Variant report

Variant	rs17680685
Chromosome Location	chr17:38588929-38588930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:38588496..38590793-chr17:38771686..38774374,2	MCF-7	breast:
2	chr17:38588540..38590112-chr17:38602415..38604178,2	MCF-7	breast:
3	chr17:38580560..38584947-chr17:38585760..38591436,7	K562	blood:
4	chr17:38581114..38584947-chr17:38588775..38591436,4	K562	blood:
5	chr17:38587923..38591705-chr17:38591977..38594441,3	MCF-7	breast:
6	chr17:38587973..38589674-chr17:38599835..38601387,2	MCF-7	breast:
7	chr17:38587058..38589515-chr17:38604299..38606675,2	K562	blood:
8	chr17:38587525..38592353-chr17:38597530..38601586,11	MCF-7	breast:
9	chr17:38587744..38590603-chr17:38590912..38592716,3	K562	blood:
10	chr17:38517929..38522150-chr17:38588397..38591798,3	K562	blood:
11	chr17:38587889..38589952-chr17:38605595..38608184,2	MCF-7	breast:
12	chr17:38588081..38591030-chr17:38591069..38592804,4	K562	blood:
13	chr17:38517929..38520889-chr17:38588435..38591798,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000183153	Chromatin interaction
ENSG00000141753	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10305288	1.00[AFR][1000 genomes]
rs10305296	1.00[AFR][1000 genomes]
rs10305303	1.00[AFR][1000 genomes]
rs11867902	0.85[EUR][1000 genomes]
rs15685	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs17557495	1.00[AFR][1000 genomes]
rs17557879	1.00[AFR][1000 genomes]
rs17617263	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17618397	1.00[AFR][1000 genomes]
rs17679038	1.00[AFR][1000 genomes]
rs17679086	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17679361	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17680217	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17680410	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17680507	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17680624	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17680704	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2012667	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2229773	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs28362321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs33998939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35783632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35898909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs41283423	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4134993	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4134998	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4135005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4135007	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4135012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4135019	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4135021	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4135027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4135030	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs45612441	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72819623	1.00[AFR][1000 genomes]
rs72819624	1.00[AFR][1000 genomes]
rs72819628	1.00[AFR][1000 genomes]
rs72819630	1.00[AFR][1000 genomes]
rs72819632	1.00[AFR][1000 genomes]
rs72819633	1.00[AFR][1000 genomes]
rs72819651	1.00[AFR][1000 genomes]
rs9891431	0.92[EUR][1000 genomes]
rs9891944	0.84[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	nsv833445	chr17:38466474-38637969	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv908223	chr17:38530799-38609187	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:38579600-38598800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr17:38583600-38589600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr17:38584000-38592600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr17:38584400-38589200	Weak transcription	Fetal Thymus	thymus
5	chr17:38584600-38600200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr17:38587800-38589400	Weak transcription	Right Ventricle	heart
7	chr17:38588200-38589000	Enhancers	Colon Smooth Muscle	Colon
8	chr17:38588200-38590600	Enhancers	K562	blood
9	chr17:38588400-38589400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr17:38588600-38589600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr17:38588600-38589600	Enhancers	Stomach Smooth Muscle	stomach
12	chr17:38588600-38589600	Weak transcription	Spleen	Spleen
13	chr17:38588600-38589800	Enhancers	HepG2	liver
14	chr17:38588600-38590400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr17:38588600-38591200	Enhancers	Fetal Stomach	stomach
16	chr17:38588600-38592600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:38588800-38590200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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