| Tag | Content |
|---|
EnhancerAtlas ID | HS023-20549 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr5:132506140-132507400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr5:132506844-132506857 | AGGGAAATCCCCT | - | 6.15 | | NFKB1 | MA0105.4 | chr5:132506844-132506857 | AGGGAAATCCCCT | + | 6.1 | | Nr2f6(var.2) | MA0728.1 | chr5:132507278-132507293 | TGAACTTCTGACCTC | - | 6.38 | | RARA | MA0729.1 | chr5:132507275-132507293 | TCTTGAACTTCTGACCTC | - | 6.88 | | REL | MA0101.1 | chr5:132506846-132506856 | GGAAATCCCC | - | 6.02 |
|
| | 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 |
| GH05I133170 | chr5 | 132506521 | 132506670 |
|
Enhancer Sequence | TTCTAACAGT CAGGTCCCTC AGCTGCAGGT CTGTTGGAGT TTGCTGGAGT TCCACTCCAG 60
ACCCTGTTTG CCTGGGTATC ACCAGCGGAG GCTGCAGAAC AGCAAATATT GCAGAACAGC 120
AAATATTTCT GCCTGATCCT TCCTCTGGAA GCCTCGTCCC AGAGGGGCAG CCGCCTATAT 180
GAGGTGTCTG TTGGCCCGTA CTGGGAAATG TCTCCCAGTT AGGCTACACG AGGGTCAGGG 240
ACACTTGAGG AGGCAGTCTG TCTGTTCTCA GAGCTCAAAC GCCATGCTGG GAGAACCACT 300
GCTCTCTTAA GAGCTGTCAG ACAGGGACGT TTAAGTCTGC AGAAGTTGTC TGCTGCCTTT 360
TGTTCAGATA TGCCCTGACC ACAGAGGTGG AGTCTAGAGG CAGTAGGCTT TGTTGAGGTG 420
TGGTGGGCTC CACCCAGTTT GAGCTTCCCT GGCTGCTTTG TTTACCTACT CAAGCCACAG 480
CAATGGCAGA TGCCCCTCCC CCAGCCAGAC TGCCTTCTGG CAGATCCATC TCAGACTGCC 540
ACAGTAGCAA TGAGCAAGGC TCTGTGGGCA TGGGAGCTAC TGAGCCAGGC ACGGGAGAGA 600
ATCACCTTGT CTGCCAGTTG CTAAGACCTT GGGAAAAGCA CTATATTTGG TCGGGAGTGC 660
CCCATTTTTC CAGGTAGCCT GTCATGGCTT CCCTTGGCTA GAAAAGGGAA ATCCCCTGAC 720
TCCTTCAGCT TTCCGGGTGA GGCGATGCCC CGCCCTGCTT CAGCTTGCCC TCCGTGGGCT 780
GCACCCACTG TGCAACCAGT CCCAATGAGA TGAACCAGGT ACCTCAGTTA GAAATGCAGA 840
AATCACCCGT CTTCTGCATC AGTCATGCTG GGAGCTGCAG ACTGGAGCTG TTCCTATTTG 900
GCCATCTTGG AACGCCCTCC TTTTTTTTTT TTTTTGAGAT GGAGTCTTGC TCTGTTGCCC 960
AGGCTGGAGT GCAGTGATGC AATCTTGGCT CACTGCAACC TCCGCCTCCT GGGTTCAAGC 1020
GATTCTACTG CATCAGCCAC CTGAGTAGCT GGGATTACAG GTGCCCACCA CTACATCCAG 1080
CTAATTTTTT GTATTTTTTA GTAGAGATGG AGTTTCGCCA TGTTGTCCAG GCTGGTCTTG 1140
AACTTCTGAC CTCAGGTGAT CCACCTGCCT TGGCCTCCCA AAGTGCTGGG ATTACAGGTG 1200
TGAGCCACCA CACCCAGCTG AAAAGAATTT TTTTTTGAGA CAGAGTCTTG CTCTGTTGCC 1260
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