Variant report

Variant	rs61150868
Chromosome Location	chr9:110516490-110516491
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:110300257..110302612-chr9:110514562..110517473,2	MCF-7	breast:
2	chr9:110515788..110518055-chr9:110572897..110574723,2	MCF-7	breast:
3	chr9:110514515..110516747-chr9:111303982..111305554,2	MCF-7	breast:
4	chr9:110246450..110254025-chr9:110510483..110522079,28	MCF-7	breast:
5	chr9:110246498..110248989-chr9:110515168..110518438,3	MCF-7	breast:
6	chr9:110241813..110245896-chr9:110516233..110519941,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136826	Chromatin interaction
ENSG00000244104	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10979099	1.00[AMR][1000 genomes]
rs56357265	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56871349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57325103	0.80[AFR][1000 genomes]
rs58669480	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58689856	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61096248	0.82[AFR][1000 genomes]
rs7035702	1.00[AMR][1000 genomes]
rs73518928	0.80[AFR][1000 genomes]
rs73518936	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73518952	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73518964	1.00[ASN][1000 genomes]
rs73653675	1.00[AMR][1000 genomes]
rs73653676	1.00[AMR][1000 genomes]
rs7849860	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427850	chr9:110456613-110632324	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv428221	chr9:110456613-110632324	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv520911	chr9:110504358-110517794	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv508561	chr9:110506336-110545367	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110512400-110517200	Weak transcription	Lung	lung
2	chr9:110512400-110518000	Weak transcription	Spleen	Spleen
3	chr9:110512400-110520000	Weak transcription	Psoas Muscle	Psoas
4	chr9:110514400-110516800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr9:110514400-110517400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr9:110514600-110516800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:110514600-110517000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr9:110514600-110517000	Weak transcription	Placenta	Placenta
9	chr9:110514600-110517200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr9:110514600-110517200	Weak transcription	Fetal Muscle Trunk	muscle
11	chr9:110514600-110517200	Weak transcription	NHDF-Ad	bronchial
12	chr9:110514600-110517400	Weak transcription	Adipose Nuclei	Adipose
13	chr9:110514600-110517400	Weak transcription	Fetal Brain Male	brain
14	chr9:110514600-110517400	Weak transcription	NH-A	brain
15	chr9:110514600-110517600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:110514600-110523200	Weak transcription	K562	blood
17	chr9:110514800-110516800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr9:110514800-110516800	Weak transcription	NHEK	skin
19	chr9:110514800-110517000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr9:110514800-110517200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:110514800-110517200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:110514800-110517200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr9:110514800-110517200	Weak transcription	HSMM	muscle
24	chr9:110514800-110517200	Weak transcription	HSMMtube	muscle
25	chr9:110514800-110517200	Weak transcription	NHLF	lung
26	chr9:110514800-110517200	Weak transcription	Osteobl	bone
27	chr9:110514800-110517400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr9:110514800-110517400	Weak transcription	Fetal Muscle Leg	muscle
29	chr9:110514800-110517400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr9:110514800-110522600	Weak transcription	Stomach Smooth Muscle	stomach
31	chr9:110515000-110517200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:110515200-110516800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr9:110515200-110516800	Weak transcription	HMEC	breast
34	chr9:110515200-110517000	Weak transcription	Small Intestine	intestine
35	chr9:110515200-110517200	Weak transcription	Fetal Intestine Large	intestine
36	chr9:110515200-110517200	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr9:110515400-110516600	Weak transcription	Hela-S3	cervix
38	chr9:110515400-110517200	Weak transcription	Fetal Intestine Small	intestine
39	chr9:110515400-110517200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr9:110515400-110517400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr9:110515400-110517800	Weak transcription	Stomach Mucosa	stomach
42	chr9:110515400-110523000	Weak transcription	Left Ventricle	heart
43	chr9:110515600-110516800	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr9:110515600-110516800	Weak transcription	A549	lung
45	chr9:110515600-110516800	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr9:110515800-110517200	Weak transcription	HUVEC	blood vessel
47	chr9:110516200-110518600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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