| Tag | Content |
|---|
EnhancerAtlas ID | HS050-49712 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr3:184183960-184184850 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr3:184184348-184184363 | GTGTTCAAGGTCAGC | + | 7.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 184184176 | 184184760 | | chr3 | 184184369 | 184184676 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I184464 | chr3 | 184182687 | 184185421 |
| Enhancer Sequence | GGGTCTGGAC AGGACATTTT CCTTGTTACC AGGGGCTCAG ACTCATCAAG AATGAGGGCT 60
AGGGTCACCC CACAGCTAGA CCATGAGGGC CGACAGAGGT GGGAGCTGAG GGCAGGGCAA 120
TTTAGAAGGA ATAGCGGAGG GAGCCAAGCA CCAGTGGTGG CCCTGAGGCC AGTAGCAGTG 180
AATGAGGTCT CTATTTCATG CTCGTAACTT CCCTCTTGTA CAGAGGCCCC CCAGATCCCT 240
GGGGGAGCTG CTCCCCACAT GTGTCCACAT TACCGTGACA TGTGGACTGT GGCAGACATG 300
GGGCTGCTCT GCTCCATTCT CCTTTGAGAA AGTATTGCTG CCCAGCCGCG AGGAGTGTGA 360
TGAGTTGACA GCCTCAGCGT CTGGGCTGGT GTTCAAGGTC AGCTGCAGCT TTTGAGCTGA 420
GATCATGCTC TTCGAGGGGT GGCCCCAGCC AGAGACTGAG CTTGATGATA AGGGCCTGGC 480
TGCTTCTGCC CTGTGAACGA CTCTTCTAAC AGAAAGTCTT GGACACCTTT GTTCCAGGGC 540
TCCCCTGGGG CCGGCCAAGC TTTGTCACAT CTGCACTGTG GTCTGGCAGC TCCCTGCCCC 600
ACCCACCTTT CCTTCCCTTT CCTCTCAGAG GCGTTGCTTA CCAATGAGGC GTGGGTATTC 660
CTGACTCTGT CTCAGCCTCT GCTTCTCAGA GAACTCCGCT GACACAGTCT GCATGGCACA 720
GTCCTCTCTG ATCTCGGAGG ACACCTGTCT TTTTTTTTTT TTGAGACTGA GTCTCGCTCT 780
GTCTCCCAGG CTAGAGTGCA GGGGCGTGAT CTCGGCTCAC TGCAACCTCC ACCTCCCGGT 840
TTCAAGCGAT TCTCCTGCCT CAGCTTCCTG AGTAGCTAGG ATTACAGGCA 890
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