| Tag | Content |
|---|
EnhancerAtlas ID | HS017-00353 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr1:17723960-17725180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:17725160-17725180 | CACCCACCCACCCACCCACA | + | 7.33 | | RREB1 | MA0073.1 | chr1:17725152-17725172 | CCCCCCCCCACCCACCCACC | + | 7.73 | | RREB1 | MA0073.1 | chr1:17725156-17725176 | CCCCCACCCACCCACCCACC | + | 8.79 | | STAT1 | MA0137.3 | chr1:17724335-17724346 | TTTCCCGGAAA | - | 6.32 | | Stat4 | MA0518.1 | chr1:17724332-17724346 | CCATTTCCCGGAAA | - | 7.82 | | ZNF740 | MA0753.2 | chr1:17725147-17725160 | CCGCCCCCCCCCC | + | 6.64 | | ZNF740 | MA0753.2 | chr1:17725150-17725163 | CCCCCCCCCCCAC | + | 6.92 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGCAGGGAG GAGCGCCATG GCATGTCGGG ACCGTTGACA GATATTACTT GCAGATACTG 60
TCAGAGGGAG TTTACTTTGC TATGACTATG CAGCTGGATC TTTTCCCCCA AGCTGGGAAA 120
GCCCTGATTA TCCAGGTTCC TAGCTGAGAG CCAATGATGG CCCAAGCATT TTGCGAGATA 180
CCTCACTACA AACCCTGCAG ATAGCCCTAT AAAACTACAA ACCCTGCAGA TAGCCCTATA 240
AAGTAAAACA CCTCTTACAT ATGAGGGTAG TGAGGCACAC AGTAAAACCG CTAGCCCAGG 300
ACAATCATTT GGGAAAATGA GTCTGAACTC CCAAGTTCAT GTGTTGCTCA TTATACTCAA 360
GCTGCCTGGG GTCCATTTCC CGGAAAATGA CATAGCTCCG CAGCCTCCTT GAAGAAGCCG 420
GCTCCTCACT TCCGAGAAGC TGAGTATCAG ACTCAAATAG ACGAGGGACT ACTCAATGCT 480
TTCTGGATGA AGTGGCCCAT CACAGCAGTC CCGAGGATGG TGTTCAGGGT CACCAAACTT 540
CAGAGATCTT AGAAGTGAAT CATTGGCTAT AAGAAGCAGA GTCTCCCCAA CTTGTAGAAG 600
GAGAAGCTTA GGCCCAGAGA AGGGTAATTT CTTGGCTGAG GTTGCATGGT CAGCAAAACT 660
GCTTCTCTCA CTGGGTCCTT AACATTCCCA GGAATGTTCC CAAGGAATGT TCTATGCCCC 720
GCACAGTGCA TGGGTACCCT GTTTTGCAAG AACAGCCCCC CTGGCATAGC AGGGTGGGTG 780
CCAGCCAGGC ATGGGGCTGA GACAGCATCT CCCAGCCCCT GGCGACAGCT TAGGTGTGTT 840
GGGTATGTGT CTGAAGCCTA TTTCAAGACC TAGGGAGACA GGTGTGTTGG GTTATGTCTG 900
AAGCCTATTT CAAGACCTAG GGAGATGCCT GGGTATTGGG CTCAGCTGGT CTGGGTTGAG 960
AAGTGCCAGA CGCTGTCTAG CCATGGGATC CTGGACTAAA GACTAGGCCA TTCCTGAGCC 1020
CCTACTTCCC CATGTGAAAA GGGAACTGCC TATTTCGTAA GGCTGGTATG AAGTGTGAGG 1080
CTCCTGGCAC ACAGCAAGTG ATGGGGATGG TAGTGGTGTC AGGCCATCAC CTACCTTCAG 1140
TATGGAAGGA AACTGGTTTT AATTCCTGAT GAGCTCTCCT TGCTCCCCCG CCCCCCCCCC 1200
CACCCACCCA CCCACCCACA 1220
|
| |
|
|
|
