Tag | Content |
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EnhancerAtlas ID | HS052-18504 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr19:13891410-13892760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:13892517-13892538 | GGGGGAGGGAGGGGCTGGAGG | + | 6.52 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 13891595 | 13891902 | chr19 | 13892025 | 13892075 | chr19 | 13892272 | 13892747 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I013780 | chr19 | 13891506 | 13893414 |
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Enhancer Sequence | TTGAACCCGG GAGACCGAGG TTGCAGTGAG CGGAAATCGT GCCATTGCAC TCGAGCCTGG 60 GCGACAGAGT GAGACTCCGT CTCAAAAAAA AAAAGAAAAA ATGGACACAG CCCACACATC 120 CATCTACGGA TGAAGGGATA AACTGAGGTC TATCCTTCAA TAGAATATTC ACCCTTGGGG 180 AGGAAGGCCA AGTGCAGTGG CTCATGCCTG TCATCCCAAC TACTTAGGAG GCTGAGGCAG 240 GAGGATCACT TGAGCCTGGG AGTTGAAGGC AGCAGTGAGC TATGATCTCA CCACTGCACT 300 CCAGCCTGGG TGACAAAGCC AGATCCCGAC TCTTAAAAAG GAATGAAGCA CTGATCCAGG 360 AAACTACAAG AATGAGCCTG AAAATAAACT AAGTGAACAA AGCGAGACAC AAAAGGCTAC 420 ATCTTGAATC GTCCCACTTA CATGAAATGT CCCAAACAGG CAAATCCATG GGGGGAGAAA 480 GCAGATGAGT GATTGCCAGG GGCTGAGGGA GCGGGAATGG GGTTTCTTTT CAAGGGGTAT 540 GAAAATGTCC TGGAGTCAGA AGTGATTGTA CAACATTGTG ATTATACTGA ACTGTGCACT 600 TTAAAATGGT GCATTAGGCC GGGCGTGGTG GCTCATAACT GTAATCCCAG AACTTTGGGG 660 GGCCAAGGCC GGTGGATCAC TTGAGGCCAG GAGTTCGAGA CCAGCATGGC CAATATGGCA 720 AAACCCCAAC TCTACTAAAA ATACAAAAAT TAGCCGGGTA TGGTGGTGAG TGCCTGTAAT 780 CCCAGCCACT TGGGAGGCTG AGGCAGGAGA ATCACTTGAA CCTGGGAGGC GGAGGTTGCA 840 GTGAGCCAAG ATGGTGCCAT TGCATGTCAG CCTGGGTGAC AGAGTGAGAC ATGGTCTCAA 900 AAAATAATTA AAATAAAATG GTGAATTTTA GCACCACCAC CCCTCCCCGC CCAAACATGC 960 AGAGAGAAAT TTCATTAAAA AGTCCTAACT TAGCATCTTG AAAAATCAGG AATCAGGGCA 1020 GTGGAAGCCG CACGCATGAG ATGGAAAGAC TGAGTAGTCT GGCGTTTCCC AAGCTGCCAG 1080 GAAGGCCCCG CCCTCATTGT TTCTGGAGGG GGAGGGAGGG GCTGGAGGAT GAATGAGGCC 1140 CAGATCTCAG ACTGAGGGAT AAGGGTAGCT CTTTCCTTTC TGGGCTTCCC TTTCACAGCC 1200 AATCCCCGGC CTCTGTTCAG GGCTGGGGAT TGGCTGTTCC AGCTTCCAGG GCACACATCC 1260 TTGAGCCCCA TCTAGGGAAC CTGGTTTCTC TGGCTGTCTG CCCACCTCAG GCAGTAATTG 1320 ACTTCTGCCC TTGGTTTTGT TTTATTTTTT 1350
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