Tag | Content |
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EnhancerAtlas ID | HS053-01869 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:85068860-85070500 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr1:85069681-85069692 | AATGAGTCACA | - | 6.62 | SOX10 | MA0442.2 | chr1:85069173-85069184 | AAAACAAAGCA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I084601 | chr1 | 85067578 | 85071085 |
| Enhancer Sequence | AGCTCAGAAA TAGCTCCCTT TCTAACCTCA TGCAGTTCAA AGAAATCACT TCTAACAAAG 60 AACAGCCCGA AAGATCAGGC TGTAAAAACA CAGATAAACA ACTCAGGCTC AGGAGATGGG 120 GAGTCTCCTA GGTAATCACC AAACTTCACA CTTATACAAT GGACCCCAGT AAAAACAGTG 180 GGCCTTAATA AGCACATTCC TTTCCTTTTA GGCACACTAA GATAGGGAAG CTAAAAGTGG 240 ACTGGGGGGA GATGCCAGCA GCTGCAGGAA GATGTCTGGG AACAGACACA GAAATTCTCC 300 CTCCCAGATA AGCAAAACAA AGCAGCACAA AGCAGCGCAG ACTAAGAGTC TGTCTACATG 360 ATCAAGGAGT GAGGTGAGAG CTGATAGAAA ACTCTACTCT ATGCACATAG CACACCTGGT 420 TCCAACTAAA TCTTTGGGCC TCAGTAAGAT AAGACACCCC CTCCTCACTA GCCCATTTAT 480 AAAAACCCTG ACATTTTTAC TACAACTTGG CAACCCACTC AGGATCCCTC TCTGTGACAG 540 AGAGCTGTTC TTTCCTTTTG CCTATTAAAC TCCTGCTCCA GTCTCACTCT GTGTATGTGT 600 GTCTGCGACT TCAATTTCCT TGGCCATGAG ACCAACAACC TTGGTATTTA CCCCAGACAA 660 TGAGGCTACT TCATTTGGGG GGCCCGTCCA GGATTTGAAG GTGAAATCAT TGGAAGAGTG 720 AGTAAAGGAG TGGACTCTCT ACTTTCATTT CCGAGGCTTC TCGTCCCCAG TTTTTATTCT 780 CTCAAAGAAC TATAAAAAAA TCGGGCATCT GTCAGCTAAT TAATGAGTCA CAAGGGCTAG 840 CCGCTAATCT TAAAGACTCA GATGTGAAGC TTGCTGGGGA GGACTTAGTC AATCCTCCAG 900 TGCCCTCAGG GTGCTGGGAA CGTTGGCTCT GTCCAAACCA GTTTCCTTTC ACTTTGCCAT 960 CACATGGGGC TGGAATAGGT CCTGGGGCAA CTGAGGATTT CTGGCCAGGG CTACACCCTG 1020 GTGTTGTCCA AAGGCTCCTG GACTGACACC AGCCTCCGAC TGCCTGACTG GGTGTCGGCC 1080 ACAAGATTGC CAAGCTTTCC TATTGCAAAT CTTATTTTCC TCCTTTCCTT TCCGAGGTCA 1140 CCATGTCTCC CATCCCCTCT CTGTACACAA TGCTGCGGGA ATTTTTATAG CCCAGAGAAA 1200 TAATTCAGTT AGGCAGGCTT AGCAACCACC TTGGCAACCA GAAATGCAGG TCAAGGGGAT 1260 TGCTGTTTTT GTGACTTTCT ACCGACAGGG GGATTTCGTG ATCCAGATCT GAAAGACTAT 1320 TTAACTCCTA ATGATAGCAC TTCCTGGGGT TGGGTAGAAG GTTATCTCCC CACCAATGAA 1380 CATCCCTCTC TCCACCTAGG CTGTTTCTTT TCCCATGTGA AGAACCAGCA CTACCCAGCC 1440 GGACTGCATA GTCCCTCTAT GAGGCGAATT AACTTTCTCC TGCTAGGAGG CATGCTGTAG 1500 GAATGGCCTG CCACATGTCA GACTTCCCTC TCTGTCCATA CGGAGGCCAA GTTACTGCCT 1560 GGTATTTCAA AGCTTGCAGC GTCACCTAGT GGAATAGGAA TCCTTTCCAT CGGCAACCTC 1620 GTCTGCCCTT TGCCAAAAGC 1640
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