| Tag | Content |
|---|
EnhancerAtlas ID | HS108-09107 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr12:19048520-19049620 | 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 | AAAGATAGGT GCCTGCTCAT TCTCTGGGAT CTCTGACCTC GAGAGGCACC AACCTGATGC 60
CAGTAGGGTC ACTCCTGTAT AGGGTGTCCG AAAACCCCTG TGGGAGGGTC TCACCCAGTT 120
GGGTGGCACG GGGACCGGGA CCCGTTTAAT GAAGCACTTT GACTGTCCCT TGGTGGAGCG 180
GGTGTCCTTC ACTGGGGTCA TCCCACTCGT CTGGGCTGCC CGGATTCCTC AGAACTACCC 240
AGAGGAAAGG CTACGTCTGC TGATCTACAG AGAATGCAGC CAACCCTCCC CTTAGGGGCT 300
CAGGCCCATG GAGATCAGGG TTCTGTCCCT GAGCCCCTGG CTGGAGTTGT TGGAGTTCCT 360
GAAGGTAGGC TCCACCCAGT GAGGAAGGAT GGGTCAGGAT CAGGCCTGAA GAGATGCTGT 420
GGCCTGAATC TGCCACAGCC AGTGTGTTGG GCTGTGGGGG ATGCCTCTTG GGACCAAGTT 480
GTCCAGCCTC CCTGGCTCCA GCCGGAAAAA AGCATGGCCT GGAGCTATAG AGATGGCTGC 540
CGCCCTTCCC CCGCCCAGGG AACTCAGCGT GTTAGGCAGT TATCAGTCCC AGTGTTGGCT 600
GCTGCCCCTC CCCCAAGGAG CTCCAAGGGC TTAGACAGCA GGCAGCCACA GCTGTGGTGC 660
TCATCGCCCC TCCCCCTGGG AACTCGGCAG CCTTAAGCAG ATTCTAGCTG AGAGACCATT 720
GAGGATCTGC ACGGCTCCAG GGTCAGAATC CTAGGCCCCA GTGGCGTGGG TTTGCGAGTG 780
GGATCTTCCG TCCGTGGGTT GCACAGTTCT GTGGAAAAAG CACGGTTTCC CACGGCTGGG 840
TAACACTCTC ACTCACCAGC TCCCTTGGCT GGGGGATGGG GGGCTCCCCT GCCCTGTGTG 900
GCTCTCAGGT GGGCCACGAC ACCACATTGC TCTTCTTTCC TCTCCATGGA TCACACTAGG 960
CACCTAGTCA GTTCTGATGA AAGAACCTAT ACCTTGGTTG CCAGTGCAGG ATTCACAGGC 1020
TATTATGGCT CTTCAATGGG AGGCTCTGAT CGCTGCTGCT TCTAGTTGGC CATCTTGGCC 1080
CCGCCCTGAT ATTTTTTATT 1100
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