| Tag | Content |
|---|
EnhancerAtlas ID | HS139-20081 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr16:1804220-1805660 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:1805631-1805646 | GAGGTCAAGAGATCG | + | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 1804864 | 1805275 | | chr16 | 1804356 | 1804420 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH16I001754 | chr16 | 1804468 | 1805630 |
| Enhancer Sequence | TCACTGAGTA TGTCGCTGGT GCTGGGAGCT GTACCAGCTA TTACCGCACT ACCTGGTGGG 60
AATTTCACAG CAAATATTCA CTAAGGAACT TATTTTTCTG TTTCACAAAT GACTAATACT 120
CAGAGAAGTT ATACTATGTG CCTTGCATTG CTGAGCGGAA TCTGGAATCC ACGCAGCTGA 180
TCTTTCTCTC CGCTCTGCTC TGCATGGACG AGGCAGCCCT CAGGAGAGAT TCCACCGATG 240
TAGTAGCCAG ATGTAGAAAC TGTCCACAAA TAGGCCGGGC ACAGTGGTTC ATGCCTGTCA 300
TCCCAGCACT GTGGGAGGCC AGGGTGGGCG GATCACAAGG TCAGGAGTTC GAGACCACTC 360
TGGCCGACGT GGTGAAACCC CATCTCTACT AAAAATACAA AAATTACCCG GGTGTGGTGG 420
CGGGCCCTGT AGTCCCAGCT ACTCAGGAGG CTGAGACAGG AGAATCACTT GAACCTGGGA 480
GGCGGGGGTT GCAGTGAACT GAGATCATGC CACTGCACTC CAGAGCGAGA CTCCGTCTCA 540
AAAAAAAAAA AAAAGAAGAA GAAAATATCC ACAAATAACC TTGAGAAAAG ACAAGCCTGT 600
GTAAGATTCA GAAGCACCAT TGAAAGACAT AAAAGAAGCT GTACACGCAG AGGGTGTTGC 660
CACGTGCCCG GACCTGAAGA CACACCCTGT GAGCTGTCTG CTGACATGAC AGGCAGCCCC 720
ACCGTTCCCA CAGGAATCCG TTCATTACCA GTAAAAATAC CCACATGCTT GTTGGAGATT 780
TTTCTGGAAC TCTATGAATG GATCTGAAGT TGATCCAGTA GAGGAAACAT GTGAGAATAT 840
CCCAGAAAAT GTGGGGAGAG AAAAAGCTTG CAGGATTCCA CATAAAGCTG CGGCAGTTGA 900
GGCAGGCAGC AACAAACCTG TGATACGAGC TCATGAGCTC AGGGCCAAGA GCCAAGACAG 960
ACCTGGAGCC ATGGGGAATT CATCTATGTA TGACAAGTAT GGCATCTCAA ACCGTGGAAA 1020
ACGGGCAGAT GAGTCAGTAA ATGTACTGCC TTAGTTGCTG CTGGTGTAAA ATGAAGTCTA 1080
AGCCTGACCT CCCCGTAAAC AGCAGTGATT TCCAGGTGGA TTAAAGATCT AAGTACACAA 1140
TTACGAGGAC AACAGAATGC AGCCGGGTGT GCTGGCACCT GTGGTCCTAG CTACTTGGGC 1200
GTCTGAAGTG GGAGGATCAC TTGAGCCTGG GAGTTCAAGG ATATAGTGAG CCATGATTGT 1260
GCCACTGCAC TCCAGCGTGG GGGACAGAGC AAGACCCTGT CTCAGAAAAA TAAGAACGTC 1320
AACAAAGGAT AGTAGAACTG GAAAAGGGGC CGGGTGCGGT GGCTCATGCC TGTAATCCCA 1380
GCACATTGGG AGGCCAAGGT GGGCGGATCA CGAGGTCAAG AGATCGAGAC CATCTTGGCC 1440
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