Variant report

Variant	rs35733341
Chromosome Location	chr11:104805207-104805208
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10466650	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10895744	0.81[EUR][1000 genomes]
rs10895752	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11226548	0.83[EUR][1000 genomes]
rs11226549	0.83[EUR][1000 genomes]
rs11226550	0.83[EUR][1000 genomes]
rs11226555	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11226557	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11226562	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11226565	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11601896	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11825902	0.81[EUR][1000 genomes]
rs12293970	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12362084	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12422201	0.83[EUR][1000 genomes]
rs15684	0.83[EUR][1000 genomes]
rs2005513	0.83[EUR][1000 genomes]
rs34436514	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4517484	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs491011	0.83[EUR][1000 genomes]
rs491945	0.83[EUR][1000 genomes]
rs518553	0.83[EUR][1000 genomes]
rs524060	0.83[EUR][1000 genomes]
rs528641	0.83[EUR][1000 genomes]
rs532705	0.83[EUR][1000 genomes]
rs532738	0.83[EUR][1000 genomes]
rs549691	0.83[EUR][1000 genomes]
rs579156	0.81[EUR][1000 genomes]
rs595395	0.83[EUR][1000 genomes]
rs625046	0.83[EUR][1000 genomes]
rs626771	0.83[EUR][1000 genomes]
rs641046	0.83[EUR][1000 genomes]
rs656251	0.83[EUR][1000 genomes]
rs870402	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv1046098	chr11:104207210-105003661	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1054456	chr11:104358924-104805251	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv531430	chr11:104380924-105194452	Genic enhancers Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv832255	chr11:104674918-104846961	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv898355	chr11:104730322-104897843	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv1040784	chr11:104763797-104855878	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	nsv468862	chr11:104774014-105243371	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv556218	chr11:104774014-105243371	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	esv3334824	chr11:104776753-104813836	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv898356	chr11:104779195-104838471	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
11	esv3385159	chr11:104786549-105051555	Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
12	nsv983232	chr11:104787454-104809055	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1041081	chr11:104797775-104912458	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs35733341	CASP4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104803400-104819000	Weak transcription	Psoas Muscle	Psoas
2	chr11:104803600-104806200	Enhancers	Primary B cells from peripheral blood	blood
3	chr11:104804000-104805600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr11:104804200-104805400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr11:104804200-104806800	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr11:104804200-104806800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr11:104804200-104806800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:104804400-104805400	Enhancers	Primary B cells from cord blood	blood
9	chr11:104804600-104805400	Enhancers	Primary T cells from cord blood	blood
10	chr11:104804600-104805600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:104804600-104806200	Enhancers	Primary T cells fromperipheralblood	blood
12	chr11:104804600-104806200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr11:104804600-104806400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr11:104804600-104807000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr11:104805000-104806200	Enhancers	Dnd41	blood
16	chr11:104805000-104806800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr11:104805200-104805400	Enhancers	Spleen	Spleen
18	chr11:104805200-104805600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
19	chr11:104805200-104805600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr11:104805200-104805600	Enhancers	Fetal Thymus	thymus
21	chr11:104805200-104805600	Enhancers	HUVEC	blood vessel
22	chr11:104805200-104805800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr11:104805200-104806000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr11:104805200-104806400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr11:104805200-104806600	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr11:104805200-104806800	Enhancers	Primary hematopoietic stem cells	blood

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