Variant report

Variant	rs12119130
Chromosome Location	chr1:180073548-180073549
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:180072424..180075289-chr1:180122422..180124952,2	K562	blood:
2	chr1:180072332..180074269-chr1:180079268..180081019,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000116260	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10913920	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10913939	1.00[CHB][hapmap]
rs12091464	1.00[CHB][hapmap]
rs12116940	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12118265	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12118985	0.84[EUR][1000 genomes]
rs12121834	0.84[EUR][1000 genomes]
rs12121845	0.84[EUR][1000 genomes]
rs12125245	0.89[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12125556	0.84[EUR][1000 genomes]
rs12125592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12125693	0.84[EUR][1000 genomes]
rs12126496	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12126967	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12127784	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12129115	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12130479	0.82[EUR][1000 genomes]
rs12130489	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12130673	1.00[ASN][1000 genomes]
rs12131200	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12133136	1.00[ASN][1000 genomes]
rs12134536	0.84[EUR][1000 genomes]
rs12138201	0.84[EUR][1000 genomes]
rs12138429	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12138974	0.83[EUR][1000 genomes]
rs12139040	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12139761	0.81[EUR][1000 genomes]
rs12140235	0.84[EUR][1000 genomes]
rs12140622	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12140868	0.84[EUR][1000 genomes]
rs12141134	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12144328	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12144346	1.00[CHB][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12144352	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12144853	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12184265	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12184270	0.82[EUR][1000 genomes]
rs16843139	0.84[EUR][1000 genomes]
rs16855125	0.81[CEU][hapmap]
rs16855268	0.83[EUR][1000 genomes]
rs16855270	0.84[EUR][1000 genomes]
rs17299006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17371159	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17371267	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17371308	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17855475	1.00[CHB][hapmap]
rs1801795	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3856049	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3889149	1.00[CHB][hapmap]
rs4460595	0.82[EUR][1000 genomes]
rs60972670	0.84[EUR][1000 genomes]
rs73034486	0.82[EUR][1000 genomes]
rs9701232	1.00[ASN][1000 genomes]
rs9701237	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429936	chr1:179790343-180214343	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv872573	chr1:179929388-180093066	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv520278	chr1:179945390-180093066	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1003739	chr1:180027760-180483292	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS 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	67 gene(s)	inside rSNPs	diseases
5	nsv535217	chr1:180027760-180483292	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
6	nsv1012558	chr1:180027960-180217613	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv535218	chr1:180027960-180217613	Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv497930	chr1:180031321-180220723	Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv533073	chr1:180031328-180217612	Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
10	nsv916937	chr1:180031328-180220685	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12119130	CEP350	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179970800-180076800	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr1:179983600-180083400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:180000800-180083400	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:180002400-180085000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:180013000-180080000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr1:180029600-180084800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:180040800-180082200	Strong transcription	Primary B cells from peripheral blood	blood
8	chr1:180042000-180082600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr1:180044800-180077200	Weak transcription	Small Intestine	intestine
10	chr1:180048800-180082200	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr1:180049000-180076800	Strong transcription	Primary B cells from cord blood	blood
12	chr1:180052800-180082600	Strong transcription	Fetal Thymus	thymus
13	chr1:180052800-180085800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:180053000-180083000	Strong transcription	Liver	Liver
15	chr1:180054000-180082600	Strong transcription	Dnd41	blood
16	chr1:180054600-180079400	Weak transcription	Fetal Brain Male	brain
17	chr1:180057600-180082600	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:180057600-180082800	Strong transcription	Adipose Nuclei	Adipose
19	chr1:180059200-180076000	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr1:180059600-180073600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:180062600-180079600	Weak transcription	Fetal Heart	heart
22	chr1:180064400-180079400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:180065000-180078400	Weak transcription	Spleen	Spleen
24	chr1:180065000-180079400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr1:180065000-180079400	Weak transcription	Psoas Muscle	Psoas
26	chr1:180065000-180079400	Weak transcription	NHLF	lung
27	chr1:180065000-180080000	Weak transcription	NHEK	skin
28	chr1:180065000-180080200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:180065200-180078600	Weak transcription	Brain Angular Gyrus	brain
30	chr1:180065400-180080000	Weak transcription	HMEC	breast
31	chr1:180066200-180079400	Weak transcription	Colonic Mucosa	Colon
32	chr1:180066200-180079400	Weak transcription	Stomach Mucosa	stomach
33	chr1:180066200-180082200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:180066400-180075200	Weak transcription	HSMMtube	muscle
35	chr1:180066400-180077200	Weak transcription	Brain Substantia Nigra	brain
36	chr1:180066400-180079600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr1:180066400-180080000	Weak transcription	Brain Germinal Matrix	brain
38	chr1:180066400-180080200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr1:180066600-180079200	Weak transcription	NH-A	brain
40	chr1:180066600-180079400	Weak transcription	Brain Anterior Caudate	brain
41	chr1:180067200-180073600	Weak transcription	HepG2	liver
42	chr1:180067800-180077400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:180067800-180078400	Weak transcription	Pancreas	Pancrea
44	chr1:180068000-180074000	Weak transcription	Ovary	ovary
45	chr1:180068000-180079600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr1:180068200-180078800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr1:180068200-180080200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr1:180068400-180074000	Weak transcription	Fetal Kidney	kidney
49	chr1:180068600-180074000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr1:180068600-180079000	Weak transcription	Hela-S3	cervix

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