Tag | Content |
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EnhancerAtlas ID | HS020-44601 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr9:33129520-33131310 |
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: 31 | ID | Coordinate | Tissue/cell |
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 | ACAAAGGGGC AGGAATCCTG GAGAGAAGCC CCGTGCTCCA CTCACTGACT GCGTCTGTAC 60 TGACTATGTA CCAGCTGTGT GGTCAGAGAG AAAGAAGGGA GGCAGACATG AGGGACTCAG 120 AGTCCGGGGG CTGGGGTGAG GCTGGAACTC AGATAATCAT CCCTTTCCAG AAAGTTCTGA 180 GCAGCCTGGG AGCAGCAGGG AAGGAGAAGT CAGCTCTATT CCAGGGGCTC CACAGAACTA 240 ATGAGGTTGG GGAGGGAAGC TTAAAAGATA GCCAGAGACA CACTAGGAAC ACAGGGGACA 300 GCATAAGCAA AGGCACACAG AGGGGAGAAC AGAGGTGTCT GGGTGGAGAT GGGGAGTCCA 360 GTGAAGTGGA GAGGAGGAGG AAGTGGCTGG AGGTAGGTCA GGGTCTCGGA TGCTAAGCTT 420 GGGCCTTCCG ACCATTTAGA CCGTTGCCTG TAGGCAGTCG TGAAATGCTA ACAGGTTTAA 480 AAGAGGAAGT AACATGGTCA GAACCAGAAA AATCCTGGGC AGCTGAGGGA GAGGAACAGA 540 GGTGCCAGAA GATATGCAAT CGGAATTGGA GAGACCAGTT CTGTGTACTG GCTGTGGGGC 600 AAAGGGCTGC CATGGTTGTG ACAAACCCAC CTGGCCAGCT GTGCCTGCAT TCCTTACTCA 660 TTTTGTAATT TTTATGATGG GCAATCCCAC AAACATTCTG CATTCCTTAA TTTAGGGCTA 720 GTGCTACCAG GTGGTGACCT GCCCTCCCTT CACCTTGAGT GAAGTCTCGT TTCCGGGTTT 780 GAGTATTAGG AAATGCAGCA TGCATCCCTG TTTGCTATGA TGTCTTCTCC TTCTGTTGCT 840 TCTTTTCTTG CTGCCGTTGA AGTTGGAATG CTATATCTTG AAATCCACGT CTCAGAGTAC 900 AAGGAGTCAA ATAGTATTCT CCCATGCTGG TGAGCTAAGG TCAGGGGTGG GAGGAGAGAC 960 CTTAAGGAAA AAGAGCAACT CTTGTTCTTC TATATCTCAA CCAGGAAAGC CTCTCCCGGC 1020 TCATTCCTTC AATATCCTTA TTTTAAGATA TAAGTTAGTA CAATAATTAC AGAGGCATAA 1080 GCCAAATGGG AGTGGTTAAC AGCTTACTAT AGACAGAGTA TGAGTCATAA CAACTTGTGA 1140 AAGTTCACTC CTGTGTGTAA AGCTTGATAC GTGGCCCTAT TTTGAAGAGG CTTATAGGCC 1200 CGGGATGGCC TCTGAGATTC TGCCACCTGG CTCACTCCAC TATCCATTAC CCTCTGACTC 1260 CAAGGAGTTC AAACCAATAG GAGGAAGGGT CCTGATGCGG GCCCTGAGTG GGGGTGCAGC 1320 AGGAGGCGGT GGGAGCCATG AAGAATTCAC CACCACAGAA GCAGGCAGAG GAAGCAGGCA 1380 GAGGAAACAG GCAGGATGAA TGGAGAGTGG AGAGGCAGGA GTGGACCCTC CTAGTAACGG 1440 CTGGTATTTA CTGAAGGTTT ACCATGAGAA GGATGCCTCA TAACCCTCCC CACCAAGGAG 1500 GAAACTGAGG CCTGCAGAGC TTAAGTAACC TGCCTGAGGT CACTGACTGT AAAGTGGCAG 1560 TGCCAGGACT GAACCCAGGC AGTCTGAGCA CACAGCACAC TCTCAGCCCT GGATACCAGA 1620 CTGTGAGCAA CACTGGGGGC ACCCTGGCCA TGAGGAGTGT CACTGATGCC CTGAGAAGGC 1680 ACTAAACCTG GAGTCAGACG CTGGGGTTTG AGCCGCAGCC CTACTGTTGT CTATGTGACT 1740 TTCGGAGCCT GTCCCTCTCT GAGCCTGTTT CCTCACCTGT GACATGGAGC 1790
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