Variant report

Variant	rs73218623
Chromosome Location	chr8:19558186-19558187
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:19552184..19554316-chr8:19556580..19558198,2	MCF-7	breast:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10091557	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10109456	0.90[EUR][1000 genomes]
rs55763426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61196448	1.00[EUR][1000 genomes]
rs73202505	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73202509	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73202513	1.00[AMR][1000 genomes]
rs73216641	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73216645	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73216651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73216656	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73218618	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73218625	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73218626	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73218631	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs73218634	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73218635	1.00[AFR][1000 genomes]
rs73218638	0.90[EUR][1000 genomes]
rs7828018	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv890627	chr8:19389865-19561997	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1021575	chr8:19430653-19623452	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1025271	chr8:19435147-19574969	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1021731	chr8:19515149-19643313	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv1021225	chr8:19554860-19586580	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19541000-19567400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr8:19548200-19559200	Enhancers	Primary B cells from peripheral blood	blood
3	chr8:19550200-19558600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr8:19550200-19558600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr8:19550400-19558400	Enhancers	Primary hematopoietic stem cells	blood
6	chr8:19551800-19558200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr8:19552400-19558600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr8:19554600-19558600	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr8:19554800-19558600	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr8:19555000-19558600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr8:19555000-19558800	Enhancers	Primary T cells from cord blood	blood
12	chr8:19555000-19558800	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr8:19555000-19559200	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr8:19555000-19573200	Weak transcription	Pancreas	Pancrea
15	chr8:19555200-19563600	Weak transcription	Adipose Nuclei	Adipose
16	chr8:19555200-19566000	Weak transcription	Lung	lung
17	chr8:19555200-19567200	Weak transcription	Fetal Brain Male	brain
18	chr8:19555200-19573600	Weak transcription	Fetal Stomach	stomach
19	chr8:19555400-19559600	Weak transcription	Right Atrium	heart
20	chr8:19555400-19563000	Weak transcription	Left Ventricle	heart
21	chr8:19555400-19563800	Weak transcription	Placenta	Placenta
22	chr8:19555400-19566000	Weak transcription	Right Ventricle	heart
23	chr8:19555600-19558600	Enhancers	Primary B cells from cord blood	blood
24	chr8:19556000-19558600	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr8:19556600-19558600	Enhancers	Primary T cells fromperipheralblood	blood
26	chr8:19556800-19558400	Enhancers	Thymus	Thymus
27	chr8:19556800-19558600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr8:19556800-19560200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:19557000-19558400	Strong transcription	A549	lung
30	chr8:19557200-19558200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr8:19557200-19558200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr8:19557200-19558200	Enhancers	Fetal Thymus	thymus
33	chr8:19557200-19558200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr8:19557200-19566200	Weak transcription	Hela-S3	cervix
35	chr8:19557800-19558200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr8:19557800-19558200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr8:19557800-19558200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr8:19557800-19558400	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr8:19558000-19558200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr8:19558000-19558200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr8:19558000-19558200	Enhancers	Small Intestine	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links