| Tag | Content |
|---|
EnhancerAtlas ID | HS150-02769 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr12:19048460-19049600 | 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 | TGTATTCATC TGGTTTGCTC TTGTGCCTGG AGATGTCAGT CAAGGAGGAT AGAGAACAGC 60
AAAGATAGGT GCCTGCTCAT TCTCTGGGAT CTCTGACCTC GAGAGGCACC AACCTGATGC 120
CAGTAGGGTC ACTCCTGTAT AGGGTGTCCG AAAACCCCTG TGGGAGGGTC TCACCCAGTT 180
GGGTGGCACG GGGACCGGGA CCCGTTTAAT GAAGCACTTT GACTGTCCCT TGGTGGAGCG 240
GGTGTCCTTC ACTGGGGTCA TCCCACTCGT CTGGGCTGCC CGGATTCCTC AGAACTACCC 300
AGAGGAAAGG CTACGTCTGC TGATCTACAG AGAATGCAGC CAACCCTCCC CTTAGGGGCT 360
CAGGCCCATG GAGATCAGGG TTCTGTCCCT GAGCCCCTGG CTGGAGTTGT TGGAGTTCCT 420
GAAGGTAGGC TCCACCCAGT GAGGAAGGAT GGGTCAGGAT CAGGCCTGAA GAGATGCTGT 480
GGCCTGAATC TGCCACAGCC AGTGTGTTGG GCTGTGGGGG ATGCCTCTTG GGACCAAGTT 540
GTCCAGCCTC CCTGGCTCCA GCCGGAAAAA AGCATGGCCT GGAGCTATAG AGATGGCTGC 600
CGCCCTTCCC CCGCCCAGGG AACTCAGCGT GTTAGGCAGT TATCAGTCCC AGTGTTGGCT 660
GCTGCCCCTC CCCCAAGGAG CTCCAAGGGC TTAGACAGCA GGCAGCCACA GCTGTGGTGC 720
TCATCGCCCC TCCCCCTGGG AACTCGGCAG CCTTAAGCAG ATTCTAGCTG AGAGACCATT 780
GAGGATCTGC ACGGCTCCAG GGTCAGAATC CTAGGCCCCA GTGGCGTGGG TTTGCGAGTG 840
GGATCTTCCG TCCGTGGGTT GCACAGTTCT GTGGAAAAAG CACGGTTTCC CACGGCTGGG 900
TAACACTCTC ACTCACCAGC TCCCTTGGCT GGGGGATGGG GGGCTCCCCT GCCCTGTGTG 960
GCTCTCAGGT GGGCCACGAC ACCACATTGC TCTTCTTTCC TCTCCATGGA TCACACTAGG 1020
CACCTAGTCA GTTCTGATGA AAGAACCTAT ACCTTGGTTG CCAGTGCAGG ATTCACAGGC 1080
TATTATGGCT CTTCAATGGG AGGCTCTGAT CGCTGCTGCT TCTAGTTGGC CATCTTGGCC 1140
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