Tag | Content |
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EnhancerAtlas ID | HS026-07535 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr12:19048600-19049740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr12:19049324-19049339 | AGTTCTGTGGAAAAA | - | 6.16 |
| | 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 |
GH12I018896 | chr12 | 19049081 | 19049190 |
| Enhancer Sequence | AGGGTGTCCG AAAACCCCTG TGGGAGGGTC TCACCCAGTT GGGTGGCACG GGGACCGGGA 60 CCCGTTTAAT GAAGCACTTT GACTGTCCCT TGGTGGAGCG GGTGTCCTTC ACTGGGGTCA 120 TCCCACTCGT CTGGGCTGCC CGGATTCCTC AGAACTACCC AGAGGAAAGG CTACGTCTGC 180 TGATCTACAG AGAATGCAGC CAACCCTCCC CTTAGGGGCT CAGGCCCATG GAGATCAGGG 240 TTCTGTCCCT GAGCCCCTGG CTGGAGTTGT TGGAGTTCCT GAAGGTAGGC TCCACCCAGT 300 GAGGAAGGAT GGGTCAGGAT CAGGCCTGAA GAGATGCTGT GGCCTGAATC TGCCACAGCC 360 AGTGTGTTGG GCTGTGGGGG ATGCCTCTTG GGACCAAGTT GTCCAGCCTC CCTGGCTCCA 420 GCCGGAAAAA AGCATGGCCT GGAGCTATAG AGATGGCTGC CGCCCTTCCC CCGCCCAGGG 480 AACTCAGCGT GTTAGGCAGT TATCAGTCCC AGTGTTGGCT GCTGCCCCTC CCCCAAGGAG 540 CTCCAAGGGC TTAGACAGCA GGCAGCCACA GCTGTGGTGC TCATCGCCCC TCCCCCTGGG 600 AACTCGGCAG CCTTAAGCAG ATTCTAGCTG AGAGACCATT GAGGATCTGC ACGGCTCCAG 660 GGTCAGAATC CTAGGCCCCA GTGGCGTGGG TTTGCGAGTG GGATCTTCCG TCCGTGGGTT 720 GCACAGTTCT GTGGAAAAAG CACGGTTTCC CACGGCTGGG TAACACTCTC ACTCACCAGC 780 TCCCTTGGCT GGGGGATGGG GGGCTCCCCT GCCCTGTGTG GCTCTCAGGT GGGCCACGAC 840 ACCACATTGC TCTTCTTTCC TCTCCATGGA TCACACTAGG CACCTAGTCA GTTCTGATGA 900 AAGAACCTAT ACCTTGGTTG CCAGTGCAGG ATTCACAGGC TATTATGGCT CTTCAATGGG 960 AGGCTCTGAT CGCTGCTGCT TCTAGTTGGC CATCTTGGCC CCGCCCTGAT ATTTTTTATT 1020 TTCTACAATG AACACATATT GTTTGGAAAA TGTATTTTAG AGCATTCTAA GTAATCAAAC 1080 AACTATCATC CTATTTAAAA AGGACTAAAT TAATTTCATA TTTTTTACAT CCTCAAACCC 1140
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