Variant report

Variant	rs62148090
Chromosome Location	chr2:100852462-100852463
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs17023659	1.00[ASN][1000 genomes]
rs17023710	1.00[ASN][1000 genomes]
rs17023791	0.87[ASN][1000 genomes]
rs17023801	1.00[ASN][1000 genomes]
rs17023820	0.87[ASN][1000 genomes]
rs17023833	0.87[ASN][1000 genomes]
rs62148077	1.00[ASN][1000 genomes]
rs62148078	1.00[ASN][1000 genomes]
rs62148079	1.00[ASN][1000 genomes]
rs62148080	1.00[ASN][1000 genomes]
rs62148082	1.00[ASN][1000 genomes]
rs62148083	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62148084	1.00[ASN][1000 genomes]
rs62148085	1.00[ASN][1000 genomes]
rs62148086	1.00[ASN][1000 genomes]
rs62148087	1.00[ASN][1000 genomes]
rs62148088	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62148089	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62148092	1.00[ASN][1000 genomes]
rs62148093	1.00[ASN][1000 genomes]
rs62148094	1.00[ASN][1000 genomes]
rs62148095	1.00[ASN][1000 genomes]
rs62150291	1.00[ASN][1000 genomes]
rs6735369	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007777	chr2:100816913-101308914	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv535844	chr2:100816913-101308914	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv834311	chr2:100816917-100990036	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100849400-100856000	Enhancers	Primary B cells from peripheral blood	blood
2	chr2:100850000-100853400	Weak transcription	Fetal Heart	heart
3	chr2:100850800-100853800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr2:100851000-100852600	Enhancers	GM12878-XiMat	blood
5	chr2:100851000-100853200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr2:100851000-100853200	Weak transcription	Fetal Lung	lung
7	chr2:100851000-100854600	Enhancers	Fetal Thymus	thymus
8	chr2:100851000-100855400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr2:100851200-100852600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:100851200-100852600	Enhancers	Dnd41	blood
11	chr2:100851200-100852800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr2:100851200-100853000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr2:100851200-100853400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr2:100851200-100853800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr2:100851200-100854800	Enhancers	Primary T cells fromperipheralblood	blood
16	chr2:100851200-100855200	Enhancers	Thymus	Thymus
17	chr2:100851400-100852600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr2:100851400-100853000	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr2:100851400-100853000	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr2:100851400-100853200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr2:100851400-100854000	Enhancers	Primary hematopoietic stem cells	blood
22	chr2:100851600-100853000	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr2:100851600-100854600	Enhancers	Primary T cells from cord blood	blood
24	chr2:100851600-100855200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr2:100851800-100852600	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr2:100851800-100853600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr2:100851800-100854000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr2:100851800-100854800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr2:100851800-100855800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:100851800-100859200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr2:100852000-100853600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:100852000-100853800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:100852000-100857000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:100852000-100859000	Weak transcription	Lung	lung
35	chr2:100852200-100854000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr2:100852200-100855800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr2:100852400-100853800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr2:100852400-100859000	Weak transcription	Spleen	Spleen

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