Variant report

Variant	rs2633560
Chromosome Location	chr3:112196896-112196897
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1155073	0.83[ASN][1000 genomes]
rs12632867	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1386895	0.97[EUR][1000 genomes]
rs1398091	0.83[EUR][1000 genomes]
rs1488259	0.83[ASN][1000 genomes]
rs1601852	0.83[ASN][1000 genomes]
rs1814052	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1873572	0.80[ASN][1000 genomes]
rs2171513	0.84[ASN][1000 genomes]
rs2171514	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2633556	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2633557	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2633562	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2633563	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2633574	0.80[ASN][1000 genomes]
rs2633579	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2633588	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2633589	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2638013	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2638015	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2638019	0.80[ASN][1000 genomes]
rs2638032	0.80[ASN][1000 genomes]
rs2705525	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2705533	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2705535	0.88[ASN][1000 genomes]
rs2705536	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2705544	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2705548	0.80[ASN][1000 genomes]
rs2705552	0.80[ASN][1000 genomes]
rs2705555	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2705562	0.80[ASN][1000 genomes]
rs2705565	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2933134	0.80[ASN][1000 genomes]
rs2969896	0.80[ASN][1000 genomes]
rs2971204	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2971205	0.88[ASN][1000 genomes]
rs3112268	0.84[ASN][1000 genomes]
rs4519670	0.90[EUR][1000 genomes]
rs4682410	0.97[EUR][1000 genomes]
rs6438079	0.97[EUR][1000 genomes]

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	nsv591294	chr3:112091220-112208750	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1010208	chr3:112098542-112227212	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1003936	chr3:112125931-112274613	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv998309	chr3:112130290-112278804	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	nsv591300	chr3:112144026-112270857	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv1006065	chr3:112147080-112276983	Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv1005323	chr3:112171990-112274613	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
8	nsv877342	chr3:112185025-112332629	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112188800-112197600	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr3:112190600-112198400	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr3:112192800-112200200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:112193000-112197800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr3:112193000-112200000	Weak transcription	Fetal Thymus	thymus
6	chr3:112193200-112201200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr3:112193800-112197000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr3:112194200-112214000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr3:112194400-112197000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr3:112194400-112198200	Weak transcription	Thymus	Thymus
11	chr3:112194400-112199800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr3:112194600-112197400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr3:112194600-112199800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr3:112195000-112198000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr3:112195200-112197000	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr3:112195200-112198200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr3:112195400-112197000	Strong transcription	Primary B cells from peripheral blood	blood
18	chr3:112195400-112200800	ZNF genes & repeats	GM12878-XiMat	blood
19	chr3:112195800-112197200	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr3:112195800-112198200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr3:112196000-112197400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr3:112196000-112198000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr3:112196200-112198200	Weak transcription	Primary T cells from cord blood	blood
24	chr3:112196400-112198600	Enhancers	Primary hematopoietic stem cells	blood
25	chr3:112196600-112197200	Enhancers	Primary B cells from cord blood	blood
26	chr3:112196600-112197400	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr3:112196600-112198000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr3:112196800-112197200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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