| Tag | Content |
|---|
EnhancerAtlas ID | HS145-16508 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:14377470-14378700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | + | 7.52 | | RFX1 | MA0509.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | - | 7.5 | | RFX2 | MA0600.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | - | 7.58 | | RFX2 | MA0600.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | + | 7.66 | | RFX5 | MA0510.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | - | 7.75 | | RFX5 | MA0510.2 | chr3:14377756-14377772 | GGTTACCATGGTAACA | + | 7.7 |
|
| | 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 |
| GH03I014332 | chr3 | 14374089 | 14378190 |
|
Enhancer Sequence | GGGCAGCACT GAGCAGCCAA GATTGTCACC GTCCCTGTTT ACAGACAAGA AATAGAAGGC 60
TACTACCCAG GAACGTGTCC ACCTTTGCAC AGCTGTGCAG CTGTCCAGGG TCAAGTTCGG 120
GCACAGGTTG TCAATCTCCA AATGCAAGTT ATTTTTACCA CGGCTAGATT AATTACCCAC 180
CTGTCTTTTA CCTGAGGGAA CAAATGAAAC AATATATGTG CAAAGGGTCT AGTACTGTGC 240
CTGGCACAAA GGAGTGCTGG TAAGCAGTTA GGATTAGATT GACTGTGGTT ACCATGGTAA 300
CACCAGACTT GTCCACTGTC CCCAACACTG GGAACTGCAG AGTAGTGGAA ACACCTGCAA 360
GCCAGAAGGA GGGGTGTTGA GCAAGAAAGT GTGGCCTCGG CATAGAAGCA TTTACATTTT 420
TCTTTTTTCT TTTTAAATCT TGTAACGATC AGTCACACTA GAGCCCCATC CCTAGGGCAG 480
AAATTTTTTT CCCTTTGAGC CTCAGTGCTG AGTACTGAAT TACACCCCCA TCCCCGCCAT 540
GTGCCAGGCA CATGATCCTC ATTGGCCCAG GCAAGCACCA CCCTCCATGC CAATTTCCTT 600
ATTTACTCTT CTCTTTTCCT GTTTGCCAAT GCAGGTGACG AACTTGGCCA GCACAGGTGA 660
CCAGTCTACA GGGTGGAATG CCTGCCCTTT TGCACGCATT CTTGCAAAAT GCATAAGCTT 720
GTATTTCTCA GTAAACTTTT CAAAGTAAAA CATTCATGCA GAAAAAAGCA CAAATGACGC 780
ATGTAGAGCT TTATGCATTT TCACAACCTG AGCACACCCG TGTCACCCAG AATGAGAAGC 840
AGAATATAAC GGGCATTGTG GAAGCCCCCA CATGCTCCTT CCCCCAAGGG GGTCACTCCC 900
CTGACTCTGA CTCCAGAAAG CAGAAGTAGC TGTCCTGTGC TCTATACAAA TGGCATCCTG 960
CACCATGTAC CCCTTGGTGC TTGGCTGCTG TTGCTCAACT GCACATCTGT GAGATTCACC 1020
CAGGTGGTTG TGTCTGGTTT GCTCTGGTTC GTTCGCTCTC ATGCTGTCAC ATATTCCCTT 1080
GTAGAAAACT ACCCCAGGCC ATTTGCCCAG TCTCCTGTTG TTAGATGTGT GGGTTGTTTC 1140
CAGCTTGGCG CTATTACAAA CAGGGCTGCA CATTCTGGAA CAAGTCCTTC GGTGATCATA 1200
AGCACACGCT TCTGTTCGGT AAACGGCTAG 1230
|
