Tag | Content |
---|
EnhancerAtlas ID | HS194-02393 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr17:79392340-79394720 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr17:79394296-79394311 | GGGTCAGACTGGCCT | + | 6.24 | EWSR1-FLI1 | MA0149.1 | chr17:79393229-79393247 | TCCTCCTTCCTGCCTCCC | - | 6.08 | EWSR1-FLI1 | MA0149.1 | chr17:79393233-79393251 | CCTTCCTGCCTCCCCTCC | - | 7.49 | Myod1 | MA0499.1 | chr17:79394198-79394211 | TGCAGCTGTTCCC | + | 6.98 |
|
| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_00395 | chr17:79390125-79398087 | Adipose_Nuclei | SE_01010 | chr17:79392619-79395878 | Adrenal_Gland | SE_01625 | chr17:79389351-79398706 | Aorta | SE_05872 | chr17:79388722-79398913 | Brain_Hippocampus_Middle | SE_26559 | chr17:79390386-79395974 | Esophagus | SE_28164 | chr17:79392457-79394609 | Fetal_Intestine | SE_29440 | chr17:79392485-79394550 | Fetal_Intestine_Large | SE_29667 | chr17:79391361-79395846 | Fetal_Muscle | SE_31439 | chr17:79390530-79395902 | Gastric | SE_34246 | chr17:79391602-79395908 | HCT-116 | SE_40858 | chr17:79390369-79395795 | Left_Ventricle | SE_42181 | chr17:79390117-79398205 | Lung | SE_44415 | chr17:79390147-79395782 | NHDF-Ad | SE_47177 | chr17:79391538-79395537 | Panc1 | SE_48277 | chr17:79391225-79395813 | Psoas_Muscle | SE_48718 | chr17:79390442-79395880 | Right_Atrium | SE_50245 | chr17:79389672-79395981 | Sigmoid_Colon | SE_51344 | chr17:79390313-79398121 | Skeletal_Muscle | SE_52635 | chr17:79390061-79395764 | Small_Intestine | SE_53447 | chr17:79391260-79395889 | Spleen | SE_54670 | chr17:79389831-79398114 | Stomach_Smooth_Muscle | SE_56968 | chr17:79392274-79394812 | VACO_400 | SE_65328 | chr17:79390158-79401315 | Pancreatic_islets | SE_67997 | chr17:79358663-79398404 | TC32 | SE_68398 | chr17:79359303-79407988 | TC71 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I081416 | chr17 | 79390540 | 79398129 |
|
Enhancer Sequence | GCCCCGACCC AGGGCAGCTG TTCATCCCGG TGCCGCTTCA ATGCCACCTT TTGCACAGCG 60 GAGGCCAAGA GCCCTTGCCA AGGTTCAGGT CAGTAAGTGG ATAAGTCTGG TGGAGGCCTG 120 AGCCCTGGGA AGCAGCATCT TTGAGGACTT GCCCAGCTGT GTGGCTCCCA TGCCCGAGAA 180 CAGAGTCTGC CAAGGTGCGC ACACCCACAG ACGTGTGTGT GTGTACGTGT GTGTACGTGT 240 GTGTGTACGT GTGTGCGTGT GTGTGTGTAC GTGTGTGTGT GTGTGTGTGT GTAGCCACTC 300 ATCCCAGACA TGTAGCACAG TCAGACCTTG TGTGTACACC CATAGTCACG TGCATATGCC 360 CAGAGACAGG TTTGCACAGA CACACCCCGT GAGTCACACA CAGTCCCTCC CCTGCCTCTG 420 TGCAAGTGTG AGTGTGTGCA AGTGTGAGTG TGTGCAAGTG TGAGGTGCAC CCCACATCTC 480 GAGTCTGGAC CACTAGTGAT TGCAGCCAGG GTGGGGGAAG CATCACTGGG TTGTATCTGG 540 GGGTTGAGCC TGCAAACACC TGCACACCCA GCATGCACCT GCCTGTCTCC CAGCCACATC 600 TGCACACTGG GGTGGCATGT GGCTGGGCCT CTAGCCCCTG CCACAGCAGC TTCTGGTCTC 660 CTGGTGCGGG CGGAGGTCCC AGAGTGGCCT CTCACCCCAG GCAGAGCCTG GTCTCCCCAC 720 CCCGTCCCTC ATTCCTCTTT CTGGGCAGCC AAATGGTCAG ATGCTACACC CCTGCCTCCA 780 AGCAGGCTGC ACCTCCCCTC TGCATCCACG CAGGAACCTG TGCAGGGCGG CTTCCTCCCC 840 GCGCTTTCCC GGAATGAGGA ATGTGGGGCA GGGCCAGCAG GGGGGCTGCT CCTCCTTCCT 900 GCCTCCCCTC CCGTCCTGCA CAGCTCCCTT GGGAGCCTGG CTCGTGGGAA GTGTGCTTGG 960 GACCGCCCAT CACTCCGTTC CCAGCCACTC CTGGTGTCCC CCGCCTGGGC GGGCCCTGTG 1020 GGGAGCGGGG AAGGTGTGGA GCGGAAGCCA GTGCCGAGGG AAGAGGGGAG CCTGAGTGGG 1080 TGTGGGTCGG GGGTGGGAGC TGACGCAGGC GGCGGGTGCA GCCGCCAGAC TCGGAGCCGG 1140 GGAGGCCCAT GCCAGCAGCC CGGCAGCTGG GCTTCCGGAA GCAGCGGGAG CCGGGAGCCT 1200 GGGAAGGGCC TCGCTGCTTC TCTGGAGCTG CCGCCATCTC AACGAGGCGT TTTTTTTTTT 1260 TTTTTTTTTT ACAACCCATT TCACAGTTTC CAGAAAAGGA GGATGCTGTC TCGGCGGCTC 1320 ACTTAACTCA AAACAAATGC TCGCTCTGCC GGCTCCGCGC CCGCCTCTCC CGGCTCCCGG 1380 GCCCTGCCGT CCTCTTGTTC CGTCTGCCTT CAGTCTGGTG CCACAGGGCG GAGCAGGGTC 1440 AGCCTGGCAG GAGAGTGGGG TGGGGCACAG TGGGCACCTG GCCATCCGAT TGCCCAGGCC 1500 CAGCCTCTGC TGTGTGGGTC CTCGGGACCC TGGATGGGGG CTGCTGGCAC GGCTGCTGGA 1560 CCGACCCTTA CAGAGGGAGT GGCTCTCCGG GGAGTCCTGG GCTCCAGGGC CCCAGCATGC 1620 TCTGTACCCC TCAGGCTGCC CAGCATGTGT TGCCCTTCTT AGCCATCCAT GGCAAGGAGC 1680 CTGGAAGACA GGTTGGCAGG AGGCAGGCTA GTTCCCATCG GCTGTCCTGG CCACTTAGGG 1740 CCACCTCTGC TGTAAGCCCA TGTGGCCAGC TCTCACCTAC TGTGTGCCGG CCTCCCCACA 1800 CAGCACCCCT GGGCCGGGGC CAGGCTCACT GGGCACCGAG ACTCCAGCCC AGCTGTTGTG 1860 CAGCTGTTCC CCAGTCTTCC CGCTGCTGGG CCACCCTGGG ACAGCAGGTC CAGGCACAGC 1920 CTGCCTCCTG GTCTAGTTGG CTGGACCTTG GGCTCCGGGT CAGACTGGCC TCCCAGGGAT 1980 GGGGCTGTGC CCGAGGACCT GAGCCACCTG GGGGTGGCCA CAGCCCTCCT GGTGTTGCTG 2040 TCTCCCGAAA CCATTTCCTC AGCTAGCCGG CCGCCCAAGC CAGGCCTCTA CAGCATCTTG 2100 GGCAGAGCTG AGGTGGCCCT GGAGCTGGGG CCAGAGCCCG GTCTGGATCT AGAGCTGCAA 2160 ACCCGGCCTG GGCCGGCTGG GCAGTGGGGG CAGCCAACTG GAGGCCAGTG TGCAGTCCTC 2220 GGTGGCCCCG CTGACACCGC ATCCCGCTTA CTGTCCCTTC CCCAGGAACA TCCTAAACTC 2280 ATGCTGCCTC CTGTGATGAG AGCTGATGGG AAGCCTGGCA GAGCGGCCCC AGGCAGGCTC 2340 TGTGTGGGGC CAGGGTGCCC TGACCATGCA CGCGGGTGGG 2380
|