCAA 720 CAATTCATGG TCCCTGTAAT GAACTCCCAC CGTTCCCGCT GTCATCCGTC GATGATGGAG 780 TGCGAGCCGG GAGCTGCAGC CCCGCGGCCG CCGAACCAAC CGCGGAGGCC AGGCAGCCTC 840 GCCCCAGGGA CCCCGCCCAC GGCGCCCTAC ACCGGCGGCC AGTCAGGGAG GCCAACGCCG 900 CGAGACGGAA GCAGCCATAC CCCGCGGGCC ACCAGTGTGG CCAGAAAAGA TCTGCAGGGA 960 TGTGAGGGCA GCTCAGAGCT GAGATCTAAG GCTGGGGCAG AACCGGACGG CGCAACAAGC 1020 TAGGGAGAAA GCATCCCCGG CGCGGGGTGC ACGGAGCCCC AGACCCCACC CGCCTCCCGC 1080 CCGGACCCCG CCTCCACTCA GGGAGCCGGG CCCCACCTCC CGCCCTAGGC CCCGCCTCCT 1140 ACCTCGGGCC CCACCTCCCG CCTAGGCCCT GCCTCCTGCC CAGGCCCTGC CCCCAACTCA 1200 GGGCCCCGCC TCCCGCCCAG GCCACGCCTC CCACTGAGGA CCCTGCCTCC CGCTCAGGGA 1260 CCCGCCTCCT GCCCGAGCCC TCCCTCCCTC CCAGGTCCTG CCTCCCGTCC AGGTCCCCGC 1320 CTCCCACTCA AGGCCCCGCC TCCCACCCAG GCCCCGCCTC CCACTCAAGG CCCCGCCTCC 1380 CACCCAGGTC CCCCCCTCTA ACCTGGGCCA CGGCTCCCAC 1420
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