Tag | Content |
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EnhancerAtlas ID | HS052-14722 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr16:70668600-70670820 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr16:70669433-70669448 | AGAGGTCAGAGGTCG | + | 7.55 | NR2C2 | MA0504.1 | chr16:70669426-70669441 | GGAGGTCAGAGGTCA | + | 8.03 | Nr2f6 | MA0677.1 | chr16:70669434-70669448 | GAGGTCAGAGGTCG | + | 6.06 | Nr2f6 | MA0677.1 | chr16:70669427-70669441 | GAGGTCAGAGGTCA | + | 7.42 | Rxra | MA0512.2 | chr16:70669427-70669441 | GAGGTCAGAGGTCA | + | 6.88 | SOX10 | MA0442.2 | chr16:70669279-70669290 | TGCTTTGTTTT | - | 6.02 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH16I070634 | chr16 | 70668595 | 70670270 |
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Enhancer Sequence | TTCCAAAGTT CCCTAATGCC CCTTTCCAGT CAGATCCTTA CCACCACCAG CCACCTGGGA 60 TAGCCACAGT TCTGATACCT ATCACCATAG ATTAGTTTAT TGGCCTGTTC TTGCATTCAA 120 ATAGCTGGAA TTATGTAGTG TGCACGCTTT TGTGTCTGGT TGCTTTTGCT CAAAATAATG 180 TTTTTGAGAT TCATCCATGT TGCTGCACAG ATCAGCAGTT CCTTTTAATT TCAGAGTAAT 240 ATTCCACTGT CTGATTATGG CACAGTTCAT ACGTCCAGTC TTCTGTTGGC AGATATTTGG 300 ATGGTTTTCA GTTTTAGAAG TGCCTATGAT TCATAGTATG AATACAGCAG CAATAGGCAT 360 TCTTGGTCAT TCGTCTTATG GCCATAGAGT TTGATTTTTC TAGGTTAAAT TCTAGGAGTG 420 GGATTGCTGG GTCAGAGTCT AGGTATGTGT TTAACTTTGT TAGAATCGCC AGTCTTCCAA 480 AATGACAATC CCAGCTTATA CTCTCAAGGG TAACGTGGAG GGCCCCATTA CCATGCATCC 540 TGAGAACTCA AACAGTGATT TTCTTGGCGA CAGATATTTT CTTTGCTCCA TAGAGGGGAT 600 AACCCCTCTG CAGAGGTTTC CATCACAGAG CTGTCAAGCT AAACACCCTC CAGCTGCTGC 660 AGCCTACCCT GCTAGTTTTT GCTTTGTTTT CTTTTGTCTC CTGCTGCTCT CAGGAAGCAC 720 AAAGGCCTGT TGGAGGCCCT TTGTCTACTG TCCCAGTACC AGTGTGGATG CTCCACAGTC 780 TGTTCTTGTG CTCTTGAGTC CCCTTGCTAG TCACAGGTCA GAGGTTGGAG GTCAGAGGTC 840 AGAGGTCGGA AGCTGGAGTC CTTCAGCAGA ACATCGGCAG CTTCCTTGAG CAGGAGCTGT 900 TTCCAGTGTT CAAGGGTCCC ATTGACTGGT CCCACGCTGG GTTTCTTTCT TGCCTTCTTT 960 CACAATCAAG TAAGTATTTT GCTCACAGAC CTCTATTGAT AGTGCAAAAA CAACAGCAAA 1020 AGGGGAAATG ATTCAAATAT AAAAGAAAAA GCCTACGTTT TTCCAAAACC CATTTTTTTA 1080 CTATTAGTAA TACGAGTGAG TAATTATAAC AATAGCAAAT ACCAAGATAG CATGTACTGT 1140 ATGCCAGCTC ATGTTCTAAG TTTTCTGTAT ATAGAAATCC AGTAAATCCT TACATAGCCC 1200 TTTGAGGTCA GAATCTCATA TCAAGCCCAT TTTACAGATG GGGAGGCTGA GGCAAAAGAG 1260 GATCCTCACC TTGCCCAAGG CAAGGTGGAG TCAGAGTTTG AACCCAAAAG GTGTAGCTTC 1320 AGGGTCTGTA TCTTTTTTTT TTTTTTTTAA TTTTTATTTT TGAGACAGTC TCGCTCTGTT 1380 GCCCAGGTTG GAGTGCAGTG GCATGATCTC AACTCAATGT AGCCTTCACC TCCCAGGTTC 1440 AAGTAATTCT CTTGCCTCAG CCTCCTGAGT AGCTGGGATT ACAGGTGTGT GCCACCACGC 1500 CCAGCTAATT TTTGTGTTCT TAGTAGAGAC AGAGTTTCTC CATATTGAGG CTGGTGTCAA 1560 ACACCTGGCC TCAAGTGATC CCCCTGCCTC AGCCTCCCAA AGTGCTGGGA TTACAGGTGT 1620 GAGCCACTGT GCCAGGCCCA GGGTCTGTAT TTTATACCTG CATGTTTTCC TTTGGTTCAT 1680 TTACAGTCTA GAAACTTAAC CACATTTATT TAAAAAGGAA ACTTTGTATC ACTAGCATAA 1740 ATGGAAGATC CACATTGCTT GACATAGATA GTAACTGTAA AAAATGAATA CTCTGACATA 1800 GTGTCGTGGC TCATGCCTAC AATCCCAGCA CTTGGGGAGG CTGAGACCAG GAGCTTGAGA 1860 CCAGCCTGGA CAACATAGCA AACCCTGTCA CACACACACA CACACACACA CACACACACA 1920 CACACACACA CAAAATTAGC TGGGCATGAT TGAGTGTACC TGTGGTCCTA GCAGTGTGGG 1980 AGGATGCCTT GAGCCCAGGA GTTCGAGGCT GCAGTGAGCC TGATTGTGCC ACTGCACTCC 2040 AGCCTTGGCA ACAGAGAGAA ACCCTGTCTC AAACAAACAA AACAAAACAA AACAAAAAAC 2100 AAAACAAAAC AGAATGAAGA AGAATACTCT AATATAACAA CATAACATGA TTCTAAATAG 2160 CACCTATTGC CCCTTCCCTA TTTTATTTTA TTTTTTTTTT GAGACGGGGT TTCGTTCTGT 2220
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