Tag | Content |
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EnhancerAtlas ID | HS191-32026 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr6:10163230-10164270 |
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 | ATAAATTTAA TCTGTAAGGG ACGAAAGTCG ATCGGGAATT ATCTCTGCCA ATGACTTGGT 60 CCAGCCAGTG AGCTTGTGAG TAAATCCTGC TTCTTCTCCA CATAACTTAA TTCCCACATT 120 TCCCTCCACT TCCACTGAAT GAAAAGAGAA GATGTTTCCA CCATAGGAAA CCACAGATAA 180 TTGAGAGAAC TTTCTAAGAT AGTTTTTCCT TTCTTCTTTT TATCCTCACT TTCTCTCCCC 240 ACTCAGAGCT TAAACAAGTG ATACATCTCT GGCTTTCCTT GCAGCCCTCC TCCCCGCCCC 300 TCCTTTTGGA TAAGCCTCAG CTTCGTGGCC TGGCATGCCG GAGAAACTGG TTCTACACAC 360 CCAGGGGGAA AATGACAGCT TTTCACCGCA AGCTGCTCAG CTCATAAATA GCGAGGGGTA 420 GCGTCCACAC ACGTCTCGAC CTGCCTCTTT CCAAACGCCT GTACAGCCAG CATGGCAGGA 480 AAGTCTTCAG AGAACATTAA CAGCTCTTTA CATAACTTTC TGTAAAGCAG CTTAGTAATG 540 TTTGCAGCCT AAACAGCCCA CAGGTGACAG CTCTGCCATT CTAATGCCTA CAAGTGAATG 600 ACCAGCTCAA CTGGGTGGTT CTTTCTTCTT CCAGAGTGGC CCTGGGAGAC AGGGAGAGGG 660 AGAAAAGAAC AGAGGTGAGC GGAGAGAGAA GTTAGCTTAG TAAAGAATGA AGTGTCCACA 720 AACCTGGCAA AGGGCCTATG ATTTTATGCC TTGAGGTAAG AAAGTCAACT GCTTTTCCTG 780 GAACTTGGTC TAAATTTAAC ACCCGCTTTT GCAAATGTCT GCTGTACGGT GAGTTGTGTG 840 AGCTCATGGT GGAAAGTGAC AAAGTAGGTA CACAGCTGAT ATAATTTATT TATAAATGCA 900 TGAGTGCCGA AAGGAGGTAA AATCATGCAG AGTTGATTTA GCTGTTGTGT TGTTCACGGA 960 AAACATGTTG CACACCAACA AAACACACAG ATGCACATCT AAATTATTTT AAAGATCACA 1020 TTTAAACCTG GAAAATACCA 1040
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