Tag | Content |
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EnhancerAtlas ID | HS179-03439 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:225878810-225880300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr1:225879781-225879792 | TGTGGATTGGG | - | 6.14 | MEF2A | MA0052.3 | chr1:225879217-225879229 | GCTAAAAATAAA | + | 6.04 | Mafb | MA0117.2 | chr1:225880032-225880044 | AAAATGCTGACT | + | 7.22 |
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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 |
GH01I225690 | chr1 | 225878701 | 225880319 |
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Enhancer Sequence | TTGAACCCGG GAAGCGGAGG TTTCAGTGAG CCAAGATGGC GCCACTGCAC TCTAACCTGG 60 GCTACAGAGA GAGATTTTAT CTCAAAAAAT AAATAAAATA AAAAAGAAGC CCAGGGACAA 120 ATGAGCCCAC CTCCACTGTA GACACTGGGA GCCACATTCT CAAAATGAGT AACTGCAGGG 180 AAGAGACAGA ATTCTCACAA GAGGGCATAT CCTCCGCCCT TCATACATTT CTCCTGTAAC 240 ACCCTTCTGG TTGAAAAGAA ATAAGAAAGC TGTGCTTGAC TTTTGCTCTA GTGCTTTTTA 300 AGATCAAGCA GGAATCTTAC ATTCTTTCAT TGCCTTTCAC ATTTCTTTTC CTTCTTCCGT 360 GTCCTCTTTC TTTTTAAATT CAGATCATTT AACAGACAAG GGTCATAGCT AAAAATAAAT 420 CTTCATTGAC CTGAGCTACC TATGATGTCA TTTACTGTAT TCATAGGTCT CCAGAGTCAA 480 CACTCCAGGC ATGTAGACAC ACACAGGAGA ATAAAACCTC AGTTCCCAGG CAGCTTCCAG 540 AAGCTGTGGC ATTGCTGTGG CCTGAGGCCT GGACTTTCCC AGGGGATAGG TATCCAGATC 600 GTTTGTGCCC TTCCATATCA CCTTTCATTC AGAGGCCTTA CCTGGATTGG TAGCCAAGCA 660 TTGATACTCA TGCCTCCCCA AAGAGGTAAG TTTTAGTAGG AAACTGAAAG AAACCAAGGC 720 CCAACAAAAT GAGGCAACTA GACGGAGTGA CTGGGGAAGT TTCCAGCCAA GTCAGATATA 780 AAATTTGTAC TGTGAAAAAC TGTTATCTGT ATTTTGGTAT TTACCAAAAA ACAGTGAGCC 840 ATGATCACTC CATGCAGTGG GTTAAACTTG TGGGAGAAGT AAATTCTGTG GTGTCAGCTC 900 AGAACAGAAC ATATTGGGAA TGCATAATAG AAAAGCAGTA CTCTCACTCA GCTTCATAAC 960 TCCAGCAAAT TTGTGGATTG GGGTTAACCA CGTCTGGAAT TCCAGAACTC AAGTTACCCA 1020 AGTGTGGCAG GCCAGGGGAA TTTCTGCGGG CTGGATGGGA AATCTTCAAA GTCAGCATTT 1080 ATTTTCATCT GCACTCAATA TTTTGGCCCA ATATGTAAGT AACTTGATGT CCATTCTTGT 1140 GTTGATAAGG AGCCTAAAAG CCTGGAACAG AGAAAGGAAA AGTTGGTCTC CACTTGGATC 1200 TCAATGTGGT CATCAGTCAT GGAAAATGCT GACTATGACC ATTCCCAATC AGCTCCTCAT 1260 GCCTGGCACT AAGAGACACT AGACACCTTG GGCTGCAATG ACTGCATTGT GCGTTTGTCA 1320 CTTTACCATA AGCTACATGA GTCCCCAGCT GGCTGTGTTA AAGTGCTCCA TCTTCCCAAT 1380 AGCCATGTGT CCCTTGACGG CAGGAACACT TTCATGTTTC TTCTGCAGCT CTCATGGTGC 1440 ACCATGTTGC TTATTCTTTT TTTTCCCTTT TTAAATTTAT TTATTTTTAG 1490
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