Tag | Content |
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EnhancerAtlas ID | HS176-20334 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:43385080-43387250 |
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) |
ZNF263 | MA0528.1 | chr2:43387224-43387245 | CCCTCCTACTCACCCACCTCC | - | 6.02 | ZNF263 | MA0528.1 | chr2:43385486-43385507 | CCCTTCAGCTCCTCCTCCTCA | - | 6.59 | ZNF263 | MA0528.1 | chr2:43387208-43387229 | TCCTCCTTTTTCTCCTCCCTC | - | 7.66 | ZNF263 | MA0528.1 | chr2:43387205-43387226 | CCCTCCTCCTTTTTCTCCTCC | - | 8.51 |
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| Number of super-enhancer constituents: 42 | ID | Coordinate | Tissue/cell |
SE_03102 | chr2:43384671-43387327 | Bladder | SE_09287 | chr2:43383934-43388379 | CD14 | SE_10736 | chr2:43385270-43387369 | CD19_Primary | SE_11722 | chr2:43384536-43388438 | CD20 | SE_11879 | chr2:43384841-43388354 | CD3 | SE_14384 | chr2:43384968-43390226 | CD4_Memory_Primary_7pool | SE_16107 | chr2:43385039-43388515 | CD4_Naive_Primary_7pool | SE_16655 | chr2:43385030-43387619 | CD4_Naive_Primary_8pool | SE_16950 | chr2:43385153-43387343 | CD4p_CD225int_CD127p_Tmem | SE_17323 | chr2:43384367-43390308 | CD4p_CD25-_CD45RAp_Naive | SE_17875 | chr2:43384151-43389961 | CD4p_CD25-_CD45ROp_Memory | SE_18565 | chr2:43384470-43389555 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19552 | chr2:43384838-43388407 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20209 | chr2:43384383-43388430 | CD56 | SE_20901 | chr2:43385124-43387775 | CD8_Memory_7pool | SE_22349 | chr2:43384494-43388457 | CD8_primiary | SE_23059 | chr2:43384055-43387389 | Colon_Crypt_1 | SE_23724 | chr2:43384477-43387342 | Colon_Crypt_2 | SE_24685 | chr2:43384340-43387340 | Colon_Crypt_3 | SE_25333 | chr2:43383856-43391948 | DND41 | SE_26374 | chr2:43384543-43388739 | Duodenum_Smooth_Muscle | SE_26557 | chr2:43384020-43387372 | Esophagus | SE_27617 | chr2:43384083-43393474 | Fetal_Intestine | SE_28536 | chr2:43383866-43393674 | Fetal_Intestine_Large | SE_30898 | chr2:43384773-43387387 | Fetal_Thymus | SE_31392 | chr2:43384365-43391297 | Gastric | SE_34919 | chr2:43383855-43388500 | HeLa | SE_38828 | chr2:43385030-43386643 | HUVEC | SE_43203 | chr2:43384366-43387389 | Lung | SE_47826 | chr2:43384619-43386674 | Pancreas | SE_47826 | chr2:43386793-43387270 | Pancreas | SE_49954 | chr2:43384504-43386643 | RPMI-8402 | SE_50052 | chr2:43384264-43393423 | Sigmoid_Colon | SE_52337 | chr2:43383845-43392633 | Small_Intestine | SE_53288 | chr2:43384755-43387396 | Spleen | SE_55101 | chr2:43384949-43387332 | Thymus | SE_56731 | chr2:43384774-43386703 | VACO_400 | SE_56731 | chr2:43386712-43387326 | VACO_400 | SE_58412 | chr2:43352450-43425007 | Ly1 | SE_61450 | chr2:43354337-43468354 | Toledo | SE_62203 | chr2:43354169-43468733 | Tonsil | SE_65350 | chr2:43384329-43388234 | 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 |
chr2 | 43385477 | 43386677 | chr2 | 43385938 | 43386506 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I043156 | chr2 | 43383741 | 43393336 |
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Enhancer Sequence | CTAGAGACGG AGTTCACTAT GCTCCTAGCC ATGTGCTGGG TGCGGGGCGA GCCCCAGATG 60 GCTCATCGCC ACGAGGTGCA GGCACAGCCT CTCCATGAGC CATCAGGAAC TCGGGGTTGC 120 ATCAAATCCC CAAAGACTTT ACTGGGCCCA CGCTAGGCAT CAGCCTGGGA TTCTCCTCCC 180 AGGTCTCCAC CAGCTGCTGA GCACAGCGGA GGTGGGGAGG CAAGAGCATG TCCTATCCTG 240 CCTCCTGGCC CCCAGCCCCA GTAACACAGA ACTAGGGTGC CTATTGTTTC AATGGCAGAA 300 ATCCCCCTCC CCTCCGACCC CTGCCCCCTG CAGCACTGCT CCCCATCACT GGGCTAAACG 360 AATGACCCGC CACTCAGCAG GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC 420 CTCCTCACCC ATCCTGACTC AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA 480 TTTGGGTGGG AAGGAGCTAT CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC 540 CTTACTGACC TGACCTTTAG CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG 600 TACACGCATG TGTGTGCACA CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT 660 GACCTGATGA AACAGTCTGG GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA 720 GCAAAAGCAG GATGTGTGTG GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG 780 GTACTGGAGG GCAAAGCGGC CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC 840 CAGAACAGGC ATTAATTCTG GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC 900 CCTTTCTTTC TCTCTCTCTC TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT 960 CAAAATTTCT CACCCACCCT CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG 1020 GCCTCTCTCA ACACCTAGGA GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC 1080 CCCTACCAGG GTTGGCCCTC TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG 1140 GCGGCCACTC CGCAGTTTCA CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT 1200 GACTCTGCAC TGCTCCCAGC ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC 1260 GTTTTTCGCC TTCATGTCTG TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT 1320 CCTGCCCATA GCGTCAGTGG CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG 1380 TGTCCTATCC TCCTGACCAT GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC 1440 CGGGTGCGAT GGCTCTCACC TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGAAGGATCA 1500 CTTGAGCTCA GGAGTTCAAG ACCAGCCTGG GCAACATGGC AAGCCCCATC TCTACAAACA 1560 ATGCAAAAAT TAGCCGGGTG TGGTGGCGTG CACCTGTAGT CCCAGTCCCA GCTACTTGGG 1620 AGGCTGAGGT GGGAGGATCA CTGGAGCCCT GGAGGTGGAG GTTGCTGTGA GCTGAGATCA 1680 CGCCACTGCA CTCCAGCCTG GGCAACTGAG GGACCTTGTC TCAAAAAAAA AAAAAAAAAA 1740 AAGATACCAT TGTTCAGAGG AGGAAGCTGA GCTGACAGAG GTCAAGGAAG ATGCATTTCT 1800 ACCCAGCTTT CAAGATTCAC TTTGGACATC ACCTTCCTCA GACTCTGCCT TCTCCTCTTC 1860 ACCGCCCCAC TACGCCCCAG GCAGGAGAAA CTGCTCCCAG CCTAGAGCCA CTGCCCGTTG 1920 TAGTGACTTC TGTTTGAGGC TGAGACCTCA GCCCCCAGGT CCTGATTTGT GCCCTCCTCC 1980 CTCAGTTTTG GGGCCTGTGA GAGTGGGTGG CTGGGCCTGG GGCTGAGTCA CTGCCTAGCC 2040 TTGCCTGCCC AGCCCCGAAC CAGGCAAGCC TCGGTGCAGG TGACCCTGCT GCCCAGAGAA 2100 GTGGGCGGCA GGAAGAATGG TCAGGCCCTC CTCCTTTTTC TCCTCCCTCC TACTCACCCA 2160 CCTCCTGGCC 2170
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