| Tag | Content |
|---|
EnhancerAtlas ID | HS023-23161 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr7:65508640-65509850 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:65509605-65509617 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr7:65509609-65509621 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr7:65509823-65509838 | TGACCTCCTGACCTC | - | 7.19 | | RARA | MA0729.1 | chr7:65509820-65509838 | TCTTGACCTCCTGACCTC | - | 6.22 | | RREB1 | MA0073.1 | chr7:65509507-65509527 | GGTGTTGGGGGGGGTGGGGG | - | 6.06 | | RREB1 | MA0073.1 | chr7:65509497-65509517 | CGGGGGTGGGGGTGTTGGGG | - | 6.69 | | RREB1 | MA0073.1 | chr7:65509499-65509519 | GGGGTGGGGGTGTTGGGGGG | - | 8.55 | | ZNF740 | MA0753.2 | chr7:65509511-65509524 | TTGGGGGGGGTGG | - | 6.37 |
|
| | 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 |
| GH07I066043 | chr7 | 65508588 | 65509970 |
|
Enhancer Sequence | GCAAAAACTT CCATTTGCAC TAGGCGCAAC GAACAAGCAC GGAAAAGACC ACGTGGAGTT 60
AAACTGTCAG AAAACCTTTT ACCCTCGCCT GTACACACCC ACACACCCCG TGCTGTTTCT 120
CCGGTCCCAG TCCTGGCTCA CATCCTTCCC TTCTCCACCC AAAAACTCGC CCCTTCCCTC 180
ACAGTGTTGA CTGTTCCCAT CAAACTCTGA GGGCAGCTCT TCGGAGTGAG GGCTCCCCAG 240
GGCCCGGTGG GGCAAGCAGA GCTCTACCTG GACCTGATTC GTCTCTCCTC CACCTACTTT 300
CAGGGCGGAC AGACTCAGGC CTTTACAGCC TGCTAAGTCC CGGGTCGGAT ACCAGGCTGG 360
GCTCCACCCC CGCACTGTGA CCCAGAAACG CTGGTAAATG AATGAGAGAA GGAGGGGGCA 420
CATTGAAAGG CAGCCGGACA CGGAGGTGCT CGGCCCCGCA CCCCAGACAC AGGTTGTGGA 480
GGTTCGGAGG GGCTTGAGTC CCGTTCGTCC CTGTCCCTAT CCCGGGGCCC TCCCGGACAG 540
GGCCAGCCAG CCCCCTGCCC TCACTTCCGT ACGAGGGTCG CCCAGTCCCC ACGGCTCTCG 600
GCTCTCAGAG GTCCAACTGT TAGGCTCCTC GCGTACCAAA AGGGACGCGT CCAGACTAGA 660
GTCTGGACTT CCATGAGGTC CAGACTCGTC GCCTCTGGCT GCCAGCAGAC AAGGAACTTC 720
ACACTCTACA GCTCTCCCCA CCGTCGCCAA CAGCGCCAAA GTGCCAGCTC CGCACGCCAA 780
GGTGCAAGCC AGGAGCGCCG CGCTTCATGC CGGGAGCTTG GCGGACTCGG AACCTCGCGC 840
CGCAGGTTCT CCTTTCTCGG GGGTGGGGGT GTTGGGGGGG GTGGGGGCGT GTTCCTGTAT 900
CCTTCGCCCA GGCCGACTTC AGACTGCTGA GCGTTTGCGG ACAGGATTAT CTCGTGTTTT 960
CTATTGTTTG TTTGTTTGTT TTGAGACGGA GTCTTGCTCT GTCGCCCAGG CTGTAGTGCA 1020
GTGGCGCGAT CTCGGTTCGC TGCAGCCTCT GCCTCCCGGG TTCAAGCAAT TCCCTGCCTC 1080
AGCCTCCCAA GTAGCTGGGA TTACAGGCAC CCGCCACCAT GCCCGGCTGA TTTTTGTATT 1140
TTTTATTAGA GACAGGGTTT CACCATCTTG GCCAGGCTGG TCTTGACCTC CTGACCTCGT 1200
GATCCACCTG 1210
|
