Variant report

Variant	rs430655
Chromosome Location	chr6:33557225-33557226
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:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33555689..33557372-chr6:33575674..33577429,2	MCF-7	breast:
2	chr6:33555453..33558278-chr6:33607870..33609566,2	K562	blood:
3	chr6:33557167..33558102-chr6:33640434..33641022,2	MCF-7	breast:
4	chr6:33556084..33559190-chr6:33561463..33564085,3	K562	blood:
5	chr6:33556676..33558804-chr6:33667221..33669587,2	K562	blood:
6	chr6:33556929..33558055-chr6:33575240..33576451,8	MCF-7	breast:
7	chr6:33557128..33558070-chr6:33729670..33730677,6	K562	blood:
8	chr6:33555432..33562879-chr6:33670455..33680174,12	K562	blood:
9	chr6:33557115..33558665-chr6:33640289..33641376,5	K562	blood:
10	chr6:33556983..33559426-chr6:33569915..33571800,2	MCF-7	breast:
11	chr6:33557066..33558559-chr6:33667900..33669281,8	K562	blood:
12	chr6:33554633..33558061-chr6:33675915..33678804,3	MCF-7	breast:
13	chr6:33557038..33558663-chr6:33565418..33568204,3	K562	blood:
14	chr6:33551039..33553771-chr6:33556676..33559187,3	MCF-7	breast:
15	chr6:33550971..33553641-chr6:33557216..33560603,4	K562	blood:
16	chr6:33556717..33560050-chr6:33586677..33588878,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000137288	Chromatin interaction
ENSG00000096433	Chromatin interaction
ENSG00000204188	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs210163	0.83[CEU][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs210202	0.80[JPT][hapmap]
rs210203	0.80[JPT][hapmap]
rs210207	0.80[JPT][hapmap]
rs210209	0.89[JPT][hapmap]
rs386906	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs419261	0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs420361	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs420628	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs422907	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462896	chr6:33534880-33588147	Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv602833	chr6:33534880-33588147	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv885770	chr6:33543409-33614127	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv830638	chr6:33551202-33711346	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs430655	FKBP5	cis	cerebellum	SCAN
rs430655	C6orf125	cis	cerebellum	SCAN
rs430655	ITPR3	cis	lymphoblastoid	seeQTL

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33548400-33557600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:33548400-33557800	Weak transcription	Right Atrium	heart
3	chr6:33548600-33560600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr6:33548800-33557800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:33553600-33558000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr6:33553800-33557400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:33553800-33557400	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr6:33553800-33557600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:33553800-33557600	Weak transcription	Left Ventricle	heart
10	chr6:33553800-33557600	Weak transcription	NH-A	brain
11	chr6:33553800-33557600	Weak transcription	Osteobl	bone
12	chr6:33553800-33557800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:33553800-33557800	Weak transcription	Esophagus	oesophagus
14	chr6:33553800-33558400	Weak transcription	Gastric	stomach
15	chr6:33553800-33560400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr6:33554000-33557400	Weak transcription	Colon Smooth Muscle	Colon
17	chr6:33554000-33557600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:33554000-33557600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr6:33554000-33557600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr6:33554000-33557600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:33554000-33557600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr6:33554000-33557800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:33554000-33557800	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr6:33554000-33557800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:33554000-33558400	Weak transcription	Fetal Kidney	kidney
26	chr6:33554000-33560400	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr6:33554000-33560400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr6:33554000-33560600	Weak transcription	Brain Angular Gyrus	brain
29	chr6:33554000-33560800	Weak transcription	Brain Hippocampus Middle	brain
30	chr6:33554200-33557600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr6:33554200-33557600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr6:33554200-33557600	Weak transcription	Liver	Liver
33	chr6:33554200-33557600	Weak transcription	A549	lung
34	chr6:33554200-33557600	Weak transcription	GM12878-XiMat	blood
35	chr6:33554200-33557600	Weak transcription	K562	blood
36	chr6:33554200-33557800	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr6:33554200-33557800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr6:33554200-33560400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr6:33554200-33560600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr6:33554200-33560800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr6:33554400-33557400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr6:33554400-33557600	Weak transcription	Primary B cells from cord blood	blood
43	chr6:33555800-33557600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:33555800-33558800	Enhancers	Brain Anterior Caudate	brain
45	chr6:33555800-33561400	Enhancers	Spleen	Spleen
46	chr6:33556400-33557400	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr6:33556400-33557600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:33556400-33557800	Enhancers	Psoas Muscle	Psoas
49	chr6:33556400-33558200	Enhancers	Fetal Intestine Small	intestine
50	chr6:33556400-33558200	Enhancers	Right Ventricle	heart

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