Variant report

Variant	rs6721881
Chromosome Location	chr2:11509193-11509194
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:11483340..11487694-chr2:11505828..11510815,5	K562	blood:
2	chr2:11484922..11486828-chr2:11507256..11509884,2	K562	blood:
3	chr2:11483074..11486945-chr2:11508769..11511659,4	MCF-7	breast:
4	chr2:11508308..11513224-chr2:11514143..11518077,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000134318	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10170598	0.86[ASN][1000 genomes]
rs10170791	0.83[ASN][1000 genomes]
rs10195908	0.86[ASN][1000 genomes]
rs10202323	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs10929734	0.88[CEU][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12692438	1.00[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs12692439	0.87[ASN][1000 genomes]
rs12692440	1.00[CHB][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs12692441	1.00[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs12993210	1.00[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs13024110	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs35029584	0.87[ASN][1000 genomes]
rs35352177	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4280434	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4533449	0.87[ASN][1000 genomes]
rs4641909	0.86[ASN][1000 genomes]
rs4668722	1.00[CHB][hapmap];0.90[JPT][hapmap];0.90[ASN][1000 genomes]
rs4668723	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6432189	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6708718	0.87[ASN][1000 genomes]
rs6708945	0.86[ASN][1000 genomes]
rs6711409	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6711414	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6716724	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs6719739	0.86[ASN][1000 genomes]
rs6756145	0.85[ASN][1000 genomes]
rs7420679	0.86[ASN][1000 genomes]
rs7595700	1.00[CHB][hapmap];0.87[JPT][hapmap];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	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6721881	ROCK2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11505400-11514400	Enhancers	Fetal Intestine Large	intestine
2	chr2:11505600-11511600	Enhancers	Fetal Intestine Small	intestine
3	chr2:11505800-11511000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:11506000-11509400	Weak transcription	Spleen	Spleen
5	chr2:11506000-11511000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr2:11506000-11514600	Weak transcription	K562	blood
7	chr2:11506800-11511000	Enhancers	HepG2	liver
8	chr2:11507200-11511200	Enhancers	Duodenum Mucosa	Duodenum
9	chr2:11507400-11516200	Enhancers	Stomach Mucosa	stomach
10	chr2:11507800-11509600	Enhancers	Fetal Stomach	stomach
11	chr2:11508000-11509800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr2:11508200-11509200	Enhancers	Fetal Muscle Leg	muscle
13	chr2:11508200-11509600	Enhancers	Placenta	Placenta
14	chr2:11508200-11510600	Weak transcription	Pancreas	Pancrea
15	chr2:11508400-11509200	Enhancers	Left Ventricle	heart
16	chr2:11508400-11509600	Weak transcription	Colonic Mucosa	Colon
17	chr2:11508400-11509800	Enhancers	Fetal Brain Male	brain
18	chr2:11508400-11510600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr2:11508400-11510600	Weak transcription	Hela-S3	cervix
20	chr2:11508400-11513400	Weak transcription	HSMMtube	muscle
21	chr2:11508400-11514800	Weak transcription	Small Intestine	intestine
22	chr2:11508600-11509200	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr2:11508600-11509200	Enhancers	Liver	Liver
24	chr2:11508600-11509800	Weak transcription	A549	lung
25	chr2:11508600-11513200	Weak transcription	NH-A	brain
26	chr2:11508600-11513600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:11508600-11514000	Enhancers	Psoas Muscle	Psoas
28	chr2:11508800-11509200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr2:11508800-11509400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr2:11508800-11509400	Enhancers	Stomach Smooth Muscle	stomach
31	chr2:11508800-11509600	Enhancers	Adipose Nuclei	Adipose
32	chr2:11508800-11509600	Weak transcription	Brain Cingulate Gyrus	brain
33	chr2:11508800-11510600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:11508800-11510800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:11508800-11510800	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr2:11508800-11510800	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr2:11508800-11511000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:11508800-11511000	Weak transcription	Fetal Lung	lung
39	chr2:11508800-11511000	Weak transcription	NHLF	lung
40	chr2:11508800-11513200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:11508800-11513400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr2:11508800-11513600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr2:11508800-11513600	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr2:11508800-11513600	Weak transcription	Osteobl	bone
45	chr2:11508800-11514400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:11508800-11514600	Weak transcription	Brain Germinal Matrix	brain
47	chr2:11508800-11514600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:11508800-11514600	Weak transcription	Right Atrium	heart
49	chr2:11508800-11515000	Weak transcription	Aorta	Aorta
50	chr2:11509000-11509400	Weak transcription	Rectal Mucosa Donor 29	rectum

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