Tag | Content |
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EnhancerAtlas ID | HS101-05354 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:69923180-69924420 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr10:69923558-69923574 | TGGGTCAAAGTGCAGC | + | 6.12 | STAT1 | MA0137.3 | chr10:69924271-69924282 | TTTCCTAGAAA | - | 6.14 | ZNF263 | MA0528.1 | chr10:69924044-69924065 | AGAGAAGGGAGGGAGAGAGGG | + | 6.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr10 | 69923511 | 69923818 | chr10 | 69924083 | 69924264 | chr10 | 69923560 | 69923873 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I068163 | chr10 | 69923385 | 69924217 |
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Enhancer Sequence | AGACCATCCT GGCTAACACG GTGAAACCCC GTCTCTACTA AAAAAAATAC AAAAAATTAG 60 CCCGGCGTGG TGGCGGATGC CTGTAATCCC AGCTACTCGG GAGGCTGAGG CGAGAGAATG 120 GTGTGAACCC GGGAGGCAGA GCTTGCAGTG AGCCAAGATC ACGCCACTGC ACTCCAGCCC 180 GGGTGACAGA GCAAGACTCC ATCTCAAAAA TAAATAAATA AATAAAAAAT AAAAGAAATC 240 CTGTCTATAG CAACAATGGG GATGCAAATC AATTCTTAAA CAGTCTTATG ATCCTAATGT 300 CAGAAATCCT ATCTATAGGA ACAAGGGGAT GCAAATGGTC AGGATCTAGT GCTACGTGAC 360 TTTTAGTGAC AAAGGAAGTG GGTCAAAGTG CAGCCTGATT AATGCTTAAC TATATTTCTG 420 TCCAGAACCT AGTATGCAAT TCTTGTCAAC CCTGTGGTTA TGGTTTCAAT ATCACACTGA 480 CTGGAATTGT GTGTCTCAAC TACCACTTAA CAAGAATAGA GTTAGCTTGA CTGGCTTAGA 540 CCAGTCATGA TTTACCATCT GAGGCTGAGA GGAACCAGCT TTCTTCAGAA CATATGACCA 600 ATCCAAGTAG AGTAGACAAA GCCAGGGTTC TATCAACAAG GAGGTAGGAG GATGAAGAGT 660 TACTGAGTAG GTACTTGCTT GGTCCACTGT GTGCTGCTGT GACCGAATAC CTGAAACTGG 720 GTGATTTTTA ATAAAGAACA GGGATTTATT TCTTACAGTT CTGGAGGCTG GAAAGCCCAA 780 GATCAAGGGG CCTGCATCTG GTGAGGGCCT TCATGCTGTG CCATTCCATG GCAGAAGGCA 840 GAAGGGCAAG AGAGCAAATG CGCAAGAGAA GGGAGGGAGA GAGGGGGCCA CTCTTACTTT 900 CATGACGAAC CCACTCCCAA GATAACAACA TGTATCCATT TATTAGGGCA GAGGCATCAT 960 GACCTAAACA CCTCCCTTTA GGCTCCACAT CCCAGCACTG AAGCATTGGG GATTGTTTCC 1020 AGCACATGAG CATTGGGGGA CATGTTCAAA TAGCAATACT CAATACTACC TGCCATGCCC 1080 CACTGGCCAG ATTTCCTAGA AACAGTCTAG TTAATTCAAT TCAATTATCA TGAAGCACTG 1140 AGATGCCTGC CAAGTTTCTC CTAATGCAAC TATTTTTTAA TAATTTTGTT TTTAATGTCA 1200 GTTCAATGGA GTGATAACTG GAGGTTTATG CTGCTGTCTT 1240
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