Variant report

Variant	rs9257167
Chromosome Location	chr6:28741734-28741735
allele	A/C
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	SUZ12	chr6:28740574-28741749	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:28739105..28742072-chr6:28746732..28748309,2	K562	blood:
2	chr6:28741705..28743702-chr6:28750039..28751986,2	MCF-7	breast:
3	chr6:28739775..28742884-chr6:28756307..28759477,3	K562	blood:

Variant related genes	Relation type
ENSG00000221191	TF binding region
ENSG00000235559	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs1233579	0.96[EUR][1000 genomes]
rs1233580	0.96[EUR][1000 genomes]
rs1233581	0.96[EUR][1000 genomes]
rs1233583	0.96[EUR][1000 genomes]
rs1233593	0.96[EUR][1000 genomes]
rs1233594	0.96[EUR][1000 genomes]
rs1233599	1.00[EUR][1000 genomes]
rs1233600	1.00[EUR][1000 genomes]
rs1233604	1.00[EUR][1000 genomes]
rs1233618	1.00[EUR][1000 genomes]
rs1233620	1.00[EUR][1000 genomes]
rs1233623	1.00[EUR][1000 genomes]
rs1238262	0.96[EUR][1000 genomes]
rs1311911	0.94[EUR][1000 genomes]
rs1311912	0.96[EUR][1000 genomes]
rs1311913	0.96[EUR][1000 genomes]
rs13194504	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13206458	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13217472	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1742743	0.94[EUR][1000 genomes]
rs3118357	0.84[EUR][1000 genomes]
rs3118359	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3118360	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3118361	0.80[EUR][1000 genomes]
rs3118364	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs3118366	0.82[EUR][1000 genomes]
rs3118367	0.84[EUR][1000 genomes]
rs3130838	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3130844	0.80[EUR][1000 genomes]
rs3130892	0.80[EUR][1000 genomes]
rs3131068	0.80[EUR][1000 genomes]
rs3131069	0.80[EUR][1000 genomes]
rs3131071	0.80[EUR][1000 genomes]
rs3131072	0.80[EUR][1000 genomes]
rs3131093	0.82[EUR][1000 genomes]
rs3131094	0.84[EUR][1000 genomes]
rs3131095	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3131096	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3131097	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3131101	0.87[AMR][1000 genomes]
rs3131335	0.82[EUR][1000 genomes]
rs3131336	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3131340	0.87[EUR][1000 genomes]
rs3131341	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3131343	0.89[EUR][1000 genomes]
rs3131345	0.84[EUR][1000 genomes]
rs3132373	0.89[EUR][1000 genomes]
rs3132374	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs3132376	0.84[EUR][1000 genomes]
rs3132378	0.87[AMR][1000 genomes]
rs3132382	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs3132384	0.84[EUR][1000 genomes]
rs3132385	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3132387	0.82[EUR][1000 genomes]
rs3132388	0.84[EUR][1000 genomes]
rs3132389	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3132391	0.84[EUR][1000 genomes]
rs3132392	0.84[EUR][1000 genomes]
rs3132393	0.82[EUR][1000 genomes]
rs3132394	0.82[EUR][1000 genomes]
rs3132395	0.82[EUR][1000 genomes]
rs3132396	0.87[EUR][1000 genomes]
rs3135293	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135294	0.85[EUR][1000 genomes]
rs3135295	0.84[EUR][1000 genomes]
rs3135298	0.82[EUR][1000 genomes]
rs3135299	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3135300	0.84[EUR][1000 genomes]
rs3135302	0.84[EUR][1000 genomes]
rs3135304	0.84[EUR][1000 genomes]
rs3135306	0.84[EUR][1000 genomes]
rs3135307	0.84[EUR][1000 genomes]
rs3135308	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135309	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135310	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135311	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135312	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135313	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135316	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3135318	0.80[EUR][1000 genomes]
rs34724414	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35044849	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35243068	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4324798	0.87[EUR][1000 genomes]
rs4947336	1.00[AMR][1000 genomes]
rs6456835	0.91[EUR][1000 genomes]
rs6908726	0.87[EUR][1000 genomes]
rs7760313	0.82[EUR][1000 genomes]
rs7761321	0.89[EUR][1000 genomes]
rs7764642	0.98[EUR][1000 genomes]
rs7766699	0.86[EUR][1000 genomes]
rs7767099	0.89[EUR][1000 genomes]
rs9257133	0.96[EUR][1000 genomes]
rs9257136	0.96[EUR][1000 genomes]
rs9257137	0.96[EUR][1000 genomes]
rs9257140	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9257183	1.00[EUR][1000 genomes]
rs9257184	1.00[EUR][1000 genomes]
rs9257187	1.00[EUR][1000 genomes]
rs9257188	1.00[EUR][1000 genomes]
rs9257189	1.00[EUR][1000 genomes]
rs9257192	1.00[EUR][1000 genomes]
rs9257217	0.89[EUR][1000 genomes]
rs9257223	0.87[EUR][1000 genomes]
rs9257227	0.84[EUR][1000 genomes]
rs9257245	0.82[EUR][1000 genomes]
rs9257262	0.84[EUR][1000 genomes]
rs9257267	0.80[EUR][1000 genomes]
rs9257272	0.84[EUR][1000 genomes]
rs9257331	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9257345	0.87[AMR][1000 genomes]
rs9393926	0.87[EUR][1000 genomes]
rs9393929	0.84[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534089	chr6:28636972-28841640	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9257167	BTN3A2///BTN3A3	Cis_chr	lymphoblastoid	RTeQTL
rs9257167	BTN3A2	Cis_chr	lymphoblastoid	RTeQTL
rs9257167	ZFP57	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28740000-28746000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
2	chr6:28740200-28741800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
3	chr6:28740200-28742000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
4	chr6:28740400-28741800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
5	chr6:28740400-28745200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:28740800-28741800	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr6:28740800-28744400	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:28741000-28745000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
9	chr6:28741200-28743800	Weak transcription	K562	blood
10	chr6:28741400-28742800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:28741400-28743600	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:28741600-28742000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
13	chr6:28741600-28742000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
14	chr6:28741600-28742000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr6:28741600-28743000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:28741600-28743000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:28741600-28744400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell

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