Tag | Content |
---|
EnhancerAtlas ID | HS048-38147 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr9:131090080-131091840 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TEAD1 | MA0090.2 | chr9:131091244-131091254 | ATGGAATGTG | - | 6.02 |
| | 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 |
GH09I128328 | chr9 | 131090403 | 131092436 |
| Enhancer Sequence | AAAAATAAAA AAAAGTATAC CAGCACTATT GTCAGCAGTT GGGATACAGT GGACAAAACC 60 AGCAAAAAGC CTGCCTTTGT GGAACTTACA TTCTAGCAGC TATGAAGAGA ACAAGTTAGT 120 GTGATAGAAG ACAGCTTTGG TATTGGGAAG GGTACAGCCA CTTCTGACTG GGTGGTCAGG 180 GCCGGCTCCT CTGAGGAGAC TTGGAAGGTA AGGAGGAGCC AACCCTGTGG AGAGCTGAGG 240 AGGAGCATTC TGAGTAGAGG GAATGGCAAG GGCAAAGGCC CCTTGTGTTT AGGAAAAGGA 300 AGGTTGACCA GTGTGGCCGC AGAGGAGGGA GTAGCAGGGA GACAGTGAGT GGGCTGGAAG 360 GGGAGCCAGG GCTGCGCCCT GTAGGCCACC AGAAGGAGGA GTCTGTATTT TGTAATAGGA 420 GCAGTAGGAA ACTTGTGGAA GGTTTTGAGC AGGACAGTAA AGTGACCTGA TTTGTAAAGG 480 ACCTTAGGAT CCAGTTGGCC CATCTTCCCT GTCCCTGTCC CATCTTCCCT CCCTCCTGCA 540 ACACAGATAC ATCCCATCAA GGCACCCCTG CCAAATGGCG AGCCAGTCTG GCTGATGGAG 600 GTGAGGGGTC TCCAAAGGTT GCCCTAGAAC AGTTTCTCAA GCCGGGCATG TTAATGTTTA 660 GGCTGGATCA CTCTTTGTTG TGGGGGCGGT CCTGAGCCTG GTAGGATGTT TAGTGGCATC 720 CCTGGCTTCT ACCCACTGGA TGCCAGGAGC ACCCCCCCGT CAAGTTGTGA CAACCACAGA 780 TGTCTCCAGA GATTACAGAT GTTCCCTGGT GGGCAGTTGA GAACCACTGC TCTGAATGGT 840 TATTGTCCCC GAGACGATGT TCTGTTCCTC ACAGTCTCCT GCACAGCTAC CTTGACGGGG 900 CGATCACCTG CACTATTTTA AACCATCTCT CTCAGATTTC ACCAGGATGC AAGTCATTTC 960 ATCAGTGGGA AACTCACCAG GGTGACCTGC CTCAAGTGCT ACACAGGGAG GGACAGTCTG 1020 AATTTCCCCC AGTCTTTAGC CCTGTCGCTG TGGAGGGGAG GGGGTAGCAG GGACAGGACT 1080 GCTAGGACAC CTTGCTCAGC CACAGCCCCA CTTGTAACCG CGCTGGCGAT TGTGACACTT 1140 GTAGAGCAAG GAAATCAGCA GCTCATGGAA TGTGAAGGAG CACCTTTGTC CCCAGAGAGA 1200 TTTAGATAAA GGTTCAAGGT GAGGCTACCC TCCCCTCCCT GAGGCTGATT TTGGTGAGAG 1260 GTGTGGTCAT CTTGTAGTAT CAAGACTACA GGCATGGGCT TGAGAATTAG GAGGAGCCTG 1320 AGTGAGAATC CTGGCTCTCT TCCCAGCTTT ACAAGCCTGG ACAAATCCTT TGACCTCGCT 1380 GAGTCTCAGG TTCCTCATCA GAAGTAAGAG GACCTCCCAT ATATCTTCCA GGGCACTTAT 1440 CGGCCTTGGT AATGGATATT AAGGCCACTG GCTTTGGAAT CCAGCAGACT TTGTTTCAAA 1500 TGCTGACTCG GCCACTTTAC TAGCTGTGTG ATCTTGGGCA AATTACTTTA TCTCTCTGAG 1560 CCTTGTTTTC CTTATTTTTA TTTATTTATT TATTTTTTTG AGTCTCGCTC TGTCACCCAG 1620 GCTGGAGGGC AGTGGCACAA TCTTGGCTCA CTGCAACCTC CACCTCCTGG CAATTCTCCT 1680 GCCTCAGCCT CCTGAGTAGC TGGGACTACA GGCGCACGCC ACCAGGCCTG GCTATTTTTT 1740 GTATTTTTAG TATAGGCGGG 1760
|
| |
|
|
|