Tag | Content |
---|
EnhancerAtlas ID | HS105-18906 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr12:56687010-56689500 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:56689088-56689103 | GAGGTCAGGAGTTCA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 56687529 | 56687725 | chr12 | 56687732 | 56688005 |
| | Number: 1 | ID | Chromosome | Start | End |
GH12I056293 | chr12 | 56687721 | 56687870 |
| Enhancer Sequence | AATTTTCTTT GATTCTCCAT CCTAGGTACA TCCAGACTCT CTCTGTCCTT CTGCATATCC 60 AGGATATGTC CTACCACATA TCCACATAAC CAACATTAAA ACCTTGGGGG AGGCTGGGCG 120 CAGTGGCTCA TGCCTATAAT CCCAGCATTT CTGAATTAAA AAGCAAGACT CTGTCTCTAC 180 AAAAAATAAT TTAAAAAATT AGAAAACAGG CTGGACACGG TGGCTCACGC CTGTAATCCC 240 AACACCTTGG GAGGCCAAGG TGGGTGGATC ACCTGATGTC AGGAGTTCAA GACCAGCCTG 300 GCCAACATGG TGACACCCCA TCTCTACTAA AAATACAAAA ATTAGCCAGG CGTGGTGGCA 360 CATGCCTATA GTCCCAGCTA CTCGGGAGGC TGAGGCAGAA TCGCCTGGAC CTGGGAGACG 420 GAGGTTGCAG TGAGCTGAGA TTGCGCCATT GCACTCCAGC CTGGGTGACA GAGCAAGACT 480 CCGTCTCAAA ATAATAATAC TAAAAAAAAT TAGAAAACAA AACAGAAAAA CCTTGCGGAA 540 GAAGCTCCTG ATTTTAACAG GGACTTCGTC CTTCATCAAC AAAAGATCAG AGCTTGCCAA 600 GCCAGCAGGA CTGGCTTAGC TGATGGAGCA AACACAATAC ACTAATAACC AGTAGGAAAA 660 AATCCTGTAC TACAGACACT TCCAATGCAG AAGGAACAAC TTGCATTCAG AGAACACGAA 720 CACAAATAGG ACAAAGGCTC CTCTCTCCCC AGAACCAGGT CAGAGAACTA AAGCCATTTA 780 ATGTGTGTGT TTCACAACGG TGATACTGGA AGTCGGTTTG GCACTACATG GTCAGGCCAC 840 TTAAAAGCCT GAGCAATCTA CAGATTTCAT ACTTTGACCT CCTTCATACT TACAGACATT 900 TCCTTAATAA TTCTACCTAA CTGTCATTTT CCAACAGTCT CTTCACGTGA ATAGTCACCG 960 ATCACTGCTG GGTGCAGTGG CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCAAGGTAG 1020 GCCGATCACC TGAGGTGAGG GGTTCAAGAC CAGTCTGGCC AAGATGGTGA AACCCTGTCT 1080 CTACTAAAAA TGCAAAAATT AGTCGGGCAC GGTGGCGCAC ACCTGTAATC TCAGCTAACC 1140 GGGAAGCTGA GAAAGGACAA TTGCTTGAAC CCAGGAGGCA GAGGTTGCAG TGAGCCGAGA 1200 TCATGCCACT GTACTCCAGC CTGGGCGACA GAGCAAGACT CTGTCTCAAA AAAAAAAAAA 1260 AAAAAAAAAA AGATGCACTG ATCACTCAGT AAGGAGGACT GCAAAAGATA CTCCTCCAGC 1320 TTCCATCTTC AGAAAGGAAT CACAAGTCTA TTTTTGTTTT TTGAGACAGA GTCTCTGTCA 1380 CCCAGGCTGG AGTGCAGTGG TGCGATCTCG GCTCACTGAA ACCTCCACCC CCTGGGTTCA 1440 AGCGATTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGATTA TAGGTGCCTG CCACCATGCC 1500 CAGCCAGGAA TCACAAGTAT TAAACTTTCC TTTCAGTAGG AACACTTACT GTTCTTTTGT 1560 TGAGACGAGT CTCACTCTAT TGCCCAGGCT GGAGTGCAGT GGCATGATCT CAGCTCACAG 1620 CAACCTCTGC CACCCGGATT CAAGTGATTC TTGTGCCTCA GCTTCCCTAG TAGCTGGGAT 1680 TACAGGCAGC TGCCACGATT GGCTGATTTT TGTATTTTTA GTAGAGACAG GGTTTCACCA 1740 TGTTGGCCAG GCTGGTCTCG AACTCCTGAC CTCAAGTGAT CTGCCCACCT CAGTCTCCCA 1800 AAGGGCTGGG ATTACAGGCG TGAGCCACTG TGCCTGGCCA ACACTTATTG TACTTTAATT 1860 TAATGAACTT TTTTTTTTTT TTTAAGAGAC AAGGTCTTGC TATGTTGCCA GGCTGATCTC 1920 AAACTACTGG GCTCAAGTGA TCCTCCTACC TCAGCCTCCC AAAGTGCTGG AATTATAGAC 1980 ATAAGCCATC ATGCCTAGCT AATAAATATT TCTTGGCCGG GCACGGTGGC TCATGCCTGT 2040 AATCCCAGCA TTTTGGGAGG CTGAGGCGGG TGGATCACGA GGTCAGGAGT TCAAGACCAT 2100 CCTGGCCAAC ATGGTGAAAC CCCATCTCTA CTAAAAATAC AAAAATTAGC CCGGCGTGGT 2160 GGCATGTGCC TGTAGTCCCA GCTACTAGGG AGGCTGAGGC AGGAGAATAG CTTGAACCCG 2220 GGAGGCAGAG GTTGCAGTGA GCCGAGATCA CACCACTGCA CTCCAGCCTG GGTGACAGAG 2280 CGAGACTCCA TCTCAAGGAA AAAAAAAAAA TTCTTGAACA CCTACTTATT ATGTGTACAC 2340 TAAGTATATA CTAGTGAATA AAGAATATAG GATCTGTCAT CATAATACTT TCTCAGGAAT 2400 TAGAAACTAT TCCCTTACTT CTGCTAGAAG TTCGTAGAAG TTTTATGGCT GGGCGCGGCA 2460 GCTCACGCCT GTAATCCCAG CACTGTGGGA 2490
|
| |
|
|
|