Variant report

Variant	rs6953328
Chromosome Location	chr7:6230940-6230941
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11973228	1.00[EUR][1000 genomes]
rs11973659	1.00[EUR][1000 genomes]
rs11974681	1.00[EUR][1000 genomes]
rs41282682	1.00[EUR][1000 genomes]
rs55681139	1.00[EUR][1000 genomes]
rs56295477	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59304454	0.90[AMR][1000 genomes]
rs6946205	0.86[EUR][1000 genomes]
rs6957628	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6974814	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73675887	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7806404	0.81[EUR][1000 genomes]
rs7807841	0.81[EUR][1000 genomes]
rs7811590	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7811721	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
2	nsv948912	chr7:5803903-6623553	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
3	nsv1034060	chr7:5814823-6745710	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
4	nsv538711	chr7:5814823-6745710	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	138 gene(s)	inside rSNPs	diseases
5	nsv1028242	chr7:5819084-6645024	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
6	nsv538712	chr7:5819084-6645024	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	127 gene(s)	inside rSNPs	diseases
7	nsv949531	chr7:5949371-6753694	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	129 gene(s)	inside rSNPs	diseases
8	nsv1021037	chr7:6070792-6426966	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	nsv538713	chr7:6070792-6426966	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	nsv530989	chr7:6176729-6438197	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
11	nsv5629	chr7:6217866-6263131	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6202400-6238000	Weak transcription	Fetal Kidney	kidney
2	chr7:6211800-6237800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:6212200-6237800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:6212600-6231000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:6212800-6238200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:6213000-6231200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:6213200-6240600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:6215800-6231400	Weak transcription	Hela-S3	cervix
9	chr7:6216800-6237000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr7:6216800-6237800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr7:6217600-6231600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr7:6218600-6231600	Weak transcription	Brain Hippocampus Middle	brain
13	chr7:6218800-6232000	Weak transcription	Stomach Mucosa	stomach
14	chr7:6219000-6233000	Weak transcription	Fetal Heart	heart
15	chr7:6219400-6231600	Strong transcription	Fetal Intestine Small	intestine
16	chr7:6219600-6238000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr7:6219600-6241800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:6219600-6243000	Weak transcription	K562	blood
19	chr7:6219800-6241800	Weak transcription	Pancreas	Pancrea
20	chr7:6220200-6232600	Weak transcription	Right Atrium	heart
21	chr7:6221400-6238400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:6222800-6235600	Weak transcription	Psoas Muscle	Psoas
23	chr7:6226800-6238200	Weak transcription	Brain Angular Gyrus	brain
24	chr7:6227000-6238600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:6227200-6237600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:6227200-6238600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:6227200-6239000	Weak transcription	HMEC	breast
28	chr7:6227400-6237600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr7:6227400-6238000	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr7:6227400-6242800	Weak transcription	A549	lung
31	chr7:6228200-6240800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr7:6228400-6235600	Weak transcription	Right Ventricle	heart
33	chr7:6228400-6238400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:6228600-6247800	Weak transcription	Colon Smooth Muscle	Colon
35	chr7:6228600-6257400	Weak transcription	Primary B cells from cord blood	blood
36	chr7:6228800-6231400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr7:6228800-6237400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:6228800-6244200	Weak transcription	NHDF-Ad	bronchial
39	chr7:6229000-6259800	Weak transcription	NHEK	skin
40	chr7:6229200-6231400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr7:6229200-6233200	Weak transcription	GM12878-XiMat	blood
42	chr7:6229200-6237800	Weak transcription	Aorta	Aorta
43	chr7:6229200-6238000	Weak transcription	Brain Cingulate Gyrus	brain
44	chr7:6229200-6241800	Weak transcription	Esophagus	oesophagus
45	chr7:6229200-6244000	Weak transcription	Fetal Muscle Leg	muscle
46	chr7:6229200-6244600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:6229200-6252200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:6229400-6231000	Weak transcription	Brain Germinal Matrix	brain
49	chr7:6229400-6231200	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr7:6229400-6233200	Weak transcription	Left Ventricle	heart

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