| Tag | Content |
|---|
EnhancerAtlas ID | HS105-72276 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:2870070-2871150 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:2871028-2871049 | CTTCACTTTCTTTTTTTTTTT | + | 6.95 |
|
| | 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 |
| GH07I002830 | chr7 | 2870119 | 2873300 |
|
Enhancer Sequence | CAAACGCAGG GGAGGTGGCC CTACAACTCT GGCAGGAGGA AGGCATGTCC CCTGTGGGGA 60
GGGCGGCTCC CAAAGAGAGA ACCTGGAGGG AATCTACAGG GCCTGAGCCC CACCTGCTTA 120
CTGCCTTCCC CAAAATCCAC CAGTCAAGCA AGTCACTCCT TCCCCGAGCA AAGGGGGATA 180
AGGGATGGCA GGAGAGGCAA GAGAATCACA GTAGCTGAGA TCTCTCTGCA AGGAAACATG 240
AGGCTAGGAA AGTGAGAATC CCACCCATCA GAGTAAAGCC CAACCTGACC TTACAGGTTT 300
ACTCGGAGGA TCAAAGACAT AACAGATAAG GTGCTTCAAA CACACAAGCT CCCTGCCAAG 360
TGGGCTATGG CGGTGTGCAC CTGTGTCCTA GCTACCCAGG AGGCTGAGGT CGGAAGATCA 420
CTTGAGCCCA GGAGGTCGAA GCTGCAGTGA GCTGTGATTG CACCACTGCA CATCAGCCTA 480
GGTGACAGAG CAAGACCCTG TCTCAAAAAA ATTAATGAAA AAAAAACAAA AAACAAAAGC 540
TCCCAATGCA CAGAGAAGGT ATCAAGGTAT CATTCCTTCC AGGCCATCTT CTCATCTCCT 600
CAGCTTCTGC AGTACCTAGC ACATAAACAC ACACTTAATA GGCATTTGTT GACTTGCTGT 660
CCCAAGATGA TTACTTTTCA TGAGGCATCT GCTTTAACTA GTGCGTTCCA GCAGTCCTGG 720
TATGTTTAAA AACAGTCTCA TTGTGCTACG GTCATACCAG ATAAGTACTG ATAAGAAAGT 780
AAATGACCGG TTTTCTATTT CTCAATTCTG ACCAGCTCAT CTCCCAGGGA GTTTTGCCTC 840
CTGGTCCACA TCACTCCATA CTTTTAACAG AGTTTTCGAT CCATATCTAT CTAATCAAGT 900
CATCAGAACC TTAGGGAAAA ACAGTTCCTC TCCCCACCCT AAAACTAAAA TTATGGAACT 960
TCACTTTCTT TTTTTTTTTT TTTTTGAGAT GGAGTCTCAC TCTGTCGCCC AGGCTGGAGT 1020
GCAGTGGCGC GATCTCTGCT CACTGCAAAC TACACCTCCC GGGTTCACGC CATTCTCCTG 1080
|
