Tag | Content |
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EnhancerAtlas ID | HS146-08117 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr2:43384900-43386660 |
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: 40 | 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_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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I043156 | chr2 | 43383741 | 43393336 |
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Enhancer Sequence | AGACCAGAAA ACTTGGAGTG GCCCTGGGGG AGCAGTGCTG TTCCCATTCT CTGTGGCAGG 60 GGCCTTGGCA GGTGCAAGAC CCAGAGTGTC CCCCCACAAC CTGAGGGGGC TGCTTCTGGA 120 CACAGAGAGC TCAGGCCTCA AATGCATCTT TTCACTAGCC TTCCTGGGTC CTGCCCATTC 180 CTAGAGACGG AGTTCACTAT GCTCCTAGCC ATGTGCTGGG TGCGGGGCGA GCCCCAGATG 240 GCTCATCGCC ACGAGGTGCA GGCACAGCCT CTCCATGAGC CATCAGGAAC TCGGGGTTGC 300 ATCAAATCCC CAAAGACTTT ACTGGGCCCA CGCTAGGCAT CAGCCTGGGA TTCTCCTCCC 360 AGGTCTCCAC CAGCTGCTGA GCACAGCGGA GGTGGGGAGG CAAGAGCATG TCCTATCCTG 420 CCTCCTGGCC CCCAGCCCCA GTAACACAGA ACTAGGGTGC CTATTGTTTC AATGGCAGAA 480 ATCCCCCTCC CCTCCGACCC CTGCCCCCTG CAGCACTGCT CCCCATCACT GGGCTAAACG 540 AATGACCCGC CACTCAGCAG GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC 600 CTCCTCACCC ATCCTGACTC AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA 660 TTTGGGTGGG AAGGAGCTAT CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC 720 CTTACTGACC TGACCTTTAG CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG 780 TACACGCATG TGTGTGCACA CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT 840 GACCTGATGA AACAGTCTGG GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA 900 GCAAAAGCAG GATGTGTGTG GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG 960 GTACTGGAGG GCAAAGCGGC CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC 1020 CAGAACAGGC ATTAATTCTG GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC 1080 CCTTTCTTTC TCTCTCTCTC TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT 1140 CAAAATTTCT CACCCACCCT CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG 1200 GCCTCTCTCA ACACCTAGGA GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC 1260 CCCTACCAGG GTTGGCCCTC TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG 1320 GCGGCCACTC CGCAGTTTCA CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT 1380 GACTCTGCAC TGCTCCCAGC ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC 1440 GTTTTTCGCC TTCATGTCTG TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT 1500 CCTGCCCATA GCGTCAGTGG CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG 1560 TGTCCTATCC TCCTGACCAT GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC 1620 CGGGTGCGAT GGCTCTCACC TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGAAGGATCA 1680 CTTGAGCTCA GGAGTTCAAG ACCAGCCTGG GCAACATGGC AAGCCCCATC TCTACAAACA 1740 ATGCAAAAAT TAGCCGGGTG 1760
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