| Tag | Content |
|---|
EnhancerAtlas ID | HS105-66739 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr5:159927780-159929110 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX5 | MA0510.2 | chr5:159928030-159928046 | CATTGCTATGGTAACA | - | 6.15 | | RFX5 | MA0510.2 | chr5:159928030-159928046 | CATTGCTATGGTAACA | + | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 159927852 | 159928388 | | chr5 | 159927861 | 159928119 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I160500 | chr5 | 159927852 | 159928388 |
|
Enhancer Sequence | AGATTTTAGA ACAATAGAAA GAAGACTTCA CAAACAGTTA AGGCTGGTTT GAGAAAGATT 60
TGTGCCTGGT GGGTAGTGAG CTGCTTGTTT CTGGGGGAGT TTAAGAAAGG ATTGCATGAC 120
CAACAGTTGG TAGATATTGC AGAGGTCTGT GAAGTACACA GGAGAAGAGG ACACTGAAAG 180
AGGAAGCGTG CATTAGGAAG GCTCTGCAAA TCAGGAACAG CAATTGAGGA CTGGCATCCA 240
AGAGCTCTCT CATTGCTATG GTAACAGTGG GGGTGGGGGT GGTAACAAGC TAATTGTGTT 300
TATAAACCTC AGCTGGGGCT TGTTTCTGAG CACTTTCTTG AGTTAAAGGT GATTCCAGGA 360
TCCTGGTCTC TGCCATGCAA CAAATCCTAA CTCCTGGGAC CAGGATCCTA TTTTGAAATT 420
GCTTATATTC CTATCTCTAG ATTCTAGCTC CTCATTAGAC TCTCTTGAGT AGGGTAGAAA 480
TTCCAATATG GGGAAACAGG TGGAGGAAAT CTGATGATCA ACCCAAACAT CTCAGGACAG 540
GAAGCTGCAT CTAGAGTAAT GAATACTAAT TTCAAACCTA TATATTGCAT TCGGTGGGTA 600
AAAGTGTGAG CGGTAGAAAC AGAAGGCTGG ATATCATCAA CTGAAGAATG AGGAGGTTCA 660
TAAATTTGGA AAGGAGAGCT TTATTTCTCA TAAAGGATTG CAGCCTGCAG GGTTGCCATT 720
CTGACAGGGT GGGAAGCATA GCCTCTGGTC AGAAGCCCAA AACAGATACT CTGAGGGTGG 780
GGCAAATGGA ATAGAAATTT ATGCTGAGCA GAGTGGTCGA ATATACATAT TCAATAAGCT 840
ATCAGAGGAA TCATGAATAT TTATGAAGGA GAAATATGCA CACGTGCAAT TGAGCTTCAT 900
CCCCCTGCTT GTGTCCCATG TACAAAAAAT GACGGTGTTA GCATGATCTA AGGGTGGAGT 960
TTTTGGCCCT TTGACATCAA AAGGTGAAGT AGACAGGAAC ACCCTTACTG TGCATTCTTT 1020
GTAGATTGGC CAGAACCACC CTGTGGTCGG TGGTCTCTTA TCGGGCAAAA AAGGAGAGGC 1080
AGCATTAGGC GGTAGACTGA TACCAGTGGT GGAGTCTTTT GAAAGGGCTG TTTTCTTTTT 1140
AAAATATTTT TAAATTTATT TTTTTATTTT CAATAGGTTT TTGGGGAACA GGTGGTGTTT 1200
GGTTACGTGA ATGAGTTCTT TAGTGGTGAT TTGTCAGATT TTGGTGCACC CATCACCAAG 1260
CAGTGTACCC TGTACCCAAT GTGTAGTCTT TTATCCCTCG CCACCCCACC CTTTCCCCGA 1320
GTCCCCAAAG 1330
|
