Tag | Content |
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EnhancerAtlas ID | HS109-14330 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr21:45626300-45629020 |
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: 25 | 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 | chr21:45626613-45628029 | 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 | GACAGTCTGG ACTGCCTGGA CAGCATGCAG ATGGGCTCTG CCCGCGGCTG CCCACGAGTT 60 CCCACCGCCC GCCCGTCCGT GGGAGAGCCA GTCCTCGTAT GTGAAGCGTA CCTGTATCCC 120 TTTACTCCGC GTACACAGGT GCCTTTGTCA CTTCTCCTTT GACCTGGCTG GCACATCTTA 180 CCGGTTTCTG CGCTAACAAT GAGTTGAAGG AAATCTTGAA CGCGCGTTCA TTTTATATCG 240 GTATCAGAGT CTGTTTATTT CTTGTTGACA CTAATCTTTG AGCATGAGTA GTTTAGTGAT 300 TGTGAAACAG AAACTTCTGG ATACAAAATC AGTCTCCTGG CTGTGACCCA ATCATCTTCG 360 CAGTTCTGAT TACCTGTGAT TAAGAAAATA AATAAGAACA CCCATTGGGG GAAGGCTTCC 420 CTCCCCCGGG CACAGCAGCT TTAAAACCGA AAGGGAAGTG GGTGCTGTGA GCAGCTCTGT 480 TCAGGCCTAA GGCCACGCAT GTGTGCCCCG TGGGGGAGAC ATGCACCAGC GAATCAGGAA 540 ACAGTGGTGA CAGCCGTTCC GGGAGGCTGA CTGGGGGTGC AGGGGTCACT TTTCTAATGT 600 GGGTGGGTCT GTGTCCCCTG CAGGAACGTG GCTGCAGCAA AGCCGGTCAG CCAGCGGTCA 660 GCTCCAGCCC CTGTCCAGGC CCTGTGGGTC CTGCTGACCA GGCTGCGGTT GTTCCCAAAC 720 CAGTTCCCAG CCCCCGCTTG CCCTACTTCC TCTCACACCA GCTCCTTCCA CCCCCTCACA 780 CCCACCTGCA GGCTCCCAGC CCAGGCTACT GACATCAATC ATGGCAATCG CTATTCCAGA 840 GGTATACGCG GTGGGTGGGG TCCGGTATCG CCTGCCATGC CTCACTCACC GGGCACCCAG 900 ATAACCTGAG GCCAGGGAGC AGCCACTCGC CCTGACCCAT GCTCCCCGGG CCCCTGAGGC 960 ACCCAGGAGG ACCACCCGGC CGCTTCTGCT CAGAGCCCAG CACCCCCGAG TCTGTGAAGA 1020 GGTCACATCT GACCACGTTT CCAGGTGGCT GCCCAGGCGT GGGTTCATGG CCGCTTCCGG 1080 TTTCCTCCTC GAGCTGAACC ACACACCTGC TCTGTCCCGG GCTTTCTGGA GGGGTTTTCC 1140 GAAGTGAGAC TGTGGGCTCC CTCCAGGGCT GGGGGCAGGA GGACACACGG GGAAGGTGGG 1200 CAAGCAGCCC CAGGCTGAGG GAGGCCTCCC CTCTGCAGCG TTTGTTCATT CATTTGTTCA 1260 TCGCTAACAC TGTCTTGGGC ATCAGGGAAA ACAGGTGTCT CTGGTCCACA TGCAGAAGAG 1320 CCACCACCGT GGCACGACTG GATGACTCAG ACCCCGGGCG GGGGGTATGA TTTGGACACA 1380 GTCATTGTCC AGGGACACAA CTTTGCCTGG ACCAGAGCTT CTCACCCCCA GGCCATTTGA 1440 AACCCCAGGG GATACTCGAC AAAGTCCAGA GACATTTTGG GTTGTTCCTT TCCAGCCCCG 1500 GCGATGGTGG GGACGTGTCC ATGTCTGTGT CCCTCCGGTC ACTCTCTCTG GCCCTCTCCC 1560 TCCCTGGGGG CAGCTGCTCT CAGCCCTCCC TGCCCCCACA TCGCCATCCT GCCTGTCCTT 1620 CTGGGCCTGC ACGTTTGTTG TGTTTGGAAG GAGCCACCAA GGAGGAGGAT GTCAATGTGC 1680 AAGTTCTCAG GGAAGCAGGC CCCGCAGCCT CCGTCAGTGT CTTCCGTCCG CAGGAAGAAC 1740 CCAGGCCTGG GTGATTCATC GGGGCCTCAG GGCCGGGAGG CACTAAATCT TCTGCAGATG 1800 TGGTAAGATC CTATCACAGC AGAAAGGGAA GGGCTAGAGT CTCAGGGAAG GTTTTGCTAG 1860 GGAGACGGGC TTGGAGGGGG CTGAGGCTCA TGGGAGCTGC AAGGGTACAG GAGGGGAGGG 1920 GACCCCAGGG CAGGTGGATG GACACCTGGG TGGGTAAGAA AAGGGCCTCT CAGAGGGCAA 1980 GGGAGGGCCA GGGAGGGAGC AGTGAGCCCT GACTGACTGT ACAAGCTTAA CTGGCTGCCC 2040 TTGTCCTGCA GGTGGTGTGG GCTGTGTGGA TTTCGGATGT GGGCCCATAA CATAGCCACA 2100 CTGCTGCAAA GCAAGTGAGT CTGAGGCAAG AAGAAGGCCC AACCTTGGGA GGCTGACCTG 2160 GAGGGCAGGC AGAGGCAGGT GGTAAGGACC TGCCTTACCT GTTGAGGTGA CAGTGGGGGA 2220 CATATTGCAA GGAAGGAGGC CCTGGATCCT CAGGATGTGG ATGGTGGGTA GAAGGGTGAC 2280 AGCTAATGGA TGTCCACCTG CACAGATGCC CACCTGCATG AGTGCCCACC TGCATGAGTG 2340 CCCACTTGTA CCAATGTCCA CCTGTACAGA TGTCCACATG CAAATGCCCA TCTGCACTGA 2400 TATCCACCTG CACAGATGCC TACCTGCATG AATACCCACT TGCCTGAAAG CCCACCTGCA 2460 CCCATGTCCA CTGGCACAAA TGCCCACCTG CACCCGTGTC CACTGGCACA AATGCCCACC 2520 TGCACAGAAG CCCACCCACA CAAATGCCCA CCTGCAAAAA TGTCCGCCTG CACAGATGTC 2580 CACCTGCATG AATGCCCACC TGTGTCCACA TGCACGAATA CCCACCTGCA CAGATGCCCA 2640 CCTGCACGGA TGCCCACCTG TACAAAGGCC TACCTGCGTG AATGTCCACC TGCATGGATG 2700 CCCACCCGCA CGGATGCCCA 2720
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