Tag | Content |
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EnhancerAtlas ID | HS145-21954 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr6:10163330-10164200 |
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) |
ZNF263 | MA0528.1 | chr6:10163515-10163536 | CCTCCTCCCCGCCCCTCCTTT | - | 6.27 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 10163466 | 10163816 | chr6 | 10163876 | 10164039 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I010162 | chr6 | 10162671 | 10165030 |
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Enhancer Sequence | CATAACTTAA TTCCCACATT TCCCTCCACT TCCACTGAAT GAAAAGAGAA GATGTTTCCA 60 CCATAGGAAA CCACAGATAA TTGAGAGAAC TTTCTAAGAT AGTTTTTCCT TTCTTCTTTT 120 TATCCTCACT TTCTCTCCCC ACTCAGAGCT TAAACAAGTG ATACATCTCT GGCTTTCCTT 180 GCAGCCCTCC TCCCCGCCCC TCCTTTTGGA TAAGCCTCAG CTTCGTGGCC TGGCATGCCG 240 GAGAAACTGG TTCTACACAC CCAGGGGGAA AATGACAGCT TTTCACCGCA AGCTGCTCAG 300 CTCATAAATA GCGAGGGGTA GCGTCCACAC ACGTCTCGAC CTGCCTCTTT CCAAACGCCT 360 GTACAGCCAG CATGGCAGGA AAGTCTTCAG AGAACATTAA CAGCTCTTTA CATAACTTTC 420 TGTAAAGCAG CTTAGTAATG TTTGCAGCCT AAACAGCCCA CAGGTGACAG CTCTGCCATT 480 CTAATGCCTA CAAGTGAATG ACCAGCTCAA CTGGGTGGTT CTTTCTTCTT CCAGAGTGGC 540 CCTGGGAGAC AGGGAGAGGG AGAAAAGAAC AGAGGTGAGC GGAGAGAGAA GTTAGCTTAG 600 TAAAGAATGA AGTGTCCACA AACCTGGCAA AGGGCCTATG ATTTTATGCC TTGAGGTAAG 660 AAAGTCAACT GCTTTTCCTG GAACTTGGTC TAAATTTAAC ACCCGCTTTT GCAAATGTCT 720 GCTGTACGGT GAGTTGTGTG AGCTCATGGT GGAAAGTGAC AAAGTAGGTA CACAGCTGAT 780 ATAATTTATT TATAAATGCA TGAGTGCCGA AAGGAGGTAA AATCATGCAG AGTTGATTTA 840 GCTGTTGTGT TGTTCACGGA AAACATGTTG 870
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