Tag | Content |
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EnhancerAtlas ID | HS047-23213 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:50936680-50937340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:50936797-50936816 | CAGTGCCCCCTTCTGGAAA | - | 6.79 | EWSR1-FLI1 | MA0149.1 | chr22:50936898-50936916 | CCTGCCTTCATCCCTTCC | - | 7.36 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I050498 | chr22 | 50936578 | 50937500 |
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Enhancer Sequence | ATCCTTTTGT GGCTTCCCAA AGTGCTAGGA TTACAGGAGT GACCGCTGTG CCTGGTCGTC 60 TCACCTTCTT TTGACATGGA GCCCCAGCCT TGGGAGGCAG ATGCTGAACC GTGTCCACAG 120 TGCCCCCTTC TGGAAATTCT CCACAAGCCA AGGTTTTGGA CAGCTCCAAT GTCTGGGGCT 180 ATGGCATTTC AGGCGGGAAG TCTCTGCAGA GAGCAGTACC TGCCTTCATC CCTTCCTAGA 240 TATTAATTCA CTTTCAGACA CATACTGAGC AGCTAGTGTG AGCTGTTACG GTGCTGGCTC 300 TGCAGACAGA GCTGCAGCGA AGACAGACGC CAACCCCACC CTCACACAGC CAATCCTGTG 360 CTAGTTTTTT CTGTAGAACC ACCACTGGGT TTCCAGTTGG TCTGGGTTAT CTGGTGAACT 420 CAGAGACTTT CGCTGTCTTC TGGACACTCC ACAACAGTCC AATCACCTGC GGGGACCCTG 480 ACCTCTGCAA ACCTCCGGGG GGTGGTTCCT TGGTTGGCCG CCCTCCTCTG ACGGCTCCGC 540 CTCCCTGCCG AGCCCTGGGA TCGTCCTCCC TGGCTCCTGC CTTCTCTCTC ATAGGATCTC 600 ATTTGTTCTG ACACACTTAT TCTCAAGCCC AGTAGTTACT CTTGAATATT GCTTATAGAG 660
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