Variant report

Variant	rs7976195
Chromosome Location	chr12:32526508-32526509
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1058640	0.92[CEU][hapmap]
rs10771940	0.91[CEU][hapmap]
rs10771941	0.94[ASN][1000 genomes]
rs10771943	0.87[CEU][hapmap];0.89[YRI][hapmap];0.80[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs10844193	0.92[CEU][hapmap];0.80[CHB][hapmap]
rs155202	0.85[JPT][hapmap]
rs1809601	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2062600	0.91[CEU][hapmap]
rs2650128	0.82[JPT][hapmap]
rs325416	0.85[JPT][hapmap]
rs325429	0.91[CEU][hapmap]
rs61927173	0.88[EUR][1000 genomes]
rs6488048	1.00[CEU][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6488049	0.91[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7135763	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7298319	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs7307458	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7312128	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7314141	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7964583	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs901599	1.00[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[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	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	nsv438201	chr12:32523455-32531212	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7976195	BICD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32475600-32532400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:32492200-32527400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr12:32492200-32530400	Weak transcription	Thymus	Thymus
4	chr12:32492400-32527200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:32492400-32532000	Weak transcription	Brain Angular Gyrus	brain
6	chr12:32494200-32533800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:32508600-32527000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:32518800-32531800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr12:32519000-32530000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr12:32519000-32530000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr12:32519000-32530000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr12:32519000-32530000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:32519000-32530200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr12:32519000-32530400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr12:32519200-32530200	Weak transcription	HSMM	muscle
16	chr12:32519200-32532000	Weak transcription	NHDF-Ad	bronchial
17	chr12:32520600-32529800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:32520800-32530600	Weak transcription	HSMMtube	muscle
19	chr12:32520800-32532400	Weak transcription	Fetal Intestine Small	intestine
20	chr12:32522400-32530000	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr12:32522400-32532200	Weak transcription	Osteobl	bone
22	chr12:32522600-32527200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr12:32522600-32529000	Weak transcription	Ovary	ovary
24	chr12:32522600-32530400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr12:32522600-32530400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr12:32522600-32535800	Weak transcription	Fetal Brain Female	brain
27	chr12:32522800-32532400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr12:32525800-32529400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:32526400-32527800	Enhancers	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links