| Tag | Content |
|---|
EnhancerAtlas ID | HS043-02022 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:92074440-92075430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:92075197-92075218 | AGGATGAAAGTGAAAGCTGGG | - | 6.13 |
|
| | 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 |
| GH01I091608 | chr1 | 92074061 | 92078134 |
|
Enhancer Sequence | TTCTCAAAAG CTGTGTATTT GTTTCCAAAG GCTGGTGCCC TGCAGTGGCC ACACGAGGAC 60
CTTCAGAATG TACACATAGT GACTAATGGT AACACTGGAA ATCATCAAAC TGCCAGGGTC 120
CTGCCAGCAC TCAGCATTTG CTCTTCCACA TGAGAAAGTC CCTACAGGGA ATGGGAGTTA 180
ATGTCAGCAT GTCAGTACAT ACAGTCTGTT CTCAGTGAAT CTGGAAGCTT GTCTTCCTAG 240
ATGCCTATGG CTGAGTCGCT GAAAAGATTT TTGACTCAGG GCTTCAGAAG ATACCTCAGT 300
GCTAAATCAC CCAGAGCAGC GTTTCAGATT CAGAAGCTGC GTCACCTGTG GGCAGAACAG 360
AACTCAGCTA CGGACTTAAA GTTCCAGAGC TCAGTAGCAT CAAAGCACAA GGGACAGAGA 420
CCCAAAGGAT CCATGAATGG GGACTGAGAC CCGAAGGATC CATGAATGAG GGCTGAGCCA 480
TGTGGTGTGT ACACACCCAC AACATGTGAG TGAGAGCTGC GCCCACAATC TCCTGTAGGT 540
CAGCCTCCAG GCCATGCAGA CAGCCCCATA CCCTAAATCC CATGTACGCC ATCTACGTTT 600
CTTCTCTCTA CTTTGTTTAA TAAATCAAAA ATTGGCTAAA GGGAGGAGGT GGTCAAGGAT 660
GCCATGACCC ACTAAACAGT CTAAACAGAA CGCAGCAATG TCACTACACT AGAGCTGGAA 720
ATGGGGTAGC AGAATGCCAG CTCCCATAGC AAACCCCAGG ATGAAAGTGA AAGCTGGGGT 780
GAAAAGGCCT AGAACTTGCT TCCAGAGCAC AGGTGACAGA ATCCCTGAAC GTGAAACATT 840
CTTCTCTCGG GGATGATGAC TTAGCACTGA GGTATCTTCT GGAGCCCTGA GTCACTCAGC 900
TCCAGGAATG ATGGGTGTGG ACCAGACTGG AAATTCACTG GACCGTTTTC AGTGTAACTT 960
GGACCCAACC TAAGCATCTG GGGGACCTGG 990
|
