| Tag | Content |
|---|
EnhancerAtlas ID | HS111-01496 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr14:90167750-90168700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr14:90168049-90168059 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr14:90168054-90168064 | GGGGCGGGGC | - | 6.02 | | RFX1 | MA0509.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | - | 6.21 | | RFX1 | MA0509.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | + | 6.22 | | RFX2 | MA0600.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | - | 6.44 | | RFX2 | MA0600.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | + | 6.4 | | RFX5 | MA0510.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | - | 6.82 | | RFX5 | MA0510.2 | chr14:90167991-90168007 | CGCTGCCATGGCAACG | + | 6.92 | | ZNF740 | MA0753.2 | chr14:90168012-90168025 | CCGCCCCCCCCCC | + | 6.64 |
|
| | 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 |
| GH14I089700 | chr14 | 90167226 | 90169650 |
|
Enhancer Sequence | CAGACAAACT GGAAAGTCTC CAAGCTCTCA GTCGCCCCAG TCGGCGGGGG AGTGAGTGGG 60
GCCGACCGGC CTTGCGGCCC TGCCACCTTT CGGGGCGACT CGGTTTCTCC ACTGACACCC 120
CCGGGCGCGA GGTCTGGTCC ATCCCGGAGT GGGAGCTAGG CAGGGACGCC ACCTGGCAGC 180
CCACTCTGGG CCCCTGGCCC GCGTTTCCCG CAGGCGCCGG CGGCGTCGGG CGCGGCCGCC 240
GCGCTGCCAT GGCAACGGCG GTCCGCCCCC CCCCCGCTTC CCGGCGCCGG CGCGCCAGCG 300
GGGCGGGGCG GGGCGGGCGT TGCTAGGAAA CCGGCGGCGG GCCGCCTCCG CGGCGCGGTC 360
TCTCGGCTTC CACCCTTCAC CTACTTCCCC TGCGGGGCCG GAGTGGGGGA GGGTCGGGGG 420
AGGCCATCGG GAAGCCACGT GGTGGCCCGG GGCCTCGCGG CTCATTCTGC GTTGCGCCGT 480
CCCTTCCAGG TCGAGTTGAC GGCCTTTTCC CCCTTGGCGT ACAAGTATTG AGTCCCGCGC 540
CCTGGGAGGG AGACGGCGCT CAGCAAATTT AGATGAATGC AACGCTTCAA CGTGGGCTCT 600
CGACCTCTGG TCCCCCATCC CCTGCCGGCT CTATTAGGAC AATGAAGTCC CCAAACTCCA 660
CTGGAGGGTT CTTCACCCAC TCTTCTTCCC CTCCAAAGGA ACCATCTCTT GAACTTCACG 720
AAATCCAGGA GCAATGCTAA GCGTTTTGTA TACATCACCT CATTTTCAAT CCTGTGAGGT 780
GGGAGCTGGG AACTTCATTT TAACAGGAAT AAAATGTGGC CTACAGCTGG TTGGGGTGGA 840
GCCAGGACTT GAAGTCCAGT TGTGCTTATT AACTTCAAGT GTCTGCCTTT TTATAATGCT 900
CAAGTTCGTC CTCTCAGCTG CCTCTTGGCT AGCCCAGCAT CCCCCTTTGC 950
|
