Tag | Content |
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EnhancerAtlas ID | HS145-10514 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr17:74263920-74264900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr17:74264281-74264296 | GTTTTCTTGAGAACT | + | 6.37 | ZNF263 | MA0528.1 | chr17:74264587-74264608 | AGTGGAGGGAGGAGGGGAAAG | + | 6.37 | ZNF740 | MA0753.2 | chr17:74264567-74264580 | GTGGGGGGGGGGC | - | 6.29 | ZNF740 | MA0753.2 | chr17:74264569-74264582 | GGGGGGGGGGCAG | - | 6.33 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_10428 | chr17:74261317-74270738 | CD19_Primary | SE_11415 | chr17:74257434-74273567 | CD20 | SE_15056 | chr17:74260072-74266530 | CD4_Memory_Primary_7pool | SE_18937 | chr17:74257700-74266466 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19565 | chr17:74259973-74266464 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21340 | chr17:74259878-74266365 | CD8_Memory_7pool | SE_23599 | chr17:74263966-74264926 | Colon_Crypt_1 | SE_24131 | chr17:74264098-74264827 | Colon_Crypt_2 | SE_24931 | chr17:74263978-74264813 | Colon_Crypt_3 | SE_27367 | chr17:74258519-74266081 | Esophagus | SE_28090 | chr17:74257585-74269455 | Fetal_Intestine | SE_29152 | chr17:74254176-74269372 | Fetal_Intestine_Large | SE_31864 | chr17:74261126-74264947 | Gastric | SE_32663 | chr17:74261503-74269696 | GM12878 | SE_43246 | chr17:74259692-74266315 | Lung | SE_47749 | chr17:74264544-74264846 | Pancreas | SE_48284 | chr17:74258480-74271528 | Psoas_Muscle | SE_50371 | chr17:74254262-74264931 | Sigmoid_Colon | SE_52552 | chr17:74254274-74270056 | Small_Intestine | SE_53757 | chr17:74260072-74269790 | Spleen | SE_55588 | chr17:74263663-74264593 | Thymus | SE_58966 | chr17:74257592-74273389 | Ly3 | SE_60322 | chr17:74239092-74270751 | Ly4 | SE_60510 | chr17:74247565-74275632 | DHL6 | SE_61026 | chr17:74257641-74276199 | HBL1 | SE_62440 | chr17:74241844-74272934 | Tonsil |
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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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Enhancer Sequence | GTAGAGACGG GGTTTCTCCA TGTTGATCAG GCTGGTCTCG AACTCCCAAC CTCAGGTGGT 60 CCGCCTGCCT CGGCCTCCCA AAGTTCAGGG ATTACAGGCG TGAGCCACTG CACCCGGCCT 120 GGCAATTTAT TTTGGACAAA GTAAGTCAAA GGAAAAAGAT CAAAAAACGA AACACTAGAG 180 ACCAGTAACA GCAAAATGGC AAAACCAGAA GTCATGAGTA ACTGATAAAT GGTTGTCCCG 240 TACATTACTG TAGATTCCCA TAGTTGGAAG CTTCCCAGTT GATAAGGAGG GCTTCCCAGT 300 TGGAAGTGGA GAAAGGCACT ACAGACTTGA AGTGGGAGGA CAAAGGTACA GGGGACAATG 360 GGTTTTCTTG AGAACTGGCC GAGAGGGCAT ATCTGGTTCA AAACCCTCAT TTTACAAAAG 420 CAGAGAGAAG CTCCAGAGAG GTTCAGGAAC TTGCCCAAGC TTACACAGGC AGGCCACCAC 480 AGGCCTGCCA GCCATCATCC CTGCTGTTCT CTGGCGGCTG TTTGAGGAGA CAGGCCTCGC 540 TGGCTGGCGG GGAACTGGGG AAGTCGGTCA CGATGCTGTG ATGCAATTGG CCTCCACCCC 600 CACCCTTCAT TCATTGTTTC CTGCTGCCGA GAAGTCATCC CCAGAGGGTG GGGGGGGGGC 660 AGGGAGTAGT GGAGGGAGGA GGGGAAAGGT CTGGGTGGGG CCAGGCCTCT GCATTGGGTC 720 CTTTGGCCTC CCCCTGAGGA CCCCTAGAAA GGCAAGGGTC AGAGCTCCCT TGGTGCCCTG 780 GGTGCTGACA TGGTGTGGGG CTCAATGGAC AGGGTGTGCT AGTGTCCCCA TTCCATGTAT 840 GTTACACACC CCCTACACAA CCTCCGGTTT CTAGCTGTGA AAGCTCCCTC TGTTTTTTTT 900 TTTTTTTTTT TTGAGACGGA GTTTTGCTCT GCCACCTAGG CTGGAGTGCA GTGACGTGAT 960 CTCAGCTCAC TACAACCTCC 980
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