Tag | Content |
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EnhancerAtlas ID | HS139-03123 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr1:145712680-145714530 |
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) |
CTCF | MA0139.1 | chr1:145713744-145713763 | TGGCCGCTAGAGGGCGCTG | + | 7.3 | Gfi1b | MA0483.1 | chr1:145713053-145713064 | AAATCACAGCT | + | 6.14 | MSC | MA0665.1 | chr1:145713159-145713169 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr1:145713159-145713169 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr1:145713159-145713169 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr1:145713159-145713169 | AACAGCTGTT | - | 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 | 145713047 | 145713169 | chr1 | 145713773 | 145714400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I145720 | chr1 | 145713284 | 145714909 |
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Enhancer Sequence | CTAGAGTCAG ACCAGGATGT TTCAGATCTG GCTTTGAAAC TTAACTATCT GTGTAATATT 60 GGGCAAGTTT CTTAATCTCT TAATGACCTA TAAAATGGTG ACAAAATATT CTCTTCCTTG 120 GGTTGTGAGG GTCAAATGAG GTCACCTATG TAAATTACTT AGCACAGTGC CTGGCAGAGA 180 GTAAGGGCTC AATAAATGAT AGCTATGATT AGTTTTATGC TTTCTTATAT TGGAATCAAT 240 GGACAGTGTT CCAGGCACAT CTACCTGCAA GACTGTGTTT AGTCCTTATA AAACACTAAG 300 CCATTATTAT TTTCTAAAAT TTATTATTTG TACGAAGCAT ATAGAGGCTT GGAGGGGACT 360 TGTGACTTGC TTAAAATCAC AGCTCCTAAG TTGGGGAGCA GGACTCTAAC CCAAGTTATG 420 AGAGTCTTTC TCTTGGAGTC CCCTTTGTCC CTCTCCTCAC AGCCGCTCAT CCATTCACGA 480 ACAGCTGTTA ACACAAGAAC GACTGTACTA AGTAATAAGG TCATAAAGTG TCAAGGGGCA 540 GCACAGGAGA AATTCTGGAT GAGGGATGTG GAAAGGCTGC AAGATGGCAA TGAAGTTAGG 600 CCTTCATAGT TGTTTGTGGG CTCTGGGGAG CTGGTGACTA AAGAATACGG TGGGTGAATT 660 AAGGTGGGGA ATGGGCTGAG GAGATCTGGC TTCCAGTCCT GGCTCCGCAC TAGGTAGCTG 720 TGGAATGTTG ACAAGGTCGT GTCCCTTCTC TAGGCGTGTT TCCTAAGGGA CTGGTGCAGC 780 GGGATGGGAG GGGCGCAGGG TAGGGACCGC TTCCAAGGAG AGAGAGGACA GGCGGGAGGG 840 GCTGATGCAG CTGGTCACTC CGCTGGAGTG GCCAGACTTC GCGGTGCCTA GGGCCGAGTT 900 GAAGAAGAGC ATGTAAGTCT GTTGTGGGCC CCTCACCAGC GCTGGGGGGC AGCGAGGTCA 960 CTGGGCAAGG ATGCTCTGGG AAGTGACCTT GGTGCCCGGG AGGGGAGCAC CCTGTTGTGA 1020 TGCAGGCGGG GCAGCGCGGA GCCGGCGGCG CTGATTTCGC ACTCTGGCCG CTAGAGGGCG 1080 CTGCCTTTCA GCCAAAGCCG AGTGACCCCC TACCTGCCCC GCGTTGGCCC GCGTCACTCC 1140 AGCCATGGGC CATCCAGCGA GCATGGGGGC TAGCCAGGGA AAGTCTAAAC TAGGAGGGGA 1200 GATGAGGGGG TGCAAAGTTG GGCCTGGTGG GTCCTGGGGA CGCAGCATGT ACTAGAGCGG 1260 CACCTGGCCC TCAACAGAGG GGAGAGCGGG TGGTCGTGAG AAGTCTGGGA ATTTTCCGGG 1320 CCCACTACAC GCCAGGGGCG GGTCTCCCCT CTTAAAACGT TGTGAGCCCC AGCGCGGGCA 1380 GGGGGGAGGG TGCCCGTGGA GTTGGCATCC TCATCTTTGA TGGTCCCCGG GGCTCCTGAG 1440 CTGCGCTGGT GGCCCCAGGG CTCGGTGCCT CTCTCAGGCG ACAGCTCACA GACGGCGGGA 1500 AACTCTTCCC TCCCGCACCT TCGGAGGCGG TCCTGGAGTC TTGTGGACTC CTGGGTTCAA 1560 ATCCAAGCTT TGTGTGACCA GCACATTGCT GGACCTCACT CAGCCTCACA TTCCTCTTGT 1620 GTTTAAAACT ACCTCATAGG AATGTGGTGA CGGTTAGATG ACACATAAAG CTTTGCCAGA 1680 GGTTTTCTGG GGAGGGTGGG GACAAGAGGG CAAGGAAGAG TCTCCATTTC CTCTGCCACC 1740 GGAGCCCGGA TCTAACCTCT CAGAGGAGCT GGAAGGTCAG CTCTGAGCTC CACAAATACC 1800 TCTGTATACA GATCTCCCAC GACACTGAAA AAGATGCCCA GAAAGATCTC 1850
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