| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13478 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr2:84967970-84969150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr2:84968930-84968945 | CCTTTCTAGAGAAAT | + | 6.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 84968192 | 84968297 | | chr2 | 84968431 | 84968925 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I084740 | chr2 | 84967965 | 84969173 |
| Enhancer Sequence | TTCCACCACC TACTACTGGG GCACTCTCCA CACTCACTGC TCAATTCTGC CTGTGGGGAC 60
CCTTCTCCCC TTCCAGAACA AGCACTTTAA TCTCACCTAA GACCAAAATG CTTGCTGTGG 120
CCACCGCTGC CAGGTTACCA AACAATGGCT CTAACCTCTC AAAATGGTGT CAGCCATGGG 180
CTTGCACCTA GAGAGTGGGG AGCCCCTCTC AGGCGAGCAG CATGGACGAG AAGCTGTGAG 240
GAGTGTGGTC CACTCAAGTC TCAGTCTCAT AGCAGCTCGT AGCAAGGCAT TGGACATTGT 300
CCTAGGTATA TATAGGAGAG CCTTGGTCCC CTTTCCCTGC TTGGCTGGGT GGCAGCAGCA 360
GTCACATCAG CCCAAACTCA GGCCAAGGAT GAGGCACAGC TCAGCACTAC ATTCTCAAAA 420
TGGTGCCTTG GGCCTGAAAA CAGGGAGGGC GGATCACTGC CCAGGCAGGC AGCATGATCA 480
AGAAGCTGTG GGGAGTGTGG TTCATTCACA TCTGTCTCAC AGCAGCCTGC TACAGAGCTG 540
TGAGTATTGT CCTAGGTATG AGTAGGATGA CCTGGTCTCC CTGTTCTTCC TTAGCCAAGC 600
AGAGGCTACA GCCACATCAG CCCAAACTAA ACAAAGCATG GAGCTCAGCC CAGCATTAAA 660
CTCTCAAAAG GGCACCTTGG GCCTGGGGCT AAAGAGGGTG GGGCACCATT CAGGCAAGCA 720
GCATAAGCAG GAAGCTGTGA GAAGTGTGGT CAACTCATAT CTCAGTCTCA ACAGCAGCTC 780
ATAGCAGGGC AGCAAGTACC CTCTAGGGGG TGCATGAGTG TGCCCGTTCT CCCCTCTCCC 840
TCCCTGGAGC AGCACAGTGG CTGCAGCTGT GTCTGTAAAT CCCCAGGATC TGGGTTCTCA 900
AAATGGCACC CAGCTGAGGC TGCACCAGGC TCGGATTCCT GTGGGATTGT GTGTGGGTTC 960
CCTTTCTAGA GAAATGTCTC TGTACAATCT TTAGGCAGTT CCATATGTCA GGCACAAGGC 1020
CCTAGTGGGT CAAGGGTTTC TCCTGTAGCC AAGATCTTAA AACCCTGTTT TGGAGCTCCA 1080
GGGATTTCCC TCTTACTGTT TCCCTGCATC CAGGACCATC TCCCAGCCCA GTCAGTTCCT 1140
GGCTGCGCAA GCTAACTTGA ACCCTCTCCT TACTTACTTC 1180
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