| Tag | Content |
|---|
EnhancerAtlas ID | HS182-14750 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr22:21931560-21932460 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr22:21932428-21932443 | GAGGTCAAGAGATCG | + | 6 |
|
| | 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 |
| GH22I021577 | chr22 | 21932048 | 21933255 |
|
Enhancer Sequence | TTTTGCATTT TTTAGTAGAG ACGGGGTTTC ATGGTGTTGG CCAGGCTGGT CGTGAACTCC 60
TAACCTCAGG TGATCCGCCT GCCTCAGCCT CCCAAATAGC TGGGATTACA GGCGTGAGCT 120
ACCGCACCCA GCCCTTGTCT TCTCTTTCAA CCTTGAAGCA GAAAGTTAAG AAAGTTGCTT 180
CTGGTGGCTG TGTAGTTTCT CCTTCTGACC CTTGCTGCAC ACATACTCTA GAATTCCAGA 240
GCTGTGTGAG GGATCTTGGA AAGCAGACAC CAGTGGCCTC TGTTTACAGA TGAGGAGGCT 300
GAAGTCAGTG GTGGAGCCAG GCCCAACATC AAGGTCCCCT GCTCTCTGGG CCTTGCTCCT 360
GCTTTTTAGA TGGTTGCTTT TGGTCTTGAG GAAGGGACAA GATGGAGAAG AAGAGGGTTC 420
ATTTCAGATT CGGTGGCTGT TTGGGTTTTG TTTGTTTTGG TTTTTAACAC TTCCAGGGCT 480
GTGTTGATTA TAGTTTTCTG TATTTCACTT TCTTGTCAGA TTTTGTCCCT ACTTTCCTAG 540
CATAGGTAGG CAGAGCGGGG AACATTCTCT TTTGACAGCC CTTATCCCAG CAGGCACATC 600
TGCAACCAAA GCAGGTGCTA ATGTCAAAGG GCTCATGGGC TAATGTCAGG GCTCATGTGA 660
TGCTCCATCT TTCTGAGAGG AGACCACCTG ACTCACGGTG AGGAAGAGGG TGTAACTCAG 720
AGGTTGAATA GCCTCTGAAC CCGTCTGAGA TGGCTTATAA AAAAGTGTTT CACACCAGCA 780
CGCCTCTCAT TAAGAACAGT CAGCGGCCGG GCACGGTGGC TCAGGCCTGT AATCTCAGCA 840
CTTTGGGAGG CTGAGGTGGG AGGATCATGA GGTCAAGAGA TCGAGACCAT CCTGGCTAAC 900
|
