| Tag | Content |
|---|
EnhancerAtlas ID | HS118-11071 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:237933550-237934700 |
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 | TGAAGCTTCT ATTCTAGTAA GACACTGGGG AGACCAACAA TATACAAGAT AAATAATAAA 60
ACACGTAGAA TGTTAGCTAT TAAGTGTTAG TATAAGAATA TTTAAAGCAA AGAGGAGAAG 120
TGGCTATGTA GTGAAGGGAG GAGGGGTGAA ATCATAGTGT CCCTGGCCAG AGAAGGATGC 180
ACTAAGAAGG TGTGAATGAA GGGTCGAAGG AAGTCAGGGA GGGAGCCATG CAAATACCTT 240
CGGGAACAGA AGGAACAGAA TGTGCACAGA CACAAAGCAG GGGTGTGTCG CGTGTTCAGG 300
GCATAGTGCA TAGGGCAGTT GGCTTGAACA GAAGGAATGG GGAAGAGAAG TAAGAGATGA 360
GTCAGTATGA CAGGGCCACT CACAGCCTCG CACGTCATGA GGACTTTGGT CTGGAAGGAG 420
TGAGCTGGAG GCCAGGGGGG AGTTTTGCTC AGAGGAATGA CATGATCTGA TTGTAACAGG 480
ATCCCTGTGG CTGACTTAAC TGACAAAACT GATATTAATT TTACTGATGT TGACAGAAGG 540
CTATAGCAAT GCAGAGGGGA GAGGGCAGGG GAGCTAGATC TGATGCAGGA GGATCATTAA 600
AAGGCTATTG TGGGGAGCTG GGAGAAGCTG ATAGGGGCTT GGAGCAGGGT GGGTTAGTAT 660
AGGGGGGAGA ATGTGACCTG ATTCTCAAGC CAACCAACAT AATCTGCTAG GTAGTTTCAT 720
GTGGGGTGTA AGAAGTAGAG AGGAATGAAC GTTCGCTCCA AACTTAAGCA ATTGGAAGAA 780
TTCACTGAAA TTGGAGACAG ATGTGAAGAA CAGGTTTGGT GGAAACATCA GAAGTCTGAT 840
TCAAACATGG TGAGCTTCAG ATGCCCACTG AATGTCCGAG AGCAGCAGAT GTCAAGGAGA 900
AGCTCAGGTG CACCAGTCTG GAATTCAAGG GGAAGGCCAG GGCCAGCGAG TATATTTGCC 960
AGTGGTCAGG ATATAGATGA TATCTAAAGC CAGGAAACAG CATGAGGTCC CGTAGGGGTG 1020
AGTGAGGACA GAAAAGAGAG GGGCTCAGAG GACTGAGCCC TGATGACTCC AACGATGACC 1080
AAGGATTACC TTGACTTTCA AGGTCAGAGA GATGAGGAGG AGCCTCAGCT GTGCTTGGGG 1140
GTGGGGTCAG 1150
|
