Variant report

Variant	rs536465223
Chromosome Location	chr1:98188908-98188909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491816	chr1:97266403-98223619	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv533039	chr1:97665736-98343102	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv530049	chr1:97883261-98384614	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv830714	chr1:98025090-98229416	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv1012958	chr1:98081528-98864746	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv871740	chr1:98165091-98322379	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv871472	chr1:98165091-98342417	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
8	nsv870596	chr1:98165091-98365310	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
9	nsv871625	chr1:98165091-98564736	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv546868	chr1:98175878-98194845	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region miRNA target site	1 gene(s)	inside rSNPs	diseases
11	nsv871050	chr1:98187755-98365310	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98148000-98192800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr1:98177200-98254600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr1:98179000-98220800	Weak transcription	Psoas Muscle	Psoas
4	chr1:98181400-98204400	Weak transcription	Osteobl	bone
5	chr1:98183600-98189600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:98183600-98279600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:98183800-98189200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:98186200-98220200	Weak transcription	Primary T cells from cord blood	blood
9	chr1:98187000-98192800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:98187200-98189000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr1:98187200-98189800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr1:98187200-98189800	Weak transcription	Dnd41	blood
13	chr1:98187200-98190200	Weak transcription	HSMMtube	muscle
14	chr1:98187200-98203000	Weak transcription	Liver	Liver
15	chr1:98187200-98206000	Weak transcription	Primary hematopoietic stem cells	blood
16	chr1:98187200-98207000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:98187200-98208400	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr1:98187200-98217200	Weak transcription	Primary B cells from cord blood	blood
19	chr1:98187200-98243400	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:98187400-98193000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr1:98187400-98203800	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr1:98188800-98189200	Strong transcription	HSMM	muscle

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