Tag | Content |
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EnhancerAtlas ID | HS113-17823 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr19:30321360-30323120 |
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) |
Foxd3 | MA0041.1 | chr19:30322524-30322536 | AAACAAACAAAC | - | 6.32 | IRF1 | MA0050.2 | chr19:30323078-30323099 | CTTTTCTTTTTCTTTTTCTTT | + | 6.02 | IRF1 | MA0050.2 | chr19:30322545-30322566 | AAAAAGAAAATGAAAATGAGT | - | 6.61 | Klf12 | MA0742.1 | chr19:30322236-30322251 | AAGATGGGTGTGGTC | - | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 30322926 | 30323060 | chr19 | 30322162 | 30322300 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I029830 | chr19 | 30321661 | 30323070 |
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Enhancer Sequence | TCCTACCACA TGTTCCACAT TTTGAAATTC AAATCACATT TATACCTTGG ACATTGTTAG 60 AAGACTATTT TTATCCCTGC TGTAATCATC TAATTTGCTG ATTACAGGTC TCAAATTGCC 120 ACAGAGAACT CAATTTTTGA AAGAATTGTC CTGTTTGATC AAATATGTTA TTCAAGCAAT 180 GCAGTCATTT GTTCCACAAG TTTACCTGCC AGGTAGAGTT AACCAGGAGT AATAGCATTA 240 GAAGCCTATA CTTAAAATCA AGCATTAGCT AATCCGCCTG CGACAATAGA GTCTTAAATA 300 TAATTTGCTG CAGATACTTC AGTTCCTGCA CCGACAGACA ATTGCAGTCT GTATCCAATG 360 AGCACAGATT TTTTCCTACC TCGTCCCAAT TCCAAATTTA ACTTCAGAAG ACTCTAATGT 420 ACTCAGTTGC ATAGGCTTAC CAGGTACTCT TTCCTGGGAG CCTCACATGG GAGGGCAACA 480 CTATCCTTTA TTCAATAAAC AGCATCCCCC ACCTTTTAAA TCATTTTCCT GATCAATGCC 540 AATTCCAAAA GTTGTGTGGT ATCTGATTAT GCAGTGCGGT TCAAGTCAAA TGCTGGCTTC 600 CTTGGGGTTG GTGAGTGAGG TGCCCTCGAT GGAGTCCCTG CTAAGTGTAC ACTGCCAGTC 660 CTGGAGACAT GAACTCAAGG GAGCCTGGGA GACCGGGGAA GCCCTGGAGT CCCCGGAGGG 720 CACTGGTATG AAATGAAAAG GTGGCACTCT AGGAGCAGAG CAGCAGCAGG ACTCAAGCTC 780 GGGAGGTGGG GCTGTGGAAT GCTCTCCAGC AGTCACAAAA GCCCTCACAA ATAGGGTAGA 840 GGAAGGCCAC ATCACAAGGG GCTTTTGCCG TCAACTAAGA TGGGTGTGGT CTCCCCCGCA 900 GCAGGAAGCC GGTGTTTGTA AGACAGGAGT GACTTGCTCA GAGCCGGTTT GGAGGAAGAG 960 GTTGATGAAC AAGTACAGAG TTATGTGTCT TTGTGCCGTA AGAAAATGAC TGTGCAAGTC 1020 GGGCGTGGTG GTGTGCACCT GTAATCCCAG CTATTGGGAG GCTGAGATGG GAAGTATCGC 1080 TTGAGCCCAG GGGTTTGAGG CTGCAGTGAG GCATGATCAC ACCACTGTAC TCCAGCCTGT 1140 GCAACAGAAC GAGACCCTAT CTCAAAACAA ACAAACAAAA AATCAAAAAA GAAAATGAAA 1200 ATGAGTGTGT AGTGTGTGGA GGACAAGCAG GCAGGCAATG AGGACATTCG TAAAATCAGC 1260 TGCATCACCA TCATTTCTAA ATGGCGCTGC CTGCATATCT CCCCAGGCCC CCGTGATTCT 1320 GCTCCTGTGC CCCTGCCCAG GCCTCTGCCT ACAGTGGCTG GACCCCACCT CCTGCAGGAG 1380 TGCACCCCTG ACGTTGGCCC ACACTGATGT CATTTCTTCA CTGGGTTCTG GAGGCAGTTG 1440 ACTCATGTGG GAAGCCGGCT CTGCCACTTC CCAGAGTGGT CTTGGGCTCT GTGCTTCATT 1500 TCTCCAAGCT TCGTGTTTCC CAGCTGTGAC CTGAGGATGA CAACATAGTG CTTCCCCCAT 1560 GGAACCGAGG GGAGATGAAA TGAGGTCACG CATAGATATG TTGAGCACAG CGCTTGGCAC 1620 ATTAAAGAGA AACAGCAAAT GACAGCTGAT CCCTCTTATT GCCACCACTG GGTTCACTGT 1680 CACTGAGCTA GGCTGTTCTG TGAAGGATTG AGCATTCTCT TTTCTTTTTC TTTTTCTTTT 1740 TTTGGGACGG AGTCTCGCTC 1760
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