Tag | Content |
---|
EnhancerAtlas ID | HS118-03226 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr11:17771490-17773610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr11:17772921-17772932 | GGGTGACTCAG | + | 6.02 | HNF4G | MA0484.1 | chr11:17773357-17773372 | TGCCCTTTGAACCCT | - | 6.03 | JUNB | MA0490.1 | chr11:17772921-17772932 | GGGTGACTCAG | + | 6.02 | RREB1 | MA0073.1 | chr11:17773133-17773153 | GGAGGTGGGATGGTTTGTGG | - | 6.13 | RUNX1 | MA0002.2 | chr11:17773387-17773398 | GTCTGTGGTTT | + | 6.62 | Rxra | MA0512.2 | chr11:17773357-17773371 | TGCCCTTTGAACCC | - | 6.04 | ZEB1 | MA0103.3 | chr11:17772166-17772177 | CCCACCTGCCC | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTCTGAGTG CCATGTGCAG GAAGAGGCCA CCATCTCAAG TGCAAGGGGA GTGTAGGGAG 60 GGGACAGGCT AAAGGAGGGT GCACAGGCCT TTGGGCCTGG CCAGGCCTGG GTTCTGATCC 120 TTCCTCTGCC TCAGTGTGGA CTCGGGCAGG TGGTGTCTGG CTGAGCCTCA GTTTCCTCGT 180 GTGTAAGATT GGATGATAGT TTGTATTTCA CAGGCTGTGG TGGGTCTCAG AGGGGCAAAG 240 CCCCCAGCAC CGTGGCTGGC ACATGGGAGA CACTCGCCAA GGGCTGGATC TGGTGACCTG 300 GGGTGCCATT GTCAGCAGGT CCTGGGTTTG GATTTTCCTG GGTATAAGGA GGCCCTGGCT 360 GAGCCACAGA GGCAGGGAGG GAGGCTGTAG AAGCCTCAGC CGGTTGCCCA CAACCTCAGG 420 GCCAGGAGCC ACCATCACCA ATGATATATT TAGAGTCACA AAGGTCAGAA ATACCAGGCG 480 CTGGCTTCCC TTCTAGGCGG CAGGAATCGT GTCTCCCGAG GCCTGGCTGT CACCAAGCAG 540 ATATTTTTTC CTGTCTGGCA GTCTGAGGAT TGGAGTAAAA GCCTGGAATG TAGGAATCAC 600 AGTGGTTTGT GCTGGCTTAC TGACACTTTC CATGTCCCCA GCCCTTTCCA AAGCCTGTGG 660 TGTGATCCTT GGGAGCCCCA CCTGCCCTGC TATTCCAGAT CACCCTGGGC CCCAATGTGC 720 ATCATCCATT CCCAACGTGC TCCGGCTCCC TGCCCTTCTG CCTTTGCTTA TTCCGTTGCC 780 TCCACTGAGA ATGCCCACTC CTCCTCCTCT GCATTTCTGA AATGGATGCT TCCTGCTAGG 840 CCGGCTCTCA TGGCTCTTCC TTTAGGGAGC CTTTCCCGAC ACCCTCTACC TCCTGGAAGA 900 GCCTGCTCTG CCCTTCATGC TTCCAGAAAA CCTTTCCTGT CTGACTTGAG GCCTTTGATC 960 CACTGACTAT CATTCTGTGA CTCTCAGACT CAACCACAAC CTCTTGGAGG ACAAGGGTCA 1020 GGTTAGGCAA TAGTAGTGCC TGTTACATAA TAGGGAATCA ATCGATCTTT GCTAAAGCTA 1080 TGTGCCCCTG TGAGGTGGAA GGGTTAGGTA GTATACCCCT CTTATTGATG AGGGAAAAAT 1140 GGCTCCCAGA GAGAATCATT TATTTGTCCA AGACCATCCA GAAGAGAGCA AGTGGTAGAA 1200 GGATTAGATC CCAGGTCTTC TTTTGAAAAT AAATCAAGAA GGTCAGCTAG AGCCATGCCA 1260 GTGTTCCTTC TGGCTCTGGG ATGCTGTGGT TCTATGGTTA AAAATGAGGT AGTGGGAGAG 1320 ACCGACGAGT AATGGACGAA TAGATGAAAG AATGGATAAA AAGACGGATA TGTGGATGGA 1380 TACAAGTGAA TGGATGGAAG GAGGGACATA TGGATTGAAG GAGACACAGC TGGGTGACTC 1440 AGTGGATGGG TAAACAAATG GCTGAGAAGG ATGGATGGAG GACCATGGAT GTGCTTCTCC 1500 TTGCGTGCCT TCAAAGCGGA AGTCCCACCT CTCACAGGAT GAACACATCC TGGACGATGG 1560 GACTTGGAAG CATGGACTTC AGGGCAGTAG GCAGAGTGGA GTGGCCCAGT ACATGTGTGC 1620 AGAAAGTGGG ACTGCCAGAT GCAGGAGGTG GGATGGTTTG TGGAGTGAGA GAGCTGGGAG 1680 CTGGGGACAG AGACTGGGCT GAGGGACTGG CCCACTCTCA AAGGTGAGAG TCCCTGATGG 1740 CAGAGAACCA GGACCAGGCT GGAAAGAAGT TCCAGGCAGA GTCATGTGGC CGGCAAGCCC 1800 TCAGGACCTG TGGTTTTCCA GACCTGCCTC TGGCCAAAGC CTGAAGGGCA GTCAGTGAGT 1860 GGGGGATTGC CCTTTGAACC CTAGGCTGTG TGAGAGAGTC TGTGGTTTCA GTCTGCTCCG 1920 GAGTAGGGAG GTCTCTCTTC CTCCTCAGGT CCCCAGCCTT GGTGAGTGAG AACCTCTGAT 1980 AGCTCAGGCA GGATGTGTTC AAGGAGGCAG TGCAGCTTCA CCAGCTGCAG AGAAGGTGCT 2040 GAGGAGGGGG CCCTCCTGAG GCCGCAGAAG ACCCTGGCTC AGGTATACCA GGATCGACCA 2100 TCTTCCCACC GCTTTTTGCT 2120
|
| |
|
|
|