Tag | Content |
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EnhancerAtlas ID | HS133-12719 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:43375650-43378300 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr17:43377099-43377114 | CATTAATCATTAAAA | + | 6.07 | Nr2f6(var.2) | MA0728.1 | chr17:43377239-43377254 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr17:43378040-43378061 | TCTCCTCTATCCTCATCCTCC | - | 6.56 | ZNF263 | MA0528.1 | chr17:43378043-43378064 | CCTCTATCCTCATCCTCCTCC | - | 7.25 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_04602 | chr17:43375838-43377196 | Brain_Anterior_Caudate | SE_04602 | chr17:43377290-43378060 | Brain_Anterior_Caudate | SE_11470 | chr17:43370585-43396257 | CD20 | SE_18500 | chr17:43377382-43378492 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23493 | chr17:43375953-43376589 | Colon_Crypt_1 | SE_24167 | chr17:43375944-43376404 | Colon_Crypt_2 | SE_25878 | chr17:43364447-43377187 | Duodenum_Smooth_Muscle | SE_26725 | chr17:43375925-43377213 | Esophagus | SE_26725 | chr17:43377358-43378325 | Esophagus | SE_30018 | chr17:43375688-43377543 | Fetal_Muscle | SE_31611 | chr17:43375930-43377146 | Gastric | SE_31611 | chr17:43377364-43378181 | Gastric | SE_32589 | chr17:43375211-43382510 | GM12878 | SE_40748 | chr17:43375640-43377290 | Left_Ventricle | SE_40748 | chr17:43377339-43378304 | Left_Ventricle | SE_44657 | chr17:43375670-43377059 | NHDF-Ad | SE_46201 | chr17:43376003-43377384 | Osteoblasts | SE_47195 | chr17:43366097-43378703 | Panc1 | SE_48714 | chr17:43375804-43377295 | Right_Atrium | SE_48714 | chr17:43377504-43378155 | Right_Atrium | SE_50169 | chr17:43375823-43377262 | Sigmoid_Colon | SE_50169 | chr17:43377351-43378286 | Sigmoid_Colon | SE_54723 | chr17:43359357-43378642 | Stomach_Smooth_Muscle | SE_59053 | chr17:43370566-43412054 | Ly3 | SE_62481 | chr17:43366079-43396493 | Tonsil | SE_65719 | chr17:43375788-43377557 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I045298 | chr17 | 43375682 | 43378039 |
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Enhancer Sequence | AAGGAGGAAA AAAGAAGCAA AAAGGACAAT AAATATAAAA TAAAAACACA AGATGGCAGA 60 AATAAGGCAA AATATTAGCA TGTCATTAAC CACAGTACAT GTGAGTAGAT TACAAAACAG 120 CAAACCAGAT TGGATTTTAA AAGATCCAGC TAGATGCTGA CTAAAAGAAA CAAAACAAAA 180 TTATCCAGAA AAGTTGGAAA TAAAGACATA GAAAGAGATG TGCCAGGCCA ATATTAACCA 240 CAAAGAAGTA ATATTCGTAT CAGACAAAAT ACTTAAGACA AAAAGATATA ATCACTTCTA 300 GGCACCCGAT AAAGAGCCTC CAAATCCAAT GACTGGAGGC AGGCTGAGGC TTTATGTTGA 360 GTAAGGTCTT GGCCCCAGAG TGTCCTGTCT AGCTGCAGAG CAAGGATCTT ATGCGTGGCA 420 GTTCCTGGGC ATGTACTAGG TCTGCTGGGT GTTGGGCCCC GTGCTGAGTG CTGGCAGTAC 480 ACTGAGGAAG AAGACACTGT CCCTTGAGGA TCTTACAGTC TACTGGGGGA AACAGACAAG 540 AAGTCAGAAG AGTTCAGTAC AATACAGGGA TGCAATGACA GAGATAGACA CACAGCAGAT 600 GTGACGGGAA CACAGAGCGA CACCTAGTCC AGCCCAGGAG GTGATGCCTG AGCTGAGTCT 660 GAAGCAGTGA GCAAGACCTG CCCAAGAAAA AGGAGAGGGT GTTCTGGGTA GAGGGGATGG 720 CAAAAGGTAA GGCACAGAGG TGAGTCAATG CAGCAATCAC CAGCAGCTTG AAGTTGTCAG 780 TGAGTAAAGC GTAAGTCAGG CAGTCCCAGG AGAGGAGGCT GCAGATGAAG TTCAGCTATC 840 AGACCATGGA CACACGCTTG ATCCTCATAT ACCCCCAGGG TTTAAATTCT CAGATGAGTG 900 AGCGGGGTAT AATTCCACAT TCCTCCCAGA CTCTTGGGGG TAAAGTTCCA GATGGCAGAA 960 GCTGCAGAGT AGGGGCAGAT GGCACTGGCC AGGCACAGTG CCTCATTCCT GTAATCCCAG 1020 CATTTTGGGA GGCTGAGGCA AGAGGATCAC TTGAGCCTGG GAGTTTGAGA TCAGCATGTA 1080 TAACATAACA AGACTGTGTC TTTATGAAAA TAAAAAAAAA GAAAAAAGAA AAGAAAATCC 1140 TGCCATTGGT ACAGAACCCC CACCCTGGCC TGGGCTAACA ATCTGACAAG TGACAGGCTT 1200 CTGAAAGGCT TGCTTCACTC TCTCCCTCAG GCGGAGAAGG AGAATGGCCA TGTGATCCCT 1260 GGGACATAGA AACAGATGTC TGAGGAAGGA GGAAGGGGCC TTACTGGGGC CTGCACTCAG 1320 GCACTGTGAG TGAAACGCAG CTGGAGGAAC CTCAGAACTG GACTCATTGG CCTGCTTGAG 1380 GCCTGCTTCC CAGGAGAGTA ATTTCTGAAT AAGCATTTCC CATTAAGGAG GATATGAAAT 1440 GTGAAGGTAC ATTAATCATT AAAATCTTAC AGATCAATTA TTAAAAAGAA ACAAATCTGA 1500 CATGCCCTCA AAAACTCAGT CTCGGCCAGG CATGGTGGCT CACGCCTGTA ATCCCAGCAC 1560 TTTCGGAGGC CGAGGCAGGT GGATCAGTTG AGGTCAGGAG TTCAAGACCA GCCTGGGCAA 1620 CATAGTGAAA CCCTGTCTCT ACTAAAAATA CAAAAATTAG CCAGGCATGG TGGCGCGTGC 1680 CTGTAATCCC AGCTACTCAG GAGGCTGAGA TGAGAGAATT GCTTGAACCT AGAGGTGGAG 1740 GTTGCAGTGA GCCGAGATCG CGCCACTGCA CTCCAGCCTG GGCAACAGAG CGAGACTCCA 1800 TCTCAAAAAA ACAAAACTCA GTCTTGCTGC CAATCCCACA GGTCAAACTG CAGGGTAAAT 1860 ACAATTTATG GGGTAAAGTT TCTGACTGTC CTGCAATTAC CACCACATGC CTGATGATGG 1920 CTGGCCGGCC CTAGCCGTGC AGAAACTACT GTCTATAAGG CCCCTTCAGA TGTTTAGGGC 1980 AATTCCCTCG CATCTATTCT ATTGGCATTG GTCTTACCCA CTTCCAGCTT CTCTCTGACC 2040 TCCCACCCTG GCGCTGAGCT AATCTTGAAA CATCGTGTAC TTAAGACAAC CTCAAGCTCA 2100 AAGACATCTG CTGGCTCTGC ACTGCTTATG GGCTCAGTCT CAGCTCTGTG GTCCATAATC 2160 TTTTTGGCCA TTGTTTCCCC AAACATAGGG TTTGGCTTTG GCCAGTCTGA TCTCTCTACA 2220 ACCCCTTGGC TACTCAACTC TCCAGGTCCC ATGTGTGCCA TGCTGTTGTG TGGGCCACCC 2280 CATACATCCT GCTTGTCCTT CAAAGGCAAG GCTCAGCCTC TACCCAGGAA GTTCCTCCCA 2340 TCAGCTCCAC TGTACAACGG CCTCCTTTTC TGCCTGCCCA CAGCACCTTG TCTCCTCTAT 2400 CCTCATCCTC CTCCTGGTCC TGACACCCCC ACTCCCTTTT ACTCATTCAA TGAAACAATG 2460 TAGATGAAGG AACTCTGGGA ACAATAAAGC ATCATAGCAA GTGAAGATAC CCACTTTTTG 2520 TGTGCACAAC TCACAGAATT GCAATCTAAG TAGGGAACAA ATTAAAAAAA ACAGAAAAAA 2580 GCATAATCAA AAATGTTTAG GGCTGAGCAT GGTGGCTTAT GCCTGTAATA CCAGCACTTT 2640 GGGAGGCCAA 2650
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