| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41914 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:139860200-139861010 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr9:139860596-139860607 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr9:139860596-139860606 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr9:139860593-139860608 | GAAGCCCCGCCCCCA | + | 6.6 | | SP2 | MA0516.2 | chr9:139860592-139860609 | GGAAGCCCCGCCCCCAT | + | 6.67 | | SP4 | MA0685.1 | chr9:139860593-139860610 | GAAGCCCCGCCCCCATT | + | 7.22 | | SPDEF | MA0686.1 | chr9:139860278-139860289 | AACCGGATGTG | + | 6.02 |
|
| | 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 |
| GH09I136965 | chr9 | 139859834 | 139861061 |
|
Enhancer Sequence | AAACCATTTC GCAGAGAAGG ACGCAGAAGC CAATGGAAAA GCTGCCAGTA GCTGCAGCTG 60
GCCTGATGTG AGCCACAAAA CCGGATGTGA CAGTAGGGTG TGAGCCAAAG TGTAAAACAC 120
CTGAGGTCCA CACGGATGTC AGTGAAGGGC TGTGCCCACC CATGGGAGAG CAGAGACAAA 180
TGATCTCGGT GCAGCAAAGT TGCAAATGTG TGTGGATTCC CCTTCCGGGG GAGGTGAGGG 240
CCACACACAG GGACTTCATC CAGAGAGGAC AGTTCAAAAA GAAAAAGACG GAGAGGTGCA 300
GGGTTAGGGT GGGGGAACCT CAGCCAGGTG ACCAAGGTCA ACATGGGCAG TGAAGGTCGC 360
GCTGATGGTG TCCCCCATGT GATGTGGTGG GAGGAAGCCC CGCCCCCATT CTCTTCCTCC 420
CGACCATCAC CGGATTCAGC GTGAGAAACT CAGCAGACGG AGCCCAACTG AGGGACGCCC 480
CACAAACACC CGAGCAGCGC CCCTCAAGGC TGCTGAGGTC ATCAAGGACC GGGAAAAGCT 540
GAGAAACGTC ACTCAGGAGG AGCCCGTGGA AGAGAGACAG AATGTCACGT GGTGTCCTGG 600
AGAGAAAGGG ACCTTCAGTA ACTAAGGGAA TCTGGAGAAA GCCTGGATGT CAGCTGACTC 660
GACGTCCCAA CACTGGCTCA CTGATTGTGA CAAAGGGACC ATGAGAATTA GGACGCCAGC 720
GAGAGGGAAA CTGGGGGAGG GGCACGCAGG AACTCCCTGA TCTGTCTTCA CATTTTTTTT 780
CTGTAAATAT AAAACATTCT ACACTGGGTG 810
|
