Variant report

Variant	rs11588242
Chromosome Location	chr1:98176656-98176657
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs17377638	1.00[LWK][hapmap]

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	esv3410855	chr1:98172764-98178562	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	inside rSNPs	diseases
11	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

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:98136200-98188800	Weak transcription	Left Ventricle	heart
2	chr1:98141800-98185400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr1:98148000-98192800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr1:98153400-98187800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:98160200-98183200	Weak transcription	Primary T cells from cord blood	blood
6	chr1:98160400-98182800	Weak transcription	Primary B cells from cord blood	blood
7	chr1:98163200-98185400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:98165800-98180200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:98166000-98183200	Weak transcription	Liver	Liver
10	chr1:98166200-98186800	Weak transcription	HSMM	muscle
11	chr1:98167400-98183000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:98167400-98185000	Weak transcription	NHDF-Ad	bronchial
13	chr1:98171600-98185400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr1:98172200-98182600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:98172600-98185400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr1:98173400-98182600	Weak transcription	Dnd41	blood
17	chr1:98173400-98185200	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr1:98175400-98176800	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr1:98175400-98185200	Weak transcription	Duodenum Mucosa	Duodenum
20	chr1:98176400-98188200	Weak transcription	Right Ventricle	heart
21	chr1:98176600-98177200	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr1:98176600-98177200	Enhancers	HUVEC	blood vessel
23	chr1:98176600-98179800	Weak transcription	Primary monocytes fromperipheralblood	blood

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