| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17690 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:133217790-133218460 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr3:133218218-133218229 | ATGTTTACATA | - | 6.32 | | Foxa2 | MA0047.2 | chr3:133218219-133218231 | TGTTTACATAGT | + | 6.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_31271 | chr3:133217053-133219475 | Fetal_Thymus | | SE_55369 | chr3:133217778-133218363 | Thymus | | SE_58435 | chr3:133156364-133225921 | Ly1 | | SE_62737 | chr3:133159951-133226397 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 133218000 | 133218200 | | chr3 | 133218200 | 133218294 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I133499 | chr3 | 133218181 | 133218350 |
|
Enhancer Sequence | CTGCCACCAC GCCCAGCTAA TTTTTGTATT TTTGAGTAGA GACAGGGTTT CGCCATGTTG 60
GCCAAGCTGG TCTCGGACTC CTGACCTCAG GTGACCCACC TGCCTCGCCC TCCCAAAGTG 120
CTGGGATTAC AGGCATGAGC CACCGTGCCC GGCCTGTTCT ATGTGTTCTT ATAGTGCAAA 180
GCATTTGTGG AAAACGTGCC CTTGTTAGAG AGTTATGTTC TTCTGTACTG GTATCTTTGT 240
ATGCCTTTTG CGTTCTAATC ATTTATTCAA CATATATTTG AGTACCTACT ACTGTAAGAC 300
AGTTTTTGGG CTCTGGTGAT ACCACAAAAT AGAAAAAGTC CTCGTTTTCA TGGTGCTTAT 360
ACTGTGTGTG TATGCTGGTG TGTGTACATA GTGTGTGTGC TGTGGCAGGT ATTTGGGTTT 420
GCTATAATAT GTTTACATAG TTACTACACA TTTCCTGCCA TTTTACTGAC AGTTAAACTG 480
GGCGGTGTTA TCTAAGTCTT TCATCTCTCT AACAAAGTGA AGAGTGAATT CTCCTTGACA 540
TTGTGTTCAC GGTATCTGGA ACCAGTTTGA ATTCTATTCA GGGCTTCAGG TTAAATTCTA 600
CATGTTGATT TTAACCCACT TTTCTGTAGC CTGAGGACAG AACTGTTAAG ATTAAATTTA 660
TGGACTTCAA 670
|
