Variant report

Variant	rs10057967
Chromosome Location	chr5:74997756-74997757
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:74997231..74999217-chr5:75000460..75002166,2	K562	blood:
2	chr5:74996831..74999207-chr5:75004311..75007242,2	K562	blood:

Variant related genes	Relation type
ENSG00000207333	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs16872768	0.92[CEU][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2112347	0.92[CEU][hapmap];0.90[JPT][hapmap];0.90[YRI][hapmap];0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2307111	0.91[CHD][hapmap];0.97[GIH][hapmap];0.91[JPT][hapmap];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs253414	0.85[MEX][hapmap]
rs34358	0.90[MEX][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34359	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34360	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34361	0.90[MEX][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs3797580	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs40060	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs42302	0.81[EUR][1000 genomes]
rs4704230	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6864091	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6874626	0.92[CEU][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6881648	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs888789	0.94[ASW][hapmap];0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[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	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv518475	chr5:74863041-75411804	Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	esv1850196	chr5:74890618-75138443	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv830353	chr5:74961520-75152609	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10057967	HMGCR	cis	parietal	SCAN
rs10057967	HMGCR	cis	cerebellum	SCAN
rs10057967	DMGDH	cis	parietal	SCAN

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74965000-74998000	Weak transcription	Fetal Brain Female	brain
2	chr5:74965200-75011800	Weak transcription	Brain Germinal Matrix	brain
3	chr5:74965400-74997800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr5:74965400-75012400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:74965400-75012400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr5:74965400-75012400	Weak transcription	Right Ventricle	heart
7	chr5:74965600-74998200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr5:74965600-74998200	Weak transcription	Fetal Heart	heart
9	chr5:74965600-75010400	Weak transcription	Gastric	stomach
10	chr5:74965600-75011400	Weak transcription	Small Intestine	intestine
11	chr5:74966000-74998400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr5:74968800-74998400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr5:74971200-75012400	Weak transcription	Aorta	Aorta
14	chr5:74971200-75012400	Weak transcription	Brain Substantia Nigra	brain
15	chr5:74974400-74997800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr5:74976600-74998200	Weak transcription	Colonic Mucosa	Colon
17	chr5:74977200-74997800	Weak transcription	Brain Angular Gyrus	brain
18	chr5:74977400-74997800	Weak transcription	NHDF-Ad	bronchial
19	chr5:74979000-75003800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:74979800-74998400	Weak transcription	Ovary	ovary
21	chr5:74980000-75012200	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr5:74981400-74997800	Weak transcription	Brain Hippocampus Middle	brain
23	chr5:74981400-74997800	Weak transcription	Spleen	Spleen
24	chr5:74981400-74999200	Weak transcription	Fetal Stomach	stomach
25	chr5:74981400-74999600	Weak transcription	Fetal Intestine Small	intestine
26	chr5:74981400-75002600	Weak transcription	Pancreas	Pancrea
27	chr5:74984200-75012400	Weak transcription	Brain Cingulate Gyrus	brain
28	chr5:74985000-74997800	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr5:74985000-74997800	Weak transcription	Brain Anterior Caudate	brain
30	chr5:74985000-74997800	Weak transcription	HMEC	breast
31	chr5:74985400-74998400	Weak transcription	HSMM	muscle
32	chr5:74985600-74998000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr5:74986400-74998400	Weak transcription	Left Ventricle	heart
34	chr5:74986600-74997800	Weak transcription	A549	lung
35	chr5:74986800-74997800	Weak transcription	Fetal Muscle Leg	muscle
36	chr5:74986800-74997800	Weak transcription	Lung	lung
37	chr5:74986800-74998200	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr5:74986800-74998400	Weak transcription	NH-A	brain
39	chr5:74986800-75000000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr5:74986800-75005800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr5:74987800-75002600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr5:74990000-74997800	Weak transcription	Colon Smooth Muscle	Colon
43	chr5:74990000-74997800	Weak transcription	Fetal Muscle Trunk	muscle
44	chr5:74990000-74997800	Weak transcription	Thymus	Thymus
45	chr5:74990000-74998200	Weak transcription	Hela-S3	cervix
46	chr5:74990000-75012000	Weak transcription	HSMMtube	muscle
47	chr5:74990000-75012400	Weak transcription	Esophagus	oesophagus
48	chr5:74990200-74997800	Weak transcription	Primary B cells from cord blood	blood
49	chr5:74990200-74997800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr5:74990200-74998000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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