Tag | Content |
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EnhancerAtlas ID | HS139-26896 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr19:41826380-41828490 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr19:41827779-41827791 | TGCCTTAGGGCA | + | 6.04 | TFAP2C | MA0524.2 | chr19:41827779-41827791 | TGCCTTAGGGCA | - | 6.32 | ZNF263 | MA0528.1 | chr19:41826385-41826406 | GCCTCCACCTCCCCATCCCCC | - | 6.28 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_01266 | chr19:41827473-41832460 | Adrenal_Gland | SE_01941 | chr19:41826114-41834937 | Aorta | SE_02341 | chr19:41827299-41835217 | Astrocytes | SE_06609 | chr19:41827940-41835020 | Brain_Hippocampus_Middle | SE_10928 | chr19:41826548-41839191 | CD20 | SE_13335 | chr19:41827590-41831869 | CD34_Primary_RO01536 | SE_14717 | chr19:41828274-41835424 | CD4_Memory_Primary_7pool | SE_20013 | chr19:41827344-41835576 | CD56 | SE_20919 | chr19:41828272-41831918 | CD8_Memory_7pool | SE_22408 | chr19:41827603-41828479 | CD8_primiary | SE_26210 | chr19:41827478-41831409 | Duodenum_Smooth_Muscle | SE_27131 | chr19:41827046-41832712 | Esophagus | SE_31885 | chr19:41826804-41832672 | Gastric | SE_37091 | chr19:41826651-41835398 | HSMMtube | SE_38093 | chr19:41826925-41835502 | HUVEC | SE_41125 | chr19:41824878-41835177 | Left_Ventricle | SE_44313 | chr19:41826974-41833634 | NHDF-Ad | SE_44950 | chr19:41827136-41832669 | NHLF | SE_45824 | chr19:41826675-41835471 | Osteoblasts | SE_48776 | chr19:41825187-41832669 | Right_Atrium | SE_50262 | chr19:41826769-41835431 | Sigmoid_Colon | SE_52575 | chr19:41827074-41832699 | Small_Intestine | SE_54849 | chr19:41827115-41832913 | Stomach_Smooth_Muscle | SE_62666 | chr19:41801738-41841748 | Tonsil | SE_65513 | chr19:41825797-41826814 | Pancreatic_islets | SE_65513 | chr19:41827124-41830643 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 41826836 | 41827141 | chr19 | 41827649 | 41828097 |
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| Number: 2 | ID | Chromosome | Start | End |
GH19I041319 | chr19 | 41825798 | 41826814 | GH19I041321 | chr19 | 41827009 | 41835422 |
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Enhancer Sequence | CCTGTGCCTC CACCTCCCCA TCCCCCAGCC CAGCATCCCA CGGCCTTTGG TCACATGCAG 60 AGCCCTTAAC AAGCTGTGGG GGTCTCCCTT TGTGGAGCTA CAAGGCCCCA AAACAGTTCC 120 AGGATGTGGG GTTGAACAGC CAAAGGAAGA GGCTGGGTGA CCTCGGACTA GCCTTGTCCA 180 TCTCAGACCC TCAGTCTCCT CACCTCTAAG GCAGGGGATG GACAGGGATG ACATATAGCT 240 CAGTATCAAT GAAACCCTGA AACACTTCCC TCCTGGCAAT GGCAGAGGCT ACTACCCCAA 300 GCCCCCCAAG TCTCCCTAGG AAGCCCAACC TCTTCCGCTT CACCTTGGAC CTCCTCATGC 360 TGCAGGAAGT AACCCCTGGC AAAGTTCATG CCCGGCATGG AGGGGCCTGC ACTGGCTGCC 420 CCCACAGTTA CAGTTGTTCA TTTCTCCAGT AGCACCCCAG GGCTGAGACA CGTGGGCCAC 480 CTGCTTTGGA AAAGGACCCA GGAGAGTGAT GTGTCAGTCA AAGATTGGTT TTGTCATTTA 540 AGGTAGCTTT GCCTTGTGGT CCCAAACACT GGGCCCAGCA GCAGAGGACC CTCCTTGGTT 600 TCACATCCAG CCCCGATGAC ATGTGAAATG TGTGACCACA CATAAGCGGA CCCTACGTCC 660 GTCCTGAGGT GGGCTCATCA GGAAAGTGGG AATTGTGATT GCCCCTGCCG TGGGGCCCAG 720 CCATGGTCAC CAGAGCCTCC TCCCATTCTG GGATCCCTGG CTCTTGAATG GAATCTGGCT 780 GCTCCACTTC CAGCCAGGCA GGCCTGCTCA GAGCCCCAGT TCCTGCACGC AAAGTGGTGA 840 GCAGAGGGCC TGGACCATGG GGACCCTCAT TCAGCAGGCA TCACTGCTGT TCCCAAGCCA 900 GGGCCCAGGA GGAAATTGGG GGTGGCAGGG ACCACAGTGT GTTGCCTCGG GAGGGCAGCA 960 GTGGCCCCGA CGTGTCCCCC ATCCGTGCAT TCAGTTGGCA TGTGCTGAGC ATCTGTGATG 1020 TCCACAGGCT CTGGGGATAA GGCGGGGACC AAAACCAACG AAAGGCTTCC CTGCCTGAAA 1080 AGGGGTCCCA CTCTAGTGAG GAAGATCTAG AATTTTCTAG CACTTCATGG TGATGGGGCC 1140 ATGAGGAAAA GTGAAGCAGT GGGAGGGGAG TGACAGGGTG GCTAGGGAAG GCCTCTCTGA 1200 GGGGCTGACA GCAAAGGCCT GCAGGAAGTG GGAGGAGCAT TCCTGGCAGA GGCCATAGTA 1260 GGTGCCAGAG CCCCCAGCAG CACCAAGGGG CAGAAGGGGC TGGAGCAGTC GCAAGGGGTC 1320 GCAAGGGGGT AGGAGATCTC TGAGTGGCCA AATCAAGCTA GGCTTGGCAA CCCAAGTGCG 1380 TGCTGCTGGG TTTACTTGCT GCCTTAGGGC ATGGGCAGCT GTCCTGCCTG TGGTCAGCTC 1440 TGGCTAATCC CGGCCTCTAT CCACTGGAGG GCAGTAGCAA GCCCCCAGTG ATGACGTCAA 1500 AATGTCAAAA TGCCGTGGGG GCAAAATTAC CCCCAAGTGG TTCTTTGTTG AGAGCCACTG 1560 CCTGCTTGAG AATGTAAGCC CATGTGTCGC CACATTTTAC AGCTTTTTAA GAAAAACTAG 1620 AGCTTTGGGG TTTTTTTTAG ACAGGGTCTC CTTTGTCACC CAGGCTGGAA TGTGGTGGTT 1680 TGATCATAGC TCACCGCAGC CTTGACCTCC TGGCCTGAAG TGAGCCTCCC GCCTCAGCCA 1740 ACTGAGTAAG CTGGGACTAC AGGTGCTCAC CACCACGCCT GGCTACTTTT TCAATTTTTT 1800 TGTAGAGACA GGGTCTCCCT TTGTTGCCCA GGGCTCCAAC TGCTGGGCTC AAGCCATCTT 1860 CCTGCCTTGG CCTCCCATAG TGCTGGGATT GCAGGCATGA GCCACCATGC CCAGCCCAGA 1920 GTTTTTGTGC AAACTCTGAT TTGGAAAATG TTCCCTTGAG TTTTAAACCC TGAGAGTTTT 1980 AAACACTATC TCCCTTGGGA GGGTCAGCTC TGACGGCTGC CAGCACATGG CCTTTGACAT 2040 CAGGGTGCCC CAGGCCTTTG ACCTGGGCAT CCGAGGGTCC CAGGGAGACC CAGTCCTTGA 2100 CAGCCTCCTC 2110
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