Variant report

Variant	rs2989753
Chromosome Location	chr9:96375728-96375729
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:96353488..96355423-chr9:96374627..96377387,2	K562	blood:
2	chr9:96375382..96377064-chr9:96378905..96380672,2	MCF-7	breast:
3	chr9:96374097..96376355-chr9:96382214..96384351,2	K562	blood:
4	chr9:96336833..96339118-chr9:96375167..96379434,3	MCF-7	breast:
5	chr9:96338137..96340211-chr9:96373633..96375791,2	K562	blood:

Variant related genes	Relation type
ENSG00000197724	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10761237	0.81[CHB][hapmap]
rs10821170	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10821171	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10821172	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10821177	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10992795	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10992796	1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13290276	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13296529	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17533702	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2254712	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2265300	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2265574	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2265575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2265576	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2989752	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2989755	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2989756	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2994365	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs2994369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2994370	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4073155	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs4743929	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4744255	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs4744258	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4744259	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56351334	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61471428	0.87[ASN][1000 genomes]
rs62573991	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62574558	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7033146	0.82[CHB][hapmap]
rs928368	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9409477	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040891	chr9:96361529-96397338	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv1044461	chr9:96362048-96397338	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv893585	chr9:96363859-96403367	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv893586	chr9:96363859-96493773	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv1055035	chr9:96372269-96402747	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv3408240	chr9:96375131-96379629	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1036609	chr9:96375217-96477641	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2989753	FAM120AOS	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96352400-96384600	Weak transcription	NHLF	lung
2	chr9:96361400-96380400	Weak transcription	Fetal Brain Male	brain
3	chr9:96361600-96379400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr9:96363200-96392000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr9:96363600-96383600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr9:96364200-96380600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:96366400-96379400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:96366600-96386600	Weak transcription	Fetal Heart	heart
9	chr9:96372800-96376000	Weak transcription	Right Ventricle	heart
10	chr9:96372800-96392000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr9:96373000-96377200	Enhancers	Psoas Muscle	Psoas
12	chr9:96373000-96379400	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr9:96373200-96376000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr9:96373400-96377000	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr9:96373400-96379400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr9:96373400-96379400	Weak transcription	Brain Anterior Caudate	brain
17	chr9:96373400-96379400	Weak transcription	Fetal Intestine Large	intestine
18	chr9:96373400-96386200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr9:96373400-96387000	Weak transcription	Fetal Brain Female	brain
20	chr9:96373400-96390000	Weak transcription	Primary B cells from cord blood	blood
21	chr9:96373600-96379400	Weak transcription	Brain Germinal Matrix	brain
22	chr9:96373800-96379000	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr9:96374200-96376400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr9:96374200-96376600	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr9:96374400-96375800	Enhancers	HMEC	breast
26	chr9:96374400-96376000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr9:96374400-96376400	Enhancers	GM12878-XiMat	blood
28	chr9:96374400-96376600	Enhancers	Colon Smooth Muscle	Colon
29	chr9:96374400-96376800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr9:96374400-96377000	Enhancers	Primary B cells from peripheral blood	blood
31	chr9:96374600-96375800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr9:96374600-96375800	Enhancers	Ovary	ovary
33	chr9:96374600-96375800	Strong transcription	Dnd41	blood
34	chr9:96374600-96375800	Enhancers	NHEK	skin
35	chr9:96374600-96376000	Enhancers	Primary T cells fromperipheralblood	blood
36	chr9:96374600-96376600	Enhancers	Left Ventricle	heart
37	chr9:96374600-96377000	Weak transcription	Fetal Kidney	kidney
38	chr9:96374600-96378000	Enhancers	Spleen	Spleen
39	chr9:96374600-96378200	Enhancers	Gastric	stomach
40	chr9:96374600-96399800	Weak transcription	K562	blood
41	chr9:96374800-96376400	Weak transcription	Primary T cells from cord blood	blood
42	chr9:96374800-96376800	Enhancers	Stomach Smooth Muscle	stomach
43	chr9:96374800-96379400	Weak transcription	Small Intestine	intestine
44	chr9:96374800-96385400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr9:96375000-96375800	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr9:96375000-96375800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:96375000-96376200	Enhancers	Lung	lung
48	chr9:96375000-96376400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr9:96375000-96376600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr9:96375000-96381600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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