| Tag | Content |
|---|
EnhancerAtlas ID | HS060-24329 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:49414270-49415460 |
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 | AGCATTCTTG GCTGGGCGCG GTGGCTCACG CCTATAATCC CAGCATTTTG GGAGGCCGAG 60
GCAGGCAGAT CACCTGAGGT CAGGAGTTTG AGACCAGCCT GGCCAACATG GAGAAACCCC 120
ATCTCTACCA AAAATACAAA ATTAGCCAGG CGTGGTGGCA CATGCCTATA ATCCTAGCTA 180
CACAGGAGCA AGAGGCAGGA GAATCGCTTG AACCCGGGAG GCAGAGGTTG TGGTGAGCCG 240
AGATCATGCC ATTGCACTCC AGCCTGGGCA ACAAGAGCGA AACTCCGTCT CAAAAAAGAA 300
AAATCAATTG AGGCCGAGCA CAGTGGTTCA TGTCTGTAAT CCCAACACTT TGGGAGACTG 360
AAGCAGGAGG AATGCTCAGG CCCAGGAGTT AAGAGACCAG CCCTGACAAC ATAGTGAGAC 420
ACTGAGAAAG GAAGGACGGA CGGAAGCATG AGAGGGGAGG GGAGAAAGAA AAGGGCCGGG 480
CGCAGTGGCT CACGCCTATA ATCCCAGCAA TCTGGGAGGC CGAAACAGGT GGACTGCTTG 540
AGAGTCCAGG AGTTCAAGAC GAGCCTGGGA AACATAGTGA AACCCTGTCT CTACTAAAAA 600
TACAAAAAAT TAGCCAGGAG CGGTGGTGCA TGCTAATCAC AGTTACTTGG GAGGCTCAGG 660
TGGGATAATC CCCTGAGCCC TGGAGGTGGA AGCTGCAGTG AGCTGAGATT GCATCACTAC 720
ACTCCAGCCT GGGGAACCCC AGTGAGACAC TGTCTCTAAA AAAAGAAGGA AAAGAAAAAA 780
AAAAAAATCA GCCAGTTGTG GTAGCATGCA CCTGTAGTCC CAGCTACCAA GGAGGCTGAG 840
GTGGGAGGAT TGCTTGAGCC CAGGAGGTGG AGGATGTGGT GAGCTATGAT TGCATCACTG 900
CACTCCAGCC TGGGTGACAG AGTGGAACCT TGTCTCAAAC TCTTATGACT CAACTACAAA 960
AAAGCAGCTT AGGTTGGTGG TCTGGCTCAG GATCTCTTGC AAGGTTGAAA TCATAAAGAA 1020
CTCTTTTTGG GCTGGGCACG GTAGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCTGAG 1080
GCAAGCAGAA CACTTGAGGT CAGGAGTTCG AGACCAGCCT GACCAACCCA GCAAAACCCC 1140
GTTTCTACAA AAAATTCAAA ACTTAGCCGG GTGTGGTGGT GGGCACCTGT 1190
|
