| Tag | Content |
|---|
EnhancerAtlas ID | HS023-19223 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr4:25332190-25333770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr4:25333302-25333323 | TGGTTCTTTCACTTTCATTTC | + | 7.67 |
|
| | 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 |
| GH04I025331 | chr4 | 25332623 | 25333812 |
|
Enhancer Sequence | AGAGACTTTG TGGCCTGCCA AGCTCCAAAT ATTTATTATC TGATCCTTTA CAGAAAGTTT 60
GCTGACCCTG CTTTTGAAGA CTTGTCTTTA AGCTTTTTAG GCAGGACTGA GCAACCTTTC 120
GTGGTTCTAG GGCTAATTTT TCCTCCCTAC TGAGGCAGTG CTCTTCTGAG TACTTGAGTA 180
CTTGTGTATT GTGAGGCATT TCCACTCTGG CTTGTTGGGA GACAAACCAT TCTGGACCTG 240
TGTGTATTTT CCAGTGATAA TTCCACCTGC TTCTGGCCAG TGGTTCTTTC CCTTGCCTTG 300
GGGAGTTTCT GCATGTGCAC ATGCTGCTCA GTACTCAGCC GAAGACTCGA GGGGAATTGT 360
CAGCTAGTCT GGAGCGTTTT TTCTCTCTCT CTCAGTGTAC AGCTTTCTGC TCTCCTGTCC 420
TCCCTGGTTA TTCGCCAGTA CTCTTTCTGT GAATTCTGGC CGCCTAGCCT CCTGGAGTGC 480
TCAGCTCTGT CTCATCAATT CCTTGGGCTG TGTTTCGGTT CTCCATCCCT GTGCTGCCAG 540
CTCTCCACAG GCAGGAAGCT GGGCAGCTGT ACCACTCACC TCTGTTCCCT TCCCTCGGGG 600
TTCACTGTTT TGGGCTGCTA GTTGTCCGAT ATCTTCAAAC TGCTTTTTCA TATATTTTGT 660
CTTTTTAAAA CTTCTTTTGA AGGCCCATGG TAAATCTGGT CTCTGTTACT CCATCATAGC 720
TGTCTGCGGA AGCTGTCAAC ATTTTTTTCT TTTAGAGACA GAGCCTCACT CTGTTGCCTA 780
GGCTGGAGTG TGGTGGCATA ATCATAGCTC ACTGCAGCCT TGAACTCCTG GGCTCAAGTG 840
ATCCTCCTGC CTCTGCCTCC TAAGTAGCTG GGACTACAGG CACATACCAC CACACCTGGC 900
TAATTTTTAA AATTTTTTGT AGAGATGGAG TCTCAACTAT GTTGCCCAGG CTGGTCTTGA 960
GCTCCTGGCC TCAAGTGATC CTCCTGTCGT GGGCTCCCAA AGTGCTGGGA TTTCAGGCGT 1020
GAGCCACTGT TCCTGGCCTG TTCAACACTG TTAGTACTTA GTGATGAGAG GTAATAGTAA 1080
ATTCAGTGTT TCTGTTGCCG AAGAGTGTTT ATTGGTTCTT TCACTTTCAT TTCATAGGGC 1140
CCTTTCTTCT ACTGGCATTC TCACTTTGAA TTACTAAGAA GTTTCTTCTA ATATCCCTCT 1200
ATCTCCTTTT TCTTTCTAGT TTTAGATAAA GCTGTCAAAA GAACAGTTAT CATAGAAATA 1260
GAAACATTTA AATTACCGGC ACGATAGCTT ATTTCTTGCT GCAACCATTC AGAATATCTA 1320
TTTGTCACTG CCTTGGGTGC TTTGAAGTGA AACTGTGCTT AGATATAAAA AGTTTAAAAC 1380
TCACTTTGAT TACATGTTAA GCTCACAGTT TTTACACTGC AGTTCCTGAA TTTAGTTCCA 1440
TCAAAACTGT ATGACTAGGC CACATGTGAT GGCTCATGCC TGTAATCCCA GCACTTTGGG 1500
AGGCCAAGGC GGGCGGATCA CCTGAGGTCA GGAGTTTGAG ACCAGCCTGG CCAACATGGT 1560
GAAACCCTGT CTCTACTAAA 1580
|
