Tag | Content |
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EnhancerAtlas ID | HS139-35184 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr22:29580100-29581750 | 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 | TAATTTTTGC AGAGACAGGA TCTCACTATG TTGCCCAGGC TGGACTTGAA TTTCTGGCCT 60 CAAGTGATCT TCCCGCCTTA GCCTCCCAAA GTGCTGGGAT TACAAGTGTG CGTCACTGTG 120 CCCAGCCTGT TATGTCCTTT CAGACACCCT GCCTCATTCC TTTTTACGAC GTGCAGTCAA 180 GCAGTTATCT GACCGTGGGT TTGTGTGTCT GTCTTTGAGG CTGGTCTTGC TGGCTCCTGC 240 ATTTCCAACA CAGAACCTGA GCTTTGGCTC AGAGTAGGCG CTCTGTAAAC ACATGTGGGA 300 CGAGTGAGGA CGTTCCCTGG ACGATGCCTG GGGTGCCCAG GCCACAGAGC TGCCATTGAA 360 TCTCCTGGGG GTTAAGGTCC ACCACGTTCC ACTCAGCAGG AAAAATTCAG AGCTGACATT 420 AATTCAGACC CCACATACGT GATTCTTACT GAGTTAGACA CCAAGACAAT CTCGCCTTTT 480 GTTGGGGCTG TGGGAGCCTT ACGTACGCCT AGAGAGAAGC CAGTCTAAAA TCAGTCGCTT 540 TTTGAAACCA TCAGCTCGAG AAATTAAGGA TTCTGTCAGC GTGCCCTGAA TTTCTGGGCC 600 CAGCAATTAA TTCCTTCTAG ATTAAAGGAT TGTTGTGTTT CTGATACATT ATTATGCGGA 660 GTGGGCTTGC TGTGAATTTT AAAACTTTAA CCAGAATCCT CATTAACTGG GACCTTTTAT 720 CTGTGTGCAA CTTCTAGAAG AGGCCAGTGG CTAGAAAGTG AGCTGATGCA TCCAAAAAAC 780 ACATTCCGGG TGTCCTGTTG CATATTCAGT CCAGGCAGCT GTTCTCCTTT CTGATGGAAA 840 CAGGGCCATT TACTTACAAT GTGCCTGGTG CCGGCTGTAT GTTGTACATT GCGCCATTGA 900 ATCATCACCT GCTCGATCAG GCAGCCACCG TCATTATTAG CTCCAGCGTA CAGGTGAAGA 960 GACTGGGGTT GAGAGAGATG GGGTCCCTGC TCAAGCCAAT GGGTGGCACA AGTCTGTCCG 1020 ACCTCCAGGC CCCATGCTTG GCTCTCAGCT TCTGTTGCTT TCCCTTCTCC GTGGATGGTG 1080 AAGACCACTG TGCGGAAGGA TGATCACAAG GCCCTTTGGG CCACCATCCA GCCAAGAGCT 1140 ATTTCATCTG TGCTGGGCTT GAGGCTCTGC TGAGCCCGAG GGAGTAGGGA GGCCCAAGGG 1200 AGCAGACCCA GTCGTGTGTG AGGCTGACTC AGGGGCTAAG AGCTCCATCC TCTGGGAACA 1260 CCCACGGGGT TCAGGGCCCA GGGAGGCCAG CCCCTGCTGT CTATCATGAG CAGGCTCTGT 1320 CCCCTCCCTA GCATCAGTCC TCCTCCTGCC ATATGTCTGG GAACCTCAGC TTCTCTCAGG 1380 CAGAGTCCAG CCTAGCTGGA GTCTCACTTT GTTGCCCAGG CTAGAGTGCA GTGGTGCCAT 1440 CTCGGCTCAC TGCAACCTTC GTCTCCCAGG TTCAAGCAAT TCTTCTGCCT CAGCCTCCCG 1500 AGTAGCTGGG ACTACAGGTA TGTGCCACCA CGCCTGGCTA ATTTTTGTAT TTTTAGTTTT 1560 GCCATGTTGG CCAGGCTGGT CTTGAACTCC TGACCTCAAG TGATCCACCT GCCTCGGCCT 1620 CCCAAAGTGT TGGGATTACA GGCGTGAGCT 1650
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