Variant report

Variant	rs10120857
Chromosome Location	chr9:13186775-13186776
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:13105793..13107889-chr9:13185268..13188197,2	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10116749	0.81[ASN][1000 genomes]
rs10125695	0.95[EUR][1000 genomes]
rs10511577	0.81[ASN][1000 genomes]
rs10756458	0.81[ASN][1000 genomes]
rs10756460	0.90[ASN][1000 genomes]
rs10809913	0.91[ASN][1000 genomes]
rs10960958	0.84[ASN][1000 genomes]
rs10960959	0.80[ASN][1000 genomes]
rs12351444	0.87[ASN][1000 genomes]
rs1331672	0.82[ASN][1000 genomes]
rs1331673	0.86[ASN][1000 genomes]
rs1331674	0.90[ASN][1000 genomes]
rs1331675	0.86[ASN][1000 genomes]
rs1556421	0.85[ASN][1000 genomes]
rs1929541	0.80[ASN][1000 genomes]
rs1999393	0.86[ASN][1000 genomes]
rs2225483	0.81[ASN][1000 genomes]
rs2274856	0.90[ASN][1000 genomes]
rs6474753	0.82[ASN][1000 genomes]
rs6474754	0.80[ASN][1000 genomes]
rs7037618	0.92[ASN][1000 genomes]
rs7040347	0.82[ASN][1000 genomes]
rs72706366	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892578	chr9:12942956-13485035	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv892583	chr9:13166139-13350478	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13121600-13225200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr9:13135400-13223600	Weak transcription	Lung	lung
3	chr9:13136000-13192400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr9:13138800-13191800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr9:13139000-13188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr9:13141000-13197800	Weak transcription	NHDF-Ad	bronchial
7	chr9:13141200-13188200	Weak transcription	NHLF	lung
8	chr9:13143600-13202200	Weak transcription	Pancreas	Pancrea
9	chr9:13145400-13203200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr9:13145400-13228600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr9:13146600-13202400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr9:13150000-13193200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr9:13153200-13194800	Weak transcription	Fetal Kidney	kidney
14	chr9:13156800-13201400	Weak transcription	Psoas Muscle	Psoas
15	chr9:13158800-13188800	Weak transcription	Fetal Heart	heart
16	chr9:13161600-13188200	Weak transcription	Fetal Stomach	stomach
17	chr9:13162200-13188200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr9:13163600-13202000	Weak transcription	Rectal Smooth Muscle	rectum
19	chr9:13164200-13188000	Weak transcription	Brain Hippocampus Middle	brain
20	chr9:13164200-13188800	Weak transcription	Brain Substantia Nigra	brain
21	chr9:13164200-13248600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr9:13164200-13258800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:13165800-13187400	Weak transcription	Brain Germinal Matrix	brain
24	chr9:13168000-13201800	Weak transcription	Colon Smooth Muscle	Colon
25	chr9:13168400-13188200	Weak transcription	Brain Cingulate Gyrus	brain
26	chr9:13168600-13188200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr9:13170000-13188200	Weak transcription	Left Ventricle	heart
28	chr9:13173000-13188800	Weak transcription	Spleen	Spleen
29	chr9:13175200-13188200	Weak transcription	Aorta	Aorta
30	chr9:13175800-13203000	Weak transcription	Fetal Intestine Small	intestine
31	chr9:13176200-13187800	Weak transcription	Placenta	Placenta
32	chr9:13176400-13186800	Weak transcription	Ovary	ovary
33	chr9:13176400-13187000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr9:13176400-13187600	Weak transcription	Stomach Smooth Muscle	stomach
35	chr9:13176400-13187800	Weak transcription	Osteobl	bone
36	chr9:13176400-13188200	Weak transcription	Fetal Muscle Leg	muscle
37	chr9:13176400-13188800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr9:13176400-13202600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr9:13176600-13191800	Weak transcription	Fetal Intestine Large	intestine
40	chr9:13177600-13197400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:13179800-13196600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr9:13180000-13188200	Weak transcription	Brain Angular Gyrus	brain
43	chr9:13180000-13193000	Weak transcription	HSMMtube	muscle
44	chr9:13180000-13202200	Weak transcription	Fetal Brain Female	brain
45	chr9:13180200-13188200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr9:13182000-13187800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr9:13182000-13188200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr9:13182000-13188400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr9:13182000-13188400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr9:13182000-13188600	Weak transcription	Brain Anterior Caudate	brain

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