| Tag | Content |
|---|
EnhancerAtlas ID | HS091-10751 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:108063400-108065720 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr12:108064315-108064326 | GCAGGGTGTGG | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 108064289 | 108064519 | | chr12 | 108064916 | 108065094 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I107671 | chr12 | 108064921 | 108065070 |
|
Enhancer Sequence | AAATAATAAT AATAATAAAT ATGATCAGCT GGGTGTGGGG GCATATGCCT GTAGTCTGAG 60
ATATTGGGAG GCTGAAGCAA GAGATTCACT TCAGCCCAGG AGTTCGAGGC CAGCCTGGGC 120
AACATAGTGA GACCCTGTCT CTAAGACAAA AAAAAAAAAA GAGAGAAGGA GGAAGAAAGA 180
GCTTTCTGGG CTAAGACAAA TGTTAGTCAT GTGTATCTGT GATGTGGTGT GATGACAGGT 240
CTACTTGTTC TGGATGTCTT TTTTTTGGTG AGTATTGTTT GGGGGAGAAA GAAGTATTGG 300
GTGGCGTGAG GATTCAATGT AGATGGACCA ATGTTTAATG GGACTGAGGA CACAGAGAGG 360
ACACAGAGCG GACACAGAGA TGTGGGAGAC AGGGTCCCTC AAGGTGCTCC TTGACACACA 420
GACACAGCTT GGGGGACTTA GTTGCTGCCA AGCCAACTCT TGGCGTGACA TGAGGTGGCA 480
GGAGTGGGGA CGGACGGCCA CTGAGGACCC ACCACCCCAG GACAGCCGGG CGCCTCTGGC 540
AGGCAGGTCC ACGGTTACTG ATTGTCATGG TCAAGCTCAG CTGGGCACTG GGTCCAGAAG 600
GAGATGTGAC TGGCCCATTT TGTGTCTTTT ATCTGAGCCT GCACCTTTCC TAACTCAGAT 660
TTTTTAAATA CTTTTTTCTT TATACTCACT TTGTTTTTCT CTGTACTAAT ACACTAACTC 720
GGATTTTTGG CTTTTATTGG GCCGAGGTCC CACCAACCTG GATGCTCAGC CTTGTTTGGT 780
AAAGCAAGAA AAGTATCTGA GAAATGTTCC CTAAAGGCTG ATTTCACCCC AAACAGTCAC 840
TCAGTGATGC GCCTCACTTA CCAAGGACAC ACCCCCAAAA GGCATCTCCT GGCCTCCGGG 900
TCTCACTCTG TTATCGCAGG GTGTGGTGGA GCAGGTGTGG TTGGGTGGCC ACCAAGATGG 960
ATTTCAGTCT CTTTCCAGGC CCAGGGAACA AGCCGAATTC GAGAGACTTG GCTTTTAGCC 1020
TCCTGTTAGA GCCAAGAAAG ACTTCAAAGA CTCAACGGCT TCTAAGGCTT TTTACATCAG 1080
CAAAGTCCTG CAAAGCCTGC AAACGAAGGC TGCTTTGAGG CCTTTCATTC TAAGGACAGA 1140
GAAGGTAAAT TCCATGGCCA CTTTCTCCAG AGCAGCAACT GGGCTCCTTC TTTTTACTTC 1200
CATGGGGAGG ACAAGAGATT CATTTGCTTT CTGTTGCTGA GAATGCTATC AAAACAAATT 1260
TTACTTTTAG CTGCAACCTT TCAAAAGCGT CTTAAGCATA AAGCACGAAA AAATCCCCAA 1320
GCTTATGTAG GCATTCTAGT TTTTTCGTGG TTGGTGTTTT TTTTTAACTG TGCCAGTTTC 1380
AGCTGAAACA TGGTTCTATT GTTTCCATTT CCCACTGTAC ATACAGCACT GAATTCTTGG 1440
GGAGCAAAAG TACGAGGGCA GATTGAGAAA CCCCAGTTCA TGAGAAGTTT GTTGTTGTGG 1500
TGGTTGTTGT TTTAGCAAAG AGAGGAAATC GGTAAATAGC TCTGATGTTG AGACAGCAGG 1560
AGGTCAGGAC ATTGAGCAAC GTGCAGGTGG GGTTGTGGAC TCAGGGCTGA GCGGCAGGGG 1620
GCGCTCCTCC CAGTGCAAGC CTTCAGAAAC ACCAGCCTTG AGTTGGACGG TTCTGGCTCA 1680
TTGTGTGGAG TCCTAAGTGG TCACACTCCA CACTCCTAAG TGGTCTGGTC ACACAGTTGT 1740
TTTAAAGAAG GGTAATGGCT CATTAGGTAG ATTTGGGTAG GATGCAGCTT GAAGTGGGGC 1800
GTAAAATCCT TTCATTGTCC AATGGGGAGG TCACAGTGCA GCAGCTACTC CTTGTACTTG 1860
GAATGAGGGA AACAGCGTAA TCTAGACTTG AACACGGGCT CAGGAACCAG GAGCGCCAGC 1920
CACAGATCTC ACTCACTCTC ACTGTTGTTT GCAACTTTGG GCAAGTCAAG TAACTTCTCT 1980
GCTGGATCAC TGCTTCTCCA ACTGTGTGAG CATTTGTAGC TTTTTCCCAA ATAAGTACTC 2040
TACTTCCTGG CTTTCCAAAG TGGAGCCGGA CAGTCGCTTC TGCATCATTG GGAGTTTGTT 2100
GGCAATGCAG AATGTCAGCC TCGATTCCAG ACCTACTACA TGGAATCTGC ATTTTAACCA 2160
GAGGCCCAGT GCTGAGCACA CTGAGGTCTG AGAAGGACTG CTCTGTTCTC CCAGGTCACT 2220
GCAATGGTAT CAGGTTCTTC TGTTCCTCTC TCTCAGAGGA TACTTGAAAT GATGCCTGAA 2280
AAAAAAGACA ATCTAGGCCA GGCATGGTGC CTCATGCTTG 2320
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