Tag | Content |
---|
EnhancerAtlas ID | HS134-32857 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr2:187685140-187686390 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr2:187685789-187685804 | TGTTAATGTTTAACA | - | 6.12 | HNF1B | MA0153.2 | chr2:187685790-187685803 | GTTAATGTTTAAC | - | 6.15 | Myog | MA0500.1 | chr2:187685530-187685541 | CTGCAGCTGTC | - | 6.62 | Tcf12 | MA0521.1 | chr2:187685530-187685541 | CTGCAGCTGTC | - | 6.14 |
|
| 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 |
GH02I186820 | chr2 | 187685541 | 187685848 |
|
Enhancer Sequence | AGTACGATGG CCGGGAAAGA GTGGCTGGAT TGTGCAGCAG CTTCTCACCA TCTCTGGCCG 60 GAAGTAACGT TCTTCACTTT CTCCCACATT TCATTGGTCA GAGCGAGTCA CAGTTCTCTG 120 CGTAACTCCA ACAGTGCTGG GAAGTATAGT TTCTTAGACA CCCAGAAAGG AACTAGATAG 180 TATTGGTGAG CACAAGTAGT ATCTACCACA AAAAGAATTG TATTTGACTT CTTTTTTCCC 240 TTTTCCCGTA ACCATCACTT CCTAAATGTT TCTTTAGTAT ATCTAATTTT CTCTATCTCT 300 ACCTGTGGCA GGTGAGAGAT GCACTGCCCA GATCAGCCTT CAAGAAAGGG CTTTTTGCCT 360 CAGCTGCTGA AAATGCTTTC GGCAGACAGC CTGCAGCTGT CTGCTTTTTG AGGGTCTGTC 420 TCAGCTGCAT GGCCTCAGCT TGGGCACTAT CTAGCCCAAG TGCACACCCT TCTTGAGATG 480 GCCTACACCC CATGATTTAT TTGTAGCAGA GTATGACTGG TGCTTTCCAA CTCTCCTCCC 540 TCTGTGAAAT CTTGTTTTCT TTCTTCAGGG AAGGGATTAG GATGAGGAGA AATTAACAAA 600 ATACCAACAT TTTAAATACA GATAAGATCA AGCCCCTTCT TTGCACATGT GTTAATGTTT 660 AACACAGACA CTGCATAACG AATTCTATTT AAGTATCTGT TTTTGGAAGA AACAACCTAT 720 GCAAGTTGAT AATGAGAAAG GTCTGAGAAA GTTGCTGATA AGATAGGGTT TAGGAGCCAG 780 ACCACTTTCA GCATACTGCA GTGGGGACCC TCTCTCTGGT AAGTGGAACA TAGACATCTC 840 TGGGCATAAG GTGGGTGAAT GCTCTGTTAT TAAAACTCTC TAGATTAGTA AGTCATGAAG 900 GTATGCCATT GGGGGTGGGG AGGGCACACA CTAGCTGGTG TGAAGTATCA GAACTTTGAG 960 AAGCACTGGG GAAATAGTTA CCATAATGAT AACAAGAACA GATGGCTATT GCTAAGCTCA 1020 TTACAACCCA AGAAAAAAAT AATGAAAAAC TATGAGCAAT TGAACACCAA ACATGAAATC 1080 CAATGCATCT TTATGATAGC TTACGAAAAC ACTCTTGTGC TGCAAGAAGG CAGAGGAAGC 1140 TGAGGAGCAG GAGTGAATGG TGTAGTAGAG CTCCAGATAA GGTTAAATGC CCCATTGAGG 1200 CAGGTCAGTT ATGACAATAT CAAGGTACGG CTGGGAAAAA TGGGACCCTG 1250
|