Tag | Content |
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EnhancerAtlas ID | HS076-28121 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr19:10589490-10590610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr19:10590046-10590061 | CTTTTCCTGAGAATA | + | 6.01 |
| | 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 |
GH19I010478 | chr19 | 10589121 | 10590829 |
| Enhancer Sequence | ATGCCTCAGT TTCCCCCATT GTAAAATCCA AATAACAATA GCTTAGGTTT ACCGAGAGGT 60 TGTTATGTGA CAAGCACTGT TTGTTTTACG TAAATCATCG AGGTAAATGC TCACAACAGC 120 CCTATTAAGT AAGTACTATT ATTATAAAAA GGGTCACAGG CATAGGCAGG GAAGGAGGTA 180 GGGCTGGGAG TCGGAGCCCG TGAGCGCCCC CTAGAGTAGG GCTAAGGGGC GGGGGGGCGG 240 GCTACAGCAG AATAGGGACC CAGCGCACTC GCAGAACGAG GGGGGAGGCG AGGCGAGAAC 300 GAGCGGGAGT TTTTTTCCCG ACTACGATTG GCTGGTGTAA TTGTCATCAC TTGAAAAGGC 360 AGCCAATGAG AGGCGCGGTC GCCTCGCTGG TGGAAGCCGA GAGCTGAGCG AAGTGAGGCG 420 TGCGGAGCCA AAGGCGCTAG AGCGATAGCG GGAGCCCCGG ACCCCGAAGC GGTTGAGGGG 480 ATCCAGGCCT CACAACGTCT TGAGAGTGGC CCCAGCGTCG TTCCTAGTCT CTTCGGCAGA 540 CCCCAGCGTC GTCCTTCTTT TCCTGAGAAT ATCCTGACAC CAGTCGCCCG TTCCAGAAGG 600 GGACACTTGG CGTCATCCCT TTTTTTCTGA GTGACCCCAG AGTCGTCCTC ACTTCCTGAG 660 GGGGATCCTG GCGTCATCCG CCCTTCTTGA GGGGACCCTG CTGTCACTAC CCTGTCCTGA 720 TGGCCAGCAC CGCATTGTCC TTTCTTCCCG CGGGAAACCC GGACATCATC CCCTCTTTCT 780 GGCGGGGACC CCCATGCCAT TATCCCCTCC TGAGGAGACC CCAGAGCCAG AGCCGTCCCC 840 CCTTCCTCAA GGCTCCCCAG CGTTGTTTCT TCTTCCCGAG AAGGGGCCTG GTGCTGTTCC 900 CCGTTTCCAG AGTGTTTCCT ATCGTTGTCC TCCCCACACT CAGAAGGCAT CTGTCATCCC 960 CCCTTTTTCT GAGATCAGTC CCTTCCTCCT TTCCAGTTTA AGGCCGACCC CTGCAAACGC 1020 TTCTGTGGCA CCCATAGATA GAAGGCCCAA AGACCCCCCT GTGCTCCCTT GCCCCCAATT 1080 GAGCAGACGG GAAGGCAAAA GACTCAGCTC ACCCCATGAA 1120
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