Variant report

Variant	rs9501035
Chromosome Location	chr6:30912414-30912415
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:30883867..30886170-chr6:30910459..30912444,2	K562	blood:
2	chr6:30912250..30916872-chr6:30917864..30923699,9	K562	blood:
3	chr6:30910646..30913427-chr6:30914373..30916457,2	K562	blood:
4	chr6:30850763..30853588-chr6:30910036..30912491,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000233529	Chromatin interaction
ENSG00000204580	Chromatin interaction
ENSG00000137411	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1049622	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1049628	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1052693	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10947111	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10947113	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10947114	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12206075	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12528271	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12697941	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13215246	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13215409	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1419693	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2074508	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2074509	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2074510	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2074511	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2074512	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2229933	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2239517	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2239518	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2240803	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2267641	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2284175	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2284176	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2285319	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2286655	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2286656	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2524236	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2894055	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3213644	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3218802	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3218803	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3218806	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3218814	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3218815	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3757339	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3869085	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3869086	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3909130	0.82[EUR][1000 genomes]
rs3916232	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41288539	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4618569	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4711247	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4711249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4713402	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6457282	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6901464	0.80[AMR][1000 genomes]
rs6924600	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7743661	0.82[EUR][1000 genomes]
rs7756521	0.82[EUR][1000 genomes]
rs7761589	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8408	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs916920	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9295928	0.92[EUR][1000 genomes]
rs9295929	0.82[EUR][1000 genomes]
rs9295930	0.89[EUR][1000 genomes]
rs9295931	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9295932	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9295933	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9295934	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9357102	0.82[EUR][1000 genomes]
rs9366761	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9368646	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9378191	0.82[EUR][1000 genomes]
rs9380200	0.82[EUR][1000 genomes]
rs9380201	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9394021	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9461638	0.82[EUR][1000 genomes]
rs9461639	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9468842	0.82[EUR][1000 genomes]
rs9468843	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9468844	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9468845	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9468846	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9468847	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9501030	0.81[EUR][1000 genomes]
rs9501032	0.82[EUR][1000 genomes]
rs9501340	0.92[EUR][1000 genomes]
rs9501342	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9501491	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
2	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
4	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
5	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
6	nsv1031677	chr6:30857542-30972865	Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv525438	chr6:30864829-30933975	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
8	nsv462743	chr6:30905313-30957766	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv601483	chr6:30905313-30957766	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9501035	HIST1H2AM	cis	cerebellum	SCAN
rs9501035	VARS2	cis	lymphoblastoid	seeQTL

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30910400-30913800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:30911000-30913800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr6:30911000-30913800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:30911000-30919000	Weak transcription	Right Atrium	heart
5	chr6:30911200-30913800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:30911200-30914000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:30911200-30914000	Weak transcription	Stomach Mucosa	stomach
8	chr6:30911400-30915000	Weak transcription	Gastric	stomach

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