| Tag | Content |
|---|
EnhancerAtlas ID | HS023-01896 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr1:167012480-167013870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH01I167043 | chr1 | 167012838 | 167014050 |
|
Enhancer Sequence | TGATGGTGGC ATTGTTTCTC TGCTCCGCTT AACTGTTCCC CGGCCAAGCC ACAGAGCTCT 60
CCTCTGTCAT GGAACAGGTT CAAAGGGACT GCAGGATGTT TTTAGTTTCA TAAAAAAGAC 120
AATGAAAGCC AGTTAGAGAA AAGACAGAAC AAGAAGATGA AAGTAACATG CTGGGAGAGG 180
AGGAAGGCTG CCCTGAGCTG ATAAACCATA TAGATTGTTC CTGAAGGGAG AGACTAAGGC 240
TCATGGTATG AATTGTACTT AAGCAACTAA CATCTTTATT TAAGGGTTCT CTCAATCTCT 300
TTCTGGGGAA AAAAAAAAAA TCTATAAGAC AGCCCAGAAC TAACATAGTT AGACCTGAGT 360
TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT AACAAGTCAC TTTAATATCC 420
CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT GCCTGGCTGA TAATGTGGCT 480
GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT AAAATTCAGT TCTTCTTTCA 540
TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC CCCACCCTGG ACAACCTCTA 600
GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC TGACTAGTTG AGATTCACTG 660
AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG CAGGGTGTTT GAAGCCTCTT 720
CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT GCAAAGCTCC TGCTCCAAGA 780
CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT GCCCGTTGGC ACAATAAGCC 840
CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA TCTCCGGTTT TGATTGCCAA 900
GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG GTGCCTCTCT ACAGAAATCC 960
ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG TTGACGTCAC CTTCGGCCAC 1020
AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT CCGCTGGTAG ACCAGGGCGT 1080
GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG CCATAGACCA GACTGACAGG 1140
GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA GGTGGAAACA GAAAAGCTTC 1200
TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG GAGAGAAAAA AAAAATCATA 1260
GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT TTCAACTGTG CAATTCCTCT 1320
TGTTGATTTT ATGAGGAAAA GGGCAGAATA GAAACATGAT GGGCTTGTTT AAAATACTTC 1380
AAAAGGGAAG 1390
|
