Variant report

Variant	rs7156664
Chromosome Location	chr14:63976756-63976757
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:63970368..63973107-chr14:63976756..63979784,4	MCF-7	breast:
2	chr14:63975181..63977761-chr14:64008340..64011639,4	MCF-7	breast:
3	chr14:63975681..63978384-chr14:64106592..64108679,2	K562	blood:
4	chr14:63975776..63978385-chr14:63991959..63994166,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000261242	Chromatin interaction
ENSG00000140006	Chromatin interaction
ENSG00000154001	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10129182	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10135999	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10220496	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11158494	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1255724	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1255728	1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1255729	1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1255732	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1255734	1.00[ASN][1000 genomes]
rs1255736	1.00[ASN][1000 genomes]
rs1255744	1.00[ASN][1000 genomes]
rs1255745	1.00[ASN][1000 genomes]
rs1255747	1.00[ASN][1000 genomes]
rs1255754	0.96[EUR][1000 genomes]
rs1255780	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1255783	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1255784	0.94[EUR][1000 genomes]
rs17101259	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28420069	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28607114	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28708979	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28744493	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61983965	1.00[ASN][1000 genomes]
rs61995015	1.00[ASN][1000 genomes]
rs6573515	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7141832	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7150291	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7150490	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7158658	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73278655	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74056132	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74056138	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74056139	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74056141	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8003274	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8005767	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs8009130	0.86[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8017413	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8021183	0.88[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs964955	0.96[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	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS 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	49 gene(s)	inside rSNPs	diseases
3	nsv530774	chr14:63591348-64029881	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription 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	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63939000-63976800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:63946200-63976800	Weak transcription	Small Intestine	intestine
3	chr14:63951000-64003200	Weak transcription	Ovary	ovary
4	chr14:63953600-63976800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:63955200-63977000	Weak transcription	Primary B cells from peripheral blood	blood
6	chr14:63955200-63977800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr14:63959000-63976800	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr14:63960000-63978000	Weak transcription	NHLF	lung
9	chr14:63960000-63983400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:63960000-64005000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr14:63960200-63977000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr14:63960200-63983200	Weak transcription	NH-A	brain
13	chr14:63960200-64008600	Weak transcription	HSMMtube	muscle
14	chr14:63960400-63980200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr14:63960400-63980600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr14:63960400-63991000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:63960600-63979800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr14:63960600-63987000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:63961000-63976800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:63962200-63977000	Weak transcription	Dnd41	blood
21	chr14:63962800-63990600	Weak transcription	Right Ventricle	heart
22	chr14:63963200-63977000	Weak transcription	Pancreas	Pancrea
23	chr14:63963200-63980400	Weak transcription	Psoas Muscle	Psoas
24	chr14:63963600-63977800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr14:63963800-63977200	Weak transcription	Primary hematopoietic stem cells	blood
26	chr14:63963800-63977800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr14:63964000-63990400	Weak transcription	Fetal Kidney	kidney
28	chr14:63964200-63981000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr14:63964800-63977000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr14:63965600-63979800	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr14:63965600-63980600	Weak transcription	Rectal Smooth Muscle	rectum
32	chr14:63966000-63980000	Weak transcription	Fetal Lung	lung
33	chr14:63966600-63983200	Weak transcription	Adipose Nuclei	Adipose
34	chr14:63966800-63983200	Weak transcription	Osteobl	bone
35	chr14:63967000-63977200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr14:63967400-63976800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr14:63967600-63986600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr14:63967600-63996400	Weak transcription	Fetal Muscle Trunk	muscle
39	chr14:63967800-63977000	Weak transcription	Fetal Intestine Large	intestine
40	chr14:63968000-63977000	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr14:63968600-63980600	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr14:63969200-63983200	Weak transcription	Left Ventricle	heart
43	chr14:63969200-63984800	Weak transcription	Lung	lung
44	chr14:63969200-63991200	Weak transcription	Right Atrium	heart
45	chr14:63970200-63977000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr14:63970200-64008600	Weak transcription	Aorta	Aorta
47	chr14:63970400-63977200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr14:63970400-63980400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr14:63970600-63980800	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr14:63970800-63979800	Weak transcription	Brain Hippocampus Middle	brain

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