Tag | Content |
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EnhancerAtlas ID | HS047-23152 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:46518120-46518990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:46518481-46518500 | TGACCACCAGGTGGCGCCT | + | 7.74 | NR2C2 | MA0504.1 | chr22:46518332-46518347 | TGACCTCTGCCCCTA | - | 6.24 |
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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 |
GH22I046122 | chr22 | 46517903 | 46519567 |
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Enhancer Sequence | CAAAGATGCT GCCGAACATG GGCCCTGGGA CCCATGCTGG GGAAGCAGGC GGGACTTGCC 60 AGTGCTCATG GCTCCCAGGC CTTGGCGTGG CCAGGGCAGG TGCACCGAAC CTCAGGCGCT 120 GGGCTCAGTC CTCCGTCCTT GCATGGCCAG GCCCCCACAT CTCCTAAGTC ACTTAAGCCC 180 AGCTGCAGGC GCTGGACAGG CGTCAGGAGC CCTGACCTCT GCCCCTACTC CAGGCCCTGC 240 CTATCTGAGG GACCTGGGGA GCTCCTACCC CTCCCTGGCC TCAGTTTCCC CAAGCTTACA 300 GGAGGACATT GAGGGTCTGG GGATGCTTTC CACACGGTTC TGGTAGCGGC GGCTTCTGGC 360 TTGACCACCA GGTGGCGCCT GGTGCCCAAT GAAGCACGTG GGGCTGGGAA GGGGCGGCCG 420 CGTGGACACC GCCCCGCTGA AGAATCAGTG TCCGGGAGGC CTGGCCGTCC CCACACCGGC 480 CCGAGGCTGA GCGGCCCTCG GGTCAAGAGC ACAGAGGTGG TGGGGTGGGT GCGCAGTGTT 540 TCCAGCACCG GCCTGGCCAC CATCGCAGGG GGGCATCTCC GGCTCGGACA GCCATATCCC 600 CCCCGGGCGG GCACAGAGCT GGGTACGGCT GGGGGCTGTG GGTGGAGGGG TGTGTAGGAG 660 GCCAGCCCCT CACCCCTCCA GTGGGGTTGC AGGAGTTCTG CCAGGCTGGG GTCTCACCCC 720 ACCTCCCTCT GTTCTCGCTT CCACTTAGCC CTGGGCTCTG CTATCCTCTG CCTCTCCCAG 780 CCTCAGTTTC CCCATATGTA AAACAGGTAA TAATCCCACC CCTTCTGTGG GTGGGTGAGG 840 CTGGCCACAG GCCAGGCCAG GAGGCCCAGC 870
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