| Tag | Content |
|---|
EnhancerAtlas ID | HS050-17866 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr12:132950300-132951150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr12:132951095-132951110 | GCAGGTCAGGGGTCA | + | 6.39 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 132950481 | 132950573 | | chr12 | 132950750 | 132951000 |
| Enhancer Sequence | CCCGTCTCTC TGCTCTGCCC AGCCAGGTCC AGCGTCCTTG AGCCAAATCT CTGCAAATGT 60
TCCAGTCAGG ACAGATTAAG TTTCACCATA AACCAGCAGC TCATCTTTAT TTCTAGGCAA 120
TTTATTTAAG AGCCTCCTAA AATCTACTAA CTTCCAGGCC GAAAATCATT TAAAATCAAA 180
TGAGTTTCCT CGCCGATAAA ACTTGAGATC ATCCTTCAGC TTTGGAGATA ATAGAACTGA 240
GCGGTCATTT CCTCCCCGCG CTGAGGGAGC TGAGTGATGG AGAGGCGGCA TAGGTCCTCC 300
GAGGAGGCCC CGTGAGCCCC ATGGCTGTTT CCCAACGCCA GCGGAAGAGG GAGGTTAGAG 360
GCTCCCTCTG CTGTTATCCT GCGGGTGGAG GAAGCCCTGA GCATCCCCTC CAGCCCCTGA 420
GGCCTGAGTC CTGGGGGGCC CCCCGCCCCC GCCAGCCCAG CCTGGCGTCA ATCCCGCTTA 480
TGCATAGCCC AGACCACCCC CTGCCCAGCG AGCTCCCCTG AGGCTCTTCC TCGTGGCAAA 540
AGAGATTCTC AGAGCCCTCT GCAGAGTGCC AAGTGCGCAG GGAAGTCACA GCTGACCCGT 600
CACCCCAGCC CCAACTGCTC AGTGCCCCAG ACCTCTCACT GCGTGTGGCC CAGGCCCTGC 660
AGAGTCTGCC CCACCCCCTC CAGCCTCCTT TCACACTTCC TCACTGCATC AGTTTGCCTT 720
TGTAGCAATA ATGCTTAGAA ACAAATCACC CGGAAACTCT GGTTTCAACC CGAGTATGTA 780
TTTAGCTCAC AAGCCGCAGG TCAGGGGTCA GGCTGGGCTC AGCAGGTGGC TCTTCTGTCC 840
TCGCCGGGGT 850
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