Tag | Content |
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EnhancerAtlas ID | HS050-50355 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr4:4981980-4983680 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr4:4983074-4983085 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr4:4983075-4983085 | CCTTTGTTTT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAACGAAACA CAGAGTTGAA ATAACTTGCT TGAAGTCAGA AAGCAAGGAC CTGGCAGAGT 60 CTGGGTTCTA ACCCGGGACT CTCCAACTCC ACATTTTTGA ACTTGCCCCA CCCCTATTCT 120 GATGTCAAAG TCCAGATCCT TCCATGAGTG TGTTGTGTGA CTTTGGTTCC ATCATTTTAA 180 ATCTCTGAAC TCACCTGGGT CTGAATTAGA TGATCTCAAA ATCTCTCTCT AGCATTAGCA 240 GATGATAGCC CCATGACTCC AGGATGCAGA TCACCTCCCG AGTGTCCCTT CCTCAGTGGT 300 TTGCATGGAA CTAAGTACAT AGTTCCACCT CCAGTTCTAC AGCCCTTGCA GATCCCCTAC 360 ACCATGGCTG TCTCACTGAT AAAGGCCAGA GCCCAAGTCT GGAAATCCAC AATCCACGCA 420 GAAAGATGGA AGGAGCCTGG GAAGAGGGAA TGAGCTCCCT CCGTGAGGCC CAGGGTCAAG 480 AGGAGCCCCT TACTGTTCCA GCCCCCACAA GGGATGGCTT TATGCTTCCT GCAGAGGGTA 540 GCCTTGCAAT GTGCATAAAT TAAGCACGGT TCAGTCTTTA TTGCCACGCA AAGCCTTGGG 600 AGGACTGTTT TATATGTCTC TGTTCTCATG GCGTTAGCAT CATATAGGCT GAAATTAATT 660 CCACCAGACG GGCTGCTCAC AAGCAGAGCC AAGAATTTCC TGGGAAGGAG TTAGGTCTGA 720 CTTTGGCAGC CGCTGTGTGC AGTGATAAAG GCGTCTCAGA CGGTCTCACA CAGCTGGGGC 780 ATCCAAGGGT ATTATATTCT TTGGCCCTCG AGGGCTATTT CTCCCTCTTC CAGAAAACTG 840 GGTGTGGAGT ATGGGCTTGG AGTCAAGGCT GATCACAGAT GGGAAATAGA CCCTGGCATT 900 CTCCCTCATC CCTGGATCAT TTGATCGATG AGGCTAGGGA ATCCCAAACA GGCCAGCCAT 960 CGTCCCTGTC TCAGAGCGCC GGAGCCATTG GGCCTGACTT CTGGGCTGGC TCACCTGCCC 1020 TGAAACCAGA CTATTACCCA CAGGAGATGG TTGCCTGAGC CCTGTGGCCT TGCTTCTGCC 1080 TTGAGTTCTG TTGGTCCTTT GTTTTGCAAA GAACTTCTAA TATGGTGTCC AATTTGAGGT 1140 ACCCCAGAGG CCGGGAAAGT AGGGGAGGTG ATATTATTAG GCATGCTAAT AATCATTATG 1200 ATAATCACCA CTATTTACCA AGTATTTCCC TCTGTACCAG CCCCCTTGGA AGCACTTTAC 1260 ACACATGAAC ACATTGCTTT GCAGAGAGGC CCATAGAGGA GAATGAAATG ACCGAGGGCA 1320 GAGACACTCC CAGGGAATCT GCTCTGTGCC AGCCTCCTCC CCAGAAATTT CACAATCCAG 1380 AACTGTTGCA AAGCTTGCAG CTTGCCAAAC ATATTGTGTT AATCTCCATC CCTTTGCTTA 1440 TGCTCTTCCA TTTATGTGTC TAGCATTCCC TGGAAAATGC CTATTCATCC CTCAAAACCC 1500 AGCTCAGGAT GCGTTTCCTT CTGCAAGCCG TGTTGTATCT CCCCAGGCTG ATTGCATCTC 1560 CATTCAACCA GCACGTATTG GGAAGATTTC AAAAGGAATA AAGAACTCTT GTCTGCACGG 1620 GAGCTTAGTT TAGTGGCTGC TGAGTCCAGT CCCTCTTCAG AGCCACTCCC CTCCCTGACT 1680 GTCCCAGCCA TCTTTCTCAC 1700
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