Tag | Content |
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EnhancerAtlas ID | HS133-26800 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:34190670-34193180 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr6:34190862-34190873 | AGCTGTGATTT | - | 6.14 | KLF16 | MA0741.1 | chr6:34191865-34191876 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr6:34191808-34191818 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr6:34191281-34191291 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr6:34191866-34191876 | GGGGCGGGGC | - | 6.02 | RREB1 | MA0073.1 | chr6:34192052-34192072 | CCCCCACCCACGCCCTCCCC | + | 6.77 | SP2 | MA0516.2 | chr6:34191278-34191295 | GAAGGGGCGGGGCGAAG | - | 6.18 | ZNF263 | MA0528.1 | chr6:34191525-34191546 | CTCCTTTCTCCTCCCTCCCCT | - | 6.01 | ZNF263 | MA0528.1 | chr6:34191521-34191542 | CTCCCTCCTTTCTCCTCCCTC | - | 6.52 | ZNF740 | MA0753.2 | chr6:34192046-34192059 | ACACCCCCCCCAC | + | 6.82 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_15387 | chr6:34190899-34193011 | CD4_Memory_Primary_7pool | SE_18188 | chr6:34190627-34193089 | CD4p_CD25-_CD45ROp_Memory | SE_19450 | chr6:34191031-34191947 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19450 | chr6:34191975-34192963 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_26784 | chr6:34190782-34192566 | Esophagus | SE_32269 | chr6:34191136-34192580 | Gastric | SE_32924 | chr6:34190866-34191738 | H1 | SE_32924 | chr6:34191898-34192442 | H1 | SE_34365 | chr6:34190859-34192745 | HCT-116 | SE_38509 | chr6:34190839-34193085 | HUVEC | SE_40020 | chr6:34190944-34192835 | K562 | SE_57546 | chr6:34192000-34192434 | VACO_503 | SE_63029 | chr6:34190859-34207435 | Tonsil | SE_65500 | chr6:34190860-34193304 | Pancreatic_islets | SE_68752 | chr6:34190784-34192504 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr6 | 34191726 | 34192136 | chr6 | 34190705 | 34191000 | chr6 | 34190903 | 34191051 | chr6 | 34192400 | 34192927 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I034223 | chr6 | 34190863 | 34193565 |
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Enhancer Sequence | AGGATGCTTT GAGCCTAGGA GTTCGAGGTT CCAGTGAGGT TCCATCATGC CACTGCGCTC 60 CAGCCTGGGC AAGAGAGCAA ACCCTTGTCT CAAAAAACAA AAAGAGCTTT TTTAGGCTGT 120 GCATCATTCC CCTCATGATT ATCATTTTTG CCCACACCCC TATTCTTGAA GAAGCAGGAT 180 GATGATGGTA AGAGCTGTGA TTTATTGAGC ACTTAATGGA TGCTAAGTCC TGTGCTGCCT 240 CACTTAGTGC TCACCCTGCT GTATAGCAAA CAGGGCCCAG GCAGGAAATG GAATCCAACC 300 AAAGGGTGCA AGAGGCTTTA ATGGAAGGAC GACAGGGGTG GGGGCAGGGT GAAGGGGATC 360 AACCTGGGTA TTGGGACCGG CAGTGATGAC AAGACACTGC AACTTCTGGG CTGAAAGGGC 420 AATGGGAAAA TGCAGTGTTC CCGAGCTGAC ATCATGAGGG GGCATAGCCA CAGTCAGACC 480 AAGGACCAAA ACAGGGCCAG GAGTACCCTG ACTTCTCTCT CGCCTCCCCT CAGGTCGGCT 540 GCATGGGTGC TGCTCAACAG AAAGCCAGCT GGTAAGGGAG CCCGGGCCAC GAAGTCGGCA 600 TGGGAGGGGA AGGGGCGGGG CGAAGGAAGA ATAACAAGCA TAGGGAAGCA GGATTATCCT 660 GCTCCATGCC ATTTCGCAGA TAAGAAGACT GAGGCCCAGA GACATGAAGT AACCTGCCGG 720 CTGCCACAGA GCTGGGAAGG TGGAGCTAGA GGAGAGCCAG GCTCTGAGGC CCTCCGCCCA 780 GCCTCCTAAT ACAATCCCAG CCTCAAGGCG CGAGCAGAGC GCGGAGCAGG CCAGCACCCC 840 ATGCTCCCGG TCTCCCTCCT TTCTCCTCCC TCCCCTCACT GCTCAGCTCT CCCACCCTCC 900 CACCTTCTGT CTGCCTTAGC TGGGCCTCCC CTGGCCTCCT CTCAAGAAGG CTGTGGCCCC 960 TTTCCTCTGT GTGCTTCCCC ACTTTGTCTC TCCCTTTTTT CTCAGTCTTC TTGTCTCCCT 1020 CACTCAGTCG CTGTCTTCAT TTCCCTCAGT CTTTCCCTAT AGCAGGCTCA CAAGGGTGCA 1080 TCCTCCTAAG GCTCAGTTTC TTTGCCATTC CCGAGCTCCG CCCCCTCTGC CCGCCGTGGC 1140 CCCGCCCCTG CCGGGCCGCC CTCCCCTGCG CTGGGCGGCG GGCCGGGTGG CAGGCGGGGG 1200 CGGGGCCCGG GCTGGCGCGG CGCCGGCCTG AGTCACACGC ATGAGGCAGC GTGAGTCAGG 1260 CGCGGAGGGA AGTCCCTGCG GAAGGGGCTT TCGGAGCTGC AGTCGAATCG CAGGGAAAGA 1320 GAAAGTGTTC GAAACGCTGC TTTGACACAG TGACCTTGTG TGAGCCCTAG CTGCACACAC 1380 CCCCCCCACC CACGCCCTCC CCGCAGACAG CAGCACGCAC ACCCCCGGCC GGCTCACGGT 1440 ACGCGGCCGC TGCCCGCACT CCCGGGTCGG GCCTGCGCGT CCCTGTGGGG TTGGGCGAGC 1500 GGGGTATCGA GGGTCCAGCA GCCTGGACCC GGCCCCTCCA CAGGGCAGTC CCTTTTCCAG 1560 CTTCCAAAAG CTAGCGTTGC TCACCTACTG CCAGACCCCA GACCCACTTC TCCCACGAGG 1620 TGTAAAGAAG GACCCCTGAG GGTCTTCCAC GTCACCTTGT GGAGCCTCGT GGAGTATGGC 1680 AGAAGGAGGA GGGCAATTTG AGGTCCTGCA GCGCCCGGGG GAACCAGGGA TGAACTCCCT 1740 CCTGCCCCCA GGCTCTCCTC CTCATCCTAG AATCAATCGA TGGGATTCAG TTACAGAAAT 1800 ATTTATTAAA CACCGACTAT ATGCCAAGTT ATAAAAACCT GGGACAAGAT GGTAAACAAA 1860 GCAGGACAGT AAACAAAATA TATTAACCCC TGCCTTTCAG GAACTGGCAT TCTAGTTAGG 1920 TGAGGGAGAT GATAAACAAA AAATAAGCAA ATGATCTAGG CTAGTGCTGC CCGATAGAAA 1980 TAGAAGGGAA GCCATGAATG TAATGTTTAA TTTTGTAGTA ACCATGTTAA GATGGTAAAA 2040 AGAAACACAT GAAATTAACT TTAATTTTTT TTTTTGAGAC CGAGTTTCGC TCTTGTTGCC 2100 CAGGCTGGAA TACAATGATG TCGACTCACC ACAACCTCTG CCTCCTGAAT TCAAGCAATT 2160 CCCCTGCCTC AGCCTCCCAA GTAGCTGGGA TTACAGGTAT TCACCACCAC TCCTGACTAA 2220 TTTTGTATTT TTGGTAGAGA TGGAGTTTCT CCATGTTGGT CAGGCTGGTC TCGAACTCCC 2280 GACCTCAGGT GATCCGCCCG CCTTGACCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA 2340 CCGCGCCTGG CCAATTTTAA TTTTTTTTTT TAAGGAACCG GGTCTTCTTA AAGGGTTCCT 2400 TAAGGAACCA GGTCTCTACT TTGTGGTCCA GGCTGGAGTT CAGTGGTGCG ATCATACCTC 2460 ACTGCGGCCT CCAACTCCTG ATGCTCCTGC CTCAGCCTTC CAAAGCCCTG 2510
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