| Tag | Content |
|---|
EnhancerAtlas ID | HS023-06701 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr13:31263990-31265450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr13:31265044-31265055 | AAGTAAACAAA | + | 6.62 | | IRF1 | MA0050.2 | chr13:31264420-31264441 | ACAGCGAAACTGAAAGAGCAC | - | 6.16 | | KLF14 | MA0740.1 | chr13:31264023-31264037 | TGCCACGCCCCCAT | + | 6.72 | | KLF16 | MA0741.1 | chr13:31264024-31264035 | GCCACGCCCCC | + | 6.62 | | Klf1 | MA0493.1 | chr13:31264564-31264575 | AGCCACACCCT | + | 6.02 | | SP3 | MA0746.2 | chr13:31264023-31264036 | TGCCACGCCCCCA | + | 6.41 | | SP8 | MA0747.1 | chr13:31264024-31264036 | GCCACGCCCCCA | + | 6.11 |
|
| | 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 |
| GH13I030689 | chr13 | 31263676 | 31265628 |
|
Enhancer Sequence | CCAACGGTTG CGTTTCCCAA GATCATCCTG GCCTGCCACG CCCCCATCTA CCTATTAAAC 60
TCCCCCACCT TCCCCAAACC CTAGCAGGCA GACACACATC GGTGGAAGAA GACAGGAGCG 120
GCTGGACATT GAAAGGACGT CGAGAGGAGC ACACCTGCAC ACCATCGACC AGCGGAACGA 180
GGCAGAGTGT GGCTGGAGCA GTCGGAGGGA AGCCTGGGCC GCTGACTCCA GGGGAAAACC 240
ATCTCCTTTC TGGCTCCCCC CTCTGCTGGG AGATACTTTC ACTGAATAAA ACCTTGCACT 300
CATTCTCCAA GCCCACCTGT GATCCGATTC TTCCTGTACA CCAAGGCAAG AACCTGGGAT 360
ACAGAAAGCC CTCTGTCCTT GTGATAAGGT AGAGGGTCTA ACTGAGCTGG TTAACACAAG 420
CTGCCTATAG ACAGCGAAAC TGAAAGAGCA CACAATAGCA CACACTCATT GGGGCTTCAG 480
GAGCTGTAAA TATCCACCCC TAGACGCTGC CATGGGGCGG GAGCCCCACA GCCTGCCCGT 540
CTAGAGGTTT GAGCAGCGGG ACACTGAAGA AGAGAGCCAC ACCCTCATCG CACGTCCTGC 600
GAGGGAGACA AGGGAACTTT TCCGGTTTCA CTTCTGCTTG GCTTGAGCTG GCACTGAAGC 660
ACCCTTTTCC CTCCTCACTG AGGGAGCAGA GGGGAAAAGC GGTAGAACTA ACAGGCTAAC 720
AATGCTCCTC CGAAAATATA TCGTATTTTT GGATCCCTAG AGATAGGTGA TCACGGCAGC 780
CGCGGAGTGC ATTTGGGTCT CCTTTCAAGA AAGAACTTGC TGCTCAGCGT TGAAGAATGC 840
AGTTGGCCAA CAGCCTCCAG CTGCTCTGTC TTCAGCATCT GCCATGGCAT CTGAGCTGAG 900
GTCATGTTCT TCCTGGGAGG TCCCCAGCAG AAGGATCACG TGGAAGCTCC ACAAGCTCCA 960
CAGATGTTCC AGGAGAGGAA TAGGCAGCAT TTGGAAGACA TATCCTGCCA TAACAGAGGG 1020
CATTTGCTAG TAGAGACAAC AAACAGCAAC AGCCAAGTAA ACAAACACAC AAGCACAAAG 1080
CACTTTCTCC CATTTCCCCT CATTGATCCT GTCCGGGTAG AAGCTGGGGA GGAAGTAGAA 1140
TAGGGTGAGG CGGGGTGGGG CTGGGGGGCC TACACCTTCT TCCTTCCCCC GCAGGTCCTG 1200
TCCCTGGGCC AGGCTTGAAC TAGGGGAATG GGAAAAGCTG TGAAGTGAAT GAGAATTAGG 1260
AGTTTTTATT TAGACTGGAC TTGAATTTTT TTTTTTTTTT TTTTTTTTTT GAGACAGAGC 1320
CTCGCTCTGT CACCCAGGCT GGAGTCCCGT GGCGCCATCT TGGCTCACTA CAGCCTCTGC 1380
CTCCCGGGTT CAAGCGATCC TCCCACCACA GTCTCCTGAG TAGCCGGGAT TACAGGTGCC 1440
TGCCACCATG CCCAGCTATT 1460
|
