Tag | Content |
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EnhancerAtlas ID | HS182-21463 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:33129080-33131810 |
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 | 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 | TTCAGGCAGG CTCCAGCTCT GCTTCCTGGC CATCGTGTGC TTACCTGTGG AGCCTTCCCT 60 CTGCAGGAAC AATCAGAAGA CCATTTGCCT TACTCTGGGG GATGGGGGGA GGTGGGAGGT 120 TCAAAATTCA AAGTGAGACC ATAAAGGTGC TGAGTCCAAA GGACCCTAAA GGAGTTTTGT 180 GACCATTAAC AATCACAAGG CTAAGGTATT AATAGGTTTT CTGCATTTTT CCTGATAAGG 240 GAGGTCACCC CAAGGACTGT CACAGGCAGC CTGTGCTCTG GTCAGCATTG AGCTGGAAGC 300 TTCGGGGAGA GGCCCAAGGG AGGGATCCTG CAAGTTCCCA AGGGTCAGGA CCTGGCCCCA 360 CTGGGAACGG AGGCTTCACT TCCAAGAGGC ACAGATTTAG GCAGAAGACC AGGAGTAGGG 420 AGTCCTGAGA CTAGGGATAA ACAAAGGGGC AGGAATCCTG GAGAGAAGCC CCGTGCTCCA 480 CTCACTGACT GCGTCTGTAC TGACTATGTA CCAGCTGTGT GGTCAGAGAG AAAGAAGGGA 540 GGCAGACATG AGGGACTCAG AGTCCGGGGG CTGGGGTGAG GCTGGAACTC AGATAATCAT 600 CCCTTTCCAG AAAGTTCTGA GCAGCCTGGG AGCAGCAGGG AAGGAGAAGT CAGCTCTATT 660 CCAGGGGCTC CACAGAACTA ATGAGGTTGG GGAGGGAAGC TTAAAAGATA GCCAGAGACA 720 CACTAGGAAC ACAGGGGACA GCATAAGCAA AGGCACACAG AGGGGAGAAC AGAGGTGTCT 780 GGGTGGAGAT GGGGAGTCCA GTGAAGTGGA GAGGAGGAGG AAGTGGCTGG AGGTAGGTCA 840 GGGTCTCGGA TGCTAAGCTT GGGCCTTCCG ACCATTTAGA CCGTTGCCTG TAGGCAGTCG 900 TGAAATGCTA ACAGGTTTAA AAGAGGAAGT AACATGGTCA GAACCAGAAA AATCCTGGGC 960 AGCTGAGGGA GAGGAACAGA GGTGCCAGAA GATATGCAAT CGGAATTGGA GAGACCAGTT 1020 CTGTGTACTG GCTGTGGGGC AAAGGGCTGC CATGGTTGTG ACAAACCCAC CTGGCCAGCT 1080 GTGCCTGCAT TCCTTACTCA TTTTGTAATT TTTATGATGG GCAATCCCAC AAACATTCTG 1140 CATTCCTTAA TTTAGGGCTA GTGCTACCAG GTGGTGACCT GCCCTCCCTT CACCTTGAGT 1200 GAAGTCTCGT TTCCGGGTTT GAGTATTAGG AAATGCAGCA TGCATCCCTG TTTGCTATGA 1260 TGTCTTCTCC TTCTGTTGCT TCTTTTCTTG CTGCCGTTGA AGTTGGAATG CTATATCTTG 1320 AAATCCACGT CTCAGAGTAC AAGGAGTCAA ATAGTATTCT CCCATGCTGG TGAGCTAAGG 1380 TCAGGGGTGG GAGGAGAGAC CTTAAGGAAA AAGAGCAACT CTTGTTCTTC TATATCTCAA 1440 CCAGGAAAGC CTCTCCCGGC TCATTCCTTC AATATCCTTA TTTTAAGATA TAAGTTAGTA 1500 CAATAATTAC AGAGGCATAA GCCAAATGGG AGTGGTTAAC AGCTTACTAT AGACAGAGTA 1560 TGAGTCATAA CAACTTGTGA AAGTTCACTC CTGTGTGTAA AGCTTGATAC GTGGCCCTAT 1620 TTTGAAGAGG CTTATAGGCC CGGGATGGCC TCTGAGATTC TGCCACCTGG CTCACTCCAC 1680 TATCCATTAC CCTCTGACTC CAAGGAGTTC AAACCAATAG GAGGAAGGGT CCTGATGCGG 1740 GCCCTGAGTG GGGGTGCAGC AGGAGGCGGT GGGAGCCATG AAGAATTCAC CACCACAGAA 1800 GCAGGCAGAG GAAGCAGGCA GAGGAAACAG GCAGGATGAA TGGAGAGTGG AGAGGCAGGA 1860 GTGGACCCTC CTAGTAACGG CTGGTATTTA CTGAAGGTTT ACCATGAGAA GGATGCCTCA 1920 TAACCCTCCC CACCAAGGAG GAAACTGAGG CCTGCAGAGC TTAAGTAACC TGCCTGAGGT 1980 CACTGACTGT AAAGTGGCAG TGCCAGGACT GAACCCAGGC AGTCTGAGCA CACAGCACAC 2040 TCTCAGCCCT GGATACCAGA CTGTGAGCAA CACTGGGGGC ACCCTGGCCA TGAGGAGTGT 2100 CACTGATGCC CTGAGAAGGC ACTAAACCTG GAGTCAGACG CTGGGGTTTG AGCCGCAGCC 2160 CTACTGTTGT CTATGTGACT TTCGGAGCCT GTCCCTCTCT GAGCCTGTTT CCTCACCTGT 2220 GACATGGAGC AGAAGTTTCT ACATTGTCTG GCCTCAGGGG TCTAGGCAAA TCCTAGCAGT 2280 GACTGAATGG GAAGCCAAGG AAGTGGAAAT GGGACATGGC CCCTACTTCA AGTAGAATGA 2340 AACCCTTGTG ACCTGCTGTA AGCGGAAGGT TGTGTAGCAT TTCAATGGGG CAGAAAGAAA 2400 TCTGATACTG AAAAGCCTGT TTGGGAACCC TTGGACTAAA TGTCTCAGAA GCCACTCCAT 2460 TTTGAGCATT ACTTCTGTCT AATCTTAAAT GGTATGTGTG TGTGTGTACA TGTGTGTGCA 2520 TGTGTATGTG TGTGTGGGAA TGAAAAGTCA AAATGACAGC AGGGTGTCTG GGCCAGGGAT 2580 AAGCTGAGAG GCTATAAAGA GGGCTAACAG CCCATAAGGT TTATTTGCTC AACAAACAGT 2640 GCAGAAAGGT CAAAACCAGG TGCTACAAAA TCCCTTTCTT CTTCTAGAAT ATAACCATAA 2700 AACAGATAAC ACAGGCAGTT CCTAATTTGT 2730
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