Variant report

Variant	rs78984713
Chromosome Location	chr8:19513092-19513093
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:12 , 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	nsv610754	chr8:19419494-19525294	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS 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	2 gene(s)	inside rSNPs	diseases
7	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
8	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
9	nsv1015448	chr8:19474715-19520367	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv6106	chr8:19499554-19544249	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv527615	chr8:19512537-19514934	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	nsv383394	chr8:19513090-19513095	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19482000-19520000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr8:19500400-19519600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:19503000-19513600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr8:19503400-19518200	Weak transcription	Primary B cells from cord blood	blood
5	chr8:19503400-19521000	Weak transcription	Pancreas	Pancrea
6	chr8:19508400-19519800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr8:19508600-19513400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr8:19509200-19519800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr8:19510000-19513400	Weak transcription	Primary T cells from cord blood	blood
10	chr8:19510600-19520600	Weak transcription	Fetal Brain Male	brain
11	chr8:19510800-19514400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:19511200-19518600	Weak transcription	Right Atrium	heart
13	chr8:19511200-19521200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:19511600-19514000	Weak transcription	Lung	lung
15	chr8:19511600-19517200	Weak transcription	Left Ventricle	heart
16	chr8:19511600-19519800	Weak transcription	Fetal Stomach	stomach
17	chr8:19512000-19514200	Enhancers	A549	lung
18	chr8:19512000-19520400	Weak transcription	NH-A	brain
19	chr8:19512200-19517200	Weak transcription	Osteobl	bone
20	chr8:19512200-19520600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:19512200-19522400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr8:19512400-19516800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:19512400-19518200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:19512400-19518800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr8:19512400-19521000	Weak transcription	Aorta	Aorta
26	chr8:19512800-19513200	Weak transcription	Placenta	Placenta
27	chr8:19512800-19513800	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr8:19512800-19514800	Weak transcription	Hela-S3	cervix
29	chr8:19512800-19517200	Weak transcription	NHDF-Ad	bronchial
30	chr8:19513000-19517200	Weak transcription	Right Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links