Tag | Content |
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EnhancerAtlas ID | HS179-24448 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr8:38507760-38509100 |
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) |
Klf1 | MA0493.1 | chr8:38508936-38508947 | GGCCACACCCA | + | 6.62 | PLAG1 | MA0163.1 | chr8:38508421-38508435 | GGGGCCTTCGGGGG | + | 6.82 |
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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 |
GH08I038650 | chr8 | 38507537 | 38509759 |
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Enhancer Sequence | CAGAATAAGC CTGACTTCTG TTAGTTAGCC TTGCTGAGCA GTCGTATTTG CTTTGGGAAA 60 GGAACAGGAG ATAAGTTGAG TAGGTAGGGT AGGGCTAGAG CATTGAATGC CAGGAGAAGG 120 TAGAGGGTAT GAATGGAAAT GGGATGAGAG CCTAAGCAAG GTTTAATTTA AAACTTCCAG 180 CAAACTGAGA TCAAAAGAAC GTGGCCTTCT AGCCAGTCTT TCCATGGAGA CAACTGAGGA 240 GCCTGGAGTG GGCAAAGGAC CCTCGGGCTT GCGGTGGCCA CGGGCACCCC AGAGGGACGG 300 AGGGCGCCAT ACCGCGGTTG CCATGTTCCT GCATGTGTTT GAAATCTGGG CTGACAAGAA 360 GAGCTGGACA ATTTTGCTCC GTTACGTATT GAATTCTCTT CTCTGTGGTA CAGGATCCCC 420 TTGAAGCGTG ACAGCTGCAA TGACTTCCAG ATGTCCGCCT CCTGTCTCCT AGCCGACTGG 480 GGTGGATGTG GTAAACTCCG CGATGGAAAC CAAAACCCCC ACCAGATGTG CCATGTCAAC 540 GTCAGCCTCG CGCACATCTG GCTTCAATGC CGGCCGCCAG CCCCAGAACA AATGGCGGCT 600 TTCCCGCTGT ATTCAGCTAG TCAGCGTTCC CCGGTTAAAA GGCGCTGGGG CAGGAACGGC 660 CGGGGCCTTC GGGGGCGCGA CGCGGCGACG CCCAGCCTGG GAAGGGGCGC GGGGCCCGTG 720 TTGGCCGCGG TGGGTCCCGG CTCCCTGGAG GCTGAGCCCC GGGCGCTCTT TCCTCGCGGC 780 GCTGCCGTGG GGTGGCCGGG AGGGCAGAAC GAGGGGCTGC GGGACGGTGT TCGGAAGAAA 840 ATCGTGCGAG TTTAAAAACA TCCAAAGTGA GCCGAGCTGG GCCCCAAGCC TCGGCCTCGC 900 GCACTCGCCA GGCCCAGGAG GCGGAGCAGG CGTCGGGACG GCGGCGACCA GAGCCTGCTG 960 GACAAGCGGG GCCGGGTGCC TCAGCCCGGC CTCCTCCTGG CCTCCCTCTC CCCAACTCAC 1020 GCATCCACCA GCAGGACCCC CTACAGGGCA GGCGCAGGAG TGAATCTTAG CTGTCATTAC 1080 TACTGAGGTG GTATTTTTCT AAATAAAAAA ATCAGACAAA TGGATATCCT GAAAACAGGA 1140 CAGAGCGTGT GAAACCTGGA CTCAGGGAAG GATGGTGGCC ACACCCAGGC CCGCTTGTCC 1200 ACGGCAGCCG GCAGGAGCGG GCACTATCAT GTTTACGAGC TGCCCTTCTA CCTACCCACG 1260 AAGTCTCATT TAGTCACAAC AGATGCTGTA TATTGGAAAA GGCCCCCAAC TGAGCACCAA 1320 AAGACTTAGG TGTGGGTCCT 1340
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