Tag | Content |
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EnhancerAtlas ID | HS133-21347 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:36860650-36863090 |
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) |
ESR2 | MA0258.2 | chr22:36862028-36862043 | GGGGCTTTGTGACCT | - | 6.02 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_01080 | chr22:36860729-36863882 | Adrenal_Gland | SE_01722 | chr22:36859233-36865838 | Aorta | SE_02575 | chr22:36860815-36864942 | Astrocytes | SE_23071 | chr22:36860789-36863201 | Colon_Crypt_1 | SE_23740 | chr22:36860819-36863050 | Colon_Crypt_2 | SE_24731 | chr22:36860747-36863197 | Colon_Crypt_3 | SE_26443 | chr22:36860643-36864808 | Duodenum_Smooth_Muscle | SE_27096 | chr22:36859292-36864834 | Esophagus | SE_27650 | chr22:36861041-36862472 | Fetal_Intestine | SE_31378 | chr22:36860668-36862998 | Gastric | SE_37504 | chr22:36860602-36869250 | HSMMtube | SE_38695 | chr22:36857456-36865052 | HUVEC | SE_41064 | chr22:36859183-36865060 | Left_Ventricle | SE_42094 | chr22:36856361-36864828 | Lung | SE_46578 | chr22:36860692-36865053 | Osteoblasts | SE_47671 | chr22:36860776-36863352 | Pancreas | SE_49127 | chr22:36860748-36864748 | Right_Atrium | SE_49784 | chr22:36860782-36864292 | Right_Ventricle | SE_50050 | chr22:36860757-36864674 | Sigmoid_Colon | SE_51467 | chr22:36856823-36865059 | Skeletal_Muscle | SE_52340 | chr22:36859997-36864647 | Small_Intestine | SE_53283 | chr22:36857017-36864617 | Spleen | SE_54687 | chr22:36859233-36871332 | Stomach_Smooth_Muscle | SE_55607 | chr22:36861828-36862276 | Thymus | SE_55607 | chr22:36862455-36862918 | Thymus | SE_57815 | chr22:36860812-36862660 | VACO_503 | SE_63127 | chr22:36801020-36866853 | Tonsil | SE_64152 | chr22:36860792-36862398 | HSMM | SE_64152 | chr22:36862456-36864808 | HSMM | SE_65459 | chr22:36859262-36864620 | 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 |
chr22 | 36860840 | 36862297 | chr22 | 36862312 | 36862636 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036457 | chr22 | 36853475 | 36869221 |
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Enhancer Sequence | TGCCTCAGCC TCCCAAGTAG CTGCGATTAC AGGCGTGCAC TGCCACGCCC GGCAAATTTT 60 TGTATTTTTA GTAGAAAAGG GGTTTCGCCA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC 120 CTCAGGTGAT CCACCCGCCT CGGCTTCCCA AAGTCCTGGG ATTACAGGCG TGAGCCACCG 180 CGCCCGGCTC CATGTTCTGT ATATTTAGAA GGAACCTGTG TGAGTGGCCA CCAAACGTTC 240 ACTCTGAACC ATGCTGGCGC TGCCTGCAGG TGAGCGTGCC TGCCCAGAGT GGTGTCTCAG 300 TTGTCTCACT GCCCACCCTG GCGCTCCGTC TCCTCTGTGG GCTGGCACCT GCTCCCTGGT 360 AGGGCGGAGC TGAGGGGCAC AAGGGAGCGT GGAAGTCAAG CAGCCAGCCC AGCAAACTCG 420 AGCTTCCACC CCTGCCGCCT CTCTGCAGGC AACCACGTGC ACTGGGTGTC AAGAAAAAAT 480 ATACAGGGGC CATATCCCGG GTTGTCTTCA GGCTCGGGAA GCCTGCGACT TTGTCCCCTT 540 TCCCCGGCTT CCCAACCTGG TGGCTAAAGG CTTCCAGCAG GTGTCTGCCA ACCCCATCCA 600 CAGTCATGGG GCCCAATGTG GCACCCAGAG AATGACCGTG GGCTGACAGC CCAGAGCCAG 660 CGGCATCCCC GGTGAGGTCA GTGTCCTGGA ATTGGTCAAA CAGGATCACC AGGAGGATTC 720 CGTGAGCACA GCCAGCATGA CTCACGGCCA TGATCAGCCT CACGGGCAGA GGCTGCCAAC 780 CTGGGATGGC CACAGCCACC GGCTCACCTT GCAGGGCAAC GCACCTTTTA AGGAGGGAGC 840 TGGAGCAGCG CCCGGGTCCT GCCTCTGGCC AAGGCCTCTG CCACACTTCT CCACGCCCAC 900 CCGGGCAGAG AGGCCAGACC CCCACTGGGT TCAAATTTGG CACCACTTTT CAGACATGAC 960 CTTGGGCAAG TCGATTTCTC TGAACTGTTT TTTTCACTTA TGATATGGAA ATAATACTTG 1020 CCTCACAAGA GTGGAATTCG ATGAGGTAAT GTGTTTAGAA AGTGCGTGGC AAACGGTGCC 1080 TTTTAAGGAG CGGCAGTGGG GTCCGGTGGA AAGGGCCAGG GCTCGGGAGT CGAGGCGCCC 1140 CAGCATTGTG CTCTGGCCCC ACCCTGGGCT CACTGGGTGT CTTTGAAAGA GTTACTCAAC 1200 CTCCGATCTG CTCTGCTCCC ACTGTGTCAA ATGAGCTGAC ACCACTTGCC TTGTTGCCTG 1260 TTGTGAGATG AAGATCACAC ACACGCCACC TTCTATCAGA TGACAGGAGG CAGCGAGGGT 1320 GGTTCCTGGG GGTGGGTGTG GAAGGCTGCC TGGCCTTGAA TCCCAGCTCA GCCACTCAGG 1380 GGCTTTGTGA CCTGGGGAAG GCTCCTCAAC CTCTCGGGGC AGGTCTCAGG TGGAATCTGA 1440 AGGGCAACGC CTTCCCGCGG GGCTGTGCTG AGCTGAGACC CTCAAAACAG TGCCAGGTAC 1500 CTGGGAGGTG CCTCCTGAGT CTGGGCAGGT CCTGCTCATC TTAACCAGGG CTTTTGGCCT 1560 TTGCAGGATG TTCACTCCAC CAGCTTCCGT CTCCACTGAC GCCAGTTGCT GGTTTTGTCC 1620 CCTCCATGTG CTTGTGACAG ACCCCAGGGT CTGGGGTCCT TCAGAGGCCA CGGGCCCCTC 1680 TCCTCCCTCG GTCTCGGCAG CCTTCCCAAG GCAGTCCTTG GGTGGGCCCC TGGAGAATGC 1740 AGACAGTTCT AATAGAACAG GGTGAGCCTC TGAGAACAGA GCAATACCAG CCCCATGGCA 1800 TCCCTGGGGC CACGGAGTAG GGTGTCAGGA TCCCCCTGCC GCCAAGCACC TGATTCACAG 1860 GAAGCTGGGG CCTCATCCAG GCAACCGAGC CCTAATGACA GCTTGGCCCT AGGAGCAAGG 1920 CAGACGGAAG GAAGGCTTTC TTGACTGGCA AGCCTGGCTC CCTTGGCACA CTCCTCTATG 1980 GCCAAGGGGA GCTGGGGGCC AAGAGGGGTT GTCTGGTCCC AAGGCCCAGA AGTTCCTGCA 2040 GGCACCCATG GGAAGGATAG CCTGATCCCC ACAGGGCCAG GCACCTGCTG GGGCAGCCAG 2100 GAGCCCTGTC AGTTGGGGAG GCCTCAGAAG GGTCAAGGGG ATCAGCTGTG GGAGCCCAGG 2160 TTTCAGAGGC AACCACGTCT GGATAGAAAC CCCAGCTCTG CATCCCATGA GCCACAGTGT 2220 CTACATCGGG GTAATGGGGA CAACAGCCTC TTGCCTTAGG AGGGCACGAG GACTGGCACA 2280 TGGCATCCTT AGAATAGCAG CCACTGCTGA CAAGCATGTT AGTGAACAGG AAGGGCTGGT 2340 TGGAGAGAGT GTTGTGGAGT TAGGGGAGGA TGTGGGGACA GTGGACAAGC CCCCTGGGAA 2400 AGGGTGACAA GTGCTCTGAG CCCACACAGA TGTGACATTG 2440
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