Tag | Content |
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EnhancerAtlas ID | HS049-05413 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr22:46518050-46518980 |
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 | TGGCTCCTAG GTGTGAACCC CAGACCTGGT CTCATTTCCT TGCTATCAAG AGTGAGGCCA 60 CTGTCTCCTA CAAAGATGCT GCCGAACATG GGCCCTGGGA CCCATGCTGG GGAAGCAGGC 120 GGGACTTGCC AGTGCTCATG GCTCCCAGGC CTTGGCGTGG CCAGGGCAGG TGCACCGAAC 180 CTCAGGCGCT GGGCTCAGTC CTCCGTCCTT GCATGGCCAG GCCCCCACAT CTCCTAAGTC 240 ACTTAAGCCC AGCTGCAGGC GCTGGACAGG CGTCAGGAGC CCTGACCTCT GCCCCTACTC 300 CAGGCCCTGC CTATCTGAGG GACCTGGGGA GCTCCTACCC CTCCCTGGCC TCAGTTTCCC 360 CAAGCTTACA GGAGGACATT GAGGGTCTGG GGATGCTTTC CACACGGTTC TGGTAGCGGC 420 GGCTTCTGGC TTGACCACCA GGTGGCGCCT GGTGCCCAAT GAAGCACGTG GGGCTGGGAA 480 GGGGCGGCCG CGTGGACACC GCCCCGCTGA AGAATCAGTG TCCGGGAGGC CTGGCCGTCC 540 CCACACCGGC CCGAGGCTGA GCGGCCCTCG GGTCAAGAGC ACAGAGGTGG TGGGGTGGGT 600 GCGCAGTGTT TCCAGCACCG GCCTGGCCAC CATCGCAGGG GGGCATCTCC GGCTCGGACA 660 GCCATATCCC CCCCGGGCGG GCACAGAGCT GGGTACGGCT GGGGGCTGTG GGTGGAGGGG 720 TGTGTAGGAG GCCAGCCCCT CACCCCTCCA GTGGGGTTGC AGGAGTTCTG CCAGGCTGGG 780 GTCTCACCCC ACCTCCCTCT GTTCTCGCTT CCACTTAGCC CTGGGCTCTG CTATCCTCTG 840 CCTCTCCCAG CCTCAGTTTC CCCATATGTA AAACAGGTAA TAATCCCACC CCTTCTGTGG 900 GTGGGTGAGG CTGGCCACAG GCCAGGCCAG 930
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