Variant report

Variant	rs1386111
Chromosome Location	chr8:91981189-91981190
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:91974810..91977533-chr8:91979660..91982481,3	K562	blood:
2	chr8:91975435..91977533-chr8:91979660..91982457,2	K562	blood:
3	chr8:91980784..91984297-chr8:91985650..91987857,3	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1003996	0.95[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10086609	0.84[GIH][hapmap]
rs10108486	0.84[YRI][hapmap];0.90[ASN][1000 genomes]
rs10108616	0.83[MEX][hapmap]
rs10112439	0.81[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.90[MKK][hapmap];0.93[TSI][hapmap];0.88[ASN][1000 genomes]
rs1011254	0.95[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.81[ASN][1000 genomes]
rs10956781	0.84[GIH][hapmap]
rs10956782	0.84[GIH][hapmap]
rs1125229	0.83[MEX][hapmap]
rs1160329	0.83[MEX][hapmap]
rs12675931	0.82[ASN][1000 genomes]
rs13265644	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.88[ASN][1000 genomes]
rs1354519	0.83[MEX][hapmap]
rs1386107	0.83[MEX][hapmap]
rs1386112	0.95[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.81[ASN][1000 genomes]
rs1463920	0.84[GIH][hapmap]
rs1486465	0.96[MEX][hapmap];0.86[TSI][hapmap]
rs1504795	0.83[MEX][hapmap]
rs1542666	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1552397	0.83[MEX][hapmap]
rs16905444	0.84[GIH][hapmap]
rs2054805	0.94[GIH][hapmap];0.90[TSI][hapmap]
rs2101378	0.83[MEX][hapmap]
rs2129260	0.83[MEX][hapmap]
rs2129261	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2255173	0.96[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2339289	1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.92[TSI][hapmap];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2339291	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2631012	0.81[ASN][1000 genomes]
rs2631014	0.81[ASN][1000 genomes]
rs2631017	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2631024	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2631027	0.86[ASN][1000 genomes]
rs2631030	0.83[ASN][1000 genomes]
rs2631033	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2677573	1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2677580	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2740782	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2740791	0.83[MEX][hapmap]
rs2740795	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2740799	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4448231	0.90[ASN][1000 genomes]
rs4634599	0.90[ASN][1000 genomes]
rs6471261	0.83[MEX][hapmap]
rs6994971	0.83[GIH][hapmap]
rs7005565	0.84[YRI][hapmap];0.90[ASN][1000 genomes]
rs7018395	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7825360	0.90[ASN][1000 genomes]
rs7828122	0.94[GIH][hapmap];0.90[TSI][hapmap]
rs997899	0.83[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028628	chr8:91680968-92418954	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv539672	chr8:91680968-92418954	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv891185	chr8:91923776-92056288	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1028201	chr8:91968527-92009964	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases
5	esv2758623	chr8:91974499-92273724	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	esv2759629	chr8:91974499-92273724	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1386111	TP53INP1	cis	cerebellum	SCAN
rs1386111	INTS8	cis	cerebellum	SCAN

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91951800-91986400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:91953400-91981400	Weak transcription	HSMM	muscle
3	chr8:91953400-91984600	Weak transcription	NH-A	brain
4	chr8:91958200-91996000	Weak transcription	Fetal Stomach	stomach
5	chr8:91964600-91989800	Weak transcription	Left Ventricle	heart
6	chr8:91964800-91996600	Weak transcription	Ovary	ovary
7	chr8:91971800-91996600	Weak transcription	Thymus	Thymus
8	chr8:91975400-91991000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:91976800-91981200	Weak transcription	Colon Smooth Muscle	Colon
10	chr8:91977400-91986400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:91977800-91981200	Weak transcription	NHDF-Ad	bronchial
12	chr8:91977800-91981400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:91977800-91996200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:91978000-91981400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:91978000-91982600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr8:91978000-91986600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr8:91978000-91996200	Weak transcription	Right Ventricle	heart
18	chr8:91978000-91996400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr8:91978400-91986600	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr8:91978600-91982400	Weak transcription	Primary T cells from cord blood	blood
21	chr8:91979200-91986400	Weak transcription	Fetal Heart	heart
22	chr8:91979200-91996600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:91979400-91981200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr8:91979400-91981200	Weak transcription	K562	blood
25	chr8:91979400-91981400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr8:91979400-91981800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr8:91979400-91982400	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:91979400-91996400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr8:91979600-91981400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr8:91979600-91981400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:91979600-91996200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr8:91979800-91981200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr8:91979800-91996800	Weak transcription	Adipose Nuclei	Adipose
34	chr8:91980000-91986600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:91980400-91983000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr8:91980400-91983000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr8:91980400-91983200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:91980800-91996400	Weak transcription	Fetal Kidney	kidney
39	chr8:91981000-91981400	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr8:91981000-91981600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:91981000-91982000	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr8:91981000-91983000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr8:91981000-91983000	Strong transcription	Fetal Lung	lung
44	chr8:91981000-91996400	Weak transcription	Osteobl	bone

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links