| Tag | Content |
|---|
EnhancerAtlas ID | HS023-15504 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr2:228647510-228648830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:228648317-228648338 | GAAACGAAAGAAAAACTAAGT | - | 6.17 | | IRF1 | MA0050.2 | chr2:228647763-228647784 | TCTGAGTTTCAGTTTCTTCAT | + | 6.2 | | IRF8 | MA0652.1 | chr2:228647767-228647781 | AGTTTCAGTTTCTT | - | 6.03 | | Nr2f6(var.2) | MA0728.1 | chr2:228647551-228647566 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr2:228648677-228648692 | TGAACTTTTGACTTC | - | 6.31 | | RARA | MA0729.1 | chr2:228648674-228648692 | TCTTGAACTTTTGACTTC | - | 6.23 |
|
| | 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 |
| GH02I227782 | chr2 | 228647192 | 228648872 |
|
Enhancer Sequence | TTAGTAGAGT GGGGGGTTTC ATCATGTTGG CCAGGCTGGT CTGAACTCCT GACCTCACAT 60
GATCTACCTG CCTCGGCCTC CCAAAGTGCT GGGATTATAG GAGTGAGCCA CCGTGCCCAG 120
CCTCTCCCAC ATTATTTCAT TCTGTACCAT GTTGTTGCTG AAGGAGCATG AGCTCTAGTG 180
CCAGGCAGAC TCACGTTTCC ATCGGGGCTC TGGGACTTAC TAGCTATGTG GCCTGCGGTA 240
GGACATAAAT TTTTCTGAGT TTCAGTTTCT TCATCTGTAA AGAAAAATGG GTGTGAATAC 300
ACTTACCTCT CCCAGTTGTT GTATGGATTG ATTTAGAAGG TGTAGACAGC TTCACTGTTC 360
ACAAGATTCA TGTGATTCTG GTATGAGTAG TTTCCAAATA TTCTGAGAGA CACAGGAGTA 420
AATAATGGAT TCAAAAGTCC CTAGCCTGGG ATTTTTTAAT GTTATGAGTT AATATTTGAA 480
AATCACTAAC AAAAAGGTCT GGAATAAAAG CCATGTTAGT GTTATGTAAA TGTTGTTTAA 540
AAAAGGAAGT TCCCTTTCTT CTTCCTTCTA TATAGTAAGG ATCTTGAGCT ATTGACTGAG 600
GTTTCAAAGT GAAGAAATGG GAAAAACCAT TTATATGGGG TTGCTAGTCA CACCAGGAGT 660
TGGGGGCAAT GCCCACCTTG GTTGGATTCT ACTGTGGTAA CAATGGACCC CACAAGACAG 720
CCAGAACTTC AAACAGCATG GAAGAGGTGG TCACTGTGCT AGCTGAGAAG TGAAACTTCA 780
TTGCGCTTTT GAAGAAATTC TGTCACCGAA ACGAAAGAAA AACTAAGTGG ATAGCAAGTA 840
GAGTTCTGCT TCTCAAAGCG TGTAGTGATT CCCCTCCCAC CCACGTAGAA TAACCACATC 900
TCAAGCACTT TCTTAAAGAT CCCTGACTGT CTGACTAGAA TATCCTCCTT GTCCACTCAA 960
TGTTTTTTTT TTGAAACAGA GTCTTTCTCT GTTGCCCAGG CTGGAGTGCA GTGGTATGAT 1020
CTTGGCTCAC TGCAACCTCC CATGTTCAAG CGATTTTCCT GCCTCAGCTT CCCCAGTAGC 1080
TGGGATTACA GGTGCCCGCC GCCATATCTG GCTGATTTTG GTATTTTTAG TAGAGATGGG 1140
GTTTCACCAT GTTGGCCAGG CTAGTCTTGA ACTTTTGACT TCAAGTGATC CACCCATCTC 1200
AGCCTCCCAA AGTGCTGGGA TCACAGACGT GAGCCACCGC ACCGGGCCTG TCCACTCAGC 1260
TTTAATCCTA GCATCGAGAC CTTTTCTGTT ATCTCATTTT TTGTCCCCTA TTTCACTTTC 1320
|
