Variant report

Variant	rs11759243
Chromosome Location	chr6:117851676-117851677
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1123836	0.88[EUR][1000 genomes]
rs11755719	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11755781	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11756993	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664604	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12665822	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1321808	0.88[EUR][1000 genomes]
rs1321809	0.88[EUR][1000 genomes]
rs1321810	0.88[EUR][1000 genomes]
rs17165	0.89[AMR][1000 genomes]
rs17573446	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17574179	0.88[EUR][1000 genomes]
rs17574269	0.88[EUR][1000 genomes]
rs17575094	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17575449	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17635492	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17636431	0.88[EUR][1000 genomes]
rs7453460	0.88[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117819800-117868800	Weak transcription	Spleen	Spleen
2	chr6:117821600-117868800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr6:117823200-117868800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:117823200-117869600	Weak transcription	Small Intestine	intestine
5	chr6:117826400-117859800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr6:117828000-117866200	Weak transcription	Esophagus	oesophagus
7	chr6:117834400-117852800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:117834400-117861800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:117834400-117863600	Weak transcription	Gastric	stomach
10	chr6:117834800-117857400	Weak transcription	Aorta	Aorta
11	chr6:117834800-117860600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr6:117835200-117868800	Weak transcription	Colonic Mucosa	Colon
13	chr6:117835400-117868800	Weak transcription	Psoas Muscle	Psoas
14	chr6:117835600-117852600	Weak transcription	HSMMtube	muscle
15	chr6:117835800-117857600	Weak transcription	Placenta	Placenta
16	chr6:117836600-117861800	Weak transcription	Pancreas	Pancrea
17	chr6:117836600-117869600	Weak transcription	Stomach Mucosa	stomach
18	chr6:117837200-117860600	Weak transcription	Fetal Muscle Leg	muscle
19	chr6:117838600-117869000	Weak transcription	Ovary	ovary
20	chr6:117842000-117854200	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr6:117842000-117860600	Weak transcription	Fetal Stomach	stomach
22	chr6:117842200-117852600	Weak transcription	Left Ventricle	heart
23	chr6:117842400-117851800	Weak transcription	Adipose Nuclei	Adipose
24	chr6:117842800-117866200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:117843600-117853000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr6:117844000-117853000	Weak transcription	Fetal Intestine Large	intestine
27	chr6:117844000-117853200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr6:117845200-117866200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr6:117845800-117868800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr6:117846800-117869600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:117847200-117852400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr6:117847400-117857600	Weak transcription	NHEK	skin
33	chr6:117847600-117861800	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr6:117848600-117856800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr6:117849000-117852400	Weak transcription	HepG2	liver
36	chr6:117849600-117852400	Weak transcription	HMEC	breast
37	chr6:117849800-117852600	Weak transcription	HUVEC	blood vessel
38	chr6:117849800-117852800	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr6:117849800-117857400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr6:117850000-117851800	Weak transcription	NH-A	brain
41	chr6:117850000-117852600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:117850000-117852600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:117851000-117851800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:117851000-117851800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:117851000-117851800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:117851000-117851800	Enhancers	Right Atrium	heart
47	chr6:117851000-117853000	Enhancers	Fetal Lung	lung
48	chr6:117851200-117851800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr6:117851200-117851800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:117851200-117851800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links