Tag | Content |
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EnhancerAtlas ID | HS065-01158 | Organism | Homo sapiens | Tissue/cell | GM18508 | Coordinate | chr12:53500320-53501940 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr12:53500681-53500692 | TCTTATCTCCT | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGGTCTGT ATTTTCATAC CTCCCACTAT TCCCAGACCA AACTGAGGGT TGGGGCTGCT 60 ATTTCTCATG GCCCAATAAC GAGATGCAGA TGAACTGGGG AGGAAGTGAG TTTTTATTTC 120 TGTAACCAGT TACAGGGAGA AGGCCTGGAA ATTATCACCA GGCCAACTAA AAATTACAAT 180 TTCCAGAGCA TATATACCTT CTAAGCTCTA CATCTATGTG TAGGTGTGCA TTCATCTAAA 240 GACATAAGTG ATTAACTTCT TTTAATCTAT AACTAAGGTC TGAGTCTTGA AGACCTTCTT 300 CTGGAGCCTC AGTAAGTTTA CTTAATCTAA ATGGGTCCAA GTGCTGGGGT GATTACCCTT 360 CTCTTATCTC CTGCTAAATA ACGGAGGTTT GGGGAGTTTC TTCAGACCCC CAGCAAAACT 420 TGTTTAATCA TGCTTTGAGG TTCAGGAAAG GCCTAGGCAA AACTCTTGGT GGGCTTTTGT 480 TACATTCCAG CCTTTGTATA AGGGCACTGG TTTTTAACAT TTAACTTAAC CACTCAGTCA 540 GTACTGAAAC AGTTGTTATG GAGGTCTGCA TTAGTGAGAC CTGCTTGTCA CAGTCCCCAC 600 TGTCAATTTA CACGATTTTT ATCATGCATG GATATTTATT TATCATGAGA ATCGCAGGGA 660 GATGGGGAGT CGTAATCTTT CTGGCTACTT CCTGCTGAGA GGGGGTCGTC GTTATGGGGC 720 ACCAAAAGCA GCAGTGGAGT GGAAGAGGTT GATTTGTTCG CAGTAGCACT CTCTGTTTCG 780 GGGCCTTGGA GGCAGCACCT GCTGAAACAT AATAGTATGT AACAGTACAT ATAAATAGGC 840 TACTGCTCTT TTCTTCTGAA GTTTAAGTTG TCTAGTCTTC AGTTTGCAGG GCTTTAAGAA 900 AGCAGAGCTT AGGTTTCAGT GATTACCAAT TAGGAAGAAT GGGGGAAAAT GGAAAAGAAA 960 GAGGAAAAAA TTGAAAACAT TATTTTGGAG ACCTGTAGCC AGAAAAGTTA GAATTTAATC 1020 CAAACTGCAG AAAATAATAA AAACTGAAAA ACATCAGGCA AGACTAGAAT TTAACAACAG 1080 ATGTACTTTT TTTTTTTTTT TTTTGAGACA GAGTCTTGGT CCGTTGCCCA GGCTGGAGTG 1140 CAGTGGCGTG ATCTTGGCTC ACTGCAACCT CCGCCTCCTG GGTTCAAGCG AATCTCCAAC 1200 CTCAGCCTCC TGAGTAGCTG GGACTACAGG CACGTGTTAC TGTGTTCGGC TCATTTTTGT 1260 ATTTTTAGTA GAGACTGGGT TTCACCGTGT TGGCCAGGCT GGTCTCGAAC TCCTGACCTC 1320 AGGCGATCTG CCCACCTTGG CCTCCCAAAG TGCTGGGATT ACAGGTGTGA GCCACTGAGC 1380 CCAGCCATAG TTTTTGAAAC ATAATTTTTC TCTCTCCAGT TTCCCATTTT TATTAAAAGA 1440 CAGATCATAG TAGGACTGGT TTGCTTTATT ATACTTGGTT TAATTATTTG TATACAGTAC 1500 AGCAAGAATA ATTAGTTTCA CATAGGCCTT TTAAATTGGC TTTGATGGAA CTTCGTTCCA 1560 TAGAAGGAAT CTGAGATAAG TCCTTTTAAA GCCGAGCCCA GCCATGGATT TGTACCAATA 1620
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