Tag | Content |
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EnhancerAtlas ID | HS116-34397 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr9:33128520-33131810 |
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) |
SPI1 | MA0080.4 | chr9:33129997-33130011 | TAAAAGAGGAAGTA | + | 7.06 | SPIC | MA0687.1 | chr9:33129997-33130011 | TAAAAGAGGAAGTA | + | 7.73 | SREBF2 | MA0596.1 | chr9:33128973-33128983 | ATCACCCCAT | - | 6.02 | ZNF263 | MA0528.1 | chr9:33129892-33129913 | GGAGGAGGAAGTGGCTGGAGG | + | 6.59 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00330 | chr9:33131315-33133010 | Adipose_Nuclei | SE_09459 | chr9:33129171-33132533 | CD14 | SE_10229 | chr9:33127769-33131935 | CD19_Primary | SE_10912 | chr9:33119344-33169982 | CD20 | SE_12090 | chr9:33130620-33131585 | CD3 | SE_18665 | chr9:33129793-33132844 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19329 | chr9:33130392-33131632 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20045 | chr9:33128349-33132443 | CD56 | SE_22416 | chr9:33128783-33132526 | CD8_primiary | SE_26031 | chr9:33129309-33132935 | Duodenum_Smooth_Muscle | SE_26859 | chr9:33129122-33131571 | Esophagus | SE_27770 | chr9:33128137-33132419 | Fetal_Intestine | SE_28724 | chr9:33128066-33132484 | Fetal_Intestine_Large | SE_31534 | chr9:33128891-33131746 | Gastric | SE_32659 | chr9:33129028-33131615 | GM12878 | SE_35029 | chr9:33129460-33130398 | HeLa | SE_35029 | chr9:33130436-33131878 | HeLa | SE_40894 | chr9:33128725-33131858 | Left_Ventricle | SE_41831 | chr9:33129685-33130482 | LNCaP | SE_41831 | chr9:33130578-33131658 | LNCaP | SE_42236 | chr9:33128546-33131800 | Lung | SE_44340 | chr9:33130634-33131475 | NHDF-Ad | SE_45731 | chr9:33130368-33132932 | Osteoblasts | SE_47814 | chr9:33129311-33130060 | Pancreas | SE_48738 | chr9:33128803-33130531 | Right_Atrium | SE_48738 | chr9:33130653-33131691 | Right_Atrium | SE_50176 | chr9:33128355-33131838 | Sigmoid_Colon | SE_52621 | chr9:33128937-33131899 | Small_Intestine | SE_53402 | chr9:33129123-33131619 | Spleen | SE_58985 | chr9:33124740-33168862 | Ly3 | SE_62118 | chr9:33106994-33169093 | Toledo | SE_62346 | chr9:33106942-33169226 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 33129600 | 33131200 | chr9 | 33129527 | 33131297 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I033127 | chr9 | 33127964 | 33132882 |
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Enhancer Sequence | AAGGGGCAAC ACTCAAACAG TGATGGTGCA GAGACACTCC CTGGCCTTCC CACTCCCATT 60 CCCCACCCCG GCAAGCTCCA AAGGGTCCAA GTGCCCGAAG GAAGGGGAGG CTACAGGACA 120 GGACCAGCCC TACCCCACTC CTCCCAAGCT CCGTTCCCAC ACACATCAAT CTGTGCACTG 180 ACAGCTGAGG TAGAAAATGG AAGGCCGGGA TGGGGGGATG GTAGAGATGA TCAAGATAGA 240 AACCAAACCA ATGAGGCCAT AAGCCCAGGC AGCTGTCCTC ACTAATGGGA TAGACCCAGG 300 AGTCTGCTTC TCCCCAGTTG ATCTTGACCT TGTGTAGGAA CCAGCTGCTT GGACCAGTGA 360 CAGAGACAAC TGCTGAGGTA GGGTGACAGA TACTCTTGCT CACTGAGGGT ACAAAGGACT 420 GTCTCCAAAT CCATCCTCAA CCAGCCTGGA ACTATCACCC CATCATCCTA AAACAGTGCA 480 CAGAAGAAAA GGAAACAGTA GAAAACTTCA AAGCCAGACA GAGTCCTCAG GGCAGCCCTC 540 CCTCCATTTC TCCACAGCCT TTCAGGCAGG CTCCAGCTCT GCTTCCTGGC CATCGTGTGC 600 TTACCTGTGG AGCCTTCCCT CTGCAGGAAC AATCAGAAGA CCATTTGCCT TACTCTGGGG 660 GATGGGGGGA GGTGGGAGGT TCAAAATTCA AAGTGAGACC ATAAAGGTGC TGAGTCCAAA 720 GGACCCTAAA GGAGTTTTGT GACCATTAAC AATCACAAGG CTAAGGTATT AATAGGTTTT 780 CTGCATTTTT CCTGATAAGG GAGGTCACCC CAAGGACTGT CACAGGCAGC CTGTGCTCTG 840 GTCAGCATTG AGCTGGAAGC TTCGGGGAGA GGCCCAAGGG AGGGATCCTG CAAGTTCCCA 900 AGGGTCAGGA CCTGGCCCCA CTGGGAACGG AGGCTTCACT TCCAAGAGGC ACAGATTTAG 960 GCAGAAGACC AGGAGTAGGG AGTCCTGAGA CTAGGGATAA ACAAAGGGGC AGGAATCCTG 1020 GAGAGAAGCC CCGTGCTCCA CTCACTGACT GCGTCTGTAC TGACTATGTA CCAGCTGTGT 1080 GGTCAGAGAG AAAGAAGGGA GGCAGACATG AGGGACTCAG AGTCCGGGGG CTGGGGTGAG 1140 GCTGGAACTC AGATAATCAT CCCTTTCCAG AAAGTTCTGA GCAGCCTGGG AGCAGCAGGG 1200 AAGGAGAAGT CAGCTCTATT CCAGGGGCTC CACAGAACTA ATGAGGTTGG GGAGGGAAGC 1260 TTAAAAGATA GCCAGAGACA CACTAGGAAC ACAGGGGACA GCATAAGCAA AGGCACACAG 1320 AGGGGAGAAC AGAGGTGTCT GGGTGGAGAT GGGGAGTCCA GTGAAGTGGA GAGGAGGAGG 1380 AAGTGGCTGG AGGTAGGTCA GGGTCTCGGA TGCTAAGCTT GGGCCTTCCG ACCATTTAGA 1440 CCGTTGCCTG TAGGCAGTCG TGAAATGCTA ACAGGTTTAA AAGAGGAAGT AACATGGTCA 1500 GAACCAGAAA AATCCTGGGC AGCTGAGGGA GAGGAACAGA GGTGCCAGAA GATATGCAAT 1560 CGGAATTGGA GAGACCAGTT CTGTGTACTG GCTGTGGGGC AAAGGGCTGC CATGGTTGTG 1620 ACAAACCCAC CTGGCCAGCT GTGCCTGCAT TCCTTACTCA TTTTGTAATT TTTATGATGG 1680 GCAATCCCAC AAACATTCTG CATTCCTTAA TTTAGGGCTA GTGCTACCAG GTGGTGACCT 1740 GCCCTCCCTT CACCTTGAGT GAAGTCTCGT TTCCGGGTTT GAGTATTAGG AAATGCAGCA 1800 TGCATCCCTG TTTGCTATGA TGTCTTCTCC TTCTGTTGCT TCTTTTCTTG CTGCCGTTGA 1860 AGTTGGAATG CTATATCTTG AAATCCACGT CTCAGAGTAC AAGGAGTCAA ATAGTATTCT 1920 CCCATGCTGG TGAGCTAAGG TCAGGGGTGG GAGGAGAGAC CTTAAGGAAA AAGAGCAACT 1980 CTTGTTCTTC TATATCTCAA CCAGGAAAGC CTCTCCCGGC TCATTCCTTC AATATCCTTA 2040 TTTTAAGATA TAAGTTAGTA CAATAATTAC AGAGGCATAA GCCAAATGGG AGTGGTTAAC 2100 AGCTTACTAT AGACAGAGTA TGAGTCATAA CAACTTGTGA AAGTTCACTC CTGTGTGTAA 2160 AGCTTGATAC GTGGCCCTAT TTTGAAGAGG CTTATAGGCC CGGGATGGCC TCTGAGATTC 2220 TGCCACCTGG CTCACTCCAC TATCCATTAC CCTCTGACTC CAAGGAGTTC AAACCAATAG 2280 GAGGAAGGGT CCTGATGCGG GCCCTGAGTG GGGGTGCAGC AGGAGGCGGT GGGAGCCATG 2340 AAGAATTCAC CACCACAGAA GCAGGCAGAG GAAGCAGGCA GAGGAAACAG GCAGGATGAA 2400 TGGAGAGTGG AGAGGCAGGA GTGGACCCTC CTAGTAACGG CTGGTATTTA CTGAAGGTTT 2460 ACCATGAGAA GGATGCCTCA TAACCCTCCC CACCAAGGAG GAAACTGAGG CCTGCAGAGC 2520 TTAAGTAACC TGCCTGAGGT CACTGACTGT AAAGTGGCAG TGCCAGGACT GAACCCAGGC 2580 AGTCTGAGCA CACAGCACAC TCTCAGCCCT GGATACCAGA CTGTGAGCAA CACTGGGGGC 2640 ACCCTGGCCA TGAGGAGTGT CACTGATGCC CTGAGAAGGC ACTAAACCTG GAGTCAGACG 2700 CTGGGGTTTG AGCCGCAGCC CTACTGTTGT CTATGTGACT TTCGGAGCCT GTCCCTCTCT 2760 GAGCCTGTTT CCTCACCTGT GACATGGAGC AGAAGTTTCT ACATTGTCTG GCCTCAGGGG 2820 TCTAGGCAAA TCCTAGCAGT GACTGAATGG GAAGCCAAGG AAGTGGAAAT GGGACATGGC 2880 CCCTACTTCA AGTAGAATGA AACCCTTGTG ACCTGCTGTA AGCGGAAGGT TGTGTAGCAT 2940 TTCAATGGGG CAGAAAGAAA TCTGATACTG AAAAGCCTGT TTGGGAACCC TTGGACTAAA 3000 TGTCTCAGAA GCCACTCCAT TTTGAGCATT ACTTCTGTCT AATCTTAAAT GGTATGTGTG 3060 TGTGTGTACA TGTGTGTGCA TGTGTATGTG TGTGTGGGAA TGAAAAGTCA AAATGACAGC 3120 AGGGTGTCTG GGCCAGGGAT AAGCTGAGAG GCTATAAAGA GGGCTAACAG CCCATAAGGT 3180 TTATTTGCTC AACAAACAGT GCAGAAAGGT CAAAACCAGG TGCTACAAAA TCCCTTTCTT 3240 CTTCTAGAAT ATAACCATAA AACAGATAAC ACAGGCAGTT CCTAATTTGT 3290
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