Tag | Content |
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EnhancerAtlas ID | HS050-14626 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:1597880-1599070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr12:1598577-1598589 | ATCTGTTTACAT | - | 6.62 | FOXP2 | MA0593.1 | chr12:1598578-1598589 | TCTGTTTACAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I001488 | chr12 | 1597779 | 1598958 |
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Enhancer Sequence | TTCTTTCCTA AAACCTGCTG TCTCCTTCGT TCTTGGTCTT ATTTGTCCAA TATCCCCAGC 60 TAGAATTGTC AGAAATGATT CTCCAGTTCT CCCTCACTTG ACACCTCCTC CTTTTAGTCC 120 TGCCTTTTGA AGAGGCTCAG ACCTGTGTGT TCCTTTCCAC GTCCCTGGCC CTCCCTTGCA 180 TCAGCCTTGC CTAACCCCCA CCTGGGCTGC GAGCAGGAGC TGCCCTTGGT GGACTCTTCC 240 TTCTGCTCAG TCTGAGAAAG TGGCGATGCT CATGTCACTG TACCATTTAA AACTGCGTGG 300 ACTCCTTTTT TGTGGTTGTG GTTTGGTTTC TAGGCAGATC ACGCTGGAAC GTCCTCACTT 360 CACGTGCTCA GTCTGGCCCT CGCGTGTGTT TTCAGCTCCA TTTCCTGTCA TTCTCCACCC 420 ACTCCCTGTG CCTTACATTC CTGCCATCCT GAGGCTTCCC TTTTCGCAAG ATCTGGGCCA 480 GGCCTGTCCC AGCCCCACGC ATCAGCCTTT GTTCTTCTGC GCTAAGCCTC CTTTGTCTTT 540 GGTCTCCCAG ACGGACTCTA GTCAGCTCTG AAGATCCAGA CCCCACGCCT CTTTAGTAGC 600 ATTTCCTCAG ACTCCTCAGG GTGAGCAGAC ACTCTTAGGG CTGCCACAGC ACATGCTCAA 660 GCCTCAGCTG CGGCCTCACT CTGCTGGGTG GTCGTTTATC TGTTTACATG CTTGTCTCCA 720 TTAACCTAAA TGTGTCTTCA GGACAAGGAC CAAATCCCAT CAGCTTTCAC CACCCAGCAC 780 AGAGTAGCGC TCAATAAAGG TTGGTTAAAA TGCTTGAAGG AATGTGAAAG AGGCTGTTAA 840 AAACAACAGG AAGTTAGAAA TATACTTACT TCTAAGCAAA GGGATTATCT TGTGTTTCTC 900 AAAGTAATCT CTTCAGCTAA ATTAGCAGGC CTCAGGTGGG TAGGCTAATG TACCGGATGA 960 AAGCGATACA CGGCAAATGG AGAAGTCCTT TAAATTCTAA GTTCCCTTAG GGCGAGGGTC 1020 GCTCCACAAG GTTAGGATCC TCTCTGAGAT CACCATGCCC CTCTCTCCTG CTCTCATGCA 1080 CGTTCATGAG CCTGTGACTT GGTGGAGAGA ACATTCTGTT TACAGTGAGA GGCCAGGACT 1140 GAAGTCACAG CTCTGCAAAA ATGATCAGCT TTCGGCCTAG AACCAGTGAC 1190
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