Tag | Content |
---|
EnhancerAtlas ID | HS105-83267 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:128136240-128137780 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr9:128137171-128137190 | GGGTGACATCTTGTGGCCA | - | 6.09 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 128136410 | 128137140 | chr9 | 128136627 | 128137500 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I125374 | chr9 | 128136680 | 128137462 |
|
Enhancer Sequence | TTTTCAGCCA CATGCCTCTG GTCCTTCTCC TTCCCCTCCA GCCAGCCCCA CTCCAGCCAC 60 TGAGAACTAT CACCTTTCCC AAAGTGCTGC CCTTTGCCGG CCTCTAAGCC TTTGCTGATG 120 CCCAGATCTG ACTGCCTCCC CCACAGTCCT TCCTCCTGCC TCAGATGGCC CTTCTGGAGG 180 AAAACCCCAG GTGCCCCCTC CTGCCTCCCT CCTCAGTGAG GCCTCACCCC CATCCCTCCC 240 TCTCCAGAGC AGTGTCTCCC TGGAGCCTGT GCTCCTAGGG GAGGGCATGC CTCCAAATGG 300 CAGGTGTCCC TAATGTTTGC AGATGGGGAT GGATGAGAGG CAGAAAGTAG CCCTTCAGGG 360 CGGGGATTCC ACCATCTTTT CCTTCCAAAT TCAGGCCCTG CTGGGACAGG AACTATCCCT 420 GTCGTGGTCC AGGGCCAGGT AGTTCTTCAC GTCCTCTGGG AAGACAGAGT GCCCCAAAGC 480 CCTTGATCTC CAGTGGGTAG AATTAGGTGG GGCAGAGGCT GTGCCACACC AGGTCACACC 540 TCTCCTGTGT CTGCTCCCAC CCCACCAAGC ACAGGGCCGG GATGAGGATG CCTGGAGCCC 600 AGCTCAGTGC CTGCCTGGGT TGCAGCCCTG ATCACACCAA AGTGTCTTGT CTGTTTGCAG 660 CCCTTTATCT GGCTAGCAGG GTTTAATTTT ACTCTGGGAA GGTGGGATTT TTGTCCCTAT 720 TTACTTATTA TTTTCGAATT TATTATCTTT AGGTGGCATC TACAAATCGG CGTCCTCTGA 780 GGGCAACAGC GCCCCGTTCT GCTAGAAATC CCGAGATTTG CAGCCACTGC AGCACGCTGC 840 CTCTGCGGCT TCTCCGCACC ATCCCCGACC CCTTCCCCCG CGAGTCTGCC GTCGGCCAGT 900 TTCCTCCCAG GCCCCGGCTT TGCTGTTCCT TGGGTGACAT CTTGTGGCCA AGGACAGGTA 960 CAAACCATTG GCTGAAAAGG AGGAGCAAAG GCAGCCCTCA GCCCTCTCTG GAGGAGCCTT 1020 GGGGCGCCTT CGAGGATGCC CAGGAGGGCA GGGGGCTCCT GAACAGGGAA TCGGCTCTCA 1080 GACCCCGAAT GGGCTTGCAC CAAGCCCTTC ATGAGACAGC TGTGGCTGGA GCCCAGAATT 1140 CACCCAGGCC CCCCGAGGCA GACACACCAG GTTCCTCTCT GCCCACCCTG CGTTGTGGCA 1200 AATAATCATT ATTCCCGATA TAAAGCTTTT CTCTAGCAGC CCAACGACAA GGTTATTATT 1260 CCAATCTTAC AGATGCAGCA ACAGCCCTGA GCCACAGCCA GTGACCTGAG CCCAGCCCAC 1320 AGGTGCCAAC ACTGTAAGAT CTCACTGGAC ACAGTCCTGA GAACTGTGGG AGCCACCTGT 1380 CCCATTCTCT GGGAAGGTGC TCTGGGGAGG CGCCTGTGTT GTTAGTCATG GCCATGCCTC 1440 GAGTTCCAAA ACCTTCTTCA TGGCCTGGCA TGGTGGCTCA CGCCTGTAAT CCCAGCACTT 1500 CGGGAGGCCA AGGCGGGCGG ATCACTTGAG GTCAGGAGTT 1540
|