Tag | Content |
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EnhancerAtlas ID | HS050-32755 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr19:8207020-8208540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:8207734-8207755 | CTCCCCCACTCCCCCTCCCCC | - | 6.69 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 8207176 | 8207880 | chr19 | 8207975 | 8208025 | chr19 | 8208093 | 8208295 |
| Enhancer Sequence | TCTGCAGGGC AGACAGATGT GGGTACCTGG CTGAGGGCTG CCCCTGTCTG GAGATCTCTG 60 CGTCTCTAAC ACCTTCTCAG CGGCCCCTGC ACCCACAGAC CAGGCTTTAC TTATGCTGCT 120 CCCTTACTAA ATAGAATATC TTTCCTCCCC TTTCCCTACC TAACGAACTC CTATTCACCC 180 TTCAAAACCC TTTTTCTTCA AAGCATTTCC TGACCAACTT CCAAGAGACC AGCACCTCCA 240 AGCCAATAAA GCTCAGGGCC TGTGTGAACA CCCTGTCTGA ACTGATGGGA CTCCTTCCCC 300 AGGCCTATCC TCCCTTCAGG CCTGGGCAGG GACCCACGGA TGCCCAGCTA AAAAGCATGT 360 CTAGTCCTTG AGCACACGCC TGGCCCTGCC ATATCGCCCA GATTTGGGGA AGGATCTGTT 420 ATCTGCCTAA ATTCTCTGGA CCCCCAACAT CACATCCCCA ATCCCCATCA GGCCCAGCCC 480 AAGGTGACCG CATTGGTTCC CCCAACCCCA GTACATGAGC CCAGATGTGA CTTCTTGGCT 540 CTCTTCTCCC AGATGTTTCC AATAAAGGAG TTAGCTCTCA AACAAGGGCA GCCGCTCCCA 600 AGAGAAGAAG CCAAACTCAC CCCCAACTCA GGCCCCGTAA GGAGGAGGGG CTTCACAGAG 660 ACCCCCACCC CCCAGCTGTC CTGATGCCCC AAGCCAAAAC GTAATTCCTG GCAGCTCCCC 720 CACTCCCCCT CCCCCTCACT CTTCTGCCAC CCAGAGCTTG GCCCGCCTCC AACAAGCCCA 780 TGTTCTAATT CTGCAGTTTC CAGAAGCCCA CCCTCAAACC CAGGTCACTT CCCCAGCCCC 840 TCCAGCTTCT AGTCCCCGGG TCGTGCCCAT CCTCACCTTC CTGGGCTGAA ACACCACATT 900 AGGCACCCAG ATGCCTCTGC ATCTGAAAAT CTCACAAGCC TGGATGTCCC TGACGCCACC 960 CACTCCGGTT CTCTTTCTCT TTCTCAGCCT CCTGTGGGCT CGGTTTTTTC TGTCCAGGCT 1020 TAAATGCCCA GGTGGCTGTC TCTGCTGGCC CTTCCTTCTC TCACGGGGAT CCTCAGCGGC 1080 ACCCTGGGCT TCAGTCCCCA TGGATGGGGC AGCCCACGCC GCCATCTCAG CCCCAGGCCT 1140 GAGTGTCCAG CTGCTTCCCA GACAACTTGC AAGTCCCTCG GCCAACACTG AGCTCAGAGT 1200 CCTCCTCCTC CCTGCCAGGG TGCGCCACTA CCTTCCCTCC AGTTTTCACC AGGTCTTGGG 1260 TTCATCCTGA CTCCCTCCTT CTTCTCTCCC CGTCCCTGCC ACACCTCACT GCTCACAAGA 1320 AAGACATCAC TGTGTCCGTT CTCCTTTTTT CTTTTCTTTT CTTTTTTTTT TTTTTTTTGA 1380 GACAGGGTTT CGCTCTGTCT TCCAGGCTGG AGTACAGTGG TGCGATCTTG GCTCACTGCC 1440 TCCCAGGTTC AAAAAATTCT CATGCCTCAG CCTTCCAAGT AGCTGGGACT ACAGGCACGC 1500 GCTACCACAC CCAGTTACAT 1520
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