Variant report

Variant	rs9395058
Chromosome Location	chr6:44984069-44984070
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 131 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs1023091	0.80[ASN][1000 genomes]
rs1041332	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1041333	0.87[ASN][1000 genomes]
rs10456119	0.82[ASN][1000 genomes]
rs10484627	0.83[ASN][1000 genomes]
rs10948183	0.83[ASN][1000 genomes]
rs10948185	0.85[ASN][1000 genomes]
rs10948186	0.85[ASN][1000 genomes]
rs10948187	0.90[ASN][1000 genomes]
rs10948188	0.89[ASN][1000 genomes]
rs10948190	0.88[ASN][1000 genomes]
rs10948193	0.90[ASN][1000 genomes]
rs10948194	0.91[ASN][1000 genomes]
rs10948197	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1150806	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1159131	0.84[ASN][1000 genomes]
rs11967188	0.90[ASN][1000 genomes]
rs12190513	0.89[ASN][1000 genomes]
rs12191518	0.85[ASN][1000 genomes]
rs12196818	0.90[ASN][1000 genomes]
rs12207620	0.80[ASN][1000 genomes]
rs12214778	0.91[ASN][1000 genomes]
rs12524069	0.84[ASN][1000 genomes]
rs12525009	0.83[ASN][1000 genomes]
rs12526711	0.83[ASN][1000 genomes]
rs12528232	0.80[ASN][1000 genomes]
rs1293598	0.80[ASN][1000 genomes]
rs13196587	0.88[ASN][1000 genomes]
rs13202529	0.85[ASN][1000 genomes]
rs13203495	0.88[ASN][1000 genomes]
rs13211229	0.89[ASN][1000 genomes]
rs13213412	0.81[ASN][1000 genomes]
rs13215618	0.81[ASN][1000 genomes]
rs13216116	0.88[ASN][1000 genomes]
rs1329710	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1329713	0.85[ASN][1000 genomes]
rs1329714	0.85[ASN][1000 genomes]
rs1329716	0.91[ASN][1000 genomes]
rs1360197	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1411148	0.80[EUR][1000 genomes]
rs1521355	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1576382	0.91[ASN][1000 genomes]
rs1578676	0.84[ASN][1000 genomes]
rs1590864	0.85[ASN][1000 genomes]
rs17339124	0.88[ASN][1000 genomes]
rs17422760	0.80[ASN][1000 genomes]
rs17424547	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1831310	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1854547	0.89[ASN][1000 genomes]
rs1971482	0.85[ASN][1000 genomes]
rs1980265	0.90[ASN][1000 genomes]
rs2396369	0.89[ASN][1000 genomes]
rs2396370	0.89[ASN][1000 genomes]
rs2396371	0.89[ASN][1000 genomes]
rs2396372	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2396375	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34808716	0.81[ASN][1000 genomes]
rs35357222	0.89[ASN][1000 genomes]
rs35813980	0.90[ASN][1000 genomes]
rs3778507	0.85[ASN][1000 genomes]
rs3799976	0.80[ASN][1000 genomes]
rs3799981	0.82[ASN][1000 genomes]
rs3799984	0.81[ASN][1000 genomes]
rs3799986	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3846896	0.80[ASN][1000 genomes]
rs4398713	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4711803	0.81[ASN][1000 genomes]
rs4711805	0.81[ASN][1000 genomes]
rs4711807	0.89[ASN][1000 genomes]
rs4711809	0.80[ASN][1000 genomes]
rs4714828	0.80[ASN][1000 genomes]
rs4714830	0.90[ASN][1000 genomes]
rs4714832	0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4714834	0.80[ASN][1000 genomes]
rs494982	0.89[ASN][1000 genomes]
rs500773	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs538801	0.83[ASN][1000 genomes]
rs55893720	0.90[ASN][1000 genomes]
rs588848	0.82[ASN][1000 genomes]
rs608941	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs636845	0.89[ASN][1000 genomes]
rs6458415	0.83[ASN][1000 genomes]
rs67001335	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs679713	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6899378	0.80[EUR][1000 genomes]
rs6903576	0.80[ASN][1000 genomes]
rs6919485	0.90[ASN][1000 genomes]
rs6923519	0.80[ASN][1000 genomes]
rs6925017	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6925467	0.85[ASN][1000 genomes]
rs718112	0.80[ASN][1000 genomes]
rs7739928	0.80[EUR][1000 genomes]
rs7742360	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7747642	0.80[ASN][1000 genomes]
rs7749865	0.90[ASN][1000 genomes]
rs7754378	0.80[ASN][1000 genomes]
rs7763421	0.82[ASN][1000 genomes]
rs7775717	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9349309	0.83[EUR][1000 genomes]
rs9357464	0.91[ASN][1000 genomes]
rs9367211	0.81[ASN][1000 genomes]
rs9367214	0.83[EUR][1000 genomes]
rs9369516	0.80[ASN][1000 genomes]
rs9369529	0.85[ASN][1000 genomes]
rs9369530	0.82[EUR][1000 genomes]
rs9381361	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9381365	0.80[EUR][1000 genomes]
rs9463054	0.90[ASN][1000 genomes]
rs9463055	0.86[ASN][1000 genomes]
rs9472407	0.84[ASN][1000 genomes]
rs9472409	0.89[ASN][1000 genomes]
rs9472411	0.88[ASN][1000 genomes]
rs9472416	0.90[ASN][1000 genomes]
rs976699	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885861	chr6:44837356-45043618	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv1024370	chr6:44878053-45251451	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	esv2758051	chr6:44879791-45056758	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	esv2759423	chr6:44879791-45056758	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv885862	chr6:44890760-45083966	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv885863	chr6:44890760-45083966	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv885864	chr6:44890760-45198796	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
10	nsv462938	chr6:44909515-45008779	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv470817	chr6:44909515-45008779	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv603007	chr6:44909515-45008779	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv1023018	chr6:44925393-45152912	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv538212	chr6:44925393-45152912	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	esv2757164	chr6:44953758-44989519	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv603008	chr6:44958372-45081821	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	esv2762589	chr6:44982992-45044580	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9395058	SUPT3H	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44966400-44993600	Weak transcription	HepG2	liver
2	chr6:44970800-44988600	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr6:44970800-44989000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr6:44971400-44988800	Weak transcription	Primary T cells from cord blood	blood
5	chr6:44974800-45004600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:44977200-44988800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:44977600-44993800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:44978600-44988600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:44980600-44989000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr6:44981600-44994800	Weak transcription	Aorta	Aorta
11	chr6:44981600-44994800	Weak transcription	Pancreas	Pancrea
12	chr6:44981800-44988200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:44981800-44988800	Weak transcription	Brain Hippocampus Middle	brain
14	chr6:44982200-44987200	Weak transcription	Dnd41	blood
15	chr6:44982600-44984200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:44982600-44989000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr6:44983000-44984600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr6:44983200-44988200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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