Tag | Content |
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EnhancerAtlas ID | HS053-02644 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:155515710-155517170 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:155517115-155517127 | TTCTGTTTACTG | - | 6.02 | STAT1 | MA0137.3 | chr1:155516701-155516712 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr1:155516701-155516712 | TTTCTGGGAAA | + | 6.32 | Zfx | MA0146.2 | chr1:155516311-155516325 | GAGGCCGAGGCGGG | - | 6.01 |
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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 |
GH01I155546 | chr1 | 155516481 | 155516776 |
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Enhancer Sequence | GCCAAGGCAG GCAGATCACT AGATGTCAGG AGTTCGAGAC CAGCCTGGCC AATGTGGTGA 60 AACCCCATCT CTACTTAAAA TACAAAAAAA CTAGCCAGGC GTGGTGGCGT GTGCCTGTAA 120 TCCCAACTAC ACAGGAGCTG AGGCAGGAGA ATCGCTTGAG CCTGGGAGAT GGAGGCTGCA 180 GTGAGCTGAG ATGGTGCCAC TGCACGCCAG CTTGGGCAAT AACACGAGAT TCCATCACCA 240 AAAAAAAAAA AAAAAACAAA AATTAGCCAG GTGTGGTGGC ATGCACCTGT GGTCCCAGCT 300 ACGTGGTAGG CTGAGGCAGG AGAATCGCTT GAACTCAGGA GGCGGAGCTT GCAATGAGCC 360 GATATCGTGC CACTGCACTC TAGCCTGGGC AACAAAGCGA GACTCTGACT CAAAAAAAAA 420 AAAAGAAATT ATTGCATTAC CATAATGGTA AAGGGGAAAG GGAGGTGAAC AGGTGACAGT 480 GAGTAAAGAT TTGCTTATAT CGTCATCTAA CCACTAGCAT TCCTTACATG AGTTTATTTC 540 CACTTTTAAG AGCACTCTGG GTTGGGCGCG GTGGCTCATG CCTATAATCC CAGCACTTTG 600 GGAGGCCGAG GCGGGCAGAT CACGAGGTCA GGAGATCTAA ACCATCCTGG CCAACACGGT 660 GAAACCAGTC TCTACTGAAA ATACAAAAAT TAGCTGGGCA TGCTGGCACA TGCCTGTAGT 720 CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATCACTTGAA CTCGGGGGGC AGAGGTTGCA 780 GTGAGCTGAG ATCACGCCAC TACACTCCAC CCTGGTGACA GAGCAAGACT CCGTCTCAAA 840 AAAAAAAGCA CTCTGGTAAA GAACAGGTAA ACAACGCAAC TGTCATTCCA TGATTTTCAT 900 AATTAAGACA CTTATATAAC AAAGAATATT GGCCTACAAT CCAAAGTGCC AGTGAACCCC 960 TTACATTCAC ATTTTATGTG CATATATACA CTTTCTGGGA AAGACTACAA AGGTTTCATC 1020 ACATTCTTTT TTTTTTTTTT TTTTTTTTTT TTGAGATGGA GACTCGCTCT GTCACCAGGG 1080 TGGAGTGTAG TGACGTGATC TTGGCTCACT GCAACCTCTG CCTCCCAAGT TCAAGCAATT 1140 CTCCTGCCTC AGCCTCCCGA GTAACTGGGA CTACAGGCAT GTGCTACCAT GCCCAGCTAA 1200 TTTTTGTATT TTTAGTAGAG ACAGGGTTTT ACCATGTTGG CCAGGATGGT TTAGATCTCT 1260 TGACCTCGTG ATCTGCCCGC CTTGGCCTCC CAAAGTGCTG GGATTATGTT TCATCATATT 1320 CTTAATGAGG GCCATGACTA CTCACCACAA CTACCATTTA AAAAAAAAAA AAGTTAAAAT 1380 CCTCTGAAGA CACATGCACA TGTGTTTCTG TTTACTGCAG CACTATTTAC AATAGCGAAG 1440 ACATGGAACC AACCCACATA 1460
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