Tag | Content |
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EnhancerAtlas ID | HS099-11845 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr2:43385100-43386970 |
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: 41 | 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_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 | GCTCCTAGCC ATGTGCTGGG TGCGGGGCGA GCCCCAGATG GCTCATCGCC ACGAGGTGCA 60 GGCACAGCCT CTCCATGAGC CATCAGGAAC TCGGGGTTGC ATCAAATCCC CAAAGACTTT 120 ACTGGGCCCA CGCTAGGCAT CAGCCTGGGA TTCTCCTCCC AGGTCTCCAC CAGCTGCTGA 180 GCACAGCGGA GGTGGGGAGG CAAGAGCATG TCCTATCCTG CCTCCTGGCC CCCAGCCCCA 240 GTAACACAGA ACTAGGGTGC CTATTGTTTC AATGGCAGAA ATCCCCCTCC CCTCCGACCC 300 CTGCCCCCTG CAGCACTGCT CCCCATCACT GGGCTAAACG AATGACCCGC CACTCAGCAG 360 GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC CTCCTCACCC ATCCTGACTC 420 AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA TTTGGGTGGG AAGGAGCTAT 480 CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC CTTACTGACC TGACCTTTAG 540 CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG TACACGCATG TGTGTGCACA 600 CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT GACCTGATGA AACAGTCTGG 660 GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA GCAAAAGCAG GATGTGTGTG 720 GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG GTACTGGAGG GCAAAGCGGC 780 CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC CAGAACAGGC ATTAATTCTG 840 GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC CCTTTCTTTC TCTCTCTCTC 900 TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT CAAAATTTCT CACCCACCCT 960 CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG GCCTCTCTCA ACACCTAGGA 1020 GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC CCCTACCAGG GTTGGCCCTC 1080 TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG GCGGCCACTC CGCAGTTTCA 1140 CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT GACTCTGCAC TGCTCCCAGC 1200 ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC GTTTTTCGCC TTCATGTCTG 1260 TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT CCTGCCCATA GCGTCAGTGG 1320 CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG TGTCCTATCC TCCTGACCAT 1380 GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC CGGGTGCGAT GGCTCTCACC 1440 TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGAAGGATCA CTTGAGCTCA GGAGTTCAAG 1500 ACCAGCCTGG GCAACATGGC AAGCCCCATC TCTACAAACA ATGCAAAAAT TAGCCGGGTG 1560 TGGTGGCGTG CACCTGTAGT CCCAGTCCCA GCTACTTGGG AGGCTGAGGT GGGAGGATCA 1620 CTGGAGCCCT GGAGGTGGAG GTTGCTGTGA GCTGAGATCA CGCCACTGCA CTCCAGCCTG 1680 GGCAACTGAG GGACCTTGTC TCAAAAAAAA AAAAAAAAAA AAGATACCAT TGTTCAGAGG 1740 AGGAAGCTGA GCTGACAGAG GTCAAGGAAG ATGCATTTCT ACCCAGCTTT CAAGATTCAC 1800 TTTGGACATC ACCTTCCTCA GACTCTGCCT TCTCCTCTTC ACCGCCCCAC TACGCCCCAG 1860 GCAGGAGAAA 1870
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