| Tag | Content |
|---|
EnhancerAtlas ID | HS023-21476 | Organism | Homo sapiens | Tissue/cell | CD8+ | Coordinate | chr6:31227420-31228600 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr6:31227951-31227967 | CTTTGTTTACCTAGTC | - | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 31228204 | 31228327 | | chr6 | 31227904 | 31228017 |
| Enhancer Sequence | TGGTGACCTA CAGATGGGGT TTTGGTGTAG ATGTCCTTTT TGTTGATGTT ATTCTTTCTG 60
TTTGTTAGTT TTCCTTCTAA CAGTCAGGAC CCTCAGCTGC AGGTCTATTG GAGTTTGCTG 120
GAGGTCCACT CCAGACCCTG TTTGCCTGGG TAACACCAGC AGAGGCTGCA GAACAGCAAA 180
TATTGCAGAA CAGCAAATGT TGCTGCCTGA TCCTTCCTCT GGAAGTTTCG TCTCAGAGGG 240
GCACCCGGCC GTATGAGGTG TCATTCGGTC CCTACTGGGA GGTGTCTCCC AGGTAGGCTA 300
CTCAGAGGTC AGCGACGCAC TTGAGGAGGC AATCTGTCCG TTCTCAGATC TCAAACTCCA 360
TGCTGGTAGA ACCACTGCTC TCTTCAAAGC TGTCAGACTG GGACATTTAA GTCTGCAGAA 420
GTTTCTGCTG CCTTTTGTTC AGCTATGCCC TGCCCCCAGA GGTGGAGTCT ACAGAGGCAG 480
GCAGGCCTTG TTGAGCTGCA GTGGGCTCCA CCTAGTTTGA GCTTCCTGCC ACTTTGTTTA 540
CCTAGTCAAG CCTCAGCAAT GGCAGACGCC CCTCCCCCAG CCTCACTGTC ACCTCCCAGT 600
TCAATTTTGG ACTGCTGTGT TAGCAGTGAG CAAGGCTCCA TGGGTGTGAG ACCCACTGAG 660
CCAGGCGTGG GATATAATCT CCTAGTGTGC CATTCACTAC AACTGTTGGA AAAGCACAGT 720
ATTAGGGTGG GAGTGTCCCG ATTTTCCAGG TACAATCTCT CATGTTTTCC CTTGGCTAGG 780
AAAGGGAATT CCCCGAGCCC TTGTGCTTCC CTGGTGAGGC AATGCCTTGC CCTGCTTCAG 840
CTCACACTCT GTGGGCAGCA CCCACTGTGT GACAAGTCCC AATGAGATGA ACCCAGTACC 900
TCAGTTAGAA ATGCAGAAAT CACCCGTCTT CTGCACCGCT CACGCTGGGA GCTGTAGACT 960
GGAGCGGTTC CTATTTGGTT ATCTTGGAAT GATCTCCCCT GGGATAATTG TTCATGACCA 1020
AAAAGGATTC TGGTAATGTA CCAGGATCTT CTCACTGTTA TGATTCTTCT GGTATAGGAG 1080
ATCTGTGATT GGCCAGGCAC AGTGGCTCAG ACTTGTAATT CCATCAGTTT CGGAGGCCAT 1140
GGTAGGAGGA TTGTTTAAGG CCAGGAGTTT GAGACCAACC 1180
|
| |
|
|
|
