| Tag | Content |
|---|
EnhancerAtlas ID | HS105-03800 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:92074430-92075860 |
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: 2 | Chromosome | Start | End |
| chr1 | 92074449 | 92074838 | | chr1 | 92075181 | 92075471 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I091608 | chr1 | 92074061 | 92078134 |
|
Enhancer Sequence | GATGAGCAGC TTCTCAAAAG CTGTGTATTT GTTTCCAAAG GCTGGTGCCC TGCAGTGGCC 60
ACACGAGGAC CTTCAGAATG TACACATAGT GACTAATGGT AACACTGGAA ATCATCAAAC 120
TGCCAGGGTC CTGCCAGCAC TCAGCATTTG CTCTTCCACA TGAGAAAGTC CCTACAGGGA 180
ATGGGAGTTA ATGTCAGCAT GTCAGTACAT ACAGTCTGTT CTCAGTGAAT CTGGAAGCTT 240
GTCTTCCTAG ATGCCTATGG CTGAGTCGCT GAAAAGATTT TTGACTCAGG GCTTCAGAAG 300
ATACCTCAGT GCTAAATCAC CCAGAGCAGC GTTTCAGATT CAGAAGCTGC GTCACCTGTG 360
GGCAGAACAG AACTCAGCTA CGGACTTAAA GTTCCAGAGC TCAGTAGCAT CAAAGCACAA 420
GGGACAGAGA CCCAAAGGAT CCATGAATGG GGACTGAGAC CCGAAGGATC CATGAATGAG 480
GGCTGAGCCA TGTGGTGTGT ACACACCCAC AACATGTGAG TGAGAGCTGC GCCCACAATC 540
TCCTGTAGGT CAGCCTCCAG GCCATGCAGA CAGCCCCATA CCCTAAATCC CATGTACGCC 600
ATCTACGTTT CTTCTCTCTA CTTTGTTTAA TAAATCAAAA ATTGGCTAAA GGGAGGAGGT 660
GGTCAAGGAT GCCATGACCC ACTAAACAGT CTAAACAGAA CGCAGCAATG TCACTACACT 720
AGAGCTGGAA ATGGGGTAGC AGAATGCCAG CTCCCATAGC AAACCCCAGG ATGAAAGTGA 780
AAGCTGGGGT GAAAAGGCCT AGAACTTGCT TCCAGAGCAC AGGTGACAGA ATCCCTGAAC 840
GTGAAACATT CTTCTCTCGG GGATGATGAC TTAGCACTGA GGTATCTTCT GGAGCCCTGA 900
GTCACTCAGC TCCAGGAATG ATGGGTGTGG ACCAGACTGG AAATTCACTG GACCGTTTTC 960
AGTGTAACTT GGACCCAACC TAAGCATCTG GGGGACCTGG AAGAGACCCA TGTCATCTGG 1020
TCTAGGCCCC AGTTCCAGGC AAATGGTAGA AAAGCTTTTC GTTATGGGAT GACTCTGATC 1080
CTGAGCTGAC AGGAGAATCC CATAGAATTG AGACGCTCCA GCACCACCTT GGATTTTGCC 1140
CCACTGTCTG GTTCTGTGAA AGAGCGAAAA AAGTCAGGAT GAATGAACCA GTGCATGAAC 1200
AAATACATCA TAGCCTTCCT TCCTCCGCAA AGGTAGAATC TTGGCAGTAG CCATCTGCCA 1260
GGGCAAGGAA TGGCCTGAGA GGGTTAGGGG AGAGGCAGAG ATGTCTAGGA AGTCATGAGG 1320
CTGCCACACA GTAGGAAGAG GAAGGCCTTC CATCTGCGGC TCCAGCCACA ATTCAGGAGA 1380
TCCCTGAGCT CCACCCATGG AAGCTTGGAC AAGCCACATC TCTGTTCCTA 1430
|
