Tag | Content |
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EnhancerAtlas ID | HS003-47974 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr9:137272010-137274950 |
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) |
GLIS2 | MA0736.1 | chr9:137272026-137272040 | GGCCCCCCGCGGTG | + | 6.16 | KLF5 | MA0599.1 | chr9:137274273-137274283 | GGGGCGGGGC | - | 6.02 | ZIC1 | MA0696.1 | chr9:137272026-137272040 | GGCCCCCCGCGGTG | + | 6.89 | ZIC3 | MA0697.1 | chr9:137272026-137272041 | GGCCCCCCGCGGTGT | + | 6.69 | ZIC4 | MA0751.1 | chr9:137272026-137272041 | GGCCCCCCGCGGTGT | + | 7.12 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00860 | chr9:137261032-137275300 | Adrenal_Gland | SE_02933 | chr9:137267847-137274105 | Bladder | SE_05812 | chr9:137261360-137282798 | Brain_Hippocampus_Middle | SE_09174 | chr9:137271959-137278823 | CD14 | SE_23121 | chr9:137273109-137276118 | Colon_Crypt_1 | SE_23757 | chr9:137272192-137272594 | Colon_Crypt_2 | SE_23757 | chr9:137273008-137273550 | Colon_Crypt_2 | SE_23757 | chr9:137273625-137275717 | Colon_Crypt_2 | SE_24707 | chr9:137267912-137275776 | Colon_Crypt_3 | SE_26524 | chr9:137261081-137273486 | Esophagus | SE_26524 | chr9:137273494-137280031 | Esophagus | SE_28276 | chr9:137272422-137275612 | Fetal_Intestine | SE_29238 | chr9:137272293-137275657 | Fetal_Intestine_Large | SE_31436 | chr9:137274124-137274990 | Gastric | SE_33498 | chr9:137264862-137274948 | H2171 | SE_34906 | chr9:137261183-137274052 | HeLa | SE_34906 | chr9:137274427-137277957 | HeLa | SE_40986 | chr9:137262434-137273204 | Left_Ventricle | SE_41556 | chr9:137243649-137273607 | LNCaP | SE_41556 | chr9:137273611-137282898 | LNCaP | SE_42130 | chr9:137261389-137273101 | Lung | SE_42130 | chr9:137273602-137275985 | Lung | SE_43440 | chr9:137267839-137274060 | MCF-7 | SE_48050 | chr9:137252285-137278501 | Psoas_Muscle | SE_50152 | chr9:137273550-137275871 | Sigmoid_Colon | SE_52424 | chr9:137273350-137275415 | Small_Intestine | SE_53315 | chr9:137273283-137275051 | Spleen | SE_65247 | chr9:137261076-137277919 | Pancreatic_islets | SE_68695 | chr9:137267831-137275219 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 6 | Chromosome | Start | End |
chr9 | 137272600 | 137273400 | chr9 | 137272238 | 137272364 | chr9 | 137272366 | 137272506 | chr9 | 137272755 | 137272852 | chr9 | 137272864 | 137273054 | chr9 | 137274039 | 137274567 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I134369 | chr9 | 137261189 | 137279971 |
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Enhancer Sequence | TGCGTGTGTT GGGGGTGGCC CCCCGCGGTG TAGGCCGGAG GTGGCGTGCC GGCCCCGTGA 60 GTCACGCCGA TCCCAGGATG GGAGTGGGGG TGGCCGGGGC ACTGTGAGCT GGCGTGCTGA 120 GGCTGGCCTG CCCGTGGCTT GGCCTGGGGG CAGGGGTAGG GTGGGGTCCT GCCCGGGTTC 180 TCCTGGAGAA CCTGGGTCAG GAGCCAGGGG CCAGATCAGG GCTGGGGACT TCGCCTGGGG 240 TCGGATAGGG GCTGGGGTGG CCATGAGAAG TGAGGAGCCT CCCATGACCC AGTGGTTGCA 300 AGGAGCAGAT GCCGCCTGTC AGGTGGGCGG CCCCCCCTGG GAGGAGGCTG CAGGCTGGGA 360 GGTAGACAGG ACGGGCCCCT CGGTGTGATG GTTGGGGTGT CCAGGGACTG GACTTGGGAA 420 GGGTTGGTGA CCTAGTGCCA TGGGGTCCCT GCTCTCTGTG GCTGCCTCTG TGGCCAGGCC 480 TTGGCCCTCC TATTGCTGCC CCACGACACC TGGCTGTGGC TTGTCCCAGC TCCTGGGCCA 540 GGTGGGGAGT GCAGCTGGCC ACCGAGCCTC ATGAAGCACC TTTCCAGTTC CCCGGCACCT 600 GGGTCTGGCC GAGGTCTGAG GCCAGAGGAA AGGCCTCCTC CAGAATCCAG GGCTGCCCGT 660 CCTGAGGTAA GGGGCTTTGA GCTGCAGGCA GACGGCACCT TCTACCCATG GCCGGATCCC 720 CCCCTGTCAA TCTGCAGTAG AGACAGCAGA GCCCCCGGGA ACCCCTCCCA GCAGCTGAGG 780 GTTCAGGGGG TGCCCCTCAC TGTACTGGGG AAATGTGGCC CCAGCGGGCA GGAGGTGCAG 840 GGCCCAGTCA GAGACTGAGT CTGAACCCGG TGGGGCCTCA GGCCAGCTCT GTGACCCGGA 900 CAAGGGGTTT TCCTTCTCTG AGCCCCAGTT GCTGCTGTCA GAGCCTGCGG TGGGCACTGA 960 TTTGAGGAAG GACAGACATG GGCTGGGAGG GTTGAGGGAG GCCCTGGAGA GGGGGACCCT 1020 GGGGAGGGAG ATCTTGGAGC TGCAGAGGCT TTGAAGAGGC AGGCGTATGG GAGTGCGTGG 1080 CCAGGTTGCC CGGCCTGGGC TGGGGGCTGG GTCCAGGGAT GCAGCTGGCC TCACCTGCTG 1140 GTAGAGCCCT GTCTGGAGGA GTTGAGCTCA GACCTTAGCT AGTGCTGACC GCGCTGGGGC 1200 AGAGTGCTGA GAGGGGCTCT CTCAGGGCCG TCTCTCAGGG CTGGGCCCTG TTGGATCTTC 1260 TAACTGTCTG AGCGGGAGAG GGAAGGCTTC CTGGAGGAGG TGTCCCTGGT AGGAAGACGC 1320 AGAGGGAATG ATTGTGTGTG CTGTAAGGGC CAGGCCCAGG GCTGAGAGGG GCTGGTGGAG 1380 ATGGTGGGGG CTGGGTGGGG CAGGACACCA TGGTCTATGT GGCGCCCGCC CTTCTCCCTC 1440 CTCCATGGCC ACAAGGCCCC TCTGGTACAG AGGGTGGTGC TGGCCTTGAG GGATCTGGCC 1500 GGCAGGTAGG CAAGTGAATG ACAGAGCCCC TCAGGTGGAC TTGGGGGTGG GGCCTCCTGG 1560 TTCTGCCTAT TTTCTTCAGC GGCCCTGGTT AGGGCTTTGA AGGGGCTTCA CTGCAAATTA 1620 GCCCCGACCT CCCCGGGGTG CCCAGCAGGG GCGCACTGCA CCTTAGGTGC TCCGTCGTGA 1680 AGTGGCCACA AGGTGCCTTT GGTGTGTGGG GCCCACAGGA TGAGTTGGAT GCAGCCTCCC 1740 GGTGGGGGCT GCTCAGGTGG TGATGAAAAC TGTACCTGTG GGCAGGTGAA GCCACCGCTC 1800 CCTCGGTGTA GCAGTCAGTG TGCCCTCCCC ACGTCTCCTC CTCTCCTTCT GTCCCTGGAC 1860 CCAGGAGTTT GGGAGAGGCC AGCGGGCCAG CTGGGCACTT TGGTCTCTGT AATGAGGACC 1920 CTCCCACCCC ACCAAGATGC ACACATGCCC TGCCAGGATG TGGGGGGGCG CAGGGCAGTG 1980 GGCTGAGCCA AGGTGTAGAT GCTGGGAGGT AAGGTTACCC TCCCCCTGGG CTGGCGTCTG 2040 CCTCCCCGCC TGCTGCTGCC CCTGTGGCCG GCCGCATGTG GGGAGGAAGG AAGAGGTTTG 2100 GGTGGTGTGT GTGTGTGTGT GTGTGTGTGC GCTTTTGACT GGGCTCGGAG GGCTCTGGCT 2160 GGGACCCAAG CTCAGGCCTT TAGCACCTTG GCTGGGAGGA GTGAGGCCTG GGGAGACAGT 2220 GGGGGCCAGG AGCTGGGTGC TGAGGAGACC AGAGCTGGGG GCTGGGGCGG GGCCAGGGCA 2280 GCTGGTAGGA AGTCCTGCCC TTGCAGCCGG TCCTGCGAGA AAGCCCCTGG CTGCTGTCTT 2340 GGCTTTGCTG GACTGGCAAG GTGGACCAGA GGCTGGGGAC TGGACACCAT GGGCCTCTGT 2400 GCACTGATGG AGCAGTAGGT GTGTGGGATT CATGGGGTGC TGGGGTGTGG ATTCACGAGG 2460 GAGGGGCCTT TTGGGTTACG AATCAGCCCC TCCAGTTATC CAGGGTGGGG TGCTGAGGCC 2520 TGAGTGGGCA GTATGAGGGT GGGCAGCTAA CTATGTAACA GCCGGGTCTC TGGGAGGCCC 2580 TGGTCTGTGG CGTTGCCGTC TCTGAGCTGG GAAGACATGT GCCTGAGAGC TGGTCCGGGG 2640 TGGCCTCTGG CTTTGGCTGG GGAGGCCCTG CCCACCTGAG AGCAGCGTTC GGCGAGTGTG 2700 GACTCTGCCC CGGTGCTGGG CGCAGCACCT GTCGAGTTCT TGGAGCGTGC CGAATGCAGG 2760 CGTAGCTTCG GGCTGTCTGG ACAGGACCTG GTTAGCGAGA CCCTGGCTGA AGGGCCCAGA 2820 AGGGGCTGCA GTGGGACTGG AGCCACCTGG CTATGCCCCT GGGCTGCTGG GATCACATGC 2880 TGTGGGTGAT TGGGCAGATG TGGCTGTGTG TGTGCACACT GTGGGGACAG ACAGGGTGGG 2940
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