Variant report

Variant	rs6737308
Chromosome Location	chr2:172872042-172872043
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:172870841..172873802-chr2:172876022..172878107,2	MCF-7	breast:
2	chr2:172749558..172752378-chr2:172870357..172872482,2	K562	blood:
3	chr2:172869928..172872436-chr2:172950140..172951979,2	MCF-7	breast:
4	chr2:172871676..172873421-chr2:172883167..172884730,2	K562	blood:

Variant related genes	Relation type
ENSG00000115840	Chromatin interaction
ENSG00000144355	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1008151	0.83[CHB][hapmap]
rs11675404	0.92[CHB][hapmap];0.81[JPT][hapmap]
rs11695630	0.83[CHB][hapmap]
rs12987931	0.92[CHB][hapmap];0.83[CHD][hapmap]
rs13020884	0.83[CHB][hapmap];0.83[CHD][hapmap]
rs1965160	0.92[CHB][hapmap]
rs1996424	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs4581870	1.00[CHB][hapmap];0.91[JPT][hapmap]
rs55653103	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62183769	0.82[ASN][1000 genomes]
rs62183770	0.82[ASN][1000 genomes]
rs62183782	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62183783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62183784	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62183785	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62183800	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62183801	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6715929	0.81[CEU][hapmap]
rs6718013	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6729945	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6730085	1.00[ASW][hapmap];0.85[CHB][hapmap];0.91[CHD][hapmap];0.98[GIH][hapmap];0.91[JPT][hapmap];0.86[TSI][hapmap];0.94[YRI][hapmap];0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6733794	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6746701	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7557612	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7584187	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.87[TSI][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7598246	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875410	chr2:172693780-172896587	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv875411	chr2:172693780-172942448	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	esv2830399	chr2:172781830-172952526	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv1012188	chr2:172855923-172928891	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv3031	chr2:172867462-172884232	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs6737308	AC068039.4	cis	Adipose Subcutaneous	GTEx
rs6737308	DYNC1I2	cis	cerebellum	SCAN
rs6737308	SLC25A12	cis	parietal	SCAN
rs6737308	AC068039.4	cis	Muscle Skeletal	GTEx
rs6737308	AC068039.4	cis	Thyroid	GTEx
rs6737308	AC068039.4	cis	Esophagus Muscularis	GTEx
rs6737308	SLC25A12	cis	cerebellum	SCAN
rs6737308	MAP1D	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172865200-172886600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:172865400-172877200	Weak transcription	Pancreas	Pancrea
3	chr2:172865400-172878000	Weak transcription	Gastric	stomach
4	chr2:172865600-172875200	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr2:172865600-172876600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr2:172865600-172877200	Weak transcription	Psoas Muscle	Psoas
7	chr2:172865600-172878000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:172865600-172897400	Weak transcription	Primary T cells from cord blood	blood
9	chr2:172865800-172876600	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr2:172865800-172877200	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr2:172865800-172877600	Weak transcription	Fetal Kidney	kidney
12	chr2:172865800-172878000	Weak transcription	Primary B cells from cord blood	blood
13	chr2:172865800-172886400	Weak transcription	Fetal Intestine Small	intestine
14	chr2:172865800-172886600	Weak transcription	Stomach Smooth Muscle	stomach
15	chr2:172866000-172872600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr2:172866000-172873600	Weak transcription	Fetal Lung	lung
17	chr2:172866000-172876400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr2:172866000-172877200	Weak transcription	Ovary	ovary
19	chr2:172866000-172877600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr2:172866000-172877800	Weak transcription	HSMM	muscle
21	chr2:172866000-172878000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr2:172866000-172886800	Weak transcription	HSMMtube	muscle
23	chr2:172866200-172876400	Weak transcription	Dnd41	blood
24	chr2:172866200-172877000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr2:172866400-172875800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr2:172866800-172882600	Weak transcription	K562	blood
27	chr2:172869600-172877200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr2:172870000-172875400	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr2:172872000-172873800	Enhancers	HepG2	liver

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