Variant report

Variant	rs7308356
Chromosome Location	chr12:50539611-50539612
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr12:50539586-50540219	MCF-7	breast:	n/a	chr12:50539895-50539902 chr12:50540010-50540018

No.	Distal block	Cell Line	Cell type
1	chr12:50535984..50537611-chr12:50539393..50542341,2	K562	blood:
2	chr12:50529914..50531795-chr12:50537950..50540041,2	K562	blood:
3	chr12:50531935..50534070-chr12:50539130..50540855,2	K562	blood:
4	chr12:50478449..50481902-chr12:50536030..50539935,3	MCF-7	breast:
5	chr12:50497375..50499657-chr12:50539250..50540993,2	K562	blood:

Variant related genes	Relation type
CERS5	TF binding region
ENSG00000066117	Chromatin interaction
ENSG00000167588	Chromatin interaction
ENSG00000139624	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1044370	0.88[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.91[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10747570	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10783342	0.91[YRI][hapmap]
rs11169294	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11169300	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11831413	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12426261	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12815871	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12824125	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12830386	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1862043	0.96[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2178173	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2358538	0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs34573394	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35549836	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35998534	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4883481	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4883482	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56709084	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs646782	0.88[CHB][hapmap]
rs6580729	0.96[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66768395	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs706791	0.88[CHB][hapmap];0.85[JPT][hapmap]
rs706792	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs706793	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs7136570	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7279	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7294548	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7297421	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7301566	0.83[ASN][1000 genomes]
rs7301649	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7301740	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7302981	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7532	0.95[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7967705	0.92[EUR][1000 genomes]
rs7967844	0.93[EUR][1000 genomes]
rs7967954	0.91[YRI][hapmap]
rs7972842	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8181679	0.91[YRI][hapmap]
rs836172	0.88[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs836177	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs836179	0.96[CEU][hapmap];0.86[CHB][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs836180	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs860698	0.88[CHB][hapmap];1.00[JPT][hapmap]

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	nsv1045327	chr12:49975040-50551375	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
2	nsv541490	chr12:49975040-50551375	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
3	nsv530671	chr12:50233858-50708991	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
4	esv3392138	chr12:50394642-50645326	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7308356	LASS5	cis	multi-tissue	Pritchard
rs7308356	CERS5	cis	Nerve Tibial	GTEx

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50517600-50548000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:50524000-50559800	Weak transcription	Right Atrium	heart
3	chr12:50524600-50541600	Weak transcription	Psoas Muscle	Psoas
4	chr12:50528800-50543000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:50529600-50542800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr12:50529800-50543000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:50529800-50559800	Weak transcription	NHLF	lung
8	chr12:50530000-50559600	Weak transcription	A549	lung
9	chr12:50530000-50560200	Weak transcription	Esophagus	oesophagus
10	chr12:50531200-50548400	Weak transcription	HUVEC	blood vessel
11	chr12:50531600-50543200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr12:50531600-50558200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr12:50531800-50544600	Weak transcription	Fetal Kidney	kidney
14	chr12:50531800-50554400	Weak transcription	K562	blood
15	chr12:50531800-50558400	Weak transcription	Fetal Brain Male	brain
16	chr12:50532000-50560200	Weak transcription	Aorta	Aorta
17	chr12:50532000-50560200	Weak transcription	Gastric	stomach
18	chr12:50532400-50541200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr12:50532400-50541400	Weak transcription	Liver	Liver
20	chr12:50532400-50559800	Weak transcription	Spleen	Spleen
21	chr12:50532800-50542200	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr12:50533200-50544800	Weak transcription	Colon Smooth Muscle	Colon
23	chr12:50533200-50559400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr12:50533400-50551200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr12:50534400-50560200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:50534600-50544800	Weak transcription	Ovary	ovary
27	chr12:50535000-50545400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:50535200-50541800	Weak transcription	Lung	lung
29	chr12:50535200-50545000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr12:50535200-50560000	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr12:50535200-50560200	Weak transcription	Right Ventricle	heart
32	chr12:50535400-50559400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr12:50535400-50560000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr12:50536400-50560200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr12:50536800-50545000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr12:50537000-50539800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr12:50537000-50544600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr12:50537200-50558200	Weak transcription	Fetal Brain Female	brain
39	chr12:50537200-50559200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr12:50537400-50543000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr12:50537400-50550600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:50537400-50559400	Weak transcription	Brain Hippocampus Middle	brain
43	chr12:50537400-50560200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr12:50537600-50559400	Weak transcription	Primary B cells from peripheral blood	blood
45	chr12:50537600-50559400	Weak transcription	Stomach Smooth Muscle	stomach
46	chr12:50537800-50544600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:50537800-50545000	Weak transcription	HMEC	breast
48	chr12:50537800-50545200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr12:50537800-50545200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr12:50537800-50547400	Weak transcription	Primary T cells from cord blood	blood

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