Tag | Content |
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EnhancerAtlas ID | HS116-21777 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr21:45625880-45628780 |
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) |
FOSL2 | MA0478.1 | chr21:45627639-45627650 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr21:45627639-45627650 | GGATGACTCAG | + | 6.14 | Myod1 | MA0499.1 | chr21:45627865-45627878 | GGGGGCAGCTGCT | - | 6.03 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_00694 | chr21:45627172-45628515 | Adipose_Nuclei | SE_03880 | chr21:45627327-45628971 | Brain_Anterior_Caudate | SE_04775 | chr21:45626030-45629668 | Brain_Cingulate_Gyrus | SE_05779 | chr21:45625585-45629669 | Brain_Hippocampus_Middle | SE_06690 | chr21:45625851-45629031 | Brain_Hippocampus_Middle_150 | SE_07737 | chr21:45627279-45628360 | Brain_Inferior_Temporal_Lobe | SE_10305 | chr21:45623380-45628791 | CD19_Primary | SE_11616 | chr21:45622912-45630050 | CD20 | SE_24239 | chr21:45625900-45626559 | Colon_Crypt_2 | SE_24239 | chr21:45626613-45628029 | Colon_Crypt_2 | SE_24239 | chr21:45628152-45628712 | Colon_Crypt_2 | SE_30176 | chr21:45627362-45628673 | Fetal_Muscle | SE_31647 | chr21:45625794-45628702 | Gastric | SE_33667 | chr21:45621645-45627097 | H2171 | SE_40890 | chr21:45625813-45629023 | Left_Ventricle | SE_42286 | chr21:45625817-45628837 | Lung | SE_48538 | chr21:45625974-45628773 | Psoas_Muscle | SE_50113 | chr21:45625833-45628971 | Sigmoid_Colon | SE_51445 | chr21:45624818-45629069 | Skeletal_Muscle | SE_52463 | chr21:45625843-45628782 | Small_Intestine | SE_56643 | chr21:45626252-45630945 | u87 | SE_59125 | chr21:45557380-45640832 | Ly3 | SE_61237 | chr21:45557180-45641526 | HBL1 | SE_61527 | chr21:45545883-45641600 | Toledo | SE_62281 | chr21:45556124-45641130 | Tonsil | SE_65639 | chr21:45625460-45628847 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH21I044205 | chr21 | 45625272 | 45628706 | GH21I005055 | chr21 | 45625955 | 45628553 |
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Enhancer Sequence | AACTCCTGAC CTCAGGCAAC CTGCCTGCCT TGGCCTCCCA AAGTGCTGGG ATTGCAGGCG 60 TGAGTCACCG TGCCCAGACA AATTAAGGCT CTTGAGACGA GGTCATCCTG GGTTATGCAG 120 ATGGACCCTG AATCCGACAC TAGCACCCGT GTGGAAGGAA CGAGAGGGAG ATTTGGGGTC 180 CGCAGAGGCA AACCACAGGA GGACGGAGTC GGAGACTGGA GCACCGCGGC CTTGATCGGG 240 GGACACCAGG GCTGCCGGCT GTGCCAGAAG GGGCTGAGGC TGGACCGGAT TCTCTCCGAG 300 TTCCCAGAAG GAGCCAGTCC TGCCGACGCC TTGATGCTGG ACTCTGGCCT CCAGAAATGT 360 GCGAGGACAA ACATCTGCGG TTTCTAGGCC CCGCCTGTGG TCCTCTGTTG CAGCAGCCTG 420 GACAGTCTGG ACTGCCTGGA CAGCATGCAG ATGGGCTCTG CCCGCGGCTG CCCACGAGTT 480 CCCACCGCCC GCCCGTCCGT GGGAGAGCCA GTCCTCGTAT GTGAAGCGTA CCTGTATCCC 540 TTTACTCCGC GTACACAGGT GCCTTTGTCA CTTCTCCTTT GACCTGGCTG GCACATCTTA 600 CCGGTTTCTG CGCTAACAAT GAGTTGAAGG AAATCTTGAA CGCGCGTTCA TTTTATATCG 660 GTATCAGAGT CTGTTTATTT CTTGTTGACA CTAATCTTTG AGCATGAGTA GTTTAGTGAT 720 TGTGAAACAG AAACTTCTGG ATACAAAATC AGTCTCCTGG CTGTGACCCA ATCATCTTCG 780 CAGTTCTGAT TACCTGTGAT TAAGAAAATA AATAAGAACA CCCATTGGGG GAAGGCTTCC 840 CTCCCCCGGG CACAGCAGCT TTAAAACCGA AAGGGAAGTG GGTGCTGTGA GCAGCTCTGT 900 TCAGGCCTAA GGCCACGCAT GTGTGCCCCG TGGGGGAGAC ATGCACCAGC GAATCAGGAA 960 ACAGTGGTGA CAGCCGTTCC GGGAGGCTGA CTGGGGGTGC AGGGGTCACT TTTCTAATGT 1020 GGGTGGGTCT GTGTCCCCTG CAGGAACGTG GCTGCAGCAA AGCCGGTCAG CCAGCGGTCA 1080 GCTCCAGCCC CTGTCCAGGC CCTGTGGGTC CTGCTGACCA GGCTGCGGTT GTTCCCAAAC 1140 CAGTTCCCAG CCCCCGCTTG CCCTACTTCC TCTCACACCA GCTCCTTCCA CCCCCTCACA 1200 CCCACCTGCA GGCTCCCAGC CCAGGCTACT GACATCAATC ATGGCAATCG CTATTCCAGA 1260 GGTATACGCG GTGGGTGGGG TCCGGTATCG CCTGCCATGC CTCACTCACC GGGCACCCAG 1320 ATAACCTGAG GCCAGGGAGC AGCCACTCGC CCTGACCCAT GCTCCCCGGG CCCCTGAGGC 1380 ACCCAGGAGG ACCACCCGGC CGCTTCTGCT CAGAGCCCAG CACCCCCGAG TCTGTGAAGA 1440 GGTCACATCT GACCACGTTT CCAGGTGGCT GCCCAGGCGT GGGTTCATGG CCGCTTCCGG 1500 TTTCCTCCTC GAGCTGAACC ACACACCTGC TCTGTCCCGG GCTTTCTGGA GGGGTTTTCC 1560 GAAGTGAGAC TGTGGGCTCC CTCCAGGGCT GGGGGCAGGA GGACACACGG GGAAGGTGGG 1620 CAAGCAGCCC CAGGCTGAGG GAGGCCTCCC CTCTGCAGCG TTTGTTCATT CATTTGTTCA 1680 TCGCTAACAC TGTCTTGGGC ATCAGGGAAA ACAGGTGTCT CTGGTCCACA TGCAGAAGAG 1740 CCACCACCGT GGCACGACTG GATGACTCAG ACCCCGGGCG GGGGGTATGA TTTGGACACA 1800 GTCATTGTCC AGGGACACAA CTTTGCCTGG ACCAGAGCTT CTCACCCCCA GGCCATTTGA 1860 AACCCCAGGG GATACTCGAC AAAGTCCAGA GACATTTTGG GTTGTTCCTT TCCAGCCCCG 1920 GCGATGGTGG GGACGTGTCC ATGTCTGTGT CCCTCCGGTC ACTCTCTCTG GCCCTCTCCC 1980 TCCCTGGGGG CAGCTGCTCT CAGCCCTCCC TGCCCCCACA TCGCCATCCT GCCTGTCCTT 2040 CTGGGCCTGC ACGTTTGTTG TGTTTGGAAG GAGCCACCAA GGAGGAGGAT GTCAATGTGC 2100 AAGTTCTCAG GGAAGCAGGC CCCGCAGCCT CCGTCAGTGT CTTCCGTCCG CAGGAAGAAC 2160 CCAGGCCTGG GTGATTCATC GGGGCCTCAG GGCCGGGAGG CACTAAATCT TCTGCAGATG 2220 TGGTAAGATC CTATCACAGC AGAAAGGGAA GGGCTAGAGT CTCAGGGAAG GTTTTGCTAG 2280 GGAGACGGGC TTGGAGGGGG CTGAGGCTCA TGGGAGCTGC AAGGGTACAG GAGGGGAGGG 2340 GACCCCAGGG CAGGTGGATG GACACCTGGG TGGGTAAGAA AAGGGCCTCT CAGAGGGCAA 2400 GGGAGGGCCA GGGAGGGAGC AGTGAGCCCT GACTGACTGT ACAAGCTTAA CTGGCTGCCC 2460 TTGTCCTGCA GGTGGTGTGG GCTGTGTGGA TTTCGGATGT GGGCCCATAA CATAGCCACA 2520 CTGCTGCAAA GCAAGTGAGT CTGAGGCAAG AAGAAGGCCC AACCTTGGGA GGCTGACCTG 2580 GAGGGCAGGC AGAGGCAGGT GGTAAGGACC TGCCTTACCT GTTGAGGTGA CAGTGGGGGA 2640 CATATTGCAA GGAAGGAGGC CCTGGATCCT CAGGATGTGG ATGGTGGGTA GAAGGGTGAC 2700 AGCTAATGGA TGTCCACCTG CACAGATGCC CACCTGCATG AGTGCCCACC TGCATGAGTG 2760 CCCACTTGTA CCAATGTCCA CCTGTACAGA TGTCCACATG CAAATGCCCA TCTGCACTGA 2820 TATCCACCTG CACAGATGCC TACCTGCATG AATACCCACT TGCCTGAAAG CCCACCTGCA 2880 CCCATGTCCA CTGGCACAAA 2900
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