Tag | Content |
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EnhancerAtlas ID | HS185-00089 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:16275240-16276830 |
Target genes | |
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 | CCAACACGAG GCAGCCGCCT CCGTATTCAG CCTGATAATA ACATGAAAAA GCCAAAAAAG 60 GGAACAAATA CAGAACACTG AAATGTGTCA TCATTTCAAA AATGAAACGA CATGGTCACT 120 TTAACATTTG TTACAAAAAG AATGCATGAC AATCTCAGAA TAAAGGACAG ATGTTTCAAT 180 TGGACATGTT GGTCTTTAAG AAAACTTTCC TATTTTCTCA TTCTCTCATG GACAGGTGAA 240 GACAAGACGG TGTTTCATCA GCCAGTGTTG CAGAACTCGG CCCCTCTCAG GCTCTGCACG 300 TACCCCATCC CCCGACAAAG CCTAGCTCTC CCTCTCTTTC TGATTCATGG GAACTACCTA 360 GAGTTGCGGA GTCTTCTGAC TCCAGAAACC TGTGTCCTGG TGGCCATCCC AGGAGAAACA 420 ACTTTGATCC TGACCCCAAG AGCTGCTGAC CTGGCCACAA CTTCTCTGTC AAGGGCCTCA 480 CTTAATGCCT GGAAATCCCA CAAGTGAAAA TGCTCAGGAA AATTCCATGG CCCAGTGCCG 540 AGCAGTCTTG AACCGCACAA GCCGTGACTA AGTAACTATC TAAAACAGCT CTCCCTCCCG 600 CCCCAACACC ACCCAGAGTG GGCGTCAACA TCAGCAATTG TCTAGGGAAA ATAAGCGGGC 660 CCTCTTTTCT AGAAAGAACC CATTTCAGAA TGTTTGAAGA GAAAAATCAA CACCCACTGT 720 CTGGGGCCAC ATTAGACAGA TTCAACTGGG CACGGCTGTC ACGCCCTGGC CCAGGATCTG 780 CTAAGGGGTA GTGAGTTCTC TGCCTACTCC TCCTCTTCTC TGAGGCCTGA GTCTGCACGG 840 GGCTGGCTCC CCGGCTTCTG GGCAGGTGAG AGGGACACTT TGGGGCTCTC CGCCCCCAGT 900 TTCGGCAGCT CTGCCCCGGC TCAGGCACTC CCCTGTGACA TCAGCATCTT GGGGGGTGAA 960 TCACTGCCGC AGCTCTGAAG CTGCTGTGGC CATGCATGGC TGTCGGGCTG TGATGAGTCC 1020 GGAGGAAGCC ACGCCCCTCA CACCAGCACA GGTCGGCCTT GAAGGGCGCC AAGGCCTCCC 1080 ACCACGTGAT GTCTGGAAAC TTTTCACAAG TGGGGGTATC TGCTGAGCGG GGGGAAGTGA 1140 CGCAACAAAT AACGGGGAGC ATGGCAGTGG CAACAGGCAT GAGCCACAGC GCACCAGCCT 1200 CCGAGCCACA AGTTCAGCGT TGCTGCTGCT GCCAGAGGCC CAGAAACAGC TGTTCCCTCC 1260 CCCTACACAT CCCCGCGCAG GCTTTGGCTC TCTCAATGAC ATTCCTAAAT GGCTGTGGCT 1320 AGAGCCCTAA GTGTAAGCAC TGGAGAGCCA GGGCCAGCCC CGAAATCAGG AGGTAAGGCC 1380 CTGGGGCAGC TGGCCCCGCA CCAAGTGCAC CAAGTGGCTG GCAGCAGCAC ACGGCCACCT 1440 GGAGCAAAGC ACAGAGGCCT TTCTCTCCTG TCCTCAGTCC CTGGAAGCAG CAGGTTCCTA 1500 TCTGTGACCT GAAGGAACGC AAGGGAGAAT CGTGGCTGCG CTGCTCCTAT GCACTGGACA 1560 TGGGGAGGCA CCAATGTCCA GCTTGTGGAT 1590
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