Tag | Content |
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EnhancerAtlas ID | HS072-01376 |
Organism | Homo sapiens |
Tissue/cell | GM19193 |
Coordinate | chr21:45626080-45629160 |
SNPs | Number: 2 | 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 | GGACGGAGTC GGAGACTGGA GCACCGCGGC CTTGATCGGG GGACACCAGG GCTGCCGGCT 60 GTGCCAGAAG GGGCTGAGGC TGGACCGGAT TCTCTCCGAG TTCCCAGAAG GAGCCAGTCC 120 TGCCGACGCC TTGATGCTGG ACTCTGGCCT CCAGAAATGT GCGAGGACAA ACATCTGCGG 180 TTTCTAGGCC CCGCCTGTGG TCCTCTGTTG CAGCAGCCTG GACAGTCTGG ACTGCCTGGA 240 CAGCATGCAG ATGGGCTCTG CCCGCGGCTG CCCACGAGTT CCCACCGCCC GCCCGTCCGT 300 GGGAGAGCCA GTCCTCGTAT GTGAAGCGTA CCTGTATCCC TTTACTCCGC GTACACAGGT 360 GCCTTTGTCA CTTCTCCTTT GACCTGGCTG GCACATCTTA CCGGTTTCTG CGCTAACAAT 420 GAGTTGAAGG AAATCTTGAA CGCGCGTTCA TTTTATATCG GTATCAGAGT CTGTTTATTT 480 CTTGTTGACA CTAATCTTTG AGCATGAGTA GTTTAGTGAT TGTGAAACAG AAACTTCTGG 540 ATACAAAATC AGTCTCCTGG CTGTGACCCA ATCATCTTCG CAGTTCTGAT TACCTGTGAT 600 TAAGAAAATA AATAAGAACA CCCATTGGGG GAAGGCTTCC CTCCCCCGGG CACAGCAGCT 660 TTAAAACCGA AAGGGAAGTG GGTGCTGTGA GCAGCTCTGT TCAGGCCTAA GGCCACGCAT 720 GTGTGCCCCG TGGGGGAGAC ATGCACCAGC GAATCAGGAA ACAGTGGTGA CAGCCGTTCC 780 GGGAGGCTGA CTGGGGGTGC AGGGGTCACT TTTCTAATGT GGGTGGGTCT GTGTCCCCTG 840 CAGGAACGTG GCTGCAGCAA AGCCGGTCAG CCAGCGGTCA GCTCCAGCCC CTGTCCAGGC 900 CCTGTGGGTC CTGCTGACCA GGCTGCGGTT GTTCCCAAAC CAGTTCCCAG CCCCCGCTTG 960 CCCTACTTCC TCTCACACCA GCTCCTTCCA CCCCCTCACA CCCACCTGCA GGCTCCCAGC 1020 CCAGGCTACT GACATCAATC ATGGCAATCG CTATTCCAGA GGTATACGCG GTGGGTGGGG 1080 TCCGGTATCG CCTGCCATGC CTCACTCACC GGGCACCCAG ATAACCTGAG GCCAGGGAGC 1140 AGCCACTCGC CCTGACCCAT GCTCCCCGGG CCCCTGAGGC ACCCAGGAGG ACCACCCGGC 1200 CGCTTCTGCT CAGAGCCCAG CACCCCCGAG TCTGTGAAGA GGTCACATCT GACCACGTTT 1260 CCAGGTGGCT GCCCAGGCGT GGGTTCATGG CCGCTTCCGG TTTCCTCCTC GAGCTGAACC 1320 ACACACCTGC TCTGTCCCGG GCTTTCTGGA GGGGTTTTCC GAAGTGAGAC TGTGGGCTCC 1380 CTCCAGGGCT GGGGGCAGGA GGACACACGG GGAAGGTGGG CAAGCAGCCC CAGGCTGAGG 1440 GAGGCCTCCC CTCTGCAGCG TTTGTTCATT CATTTGTTCA TCGCTAACAC TGTCTTGGGC 1500 ATCAGGGAAA ACAGGTGTCT CTGGTCCACA TGCAGAAGAG CCACCACCGT GGCACGACTG 1560 GATGACTCAG ACCCCGGGCG GGGGGTATGA TTTGGACACA GTCATTGTCC AGGGACACAA 1620 CTTTGCCTGG ACCAGAGCTT CTCACCCCCA GGCCATTTGA AACCCCAGGG GATACTCGAC 1680 AAAGTCCAGA GACATTTTGG GTTGTTCCTT TCCAGCCCCG GCGATGGTGG GGACGTGTCC 1740 ATGTCTGTGT CCCTCCGGTC ACTCTCTCTG GCCCTCTCCC TCCCTGGGGG CAGCTGCTCT 1800 CAGCCCTCCC TGCCCCCACA TCGCCATCCT GCCTGTCCTT CTGGGCCTGC ACGTTTGTTG 1860 TGTTTGGAAG GAGCCACCAA GGAGGAGGAT GTCAATGTGC AAGTTCTCAG GGAAGCAGGC 1920 CCCGCAGCCT CCGTCAGTGT CTTCCGTCCG CAGGAAGAAC CCAGGCCTGG GTGATTCATC 1980 GGGGCCTCAG GGCCGGGAGG CACTAAATCT TCTGCAGATG TGGTAAGATC CTATCACAGC 2040 AGAAAGGGAA GGGCTAGAGT CTCAGGGAAG GTTTTGCTAG GGAGACGGGC TTGGAGGGGG 2100 CTGAGGCTCA TGGGAGCTGC AAGGGTACAG GAGGGGAGGG GACCCCAGGG CAGGTGGATG 2160 GACACCTGGG TGGGTAAGAA AAGGGCCTCT CAGAGGGCAA GGGAGGGCCA GGGAGGGAGC 2220 AGTGAGCCCT GACTGACTGT ACAAGCTTAA CTGGCTGCCC TTGTCCTGCA GGTGGTGTGG 2280 GCTGTGTGGA TTTCGGATGT GGGCCCATAA CATAGCCACA CTGCTGCAAA GCAAGTGAGT 2340 CTGAGGCAAG AAGAAGGCCC AACCTTGGGA GGCTGACCTG GAGGGCAGGC AGAGGCAGGT 2400 GGTAAGGACC TGCCTTACCT GTTGAGGTGA CAGTGGGGGA CATATTGCAA GGAAGGAGGC 2460 CCTGGATCCT CAGGATGTGG ATGGTGGGTA GAAGGGTGAC AGCTAATGGA TGTCCACCTG 2520 CACAGATGCC CACCTGCATG AGTGCCCACC TGCATGAGTG CCCACTTGTA CCAATGTCCA 2580 CCTGTACAGA TGTCCACATG CAAATGCCCA TCTGCACTGA TATCCACCTG CACAGATGCC 2640 TACCTGCATG AATACCCACT TGCCTGAAAG CCCACCTGCA CCCATGTCCA CTGGCACAAA 2700 TGCCCACCTG CACCCGTGTC CACTGGCACA AATGCCCACC TGCACAGAAG CCCACCCACA 2760 CAAATGCCCA CCTGCAAAAA TGTCCGCCTG CACAGATGTC CACCTGCATG AATGCCCACC 2820 TGTGTCCACA TGCACGAATA CCCACCTGCA CAGATGCCCA CCTGCACGGA TGCCCACCTG 2880 TACAAAGGCC TACCTGCGTG AATGTCCACC TGCATGGATG CCCACCCGCA CGGATGCCCA 2940 CCTGCACAGT TATCCATCTG AACAGCCCTC TGGTGCCTCC TTTTGCTTGC ACATGTTCAA 3000 ATCCTCCCAG TCCTACAGTC GATTGTTCCT AGTTGGGGTC ATTCTGGGCA TGTTATTCTA 3060 AAACTTGTTT TTTCCCGTCT 3080
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