Variant report

Variant	rs10196933
Chromosome Location	chr2:112951702-112951703
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:112951422..112953585-chr2:112957431..112959330,2	K562	blood:
2	chr2:112950076..112952216-chr2:112954014..112957204,3	K562	blood:
3	chr2:112944701..112946678-chr2:112951279..112953593,2	K562	blood:
4	chr2:112947735..112949469-chr2:112950184..112952276,2	MCF-7	breast:
5	chr2:112945476..112947826-chr2:112951258..112953580,3	MCF-7	breast:
6	chr2:112950076..112953760-chr2:112955704..112959330,4	K562	blood:
7	chr2:112951584..112954531-chr2:112972877..112975539,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10169159	0.81[ASN][1000 genomes]
rs10177573	0.94[CHB][hapmap];0.81[ASN][1000 genomes]
rs10183121	1.00[CHB][hapmap];0.88[JPT][hapmap];0.89[ASN][1000 genomes]
rs10191002	0.94[CHB][hapmap]
rs10205038	0.94[CHB][hapmap]
rs10211300	0.88[CHB][hapmap];1.00[YRI][hapmap]
rs10439391	0.94[CHB][hapmap];1.00[YRI][hapmap]
rs10864903	0.94[CHB][hapmap]
rs11123131	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11123132	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11674953	0.94[CHB][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes]
rs11689487	0.81[AMR][1000 genomes]
rs11691431	0.94[CHB][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes]
rs11903741	0.94[CHB][hapmap]
rs12620553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12711738	0.94[CHB][hapmap];0.81[ASN][1000 genomes]
rs12711739	0.94[CHB][hapmap]
rs13387611	0.94[CHB][hapmap]
rs13407329	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34623958	0.81[ASN][1000 genomes]
rs4299347	0.94[CHB][hapmap];1.00[YRI][hapmap]
rs4352239	0.94[CHB][hapmap];1.00[YRI][hapmap]
rs4392265	0.81[ASN][1000 genomes]
rs4399734	0.94[CHB][hapmap]
rs4430968	0.94[CHB][hapmap]
rs4446076	0.81[ASN][1000 genomes]
rs4450606	0.94[CHB][hapmap]
rs4456711	0.94[CHB][hapmap]
rs4507112	0.94[CHB][hapmap]
rs4522611	0.94[CHB][hapmap]
rs4525706	0.94[CHB][hapmap]
rs4542853	0.94[CHB][hapmap];1.00[YRI][hapmap]
rs4578863	0.94[CHB][hapmap];1.00[YRI][hapmap]
rs4622729	0.94[CHB][hapmap]
rs4849056	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4849057	0.81[AMR][1000 genomes]
rs6542045	0.94[CHB][hapmap]
rs6542050	0.81[ASN][1000 genomes]
rs6542051	0.94[CHB][hapmap]
rs6706874	0.81[ASN][1000 genomes]
rs6733138	0.94[CHB][hapmap]
rs6745942	0.81[ASN][1000 genomes]
rs6751146	0.94[CHB][hapmap]
rs6758110	0.94[CHB][hapmap]
rs6761599	0.93[CHB][hapmap]
rs72831684	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7557281	0.94[CHB][hapmap]
rs7557862	0.93[CHB][hapmap];0.80[JPT][hapmap]
rs7571435	0.94[CHB][hapmap];0.81[AMR][1000 genomes]
rs7591439	0.94[CHB][hapmap]
rs7598168	0.94[CHB][hapmap]
rs7600338	0.94[CHB][hapmap];1.00[YRI][hapmap]
rs7601200	0.94[CHB][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874863	chr2:112591224-113157344	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer 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	57 gene(s)	inside rSNPs	diseases
2	nsv874864	chr2:112617280-113104142	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv874865	chr2:112623098-113049274	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
4	esv3422414	chr2:112883450-113200285	Strong transcription Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv874866	chr2:112906599-112991098	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv582703	chr2:112920219-113100014	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
7	nsv874867	chr2:112930064-113038409	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
8	esv1805614	chr2:112949713-113048705	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112914600-112972800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:112943200-112952200	Weak transcription	Fetal Lung	lung
3	chr2:112945200-112970600	Weak transcription	Fetal Stomach	stomach
4	chr2:112946400-112951800	Weak transcription	K562	blood
5	chr2:112946400-112953800	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr2:112946800-112952200	Enhancers	Primary T cells from cord blood	blood
7	chr2:112947200-112951800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr2:112948200-112953800	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr2:112950000-112952000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr2:112950000-112952000	Weak transcription	HUVEC	blood vessel
11	chr2:112950600-112951800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr2:112951200-112953800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr2:112951400-112953800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr2:112951600-112953000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr2:112951600-112953200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr2:112951600-112953600	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr2:112951600-112953600	Enhancers	Thymus	Thymus
18	chr2:112951600-112953800	Enhancers	Primary T cells fromperipheralblood	blood
19	chr2:112951600-112953800	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr2:112951600-112954400	Enhancers	Fetal Thymus	thymus

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