| Tag | Content |
|---|
EnhancerAtlas ID | HS003-47325 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr9:117313910-117315340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr9:117315320-117315337 | TCAATTCCTAGAAAAAA | - | 6.15 | | KLF4 | MA0039.3 | chr9:117314906-117314917 | CCACACCCTCC | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 117314027 | 117315316 | | chr9 | 117314293 | 117314590 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I114550 | chr9 | 117312897 | 117316577 |
|
Enhancer Sequence | GTCTCAAACT CCTGGCCTCA AGCGATCCTC CCACCTTGGC CTCCCAAAGT ACTGGGATTA 60
CAGGCGTAAG CCACTGCACC CAGCCTCACA CACTCTGAAT TATGTGGGGT GGGGTCCTAA 120
CTAACTCACT GAGCCTCCCA AGCCAAACTC AACCGCAGCT ATTCTCCATC CCAAAAGTGG 180
GAAGGAGCTG CCTATTGAGG GAGAGGTGGG CCTTCTTCCC ATTCTCCATC TTCACCTACA 240
AGCTATCCAC TATGCAGGGG CTGCTTGGAG TTTTAACACT GATCCAGTAG CTCACCTGGC 300
TCTTGCCTAA GTAAATTACC TTTCTCCCTT GGGGTTGGGG AGGTGTGGGT CTGGGTGGTG 360
GGCACTGGCT TTACCTCCAG CTCAGCTCCT TCTCTTTGGT CCCGCCTCCC AGGGTTTTAT 420
GTGTCCATAT AACCACTGAC TCAGGGTCAG CTTTTTCCAG TCTAGTGCGT CAGCACAAGT 480
GAGTGATAGA GCCTGAAGGC CATTACTCAG GGGAGGATGG TGGTGAGTCA TCACGAGAGA 540
CTCCTTCCCT AGTCTGGCCA CTCTGCTCCA AGCTGTGCTG GGAGACAGAG AATAATAACA 600
CCTTTTGGAC TGGCCTTTTA AAAATAGAAA CAATGGAGTC TGTGGCTTTA GGAGGAGAGG 660
TCCTGGGAGT CAGAAGCTCA GTCCTGCTAG CTTGTCATTC CTTGGAGGAT GCTGGCTACT 720
ACTTTGCCCA CCGGTAATTG AGGGTGTTGC CCTTGGCCAT TTGGGGTGGG CTTTCTGAGT 780
CTTTTAGAGG TTGCAGAATC TTACATGTGC TATAAACCAA GGACACACCC TACCCAAAAT 840
TTATATACAC ATTCATGCAA AATGTGTCAT GCAATCTCAG GGTTTCATGG AACCCGCTGA 900
CACCCAGTCA TGGGCTCCTG GCAATGAATT CCTGATCTCT GGGCTCTATT TGTCTAATAA 960
TTCTATGAAA TATGTTTCTT CCAAATTCTA TACTCCCCAC ACCCTCCATA AAATCATTTT 1020
TTAAAACATT TTTTTGTCTT CATTTATTTA AGAAACATTT ATTGAGTGCT ACCCACTCCT 1080
GTGGAAAAGT CCAGTATTGC TGGGAGAGAG AAAAGAGGAA AGGCCTCCAC CTGGGGTGTC 1140
TGCAAGAAGG GCACGGACAT TGGAGGTGCA GATGCACTGA AGAACTGATG GGCAAGCAAG 1200
ATAGATGGTC AAGGTTGGCA CTCAGAGGGG TGACCGTTAC CCGCCCCTCC ACCCCTTTCC 1260
CCGGCTTGTT GTAAGGGCAA GATCCTTCCC TCAACTCCAG AAATGAGTCA TCATGTGTCT 1320
ATGCCAGCCC TGGCAATCCC ATTCCCCTTT TTGAGTGTTT CCAACCCCAG TTTTGGACAA 1380
AGAGACCTAA GGGAAGTCAG TGTGCGACCC TCAATTCCTA GAAAAAAGAC 1430
|
