Tag | Content |
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EnhancerAtlas ID | HS116-14769 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr17:39930660-39933100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr17:39931738-39931749 | GGCCACACCCA | + | 6.62 | Nr2f6(var.2) | MA0728.1 | chr17:39931136-39931151 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr17:39930804-39930819 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr17:39932105-39932126 | CCCTTCTTTCCTGCCTCCTCC | - | 7.34 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_23177 | chr17:39930804-39931144 | Colon_Crypt_1 | SE_23177 | chr17:39931205-39933035 | Colon_Crypt_1 | SE_23845 | chr17:39930822-39931135 | Colon_Crypt_2 | SE_23845 | chr17:39931224-39932687 | Colon_Crypt_2 | SE_24826 | chr17:39930708-39931158 | Colon_Crypt_3 | SE_24826 | chr17:39931195-39932773 | Colon_Crypt_3 | SE_26576 | chr17:39930776-39933078 | Esophagus | SE_27684 | chr17:39927545-39932901 | Fetal_Intestine | SE_28604 | chr17:39927417-39935020 | Fetal_Intestine_Large | SE_31640 | chr17:39930793-39933070 | Gastric | SE_35990 | chr17:39927477-39932923 | HMEC | SE_40900 | chr17:39930739-39935638 | Left_Ventricle | SE_41716 | chr17:39930816-39931170 | LNCaP | SE_41716 | chr17:39931399-39932763 | LNCaP | SE_42558 | chr17:39927553-39935131 | Lung | SE_47748 | chr17:39931607-39931978 | Pancreas | SE_48895 | chr17:39931209-39932999 | Right_Atrium | SE_49575 | chr17:39931505-39932598 | Right_Ventricle | SE_50269 | chr17:39927482-39933094 | Sigmoid_Colon | SE_52578 | chr17:39930767-39933072 | Small_Intestine | SE_56909 | chr17:39931351-39932702 | VACO_400 | SE_57643 | chr17:39931949-39932569 | VACO_503 | SE_64699 | chr17:39927854-39931238 | NHEK | SE_64699 | chr17:39931275-39932337 | NHEK | SE_65762 | chr17:39926307-39935230 | Pancreatic_islets | SE_68966 | chr17:39931400-39932838 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I041771 | chr17 | 39927532 | 39936603 |
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Enhancer Sequence | CTGCAACCTC CACCTCCTGG GTTCCAGTGA TTCTCCTGCC TCAACCTCTG AAGTAGCTGG 60 GACTACAGGT GTGCACCACC ACGCCTGGCT AATTTTTGTA TTTTTAGTAA AGACCGGGTT 120 TCCCCATGTT GGCCAGGCTG GTCTTGAACT CCTGACCTCA GGTGATCCGC CCACCTCAGC 180 CTCCCAAAGT GCTGGGATTA TAGGCTTGGG CCACTGTGCC TGGCTTTATT CCCAATTTCT 240 AGGTGAAGAA GCTGTGCCTG CACACTGAGA AAATGGCAGC ACTTGTGGTA GGAACAGCAT 300 CCAGTCCACT AGACAAGCCT GGGTGGAGCT GAGCCCTCTT GCCAAGGGGA GGAGGGGACC 360 AAGGTGCTTG CAGATGGAAG CAGAGCACTC GGCTGCAAAT CAAGTGTCCC AGGTTCGGGT 420 GCGGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC AAGGCGGGCA GATCACGAGG 480 TCAGGAGTTC AAGACCATCC TGGTCAACAT GGTGAAATCC TGTCTCTACT AAAAAAGTAC 540 AAAAATTAGC CAGGCATGGT GGTGTGCACC TGTAATCCCA GCTACTCGGG AGGCTGGGGC 600 GGGAGAATTG CTTAAACCAG GGAGGTGCAT GTTGCAGTGA GCCGAGACTG CGCCACTGCA 660 CTTCAGCCTG GCTGACAACA GAGCAAGACC CTGTCTCAAA AAAAAAAAAA AAGAGTCCCA 720 GGTTCTAGTC CCAGCTCTGC CACAAACTTG CTGGGTGTCC TTGTGTCCCT GGATCTCAAA 780 GGAATGTTGA TGTCTAAGAT TCTAGAAATA AAAAAACAGG ATTCCCACAA CAGACAGAAG 840 AAGGCTGGGG GTGGGCAACG TCAGAGTTGG GAACCAGTTC AGAGAGAGGA CACACTCCAG 900 AACTCCTCCT GAGGAAGGGG TCACGGGAGC TATTCCTGCA ACAGGAAGGC TGGAAGTCAG 960 ACCTCAGGCA GGACTGTCAA CCAGCCCCAC CCTTCTCCTT ACCTACTGCC CAGGAGAACA 1020 AAGGAACTTC TCTCACAAGA AACAAAAGTG CTGGTTTTAC AGTTCCCAGG GTGGAGGGGG 1080 CCACACCCAG TTCAGTCTTG TCCCTCTCCA CCCTGGACCT GGAGTCAGAC CTCCTGCAAT 1140 GCCCCTGGAC AGAGCCAGGG TGGAAGCGAG AGAGACAGAC GCAGGCCCTG CCCACTCATC 1200 CCAGCCAGAG ACGGGCAGGG ACAGAGACAG GGCGGGTTTC TGAGTTGAAT GGGGGGCCTT 1260 TGTTTAGAGC GTGCTCTATT GTTAGCAGCA CGGGAGGAAG AAGCCAGATC AGAGACTGTA 1320 GGGACAGCCC AAGGACAGGA AGAAGGAAGA CGGGCCCTGG AGAGGGGGTG CAGAGGACCC 1380 TTCCCCATGG GACCCACACC AGGTAAGTGT GAGCAAGTAA TAAGGCTAGA CTGGGTGCAC 1440 CCCTACCCTT CTTTCCTGCC TCCTCCTCTG CGCAGCCAAC CCAGAGGGCT GGCACCGGGC 1500 ACCCTAAATC CAAGACTGAC CTGGCAGAGT GTGGCCCAGC CCTGACATTA AAAATAGCCC 1560 CACCAGAGCT ACACCAGGCT CCTTCCCCAG CCGGCACCTG CCAAGGACAG TCAGCAATGG 1620 GCACATCTAG GCTGGGTTGC AGGGCACCAA GTGCCAAGAC ACCTGGAAAT AAGGACAGGA 1680 GTGGGTTACC CCAGAGGCCG TGCTGGAAGC AGACTCAGAA GCATTGCATT TGGGAACAGA 1740 GGAGCAGGGC GGAGCAGGGC AGGGCTGGGT CCCCCAGAGG TTCCTTAGGC TAGAGGCCAG 1800 CACCCTGTGC AGACACAGGT CCCCAGGCTC AGACAGCGAC AGGGTGAGCA CAGGATTCTG 1860 AGTGAGGAGA GGGGCTCAAT TTCCTTAAGC CTCATTTTCT CATCTGTAAA ATGGAGATGA 1920 TCAAGTGACT TCTTTTGTCA CTGTGACTCT GGAAGCCCTC TGTCCACAGG AAAGGCATGC 1980 ATTCTCATGC TAGAAGAACA AAGAGATGGC AGAGGAGGCG GAAGCCAGCT GGCGCAGTGG 2040 CTCGTGCCTA TAATCCCAGC ATTTTGGAAG GCGGAGGTGG GAGGGTCGTT TGAGCCCAGG 2100 AGTTCGAAAC CAGCCTGGGC AACATAGTAA GACCCTGTCT CTACAAAAAA TAAAAAGAAA 2160 TTAGCCGGGC ATGGTGGCAT GCACCTGCAG TCCCAGCTAC TCTGGAAGCT GAAGCATCAC 2220 TTGAGCCCAG GTGATTGAGG CTGCAGTGAG CCAGGATCAT GCCACTCCAG CCTAGGCAAC 2280 AGAGCGAGAC CGTGTCTCAA AACAAAAAGG TGAGGGGGCC AGGCGCGGTG GCTCACGCCT 2340 GTAATCCCAG CATATTGGGA GGCCAAGGTG GGTGGATCAC AAGGTCAGGA GTTTGAGACC 2400 AGCCTGGCCA ACATAGTGAA ACCCCATCTC TACTAAAAAT 2440
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