Tag | Content |
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EnhancerAtlas ID | HS113-35251 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr7:148771630-148773030 |
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) |
Lhx3 | MA0135.1 | chr7:148771929-148771942 | AAATTAATTATTT | + | 6.78 |
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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 |
GH07I149074 | chr7 | 148771210 | 148772523 |
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Enhancer Sequence | CTGCACAGAG AAGTCAGACA GGGTAGTTTG GCTTCCTGAA TTTAAAGCAC ACTAAGTTTC 60 TAAATTTCTC AACATTCACT CCTGGGACAA AGTATGAGAA CAACATGTCA AAAAAAAAAA 120 AACAGGTTTA CACAAAGATG AAAAAACCGC CTACACATCC TAACAATGCC TCCTAGTCTG 180 TCTGGGCATG TTAGATCAGG TATGTTGTTT TAATTTTGTC ATGTTCCCCA CACATTTAGC 240 AATGCTGTAT TTTGTCCAAA AACAAAATGG CTAATGCTAT ATATATATAT ATATTTTTAA 300 AATTAATTAT TTATTTTTTG AGATGGGTTC TCACTCCAGT TGCCAAGGCT GGAGTGCAGT 360 GGTGCAATCA TGGCTCACTG TAGCCTCGGC TTCCTGGGCT CAGGTAATTC TTCAACCTCA 420 GCCTGGGACT ACAGGCACGC ACCACCAGGC CAAGCTAATT TTCGCATTTT TAGTGGAGAC 480 GGGTTTCACC GTGTTGCCCA GGCTGGTTTC AAATTCCTGT GCTCAAGCAG TCTGCCTGCC 540 TTGGCCTCCC AAAGTGCTGG GATTACAGGC ATAAACCACT GCGCCCAGCC TTCAATATTC 600 TTAATAGTGA TTTATTAACA GCCAGATCAT AGGGTCCAAT TTTAAAGCAA GTTGGTTATG 660 GCAAAAATGC GGTCAAAAAG GAGTTTTTAA AATAATGCTT TAAGTTATTA TTACTATTGT 720 TTTAGATAGG GTCTCACTCT GTCTCTCAGG CTGGAATGCA GTGGCATGAT CACAGCTTAC 780 TGCAGCCTCA ACCTCCTGGG CTCCAGTGAT CTGCCCACCT CAGCCTCCTG AGTAGCTGGG 840 ACTACAGGCA AGAGCTACCA CACTGGCTAA TTTTTTTTAT TAGTTTCTGA AATGGGGTCT 900 CACTATGTTG CCCAGGCTAA CCTCAAACTC CTGGACTCAA GTAGTCTTAC CCCACCCTGG 960 AGTCTCAAAG TGCTGCGATT ACAGGCATGA GCCACCGCAC CTGGCCAGTG GTTTAACTTA 1020 TTAGAAATAT TTCTGGCACA TGGAGAAGGA GAAAAATATA CAAAAACCTG GATGCCATCT 1080 AACTTTGTCA AATCCTACTG TGCTGACACA CTTCAGGTTT TTTTTTTTTT TTTTTTTTTT 1140 TTTTTGATAG AGTCTCACTG TGTCTCCCAG GCTGAAGTGC AGTGGTGCAA TCATAGCTCA 1200 TTGCAGCCTC AACCTCCTGG GCTCAAGTAA TCCTCCCACC TCAGCCTCCT GACAGCTGGG 1260 ACTACAGGCG GGAGCCACCA TGCTCAGCTA ATTTTTAAAT TTTTTGTAGA GAGAGGGTCT 1320 CCCTAGTTTG TCCAGGCTGG TCTCAAACTT CTCAGCCCAA GATATCCTCC TACCTCAGCC 1380 TCCGAAAGTG CTGGGATTAT 1400
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