Tag | Content |
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EnhancerAtlas ID | HS148-09369 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr2:43385440-43387230 |
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 | 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 | AATGACCCGC CACTCAGCAG GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC 60 CTCCTCACCC ATCCTGACTC AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA 120 TTTGGGTGGG AAGGAGCTAT CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC 180 CTTACTGACC TGACCTTTAG CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG 240 TACACGCATG TGTGTGCACA CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT 300 GACCTGATGA AACAGTCTGG GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA 360 GCAAAAGCAG GATGTGTGTG GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG 420 GTACTGGAGG GCAAAGCGGC CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC 480 CAGAACAGGC ATTAATTCTG GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC 540 CCTTTCTTTC TCTCTCTCTC TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT 600 CAAAATTTCT CACCCACCCT CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG 660 GCCTCTCTCA ACACCTAGGA GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC 720 CCCTACCAGG GTTGGCCCTC TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG 780 GCGGCCACTC CGCAGTTTCA CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT 840 GACTCTGCAC TGCTCCCAGC ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC 900 GTTTTTCGCC TTCATGTCTG TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT 960 CCTGCCCATA GCGTCAGTGG CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG 1020 TGTCCTATCC TCCTGACCAT GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC 1080 CGGGTGCGAT GGCTCTCACC TGTAATCCCA GCACTTTGGG AGGCCGAGGC AGAAGGATCA 1140 CTTGAGCTCA GGAGTTCAAG ACCAGCCTGG GCAACATGGC AAGCCCCATC TCTACAAACA 1200 ATGCAAAAAT TAGCCGGGTG TGGTGGCGTG CACCTGTAGT CCCAGTCCCA GCTACTTGGG 1260 AGGCTGAGGT GGGAGGATCA CTGGAGCCCT GGAGGTGGAG GTTGCTGTGA GCTGAGATCA 1320 CGCCACTGCA CTCCAGCCTG GGCAACTGAG GGACCTTGTC TCAAAAAAAA AAAAAAAAAA 1380 AAGATACCAT TGTTCAGAGG AGGAAGCTGA GCTGACAGAG GTCAAGGAAG ATGCATTTCT 1440 ACCCAGCTTT CAAGATTCAC TTTGGACATC ACCTTCCTCA GACTCTGCCT TCTCCTCTTC 1500 ACCGCCCCAC TACGCCCCAG GCAGGAGAAA CTGCTCCCAG CCTAGAGCCA CTGCCCGTTG 1560 TAGTGACTTC TGTTTGAGGC TGAGACCTCA GCCCCCAGGT CCTGATTTGT GCCCTCCTCC 1620 CTCAGTTTTG GGGCCTGTGA GAGTGGGTGG CTGGGCCTGG GGCTGAGTCA CTGCCTAGCC 1680 TTGCCTGCCC AGCCCCGAAC CAGGCAAGCC TCGGTGCAGG TGACCCTGCT GCCCAGAGAA 1740 GTGGGCGGCA GGAAGAATGG TCAGGCCCTC CTCCTTTTTC TCCTCCCTCC 1790
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