Variant report

Variant	rs7725717
Chromosome Location	chr5:75983462-75983463
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10514071	1.00[CHB][hapmap]
rs11951337	0.82[YRI][hapmap]
rs2303162	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs34653273	0.81[ASN][1000 genomes]
rs35787934	0.81[ASN][1000 genomes]
rs3764935	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs3776771	0.86[ASN][1000 genomes]
rs3776773	0.81[ASN][1000 genomes]
rs3815778	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs56215827	0.91[AFR][1000 genomes]
rs7708326	1.00[YRI][hapmap];0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019669	chr5:75836365-76477788	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1035135	chr5:75927027-76092058	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75943800-75986600	Weak transcription	Gastric	stomach
2	chr5:75945200-76001000	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr5:75946400-76001000	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr5:75947800-75992000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr5:75948000-76004600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr5:75949200-75986600	Weak transcription	GM12878-XiMat	blood
7	chr5:75950800-75999400	Weak transcription	Ovary	ovary
8	chr5:75951800-76001400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:75953400-75986000	Weak transcription	Spleen	Spleen
10	chr5:75955000-75996600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr5:75956800-75984200	Weak transcription	Fetal Kidney	kidney
12	chr5:75963400-75987400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr5:75965800-75986600	Weak transcription	Colonic Mucosa	Colon
14	chr5:75967000-75991200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr5:75969800-75986600	Weak transcription	Stomach Mucosa	stomach
16	chr5:75969800-75999600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr5:75971200-75991000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr5:75971400-75986600	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr5:75971400-75991200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:75973200-75989600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr5:75973800-75991400	Weak transcription	Fetal Thymus	thymus
22	chr5:75974200-75984800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr5:75975000-75989000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr5:75975400-75986200	Weak transcription	Fetal Stomach	stomach
25	chr5:75975600-75999600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr5:75977600-75987000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr5:75977600-75991000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr5:75977600-76003400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr5:75978000-75985600	Weak transcription	Aorta	Aorta
30	chr5:75978400-75984400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr5:75978400-75989600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr5:75978400-76001600	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr5:75978400-76004400	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr5:75978600-76003400	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr5:75979000-75985600	Strong transcription	Placenta	Placenta
36	chr5:75979600-75983600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
37	chr5:75979600-75986200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr5:75979800-75996200	Strong transcription	Liver	Liver
39	chr5:75980600-76002600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr5:75980800-75987000	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr5:75980800-75989600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr5:75980800-76000200	Strong transcription	Primary hematopoietic stem cells	blood
43	chr5:75981000-75986000	Strong transcription	Primary B cells from cord blood	blood
44	chr5:75981000-75986600	Weak transcription	Lung	lung
45	chr5:75981000-75986600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr5:75981000-75988600	Weak transcription	Pancreas	Pancrea
47	chr5:75981200-75984000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:75981200-75985600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr5:75981200-76001600	Weak transcription	Primary B cells from peripheral blood	blood
50	chr5:75981600-75984000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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