| Tag | Content |
|---|
EnhancerAtlas ID | HS047-19411 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr2:97222150-97223260 | 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 | CAAGATCGTG CCATGCACTC CAGCCTGGGC GACAGAGTGA GACTGTCAAA AAAAAAAAAG 60
GAAGAAAGAA AAGAAAGAAA TCAGCACGTG CTACACATCA GGGCTCCCCC CGCCCCCAGC 120
CAGGGGTCAA TCACCTAACA GCACGCACTG CCGACTCAGC TCCAACTGCC TTCTCTCCCT 180
GGGGTCCCGC TTCAGGATGC ATTGTGAGGG GAGAATCTTA TCTGAGGCCT CTGCTTACCC 240
GGTAACCTCT GAGGCTGTTA CCTCAGAGGA GGTGTGTCTT CCGTAGACCA AGACAGTAGC 300
TGCTGTGCTG GGTGACGCCA GGTGCATACC CTTCTCTTGG CCTCCATTCC CTCACCTGTG 360
ATATGGAAAT GAGTCACTCC TACCTCAAGA GTGGTGGGCA TTTAGTGAAA GTGCTCTGTA 420
AACTAAAGTT CTGATGAATG TGGATCATCA CCTCCTTCCC CACCAGCAGT TCTGCTCTAC 480
CAGCCTGACC GCCCCGTGCC CTGCCCTTTA CCTCACTGCT TTTTAACATT CCCGCTCTCC 540
CGCCTGGCTT CTGACTCACA GTCACACTGA ACTTTGGATC CTGTCAGCAT CTGAGTCAAG 600
TATGGCAAGT CACTTCCCCC CAGGTATCAA CTTTGACTGA TGGTGGCTGT CTGCAGCTTG 660
GGGCTGACTC AGTGTGACAG TGATGCAATT GATTAGTAAT GTCTGCCAAG GCCACAGGCA 720
GCGGTGCGGA GGCTCACCAG CCACTTAGTT GCCATCTCTG TCTACATGCA TGATGATCTA 780
ATCGTGCCTG ATGATGGTCT GTCTGATGTA GGTCCTGACC TCACTGCCAC ATCTTAGCCA 840
CAGCTCCTGT GCAGAGCTGC CTAGTTTCTC TCCCACATGA GCAAGGGTTG TGGAGGAGCA 900
GGTCTTGGAT TGGGCAGTCA AATCCTTGGC CTTGAGCTAC AGAGTTTGAT CCCTGGGTAG 960
TCGTCAGGGA GGCTGCCTCT TGGGAGAAAC CCAGGTAGGC TGTCCAAAAA CCAGAAAGGT 1020
CTTTCCACAG CAGCTGGAGA GGGATGATCT AGGATCCACA CCAATAGGAT AGAGTATAAG 1080
TGGAACAATT CTGGTGTCAT TTGTAGAGTA 1110
|
| |
|
|
|
