Variant report

Variant	rs8014337
Chromosome Location	chr14:70152769-70152770
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:70135430..70139006-chr14:70149542..70153148,4	MCF-7	breast:
2	chr14:70145323..70149322-chr14:70149877..70152985,4	MCF-7	breast:
3	chr14:70145783..70147481-chr14:70150839..70153157,2	K562	blood:
4	chr14:70151659..70153320-chr14:70179595..70181137,2	MCF-7	breast:
5	chr14:70148349..70149989-chr14:70151546..70154474,2	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11844109	0.84[AFR][1000 genomes]
rs11844442	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs11845451	1.00[AFR][1000 genomes]
rs11846535	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11847303	1.00[ASW][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs11848538	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11849303	0.94[AFR][1000 genomes]
rs6573896	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs7155876	0.94[AFR][1000 genomes]
rs7156989	0.82[AFR][1000 genomes]
rs7160036	0.82[AFR][1000 genomes]
rs8004755	1.00[AFR][1000 genomes]
rs8009791	1.00[AFR][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	nsv1049280	chr14:70036804-70172630	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv542124	chr14:70036804-70172630	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
4	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70146600-70153200	Enhancers	Colon Smooth Muscle	Colon
2	chr14:70146800-70153200	Enhancers	Duodenum Smooth Muscle	Duodenum
3	chr14:70146800-70153600	Enhancers	Fetal Muscle Leg	muscle
4	chr14:70146800-70153800	Enhancers	Brain Anterior Caudate	brain
5	chr14:70146800-70155600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr14:70147000-70152800	Enhancers	Primary B cells from peripheral blood	blood
7	chr14:70147000-70153000	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr14:70147000-70153200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr14:70147200-70152800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr14:70147200-70152800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:70148200-70152800	Enhancers	Left Ventricle	heart
12	chr14:70148200-70152800	Enhancers	Spleen	Spleen
13	chr14:70148200-70153000	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr14:70148400-70152800	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr14:70148400-70156800	Enhancers	HepG2	liver
16	chr14:70148600-70153000	Enhancers	Primary T cells fromperipheralblood	blood
17	chr14:70148600-70153000	Enhancers	Psoas Muscle	Psoas
18	chr14:70148600-70153000	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr14:70148600-70155800	Enhancers	Fetal Thymus	thymus
20	chr14:70148800-70152800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr14:70148800-70152800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr14:70148800-70153000	Enhancers	Small Intestine	intestine
23	chr14:70148800-70153200	Enhancers	Brain Angular Gyrus	brain
24	chr14:70148800-70153600	Enhancers	Brain Substantia Nigra	brain
25	chr14:70148800-70156600	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr14:70149000-70152800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr14:70149000-70152800	Enhancers	Duodenum Mucosa	Duodenum
28	chr14:70149000-70152800	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr14:70149000-70153200	Enhancers	Adipose Nuclei	Adipose
30	chr14:70149000-70153400	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr14:70149000-70153600	Enhancers	Rectal Smooth Muscle	rectum
32	chr14:70149200-70153600	Enhancers	Brain Cingulate Gyrus	brain
33	chr14:70149200-70156200	Enhancers	Brain Hippocampus Middle	brain
34	chr14:70149400-70152800	Enhancers	Esophagus	oesophagus
35	chr14:70149400-70152800	Enhancers	Right Atrium	heart
36	chr14:70149600-70153000	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr14:70149800-70152800	Enhancers	Fetal Muscle Trunk	muscle
38	chr14:70149800-70152800	Enhancers	Gastric	stomach
39	chr14:70149800-70152800	Enhancers	Lung	lung
40	chr14:70149800-70152800	Enhancers	Pancreas	Pancrea
41	chr14:70149800-70153000	Enhancers	Liver	Liver
42	chr14:70149800-70153200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr14:70150000-70154400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:70150200-70154200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:70150200-70161000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr14:70150400-70153000	Enhancers	Fetal Heart	heart
47	chr14:70150600-70153400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr14:70150800-70153600	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr14:70150800-70159800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:70151000-70155200	Weak transcription	Primary hematopoietic stem cells	blood

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