| Tag | Content |
|---|
EnhancerAtlas ID | HS059-11767 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr12:117588110-117589170 |
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 | chr12:117588550-117588571 | AATTTGAAAGCGAAAGCCAAA | - | 6.68 | | IRF2 | MA0051.1 | chr12:117588554-117588572 | TGAAAGCGAAAGCCAAAG | + | 6.6 |
|
| | 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 |
| GH12I117151 | chr12 | 117588981 | 117589170 |
|
Enhancer Sequence | TTTAACGTTC AGCTACCCCA AAATATATGA ATAAATACTA TGGAAACACT ACCCATGAGT 60
CCTGTGTGGG CACCTGTCCT GTCCTGATCC GGTCTTCCTC TCCAAGAGAA AAGCACCATC 120
GGTGCCAGTG TGTCGCTGCA GTCCTCCTGT GAGCACACAC ATAGGCAGCT AGATACCCTA 180
AGTATACTTA AAATTTAGTA CTGCTTTATG TGTGTGTACT TAAACAAAAC GTATTCTAAC 240
CACTCACCCG CAACTGGCTT ATTCAATTGC AGCTTAGTAT TCATTCCAGT CTGCATAGAC 300
CCCAGGCTAC TAGAAGACTC CTTGTGAATG ACAATTGTCT TGCTATTTTA ACAAAGGGGC 360
CAAAGACCTC CTTGTACACG TGTGGAGGGA TCGAGGTGGA ACTGCTAGGC TGGAAGAGAA 420
TGTGTGCTTG AGATTTTTAC AATTTGAAAG CGAAAGCCAA AGCATCCTCT GACATGTTTG 480
TGCCACTTAA CACTCAACCC CACCCCCATG CAGGGGATCC CCATTCACCT CACCACACTT 540
GCCAGCAGGT ACAGCTGGCC ATGGACTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTCAG 600
GCGGGAGGAC TGTATGGGTG GAAAGTTGAG TTTGGAAGTA TCAAATAAGT TTGTGTGTGT 660
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTCG GGCGGGGAGG ACTGTATGGG 720
TGGAAAGTTG AGTTTGGAAG CATCAAATAA GTTATGGAAA AGGGAACCAA CGTTTGTCGA 780
GGACATGCCA TGTGCCAAGC ATTGTACAGG TGCTTTACCA TTACAGACAA AACTTAAGAA 840
CGAGATTTTC ACATGGTAGT TGAATTCCTG GCCTTTCAAT ACGGCGGCTG ACCTAGACTC 900
GGAGCTTCCG AGAAGTCCAG AAGGAGGCGG GACAGGAGCG GCACTCTCCC ACCCAGGGCC 960
ATGAAAGTAT CAAAGCGCGC CCCCTTGTGG GAACACAACA TTACACACAT GCAAGATGCC 1020
GGACATCCCA TTAGGGTTTA GGTGAGAGAG TACACACCGG 1060
|
