| Tag | Content |
|---|
EnhancerAtlas ID | HS047-22374 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr22:19718090-19718950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:19718333-19718352 | CAGGCACCAGAGGGCGCTC | + | 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 |
| GH22I019729 | chr22 | 19717312 | 19719321 |
| Enhancer Sequence | GAGTGAGCGA GCGAGTGAGT GAGGCCCTGC AAGATGGTCA TCTGTCTTGT CCCGCAAAGG 60
CCAAGACAAA CGCCGTGTCA GCGGCAGCCT CTCCAACCCA GTCTGTGATG GCCAGTGGTG 120
GTCAGTGAGG GCTGGGCCGC GAGGCTCACA GCTCAGGCCG CACCCGCCGG TTTCACAGAC 180
CGGCCAGGAA GCTCCCAGGG CGAGGGCCTA GTCGTGTCCT CCCCATGGGC GAGCAACCCT 240
AGGCAGGCAC CAGAGGGCGC TCGCGGTCTG CAGAAAACGC TGGCTAAGGG GGGAGCGCGG 300
AAAGAGGTGG GCACTGTGGG TGCAGACAGC TGGGGTCCGC GGAGAAACGA AGGCCTGGAG 360
CGGGGGCGCT GGGTTGTCCA GGCTGGCGGC GAGCTGCACC GAGTGGGACG GGCAGGCTGC 420
CCCTAGTGAG GGCGGGGAGG GTGTCGCCGC GTGGCGGCTG ACAGACGGGG CGGGATGAGC 480
GTAGCCCCCG CCCCTGCCCT GGTGCACTGA CAGCCTGTCA GCCGGGAAGA TAAGGGACTT 540
CTTCCGCTGG GCGTGGGGTG GGGGTCAACC CAGGTGCGCT GTCCCCCTCC CGCTGGTGTT 600
TGCTCGGTAA ACACTTATTG GGCCCCGGGC TGTGCACACC GCCGCGGGGG AGGGGCGGGC 660
GACCTGAAGG CCTGGACTCC ATGGCCTCTG CCAGGGATGC CGGGTCCATG GGCCATCAAT 720
GATGCAGGAA AAGAGGCTCT GTCACCTCTG GCCCCGCCTG GAGAGAGTTG CCTGTGGGGT 780
CCTTCGTGGG CCCCCTCCAG CCTGGGGTGG CCCTAGCCTC AGCTTCAGAG CTGGGCTGAC 840
CCCCGACTAG CCGAGGCATT 860
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