Tag | Content |
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EnhancerAtlas ID | HS103-03822 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr11:12387400-12388600 |
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) |
FOXA1 | MA0148.4 | chr11:12387964-12387980 | CACAGTGTAAACAAAG | + | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I012366 | chr11 | 12387548 | 12388368 |
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Enhancer Sequence | ATTGCTTGAA CCCAGGAGGC AGAGTTTGCA GTGAGCCAAG ATCATGCCAC TGCACTCCAG 60 CCTGGGCAAC AGAGTGAGAC TCAGTCTAAA AAAAAAAAAA GAAAAAAGGG CGCTTTTAAG 120 ATGGCCAAAT AAGAACAGCT CCGGTTTGCA GCTCCTAGCG AGATCGATAC AGAAGACAGG 180 TGATTCTTGC ATTTCAAACT GAGGTATCTG GTTCCTCTCA TTGGGACTGG TTGGACAGTG 240 GATGCAGCCC ATGGAGGGCG AGCTGAAGCA GGGCAGGGCA TCGCCTCACC CAGGAAGTGC 300 AAGGGGTCAG GGGACTTCCC TTTCCTAGCC AAGGGAAGCC ATGGCAGACT GTACCTGGAG 360 AAACTGTACA CTCCTGACCA AATACTGCGC TTTCTCCACA GTCTTAGCAA CTGGCAGACC 420 AGGAGATACC CTCCCATGCC TGGCTTAGTG GGTCCCACGC CCACGGAGCC TTGCTCACTG 480 CTAGCACAGC AGTCTGAGAT CGACCTGCGA TGCTGCAGAT TGGCGGGGGG AGGGGCGACT 540 GCCACTGCTG AGGCTTGAGT AGCTCACAGT GTAAACAAAG AGGCCAGGAA GCACGAATTG 600 GGTGGAGCCC ACTGCGGCTC AGCAAGGCCT ACTGCCTCTG TAGATTCCAC CTCTGGGGCA 660 GGGCATAATA GAACAAAAGG CAGCAGACAG CTTCTGCAGA CTTAAACATC CCAGTCTGAC 720 AGTTCTGAAG AGGGCAGTGG TTCTCTCAGC ATGGTGTTCG AGTTTCGAGA ACGGACAGAC 780 TGCCTCCTCA AGTGGGTTCC TGACCCCCGT GTAGCCTGAC TGGGAAACAT CTCCCAGTAG 840 GGGCCAACAG ACACCTCAAT CAGGCGGGTG CCCCTCTGGG ATGAAGCTTC CAGAGGAAGG 900 ATCAGGTAGC AATACTTGCT GTTCTGCAGC TTCCGCTGGT GATACCCAGG CGAACAGCAT 960 CTGGAGTGGA CCTCCAGCAA ACTCCAACAG ACCTGCAGCT GAGGGGTCTG ACTGTTAGAA 1020 AACTAACAAA CAGAAAGGAA TAGCATCAAT ATCAACAAAA AGGACATCCA CACCAAAACC 1080 CCATCTGTAG GTCACCAACA TCAAAGATCA AAAACCACAA AGATGGGGAG AAGCCAGAGC 1140 AGAAAAGCTG AGAATTCCAA AAAACAGAGT GCCTCTTCTC CTCCAAATGA TCACAGCTCC 1200
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