Tag | Content |
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EnhancerAtlas ID | HS050-56480 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr5:168893790-168895380 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr5:168894279-168894295 | AATTGTTTACTTAACC | - | 7.01 | ZNF263 | MA0528.1 | chr5:168894532-168894553 | GGAGGAGAAGGAAGTGAAGGC | + | 6.13 | ZNF263 | MA0528.1 | chr5:168894529-168894550 | GAAGGAGGAGAAGGAAGTGAA | + | 7.1 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTTGTACAA TCTCATGTGA TCCTCACATC AACTCTGAGG TAGGGACTAT TTCCTCTTTC 60 ACATTTTACA TACGAGAAAA CTGAGAAACA GGGCTATTAA GTTACTTGCC TAAGTTAACA 120 CAATCAGTAA AGGGTAGAGC AGGATTCAGA TAGACCAGCC CAGGGTCCAC ACACCCTGGA 180 ATTTCTTTAC ATAACCTTTT AGTTCACAAA TCAGCTTCTC TTTTCTTGAA GAAACCAACA 240 AGCAGCACTA TTTGTGTTAC AAAAACAGTT TTACATACAA ATTGTTTTCA TGTAAATGTA 300 TATGAATTTG TTCCATGAAT GCTCTTTATT GCATCCTGGC CTTGACGCAG GACCTAATTA 360 ATCGTCTCTT TGGTTCCCCC ATTATTCTCT CTGGCAATCA CAAATCCCTC TCTAAAAAGA 420 AAACCTTCAA GTCTGGCTCT AAGAGGAAGG CTGGGGGAGA AAAGGAGGGG CCTTGTTCCT 480 GTTTGAATCA ATTGTTTACT TAACCCTGTG GCTGAAATAT AAACAATTTT TTTAAGGCTA 540 AAGAGAGAAT TAAATTATTT CAATATAATG ACTGAGAAGG GAGAGAGCCA AAGTCTGATG 600 AGGTCTGAAT GTGCATGAAA GCACCCACTA TTTTTCATAC TTTTTCTTAT ATACTGTGTT 660 AAAAGTGTGG AGGGAGAGAA AGATGAAGGG AAGGGTAGAG AAAGAGAAAG GGATGAATAA 720 GAGAGAGAGG AGGAAAAGTG AAGGAGGAGA AGGAAGTGAA GGCAGCTCCA GGCACCTTGC 780 CCAACTCCTT GGAGATAAAG TTAACGTTTG TTCGCTTGTC TGAATAAACA AAGCTAGTCT 840 GATACTCATC TGATAGTCTC AGTTAAGTCA GTACTGAAAT AGTTGTAAAC TGAAAATACT 900 GAAAGATTTG CACACTGGTT GGTTAGTATC CATTGCTCCC ACCCATCACA CTGGGGGCTT 960 GGTCCATCCC CCATGACCAA GACGTCCACA CCACCCTGCA ACCAAAAGAG TATGCCTAAT 1020 ACTGCAGGGA GCTCCCGGGG CCTCCTCCAG TACCAAGTGG GCATTGGCCA ATCTTCCTGC 1080 CCTATAGGTT GTAAAATATT TTAAATATCA CCCCTGTGCA GAAATCCTTA TTCTGCAGCC 1140 TGGGAATGAG GTTGCCATTC TCCCTAGTCT TCCTCTCTTT GTTCACTCCT AACTGTCACT 1200 GGTTGAGCAT CTGATGGTCT GAGAACAACA GTCACCAGGT CAGTCTGATG TCAGTCGTTA 1260 ACTTGCCTTT GGTCCCATGC TCTCACTGCC CTATACTCAA AACGATCATA GCTAGAGGGG 1320 ATTGTGTGGG CATGGAGGTG ATGGACAGGC TGGGAGAGAG CGGGGGAATG GGGCAGGGTC 1380 ACTGTAAAGT TTTGAGGGTG AGAAGAAAAA CCAGAAGCCT TCTTGTTCAC ATAAAAAAAG 1440 AATTCATATG ACTCCCTGTT TTGGGTGCTG TACAGTTTAT ATGATGTCAC ACAGTTTGTA 1500 AAACTCACAT GCATGATCTC ACTTGATCTT CATGCCAAAT CTTTTGGTAG GCAGAGCAGG 1560 GGTGATGATT CTATTTTCAC AGAGAAGGAA 1590
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