| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00033 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:1050220-1051430 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:1050244-1050265 | GAGGGAAGGGTGGGAGGGGGA | + | 6.65 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GATACACTGG ACTTTGGGGA CTCGGAGGGA AGGGTGGGAG GGGGACAAGG ATAAAAAGCT 60
ACAAATAGGG TGCAGTGCGT ACTGCTCGGG TGATGGGAGC ACCAAAATCT CACAAATCAC 120
CACTAAAGAG CTTACCCATG TAACCAAGTA ACCAAACACC ACCTGTACCC CAGTAACTTA 180
CGGAAAAATA AAAGAGGAAG ACGCAGCTCT GCCTTCTCTG CACACCCTGG TAATACTAAG 240
AAAAATGAAA ACCAAAAAAA GGAGGCCAAG TTTGACATCC TGAAATTTAA CAGGACGAGG 300
CGGCTAAGAA TTCAGCCACA AAATAGTTCC CGGGGAAGAA GCCGCGTTTG CTTTGAAACG 360
CGGTAAGAAA TGCCCCCGAA CACCTGGGCT TAAATTACAC CCAAACTCAA TCATCGACTC 420
GCTGCCACCG GAACACGCGC TCCCGAAAAA CTGCACCCCG ACTAGCCCTC GGCTACTCCA 480
GGTGACAAAC GGACAAAAAC AAATCCTAAA GCCTCGCGGG AAAAAGACCT GAATCGTGGC 540
CGACTTCTAG GACACCGGGG ACCGCGCCGG TGCCCCCACT CCCGGCTGCC GGGAAGGCGA 600
GGCGAACGCG CCCCCTTTCT TCCCCCGGGC GCCCGTCCCA TCCCCTCCCC AGGGACCCCC 660
TCCCTGCCCC GAGAACCCCC TCCCCTCCCC AGGTGCCCCC TCTCCCCCAG AGACCCCCTC 720
CCCTCCCCAG GGACCCCCTT CCCTGCCCCG GGAACCCTTC CCCTCCCCAG GGACCCCCCT 780
CCCTCCCCAG GGACCCCCTC CCCTCCCCAG GGACCCCCTT CCCTGCCCCG GGAACCTTTC 840
CCCTCCCCAG GGACCCCCCC TCCCCGCTCC GGGAACCCCC TCCCCTCCTT AGGGACCCCC 900
TCCCCACCCC TCCCCGGGGT CCCCCTGCCC TCCTCAGACG CCCCTTCCCC TCCCCAGGCG 960
TCCCGCTCAG CCCGGGCGCC TTTCCCCCAT AGGACCGCGG CCAGGCTCGT TGGGAGGCGG 1020
CGACGAGGAC GCGGGCCCAG GCGCTGGCGG CTCCTCCGCG CGCCGCACAA TGGGGGACGC 1080
GCAGGGAACG TCCCTCGGGC CGGGCCAGGG CCGCCGACCT TTGTCTGCCT CTCGCACTCC 1140
CTGCGCCGAC CCGGCCGCCC AGACGGACCC CAGCGCCCCA ACCCGCTACC CTCACGCCTG 1200
CCCCCAGCCC 1210
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