Variant report

Variant	rs10815534
Chromosome Location	chr9:7173215-7173216
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	chr9:7166311..7168822-chr9:7171544..7173706,2	K562	blood:
2	chr9:7169706..7171250-chr9:7171522..7173272,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1041288	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10758842	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976118	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10976119	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1467700	0.97[ASN][1000 genomes]
rs1887870	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1887872	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1928211	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2011128	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2014332	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2104682	0.96[ASN][1000 genomes]
rs2248904	0.94[ASN][1000 genomes]
rs2381571	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2381572	0.96[ASN][1000 genomes]
rs2494241	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2494242	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2770728	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2770729	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2770730	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2770733	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2770735	0.96[ASN][1000 genomes]
rs2770737	0.96[ASN][1000 genomes]
rs2770742	0.84[AMR][1000 genomes]
rs2770745	0.84[AMR][1000 genomes]
rs2770756	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2770760	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2820910	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2820918	0.84[AMR][1000 genomes]
rs2820919	0.84[AMR][1000 genomes]
rs2820922	0.96[ASN][1000 genomes]
rs2820924	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2820925	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2820930	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2820934	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3753003	0.98[ASN][1000 genomes]
rs3829103	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7022345	1.00[ASN][1000 genomes]
rs7029684	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7036627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs913591	0.94[ASN][1000 genomes]
rs943925	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
7	nsv892191	chr9:7150997-7173752	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv892192	chr9:7153009-7257340	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
9	nsv528873	chr9:7163530-7177936	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7147400-7174600	Weak transcription	NHEK	skin
2	chr9:7148600-7185400	Weak transcription	HMEC	breast
3	chr9:7149600-7185400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr9:7149600-7186200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr9:7150400-7175800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr9:7151800-7188600	Weak transcription	Colonic Mucosa	Colon
7	chr9:7154400-7174400	Weak transcription	Aorta	Aorta
8	chr9:7160800-7174400	Weak transcription	Fetal Stomach	stomach
9	chr9:7160800-7175200	Strong transcription	Primary B cells from cord blood	blood
10	chr9:7160800-7182000	Weak transcription	Dnd41	blood
11	chr9:7162600-7181600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr9:7162600-7182200	Weak transcription	Small Intestine	intestine
13	chr9:7163200-7177800	Strong transcription	Primary B cells from peripheral blood	blood
14	chr9:7163400-7180600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr9:7163800-7179000	Strong transcription	Primary T helper cells fromperipheralblood	blood
16	chr9:7164000-7174600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr9:7164000-7176200	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr9:7164600-7178000	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr9:7165800-7174600	Weak transcription	Ovary	ovary
20	chr9:7165800-7176200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr9:7165800-7179400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr9:7165800-7183800	Weak transcription	Esophagus	oesophagus
23	chr9:7165800-7185400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr9:7166000-7175600	Weak transcription	Colon Smooth Muscle	Colon
25	chr9:7166200-7181000	Weak transcription	Hela-S3	cervix
26	chr9:7166400-7173600	Weak transcription	Spleen	Spleen
27	chr9:7166400-7174600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr9:7166400-7176800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr9:7167200-7185600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr9:7167600-7174400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:7168000-7174600	Weak transcription	Pancreas	Pancrea
32	chr9:7168200-7176400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr9:7169200-7173400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr9:7169200-7183000	Strong transcription	Primary T cells from cord blood	blood
35	chr9:7169400-7173800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr9:7169400-7176600	Strong transcription	Fetal Intestine Large	intestine
37	chr9:7169600-7175000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr9:7169600-7176400	Strong transcription	Duodenum Mucosa	Duodenum
39	chr9:7169600-7176600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr9:7169600-7176800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr9:7169800-7173400	Strong transcription	Fetal Thymus	thymus
42	chr9:7169800-7173600	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr9:7169800-7176600	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr9:7169800-7176600	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr9:7169800-7176800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr9:7169800-7177600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr9:7170000-7176400	Strong transcription	Adipose Nuclei	Adipose
48	chr9:7170000-7176400	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr9:7170200-7174400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr9:7170800-7176600	Enhancers	Placenta	Placenta

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