| Tag | Content |
|---|
EnhancerAtlas ID | HS060-10658 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:90167620-90168720 |
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 | CAGACGTGCG TATGCGTGTG TGCACACGCG TGCAGTCTTG ACTAGGTGTG GAAAAAAGGT 60
CCGAAGAGAT TCCAAAATCA AAAAAATTCC CTTGGCCTAC TCCGGCCCCG AAGACCAACT 120
CAGACCCCAC CAGACAAACT GGAAAGTCTC CAAGCTCTCA GTCGCCCCAG TCGGCGGGGG 180
AGTGAGTGGG GCCGACCGGC CTTGCGGCCC TGCCACCTTT CGGGGCGACT CGGTTTCTCC 240
ACTGACACCC CCGGGCGCGA GGTCTGGTCC ATCCCGGAGT GGGAGCTAGG CAGGGACGCC 300
ACCTGGCAGC CCACTCTGGG CCCCTGGCCC GCGTTTCCCG CAGGCGCCGG CGGCGTCGGG 360
CGCGGCCGCC GCGCTGCCAT GGCAACGGCG GTCCGCCCCC CCCCCGCTTC CCGGCGCCGG 420
CGCGCCAGCG GGGCGGGGCG GGGCGGGCGT TGCTAGGAAA CCGGCGGCGG GCCGCCTCCG 480
CGGCGCGGTC TCTCGGCTTC CACCCTTCAC CTACTTCCCC TGCGGGGCCG GAGTGGGGGA 540
GGGTCGGGGG AGGCCATCGG GAAGCCACGT GGTGGCCCGG GGCCTCGCGG CTCATTCTGC 600
GTTGCGCCGT CCCTTCCAGG TCGAGTTGAC GGCCTTTTCC CCCTTGGCGT ACAAGTATTG 660
AGTCCCGCGC CCTGGGAGGG AGACGGCGCT CAGCAAATTT AGATGAATGC AACGCTTCAA 720
CGTGGGCTCT CGACCTCTGG TCCCCCATCC CCTGCCGGCT CTATTAGGAC AATGAAGTCC 780
CCAAACTCCA CTGGAGGGTT CTTCACCCAC TCTTCTTCCC CTCCAAAGGA ACCATCTCTT 840
GAACTTCACG AAATCCAGGA GCAATGCTAA GCGTTTTGTA TACATCACCT CATTTTCAAT 900
CCTGTGAGGT GGGAGCTGGG AACTTCATTT TAACAGGAAT AAAATGTGGC CTACAGCTGG 960
TTGGGGTGGA GCCAGGACTT GAAGTCCAGT TGTGCTTATT AACTTCAAGT GTCTGCCTTT 1020
TTATAATGCT CAAGTTCGTC CTCTCAGCTG CCTCTTGGCT AGCCCAGCAT CCCCCTTTGC 1080
TGTCCAAACA CCCACACCAG 1100
|
