Tag | Content |
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EnhancerAtlas ID | HS017-21487 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr21:45625790-45629120 |
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: 2 | Chromosome | Start | End |
chr21 | 45625876 | 45628728 | chr21 | 45626600 | 45628736 |
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| Number: 2 | ID | Chromosome | Start | End |
GH21I044205 | chr21 | 45625272 | 45628706 | GH21I005055 | chr21 | 45625955 | 45628553 |
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Enhancer Sequence | CTGGGATTAC AGGCACCCAC CACCACACCC AGCTAATTTT TGTATTTTTA GTAGAGATGG 60 GGTTTCACTA TGCTGGCCAG GCTGGTCTTA AACTCCTGAC CTCAGGCAAC CTGCCTGCCT 120 TGGCCTCCCA AAGTGCTGGG ATTGCAGGCG TGAGTCACCG TGCCCAGACA AATTAAGGCT 180 CTTGAGACGA GGTCATCCTG GGTTATGCAG ATGGACCCTG AATCCGACAC TAGCACCCGT 240 GTGGAAGGAA CGAGAGGGAG ATTTGGGGTC CGCAGAGGCA AACCACAGGA GGACGGAGTC 300 GGAGACTGGA GCACCGCGGC CTTGATCGGG GGACACCAGG GCTGCCGGCT GTGCCAGAAG 360 GGGCTGAGGC TGGACCGGAT TCTCTCCGAG TTCCCAGAAG GAGCCAGTCC TGCCGACGCC 420 TTGATGCTGG ACTCTGGCCT CCAGAAATGT GCGAGGACAA ACATCTGCGG TTTCTAGGCC 480 CCGCCTGTGG TCCTCTGTTG CAGCAGCCTG GACAGTCTGG ACTGCCTGGA CAGCATGCAG 540 ATGGGCTCTG CCCGCGGCTG CCCACGAGTT CCCACCGCCC GCCCGTCCGT GGGAGAGCCA 600 GTCCTCGTAT GTGAAGCGTA CCTGTATCCC TTTACTCCGC GTACACAGGT GCCTTTGTCA 660 CTTCTCCTTT GACCTGGCTG GCACATCTTA CCGGTTTCTG CGCTAACAAT GAGTTGAAGG 720 AAATCTTGAA CGCGCGTTCA TTTTATATCG GTATCAGAGT CTGTTTATTT CTTGTTGACA 780 CTAATCTTTG AGCATGAGTA GTTTAGTGAT TGTGAAACAG AAACTTCTGG ATACAAAATC 840 AGTCTCCTGG CTGTGACCCA ATCATCTTCG CAGTTCTGAT TACCTGTGAT TAAGAAAATA 900 AATAAGAACA CCCATTGGGG GAAGGCTTCC CTCCCCCGGG CACAGCAGCT TTAAAACCGA 960 AAGGGAAGTG GGTGCTGTGA GCAGCTCTGT TCAGGCCTAA GGCCACGCAT GTGTGCCCCG 1020 TGGGGGAGAC ATGCACCAGC GAATCAGGAA ACAGTGGTGA CAGCCGTTCC GGGAGGCTGA 1080 CTGGGGGTGC AGGGGTCACT TTTCTAATGT GGGTGGGTCT GTGTCCCCTG CAGGAACGTG 1140 GCTGCAGCAA AGCCGGTCAG CCAGCGGTCA GCTCCAGCCC CTGTCCAGGC CCTGTGGGTC 1200 CTGCTGACCA GGCTGCGGTT GTTCCCAAAC CAGTTCCCAG CCCCCGCTTG CCCTACTTCC 1260 TCTCACACCA GCTCCTTCCA CCCCCTCACA CCCACCTGCA GGCTCCCAGC CCAGGCTACT 1320 GACATCAATC ATGGCAATCG CTATTCCAGA GGTATACGCG GTGGGTGGGG TCCGGTATCG 1380 CCTGCCATGC CTCACTCACC GGGCACCCAG ATAACCTGAG GCCAGGGAGC AGCCACTCGC 1440 CCTGACCCAT GCTCCCCGGG CCCCTGAGGC ACCCAGGAGG ACCACCCGGC CGCTTCTGCT 1500 CAGAGCCCAG CACCCCCGAG TCTGTGAAGA GGTCACATCT GACCACGTTT CCAGGTGGCT 1560 GCCCAGGCGT GGGTTCATGG CCGCTTCCGG TTTCCTCCTC GAGCTGAACC ACACACCTGC 1620 TCTGTCCCGG GCTTTCTGGA GGGGTTTTCC GAAGTGAGAC TGTGGGCTCC CTCCAGGGCT 1680 GGGGGCAGGA GGACACACGG GGAAGGTGGG CAAGCAGCCC CAGGCTGAGG GAGGCCTCCC 1740 CTCTGCAGCG TTTGTTCATT CATTTGTTCA TCGCTAACAC TGTCTTGGGC ATCAGGGAAA 1800 ACAGGTGTCT CTGGTCCACA TGCAGAAGAG CCACCACCGT GGCACGACTG GATGACTCAG 1860 ACCCCGGGCG GGGGGTATGA TTTGGACACA GTCATTGTCC AGGGACACAA CTTTGCCTGG 1920 ACCAGAGCTT CTCACCCCCA GGCCATTTGA AACCCCAGGG GATACTCGAC AAAGTCCAGA 1980 GACATTTTGG GTTGTTCCTT TCCAGCCCCG GCGATGGTGG GGACGTGTCC ATGTCTGTGT 2040 CCCTCCGGTC ACTCTCTCTG GCCCTCTCCC TCCCTGGGGG CAGCTGCTCT CAGCCCTCCC 2100 TGCCCCCACA TCGCCATCCT GCCTGTCCTT CTGGGCCTGC ACGTTTGTTG TGTTTGGAAG 2160 GAGCCACCAA GGAGGAGGAT GTCAATGTGC AAGTTCTCAG GGAAGCAGGC CCCGCAGCCT 2220 CCGTCAGTGT CTTCCGTCCG CAGGAAGAAC CCAGGCCTGG GTGATTCATC GGGGCCTCAG 2280 GGCCGGGAGG CACTAAATCT TCTGCAGATG TGGTAAGATC CTATCACAGC AGAAAGGGAA 2340 GGGCTAGAGT CTCAGGGAAG GTTTTGCTAG GGAGACGGGC TTGGAGGGGG CTGAGGCTCA 2400 TGGGAGCTGC AAGGGTACAG GAGGGGAGGG GACCCCAGGG CAGGTGGATG GACACCTGGG 2460 TGGGTAAGAA AAGGGCCTCT CAGAGGGCAA GGGAGGGCCA GGGAGGGAGC AGTGAGCCCT 2520 GACTGACTGT ACAAGCTTAA CTGGCTGCCC TTGTCCTGCA GGTGGTGTGG GCTGTGTGGA 2580 TTTCGGATGT GGGCCCATAA CATAGCCACA CTGCTGCAAA GCAAGTGAGT CTGAGGCAAG 2640 AAGAAGGCCC AACCTTGGGA GGCTGACCTG GAGGGCAGGC AGAGGCAGGT GGTAAGGACC 2700 TGCCTTACCT GTTGAGGTGA CAGTGGGGGA CATATTGCAA GGAAGGAGGC CCTGGATCCT 2760 CAGGATGTGG ATGGTGGGTA GAAGGGTGAC AGCTAATGGA TGTCCACCTG CACAGATGCC 2820 CACCTGCATG AGTGCCCACC TGCATGAGTG CCCACTTGTA CCAATGTCCA CCTGTACAGA 2880 TGTCCACATG CAAATGCCCA TCTGCACTGA TATCCACCTG CACAGATGCC TACCTGCATG 2940 AATACCCACT TGCCTGAAAG CCCACCTGCA CCCATGTCCA CTGGCACAAA TGCCCACCTG 3000 CACCCGTGTC CACTGGCACA AATGCCCACC TGCACAGAAG CCCACCCACA CAAATGCCCA 3060 CCTGCAAAAA TGTCCGCCTG CACAGATGTC CACCTGCATG AATGCCCACC TGTGTCCACA 3120 TGCACGAATA CCCACCTGCA CAGATGCCCA CCTGCACGGA TGCCCACCTG TACAAAGGCC 3180 TACCTGCGTG AATGTCCACC TGCATGGATG CCCACCCGCA CGGATGCCCA CCTGCACAGT 3240 TATCCATCTG AACAGCCCTC TGGTGCCTCC TTTTGCTTGC ACATGTTCAA ATCCTCCCAG 3300 TCCTACAGTC GATTGTTCCT AGTTGGGGTC 3330
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