Variant report

Variant	rs1264350
Chromosome Location	chr6:30796545-30796546
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30795970..30796922-chr6:31036758..31037281,2	K562	blood:
2	chr6:30795677..30797852-chr6:30845172..30846174,17	K562	blood:
3	chr6:30794974..30797453-chr6:30880816..30883631,3	MCF-7	breast:
4	chr6:30795961..30796892-chr6:31051647..31052371,2	K562	blood:
5	chr6:30787789..30791714-chr6:30792255..30797305,10	K562	blood:
6	chr6:30766881..30768729-chr6:30796268..30797854,2	MCF-7	breast:
7	chr6:30735516..30738178-chr6:30794315..30796554,3	MCF-7	breast:
8	chr6:30796298..30796948-chr6:31010213..31011129,3	MCF-7	breast:
9	chr6:30794499..30796682-chr6:30796946..30799909,4	K562	blood:
10	chr6:30796384..30798794-chr6:30876100..30879027,2	MCF-7	breast:
11	chr6:30796239..30796891-chr6:30844046..30844747,2	K562	blood:
12	chr6:30792900..30798152-chr6:30848587..30855236,10	MCF-7	breast:
13	chr6:30796064..30796722-chr6:30881441..30882257,2	MCF-7	breast:
14	chr6:30796027..30796900-chr6:30881469..30882333,4	MCF-7	breast:
15	chr6:30794216..30799803-chr6:30838849..30846731,16	K562	blood:
16	chr6:30793814..30798702-chr6:30880453..30884092,5	K562	blood:
17	chr6:30787837..30792214-chr6:30792255..30797817,7	K562	blood:
18	chr6:30795223..30797850-chr6:30849493..30851248,2	K562	blood:
19	chr6:30796035..30796933-chr6:31047284..31048260,5	K562	blood:
20	chr6:30795972..30796653-chr6:31011334..31012075,2	K562	blood:
21	chr6:30794896..30797869-chr6:30842153..30843762,2	K562	blood:
22	chr6:30795980..30796892-chr6:30881457..30882601,3	K562	blood:
23	chr6:30795938..30797474-chr6:30860492..30861360,6	K562	blood:
24	chr6:30709015..30713327-chr6:30792572..30798179,6	K562	blood:
25	chr6:30703666..30722133-chr6:30776009..30801352,184	MCF-7	breast:
26	chr6:30796286..30797094-chr6:31038583..31039101,2	MCF-7	breast:
27	chr3:63497233..63499254-chr6:30795355..30797782,2	MCF-7	breast:
28	chr6:30792780..30797161-chr6:30880651..30883443,6	K562	blood:
29	chr6:30795972..30797365-chr6:30845047..30846130,14	MCF-7	breast:
30	chr6:30780598..30803497-chr6:30842531..30855110,80	MCF-7	breast:
31	chr6:30796535..30799180-chr6:30856343..30859199,3	MCF-7	breast:
32	chr6:30795918..30796957-chr6:30845184..30846122,7	MCF-7	breast:
33	chr6:30796462..30798109-chr6:30809712..30812488,2	K562	blood:
34	chr6:30796335..30796872-chr6:31055400..31055943,2	K562	blood:
35	chr6:30792427..30796566-chr6:30845190..30846951,4	MCF-7	breast:
36	chr6:30703055..30723531-chr6:30783853..30800217,151	MCF-7	breast:
37	chr6:30796461..30798105-chr6:30865985..30868433,2	MCF-7	breast:
38	chr6:30796002..30796914-chr6:30849773..30850471,2	K562	blood:
39	chr6:30794295..30796763-chr6:31046294..31048518,2	K562	blood:
40	chr6:30733982..30738634-chr6:30792613..30796884,6	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000137331	Chromatin interaction
ENSG00000204580	Chromatin interaction
ENSG00000272273	Chromatin interaction
ENSG00000228022	Chromatin interaction
ENSG00000263608	Chromatin interaction
ENSG00000137411	Chromatin interaction
ENSG00000214894	Chromatin interaction
ENSG00000201988	Chromatin interaction
ENSG00000213780	Chromatin interaction
ENSG00000137312	Chromatin interaction
ENSG00000264594	Chromatin interaction
ENSG00000237775	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs11757306	0.86[ASN][1000 genomes]
rs11758183	0.86[ASN][1000 genomes]
rs1264351	0.81[EUR][1000 genomes]
rs1264373	0.81[EUR][1000 genomes]
rs2524266	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28744105	1.00[ASN][1000 genomes]
rs3094086	0.87[EUR][1000 genomes]
rs3095152	0.87[EUR][1000 genomes]
rs3095153	0.85[EUR][1000 genomes]
rs3095338	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3132580	0.88[EUR][1000 genomes]
rs3132581	0.88[EUR][1000 genomes]
rs55745908	0.86[ASN][1000 genomes]
rs57065637	1.00[ASN][1000 genomes]
rs57817411	1.00[ASN][1000 genomes]
rs58554612	1.00[ASN][1000 genomes]
rs58594197	1.00[ASN][1000 genomes]
rs6457281	0.86[ASN][1000 genomes]
rs6930910	0.86[ASN][1000 genomes]
rs73425726	1.00[ASN][1000 genomes]
rs73432796	1.00[ASN][1000 genomes]
rs73432800	1.00[ASN][1000 genomes]
rs73434604	1.00[ASN][1000 genomes]
rs73434608	1.00[ASN][1000 genomes]
rs73437885	1.00[ASN][1000 genomes]
rs7746003	0.86[ASN][1000 genomes]
rs7751952	0.86[ASN][1000 genomes]
rs7759803	0.86[ASN][1000 genomes]
rs9262174	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	esv3430377	chr6:30443802-30814426	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	967 gene(s)	inside rSNPs	diseases
5	esv2758041	chr6:30644693-30816319	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
6	esv2759413	chr6:30644693-30816319	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	223 gene(s)	inside rSNPs	diseases
7	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
8	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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1264350	HLA-C	Cis_1M	lymphoblastoid	RTeQTL
rs1264350	HIST1H2BM	cis	cerebellum	SCAN

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30782000-30797000	Weak transcription	Gastric	stomach
2	chr6:30794400-30798400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:30794400-30798400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:30794600-30796600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:30794600-30796800	Enhancers	Fetal Intestine Large	intestine
6	chr6:30794600-30796800	Enhancers	Stomach Mucosa	stomach
7	chr6:30794600-30796800	Enhancers	HUVEC	blood vessel
8	chr6:30794600-30796800	Enhancers	NH-A	brain
9	chr6:30794600-30797200	Enhancers	HMEC	breast
10	chr6:30794600-30797400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:30794800-30796800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:30794800-30796800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:30794800-30796800	Enhancers	GM12878-XiMat	blood
14	chr6:30794800-30797000	Enhancers	NHLF	lung
15	chr6:30794800-30797200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:30794800-30797200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:30794800-30797200	Enhancers	Colonic Mucosa	Colon
18	chr6:30794800-30797200	Enhancers	Psoas Muscle	Psoas
19	chr6:30794800-30797400	Enhancers	Placenta	Placenta
20	chr6:30794800-30797800	Enhancers	Dnd41	blood
21	chr6:30795000-30796600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:30795000-30798800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:30795000-30799000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr6:30795200-30798800	Flanking Active TSS	Thymus	Thymus
25	chr6:30795400-30797000	Enhancers	Esophagus	oesophagus
26	chr6:30795600-30797800	Enhancers	Primary hematopoietic stem cells	blood
27	chr6:30795600-30798000	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr6:30795800-30796800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:30795800-30796800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr6:30795800-30796800	Enhancers	Aorta	Aorta
31	chr6:30795800-30796800	Enhancers	Brain Cingulate Gyrus	brain
32	chr6:30795800-30796800	Enhancers	Brain Hippocampus Middle	brain
33	chr6:30795800-30796800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr6:30795800-30796800	Enhancers	Fetal Heart	heart
35	chr6:30795800-30796800	Enhancers	Placenta Amnion	Placenta Amnion
36	chr6:30795800-30796800	Enhancers	Right Atrium	heart
37	chr6:30795800-30796800	Enhancers	Right Ventricle	heart
38	chr6:30795800-30797000	Enhancers	Brain Angular Gyrus	brain
39	chr6:30795800-30797000	Enhancers	Brain Substantia Nigra	brain
40	chr6:30795800-30797000	Enhancers	Fetal Kidney	kidney
41	chr6:30795800-30797000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr6:30795800-30797000	Enhancers	Fetal Muscle Leg	muscle
43	chr6:30795800-30797000	Enhancers	Fetal Stomach	stomach
44	chr6:30795800-30797000	Enhancers	Left Ventricle	heart
45	chr6:30795800-30797000	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr6:30795800-30797000	Enhancers	NHDF-Ad	bronchial
47	chr6:30795800-30797200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr6:30795800-30797600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr6:30795800-30797600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
50	chr6:30795800-30798000	Enhancers	HUES6 Cell Line	embryonic stem cell

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