Tag | Content |
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EnhancerAtlas ID | HS051-18109 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr21:45626010-45628960 |
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 | AATCCGACAC TAGCACCCGT GTGGAAGGAA CGAGAGGGAG ATTTGGGGTC CGCAGAGGCA 60 AACCACAGGA GGACGGAGTC GGAGACTGGA GCACCGCGGC CTTGATCGGG GGACACCAGG 120 GCTGCCGGCT GTGCCAGAAG GGGCTGAGGC TGGACCGGAT TCTCTCCGAG TTCCCAGAAG 180 GAGCCAGTCC TGCCGACGCC TTGATGCTGG ACTCTGGCCT CCAGAAATGT GCGAGGACAA 240 ACATCTGCGG TTTCTAGGCC CCGCCTGTGG TCCTCTGTTG CAGCAGCCTG GACAGTCTGG 300 ACTGCCTGGA CAGCATGCAG ATGGGCTCTG CCCGCGGCTG CCCACGAGTT CCCACCGCCC 360 GCCCGTCCGT GGGAGAGCCA GTCCTCGTAT GTGAAGCGTA CCTGTATCCC TTTACTCCGC 420 GTACACAGGT GCCTTTGTCA CTTCTCCTTT GACCTGGCTG GCACATCTTA CCGGTTTCTG 480 CGCTAACAAT GAGTTGAAGG AAATCTTGAA CGCGCGTTCA TTTTATATCG GTATCAGAGT 540 CTGTTTATTT CTTGTTGACA CTAATCTTTG AGCATGAGTA GTTTAGTGAT TGTGAAACAG 600 AAACTTCTGG ATACAAAATC AGTCTCCTGG CTGTGACCCA ATCATCTTCG CAGTTCTGAT 660 TACCTGTGAT TAAGAAAATA AATAAGAACA CCCATTGGGG GAAGGCTTCC CTCCCCCGGG 720 CACAGCAGCT TTAAAACCGA AAGGGAAGTG GGTGCTGTGA GCAGCTCTGT TCAGGCCTAA 780 GGCCACGCAT GTGTGCCCCG TGGGGGAGAC ATGCACCAGC GAATCAGGAA ACAGTGGTGA 840 CAGCCGTTCC GGGAGGCTGA CTGGGGGTGC AGGGGTCACT TTTCTAATGT GGGTGGGTCT 900 GTGTCCCCTG CAGGAACGTG GCTGCAGCAA AGCCGGTCAG CCAGCGGTCA GCTCCAGCCC 960 CTGTCCAGGC CCTGTGGGTC CTGCTGACCA GGCTGCGGTT GTTCCCAAAC CAGTTCCCAG 1020 CCCCCGCTTG CCCTACTTCC TCTCACACCA GCTCCTTCCA CCCCCTCACA CCCACCTGCA 1080 GGCTCCCAGC CCAGGCTACT GACATCAATC ATGGCAATCG CTATTCCAGA GGTATACGCG 1140 GTGGGTGGGG TCCGGTATCG CCTGCCATGC CTCACTCACC GGGCACCCAG ATAACCTGAG 1200 GCCAGGGAGC AGCCACTCGC CCTGACCCAT GCTCCCCGGG CCCCTGAGGC ACCCAGGAGG 1260 ACCACCCGGC CGCTTCTGCT CAGAGCCCAG CACCCCCGAG TCTGTGAAGA GGTCACATCT 1320 GACCACGTTT CCAGGTGGCT GCCCAGGCGT GGGTTCATGG CCGCTTCCGG TTTCCTCCTC 1380 GAGCTGAACC ACACACCTGC TCTGTCCCGG GCTTTCTGGA GGGGTTTTCC GAAGTGAGAC 1440 TGTGGGCTCC CTCCAGGGCT GGGGGCAGGA GGACACACGG GGAAGGTGGG CAAGCAGCCC 1500 CAGGCTGAGG GAGGCCTCCC CTCTGCAGCG TTTGTTCATT CATTTGTTCA TCGCTAACAC 1560 TGTCTTGGGC ATCAGGGAAA ACAGGTGTCT CTGGTCCACA TGCAGAAGAG CCACCACCGT 1620 GGCACGACTG GATGACTCAG ACCCCGGGCG GGGGGTATGA TTTGGACACA GTCATTGTCC 1680 AGGGACACAA CTTTGCCTGG ACCAGAGCTT CTCACCCCCA GGCCATTTGA AACCCCAGGG 1740 GATACTCGAC AAAGTCCAGA GACATTTTGG GTTGTTCCTT TCCAGCCCCG GCGATGGTGG 1800 GGACGTGTCC ATGTCTGTGT CCCTCCGGTC ACTCTCTCTG GCCCTCTCCC TCCCTGGGGG 1860 CAGCTGCTCT CAGCCCTCCC TGCCCCCACA TCGCCATCCT GCCTGTCCTT CTGGGCCTGC 1920 ACGTTTGTTG TGTTTGGAAG GAGCCACCAA GGAGGAGGAT GTCAATGTGC AAGTTCTCAG 1980 GGAAGCAGGC CCCGCAGCCT CCGTCAGTGT CTTCCGTCCG CAGGAAGAAC CCAGGCCTGG 2040 GTGATTCATC GGGGCCTCAG GGCCGGGAGG CACTAAATCT TCTGCAGATG TGGTAAGATC 2100 CTATCACAGC AGAAAGGGAA GGGCTAGAGT CTCAGGGAAG GTTTTGCTAG GGAGACGGGC 2160 TTGGAGGGGG CTGAGGCTCA TGGGAGCTGC AAGGGTACAG GAGGGGAGGG GACCCCAGGG 2220 CAGGTGGATG GACACCTGGG TGGGTAAGAA AAGGGCCTCT CAGAGGGCAA GGGAGGGCCA 2280 GGGAGGGAGC AGTGAGCCCT GACTGACTGT ACAAGCTTAA CTGGCTGCCC TTGTCCTGCA 2340 GGTGGTGTGG GCTGTGTGGA TTTCGGATGT GGGCCCATAA CATAGCCACA CTGCTGCAAA 2400 GCAAGTGAGT CTGAGGCAAG AAGAAGGCCC AACCTTGGGA GGCTGACCTG GAGGGCAGGC 2460 AGAGGCAGGT GGTAAGGACC TGCCTTACCT GTTGAGGTGA CAGTGGGGGA CATATTGCAA 2520 GGAAGGAGGC CCTGGATCCT CAGGATGTGG ATGGTGGGTA GAAGGGTGAC AGCTAATGGA 2580 TGTCCACCTG CACAGATGCC CACCTGCATG AGTGCCCACC TGCATGAGTG CCCACTTGTA 2640 CCAATGTCCA CCTGTACAGA TGTCCACATG CAAATGCCCA TCTGCACTGA TATCCACCTG 2700 CACAGATGCC TACCTGCATG AATACCCACT TGCCTGAAAG CCCACCTGCA CCCATGTCCA 2760 CTGGCACAAA TGCCCACCTG CACCCGTGTC CACTGGCACA AATGCCCACC TGCACAGAAG 2820 CCCACCCACA CAAATGCCCA CCTGCAAAAA TGTCCGCCTG CACAGATGTC CACCTGCATG 2880 AATGCCCACC TGTGTCCACA TGCACGAATA CCCACCTGCA CAGATGCCCA CCTGCACGGA 2940 TGCCCACCTG 2950
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