Tag | Content |
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EnhancerAtlas ID | HS139-17922 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr15:31688540-31691810 |
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) |
Nr2f6(var.2) | MA0728.1 | chr15:31688580-31688595 | TGATCTCTTGACCTT | - | 6.93 | RREB1 | MA0073.1 | chr15:31689423-31689443 | TGGGGCGGGGTGGGGTGGGG | - | 6.8 | RREB1 | MA0073.1 | chr15:31689428-31689448 | CGGGGTGGGGTGGGGTGGGG | - | 7.29 | SOX10 | MA0442.2 | chr15:31689068-31689079 | GTCTTTGTTTT | - | 6.14 | TCF7L2 | MA0523.1 | chr15:31691093-31691107 | TCCCTTTGATCTGC | - | 6.39 | Tcf12 | MA0521.1 | chr15:31690588-31690599 | AACAGCTGCTG | + | 6.32 | Zfx | MA0146.2 | chr15:31691778-31691792 | CAGGCCTAGGCCTG | + | 6.06 | Zfx | MA0146.2 | chr15:31691778-31691792 | CAGGCCTAGGCCTG | - | 6.06 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_05780 | chr15:31689449-31691257 | Brain_Hippocampus_Middle | SE_23077 | chr15:31688850-31691343 | Colon_Crypt_1 | SE_23726 | chr15:31689048-31691227 | Colon_Crypt_2 | SE_24682 | chr15:31688786-31691298 | Colon_Crypt_3 | SE_27847 | chr15:31688638-31690893 | Fetal_Intestine | SE_28890 | chr15:31688607-31690709 | Fetal_Intestine_Large | SE_33429 | chr15:31688633-31696710 | H2171 | SE_40604 | chr15:31688686-31691276 | Left_Ventricle | SE_42098 | chr15:31688575-31691486 | Lung | SE_48562 | chr15:31688907-31691341 | Right_Atrium | SE_50055 | chr15:31688901-31691529 | Sigmoid_Colon | SE_51258 | chr15:31688681-31691220 | Skeletal_Muscle | SE_52342 | chr15:31688564-31691253 | Small_Intestine | SE_53298 | chr15:31688681-31691322 | Spleen | SE_65426 | chr15:31688919-31690873 | Pancreatic_islets | SE_67090 | chr15:31688633-31696710 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 31688659 | 31690666 | chr15 | 31689645 | 31689781 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I031395 | chr15 | 31688092 | 31692369 |
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Enhancer Sequence | TAGTAGAGAC AGGGTTTCAC CATGTTGGCC AGGATGGTCT TGATCTCTTG ACCTTGTGAT 60 CTGCCTGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCT TGAGCCACCG CGCCCGGCCT 120 AGGGTTTTTA AGGATAATTT GGTGGTTGGG GGGCAGCCAG TGAGTTGGGA GTGCTGATTG 180 GTCAGTGATG AAATCTTAGG GAGTCGAAGC TGTCTTCTTG CATTGAGTCA GTTCCTGGTT 240 TGGGGCCACA AGATCAGATG AGCCAGTTTA TTGACCTGGG TGGTGCCAGC TGATCCATGG 300 AGTACAGGGT CTGCAAAATA TCTCAAGCAC TGATTTTAGG GATCTTAGGC TTTACAATAG 360 TGATGTTATC CCCAGAAGCA ACTTGGGAAA GTCAGAATCT TGTAGCCTCC AGCTGCGTGA 420 CTCCTAAACC ATAATTTCTA ATTTTTTGGC TAATTTATTA GTCCTAGCTA CAAAGGCAGT 480 CTAGTCCCTA GGCAGGAAGG AGGTCTGCTT TGGGAAAGGG ATGTTACAGT CTTTGTTTTA 540 AACTATAAAC TATAAACCAA GTTTTCTCCC AAAGTTAGTT CAGCTTACAC CTAGGAATGA 600 ACAAGGACAG CTTGGAGGTT AGAAGCAAGA TGGAGTTAGT TAAGTCAGAT CTCGTTCACT 660 GTCTGGGTTA TAATTTTGCA GTGGTGGTTT CAACAGTGGC TCAGGGGCTG GTGCCTGTCC 720 CTACCCTGAG CCCAGAGGAC ACTTTCCGTC CTCCAGTCCA GGTTTTTCGT TTGACTTTGC 780 CACAGGAACA TTTGCCAGGG GTCATTTCCC AGGCGGAAAT GGGCAAAGGG GGGTTGGGAA 840 CAAGCCTGAG GCCCTGAGGC CAAGAGGGTG TCCAGGTTCA GGGTGGGGCG GGGTGGGGTG 900 GGGTGGGGCG GGCAGGGCAG GGCAGGGCAG GGGTGCACGT GGCAGGGTGG GCAGGCTTCC 960 CGGCGCTCCG CTCAGGCCAC GCCCAGCGCC AGCATAATTA CCGGGAGAAT AATTACGAGC 1020 CCAGAGAGCC GCCGACCCCG CCCATTGCCG ACCATTCTCA GGCCTGGGGC GGTGGCGCCC 1080 TCTCCTCCTC AGTGACGCGC ACTTGCAAAG GCTGCAGGCC AAGAGGTCCA GACGCCTCGG 1140 AGTGGGAGGG GCCGTGGCCT GCCAACGTTG TCTGTCCTCA AGGGAGGGGC GCTGGGAAGT 1200 TCCTGGGCCT GTTTCCCCTT TGGGGTCAGG GCTGCCTCTT GCTTCCAGCT CTAGCAGCTG 1260 CTAGCAAGTC CTTTAACATC CCTGAGCCTC AGTTTCCCCA TCTATAAAAT GAAGATGGAT 1320 TTGTTGAGGA CTAAATGAGC TACTCTTTGT ACAGTGTGAG GCTGATTTTG TAACATTATT 1380 ATTATTATGT TATTTTCAAC CATACCCAGT GGCCAGCAGC TCCTGGCACA TCATAAATGT 1440 CAGAGGGATG AACTACACAG ATGAGGACGT GGAGGGGGTC AGAGTTAGGA GCTGGATGTG 1500 GGGTCTGCAG ACTTCTCTGG TCTTTGGGGG TGGCGGCGGG GGGGGTGGTG ATCCACTCTC 1560 CCTGGGGAAT TCTTCAGTCT TTCTCTCCTG TGCCTCAGCC TGAGGGCCTC TGGCAAGTGC 1620 CTCTCCAGGA AAACACCACC TCCCAGCTGC TCTCCGGGTC GACCCTGAGT TTATCTTGGG 1680 TTTTACGCAG TCCGGGGCCA GTAATTAGCC TAATAAGGAG CCTGCTAGGC CTGCGTCTCT 1740 GCTCAGGCTC CGATAGTTAC CCAGTAATTT ACCTGATCTC TCGGATAAGG CCTTTGCCTG 1800 GACAGGTTCC CACCACAAAG CACAGGATGC TCCTGCTCGG GCGGGGCCTT AATTGGTGGT 1860 GTTTTCAGAG ATTCTCCAAC CCTAGTTGAA AGGAGCCCAG GCCTCAGAGG CACAACCATG 1920 GCCATCACAG CAAGGAAACA GCCCAGGTGT TAGGGGACAG GGCTGCACCA GGACACAACA 1980 GACCAGACAC GGCAGCACTG ACGAGTTTAG AAGGCGTATG GGGGTGGCAG CAGAAGCTGC 2040 CAAACCAAAA CAGCTGCTGG CATTTCGTGT GTAGTGGCTG GGAGCAGAGC GTGGTGGGCA 2100 ATGAGGGAGC CAACTTGGCC CTGGGGCCAA CCCCGCAGCC TACACCCAGG CTCTGGCCAG 2160 CGCCTATTTC AGGGGCATGC TCGGTGCTGC TGCCTGGCCC CCAGGGTACT CCCAGAGCAA 2220 GAGCCCACTG GCTCCTGGAC CCCAGTGGAG AAGCAGCGAC CCCTTCCATC CCAGGGCTCA 2280 AGCTCAGGGC TCCGAGCCCT CCCAGCCACC TTTGTCCCCA GGCACAGTAC CACATCAGGA 2340 GTGTCTGACT TTGGAGCAGG CCCCCAGGCC TTGGAAAGAT CAAGCAGGAG GCCAAGGCTG 2400 TTGGAGCTGA GAAGCAGGAA GAGTCAACCA TGCACGGTGC CCTCCTCCCT CTCCCCCAGG 2460 GCAGCTATAG GACTCTGTGG GTGGGAAGAG CCTGCAGCCA GGCCAAGAAG CCGTGGGCAA 2520 GCCCTACAGT CGCCTAGTGC TCGCCTACAC AGCTCCCTTT GATCTGCCCC ACTGGGCGGG 2580 GCTGTGTCAT CTACTGGGTT TTCCCTGGAG CCTGTGCCCA GGGAAGCTCA GTGTCACACA 2640 GCCCCAAGCA TCCTGTGTGT CCCTGGCAGA GTGCGAGCCC CTTATCCTGC CTCAGTGAAG 2700 AGGACGGTGC TGGCTGCCCT AGAGGATGTC AGCACCAGAT GGAGAAGCAG AGCAGACTCC 2760 ACTGGGCAAA GTTGCAATCA CCCTCTGAGA GGAGCTGAGC TCCCTCTGAA AACAAGGGGC 2820 CCCTTAGCCC CACAAATGTG GGGGCAACCC ACATGGCAGG GAATTGCATC CCTGAGTTTT 2880 CCCCCTGCGG CTGGAGTGCA ATGGCGCAAT CTTGGCTCAC TGCAACCTCT GCCTCCCAGG 2940 ATCAAGCGAT TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ATTAGCCCAG CTAATTTTTG 3000 TATTTTTAGT AGAGACGGGG TTTCATCATG TTGGGCAGGC TGGTCTCAAA CTCCTGACCT 3060 CAGGTGATCC ACCCACCTCG GCCTCCCAAA GTGCTGGGAT TATAGGTGTG AGCCACCGTG 3120 CCCAGCCTAT CTCTGAGTTT TTTGCAGTCA GCTGTGCCAA ACCACCACAC ACTGCCCTTG 3180 GTTTCCCAGA GCCATCCTGC CCACACAGGG GATTCCTTGA CACCCACTGC TCCAGGTCCA 3240 GGCCTAGGCC TGCCCCCTCT ACTCCTAGAT 3270
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