| Tag | Content |
|---|
EnhancerAtlas ID | HS182-15894 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr3:49414590-49415470 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr3:49414695-49414713 | GAAAGGAAGGACGGACGG | + | 6.64 | | EWSR1-FLI1 | MA0149.1 | chr3:49414699-49414717 | GGAAGGACGGACGGAAGC | + | 6.8 | | ZNF263 | MA0528.1 | chr3:49414712-49414733 | GAAGCATGAGAGGGGAGGGGA | + | 6.16 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_18986 | chr3:49414110-49416419 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | 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 |
| GH03I049377 | chr3 | 49414635 | 49417768 |
|
Enhancer Sequence | CAGTGGTTCA TGTCTGTAAT CCCAACACTT TGGGAGACTG AAGCAGGAGG AATGCTCAGG 60
CCCAGGAGTT AAGAGACCAG CCCTGACAAC ATAGTGAGAC ACTGAGAAAG GAAGGACGGA 120
CGGAAGCATG AGAGGGGAGG GGAGAAAGAA AAGGGCCGGG CGCAGTGGCT CACGCCTATA 180
ATCCCAGCAA TCTGGGAGGC CGAAACAGGT GGACTGCTTG AGAGTCCAGG AGTTCAAGAC 240
GAGCCTGGGA AACATAGTGA AACCCTGTCT CTACTAAAAA TACAAAAAAT TAGCCAGGAG 300
CGGTGGTGCA TGCTAATCAC AGTTACTTGG GAGGCTCAGG TGGGATAATC CCCTGAGCCC 360
TGGAGGTGGA AGCTGCAGTG AGCTGAGATT GCATCACTAC ACTCCAGCCT GGGGAACCCC 420
AGTGAGACAC TGTCTCTAAA AAAAGAAGGA AAAGAAAAAA AAAAAAATCA GCCAGTTGTG 480
GTAGCATGCA CCTGTAGTCC CAGCTACCAA GGAGGCTGAG GTGGGAGGAT TGCTTGAGCC 540
CAGGAGGTGG AGGATGTGGT GAGCTATGAT TGCATCACTG CACTCCAGCC TGGGTGACAG 600
AGTGGAACCT TGTCTCAAAC TCTTATGACT CAACTACAAA AAAGCAGCTT AGGTTGGTGG 660
TCTGGCTCAG GATCTCTTGC AAGGTTGAAA TCATAAAGAA CTCTTTTTGG GCTGGGCACG 720
GTAGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCTGAG GCAAGCAGAA CACTTGAGGT 780
CAGGAGTTCG AGACCAGCCT GACCAACCCA GCAAAACCCC GTTTCTACAA AAAATTCAAA 840
ACTTAGCCGG GTGTGGTGGT GGGCACCTGT AATCCCAGTT 880
|
