Tag | Content |
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EnhancerAtlas ID | HS156-08227 | Organism | Homo sapiens | Tissue/cell | P493-6 | Coordinate | chr22:29579880-29582170 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr22:29581682-29581697 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTATCTGCC AGGCCCTGTC ATCTAAATTA GGGCCCTATT GTCCTCTCTC TTTTTTTTTT 60 TTTTTTAAGA CAGGGTCTTG TTCTGTCACC CAGGCTGGAG TGCAAGGGTG CAATCACGGC 120 TCACTGCAGC CTCAACCTCC CTGGCTCAAG CAATCCTCCT GCCTCAGCCT TCTGAGCAGC 180 TGAGACCACA GGCATGCACC ACCATACCCA GGTAATATTT TAATTTTTGC AGAGACAGGA 240 TCTCACTATG TTGCCCAGGC TGGACTTGAA TTTCTGGCCT CAAGTGATCT TCCCGCCTTA 300 GCCTCCCAAA GTGCTGGGAT TACAAGTGTG CGTCACTGTG CCCAGCCTGT TATGTCCTTT 360 CAGACACCCT GCCTCATTCC TTTTTACGAC GTGCAGTCAA GCAGTTATCT GACCGTGGGT 420 TTGTGTGTCT GTCTTTGAGG CTGGTCTTGC TGGCTCCTGC ATTTCCAACA CAGAACCTGA 480 GCTTTGGCTC AGAGTAGGCG CTCTGTAAAC ACATGTGGGA CGAGTGAGGA CGTTCCCTGG 540 ACGATGCCTG GGGTGCCCAG GCCACAGAGC TGCCATTGAA TCTCCTGGGG GTTAAGGTCC 600 ACCACGTTCC ACTCAGCAGG AAAAATTCAG AGCTGACATT AATTCAGACC CCACATACGT 660 GATTCTTACT GAGTTAGACA CCAAGACAAT CTCGCCTTTT GTTGGGGCTG TGGGAGCCTT 720 ACGTACGCCT AGAGAGAAGC CAGTCTAAAA TCAGTCGCTT TTTGAAACCA TCAGCTCGAG 780 AAATTAAGGA TTCTGTCAGC GTGCCCTGAA TTTCTGGGCC CAGCAATTAA TTCCTTCTAG 840 ATTAAAGGAT TGTTGTGTTT CTGATACATT ATTATGCGGA GTGGGCTTGC TGTGAATTTT 900 AAAACTTTAA CCAGAATCCT CATTAACTGG GACCTTTTAT CTGTGTGCAA CTTCTAGAAG 960 AGGCCAGTGG CTAGAAAGTG AGCTGATGCA TCCAAAAAAC ACATTCCGGG TGTCCTGTTG 1020 CATATTCAGT CCAGGCAGCT GTTCTCCTTT CTGATGGAAA CAGGGCCATT TACTTACAAT 1080 GTGCCTGGTG CCGGCTGTAT GTTGTACATT GCGCCATTGA ATCATCACCT GCTCGATCAG 1140 GCAGCCACCG TCATTATTAG CTCCAGCGTA CAGGTGAAGA GACTGGGGTT GAGAGAGATG 1200 GGGTCCCTGC TCAAGCCAAT GGGTGGCACA AGTCTGTCCG ACCTCCAGGC CCCATGCTTG 1260 GCTCTCAGCT TCTGTTGCTT TCCCTTCTCC GTGGATGGTG AAGACCACTG TGCGGAAGGA 1320 TGATCACAAG GCCCTTTGGG CCACCATCCA GCCAAGAGCT ATTTCATCTG TGCTGGGCTT 1380 GAGGCTCTGC TGAGCCCGAG GGAGTAGGGA GGCCCAAGGG AGCAGACCCA GTCGTGTGTG 1440 AGGCTGACTC AGGGGCTAAG AGCTCCATCC TCTGGGAACA CCCACGGGGT TCAGGGCCCA 1500 GGGAGGCCAG CCCCTGCTGT CTATCATGAG CAGGCTCTGT CCCCTCCCTA GCATCAGTCC 1560 TCCTCCTGCC ATATGTCTGG GAACCTCAGC TTCTCTCAGG CAGAGTCCAG CCTAGCTGGA 1620 GTCTCACTTT GTTGCCCAGG CTAGAGTGCA GTGGTGCCAT CTCGGCTCAC TGCAACCTTC 1680 GTCTCCCAGG TTCAAGCAAT TCTTCTGCCT CAGCCTCCCG AGTAGCTGGG ACTACAGGTA 1740 TGTGCCACCA CGCCTGGCTA ATTTTTGTAT TTTTAGTTTT GCCATGTTGG CCAGGCTGGT 1800 CTTGAACTCC TGACCTCAAG TGATCCACCT GCCTCGGCCT CCCAAAGTGT TGGGATTACA 1860 GGCGTGAGCT ATCGCACCTG GCCAGCCTGG CTGTCCTGAT GGCAGAACCG GAGCCCAGAT 1920 GCAGCCCTTT GAGGGAGAGA CTTCCAGGCC CTATGTCAGA TGCTTACTGA ACATCTCCAA 1980 ATGAGCCTGG GTCTCCCGGC ATAGCAGCAA CTTCCCACTT TGGTTTACAC AGGTTTATAT 2040 ACACACAGTG TTTATGCACA CAGCTACTTC CTCACCCCTG CGTGCCTGGA ACCAGCGCTC 2100 CCCAGCCCAG TGTGCACCCC AGGCCAAGAG CCAGGCCATC ACTCCCACAG TGGGCTTCCC 2160 CTAGGGCCCT GGGATCTTCT AGAAACCTTA GAAACTCAAA AGGAGTCAGG ATTCCAGGAG 2220 TTCTGGCATC CCTAAGTAAA GTGCCCCTTT CGAGCTCCCC AGAGAAAGGA GCCAGGCAGC 2280 CCCGGAGAAC 2290
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