| Tag | Content |
|---|
EnhancerAtlas ID | HS050-61180 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr7:445320-446330 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr7:445617-445635 | GACTTGCTTTCGCTTCCC | - | 6.14 | | RUNX1 | MA0002.2 | chr7:445375-445386 | AAACCACAGAA | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGTGCATCT GAGATGTGTG TGGTTTTCCA CACGCGTGCG ATATGTGGAT ATTCAAAACC 60
ACAGAATTTA AAAGTAGGTT CTGCCTAGAC TGGGAGCCAC GTATGTCCAG GGTGGAGGCC 120
ACACAGCCCC CTGGCCCACA GCACCCTCCT GGCCGTGGCC ATGCCCCTTC ACCACCCCAG 180
GACCACACTA TTGACCTGAG TGCAGCTCCC TGAGCGGTGA CGGGGGAGTC CACCTGCTGA 240
GGGAAGTGAG GGGAGTCTGT GGGACGCCCA GCTCTCCAAG GCATGGCAGG AGCTCCGGAC 300
TTGCTTTCGC TTCCCGCCTC TCAGGCCCTG GGCCTGAACC CCCACACCCC CCATGGAGGG 360
GCCGTTCCCC TCTGAGGCCG AGCCTGGCCC CCCCAGAGCA TCTGTCTCTG AGTCTGTGCC 420
TGTCCCTCTG CGAAGGTGAA GTCCAGACAG CTTTGAAGCC CCCATGCCCC CATCCTCGGG 480
GTGGCCCGGG ACCAAAGACG AGGCAGGAGC CAGCTGTCAG AGTCTCTGGA ACCCAGCAGG 540
AGAGGGTAAG GGCTGGACTA CCAGCTGGTG TTTTGAAAGA ATGAAGACCT GCAGCTCCAG 600
GGGGAGGGCC TGGCCTGGCC AGCCGCCGAG CCTCCACCCC CTCACCAGAA ACCCCTTGGG 660
CTGCGGGCCA CCGCCTGACT CTCCCTCCCT CCTCCAGACC ACCCTGGTAC TCACTCAACC 720
TGCCTTCGCC AAGAGCTGGG GGCGGGGAAT CTTTTGCATG ACCGGCCCTG GGCCTGACTC 780
CTCTGGTGCA GGAAGAAGCA GATCCAGCAA GGGGGTCCTC CCATCCCTGG TGGGGCCAAA 840
CCTTCTCCAA CAAGCCCTCA GACAGAGCAG TGTACGGAGG CTTCCTTTGA ATGTCGAGGT 900
TTTCCAAAGA TCAAAACAGA AAGCAAGGTA TTTTGGAAAC ACCTCATGTG CCAACTAATT 960
AAGTGTCTGG CTGTTAGCAA GCCCCTCACA GAGGAGGGAA GAGCCAGCCG 1010
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