Variant report

Variant	rs10815525
Chromosome Location	chr9:7130193-7130194
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:7128721..7131684-chr9:7133933..7136070,2	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10448243	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10758825	0.81[EUR][1000 genomes]
rs12341169	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12343146	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13289983	0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13292853	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1407863	0.81[EUR][1000 genomes]
rs1407865	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4740872	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7856110	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7858509	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7861396	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7871016	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892166	chr9:6602821-7222495	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1023906	chr9:6731786-7372132	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv613259	chr9:7032776-7541338	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1015874	chr9:7048807-7434890	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv539971	chr9:7048807-7434890	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv869932	chr9:7068359-7133384	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv892189	chr9:7091968-7150997	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv892190	chr9:7094860-7186074	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7103000-7148600	Strong transcription	Primary B cells from peripheral blood	blood
2	chr9:7104200-7148200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr9:7104400-7135400	Weak transcription	Fetal Muscle Leg	muscle
4	chr9:7104400-7137600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr9:7104400-7144600	Weak transcription	Brain Anterior Caudate	brain
6	chr9:7104600-7148000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr9:7104800-7138200	Weak transcription	HSMM	muscle
8	chr9:7104800-7142800	Weak transcription	Osteobl	bone
9	chr9:7104800-7153200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:7105000-7133600	Weak transcription	Fetal Stomach	stomach
11	chr9:7105000-7146600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr9:7105200-7130200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr9:7105600-7133200	Weak transcription	Ovary	ovary
14	chr9:7105600-7136800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr9:7106200-7147600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr9:7113400-7147800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:7116000-7134800	Weak transcription	Brain Substantia Nigra	brain
18	chr9:7116200-7145200	Weak transcription	Colon Smooth Muscle	Colon
19	chr9:7118200-7147800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr9:7118600-7136600	Weak transcription	NHDF-Ad	bronchial
21	chr9:7119000-7133600	Weak transcription	Placenta	Placenta
22	chr9:7119000-7144600	Weak transcription	Right Ventricle	heart
23	chr9:7119200-7136400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr9:7119200-7139800	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr9:7121600-7148000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr9:7121800-7148800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr9:7122000-7131800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr9:7122000-7137200	Weak transcription	K562	blood
29	chr9:7122000-7137800	Strong transcription	Primary T cells from cord blood	blood
30	chr9:7122000-7149000	Strong transcription	Primary B cells from cord blood	blood
31	chr9:7123000-7137400	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr9:7123400-7137600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr9:7123600-7131400	Strong transcription	Liver	Liver
34	chr9:7123800-7144600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr9:7124000-7147800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr9:7124400-7146600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr9:7124600-7137000	Weak transcription	Brain Angular Gyrus	brain
38	chr9:7125400-7144400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr9:7125400-7146400	Weak transcription	HMEC	breast
40	chr9:7125800-7146400	Weak transcription	NHEK	skin
41	chr9:7126000-7146400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr9:7126200-7139800	Weak transcription	Hela-S3	cervix
43	chr9:7126600-7137400	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr9:7126800-7136600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:7127200-7133800	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr9:7127400-7130200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr9:7127400-7136600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr9:7127600-7130400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:7127600-7130600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:7127600-7135000	Weak transcription	NH-A	brain

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