Tag | Content |
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EnhancerAtlas ID | HS091-21712 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr18:265530-267960 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr18:266755-266770 | TGAACTCTTGACCTC | - | 7.64 | Nr5a2 | MA0505.1 | chr18:266747-266762 | GCTGGCCTTGAACTC | - | 8.25 | RARA | MA0729.1 | chr18:266752-266770 | CCTTGAACTCTTGACCTC | - | 7.63 | Zfx | MA0146.2 | chr18:266780-266794 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CTAAAAAAAA ATTAAAATGG CAAATAATTG TAAAGATTTT GCTTATTATT TGCTGAAAAA 60 TATATCGTTC ATTGATAGTG TATCTTACTA ACTAAAAAAT GCTTATACCT GGGAAAAATT 120 ACCTATCAGT CATTCTCTCA GTAATCCTTA TTCCAATGCT ACTTCATGAT ACGGATCCTC 180 ATCACTTTAA ATCTGGCAAG AGCTTCCTTG CTGGACTTTT TCATTCTAGG TGATATTTCT 240 GTCTCTTTAA ATATCACATT CATGAGTATT GTGCTTACAA AAAAAAAAAA TCTCCATATG 300 GCTCCTTATT TGCCCGTTTT AGTTTTGAAG CTTCATAGAT CCCTCAAGGT CCTTGATAAT 360 GTTATCCCAA TTTACCCAAA CTTAATTCCC AATACTCCCT AACACATACT TTGCACTAAA 420 GTCTAGCCAT TTTTCATCAC TTTATATCAA ACTCATTCTA CTGTATTCAC ACATTCATGT 480 TGCTCTTCCT ACCTGCTCAT CCAAATTCTA TCCATTCTCC CACACCCATG TCAGGTCTCG 540 CCTCCTGGAG GTATCTTGTT CAGTCCCTGA CACGTAGCAC TCAATAAAAC CATGCTGACA 600 ATCTGTAGAT TGTTTTAAAG TAATCATAAC TTAAAGACAA AAATATTGCA AAAGGCATTC 660 ATTCTATGAA CACTCACATA CACTTAGAAA GTCATCTTAT TACCTCACAG GAATTAGATC 720 TATCCTAAAT GTGTCCATTC CTTGCTCTGC CACTAACAGG CTGAGTAATT TGGGGCCTGT 780 TCCTTTATCT CTTTGTGCTT CATTTTCGTC ACCAGTTAAA TAAGAGGGTT TTTGTAGATT 840 TTTACTACCA GCAGCAGCTA CAGTGGCATC ACCTAGGAAG CTGGTAGAAA TGCAAAATCT 900 CAGGCTCCCT TCCACACTTA CTGAACAAGA ATCTGCATTT CACAAGAAGC TTGAGAAACA 960 CTGAACTAGA TGATCTCCAA TTTCATGGTC CTTTTCAGGG CTAGTATGAT TTTTTTTTTT 1020 TTTTTTGAGA TGGAGTCTCC CTCTGTTGCC CAGGTGTTGT GCACTGGCAT GATCTTGGCT 1080 CACTGCAACC TCCGCTGTCC GGGTTCAAGC GATTCTCCTG CCTCAGCCTC CCAAGTAGAT 1140 GGGATTACAG CGCCCACCAC CACGCCTGGC TAATTTTCGT ATTTTTAGTA GAGACGGGGC 1200 TTTGCCATGT TGGCCAGGCT GGCCTTGAAC TCTTGACCTC AGGTGATCCG CCCGCCTCGG 1260 CCTCCCGAAG TACTGCATTT ACAGGCGTGA GCCACTGCGC CCGGCCGCCA ATATGATCTT 1320 GGATAGTCCT AACAGTTACT CTTAGCAGGC TTTCAAAGCA CCAGAGATTG CAGCAAAACG 1380 CACACAAAGA AAATGATTAT GATGACATAC ACAAAATATA ATCCATTTAA AAAAAACCTC 1440 ACACTGTGTG TGTGTGTATA TATATATTAT ACGTATACGT ATATATATGT ATATATATAT 1500 ATATATAACC CTGCAAACAA GAAAACTACT TACTACAAAG GATGAATTTT TCTTTCACAC 1560 AATTTTCATC CTGGCATCCC TATAACTACC AAAACACAGC CGAATATCTG AGAAATGTTG 1620 GTGCAAATGC TAGAGACGAA TAGAGTCAGG CAACTTAAAA GTGTTCTTCA TACTTACGTT 1680 GCTGTGACGA GCAACATAAA AAGAACAGAG TGTCTAAAGT CAGAAAAACC ACTGAAGTCA 1740 CAACTTTTTG GGGGGTGTCA GCTTCTACCT CATGTACCAG GAATAACCAA CTTAGCCTAC 1800 TTCACAGTGT TACTCTAATA GTTAAATGAG AAAGTGATCT GTCAAGTGTT TCCCAAATGC 1860 TCAAAACCAC CCTTCCACAT TGAGCAAGAA TAAAATAGCA TCTGGTTACC CTTCCCAAGG 1920 TGATCTATCT GCCTTTTCCC GCTTAGGATC TCATCGATCG CTTAGGAGTT AGACACGGTG 1980 GGTTAAGGGG TGGTGAAGAG ACGGCGGGAA CAAGCACTTG GTAGCTCAGA AGGCTAGGGC 2040 GGGAGCCAGG TCTTTGGACT GAAACCACTC CCACCCTCCC CCTTCAGCAG CTCCCCTTCC 2100 CCTTCTCGAG ACACCTGCCC CACTAAACGA GCTGAGAGGA TGGACCCAAC CAGCAGTAGT 2160 CTGCAGGTGG GCACTCCAAG CGGGGAGCCG AGGCGCCCAG CACGCAGTCC GGGGACCCGC 2220 TGGAGGGTGG GCGGAGGCGG ACGGCCCAGC CCACAAAGAA GAGGCGGGTA GTGCGTCTTT 2280 CCCTACCCCT CAACCTCCGA CGGGGCCCGG AGCGGACGCT GAGGCGGACA CACCTCTGTC 2340 TCACTTTACC CCAGGGCAAA ATTCGAGTAA TTTCAGGGAG AAGAGGACAA AGCATAGCGC 2400 CGGGTCAGGC CTGCACCCTC CCCTCTACAG 2430
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