Tag | Content |
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EnhancerAtlas ID | HS194-00033 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr1:16275350-16276850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | SP1 | MA0079.4 | chr1:16276264-16276279 | GAAGCCACGCCCCTC | + | 6.67 | SP4 | MA0685.1 | chr1:16276264-16276281 | GAAGCCACGCCCCTCAC | + | 6.35 | ZNF263 | MA0528.1 | chr1:16276035-16276056 | TTCTCTGCCTACTCCTCCTCT | - | 6.37 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_01097 | chr1:16275403-16279590 | Adrenal_Gland | SE_01987 | chr1:16272432-16279631 | Aorta | SE_02709 | chr1:16274610-16280662 | Astrocytes | SE_03452 | chr1:16275260-16277700 | Brain_Angular_Gyrus | SE_04408 | chr1:16274061-16278759 | Brain_Anterior_Caudate | SE_05249 | chr1:16273948-16279656 | Brain_Cingulate_Gyrus | SE_06124 | chr1:16270812-16279644 | Brain_Hippocampus_Middle | SE_07342 | chr1:16272948-16278751 | Brain_Hippocampus_Middle_150 | SE_08131 | chr1:16272535-16279679 | Brain_Inferior_Temporal_Lobe | SE_18522 | chr1:16273733-16281386 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19255 | chr1:16273419-16281362 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_27189 | chr1:16274173-16281550 | Esophagus | SE_36664 | chr1:16274460-16277822 | HMEC | SE_38820 | chr1:16274752-16281466 | HUVEC | SE_40080 | chr1:16274659-16281418 | K562 | SE_45001 | chr1:16274543-16280813 | NHLF | SE_45986 | chr1:16274066-16281079 | Osteoblasts | SE_47059 | chr1:16275327-16277770 | Ovary | SE_55849 | chr1:16274274-16283539 | u87 | SE_61132 | chr1:16274043-16303645 | HBL1 | SE_64852 | chr1:16274416-16281190 | NHEK | SE_67570 | chr1:16274274-16283539 | u87 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I015947 | chr1 | 16274011 | 16281336 |
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Enhancer Sequence | CATGGTCACT TTAACATTTG TTACAAAAAG AATGCATGAC AATCTCAGAA TAAAGGACAG 60 ATGTTTCAAT TGGACATGTT GGTCTTTAAG AAAACTTTCC TATTTTCTCA TTCTCTCATG 120 GACAGGTGAA GACAAGACGG TGTTTCATCA GCCAGTGTTG CAGAACTCGG CCCCTCTCAG 180 GCTCTGCACG TACCCCATCC CCCGACAAAG CCTAGCTCTC CCTCTCTTTC TGATTCATGG 240 GAACTACCTA GAGTTGCGGA GTCTTCTGAC TCCAGAAACC TGTGTCCTGG TGGCCATCCC 300 AGGAGAAACA ACTTTGATCC TGACCCCAAG AGCTGCTGAC CTGGCCACAA CTTCTCTGTC 360 AAGGGCCTCA CTTAATGCCT GGAAATCCCA CAAGTGAAAA TGCTCAGGAA AATTCCATGG 420 CCCAGTGCCG AGCAGTCTTG AACCGCACAA GCCGTGACTA AGTAACTATC TAAAACAGCT 480 CTCCCTCCCG CCCCAACACC ACCCAGAGTG GGCGTCAACA TCAGCAATTG TCTAGGGAAA 540 ATAAGCGGGC CCTCTTTTCT AGAAAGAACC CATTTCAGAA TGTTTGAAGA GAAAAATCAA 600 CACCCACTGT CTGGGGCCAC ATTAGACAGA TTCAACTGGG CACGGCTGTC ACGCCCTGGC 660 CCAGGATCTG CTAAGGGGTA GTGAGTTCTC TGCCTACTCC TCCTCTTCTC TGAGGCCTGA 720 GTCTGCACGG GGCTGGCTCC CCGGCTTCTG GGCAGGTGAG AGGGACACTT TGGGGCTCTC 780 CGCCCCCAGT TTCGGCAGCT CTGCCCCGGC TCAGGCACTC CCCTGTGACA TCAGCATCTT 840 GGGGGGTGAA TCACTGCCGC AGCTCTGAAG CTGCTGTGGC CATGCATGGC TGTCGGGCTG 900 TGATGAGTCC GGAGGAAGCC ACGCCCCTCA CACCAGCACA GGTCGGCCTT GAAGGGCGCC 960 AAGGCCTCCC ACCACGTGAT GTCTGGAAAC TTTTCACAAG TGGGGGTATC TGCTGAGCGG 1020 GGGGAAGTGA CGCAACAAAT AACGGGGAGC ATGGCAGTGG CAACAGGCAT GAGCCACAGC 1080 GCACCAGCCT CCGAGCCACA AGTTCAGCGT TGCTGCTGCT GCCAGAGGCC CAGAAACAGC 1140 TGTTCCCTCC CCCTACACAT CCCCGCGCAG GCTTTGGCTC TCTCAATGAC ATTCCTAAAT 1200 GGCTGTGGCT AGAGCCCTAA GTGTAAGCAC TGGAGAGCCA GGGCCAGCCC CGAAATCAGG 1260 AGGTAAGGCC CTGGGGCAGC TGGCCCCGCA CCAAGTGCAC CAAGTGGCTG GCAGCAGCAC 1320 ACGGCCACCT GGAGCAAAGC ACAGAGGCCT TTCTCTCCTG TCCTCAGTCC CTGGAAGCAG 1380 CAGGTTCCTA TCTGTGACCT GAAGGAACGC AAGGGAGAAT CGTGGCTGCG CTGCTCCTAT 1440 GCACTGGACA TGGGGAGGCA CCAATGTCCA GCTTGTGGAT CAAGACCTGA AGGGCACAAA 1500
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