Variant report

Variant	rs2451754
Chromosome Location	chr6:26651809-26651810
allele	C/G
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	MAFK	chr6:26651708-26651920	Hela-S3	cervix:	n/a	chr6:26651798-26651813
2	TCF7L2	chr6:26651664-26651864	HepG2	liver:	n/a	n/a
3	MAFK	chr6:26651670-26651957	HepG2	liver:	n/a	chr6:26651798-26651813
4	MAFF	chr6:26651628-26651970	HepG2	liver:	n/a	chr6:26651796-26651814
5	MAFK	chr6:26651787-26651811	H1-hESC	embryonic stem cell:	n/a	n/a
6	MAFK	chr6:26651627-26651982	HepG2	liver:	n/a	chr6:26651798-26651813

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:26649496..26653282-chr6:26658132..26661743,4	MCF-7	breast:

Variant related genes	Relation type
ZNF322	TF binding region
ENSG00000181315	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs2451714	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2451715	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2451716	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2451717	0.82[ASN][1000 genomes]
rs2451739	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2451742	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2451746	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2451749	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2451752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2451753	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2494691	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2494705	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2494706	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2494710	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2494711	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2494714	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2494715	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2498342	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2498343	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3800302	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3807029	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4591839	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6902411	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6911540	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6915555	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6919391	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6931849	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9379902	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9379903	0.90[EUR][1000 genomes];0.82[ASN][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	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs2451754	RP11-457M11.2	cis	lung	GTEx
rs2451754	ZNF322	cis	Adipose Subcutaneous	GTEx
rs2451754	ZNF322	cis	Nerve Tibial	GTEx
rs2451754	ZNF322	cis	Thyroid	GTEx
rs2451754	RP11-457M11.2	cis	Nerve Tibial	GTEx
rs2451754	RP11-457M11.2	cis	Artery Tibial	GTEx
rs2451754	RP11-457M11.2	cis	Thyroid	GTEx
rs2451754	RP11-457M11.2	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26633000-26658000	Weak transcription	Fetal Brain Male	brain
2	chr6:26641400-26659000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:26641400-26659000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:26643400-26652000	Weak transcription	Fetal Stomach	stomach
5	chr6:26643400-26652600	Weak transcription	Ovary	ovary
6	chr6:26643400-26657600	Weak transcription	Right Ventricle	heart
7	chr6:26643400-26658800	Weak transcription	Pancreas	Pancrea
8	chr6:26643400-26659000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:26643400-26659000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr6:26643400-26659000	Weak transcription	Aorta	Aorta
11	chr6:26643400-26659000	Weak transcription	Lung	lung
12	chr6:26643400-26659400	Weak transcription	Esophagus	oesophagus
13	chr6:26643400-26659400	Weak transcription	Gastric	stomach
14	chr6:26643600-26654000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:26643600-26655600	Weak transcription	Left Ventricle	heart
16	chr6:26643600-26657600	Weak transcription	Psoas Muscle	Psoas
17	chr6:26643600-26658000	Weak transcription	Rectal Smooth Muscle	rectum
18	chr6:26643600-26658200	Weak transcription	Brain Germinal Matrix	brain
19	chr6:26643800-26657800	Weak transcription	Stomach Smooth Muscle	stomach
20	chr6:26643800-26658400	Weak transcription	Fetal Heart	heart
21	chr6:26643800-26658400	Weak transcription	Small Intestine	intestine
22	chr6:26644000-26652000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr6:26644000-26654000	Weak transcription	Brain Anterior Caudate	brain
24	chr6:26644000-26656000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr6:26644000-26657600	Weak transcription	Colon Smooth Muscle	Colon
26	chr6:26644000-26657600	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr6:26644000-26658000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr6:26644000-26658000	Weak transcription	Brain Cingulate Gyrus	brain
29	chr6:26644000-26658200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr6:26644000-26658400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr6:26644000-26658400	Weak transcription	Fetal Muscle Leg	muscle
32	chr6:26644200-26658000	Weak transcription	Brain Hippocampus Middle	brain
33	chr6:26644600-26653200	Weak transcription	Placenta	Placenta
34	chr6:26644600-26657600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr6:26644600-26658000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr6:26644600-26659000	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr6:26644800-26652000	Weak transcription	Fetal Muscle Trunk	muscle
38	chr6:26644800-26652600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr6:26644800-26652800	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr6:26644800-26653400	Weak transcription	Fetal Thymus	thymus
41	chr6:26644800-26654000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr6:26644800-26657600	Weak transcription	Brain Angular Gyrus	brain
43	chr6:26644800-26658000	Weak transcription	Thymus	Thymus
44	chr6:26644800-26658000	Weak transcription	Hela-S3	cervix
45	chr6:26644800-26658400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr6:26644800-26658400	Weak transcription	HUVEC	blood vessel
47	chr6:26644800-26658400	Weak transcription	NH-A	brain
48	chr6:26645000-26652600	Weak transcription	Osteobl	bone
49	chr6:26645000-26652800	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr6:26645000-26653000	Weak transcription	Fetal Kidney	kidney

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