Variant report

Variant	rs61604633
Chromosome Location	chr18:12297931-12297932
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr18:12295731..12298495-chr18:12304376..12306859,2	MCF-7	breast:
2	chr18:12293630..12298544-chr18:12303108..12309947,8	K562	blood:
3	chr18:12297799..12300084-chr18:12375103..12377083,2	K562	blood:

Variant related genes	Relation type
ENSG00000176014	Chromatin interaction
ENSG00000141385	Chromatin interaction
ENSG00000199702	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10853224	0.83[EUR][1000 genomes]
rs11080567	0.83[EUR][1000 genomes]
rs11267036	0.87[EUR][1000 genomes]
rs11548177	0.89[EUR][1000 genomes]
rs11660222	0.83[EUR][1000 genomes]
rs11661431	0.80[ASN][1000 genomes]
rs12455756	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12455885	0.84[ASN][1000 genomes]
rs12607250	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12607321	0.81[EUR][1000 genomes]
rs12607378	0.83[EUR][1000 genomes]
rs12954560	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12960267	0.87[EUR][1000 genomes]
rs12960302	0.81[EUR][1000 genomes]
rs12963761	0.89[EUR][1000 genomes]
rs12965912	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28625182	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34685983	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35242253	0.83[EUR][1000 genomes]
rs35959277	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4796958	0.82[EUR][1000 genomes]
rs4796960	0.83[EUR][1000 genomes]
rs4796962	0.81[EUR][1000 genomes]
rs4796963	0.87[EUR][1000 genomes]
rs4797673	0.83[EUR][1000 genomes]
rs4797674	0.83[EUR][1000 genomes]
rs4797675	0.83[EUR][1000 genomes]
rs58136410	0.87[EUR][1000 genomes]
rs62097556	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6505749	0.87[EUR][1000 genomes]
rs6505751	0.83[EUR][1000 genomes]
rs7244254	0.83[EUR][1000 genomes]
rs7244709	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7504558	0.89[EUR][1000 genomes]
rs7504575	0.89[EUR][1000 genomes]
rs7505208	0.83[EUR][1000 genomes]
rs7505255	0.87[EUR][1000 genomes]
rs7505626	0.87[EUR][1000 genomes]
rs8083882	0.83[EUR][1000 genomes]
rs8087843	0.87[EUR][1000 genomes]
rs8098040	0.83[EUR][1000 genomes]
rs8099636	0.83[EUR][1000 genomes]
rs9303766	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9303767	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9303768	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9652931	0.87[EUR][1000 genomes]
rs9807444	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9945901	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9946172	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9946217	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9946347	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9949054	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9954945	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9958069	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9958525	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9964163	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063125	chr18:12046892-12918251	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
2	nsv491873	chr18:12159445-12739784	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
3	nsv909400	chr18:12201374-12585545	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	nsv909401	chr18:12211483-12312075	Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
5	nsv909402	chr18:12211483-12325222	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	nsv909403	chr18:12231060-12325222	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv1061545	chr18:12235999-12328405	Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
8	esv2758471	chr18:12240681-12499525	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	esv2758714	chr18:12240681-12499525	Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	nsv576496	chr18:12247872-12490502	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
11	nsv1058661	chr18:12280366-12313865	Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs61604633	TUBB6	Cis_1M	lymphoblastoid	RTeQTL
rs61604633	MC1R///TUBB3	trans	lymphoblastoid	RTeQTL
rs61604633	TUBB6	cis	Whole Blood	GTEx
rs61604633	TUBB6	cis	multi-tissue	Pritchard

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12289000-12304800	Weak transcription	Pancreas	Pancrea
2	chr18:12289200-12306400	Weak transcription	Right Atrium	heart
3	chr18:12289400-12298200	Weak transcription	Fetal Heart	heart
4	chr18:12289400-12306400	Weak transcription	NHLF	lung
5	chr18:12291600-12301600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr18:12294400-12306200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr18:12296200-12299200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr18:12296800-12302000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr18:12297000-12300600	Weak transcription	K562	blood
10	chr18:12297200-12302000	Weak transcription	Placenta Amnion	Placenta Amnion

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