Tag | Content |
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EnhancerAtlas ID | HS176-05656 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:82220340-82221760 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 41 | ID | Coordinate | Tissue/cell |
SE_00012 | chr10:82211895-82238814 | Adipose_Nuclei | SE_03133 | chr10:82218882-82221533 | Bladder | SE_03722 | chr10:82219975-82221722 | Brain_Angular_Gyrus | SE_04012 | chr10:82217181-82228773 | Brain_Anterior_Caudate | SE_05643 | chr10:82217090-82229822 | Brain_Cingulate_Gyrus | SE_06016 | chr10:82217051-82229868 | Brain_Hippocampus_Middle | SE_08270 | chr10:82217071-82229796 | Brain_Inferior_Temporal_Lobe | SE_09209 | chr10:82213893-82229394 | CD14 | SE_12039 | chr10:82218775-82221502 | CD3 | SE_14580 | chr10:82213988-82229858 | CD4_Memory_Primary_7pool | SE_17018 | chr10:82217189-82221723 | CD4p_CD225int_CD127p_Tmem | SE_17363 | chr10:82212715-82235520 | CD4p_CD25-_CD45RAp_Naive | SE_17861 | chr10:82212598-82235299 | CD4p_CD25-_CD45ROp_Memory | SE_18324 | chr10:82213958-82235661 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19180 | chr10:82214007-82229473 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20438 | chr10:82214073-82221846 | CD56 | SE_20998 | chr10:82217088-82221568 | CD8_Memory_7pool | SE_21854 | chr10:82219051-82221041 | CD8_Naive_7pool | SE_22113 | chr10:82216880-82221477 | CD8_Naive_8pool | SE_22394 | chr10:82214028-82235411 | CD8_primiary | SE_23676 | chr10:82217307-82223095 | Colon_Crypt_1 | SE_23916 | chr10:82220134-82221914 | Colon_Crypt_2 | SE_26561 | chr10:82217136-82235180 | Esophagus | SE_31654 | chr10:82217547-82222320 | Gastric | SE_36281 | chr10:82217471-82221910 | HMEC | SE_38806 | chr10:82217205-82230050 | HUVEC | SE_39636 | chr10:82219989-82223197 | Jurkat | SE_40835 | chr10:82217112-82229768 | Left_Ventricle | SE_41793 | chr10:82219983-82221776 | LNCaP | SE_42164 | chr10:82217114-82229807 | Lung | SE_47902 | chr10:82220097-82221706 | Pancreas | SE_48782 | chr10:82217123-82222157 | Right_Atrium | SE_50150 | chr10:82217126-82229850 | Sigmoid_Colon | SE_52532 | chr10:82217154-82229636 | Small_Intestine | SE_53353 | chr10:82217368-82229838 | Spleen | SE_55160 | chr10:82217607-82221978 | Thymus | SE_56703 | chr10:82219810-82226083 | u87 | SE_57601 | chr10:82220014-82221676 | VACO_503 | SE_58559 | chr10:82213055-82265607 | Ly1 | SE_62319 | chr10:82212748-82296810 | Tonsil | SE_64280 | chr10:82217133-82223532 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 82220600 | 82221200 | chr10 | 82221200 | 82221635 |
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Enhancer Sequence | GTGTAAGAGT AGGGGACAGG TTTCTCTCCT TGTAGGTGTC CCTTCTTGTA AGTGTCACTC 60 TCTTTTTTTC CAGAAACCTT GGTCCTTTTC AGCATCTGCT GGCCCCTTGT CCCTTGGCTC 120 CCTTGCTCTT GGCCTGCTGG ATTTCCCCTC TGCACCCAGG AAATCGCATG GACCTGGGTC 180 CTTGTTTCCC TACAGCCCAC CAATTTTGCT GCTTTTTTCT GCCCCCTGAA GCTGAGCTCC 240 TGCTGCAATT TGTGTTCCCT GCTCTCCCTG TCCTGGGCAA ACCAGTCTGA CAACTTTGTG 300 GTTCTCGCTC CCGCCTCCAT CAGCCTGGGG ATTGACTGTC CCATTTGTCT GAGCTGGGCA 360 GAGGGAGGTG CTGTGGGGGA TCTCTTCCTC TTGCCTGGAC TGCACACTCC TGCTGCCTTC 420 TAGCCGGAGC TCCTGGGCAT TTTGCCTATG GGAGCTTCAC CAGCTTCCTT CTGTCTGAGG 480 CCTACAAGTC CCTGCCTCCA GCCTACCTTG TTCCTCCTCC ATGAGTGAGG CTCCTCCTTT 540 TCTCTCTGGC CCTCCTGTCT ACTTGATCAG ACTCTGCCTC TCTTGAGGGC CGGCTCCCTC 600 CAGCCTACCC TGCACAGGTG ACCCTGTTTG GCCTGCCTCC TTTTCTTGAG GCTGATCTTG 660 TCTCAACAGT CAGCTTTTCA GGAACCAGGC CCTTGCTGTT GTAAGGAAAA CCTGTCGGCT 720 GTGGATGGGG CCTTCCCTCC TTCCTAAAGG CTCTGTAGCC AGCTTCCACC CTTGCAGTGG 780 AACAGTGGTG GTGCCAGAAC CCTGCTCTCT GCAGCCATCC TGCCTACCAC AGTCATTGTG 840 TTTTGTAACT CTAGTAGCTT CTTGTGAAAT ACAAGTGATG GTATAAACGT GGATAGGTTT 900 TTGAGGGGGG CATGCCAAAA TCAGAGTTGG TGGTAGTGGT GGGGGATTCA TTCCCAAGGG 960 CTCTGGGGTG CTAAGTGTGT GAGCAAAGAG GAACAAGTGG CATGTGCCCA GGATGGGGTG 1020 GGGCGGGCAG GTTTAGTTGA GGGCTCCTCT GGTGTAGGGT AGCCCTGACG CTCCCCTCCA 1080 TGGCATGACT GATGAGGTGG CAAAGGCAGG TGCCAGGATT TGGTGTGTTG AAGATTAGTG 1140 CCTGGGTTGG GCTCTGCTCA CTCCTGCAGA AAGACGGTTG GAGAGGGGCT GGTCTTGGTT 1200 TCACAGAGGA TTGTGGGATT ACAGGCAAGA CCTGCTGAGG GCTTGCACTG AGCCACCGAG 1260 AGGAGCAGAA AGAGATACGA GGGCTTCAGG TGCCAGTATG GTTCTCACTG TTGTGAGATC 1320 TCATTTGTGC CTTTTTTTTT TTTCCTTCAG ACAGGGTCTC ACTCTGTTGC CCAGGCTGGA 1380 GTGCAGTGGC CCTATCACAG CTCACTGAGG CCTCCACCTT 1420
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