| Tag | Content |
|---|
EnhancerAtlas ID | HS136-13051 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr22:45817170-45818160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr22:45817229-45817242 | TAATTAATTATTA | + | 6.18 | | Lhx3 | MA0135.1 | chr22:45817362-45817375 | TAATTAATTATTA | + | 6.18 | | Lhx3 | MA0135.1 | chr22:45817226-45817239 | AAATAATTAATTA | - | 6.71 | | RARA | MA0729.1 | chr22:45817654-45817672 | CCTTGACCCCTTCACCTC | - | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTCAAATAAT AATAATACTA TTATTATTAT TAATACTATT ATTAATAATA ATAATTAAAT 60
AATTAATTAT TATTTAAATG CCACCTATAG GCCATCATTT CCCAGGTTTA TACCTCCAGC 120
CTGGACTCTT CCCTGAATCC AGACTCATAA ATTCATCTAA CTTCTCTTGG ATGTCTAATG 180
CACTTGGATG TCTAATTAAT TATTATTATT AATAATAGTA TTATTAATAA TAATAATAGT 240
ATTATTAATA ATATTAATAA TAATAATAGT ATTATTAATA ATAGTATTAT TAATAATAAT 300
AATAGTATTA TTAATAATAA TAATGTTATT ATTCTGCAAA GGAGGTATGT CCTGCTTCAC 360
AGGTAAGGAC ACAGGCTCAG CAAGGCTAAG TAATAGTTGA GGTTAACAGA GCTCGGAAAT 420
GTCTGGGCTG GGATGTGAGC CTCCTCTGAC TCCAAATCTT CACATTTTGC TTTTGGACCT 480
TCTACCTTGA CCCCTTCACC TCCTACTCTT CCTCTTTCTC TTACTCATTG GCCTGACCAA 540
GTCCTCCTGC CACTCCACAG TATCTGTCAT CTGGCCCCAC TTCCTCCATA GAGTCCTGTC 600
TGGTTTCTTG CTCTTTCACT TCTGGATTCC CCTGAATCCT TTCCCAAAAC CTCTGCACCT 660
GCTCCCAACC CACTTCTTTT GTCCTGCAGG TCTCAAACGT CATTTCTTGG GGCTGTAGAG 720
TATCTCTTGC CCACTGTAAG GATGTAGCTG CCTCAGGATA GAGCAGGACA GCAAGGGGCA 780
CACCACCAGC CTGTCCCAGG ACCCCAGCAT AGTAGTGATC ACTAGCACTC ATCTGGGAGC 840
TTGACTCTCC CACAGCCTTC AGAGGCAGGT CCTGTCATTA TTGTTCCCGT CCTCATGCTC 900
ATGGCTAAGG ACGTGGTAGG AGGCAAAGGC ACGAACGGCC ACACGTGGGA AGGTGCTCCT 960
GTGGCCAGGT CGATCTGATT GCTTCTTGCC 990
|
