| Tag | Content |
|---|
EnhancerAtlas ID | HS050-70906 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr9:136361660-136362960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr9:136362794-136362805 | ATGACCTTGAC | - | 6.32 | | Esrrg | MA0643.1 | chr9:136362794-136362804 | ATGACCTTGA | - | 6.02 | | GLI2 | MA0734.2 | chr9:136361893-136361908 | CCAGGTGGGTGGTCT | - | 6.59 | | Nr5a2 | MA0505.1 | chr9:136362793-136362808 | GATGACCTTGACCTT | - | 7.16 | | SREBF2 | MA0596.1 | chr9:136362855-136362865 | ATGGGGTGAT | + | 6.02 | | Stat6 | MA0520.1 | chr9:136361778-136361793 | CTCTTCCTGAGAAAT | + | 7.8 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTCCACCAC TGAGCTGAGC TTTGAAGCCC CCAGAGCTCA ACTCTCCTGT TTCCTCTTCC 60
GTTTCTGCAA GACTCTTTCC TATCAGAACA GAAGGCGAGT GCCCGTTGGG CCCTTCTGCT 120
CTTCCTGAGA AATGGAACTC GTCCCCAGAC TGCCTCCCTC CTTCTTTTTG AAAGTCCAGA 180
CACAATGTGT CTCGGTCAGG CATGACACGC CTGGGGGTCT GGCCCCGAAA TGGCCAGGTG 240
GGTGGTCTTT GGGTCAGTGA CACTCTGGCT TTGAAATCTC CCCCAGATGC ACTTGGAACA 300
AGGGACTCCA TGGGAAGACC CCCCAGATCG GGGTGGAGTC AGCCCCACAC CTCTCTCTGG 360
GTGGCTGATA TTTCAAAACT TGTAGCTCTC CAGACAGTGG CCGGGGAGCC TCTCCGTGGC 420
GGGGGTGCGC ACCCTCCCTT GGCAGCCTTG CCTGAGCTCG GGAGGCTCTC TGGTGTCTGA 480
GGCTGAGAGC CCGGTCTGCT GTTCAAGCCA TGCTTTCTCC CGTCTGTCCC GTGTCCATGC 540
ACATGTCCAT GCACTTACGA TGGCCCTTAG GGTGAGGCAG GAGGAGGCTT CGTGGGATTA 600
GACATTGCCA CAGCGTCTGC ATAAGTTGAG GGTGGCGCTG TCACTGTTCA GGGCCCCCCG 660
ACCCTGCCCC TGAAGCCGGT TGGCCTGAAA TGCAGAGTCG ATGACCTGGA GCCGGCCCCT 720
GGCCTCTGAG AAGCTGAGCT GCGGCTGACT TGGCCTTTCC TCCATCGGAG GCTGAAATCC 780
ACGACTCTCA CCAGCCGGCT GGGGGCTGGG GGTGGAGCGG CGTCCAGGCA TCCGGGAAGG 840
ACTCTAGGGG TCTGACTGAT GGACTGAGGG TACGGCCCTC CCAGGAGTTC CTGTCCACCC 900
TGTCTCAGTG TGGACTGACC TGGAGGTCTG GGATGTGACA GGCTTGGAAA ATGATGCGGT 960
GATCCTGCCT GGAGGGTGTT CACGACAGAC TGCATGCTAA GATGGCGCTG GGGGGCGGGT 1020
TACAGAAGAC AGTGTTGTAT GATCCTAATT ATGCACAGGA CAGGGCACAG CGGTCAAGAC 1080
CATGGGCATT GGAGCCTGCT GTCAGAGCTC AAGTCCAGCC CTGTCGCTTT CCAGATGACC 1140
TTGACCTTGG ACATGCTGCC AAACGGCCCT GCACTTCAGT GCCTTCAGCT GCAAAATGGG 1200
GTGATGCCCA CACCTGTCAC TCAGGGGTAT TGCGCAGGTT AAATGAGTCA ATACGTGGAG 1260
CAGACTTAGA ACAGCAGCCC TACGTAAGTG ACCACAGAGA 1300
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