Tag | Content |
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EnhancerAtlas ID | HS073-08179 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr2:43385400-43386570 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I043156 | chr2 | 43383741 | 43393336 |
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Enhancer Sequence | CTGCCCCCTG CAGCACTGCT CCCCATCACT GGGCTAAACG AATGACCCGC CACTCAGCAG 60 GTGACGACTT ACTCCTCCTT GGCCGGCCCT TCAGCTCCTC CTCCTCACCC ATCCTGACTC 120 AGAGGCCTGT CAGCTGCCAC TGCCCCCGAG GCCTGGCAGA TTTGGGTGGG AAGGAGCTAT 180 CTGGGTGCCA GGACCTGAGG GGCTGGCCAT GCCCTCACTC CTTACTGACC TGACCTTTAG 240 CAGGGCCTCT GAGCATTCTC TGATCTAGAA ATGCCACATG TACACGCATG TGTGTGCACA 300 CACACACAAA CACCCACACA CTCACACCCA GCCGCTCTAT GACCTGATGA AACAGTCTGG 360 GTGCAGGGCT GAGGCAGGCC AGGGAGGAGA GTTAGACTGA GCAAAAGCAG GATGTGTGTG 420 GAGCAGCCTC CTGGCCTCTC TCCCGCAGAG GCACTTCCTG GTACTGGAGG GCAAAGCGGC 480 CCGGGGTTGG GAAAGAGACC GGTGCTGCTT GCTCCCTCTC CAGAACAGGC ATTAATTCTG 540 GCTGCCCCTT GGTATTGGCC TCCAACTTTA TAGTTCTCTC CCTTTCTTTC TCTCTCTCTC 600 TCCTACACAC ACCCCTCTAG ACTCCTCCCC TGCACCTCCT CAAAATTTCT CACCCACCCT 660 CACCCCACAG AAGGAGCATC AAAGCCCCAC ATAGCCTCTG GCCTCTCTCA ACACCTAGGA 720 GTTGAGATCA GGCCCTTGTG GCCCAGTCTT GGGGACTTCC CCCTACCAGG GTTGGCCCTC 780 TTGGGTCCAC GCCTCTTTGG CTAGACTTCT GATCGCTCTG GCGGCCACTC CGCAGTTTCA 840 CCACGCCTGC TCCTGCCTGC AACACACAGA AGTTGGCAGT GACTCTGCAC TGCTCCCAGC 900 ACCCCGGATG GCTCAGGGCT GTGGCATTTT GTTTTCTTTC GTTTTTCGCC TTCATGTCTG 960 TGCTGTTCAC TGTGCCTGAA ATCCCCTCCC CGCTAACCCT CCTGCCCATA GCGTCAGTGG 1020 CCCACATGTC AGCACCCAGC ACTTACCACT AGCGAGGCTG TGTCCTATCC TCCTGACCAT 1080 GCCAATGAAA AAAGTCCCAT TAATTATACC CACTGTTGGC CGGGTGCGAT GGCTCTCACC 1140 TGTAATCCCA GCACTTTGGG AGGCCGAGGC 1170
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