| Tag | Content |
|---|
EnhancerAtlas ID | HS099-20874 | Organism | Homo sapiens | Tissue/cell | HSMMtube | Coordinate | chr7:101257650-101259100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:101257940-101257961 | GAGGGAGGGGTGAAGGGGAGG | + | 6.25 |
| | | 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 |
| GH07I101614 | chr7 | 101257374 | 101258941 |
| Enhancer Sequence | GTCACAGTTT CCAGCTCTCC AAGCCGGGGA CTTTTCACAG ACTCTGTTTC AACCAGAGCC 60
TCCACCGTGG CCTGTCTGGC CTGCCTGGCC TGCAGCCACA GATCCAGGTC CCATGTCCCA 120
AGGCAGTGCC TTCAGTTCCC AAATTAGGTC CCCAAAGGGT CTTCCCAGCC TTGTCCTTGC 180
ACTGGTGAGA GAGAAAGTGG TTGACAGTAG AGGGAGGGCT TGGGGTTACT CCGGGGGTGA 240
CTCTGATGCC TCCCCAGGTC CCCAGGATGG AGGTAGGAGC CACAGACCCC GAGGGAGGGG 300
TGAAGGGGAG GACTGTGGAC TGCAGCAACC CTCAGCATCC CCTCCCCATC CCAGGGGAGT 360
ATGTGACTCA TGGTCTTGGA GTTGAGAATG TGTGAGACGG GACAGACCCT CTCCACCTCC 420
ACCCCTGCTG CGTCTGCCCT CTCCCTTTGA GATGCGAGAA TCTCAAAACC AGCAAAACTA 480
GCCTCAAAAT GAAGGCTGGC AGCATTACAG TAATTGATCA GGAAGCCTGG GCCTGGGGAG 540
GAATCTCACC TGCCCCAGGC CACCCTCAGG TCCAGCAAGG TTCTGAAGGG ACTGCGTCGG 600
CACAGCTCAG AGGTCAGCCC TGAATCTTGG GTCCTGGGAA GGCTGCCACT CCCCCGCCCA 660
CTCCTGCCTG CAATTCTTGG CTCTCTGTTC CCTTGCTGTC ACTGGGTGGG GCACCCCTAC 720
CCTCATGATG GCAGCCCCGG TGCCTGCCAG ACAGCTGCCT GCAGCCACTT CCCCTTCATG 780
CATTCCAAGT GAGCTGGTCA CTTTCCCCAA TCCTTACTGC CCTCTTGCCC GAGGCGGTGC 840
TGGCTACGAT CTGGCTCAGT CCTCTCCCCA GACCCTGGAT CCTATGGGCA CTGGCCCCTG 900
GCTCTTTGCT TATCTGTCCG CCCGACTCCA TCTCGACGGC CATGACCCTC CTGGGAGCTG 960
CAACCCTCTC CTCTCCTTCT CCAGGCTGGC CTCCATGGTG TCCTTGCCTA ACTCCTCCTC 1020
AGGTTCTCCC ATGCTCCCAG GGCAGACGCA GGGTCCAGGG GCTAGGGTGT GAGCGCTCCC 1080
CCAGAGGCCC CGCCTGCCGC TCTGTGCTCA GTCTCCCCTA CACCACCTCC ACCCGCACCC 1140
TCCAGCTGCA GCCAACTCTG AACAAACATG CACATGCCAA GCCCTGGCCC TCCAAGCTCT 1200
CTGTTCCCTC ATCTAGAATG CTGTTCCCCC CCTAGCCTGG GCAACCTGCA GTCATTCTTC 1260
AAGATCTGCC TTTGCCCCCA CACCCACCCC ACTAGGAAGC TCTCCTGGAG TGACCCACCA 1320
CTTCTTCTTT TTTTTTTTTT TTTTGAGACA GTCTCACTCT GTCGCCCAGT CTGGAGTGCA 1380
ATGGCGTGAT CTCGGCTCAC TGCAACCTCC ACTTCCTGGG TTCGAGCGAT TCTCCTGCCT 1440
CAGCCACCAG 1450
|
| |
|
|
|
