| Tag | Content |
|---|
EnhancerAtlas ID | HS017-22142 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr22:41405350-41406150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr22:41405697-41405708 | GGGCGGGAAGA | + | 6.14 | | ESR2 | MA0258.2 | chr22:41405669-41405684 | GGGCCAAGCTGACCT | - | 6.52 |
|
| | 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 |
| GH22I041008 | chr22 | 41404931 | 41406002 |
|
Enhancer Sequence | CCTCACACTC CTGGGCTCAA GCCATCTTCC ACCTCAGCCT CCCAAAGTGC TAGGGTTACA 60
TGCATGAGCC ATCACATCTG GCTCCCACGG GGGGTTTTGT AAACTGAACA AAGGGAGCTC 120
CCTTTCCCCA GCAATTCATC CCTGGAGTCC ATATGAACCA ATGTTCCTCA TTTACAGCAG 180
AAAAAGCAGC TTCCCATGCT CTAACCCCTG CCTGCTCCTC AGCTGAATGA GGCTGACAGG 240
TGCACACCCT GCAGCATCCT GCACCTCACC AGGTAAACAG GCCTGAAAGA GGGAGGCCAT 300
GGGTGTGGGC ACAGGCTCAG GGCCAAGCTG ACCTCGCAAA GGCTGAGGGG CGGGAAGAAC 360
AGGAGGAAGT GTGGGCAATG GGGAGCTGCT GGGTCTGGAG CAATTACCAT TGCCACATGG 420
TGAAGACACC AGCCCAGAGG CTGACCTGGG GCTGAGCAGA GCCCAGCAGT AGGGTAGGAA 480
GGGGCCCACC CTTGCTCCTC CAGCTCCCTT TTCTCCCCAC CCCTCAACCC CAAACTCTGT 540
CCCTCCTCCT CACTGCCCTG CTGTCAGTTC ACCTCCTTTA ACCCTTTCCT CCCGTGCCTC 600
CCAAGGAAAA GGGGAAACTA ACAGGCCAAC TGATCTTCAA CGGCCATGGA GCTTCGTTTC 660
TTAAAAATTC ATTAAGAGGC CAGGCGCAGT GGCTCATGCC TGTAATCCCA GCACTTTGGG 720
AAGCCAATGG AGGTGGATCA CTTGTGGTCA GGAGTTCGAG ACCAGCCTGG TCAACATGGT 780
GGAACCCCGT CCCTACAAAA 800
|
