| Tag | Content |
|---|
EnhancerAtlas ID | HS187-01601 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:155484370-155485280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:155484541-155484552 | GAAGATAAGAA | - | 6.02 |
|
| | 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 |
| GH01I155514 | chr1 | 155484501 | 155484650 |
|
Enhancer Sequence | GAAATGTTAG ACTAAAAGCA AATTCAAGCG ATCTTCTTAT TTGGGTTTAA AATGGGTCAT 60
AAAGCAGTGG AGACGATTTG CAACATCAAC AACGCATTTG GCCCAGGAAC TGCTAATGAA 120
TGTACAGTAC AGCGGTGGTT CAGGAAGTTT TGCAAAGGAG GTAAGAGCCT TGAAGATAAG 180
AAGCACAGTG GCTGGCTGTC AGAAGCTCAC AACAACTGAG AGCAATCATC GAAACTGATC 240
CTCTTTTAAC TACACGAGAA GTTGCCGAGG AACTCGGCAA CTTCAACCAT TCTACAGTCA 300
TTCGGCATTT TACACACCAA CAAGGAAAAA TTTCTCAGAC TGTGATGTGT GACAAAAAGT 360
GGATTTTATA TCACAACCGG CAACAACCAG ATCAGTGGTT GGACCCAGAA GAAGCTCCAA 420
AGCACTTTTC AAAGCCAAAC TTGCACCAAA AAAGGTCATG GTCACCGTTT GGTGGTCTGC 480
TGCCAGTCTG ATCCACTATA CCTTTCCAAA TGCCAGCGAA ACCATTACAC CTGAGACGTA 540
TGCTCAGCAA ATTGATGAGA TGTACCAAAA ACTGCAATGC CTGCCGCCAG CACTGATCAA 600
CAAAAAGAGC CCAATTCTTC TCCAGGACAA CGCCTGACTA CATGTCACAC AATCAATGCT 660
TCAAAAGTTG GACGAATTGG ACTACTAAGT TTTGCCTCAC CTGACATATT CAACCGACCT 720
CTCGTCAACC AGCTACCACT TCTTCAAGCA TCTCAACAAT TTTTTGCAGG GAAACAGCTT 780
CCACAACCAG CAGGATGCGT AAAATCCTTC CCAAGAGTTT GTTGAATCCA GAAGCACAGA 840
TTTTTATGCT ACAGGATTAA ACAAACTGAT TTCTTTTTGG CACAAACTTT TATTGTAATG 900
GTTCCTATTT 910
|
