Tag | Content |
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EnhancerAtlas ID | HS197-13896 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr22:36860540-36863090 |
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: 3 | Chromosome | Start | End |
chr22 | 36860840 | 36862297 | chr22 | 36860580 | 36860638 | chr22 | 36862312 | 36862636 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036457 | chr22 | 36853475 | 36869221 |
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Enhancer Sequence | TTATTATTAT TATTTTTGAG ATGGAGTCTT GCTCTGTTGC CCAGACTAGA GTGCAATGGT 60 GTGTTCTCAT CTCACCGCAA CCTCTGCCTC CCAGGTTCAA GCGATTCTCC TGCCTCAGCC 120 TCCCAAGTAG CTGCGATTAC AGGCGTGCAC TGCCACGCCC GGCAAATTTT TGTATTTTTA 180 GTAGAAAAGG GGTTTCGCCA TGTTGGCCAG GCTGGTCTCG AACTCCTGAC CTCAGGTGAT 240 CCACCCGCCT CGGCTTCCCA AAGTCCTGGG ATTACAGGCG TGAGCCACCG CGCCCGGCTC 300 CATGTTCTGT ATATTTAGAA GGAACCTGTG TGAGTGGCCA CCAAACGTTC ACTCTGAACC 360 ATGCTGGCGC TGCCTGCAGG TGAGCGTGCC TGCCCAGAGT GGTGTCTCAG TTGTCTCACT 420 GCCCACCCTG GCGCTCCGTC TCCTCTGTGG GCTGGCACCT GCTCCCTGGT AGGGCGGAGC 480 TGAGGGGCAC AAGGGAGCGT GGAAGTCAAG CAGCCAGCCC AGCAAACTCG AGCTTCCACC 540 CCTGCCGCCT CTCTGCAGGC AACCACGTGC ACTGGGTGTC AAGAAAAAAT ATACAGGGGC 600 CATATCCCGG GTTGTCTTCA GGCTCGGGAA GCCTGCGACT TTGTCCCCTT TCCCCGGCTT 660 CCCAACCTGG TGGCTAAAGG CTTCCAGCAG GTGTCTGCCA ACCCCATCCA CAGTCATGGG 720 GCCCAATGTG GCACCCAGAG AATGACCGTG GGCTGACAGC CCAGAGCCAG CGGCATCCCC 780 GGTGAGGTCA GTGTCCTGGA ATTGGTCAAA CAGGATCACC AGGAGGATTC CGTGAGCACA 840 GCCAGCATGA CTCACGGCCA TGATCAGCCT CACGGGCAGA GGCTGCCAAC CTGGGATGGC 900 CACAGCCACC GGCTCACCTT GCAGGGCAAC GCACCTTTTA AGGAGGGAGC TGGAGCAGCG 960 CCCGGGTCCT GCCTCTGGCC AAGGCCTCTG CCACACTTCT CCACGCCCAC CCGGGCAGAG 1020 AGGCCAGACC CCCACTGGGT TCAAATTTGG CACCACTTTT CAGACATGAC CTTGGGCAAG 1080 TCGATTTCTC TGAACTGTTT TTTTCACTTA TGATATGGAA ATAATACTTG CCTCACAAGA 1140 GTGGAATTCG ATGAGGTAAT GTGTTTAGAA AGTGCGTGGC AAACGGTGCC TTTTAAGGAG 1200 CGGCAGTGGG GTCCGGTGGA AAGGGCCAGG GCTCGGGAGT CGAGGCGCCC CAGCATTGTG 1260 CTCTGGCCCC ACCCTGGGCT CACTGGGTGT CTTTGAAAGA GTTACTCAAC CTCCGATCTG 1320 CTCTGCTCCC ACTGTGTCAA ATGAGCTGAC ACCACTTGCC TTGTTGCCTG TTGTGAGATG 1380 AAGATCACAC ACACGCCACC TTCTATCAGA TGACAGGAGG CAGCGAGGGT GGTTCCTGGG 1440 GGTGGGTGTG GAAGGCTGCC TGGCCTTGAA TCCCAGCTCA GCCACTCAGG GGCTTTGTGA 1500 CCTGGGGAAG GCTCCTCAAC CTCTCGGGGC AGGTCTCAGG TGGAATCTGA AGGGCAACGC 1560 CTTCCCGCGG GGCTGTGCTG AGCTGAGACC CTCAAAACAG TGCCAGGTAC CTGGGAGGTG 1620 CCTCCTGAGT CTGGGCAGGT CCTGCTCATC TTAACCAGGG CTTTTGGCCT TTGCAGGATG 1680 TTCACTCCAC CAGCTTCCGT CTCCACTGAC GCCAGTTGCT GGTTTTGTCC CCTCCATGTG 1740 CTTGTGACAG ACCCCAGGGT CTGGGGTCCT TCAGAGGCCA CGGGCCCCTC TCCTCCCTCG 1800 GTCTCGGCAG CCTTCCCAAG GCAGTCCTTG GGTGGGCCCC TGGAGAATGC AGACAGTTCT 1860 AATAGAACAG GGTGAGCCTC TGAGAACAGA GCAATACCAG CCCCATGGCA TCCCTGGGGC 1920 CACGGAGTAG GGTGTCAGGA TCCCCCTGCC GCCAAGCACC TGATTCACAG GAAGCTGGGG 1980 CCTCATCCAG GCAACCGAGC CCTAATGACA GCTTGGCCCT AGGAGCAAGG CAGACGGAAG 2040 GAAGGCTTTC TTGACTGGCA AGCCTGGCTC CCTTGGCACA CTCCTCTATG GCCAAGGGGA 2100 GCTGGGGGCC AAGAGGGGTT GTCTGGTCCC AAGGCCCAGA AGTTCCTGCA GGCACCCATG 2160 GGAAGGATAG CCTGATCCCC ACAGGGCCAG GCACCTGCTG GGGCAGCCAG GAGCCCTGTC 2220 AGTTGGGGAG GCCTCAGAAG GGTCAAGGGG ATCAGCTGTG GGAGCCCAGG TTTCAGAGGC 2280 AACCACGTCT GGATAGAAAC CCCAGCTCTG CATCCCATGA GCCACAGTGT CTACATCGGG 2340 GTAATGGGGA CAACAGCCTC TTGCCTTAGG AGGGCACGAG GACTGGCACA TGGCATCCTT 2400 AGAATAGCAG CCACTGCTGA CAAGCATGTT AGTGAACAGG AAGGGCTGGT TGGAGAGAGT 2460 GTTGTGGAGT TAGGGGAGGA TGTGGGGACA GTGGACAAGC CCCCTGGGAA AGGGTGACAA 2520 GTGCTCTGAG CCCACACAGA TGTGACATTG 2550
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