| Tag | Content |
|---|
EnhancerAtlas ID | HS012-17099 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr2:237933460-237934460 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr2:237933901-237933915 | AAGAGATGAGTCAG | + | 6.25 | | TBX21 | MA0690.1 | chr2:237933736-237933746 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr2:237933736-237933747 | AAGGTGTGAAT | + | 6.02 |
|
| | 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 |
| GH02I237024 | chr2 | 237933361 | 237935587 |
|
Enhancer Sequence | ATTGTATAGC TATTTATTGA GTTCCAACTA TGGGTTGGGC TCTGTTTCTA TTTCTGGGGT 60
GGGAAAGCTG TCAAAAAAAA CCCTGCATCA TGAAGCTTCT ATTCTAGTAA GACACTGGGG 120
AGACCAACAA TATACAAGAT AAATAATAAA ACACGTAGAA TGTTAGCTAT TAAGTGTTAG 180
TATAAGAATA TTTAAAGCAA AGAGGAGAAG TGGCTATGTA GTGAAGGGAG GAGGGGTGAA 240
ATCATAGTGT CCCTGGCCAG AGAAGGATGC ACTAAGAAGG TGTGAATGAA GGGTCGAAGG 300
AAGTCAGGGA GGGAGCCATG CAAATACCTT CGGGAACAGA AGGAACAGAA TGTGCACAGA 360
CACAAAGCAG GGGTGTGTCG CGTGTTCAGG GCATAGTGCA TAGGGCAGTT GGCTTGAACA 420
GAAGGAATGG GGAAGAGAAG TAAGAGATGA GTCAGTATGA CAGGGCCACT CACAGCCTCG 480
CACGTCATGA GGACTTTGGT CTGGAAGGAG TGAGCTGGAG GCCAGGGGGG AGTTTTGCTC 540
AGAGGAATGA CATGATCTGA TTGTAACAGG ATCCCTGTGG CTGACTTAAC TGACAAAACT 600
GATATTAATT TTACTGATGT TGACAGAAGG CTATAGCAAT GCAGAGGGGA GAGGGCAGGG 660
GAGCTAGATC TGATGCAGGA GGATCATTAA AAGGCTATTG TGGGGAGCTG GGAGAAGCTG 720
ATAGGGGCTT GGAGCAGGGT GGGTTAGTAT AGGGGGGAGA ATGTGACCTG ATTCTCAAGC 780
CAACCAACAT AATCTGCTAG GTAGTTTCAT GTGGGGTGTA AGAAGTAGAG AGGAATGAAC 840
GTTCGCTCCA AACTTAAGCA ATTGGAAGAA TTCACTGAAA TTGGAGACAG ATGTGAAGAA 900
CAGGTTTGGT GGAAACATCA GAAGTCTGAT TCAAACATGG TGAGCTTCAG ATGCCCACTG 960
AATGTCCGAG AGCAGCAGAT GTCAAGGAGA AGCTCAGGTG 1000
|
