| Tag | Content |
|---|
EnhancerAtlas ID | HS023-17471 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr22:46816700-46818180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr22:46817184-46817204 | AGTGAGGGGTTGGGTGGGGT | - | 6.72 | | TCF3 | MA0522.2 | chr22:46817719-46817729 | AACACCTGCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr22 | 46816877 | 46816935 | | chr22 | 46817496 | 46817954 | | chr22 | 46817206 | 46817404 | | chr22 | 46817160 | 46817536 | | chr22 | 46817839 | 46817894 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046420 | chr22 | 46816560 | 46817989 |
|
Enhancer Sequence | GCCTGCATCC CACTAAGGGG TGACATGCTC AGTATCTGTG TGATAAGGTG AAGGTGGGGA 60
GAGGGCTGAA TTGGGGGACA GAGCATGGAA GCGCCTGGAT AAGACAGGGA GAAGGTGGGG 120
GCCGGGGATG GTCACGGCAG GAAAACGCGA CAGCCCTCGG ATGGCACGTC CCAGAGCAGC 180
GGATACACGG GTGGGTGAGA GATGCTGGGT CCATGGCTCC GCCTAAACCC GGCCCTCCCA 240
TCATCTACTC TGTGCTTCAG TTTCCTCATC TGTGAAACAG CAACAGCACC TCCTCCTCCA 300
GGAGCTAACA TGAGGATCAC GTGGGGGACA CACATGAGCC TGGCACAAGA CAGGACATCA 360
GCCAGTACAC TTCAGCCACC ACCACCCTCC CTGCCGAGGT GCTGGGGGGG TAGAGGCGGG 420
AAAGGCCAGG AGCCCAGAGA GGGGAGGGAG GCAGCCGTGG CACAGTGCAT CTCAGAGCCC 480
CAGCAGTGAG GGGTTGGGTG GGGTGGGAAG GATGGGGGTG AGACAGAGGC TGCTGGAGGA 540
CAGTGGCTAT GATGCCAGAC AGGAAGCAAC CTCAGCCGGG CGTGAAACTG AGGGCTGCTC 600
CAGCCCTGGG GCGACTTTCC ATAACAGGGT TCTGTAACAC AAAGGCCCAG GGTGGGGCGG 660
CGCTTGCCTC CGAGAATCAC CACGTTTCCA TAGCAGGTGA CTTTCTACCA CCTGACCAGG 720
CCTGTGTTTG GGAACGGAAA CCAAGTGACT TATCTGTCAC ATCACATAGC AGCATCGGGG 780
CAGCCCCCAC CTGCCACAGC GCCTGCAAGC AGGGCCCTGC ACCACCTTTC TGGCAGAGCT 840
CGCTAGCCAC CTGAAGACCC CTCTATCGGC TTCTATGCCC CCATCACTTG GGCTCAAGGA 900
GGCAGGAACA TCCTGAGTCC GAGATGCAGG GTAAGTAAAG GCAGTGGCCG CCGACTTCAC 960
CAACTGATGG GAGCACGTGC AGACTGCCTT AGCAGAGGCC CCACTAGTGG ATTTGACAGA 1020
ACACCTGCTG GGGCTGGAGA AGCCAGGGAA GCTCACGAAG GGCGTGACCT TTCACGCAGC 1080
CACGGAACAC CTGGGGAGCA TCCCCATCCC CTCCTCTTAA ACACGGAACT TCCTATGAGA 1140
CAGAATCAAA GCCAACAAGG CCCTGAGGGC AAAATTACCA GCCTGCATGG CCACCTCCTT 1200
TATCATAAGG ATTTTACATA CTTTGCAAGG CTTAATTAAC TTTGTAAAAG TTTAGCTTCT 1260
TTATCTTACA TATTCTGTAT ATCCAATTAT CTTTTTGTTT ATTTTTTTTG TTTTATTTTT 1320
GAGACAGAGT CTCACTCTGT CGCCCAGGCT AGAGTGCAGT GGCACGGTCT TGGCTCACTG 1380
CAACCTCTAC CTCCCAGGTT CAAGAGATTC TCCTGCCTCA GCCTCCCGAG TAGCTGAGAT 1440
TATGGGCACC TGCCACCACG CCCGGCTAAT TTTTTTGTAT 1480
|
