Variant report

Variant	rs17250953
Chromosome Location	chr17:45821844-45821845
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:45811931..45814457-chr17:45821701..45824432,2	MCF-7	breast:
2	chr17:45770256..45772710-chr17:45820237..45822227,2	MCF-7	breast:
3	chr17:45819448..45824573-chr17:45826000..45830135,4	K562	blood:
4	chr17:45769360..45771428-chr17:45820876..45822784,2	K562	blood:
5	chr17:45762090..45764390-chr17:45820597..45823079,2	K562	blood:

Variant related genes	Relation type
ENSG00000198933	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12450008	0.92[EUR][1000 genomes]
rs12451682	0.92[EUR][1000 genomes]
rs12452307	0.92[EUR][1000 genomes]
rs16946878	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17244544	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17772855	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17773055	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41407050	0.92[EUR][1000 genomes]
rs72648867	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72648868	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72648869	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498122	chr17:45763853-46064327	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv2071	chr17:45801503-45844229	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17250953	C17orf57	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45811400-45822000	Weak transcription	Right Atrium	heart
2	chr17:45819200-45824000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr17:45819600-45823000	Genic enhancers	Primary T cells fromperipheralblood	blood
4	chr17:45820400-45822000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr17:45820400-45824000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr17:45820600-45822000	Weak transcription	Primary B cells from peripheral blood	blood
7	chr17:45820600-45822000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr17:45820600-45822400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr17:45820600-45822800	Weak transcription	GM12878-XiMat	blood
10	chr17:45820600-45823600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr17:45820600-45823800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr17:45820600-45826200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr17:45820600-45830400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr17:45821200-45823800	Enhancers	Dnd41	blood
15	chr17:45821600-45822000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr17:45821600-45822800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr17:45821600-45822800	Strong transcription	Spleen	Spleen
18	chr17:45821600-45823800	Enhancers	K562	blood
19	chr17:45821600-45824400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr17:45821800-45822000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr17:45821800-45823400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr17:45821800-45823600	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr17:45821800-45823600	Strong transcription	Primary T helper cells fromperipheralblood	blood

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