| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13611 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr2:97222160-97223120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:97222209-97222227 | GGAAGAAAGAAAAGAAAG | + | 6.04 |
| | | 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 |
| GH02I096556 | chr2 | 97222117 | 97223446 |
| Enhancer Sequence | CCATGCACTC CAGCCTGGGC GACAGAGTGA GACTGTCAAA AAAAAAAAAG GAAGAAAGAA 60
AAGAAAGAAA TCAGCACGTG CTACACATCA GGGCTCCCCC CGCCCCCAGC CAGGGGTCAA 120
TCACCTAACA GCACGCACTG CCGACTCAGC TCCAACTGCC TTCTCTCCCT GGGGTCCCGC 180
TTCAGGATGC ATTGTGAGGG GAGAATCTTA TCTGAGGCCT CTGCTTACCC GGTAACCTCT 240
GAGGCTGTTA CCTCAGAGGA GGTGTGTCTT CCGTAGACCA AGACAGTAGC TGCTGTGCTG 300
GGTGACGCCA GGTGCATACC CTTCTCTTGG CCTCCATTCC CTCACCTGTG ATATGGAAAT 360
GAGTCACTCC TACCTCAAGA GTGGTGGGCA TTTAGTGAAA GTGCTCTGTA AACTAAAGTT 420
CTGATGAATG TGGATCATCA CCTCCTTCCC CACCAGCAGT TCTGCTCTAC CAGCCTGACC 480
GCCCCGTGCC CTGCCCTTTA CCTCACTGCT TTTTAACATT CCCGCTCTCC CGCCTGGCTT 540
CTGACTCACA GTCACACTGA ACTTTGGATC CTGTCAGCAT CTGAGTCAAG TATGGCAAGT 600
CACTTCCCCC CAGGTATCAA CTTTGACTGA TGGTGGCTGT CTGCAGCTTG GGGCTGACTC 660
AGTGTGACAG TGATGCAATT GATTAGTAAT GTCTGCCAAG GCCACAGGCA GCGGTGCGGA 720
GGCTCACCAG CCACTTAGTT GCCATCTCTG TCTACATGCA TGATGATCTA ATCGTGCCTG 780
ATGATGGTCT GTCTGATGTA GGTCCTGACC TCACTGCCAC ATCTTAGCCA CAGCTCCTGT 840
GCAGAGCTGC CTAGTTTCTC TCCCACATGA GCAAGGGTTG TGGAGGAGCA GGTCTTGGAT 900
TGGGCAGTCA AATCCTTGGC CTTGAGCTAC AGAGTTTGAT CCCTGGGTAG TCGTCAGGGA 960
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