Tag | Content |
---|
EnhancerAtlas ID | HS136-04769 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr12:69432900-69434680 |
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 | chr12:69434574-69434595 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | IRF1 | MA0050.2 | chr12:69434568-69434589 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | Nr2f6(var.2) | MA0728.1 | chr12:69434240-69434255 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr12:69433436-69433451 | CGATCTCTTGACCTC | - | 6 | SOX10 | MA0442.2 | chr12:69434094-69434105 | AAAACAAAGAC | + | 6.14 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 69433704 | 69434066 | chr12 | 69433721 | 69434090 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I069039 | chr12 | 69433580 | 69434090 |
|
Enhancer Sequence | AGTTATTAGT CCAACATAAC TGTGATTTTG AACACTTATT TATTGGGCAC CTCTTCTGTG 60 CTAGGTGCAA GGGTTATCTC CTGTAATCTT TATAACAATG AAATCAATAC TATTATTATC 120 CAATTATGTA ACCAAGGAAA CTGATGCTTA GCAAGGTTAA GTAGCTTTCT CAAGGTCAAG 180 GTGAGTGGTG GAGCAAGCAG GTAAACCCAT GTGTGTCTAA GGCCACAGCC TATGCTCTAG 240 TCACCAGGTA ATCATTGATC TCTCTGGAAT ATCCACAGTT GGAAAGCAAG GACTTTGCAA 300 CTTGCTGCTG AATGTATTTC TTTTCTTTTC TTTTTTTAGA CCGAGTCTCG TTCTGTCACC 360 AGGCTGGAGT GCAGTGGCGC AATCTCGGCT CATTGCAACC TCCACCTCCC AGGTTCAAGT 420 GAGTCTCCTG CCTCAGCCTC CCCAGTAGCT GGGACTACAG GCGCACACCA ACACACCCAG 480 CTAATTTTTG TATTTTTAGT AAAGACGGGG TTTCACCATG TTGGCCAGGA TGGTCTCGAT 540 CTCTTGACCT CGTGACCCAC CCACCTTGGC CTCCCAAAGT GCAGGGATTA TAGGTGTGAG 600 CCGCTGTGCC CAGCCGCCGC TGAATGTATT TCTTACCACC AATCTGTTCA GTCATTACTA 660 TTCCTTCCCC CTTTCCTAAG TACCATGGGA AATGAAGCAT AAAGCACTCA AAGTCCAAGG 720 AAAAGGCAAC ATTCAGGATT CAGTTCCAGA ATGTCTGCCT CTTCCAGACC CATGCTCCCA 780 CCAGTTGGCC ATGCATTCTC AACTTGCATG CCTATGTCAT CTGTCTCTTC TGACCCTGAA 840 GAAAGCTTCT ATTCACTCCA TGAGCACCTG CACCTTCACT GAGTCAATAG TGAGTGGCTG 900 CTATCTGCAC CAAAATCCAT TGCTCAATAT TCTTTCTTCT CCATTCCAAA TGGTTCCTCA 960 TTTCTGTGAA AGCCCACATG GTCTTACCAT ATGTCTCGTT GTCTTGGTAG TAAACGCATT 1020 TTTAAAAACA AATATGTCAG CATCATTTTG TTTTTTTTCA TTAGTGGTCT CATGTTACAG 1080 TCATAACAGG TTGCATAATG GTTACATCTA GTACAAAATA ATGCTATTGT GTTTTCTCTT 1140 GGAGGCTGTT ATCTAGTTAC ATTGCTTGTG ACTAGCTAAG GAGGATATTG TAGAAAAACA 1200 AAGACCTTCA AGGTAGACAG ACCTGACTCT GAATTCTGAC TTTATCATCC ATTCATTTAA 1260 AAATATTTAT TCAAGGCCAG GCGCGGAGGC TCATAGCTGT AGTCCCAGCA CTTTGGGAAG 1320 CCGAGGCGGA TGGATCACCT GAGGTCAGGA GTTCAAGACC AGCCATGGTC TTGAAATCCC 1380 ATCTCTACTA AAAAATACAA AAAATTCGTT AGGTGTGGTG GCACACGCCT GTAATCTCAG 1440 CTACTTGGGA GGCTGAGGCA GGAGAATTGC TATATATATA TATTCCTGGT ACGTAGTAGG 1500 TCCTGAATAA ATATGTATAT ATACTCCAAT TTTAACATTT CCTATGCCCC TTCCCTGCTT 1560 TATTTTTCTC CTCAGCATAT CATTGGCTAA TATAGCTTTT TCTCCTCATT TGTCTTGATT 1620 AATGTCTATC TCACTCCACT TGAACATAAG CTCCATGAAG ACAGTGTTTT TTTCTTTTTC 1680 TTTTTCTTTT TTTTTTTAAT ACAGTCTTGC TCTGTTGCCC AGGCTGGAGT GCAGTGGCTC 1740 AATCACAGCT CACTGCAGCC TCGAACTTCT GGGCTCGAGC 1780
|