Variant report

Variant	rs6913595
Chromosome Location	chr6:128373007-128373008
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10046119	0.80[EUR][1000 genomes]
rs11962156	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17055223	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17055231	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1883810	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35335036	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4265047	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4339480	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4345415	0.91[EUR][1000 genomes]
rs4421216	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4498384	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4598101	0.92[EUR][1000 genomes]
rs4895829	0.95[EUR][1000 genomes]
rs4897239	0.95[EUR][1000 genomes]
rs4897240	0.95[EUR][1000 genomes]
rs4897241	0.83[EUR][1000 genomes]
rs4897242	0.85[EUR][1000 genomes]
rs4897243	0.95[EUR][1000 genomes]
rs6569520	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6569521	0.93[EUR][1000 genomes]
rs6569522	0.93[EUR][1000 genomes]
rs6569523	0.92[EUR][1000 genomes]
rs6913095	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6928445	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6928496	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6928512	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6938574	0.92[EUR][1000 genomes]
rs7756639	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7757761	0.82[EUR][1000 genomes]
rs7758689	0.82[EUR][1000 genomes]
rs7769691	0.93[EUR][1000 genomes]
rs7774703	0.92[EUR][1000 genomes]
rs9321106	0.80[EUR][1000 genomes]
rs9321107	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9321108	0.99[EUR][1000 genomes]
rs9321109	0.97[EUR][1000 genomes]
rs9375546	0.86[EUR][1000 genomes]
rs9388616	0.81[EUR][1000 genomes]
rs9402016	0.84[EUR][1000 genomes]
rs9482857	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9482858	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9482859	0.80[EUR][1000 genomes]
rs9482860	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9482861	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9482862	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9482863	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9482864	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9482865	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9482866	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9482867	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9482868	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9482869	0.81[EUR][1000 genomes]
rs9482871	0.95[EUR][1000 genomes]
rs9482872	0.84[EUR][1000 genomes]
rs9491904	0.80[EUR][1000 genomes]
rs9491905	0.80[EUR][1000 genomes]
rs970363	0.80[EUR][1000 genomes]
rs970364	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033443	chr6:128306654-128899203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv538440	chr6:128306654-128899203	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv604643	chr6:128359362-128493991	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128289000-128431000	Weak transcription	Psoas Muscle	Psoas
2	chr6:128293600-128374400	Weak transcription	Pancreas	Pancrea
3	chr6:128311600-128387200	Weak transcription	NH-A	brain
4	chr6:128311800-128378400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:128320800-128388200	Weak transcription	NHEK	skin
6	chr6:128326600-128388200	Weak transcription	HMEC	breast
7	chr6:128337400-128378400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr6:128341200-128374400	Weak transcription	HSMMtube	muscle
9	chr6:128342600-128388600	Weak transcription	Fetal Brain Female	brain
10	chr6:128347000-128374400	Weak transcription	Esophagus	oesophagus
11	chr6:128347000-128405200	Weak transcription	Lung	lung
12	chr6:128350000-128401000	Weak transcription	Small Intestine	intestine
13	chr6:128350400-128374200	Weak transcription	Gastric	stomach
14	chr6:128350600-128374200	Weak transcription	Fetal Stomach	stomach
15	chr6:128351400-128378600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:128351400-128385000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr6:128351600-128375000	Weak transcription	Brain Anterior Caudate	brain
18	chr6:128352400-128378400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:128353200-128388400	Weak transcription	NHLF	lung
20	chr6:128353400-128374400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:128353400-128378600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr6:128353400-128378600	Weak transcription	Osteobl	bone
23	chr6:128353600-128374400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:128353600-128374400	Weak transcription	Aorta	Aorta
25	chr6:128353600-128378400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr6:128353600-128378600	Weak transcription	Left Ventricle	heart
27	chr6:128354000-128378400	Weak transcription	Primary B cells from cord blood	blood
28	chr6:128354200-128384800	Weak transcription	Fetal Lung	lung
29	chr6:128355600-128385400	Weak transcription	Primary T cells from cord blood	blood
30	chr6:128359600-128378600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr6:128361200-128388000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr6:128361800-128378400	Weak transcription	Fetal Thymus	thymus
33	chr6:128362000-128385200	Weak transcription	Brain Angular Gyrus	brain
34	chr6:128362000-128385200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr6:128363200-128378000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:128363800-128378400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:128367600-128384400	Weak transcription	Brain Cingulate Gyrus	brain
38	chr6:128367600-128398000	Weak transcription	HUVEC	blood vessel
39	chr6:128368200-128385000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:128368400-128388000	Weak transcription	Fetal Muscle Leg	muscle
41	chr6:128369400-128378600	Weak transcription	Stomach Smooth Muscle	stomach
42	chr6:128369800-128388000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr6:128370000-128374400	Weak transcription	Ovary	ovary
44	chr6:128370000-128378400	Weak transcription	HSMM	muscle
45	chr6:128370000-128385000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr6:128370000-128388000	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr6:128370000-128412600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr6:128370800-128388000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:128371400-128374000	Weak transcription	Fetal Intestine Large	intestine
50	chr6:128371400-128374400	Weak transcription	Fetal Intestine Small	intestine

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