Variant report

Variant	rs6928210
Chromosome Location	chr6:118699394-118699395
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10456917	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10457330	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10457331	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10457335	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10457337	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10457338	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11153732	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11153734	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11153748	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11153752	0.84[EUR][1000 genomes]
rs11153753	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11755121	0.84[EUR][1000 genomes]
rs12192682	0.81[EUR][1000 genomes]
rs12192964	0.83[ASN][1000 genomes]
rs12194555	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12197337	0.80[EUR][1000 genomes]
rs12199463	0.85[EUR][1000 genomes]
rs12205899	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12206329	0.82[EUR][1000 genomes]
rs12211576	0.81[EUR][1000 genomes]
rs12214483	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12660455	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12665409	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13219555	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1344178	0.80[ASN][1000 genomes]
rs2077162	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2078079	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2078383	0.80[ASN][1000 genomes]
rs2213856	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2213857	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2356183	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2356492	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28655926	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34479834	0.85[EUR][1000 genomes]
rs35730412	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3752581	0.81[EUR][1000 genomes]
rs3798420	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3890198	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3951042	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3951043	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4027880	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56403768	0.92[ASN][1000 genomes]
rs57813349	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57912492	0.92[ASN][1000 genomes]
rs6569013	0.84[ASN][1000 genomes]
rs6569014	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6569015	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6569017	0.80[ASN][1000 genomes]
rs6569020	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67832971	0.84[EUR][1000 genomes]
rs6903459	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920640	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6925641	0.84[EUR][1000 genomes]
rs6936178	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7453914	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7746778	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7757815	0.80[ASN][1000 genomes]
rs7757943	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7764272	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7764280	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7767864	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7772214	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9320648	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9320649	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9320650	0.80[ASN][1000 genomes]
rs9489355	0.86[ASN][1000 genomes]
rs973944	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv532051	chr6:118551027-119044197	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats 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	9 gene(s)	inside rSNPs	diseases
3	nsv1020463	chr6:118593028-119146363	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv604554	chr6:118631282-118716318	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv830787	chr6:118631902-118805106	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1025403	chr6:118635123-119122551	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
7	nsv1025456	chr6:118669672-119058789	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv1027444	chr6:118687556-119121660	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
9	nsv538428	chr6:118687556-119121660	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv949321	chr6:118692304-119137658	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
11	nsv432958	chr6:118692307-119010307	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
12	nsv604555	chr6:118695049-118856822	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
13	nsv1034448	chr6:118698169-119016383	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118688200-118700200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:118691400-118700400	Enhancers	Fetal Heart	heart
3	chr6:118694200-118699600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr6:118698200-118699600	Enhancers	Fetal Thymus	thymus
5	chr6:118698200-118699800	Enhancers	Thymus	Thymus
6	chr6:118698800-118699800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:118698800-118700400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr6:118699000-118699400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr6:118699000-118699400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:118699000-118699400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:118699000-118699400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
12	chr6:118699000-118699400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
13	chr6:118699000-118699600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr6:118699000-118699600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:118699000-118699600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:118699000-118699600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:118699000-118699600	Enhancers	Fetal Muscle Trunk	muscle
18	chr6:118699000-118699600	Enhancers	Fetal Muscle Leg	muscle
19	chr6:118699000-118699600	Enhancers	Psoas Muscle	Psoas
20	chr6:118699000-118699600	Enhancers	Right Atrium	heart
21	chr6:118699000-118699800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr6:118699000-118699800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr6:118699000-118700000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr6:118699200-118699400	Enhancers	Left Ventricle	heart

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