Variant report

Variant	rs7972934
Chromosome Location	chr12:66666893-66666894
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	chr12:66665436..66668089-chr12:66696028..66698258,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000127311	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10748037	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs10784519	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10784520	0.83[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10878396	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs10878397	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10878402	0.83[CEU][hapmap]
rs10878403	0.83[CEU][hapmap]
rs11176115	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11176117	0.89[EUR][1000 genomes]
rs11176120	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11176125	0.83[CEU][hapmap]
rs11610967	0.81[CHB][hapmap]
rs1168324	0.95[EUR][1000 genomes]
rs12146776	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12371662	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12423377	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12818303	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12822967	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1603244	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1816562	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2047236	0.86[EUR][1000 genomes]
rs2047237	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2088169	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2118137	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs289065	0.98[EUR][1000 genomes]
rs6581669	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs7137005	0.98[EUR][1000 genomes]
rs7137378	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7138034	0.87[EUR][1000 genomes]
rs724739	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs724742	0.91[CEU][hapmap];0.98[EUR][1000 genomes]
rs7308068	0.86[CEU][hapmap]
rs7315361	0.96[CEU][hapmap];0.96[EUR][1000 genomes]
rs7959802	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs9971666	0.90[EUR][1000 genomes]

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	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv899216	chr12:66563835-66716844	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer 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
4	nsv976747	chr12:66663300-66669568	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7972934	HELB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66663600-66667400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr12:66663800-66667000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr12:66663800-66667400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:66664400-66673000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr12:66664600-66669800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr12:66664600-66672800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:66664600-66672800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr12:66664600-66673000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr12:66664800-66669600	Weak transcription	Primary T cells from cord blood	blood
10	chr12:66665800-66668800	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr12:66665800-66668800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:66665800-66668800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr12:66666600-66667000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr12:66666600-66667200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr12:66666800-66667400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr12:66666800-66667600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr12:66666800-66667600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr12:66666800-66667600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr12:66666800-66667600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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