| Tag | Content |
|---|
EnhancerAtlas ID | HS091-10888 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:112053120-112055450 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr12:112054272-112054283 | TATTGTGCAAT | - | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr12:112054546-112054561 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I111616 | chr12 | 112054221 | 112054370 |
|
Enhancer Sequence | TAGAGTACAA TGGCATGATC ACAGTCACTG CAGCCTTCAC CCCCGGGCTC AAGCAATCCT 60
CCCACCTCAG CCTCCCCAGT AGCTGAGACC ACAGGCACGC ACTACCAGGC CTGGCTAATT 120
TTTGTATTTG TTGTAGAGCC AGGGTCTCCC TGTGTTACCC AGGCTGGTCT TGAACTCTGC 180
ACAGGCACTT TTCAGGTCTT TTCTTGTGTC ACATTTTCTA ATGTCACATT AGCCAAAGCA 240
AGACATGTGG CCAAACACAA AATTTGAGGG GTAGGGAAAT ATACAGCCAA ATAACTTTGC 300
AAAGGATGGG CATGTAGGGA GGAACCAATT GGTGGCTTTT TTGTGTAATC ATCACAATTG 360
GAGGCGAGAT ATTTGAATAT CAATACAAAA ACTTTTATTC TTTCTTTATT TACTTTTTGA 420
GACGGAGTCT CGCTCTGTCG CCCAGGCTGG AGTGCAGTGT CGTGATCTTG GCTCACTGCA 480
AGCTCCGCCT CCCGGGTTCA TGCCATTCTC CTGCCTCAGC CTCCCAAGTA GCTGAGACTA 540
CAGGCGCCCG CCACCACGCC CAGCTAATTT TTTTGTATTT TTAGTAGAGA TGGGGTTTCA 600
CCGTGTTAGC CAGGATGGTC TGGATCTCCT GACCTCATGA TCCGCCCACC TCGCCTCCCA 660
AAGGCTGGGA TTACAGGCGT AAGCCACCAC GCCTGGCCGA AAACTTGTTC TTTTAACAAG 720
ATGCCTTCCG GAATGCAGAA CAAAGCTGAG AAGCCTTCTT TTAACAACCT GATGATTTCC 780
AAACTCTAGA TTCTTGGTCA TCTCACCCTG GACTATTAGA ACCATCCTGA TGAAAATAGC 840
ACCAGGTATA GTTTCTGCAC AGCTGCTTGT CCAGAAATGT GTGACCTTGG GAAGGTCATC 900
CTCATTGTTC TTCATCGAAA ACAAGGGGTT ATACTAGATC TTCTCAAATT GCAAGGAACC 960
TTTCAGAGGT CATGTTTCAG GAAAATGAAA GAACAGGCCA TATGTGGAAT GGCCCAATCG 1020
CTGCCTGTAG AGATAAGACA GCCAGAGAGG CTGAAATTTT CAGCTTTCAT CCAGATTTTG 1080
GCATGGGCTG TGAGTCTATG ATTTTTCAAC TTTTCCTTCT CGTAGGCTTG TTTAAACCCT 1140
TTGATCTCAT TTTATTGTGC AATATTATTA CACCACTTTA CAAATAGACC ATTTATTCCA 1200
GGCTGACCGT AAAAGTCATT CCCGGCTGGG TGCAGTGGCT CAAGCCTGTA ATCCCAATAC 1260
TTTGGGAGTT CGAGGCAGGC AGATCACCTA AAGTCAGGAG TTCGACACCA GACTGACCAA 1320
CATGTAGAAA CCCCGCGTCT ACTAAAAATA GGAAAATTAG GACCTGGCAC AGTGGCTCAC 1380
ACCAGTAATC CCAGCACTTT CGGAGGCCAA GACGGGCGGA TCACCTGAGG TCAGGAGTTC 1440
ATCACCAGCC TGGCCAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA AAATTAGCCA 1500
GGAGTGGTGG CACATGCCTG TAATCACACC TACTCGGGAG CATGAGGCAG GAGATCTGCT 1560
GGAACCCAGG AGGCGGAGGT TGTAGTGAGC CGAGATCGTG CCACTGCACT CCAGCCTGGG 1620
AGACAGAGTG AGACTCCGTT AAAAAAAAAA AAAATAGGCC GGGCGTGGTG GCTCACGCCT 1680
GTAATCCCAG CACTTTGGGA GGCCGAGGCA GGCAGATCAT GAGGTCAGGA GATTGAGACC 1740
ATCTGGCTAA CATTAGTGAA ACCCCATCTC TACTAAAACT ACAAAAAAAT TAGCCGGCTG 1800
TGGTGGCGGG CACCTGTAGT CCCAGCTACT CGGGAGGCTG AGGCAAGAGA ATGGCGGGAA 1860
CCCTGGAGGC AGAGCTTGCA GTGAGCCGAG ATCATGCCAC TGCACTCCAG CCTGGGAGTG 1920
CAGACAGAGC GAGACTCCAT CTCAAAAATA ATAATAATAA CAATAATAAT AAAAGTACAA 1980
AAATTAGCCA GCGTGGTGGC AGGCGCCTGT AATCTGAGCT ACTATGGAGG CTAAGGCAGG 2040
AGAATTGCTT GAACTCAGGA GGCCAAGATT GCAGTGAGTC AAGACGGCAC CACCGCACTC 2100
CAGCCTGAGC AACAGAGCGA GACTCCATCA CAAAAAAAAA AAAAAAAGTT ATTTCTGTCC 2160
CCTATGGCTT GAAGGGCACT CATACTCATA GTTAGCAGAA TCTTCAATAA TACTAGAGCT 2220
TAAATGGGAG AGAGTCATAC AGTAGATGCT TGAAAATGTT CAAATAAATG AAGGCCAGGA 2280
GGCTGGATGC AGTGACTCAC ACCTGTAATC CTAGCACTTT GGGAGGCCAA 2330
|
