| Tag | Content |
|---|
EnhancerAtlas ID | HS052-08067 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr12:2892980-2893990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:2893344-2893363 | TGCTGCCCTCTCCTGGCAA | - | 6.62 | | Zfx | MA0146.2 | chr12:2893013-2893027 | CCGGCCTCGGCCTC | + | 6.28 |
|
| | 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 |
| GH12I002784 | chr12 | 2893167 | 2893436 |
|
Enhancer Sequence | ACTGATCTCG AACTCCTTAC CTCAAGTGAT CCGCCGGCCT CGGCCTCCCA AAGTGCTGGG 60
ATTACAGGCG TGAGCCACTG CGACTGGCCT CTGCTGAGTG TTTTCTGATA CCCCTCCTGG 120
GAACCCCACA CTCCCCTGAA GAGCCTTCTG CCCCAGCGCC TCGCCCCGCT GGTCCTGTAT 180
GTTTCCATGG CTGCCTCGCC CTCTTAGACC ACAGCCTCCT GCAAAGTAGG GCCCCGTATC 240
TCAGTTGGCT TTGCGCTCCC AGTGCCTGGC ACAGAGCCTG GCTCCCATGA GCACTCAACG 300
ACCCTTGAAA ATTGACCGGA ATCCCGGACA GCGCCGAGGT AGCGCGGGGA ACGGGAGCGT 360
GATCTGCTGC CCTCTCCTGG CAATGTGAAG CATTGTCCTA AGCACAGACA CTTCCCTCTC 420
CGCTGTACAA AAACAACTGC AGGATCGGGA AGCTGGAAAA GGAGCTGATG GAGGATGGGG 480
GATATGGATG CTGTCTAAGA GACAAACTGG ATTGAGGGGT TGCTGAGACT CTGCCATCTC 540
CCACACTTTT CCCACGTTCG TGGACGCAGG GGCGAGGTGA GTGCTTTCAA AGGAGGATGC 600
ATCCTCAGAG AGGCTCTCGC TCCCCCCATC AAACCCTATA CTCTTGGATG AGATCTCGCT 660
TGTCAATATA TGCGGTTGCC ATGTTGTAAC TATCACTGCA CCTTTAATTC ACTTCAGTGA 720
GCGATCACTG AGTTTTTTCC ACCATTGTTG TAAAATTTGT TTTGCTCTTG TGTGTAAAAA 780
GACTGTGAAT TTAACCACTG GCTTCTCCTG ATATTAACTC GGCTTTCTAC GGCTGGGAGG 840
TTGTCTCTGA CATTCTGGGT TTCTCAGCCT TCTGTCAAAA TCCAAATACA GTCAGTCCGC 900
AGTATACGTG GGGGACTGGC TCCAGGACCC TCCCTTGAAG ATACTAACAT CACAGGTGCT 960
CAAGCCCCTG ATACAGAATG GCACAGCGTT TGCAGACAAC CTATGCACAC 1010
|
