| Tag | Content |
|---|
EnhancerAtlas ID | HS091-10705 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:105776350-105777800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:105777300-105777319 | TACTTCCCCCTGGTGGACT | - | 6.3 | | FOS | MA0476.1 | chr12:105776556-105776567 | TCTGACTCATT | + | 6.32 |
|
| | 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 |
| GH12I105382 | chr12 | 105776296 | 105777580 |
|
Enhancer Sequence | GACAGGAAAT ACTGGCTTTC TGTTTGTGAT GAAATGCAAA TTCCTTATGT ATTTTTCCAA 60
AATGTTTAAA ATGAGGCTTT TGTAATCAGA AGTATATAAG CCCCCTTCCC CCAAAGAAAA 120
TGATTATTCT ACTGCCCGTC TTGACTGTAT TCTTACTTGG GGGCAGGGTG GGTGGCGTGA 180
ACAGGGAGAG CTAATCTCTC CTTCTTTCTG ACTCATTCCA CAGTCAATCC TTTTTCTTAT 240
TATTTTCCAA AGGCATGAGG ACCTTCCATG TTCCGAAACC ATTGTCCAGA GTATTTCTTC 300
TGGACTATTT TCCACTTCCT TCCATCTGAC CGGCCAGCTG TTCTGCATTT GTAAAAGCTG 360
GTTTCTGATG TCATCTCTAG GCAGGACCGC TCCCTCCCTC TCCTGCACTC CTATACTTCG 420
TGGCATATCC GCCCCAAGAT AACACTTGTC ACTCTGTTTT CCAAATTCAG TTTCATTCAT 480
TTGCTTCACA TGTGCACTGA GCCCACTGAC TTCTTTCCCT GTCTGTTGCC AGCACTGGAG 540
ACCAAGCCTG CACGCTTTGG CCCAGACCAT CTCATTCACC TTTTAACACA GAATCAGGGT 600
GAGTGGAGAG TGGGGGAGTG GTGTGGTGGG TCTTTGCCTC TCGCTGTTCA GTGAACTTCA 660
TGCCTGTCCT CCTGATCCCC AGCGCTAACA CAGGGTCAGG CTCGCGGGAG TGAACAACCA 720
CCATTTATCT CCGGCTTGTT GGGGGAAGCC CTTTCATTTA CTTGACAGTT TACCTGTCAA 780
TTTTACGTGC GTGGTCATTT TTAATCCTCT GCACTTTCAG GTAATAGGAA AATAATTTGA 840
ATCAAGTTCT TCCTTCACCA TTGGCGTAAA ATCGGTGATT AAACTTTTAA TATTTAACGT 900
CTTAAAAAAA ATTCCCCGGG CTAGCGTCAT GCCTAAGTAA TGCATGCATC TACTTCCCCC 960
TGGTGGACTC ATCTTCTAAT AGCAGCTTTG TTTTCCCCCC TTTATTATTG GCAGGAGTAA 1020
TCCATCTCTC ACTTTCCTTA ACACAGATAT TCATGGATTG CAGGATTCAG CAGTGTCTTC 1080
ATAATAGCAG GAAGTTTATG TTCTGGCTTT GCCACTTACT AGCTGTGTAA CTTGGGCAAT 1140
TTACTTAACT TCTCTGCGTC TCGGTTTCTT AACCTGTAAA ATGGAGACAG TATCAATAAT 1200
AAAATATTAA AAACGAATAC ATATCAAGTG CTTACTACAT GGCATGTATG AACTCATTAA 1260
ATTTCTACAA AAATCCTATT ACATAAGATT TAAAATGTCC TGGCCGGGCA CGGTGGCTCA 1320
CGCCTGTAAT CCCAGCACTT TGGGAGGCCG AGGCAGGCGG ATCACGAGGT CAGGAGATCG 1380
AGACCATCCT GGCTAACATG GTGAAACCCC ATCTCTACTA AAAAATACAA AAAATTAGCC 1440
GGACGTGGTG 1450
|
