Variant report

Variant	rs528267194
Chromosome Location	chr8:131851225-131851226
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv612294	chr8:131645079-131923377	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv891448	chr8:131668278-131968469	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS 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
3	nsv831462	chr8:131704119-131895793	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1034107	chr8:131740146-131985765	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv539747	chr8:131740146-131985765	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1030881	chr8:131801472-132654822	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	esv1011202	chr8:131844314-131853745	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3480049	chr8:131848970-131854668	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3511351	chr8:131849620-131853818	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3511349	chr8:131850020-131853768	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3480051	chr8:131850352-131853039	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	nsv512069	chr8:131850473-131852744	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv6594	chr8:131850522-131852969	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3480053	chr8:131850621-131852837	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3511348	chr8:131850644-131852848	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3511350	chr8:131850648-131852831	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	nsv824730	chr8:131850658-131852417	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	nsv821256	chr8:131850658-131852863	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	nsv824732	chr8:131850658-131852863	Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3511347	chr8:131850661-131852775	Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv3480050	chr8:131850671-131852809	Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv3480054	chr8:131850679-131852819	Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv3480048	chr8:131850683-131852762	Weak transcription	n/a	n/a	inside rSNPs	diseases
24	nsv819677	chr8:131850688-131852515	Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv3511353	chr8:131850689-131852787	Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv1793218	chr8:131850712-131852954	Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv1813923	chr8:131850712-131852954	Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv1822501	chr8:131850712-131852954	Weak transcription	n/a	n/a	inside rSNPs	diseases
29	esv1828542	chr8:131850712-131852954	Weak transcription	n/a	n/a	inside rSNPs	diseases
30	esv1000595	chr8:131850749-131852737	Weak transcription	n/a	n/a	inside rSNPs	diseases
31	esv3480055	chr8:131850750-131852739	Weak transcription	n/a	n/a	inside rSNPs	diseases
32	esv3511354	chr8:131850750-131852739	Weak transcription	n/a	n/a	inside rSNPs	diseases
33	nsv396197	chr8:131850751-131852738	Weak transcription	n/a	n/a	inside rSNPs	diseases
34	esv19407	chr8:131850764-131852855	Weak transcription	n/a	n/a	inside rSNPs	diseases
35	nsv824733	chr8:131850779-131852417	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131842600-131858400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr8:131843800-131858200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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