Variant report

Variant	rs4921640
Chromosome Location	chr8:19283397-19283398
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:19283299..19285964-chr8:19292652..19294945,2	MCF-7	breast:
2	chr8:19275354..19278233-chr8:19280534..19283813,3	MCF-7	breast:
3	chr8:19279205..19280725-chr8:19282957..19284991,2	MCF-7	breast:
4	chr8:19277716..19280530-chr8:19280967..19283858,2	MCF-7	breast:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17407449	0.89[ASN][1000 genomes]
rs4921639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4922024	0.89[ASN][1000 genomes]
rs5009989	0.96[CEU][hapmap];1.00[CHB][hapmap];0.81[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6586829	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6980861	0.96[CEU][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015395	chr8:18489538-19370258	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv429907	chr8:18578720-19398220	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv949745	chr8:18826830-19363963	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv1016482	chr8:18834807-19339487	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	nsv533109	chr8:18845845-19456780	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers 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	20 gene(s)	inside rSNPs	diseases
6	nsv1016993	chr8:18855623-19311731	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	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
8	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
9	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
10	nsv610751	chr8:19226335-19284889	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
11	esv3693374	chr8:19241970-19359184	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
12	esv34007	chr8:19252602-19482098	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
13	nsv610752	chr8:19254816-19311496	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
14	nsv1022344	chr8:19270143-19324083	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19266600-19283800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr8:19267200-19297000	Weak transcription	Brain Substantia Nigra	brain
3	chr8:19267400-19283600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr8:19267800-19295600	Weak transcription	Brain Hippocampus Middle	brain
5	chr8:19268000-19283800	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr8:19270200-19288800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr8:19271000-19284200	Weak transcription	Thymus	Thymus
8	chr8:19271800-19283400	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr8:19271800-19305200	Weak transcription	Pancreas	Pancrea
10	chr8:19275800-19287200	Weak transcription	Gastric	stomach
11	chr8:19275800-19288600	Weak transcription	Aorta	Aorta
12	chr8:19275800-19295600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr8:19276200-19283400	Weak transcription	Ovary	ovary
14	chr8:19277600-19295600	Weak transcription	Hela-S3	cervix
15	chr8:19277600-19307800	Weak transcription	Fetal Stomach	stomach
16	chr8:19277800-19283600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr8:19277800-19300200	Weak transcription	Primary B cells from peripheral blood	blood
18	chr8:19278000-19304800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr8:19278600-19283600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr8:19278600-19283800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr8:19279600-19290600	Weak transcription	Primary B cells from cord blood	blood
22	chr8:19280800-19284800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr8:19280800-19285000	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr8:19281000-19285000	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr8:19281000-19285000	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr8:19281400-19283800	Enhancers	Primary T cells fromperipheralblood	blood
27	chr8:19281800-19283400	Weak transcription	Spleen	Spleen
28	chr8:19281800-19283600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr8:19281800-19283800	Strong transcription	Placenta	Placenta
30	chr8:19281800-19296800	Weak transcription	Lung	lung
31	chr8:19282200-19283400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr8:19282200-19283400	Weak transcription	Left Ventricle	heart
33	chr8:19282400-19283400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr8:19282400-19283400	Weak transcription	Right Atrium	heart
35	chr8:19282400-19283600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr8:19282400-19283600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr8:19282400-19283600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr8:19282400-19284400	Enhancers	Primary T cells from cord blood	blood
39	chr8:19282400-19286400	Weak transcription	Esophagus	oesophagus
40	chr8:19282400-19292200	Weak transcription	Fetal Brain Male	brain
41	chr8:19282400-19294800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr8:19282800-19287200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:19283000-19283800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:19283200-19283600	Genic enhancers	A549	lung
45	chr8:19283200-19283600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr8:19283200-19283800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr8:19283200-19284800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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