| Tag | Content |
|---|
EnhancerAtlas ID | HS069-05507 | Organism | Homo sapiens | Tissue/cell | GM18951 | Coordinate | chr22:19717860-19718950 | 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 | CCCCATGGGC CAGGCCCTCC ATGCCTTTGC CCGCGCCAGT CCCTCCACGG GGCACGCCCT 60
TCCCGCTGTG GCTACTCCTC AATCTTAGAG GCCCCTCCCA AGCCCATTCT CACAGAGCTT 120
CCTAGGCCTG CCCTGGCCTG ACACATAGTG CAGGACAGTG TCCAGGCCTG TGTCCCCAAG 180
ACCCATCTGG GGTTCAAGCC ACATCTTGGG CCTATACACA GCCAGCTAGT GAGTGAGCGA 240
GCGAGTGAGT GAGGCCCTGC AAGATGGTCA TCTGTCTTGT CCCGCAAAGG CCAAGACAAA 300
CGCCGTGTCA GCGGCAGCCT CTCCAACCCA GTCTGTGATG GCCAGTGGTG GTCAGTGAGG 360
GCTGGGCCGC GAGGCTCACA GCTCAGGCCG CACCCGCCGG TTTCACAGAC CGGCCAGGAA 420
GCTCCCAGGG CGAGGGCCTA GTCGTGTCCT CCCCATGGGC GAGCAACCCT AGGCAGGCAC 480
CAGAGGGCGC TCGCGGTCTG CAGAAAACGC TGGCTAAGGG GGGAGCGCGG AAAGAGGTGG 540
GCACTGTGGG TGCAGACAGC TGGGGTCCGC GGAGAAACGA AGGCCTGGAG CGGGGGCGCT 600
GGGTTGTCCA GGCTGGCGGC GAGCTGCACC GAGTGGGACG GGCAGGCTGC CCCTAGTGAG 660
GGCGGGGAGG GTGTCGCCGC GTGGCGGCTG ACAGACGGGG CGGGATGAGC GTAGCCCCCG 720
CCCCTGCCCT GGTGCACTGA CAGCCTGTCA GCCGGGAAGA TAAGGGACTT CTTCCGCTGG 780
GCGTGGGGTG GGGGTCAACC CAGGTGCGCT GTCCCCCTCC CGCTGGTGTT TGCTCGGTAA 840
ACACTTATTG GGCCCCGGGC TGTGCACACC GCCGCGGGGG AGGGGCGGGC GACCTGAAGG 900
CCTGGACTCC ATGGCCTCTG CCAGGGATGC CGGGTCCATG GGCCATCAAT GATGCAGGAA 960
AAGAGGCTCT GTCACCTCTG GCCCCGCCTG GAGAGAGTTG CCTGTGGGGT CCTTCGTGGG 1020
CCCCCTCCAG CCTGGGGTGG CCCTAGCCTC AGCTTCAGAG CTGGGCTGAC CCCCGACTAG 1080
CCGAGGCATT 1090
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