| Tag | Content |
|---|
EnhancerAtlas ID | HS098-51873 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:44265000-44266110 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr7:44265179-44265194 | GGCACCCAGGGTGGA | + | 6.7 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr7 | 44266048 | 44266102 | | chr7 | 44265119 | 44265222 | | chr7 | 44265366 | 44265766 | | chr7 | 44265932 | 44266034 |
|
Enhancer Sequence | GCCTCCCTCC TTGAGTTCTG GTCGCCCAGG CACCCCGACC CTATCAGCAT CAAGAACCTG 60
GCCTCTCCCC TCAGCTGCTT GCCTCTGATC CCCTCAGTCA ACCCCTGCTG GGGGTCCTCA 120
GCCGACCACA GAAGCTCTGG GGGTGAGTAC CCCTCCAGGG GCTGCCCCCT GCTCTCTCGG 180
GCACCCAGGG TGGATCCAGT GCCCCTTTGA GCCTGCAGCC TGCATCCCCC TCCTCGAGCC 240
GCTGCTCCTG TGGGTTCACT CTCCCCACAC CCTTCTGCCC TGGCCGCCTG CAGCAGCCCC 300
CAGGCCCAGC CTGCAGAGGG GACGGTGGCA AGCAGACCCC ACCTGTCCCT CAAGTACTTA 360
CCTAGCCACT GCCCTGCCAT GCCGAGCCCG TGGCCCAGCA GCCTCTTCTC TAAGAGTATC 420
TCCACACCAC CCCCAGTCTG GTGTCTCCCC ACAGGTGGGG GTGGCAGCAG CCCTGGGATG 480
TCATCCATCC CTGTAAGTGA TACTGCGGGT AGTCGGCAGA CAGACCGGGA GGTGGCCCAG 540
CCTGGCTCCT CCCTGGCCGG GGAGGCTGCC CAGCCTGTGC TTCCTGTCCC GCCCGCTCTG 600
TTTCAGCCTG GCCCCAGCTG CCCCCCAGAT CCGCGCCTCC CGATCCCCAC CTGCTCCCTG 660
CTGTCTGGAC TTGGACAGCT CTAATGCTAG AGCGTCTCAG GCCGGGACTG ACACTTTTCT 720
GTCCCGGCCC AGCAGGTCCA CCTTGACCCA AGCCAGCAGC TCCTGGCGTG CTAGCCCTTG 780
CCACACGCGC AGACCCTTTG CCACCCATTC CCCTCCCATC AGGAGAAAGC TGTGGACCTC 840
AGGGTTGCGA ATGCTGGGGT CGGCAACAAA CCTGCTCTTT CGGACGCTCT TCCTATACAC 900
ATATGTCATA CACACTTCAT AACCATAACC TCCATTTTCT GAGACCCAGT GGCACCTTCA 960
TGTGCTTCAA AGCAATTCCC TGGGACCCAG CAGAGGGATC CTGTGCCCCG CCCTCCTCCG 1020
CAAGAATGGC CCTTCCCAGA GCACCACTGC CAGGCTCGCA CGCCCCGAGC CCCTCCGGGC 1080
AGCCGCTGCC ACGGCCACTC AAGGTGCTAC 1110
|
