Variant report

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11742341	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs11742370	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs16875128	0.83[CEU][hapmap]
rs17713759	0.86[CEU][hapmap];1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs17713940	0.86[CEU][hapmap];1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs2059798	0.86[CEU][hapmap];1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs2081850	0.86[CEU][hapmap];1.00[CHB][hapmap]
rs2913627	0.83[EUR][1000 genomes]
rs2913628	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs2913629	0.83[EUR][1000 genomes]
rs2913630	0.87[CEU][hapmap];0.84[EUR][1000 genomes]
rs2913631	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs2913632	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs2964429	0.86[CEU][hapmap];1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs35061588	0.80[ASN][1000 genomes]
rs55819445	0.80[ASN][1000 genomes]
rs72724162	0.80[ASN][1000 genomes]
rs72724173	0.82[ASN][1000 genomes]
rs919245	0.80[ASN][1000 genomes]

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	nsv1024784	chr5:4980979-5391231	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1032719	chr5:5102763-5387406	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv537621	chr5:5102763-5387406	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:5185200-5262800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:5200200-5252800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr5:5224400-5253800	Weak transcription	Fetal Kidney	kidney
4	chr5:5230200-5255400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:5234600-5252600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr5:5236800-5255400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:5238000-5250200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr5:5238400-5246000	Weak transcription	Fetal Muscle Leg	muscle
9	chr5:5239000-5246600	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr5:5239400-5263000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:5240800-5247400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr5:5240800-5263000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr5:5241400-5248600	Strong transcription	NH-A	brain
14	chr5:5242400-5253800	Weak transcription	Pancreas	Pancrea
15	chr5:5242600-5250000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:5244600-5248200	Strong transcription	Ovary	ovary
17	chr5:5244600-5252800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr5:5244600-5266400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr5:5245400-5252600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:5245600-5248400	Enhancers	Fetal Brain Male	brain

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