| Tag | Content |
|---|
EnhancerAtlas ID | HS050-62904 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr7:72824340-72825700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr7:72825087-72825098 | GGGCGGGAAGG | + | 6.62 |
| | | 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 |
| GH07I073410 | chr7 | 72824530 | 72825543 |
| Enhancer Sequence | AAAGCCTGAG TCACAGGGAG AGGCTTCTCC CCAGCCCCTG GGAAGCCGAA GAAGCCCTGG 60
CCAGGCCGGC TCCCAAACTC ACGGGTCCTG CTAGGCACCT GCTGTCACTC TCACTACCGA 120
CCTGGGAGAA GGCAATGGCC CATTTATGAC ACTGGAGGCG AGGGCCATGC ACCCCCTAAG 180
CAGGCAGCAC CTCTGGAGCC ATTCTGCAGC TGGAGGTTCA TTTCCTTCCT GATGTCATAG 240
TGCTCCAAGG TGGCACAGCC AGGACGGGAG CCTAGGGAAT TGTCATCCAC CCTGGAGCAC 300
TTTCCGTCTC TCAGCGGCTG TCCCAGCCCT GCACTCAGGC AATTCCTGCG GGAATCGGTG 360
GCCCCTGGGC GTCCTGGATG GGGAACCACA GCCCCTGAGG CAGAGCGGCA CAAACCCTCC 420
AGTGGATCCC GTTCTCTTCT CCCAGGGATC AATGAAGCCC AGGGTGTGGG GGCTCAGCCT 480
TGGTGTCCCG GCCCCTGTGG TCACACAGCA GCTATTGCTA TGGGGTTGGG ATGCAGGGAG 540
GAAAAGCCCA GCGTCCCCCT TTCCACCCCA GGCCCCAACT TCTCTGTATT TGTTTATTTA 600
CCTTGGAAAA AGCCCCACAG CCCAGGCAGG AAATGGGCCA ATTCCAGGAG GCCGGGCCGG 660
GGAACAAGGA GCTACATTGT GCTCGGGCGG TGGCTCCCCA CCCGGGCCTG CCAGGAGCCC 720
AGAGGTGGGG GGGTCTGCAT GGGGACCGGG CGGGAAGGAG GCGTGGGGCT GAGGGGCTGC 780
CAGTACTCCC AACCAGCCAG CGTGTGAAAA GGCTTCTGTG CAGGGGGTGG GATGGGGGCT 840
GTGGCTCCCC GTCCCACCTG GGAATGAACA GAGGCTGGGC AGTGGGGGAG GCAGACGCTG 900
GGCTGGGGCT GGACCCCGGT CTTGACCCAG GGCCCACCTG GCACTGATCT GCCTGCCCAA 960
GGCAGACCCT GGCCTGGGAA CCCCATCTCC TTGGGCTGAG ATCCCACCCT GTGGCTGGAG 1020
AATGTTCCCG CCCTCGGCCT CCCTTCTGGG GTCTCAACTC CTGCCAGGCA GCTGGCCTGA 1080
CCTCAGACTG CCCCTAGCCC AAGGCTGGGG GCTGGAGAGC CCTGTGGTCA GAGCCCTCCC 1140
CTCCATGCCC AAGCCCAGGC TGGCACTGGG GCTGATGTCA TCATGGGGGC GGCTTGAGGA 1200
GGGCTGAGCT CTCCCTGACC CTAGACTCTT CTTTACTAAC AGGCTAGTGT CCATATGGAT 1260
GGATCATTCA TTCACTCATT CGTTTATTTA ATACACTCCC TGTCTGTTCG ACGCACACTC 1320
CCCTTCTCTC CACTTCTGGC CCCGTTTCCT CTAATCCTTC 1360
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