Variant report

Variant	rs10205315
Chromosome Location	chr2:54314001-54314002
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10166363	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10169648	0.84[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10172916	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10176342	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10176406	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10192403	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10208690	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11675345	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11676433	1.00[ASN][1000 genomes]
rs11677951	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11687470	1.00[ASN][1000 genomes]
rs11688581	1.00[ASN][1000 genomes]
rs11695936	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13394575	0.81[AFR][1000 genomes]
rs13418039	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13418658	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13418839	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13429859	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1559039	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1559040	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17045513	0.81[AFR][1000 genomes]
rs17189638	1.00[ASN][1000 genomes]
rs2112125	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28368466	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28416116	1.00[ASN][1000 genomes]
rs34433964	0.81[AFR][1000 genomes]
rs35641543	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55666400	1.00[ASN][1000 genomes]
rs55672362	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55820614	1.00[ASN][1000 genomes]
rs56374740	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61572658	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6721034	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67951010	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72799283	1.00[ASN][1000 genomes]
rs72799301	1.00[ASN][1000 genomes]
rs72800709	1.00[ASN][1000 genomes]
rs72800719	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800725	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800729	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800732	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800738	1.00[ASN][1000 genomes]
rs72800739	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800741	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800746	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800751	0.87[EUR][1000 genomes]
rs72800752	1.00[ASN][1000 genomes]
rs72800759	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800765	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800772	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72800775	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7571660	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7586592	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs998381	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001246	chr2:54195654-54434832	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
2	nsv1003205	chr2:54220049-54700843	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2762639	chr2:54220049-54700855	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1011790	chr2:54220049-54714553	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv1002891	chr2:54227005-54682169	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv535722	chr2:54227005-54682169	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv1011690	chr2:54255361-54700843	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	nsv431069	chr2:54260132-54434049	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv1010175	chr2:54292951-54343466	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54280800-54315000	Weak transcription	Adipose Nuclei	Adipose
2	chr2:54280800-54315200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:54280800-54331000	Weak transcription	Aorta	Aorta
4	chr2:54289800-54317600	Weak transcription	Primary B cells from cord blood	blood
5	chr2:54291200-54342000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr2:54294800-54315000	Weak transcription	Fetal Intestine Small	intestine
7	chr2:54302800-54317800	Weak transcription	Left Ventricle	heart
8	chr2:54305000-54315000	Weak transcription	Fetal Intestine Large	intestine
9	chr2:54305000-54315200	Weak transcription	Pancreas	Pancrea
10	chr2:54305400-54321600	Weak transcription	Lung	lung
11	chr2:54306600-54315400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr2:54307400-54319400	Weak transcription	Primary T cells from cord blood	blood
13	chr2:54309000-54315200	Weak transcription	Fetal Muscle Leg	muscle
14	chr2:54309000-54317600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr2:54309200-54315400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:54309200-54315600	Weak transcription	Esophagus	oesophagus
17	chr2:54309400-54315000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:54309400-54315000	Weak transcription	NHEK	skin
19	chr2:54309400-54315200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:54309800-54315000	Weak transcription	HMEC	breast
21	chr2:54310800-54315200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr2:54310800-54315200	Weak transcription	NH-A	brain
23	chr2:54311000-54314600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:54311000-54315000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr2:54311000-54315200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr2:54311000-54315200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:54311000-54315200	Weak transcription	Right Atrium	heart
28	chr2:54311000-54317800	Weak transcription	Brain Anterior Caudate	brain
29	chr2:54311000-54317800	Weak transcription	Brain Hippocampus Middle	brain
30	chr2:54311000-54324200	Weak transcription	HSMMtube	muscle
31	chr2:54311800-54317600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr2:54312000-54315200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:54312200-54315200	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:54312600-54315200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:54313800-54315000	Weak transcription	HepG2	liver
36	chr2:54313800-54315400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr2:54314000-54315200	Weak transcription	K562	blood

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