Variant report

Variant	rs699863
Chromosome Location	chrX:65452795-65452796
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1011526	0.86[CEU][hapmap];0.84[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs1028348	0.93[MEX][hapmap]
rs1068536	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1068537	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1068538	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs1090752	1.00[CEU][hapmap]
rs1090842	1.00[CEU][hapmap]
rs1091486	0.86[CEU][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs12395548	1.00[ASW][hapmap];0.85[CEU][hapmap];0.83[GIH][hapmap];0.89[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs1264212	0.86[CEU][hapmap];0.84[GIH][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap]
rs1264216	0.86[CEU][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs1264218	0.86[CEU][hapmap]
rs1325561	1.00[ASW][hapmap];0.86[MEX][hapmap]
rs1415297	0.85[CEU][hapmap];0.83[GIH][hapmap];0.86[TSI][hapmap]
rs1456803	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1456804	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1456806	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs17301659	0.85[CEU][hapmap]
rs1989028	0.86[CEU][hapmap];1.00[YRI][hapmap]
rs2054179	1.00[CEU][hapmap]
rs2198868	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs2198869	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs2206203	1.00[ASW][hapmap];0.86[CEU][hapmap];0.84[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs4827365	1.00[CEU][hapmap]
rs4827449	1.00[ASW][hapmap];0.86[MEX][hapmap];1.00[YRI][hapmap]
rs585069	0.86[MEX][hapmap]
rs586789	0.86[MEX][hapmap]
rs587657	0.86[MEX][hapmap]
rs5918587	0.86[MEX][hapmap]
rs5918594	0.83[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs5918974	0.86[MEX][hapmap]
rs5919024	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs5919069	1.00[ASW][hapmap];0.85[CEU][hapmap];0.83[GIH][hapmap];0.89[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs5964488	1.00[ASW][hapmap]
rs5964495	0.86[CEU][hapmap]
rs5964499	0.86[CEU][hapmap]
rs5964500	1.00[ASW][hapmap];0.86[CEU][hapmap];0.84[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs5965105	1.00[ASW][hapmap];0.86[CEU][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs5965106	0.85[CEU][hapmap];0.84[GIH][hapmap];1.00[MEX][hapmap]
rs5965110	0.86[CEU][hapmap];0.86[TSI][hapmap]
rs606886	0.86[MEX][hapmap]
rs651494	1.00[CEU][hapmap]
rs6624844	0.86[MEX][hapmap]
rs6624875	0.86[CEU][hapmap];0.84[GIH][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap]
rs6624876	0.84[CEU][hapmap]
rs670546	0.86[MEX][hapmap]
rs7054364	0.86[CEU][hapmap];0.84[GIH][hapmap];1.00[MEX][hapmap];0.86[TSI][hapmap]
rs7062799	0.85[CEU][hapmap];0.84[GIH][hapmap];1.00[MEX][hapmap]
rs707298	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs707302	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs708966	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs708968	1.00[CEU][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs708969	1.00[CEU][hapmap];0.83[GIH][hapmap];0.92[MEX][hapmap];0.95[TSI][hapmap]
rs760866	0.86[CEU][hapmap]
rs760867	0.91[ASW][hapmap];0.86[MEX][hapmap]
rs7891437	1.00[ASW][hapmap];0.86[CEU][hapmap];0.84[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap]
rs806537	0.91[CEU][hapmap]
rs806538	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs806607	1.00[ASW][hapmap];0.86[CEU][hapmap];0.92[GIH][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.95[TSI][hapmap]
rs806608	0.86[CEU][hapmap];0.92[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs806609	0.86[CEU][hapmap]
rs806610	0.86[CEU][hapmap];0.92[GIH][hapmap];0.91[TSI][hapmap]
rs809363	0.92[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3429625	chrX:64787230-65458721	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv995042	chrX:65121634-65953299	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Strong transcription Active 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	40 gene(s)	inside rSNPs	diseases
3	nsv916393	chrX:65269672-65521616	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv3350331	chrX:65287003-65495627	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:65436400-65453000	Weak transcription	K562	blood
2	chrX:65436400-65454200	Weak transcription	Duodenum Mucosa	Duodenum
3	chrX:65437600-65466400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chrX:65446800-65468800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chrX:65448200-65462200	Weak transcription	Fetal Intestine Large	intestine
6	chrX:65450200-65468000	Weak transcription	Rectal Mucosa Donor 31	rectum

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