| Tag | Content |
|---|
EnhancerAtlas ID | HS091-10789 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:109865680-109867150 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:109866005-109866024 | CTGCCACCAGGGGGCAGCC | + | 7.69 | | Nr2f6(var.2) | MA0728.1 | chr12:109866797-109866812 | GAGGTCAGAAGTTCA | + | 6.38 | | RARA | MA0729.1 | chr12:109866797-109866815 | GAGGTCAGAAGTTCAAGA | + | 6.88 | | REST | MA0138.2 | chr12:109867047-109867068 | AGCACTGTCCTAGGTGCTGGG | - | 7.39 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 109865808 | 109866435 | | chr12 | 109866601 | 109866754 | | chr12 | 109866815 | 109866908 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I109428 | chr12 | 109865941 | 109866090 |
|
Enhancer Sequence | CTCTACAAAA AAAAAAAAAA AAAAAAAAAA AAAAATATAT ATATATATAT ATATATATAT 60
ATTAGATGGG TGTGGTGGTA CACACCTGTA GTCCCAGCTA CTCAGAAGGC TGAGGTGGGA 120
GGATCACCTG AGCCTGGGAG GTTGAGGCTG CGGTGAACTT GAGATCGTAC CACTGCACTC 180
CAGCCTGGGT GACAGAATGA GAACCATCTC AAAAACAAAA CAAAACAACA AAAAAAAAAA 240
CTCACAAAAA TTCAGTTTAC CATCTTCTGT TCATTTCACT AATCCCTGAC TGTTTACAGT 300
CAAGGGCAAG GCCAAGTGCG TAGATCTGCC ACCAGGGGGC AGCCGTGGGC AGTGCCCCAC 360
AGGCCTCTGA ATTAGCAGGA GAAGCTAAGT CCATTTGTGA CCGTAGGGCC TGGTTTAGTG 420
CCTTAGCGCA ACGGGCTGTC AAGAGCAGCA GGTTAGCGGT GGGGACATGG GTTTTCAAAC 480
CACATGAACT TGGATCATAA TCCTCATTCT CTTATAGCTG TGACCTGTCA TTTCCCTTAT 540
CTGTAGGATT AAATTGTCTG GGATCAGGGA GTTTGTAAAG ATTTAATGAA CTATTTCTAC 600
GCCTACTCTC ACCATCCCCC AAATTGCTTA TACACCAACA CTTCTTCAAT GATGGGCTGT 660
GTGTGAATTT ATGCTACCAA AATAGCAACA CACTCTCAAG CATAATAAAT GGTCACTTTG 720
TTGGGTCAGA ATGGTTGAAT AGCAGAAATT TCATGTGGTT CAACCAATAT TTTGAGTGTA 780
GTCATTTGAG ACTCTTTGCC TTTATTTTTC CTGGATGTAC CTCCTTTGCC CACCATTTTT 840
GCCCATCCGC TACTTATTCA TTCATCTTCA TCCCAAATCT GACTTCTGCG GCAGATGGCA 900
GGGCAACAGC CACTGCCCAC CTCACCCCCC TCCAAACATA TACACACTTG ATGTTCCCAT 960
CTACCTGTGT TTTTTTGAAC TTCATACATC TCTTGTCTAT TTTTGCTGCT TTCTGAGGCT 1020
CATTCATTCT TTCCATAAAA TCTAGTGAGC AGGCCGGGCA TGTTGCCTCA CACCTGTAAT 1080
TCCAGCACTT GGGGAGGCCA AGGTGGGCAG ATCACTTGAG GTCAGAAGTT CAAGACCAGC 1140
CTGACCAACA TGGTGAAATC CTGTCTGCTA AAAACACAAA AATCAGCCAG GCATAGTGGC 1200
GCATGCCTGT AATTCCAGCT ACTCAGGAGG CTGAAGCATG AGAATCATTT GAACCCGGGA 1260
GGCAGAGGTT GCAGTGAGCT GAAATCACAC CACTGCACTC CAGCCTGGGT GATAGAATGA 1320
GACTCTGTAT CAAAACAAAC AAAAACTGGT GAGCAGCTAT CTGAGCTAGC ACTGTCCTAG 1380
GTGCTGGGGT GATGTCAGAG AACAGAACAG ACCCCATCCC TGTCCTCATG GAATTTACTT 1440
TCTATGGGGG AGACCAACAA TAACAAAGAC 1470
|
