Tag | Content |
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EnhancerAtlas ID | HS139-03180 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:150166150-150167860 |
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) |
FOSL1 | MA0477.1 | chr1:150166345-150166356 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr1:150166345-150166356 | GGTGACTCATG | + | 6.02 | RARA(var.2) | MA0730.1 | chr1:150167433-150167450 | TGGTCATGAGAAGGTCA | + | 6.09 | Twist2 | MA0633.1 | chr1:150167427-150167437 | AACATATGGT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 150166670 | 150167023 | chr1 | 150166245 | 150166384 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I150193 | chr1 | 150165894 | 150167634 |
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Enhancer Sequence | TGATCTCAAT CTCGACCTCG TGATCCGCCG CCTCGACCTC CCAAAGTGCT GGGATCATAG 60 GCGTAAGCCA TTGCGCCCGG CCAACTCCAG CCATTTTTAA GCTATACTTA AGATCTTTCT 120 GTCTTACATT TCTGTAATGA GACAGCTAAT CACAACTAAG CGGGTTGGTT ATAAAGATCT 180 AAACCGGCCG GGCGCGGTGA CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGTGG 240 GCGGATCACG AGGTCAGGAG ATCCAGACCA TCCTGGCTAA CAGTGAAACC CCGTCTCTAC 300 TGAAAATACA AAAAATTAGC CAGGCATGGT GGCGGACGCC TGTAGTCCCA GCTACTCGGG 360 AGGCTGAGGC AAGAGAATGG CATGAACCTG GAAGGCGGAG CTTGCAGTGA GCTGAGATCG 420 CACCACTGCA CTCCATCCTG GGCGACAGAG TGAGACTCCG TCTCAAAAAA AAAAAAAAAA 480 AAAAAAGACC TAAACCGACA TTGTAAGCAA GACAATGCTA CAAAATATGG AAGACACAAA 540 GAGAGTTCCT ACCCTCCAGA GAATTTCCCT GAGACGAGTA CTGCCTTTCA GTTTTCTCTG 600 TTGTGGGGAC AGAAAGAATA ATGGTAAGAG GCTGAGTAAT GGCTGCATCA TGAGGGTAGT 660 CTAGACAAGC AACCCATGGA TATGCAAGAG AAAGACTGTC TCCAGGGGTC CATGAAAGAG 720 ACTGCCTGAA GGTGGGTGGG ATCTTGATGA GATGGAAAAC CTTCCAGGCA GAGGGAAAAG 780 TGTGAGCAAA GACAGAGAGA TTTGTGTATT CATTTCCCAG GGCTGCTGGA ACAAGGTACC 840 ACAAACTGGG TGGCTTAAAA CAGCAGAAAT CTCTCACAGT TCTGAAGGCC AGAAGTCTGA 900 CATAGAGTTG TGGGTGGGGC AATACTTTCT CTGAAGGCTC TAAGAGAGGA TTTTCCTTGC 960 TGCTTCTTAG CTTCTGGTGG TTGCAGACAA TTCTTGGCAT TCTTTGGTTT GTAGACACAC 1020 ATCACTCCAA TCTCTGCCTC CACCGTGATA TGTTGTTTTC TTTATATGTC TCTCTGTTCA 1080 CATGCCCCCC AGCTCTGCGT CTGTATCTAT ATCTCCTCCT CTCATAGGTA CATAGCTTAT 1140 ACTGGATTAG AGCCCACCCA CCCACTAGGA CATCATCTTA ACTACATCTA CAATGACTCT 1200 ATCTCCAAAT AAGGTCACAT TCATAGGTAG GCATTAGAAC TTGAACATAT CTTTTTGAAG 1260 GACACAATTC AACCCACAAC ATATGGTCAT GAGAAGGTCA GTGTGGTCAG AAAGTAGAGT 1320 ATATCTAGGG AAAGAGTGGA AGTAACTCAG GAAGAAGGGG CTGGAGTATA GAGAACCTTG 1380 ATGAATAAGC AATGAGGGTG CACAGAATAT ATATATATAT TTTTTCGAGG CAGAGTTTCA 1440 CTCTTGTTGC CCAGCTGGAG TTGCAATGCA CGATCTTGGC TCACTGCAAC CTCTGCCTCC 1500 CGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGGATTACA GGCATGTGCC 1560 ACCACACCTG GCTAATTTTG TATTTTTAGT AGAGACAGGG TTTCTCCATG TTGGTCAGGC 1620 TAGTCTTGCA CTCCTGACCT CAGGTGATCT GCCTGCCTTG GCCTCCCAAA GTGCTGGGAT 1680 TACAGGCGTG AGCCACCACG CCCAGCCATT 1710
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