Tag | Content |
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EnhancerAtlas ID | HS191-07187 | Organism | Homo sapiens | Tissue/cell | Trophoblast | Coordinate | chr11:67745770-67747280 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:67745863-67745884 | GGGGGAGGGGGGGAGAGGATA | + | 6.24 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I067978 | chr11 | 67746341 | 67746530 |
| Enhancer Sequence | TCCTAATATC CAAGAAGGCA GAGGATGGCA TTACTCCCAA TAAAGCAGTG GGTGTACACT 60 ACCCCTGTGT TATTGCCTCT AATATCCGGG GCCGGGGGAG GGGGGGAGAG GATAACATTC 120 CCTCAAATGT AGCAGGTGGT TTGACGCCCC TCGTGGTGTT GTTTTACATA TCCATCGCGG 180 AAGACAATAA TACTATTTTG ATAGTCCGAT TCATCCCCTC CACCTTTCCG GAACTCTGAG 240 GCCGGGAGGC AGCAGGCAAT TTCCGTGTGA TCCCCAATTC CTTTGCCGTC TTCTGTAGCA 300 AGTCAGCCAC AAACGCAGGC CCGTTATCTG AGCCGATCCG GAAGGGCAGT CCCAATCTAC 360 GAATCAGATC TCGAAGAAGC ACACGGGTTA CTTCACGAGC TTTCTCAGTT GTGTTGGATA 420 AGCCTCCACC CACCCAGAGT AGGTACGGCC AAGAACTAGT AAATACTTGT TACCTCCACA 480 CTTTGGCATC TCTGTGAAGT CTACCTGGAG ATCTTCTAAG GGGGCTGCTC CATAAGCTTG 540 TATGCCGGGT GGAACGGCTG GACCTTGCCT CGCTTTATGC TGTCGGCAGG TAACACACCG 600 CTGCCTCACC GTTTTGGCAA GGGCTGAGAA ACGCGAGATG TAGAAATACC GGCCTAACAA 660 CTTTTCCAGT GACTCCTGAC CTCGATAGGT GGTTTCTTGC ACAGCCAGTA CAACTGCAGC 720 TCCTAGCAGC TGTGGCGCAG CTACTCTCCA TCCTTCCTCC ATCACTTGTC CTTCCCTCTA 780 CCTGGACAAA GTCCTTTTCT TCTTTAGAAT AAGCAGGTCC AAGATCAGGT GCTTGAGGGA 840 GCAGAGGAGC TGTGACTGAT GCCTGGAAAC GGGCAGATGC TGCTTTTCCA GCCTATGAGT 900 CAGCGCGGGA ATTCCCCAAG CCCACCAAGG TGGAAGCTCG CTGGTGTCCC CTGCAATGCA 960 TAACTGCCAC CTTGTGGGGT TTCCATACTA CTTCTAATAC ATAGAAGATT TCTGGTTGAT 1020 ATTTTCTGTC TTTTACCCCA GAGTTTAATA GGCCCTTTTC TTTCTATCAC GCTCCATGCA 1080 TGTGAAGGGT TCAAAAGACA TACCGAGAAT CAGTGTAAAT GTTGACAGTC TCACCCTCAC 1140 TGAGCTCTAA GGCCCAAATG AAAGCAATGA GTTCAGCTTT CTGGGCTGAA GTGGCCTGGG 1200 GCAACGATCT GGCTTCAACA ACAGTGTCCA GGGTTATCAC TGCATACCCT GCACCTCTCT 1260 CTCCTTGGGG GTTGAAGAAG CTGCTCCCAT CCACGTATAG TTCCCAGTCT ACTGATGCCC 1320 AAGGCTGGTC CCAGAAGTCA GGTCTGCTAG AGTCAACTGA GTCCAACACT TCTACACAAT 1380 CATGCTCGAC GGGGCTCTCT GATAGCGGGA GCAAGGTGGC AGGGTGTTAC AAACTTCAAT 1440 GGTTACACGG GGATTTTCAC AGAGCAAACT TTGGTACTTG GTGAGTCTGG CATTCATTAG 1500 CCAATGATGT 1510
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