Tag | Content |
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EnhancerAtlas ID | HS060-19084 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:43385260-43387000 |
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 | chr2:43385486-43385507 | CCCTTCAGCTCCTCCTCCTCA | - | 6.59 |
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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 | AGGTCTCCAC CAGCTGCTGA GCACAGCGGA GGTGGGGAGG CAAGAGCATG TCCTATCCTG 60 CCTCCTGGCC CCCAGCCCCA GTAACACAGA ACTAGGGTGC CTATTGTTTC AATGGCAGAA 120 ATCCCCCTCC CCTCCGACCC CTGCCCCCTG CAGCACTGCT CCCCATCACT GGGCTAAACG 180 AATGACCCGC CACTCAGCAG GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC 240 CTCCTCACCC ATCCTGACTC AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA 300 TTTGGGTGGG AAGGAGCTAT CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC 360 CTTACTGACC TGACCTTTAG CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG 420 TACACGCATG TGTGTGCACA CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT 480 GACCTGATGA AACAGTCTGG GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA 540 GCAAAAGCAG GATGTGTGTG GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG 600 GTACTGGAGG GCAAAGCGGC CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC 660 CAGAACAGGC ATTAATTCTG GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC 720 CCTTTCTTTC TCTCTCTCTC TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT 780 CAAAATTTCT CACCCACCCT CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG 840 GCCTCTCTCA ACACCTAGGA GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC 900 CCCTACCAGG GTTGGCCCTC TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG 960 GCGGCCACTC CGCAGTTTCA CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT 1020 GACTCTGCAC TGCTCCCAGC ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC 1080 GTTTTTCGCC TTCATGTCTG TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT 1140 CCTGCCCATA GCGTCAGTGG CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG 1200 TGTCCTATCC TCCTGACCAT GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC 1260 CGGGTGCGAT GGCTCTCACC TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGAAGGATCA 1320 CTTGAGCTCA GGAGTTCAAG ACCAGCCTGG GCAACATGGC AAGCCCCATC TCTACAAACA 1380 ATGCAAAAAT TAGCCGGGTG TGGTGGCGTG CACCTGTAGT CCCAGTCCCA GCTACTTGGG 1440 AGGCTGAGGT GGGAGGATCA CTGGAGCCCT GGAGGTGGAG GTTGCTGTGA GCTGAGATCA 1500 CGCCACTGCA CTCCAGCCTG GGCAACTGAG GGACCTTGTC TCAAAAAAAA AAAAAAAAAA 1560 AAGATACCAT TGTTCAGAGG AGGAAGCTGA GCTGACAGAG GTCAAGGAAG ATGCATTTCT 1620 ACCCAGCTTT CAAGATTCAC TTTGGACATC ACCTTCCTCA GACTCTGCCT TCTCCTCTTC 1680 ACCGCCCCAC TACGCCCCAG GCAGGAGAAA CTGCTCCCAG CCTAGAGCCA CTGCCCGTTG 1740
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