Variant report

Variant	rs7312698
Chromosome Location	chr12:32554695-32554696
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1045751	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10771942	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10771943	0.82[ASN][1000 genomes]
rs10844197	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10844198	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1128591	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12367488	0.87[EUR][1000 genomes]
rs167806	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs186568	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs188978	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs188979	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2062600	0.99[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2253235	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2253237	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2253247	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2450506	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2455004	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2455005	0.82[EUR][1000 genomes]
rs2632326	0.87[EUR][1000 genomes]
rs2632330	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2632337	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2632363	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2651365	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2651366	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2651367	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2651368	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2651371	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2651372	0.88[EUR][1000 genomes]
rs2651374	0.88[EUR][1000 genomes]
rs2651375	0.88[EUR][1000 genomes]
rs2651376	0.88[EUR][1000 genomes]
rs2651377	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2651380	0.87[EUR][1000 genomes]
rs2728675	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2728676	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2728678	0.90[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2728679	0.84[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2728681	0.80[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs2728689	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2728690	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2733683	0.93[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2733694	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2733696	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2733698	0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2733703	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2733704	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2733705	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2931554	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs325418	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs325419	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs325420	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs325421	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs325423	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs325424	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4931622	0.97[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs4931624	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4931625	0.95[ASN][1000 genomes]
rs56146365	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61927173	0.82[ASN][1000 genomes]
rs7298319	0.82[EUR][1000 genomes]
rs7298381	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7315762	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7315797	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7963401	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv558171	chr12:32287259-32559693	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv469346	chr12:32531220-32587465	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv558188	chr12:32531220-32587465	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1054191	chr12:32534619-32733066	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv541455	chr12:32534619-32733066	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	esv3342938	chr12:32551041-32716745	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7312698	BICD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32551200-32554800	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr12:32551800-32554800	Active TSS	H1 Cell Line	embryonic stem cell
3	chr12:32551800-32555200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:32552000-32554800	Active TSS	Fetal Intestine Small	intestine
5	chr12:32552000-32555200	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr12:32552000-32555400	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr12:32553000-32554800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:32553200-32555600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:32553400-32555200	Active TSS	Duodenum Mucosa	Duodenum
10	chr12:32553400-32555200	Weak transcription	Lung	lung
11	chr12:32553400-32572200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr12:32553400-32572200	Weak transcription	HSMMtube	muscle
13	chr12:32553400-32572400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:32553600-32554800	Enhancers	Liver	Liver
15	chr12:32553600-32555000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:32553600-32555200	Weak transcription	Gastric	stomach
17	chr12:32553600-32555200	Weak transcription	Pancreas	Pancrea
18	chr12:32553600-32556000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr12:32553600-32572600	Weak transcription	Esophagus	oesophagus
20	chr12:32553800-32556000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr12:32553800-32571600	Weak transcription	Left Ventricle	heart
22	chr12:32554000-32554800	Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr12:32554000-32555200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr12:32554000-32555200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr12:32554000-32572200	Weak transcription	Right Ventricle	heart
26	chr12:32554200-32555000	Weak transcription	HUVEC	blood vessel
27	chr12:32554200-32555200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr12:32554200-32555600	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr12:32554200-32556000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr12:32554200-32556000	Enhancers	NHEK	skin
31	chr12:32554200-32559600	Weak transcription	A549	lung
32	chr12:32554200-32561200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr12:32554200-32566400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr12:32554200-32571800	Weak transcription	Ovary	ovary
35	chr12:32554200-32573800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:32554400-32554800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr12:32554400-32555200	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr12:32554400-32555200	Enhancers	Placenta	Placenta
39	chr12:32554400-32555800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:32554400-32556800	Weak transcription	Colonic Mucosa	Colon
41	chr12:32554400-32559800	Weak transcription	Psoas Muscle	Psoas
42	chr12:32554600-32554800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:32554600-32554800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr12:32554600-32555000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr12:32554600-32555200	Weak transcription	Adipose Nuclei	Adipose
46	chr12:32554600-32555200	Weak transcription	Stomach Mucosa	stomach
47	chr12:32554600-32555200	Weak transcription	HMEC	breast
48	chr12:32554600-32555600	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr12:32554600-32556000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:32554600-32556200	Weak transcription	Placenta Amnion	Placenta Amnion

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