Tag | Content |
---|
EnhancerAtlas ID | HS063-03708 |
Organism | Homo sapiens |
Tissue/cell | GM18505 |
Coordinate | chr2:97628050-97629490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:97628170-97628191 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | REL | MA0101.1 | chr2:97628343-97628353 | GGGGATTTCC | + | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 2 | ID | Chromosome | Start | End |
GH02I096962 | chr2 | 97628301 | 97629334 | GH02I096963 | chr2 | 97629400 | 97630716 |
|
Enhancer Sequence | ATACAAAAGG GAGGCTGAGG CAGGAGAATT GCTTGAACCT GGGAGGTAGA GGTTGCAGTG 60 AACCAAGACT GTGCCATTGC ACTCCAGCCC TGGCAACAGT GCAAGACTTC GTCTCAAGAA 120 AAAAAAAAAA AGAAAGAAAG AAAGAAAGAA AAAAAAGCCT ATAAGAACTA GGCTAATCTA 180 CAAAGGGGTC CTGTCCCTGT CCCTAAAACC ATCTTTTAAA GGGACTTCTG TGATGCTGGC 240 TGTAATGTAT GTGCATTATT AAGAGTCCTG AGGCGACTCT TATACATCTA ATTGGGGATT 300 TCCTGTGCAG CCTAGAGCTG AGAATAAAGG ATGATGTTGT GGTTTAAATA TCTGCCTCTG 360 CCCCAGGCTC AGCACACACG CAAGGTCTTT TAACTTTAAG AAATGGAGAA TTGAGGATGT 420 CACCCATTCA AGATGCAAGC CGATTGTTAG AGCATGCACA GATGCTTGCT CGGGACTGTC 480 AGGGGTCCTT TCTGTGACGG GCAGTTGTGG CAATTAGATG ACGCCTTGTC TGGCAGGCAG 540 TGGTCAGCCC CCACCCTAAG CATCCCTTCC TGACCTGCAC CCCCTTCCCT GGCCCTATTC 600 AGGGATGAAG AGGCTGCTGG CTTTGTACAC TGGTGAATGA CTTTTGTAAA GCAGAAAGCT 660 GAACAGTCCC ATCCAGATGA TCCCACATCA AAACCACCAC CTCAAAGTGG CTGCTGTCAA 720 AGAGGCTTTC TCAAAGCACC ACTAGAAAAC GTCATGCGCC CAGCAAATTA CCAGTGTTTT 780 CAAAGCCAGG ACTACCTTCT GCGTTAAGCT GGTTGCACAG ATAACTTCCT TTCTGTGAGG 840 AGTTTCAAAA CATCCAAGCC ATGACTTCCG GAATGCTGGA GGTACTCAGT AGAAAGATAC 900 AGAGCTGGAA GAATTACTCT TGCTGCAGAG ATTTTTAAAA AGGTTTTAAA AGGTTTGATT 960 CCATGGCTAT GTAGCTAGTG AGTGGAGAAC CTGGAAACCA AATCCATGCA CCTCAGCTCA 1020 GAGAGAAAGT TGCTTTCATC AAATATAATG CTGCCAAAGT GCTCTTGCCG AGGAAGGCCT 1080 TTGGCCCTAA ACACGCTAAT TAAATTCAGT CTACATGCCC CACCATGCCC ATCCACATGC 1140 TTCCTGCAAC ATCAGACAGG AAGCAGCACC TGCCTCGTGG GAGTCCATGT GGGACGTCAT 1200 GGCCGGCTGC CTTTCCCTGG AACTCTGGGC AGTGTGTGAG GAGCTCTCTT TGTCCACCTG 1260 GGACGGCTGC TCAAATCCCA ACACATTCCT AAACTTTCAC CATAAAAACT GGCACCAGTC 1320 AGGAGGCAGG GGTCCTTCTA ATTTGGGCCA GGCAAAGTAC AGCCTGCAGG CCGAGTCCTG 1380 TGTGGGGCCT GTTTCTGCAA CAAGGGCTCA CTGCAGCACA GCCATGCGCC TTCATTCACC 1440
|