Variant report

Variant	rs7881798
Chromosome Location	chrX:110337384-110337385
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10521531	1.00[CEU][hapmap]
rs1159650	1.00[CEU][hapmap]
rs12116264	1.00[CEU][hapmap]
rs1339302	1.00[CEU][hapmap]
rs1339303	1.00[CEU][hapmap]
rs1339304	1.00[CEU][hapmap]
rs1361320	1.00[CEU][hapmap]
rs16986368	1.00[CEU][hapmap]
rs16986378	1.00[CEU][hapmap]
rs16986384	1.00[CEU][hapmap]
rs16986385	1.00[CEU][hapmap]
rs1884552	1.00[CEU][hapmap]
rs1884554	1.00[CEU][hapmap]
rs1884555	1.00[CEU][hapmap]
rs2050750	1.00[CEU][hapmap]
rs2050751	1.00[CEU][hapmap]
rs2066102	1.00[CEU][hapmap]
rs2208017	1.00[CEU][hapmap]
rs2208018	1.00[CEU][hapmap]
rs2208020	1.00[CEU][hapmap]
rs4341302	1.00[CEU][hapmap]
rs4384152	1.00[CEU][hapmap]
rs4514174	1.00[CEU][hapmap]
rs5942719	1.00[CEU][hapmap]
rs5942720	1.00[CEU][hapmap]
rs5942721	1.00[CEU][hapmap]
rs5943130	1.00[CEU][hapmap]
rs5943132	1.00[CEU][hapmap]
rs5943137	1.00[CEU][hapmap]
rs5985318	1.00[CEU][hapmap]
rs5985586	1.00[CEU][hapmap]
rs5985587	1.00[CEU][hapmap]
rs5985588	1.00[CEU][hapmap]
rs5985590	1.00[CEU][hapmap]
rs6642857	1.00[CEU][hapmap]
rs6642860	1.00[CEU][hapmap]
rs6642862	1.00[CEU][hapmap]
rs6642870	1.00[CEU][hapmap]
rs7879757	1.00[CEU][hapmap]
rs994591	1.00[CEU][hapmap]

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	nsv532899	chrX:110117241-110419226	Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv428712	chrX:110184832-110358638	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3337751	chrX:110217889-110429181	Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:110330400-110338800	Weak transcription	Brain Germinal Matrix	brain
2	chrX:110331200-110338800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chrX:110333600-110338800	Weak transcription	Pancreas	Pancrea
4	chrX:110334400-110338400	Weak transcription	Pancreatic Islets	Pancreatic Islet

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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