Variant report

Variant	rs62533897
Chromosome Location	chr9:7079383-7079384
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	chr9:7074844..7076869-chr9:7078894..7081188,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1407856	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs16925220	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16925247	0.88[EUR][1000 genomes]
rs16925266	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16925288	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16925292	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4740869	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4742299	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55787411	0.82[AMR][1000 genomes]
rs56348300	0.87[EUR][1000 genomes]
rs61075062	0.85[EUR][1000 genomes]
rs62533860	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62533862	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62533899	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs62533900	0.82[AMR][1000 genomes]
rs62534433	0.84[EUR][1000 genomes]
rs62534436	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62536961	0.80[AMR][1000 genomes]
rs62536962	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7019027	0.87[EUR][1000 genomes]
rs73639964	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73639965	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[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	nsv466117	chr9:7030268-7084558	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv613258	chr9:7030268-7084558	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	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
6	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
7	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
8	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

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7012200-7111200	Weak transcription	Colonic Mucosa	Colon
2	chr9:7028800-7086400	Weak transcription	Right Ventricle	heart
3	chr9:7029000-7081200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:7034000-7103600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr9:7043400-7103600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr9:7050000-7082200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr9:7051600-7103200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr9:7052600-7086400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr9:7053000-7086600	Weak transcription	Fetal Intestine Large	intestine
10	chr9:7053200-7084400	Weak transcription	Brain Hippocampus Middle	brain
11	chr9:7053200-7099200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:7058400-7088600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr9:7058600-7085000	Weak transcription	Brain Anterior Caudate	brain
14	chr9:7059400-7082000	Weak transcription	Fetal Stomach	stomach
15	chr9:7061200-7104600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr9:7061600-7103600	Weak transcription	Spleen	Spleen
17	chr9:7062800-7096400	Weak transcription	Fetal Intestine Small	intestine
18	chr9:7066200-7096200	Weak transcription	Stomach Mucosa	stomach
19	chr9:7067000-7088000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr9:7067200-7082600	Strong transcription	Primary B cells from peripheral blood	blood
21	chr9:7067200-7103600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr9:7068400-7103600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:7071200-7087400	Strong transcription	Primary B cells from cord blood	blood
24	chr9:7072000-7082200	Weak transcription	Small Intestine	intestine
25	chr9:7072000-7088600	Strong transcription	Primary T cells from cord blood	blood
26	chr9:7072200-7080800	Weak transcription	Fetal Heart	heart
27	chr9:7073600-7099200	Weak transcription	NHEK	skin
28	chr9:7074600-7079400	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr9:7074600-7089800	Weak transcription	Fetal Muscle Trunk	muscle
30	chr9:7074800-7079400	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr9:7075000-7081800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr9:7075000-7097800	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr9:7075200-7082800	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr9:7075400-7080800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:7075400-7086400	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr9:7075400-7088400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:7075600-7082600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr9:7075600-7105800	Weak transcription	NHLF	lung
39	chr9:7076200-7079400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:7076200-7079400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr9:7076200-7080000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr9:7076200-7080000	Strong transcription	Fetal Thymus	thymus
43	chr9:7076400-7079400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr9:7076400-7080200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr9:7076400-7081000	Strong transcription	Liver	Liver
46	chr9:7076600-7103600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr9:7077000-7086400	Weak transcription	Hela-S3	cervix
48	chr9:7077000-7098000	Weak transcription	Colon Smooth Muscle	Colon
49	chr9:7077200-7085000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr9:7077400-7082200	Weak transcription	Ovary	ovary

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