| Tag | Content |
|---|
EnhancerAtlas ID | HS095-28378 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr7:101257930-101258920 | 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 | CACAGACCCC GAGGGAGGGG TGAAGGGGAG GACTGTGGAC TGCAGCAACC CTCAGCATCC 60
CCTCCCCATC CCAGGGGAGT ATGTGACTCA TGGTCTTGGA GTTGAGAATG TGTGAGACGG 120
GACAGACCCT CTCCACCTCC ACCCCTGCTG CGTCTGCCCT CTCCCTTTGA GATGCGAGAA 180
TCTCAAAACC AGCAAAACTA GCCTCAAAAT GAAGGCTGGC AGCATTACAG TAATTGATCA 240
GGAAGCCTGG GCCTGGGGAG GAATCTCACC TGCCCCAGGC CACCCTCAGG TCCAGCAAGG 300
TTCTGAAGGG ACTGCGTCGG CACAGCTCAG AGGTCAGCCC TGAATCTTGG GTCCTGGGAA 360
GGCTGCCACT CCCCCGCCCA CTCCTGCCTG CAATTCTTGG CTCTCTGTTC CCTTGCTGTC 420
ACTGGGTGGG GCACCCCTAC CCTCATGATG GCAGCCCCGG TGCCTGCCAG ACAGCTGCCT 480
GCAGCCACTT CCCCTTCATG CATTCCAAGT GAGCTGGTCA CTTTCCCCAA TCCTTACTGC 540
CCTCTTGCCC GAGGCGGTGC TGGCTACGAT CTGGCTCAGT CCTCTCCCCA GACCCTGGAT 600
CCTATGGGCA CTGGCCCCTG GCTCTTTGCT TATCTGTCCG CCCGACTCCA TCTCGACGGC 660
CATGACCCTC CTGGGAGCTG CAACCCTCTC CTCTCCTTCT CCAGGCTGGC CTCCATGGTG 720
TCCTTGCCTA ACTCCTCCTC AGGTTCTCCC ATGCTCCCAG GGCAGACGCA GGGTCCAGGG 780
GCTAGGGTGT GAGCGCTCCC CCAGAGGCCC CGCCTGCCGC TCTGTGCTCA GTCTCCCCTA 840
CACCACCTCC ACCCGCACCC TCCAGCTGCA GCCAACTCTG AACAAACATG CACATGCCAA 900
GCCCTGGCCC TCCAAGCTCT CTGTTCCCTC ATCTAGAATG CTGTTCCCCC CCTAGCCTGG 960
GCAACCTGCA GTCATTCTTC AAGATCTGCC 990
|
| |
|
|
|
