Tag | Content |
---|
EnhancerAtlas ID | HS136-01137 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:152491920-152493260 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HLTF | MA0109.1 | chr1:152493095-152493105 | ATATAAGGTT | - | 6.02 | SPIC | MA0687.1 | chr1:152492536-152492550 | AGAAAGAGGAAGCA | + | 6.04 | STAT1 | MA0137.3 | chr1:152492059-152492070 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr1:152492059-152492070 | TTTCTGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chr1:152492059-152492073 | TTTCTGGGAAAGAG | + | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTTTGTTAAG AAAACTGAAA GATAGAGCTG TTAGGTAGCC ATCCTAGGAT TTCCCAGCTT 60 GTAATAGGAA GAACAAGGTT TTGTACTGGA GACATTTTCC TCTGAAGTCA ATGTTCTGAA 120 CATTGTGCTA CAGTCTGCAT TTCTGGGAAA GAGGGGAGTA GTCTCAAGCT TGGACTAGGG 180 GAGGAGAAAG GGGTCTCAAG GGAGTGGTGT TGATATTGAA AGACCCTGAG GACACATCTT 240 CAGAGAAGGA GATAGGAGGC CAGATCATGG ATGGTTTGGA GTGCCAAATC AAGGAGTTTC 300 AACTATCTCA TATTTGTGGA GTATGGTGGT AGGAAAATGG CTTTGAAAGA AGTACATTAG 360 AGAGATAAAA GTTGGTTTAT ATAACATCTA GAGTACTCTC TGACATGACC CTAAGATTAA 420 TTAGGCAGCA ATGATTAAGG TGCTCCAGAA GAGGAAGTTA ATGGAGAGAT TACCTCTGTG 480 AGCAGGTGCA ATGGCCCAGG CATGAAATGA AGATCTGAAC CTGGCACATG GCAGTCATTA 540 CAAAAAGGAA ATGACTGTTG TGAAAAGCAT TTGTCCAGAA GGAAGAGGGA TAGAATCAGG 600 TGATGTATTG GGGTTGAGAA AGAGGAAGCA ACTGGGGTGT CTCTGAGGTT TTGTGCCTTG 660 TGCCTGGGAA ATGATGACAG CATTGACAAA ATAGAGAAGT CAGGAGAAAG AACAAGTGTG 720 AGGAGGAGAG GTAAGTTTGG TCCAAGATGT GTTGGGTTTG ACGTGCTGGC AGGACATGAC 780 CATGTGACAG TGATGTGGGG CTGGAACTTC AGACTCAGAA TCCTTGAACA TTGACATAAA 840 CACAATTAAG ATAAATGGTA ATAAGCCTTA TGCAGCTTGG AGTCAAATCT TTGGGAATGA 900 ATGCAGTCCT ATTTCTGCAG TGAAGGTTAT GAGAAAATAG ACTTGGTCTG TCTTGTTCAT 960 TGCAGCAACC TCAGTGCAAA GAACAGAGAC CTAGGCAAGT AAAGGCACTC AGTGAATATG 1020 TGTTGAGTAA GTCAATAAAT AAAACAGCAA GACAGAGTGC CCAAGACTTG AGTTGAGGGA 1080 GAAACGAAGC AGAAAGGAGG AAGTTGAATT CCGATCGAAG GGGGCAAAGA TGATGAAGTC 1140 AGAGAAATTA CTCAGATATT TGGCCTCAAC AATTCATATA AGGTTACTTT AAAGTCTTAT 1200 GTTCTAGGAA TCTGGGCAGA AGGGAACCAG CACGATGCAA GAATGCAGAA GCTAAAGAAT 1260 GTCAACCAGT CAGGGTCTTC CTTCCCACTG CGCGATCTAT CTTTGGCATC TTTAAACCAT 1320 TGAACAGTTA TAGTAGGAAA 1340
|