Tag | Content |
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EnhancerAtlas ID | HS194-02301 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr17:74705060-74706680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZBTB33 | MA0527.1 | chr17:74705329-74705344 | CTCCCGCGAGACCTC | + | 6.42 | ZNF263 | MA0528.1 | chr17:74706053-74706074 | GGGGGAGTGGGGGTAGGAGGG | + | 6.25 | Zfx | MA0146.2 | chr17:74706591-74706605 | GAGGCCGCGGCCCC | - | 6.59 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00954 | chr17:74703516-74707876 | Adrenal_Gland | SE_01807 | chr17:74703603-74707092 | Aorta | SE_02729 | chr17:74704492-74707098 | Astrocytes | SE_04253 | chr17:74703497-74707109 | Brain_Anterior_Caudate | SE_26767 | chr17:74703420-74707961 | Esophagus | SE_28742 | chr17:74703707-74706827 | Fetal_Intestine_Large | SE_29859 | chr17:74703313-74708323 | Fetal_Muscle | SE_37069 | chr17:74703353-74708382 | HSMMtube | SE_39328 | chr17:74703858-74707032 | IMR90 | SE_40719 | chr17:74701539-74708204 | Left_Ventricle | SE_42350 | chr17:74703494-74708386 | Lung | SE_44481 | chr17:74703731-74706862 | NHDF-Ad | SE_45218 | chr17:74704075-74706878 | NHLF | SE_45997 | chr17:74703535-74707090 | Osteoblasts | SE_46847 | chr17:74704708-74707799 | Ovary | SE_48029 | chr17:74704698-74707767 | Pancreas | SE_48607 | chr17:74703319-74708389 | Right_Atrium | SE_49540 | chr17:74703625-74707767 | Right_Ventricle | SE_50328 | chr17:74703705-74707970 | Sigmoid_Colon | SE_51951 | chr17:74703990-74707054 | Skeletal_Muscle_Myoblast | SE_56072 | chr17:74703596-74708429 | u87 | SE_63747 | chr17:74703781-74707062 | HSMM | SE_67575 | chr17:74703596-74708429 | u87 | SE_68515 | chr17:74692690-74734995 | TC71 | SE_68516 | chr17:74692690-74734995 | TC71 | SE_68517 | chr17:74692690-74734995 | TC71 | SE_68518 | chr17:74692690-74734995 | TC71 | SE_68519 | chr17:74692690-74734995 | TC71 | SE_68520 | chr17:74692690-74734995 | TC71 |
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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 | TTCACCCAGA CAGTGGCAAA TTATGCGAGT GGCCCTATTT AAACACCACT GAACCTATTC 60 CTGTAGGTAC CATGTGCTGA GAGCCGAAAG CCTTGTAGAA AGTTCTTTAA GCGCTGTGCC 120 CCACAGGATT GAGCTAAGAC AGGGCGCCGC TAAAGGACAT TTTGCACTTC AGTCCAGAGC 180 CTGGTGTGGG TGATAAAGGG CCAGCCCTGT AAGGCCAGGA CTGACTGAGT GTGCATGACG 240 GCTCCAGAAC TGTCTAAAGG CCTCTCCTGC TCCCGCGAGA CCTCGATGGA GGCAGGAATC 300 CCAAATATGG GAGCAAACAC AACAGATCAG CACATGTCCA AACCGCGCCC CCTCCACCAT 360 CACCGCGTGA GGTCTGGAAG CCCACCCCAA GCAAGAACGG CAGGGCCTGC CCCTGCTCCA 420 CCCCATTAAA TGTGGCTGGT TAGAATCCTC TCTAATGACA CAATTAGTCA CCCACTTGTC 480 AAGCAAAGCG CCTGCTCAGA GGGGGTCTGG CGCACTTACT CAGCAAAGAG AAATGCCTCT 540 GAGCACAGCC TGGCTGCCTC CTCCTCCCCC GAAGGGCTTC TCTCCAGGGT AAACCATTGT 600 GTCCAGCACA GGACAGAGTG GGCACGCAGA CACGCAGGCA CGCTGACAAT GCGCATCCCG 660 GCTCTCCTCC CTTCCAAGAA AAGGAGCTCA GGGGTAAGAA CAAGGGATTA CAATCCGACT 720 CGGAGACCCT GGCGGTGGCC TGGACCGGCC AAGCGTGGTG AACTCCAGGG AACATGGGCA 780 CACAGTGTAG GGGCTGGGAT GAGTGGATGA GGGAAATCCG ACTCCTCTCA GATATCCACA 840 GGCAGGACAA GGTGGCCAAG GCCGAGCTGA TGGACAGCAT GGCGGGAGGC CTGGGGCAGA 900 GGCAGGGAGG GCCGCTTTGG GGTGCTCACT GGTGCTCCAG GAGGGCTTTA TCCTGCATCT 960 TCACTCCATC CAGGCCCAGC TTACCTACAA CCCGGGGGAG TGGGGGTAGG AGGGTGTTAG 1020 ATGTGTAGCT TGAAAACGAC AATAAAAAGG ACTGCTGGGA TCGGGTGCCT TTTCTTTCAG 1080 TCCCAGCCCA CGGGCTTCAC AAAACGCCAC AGCACTGACT CTGAAATCTG GACTTCAAAT 1140 TGGCTGAAAA AGAAAAGCCA GCTTTCCTCC CTCGCCCCCC GAAAGTCCTA CTTTTTAAAC 1200 ATCAAGATAA CTCTCATGGC AGGCCTGGAA ATAAGCCACA GGCACGTGGA TTTGGGAACC 1260 GGTGGGCGGG AGGGGTCAGA AGTGGGTGAG GAGCAAAATT CCAAGCCCTG GTCCCGAGGC 1320 CTGGGAGCCA GCAGCTGCGG AGCACGCCCT GGGCTGGGAG AGGCCGAGGG GAGGGGAGAG 1380 CAAAACACCT CCAAACAAAC TCCTTCGGGC TCGCCCCTCG CCACACTTTC TGGGGGAGGG 1440 CGGCGAGTTT GCGGGGCTGC GGCTTAGCAT GGCGGGACCT GCATTTCCTG CGGGCCGCGG 1500 GTTCTGCGCT TCCTGGGGGC AGCCTGGGCT GGAGGCCGCG GCCCCGCTCC CTGGCTCGGC 1560 GGGGAACGGC AGCGGCAGCC GGAGCCCCGG GGGTGGGGAG GGGGCCGCGA GGGCCCCGGT 1620
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