Variant report

Variant	rs10143208
Chromosome Location	chr14:35290364-35290365
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:35288901..35291358-chr14:35341201..35343506,2	MCF-7	breast:
2	chr14:35289257..35291894-chr14:35296561..35298664,2	MCF-7	breast:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10131554	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10146953	1.00[AMR][1000 genomes]
rs10147300	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10147386	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10147966	1.00[AMR][1000 genomes]
rs10148768	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10149825	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10151586	1.00[AMR][1000 genomes]
rs10162531	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28489895	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28571108	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28612125	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28613490	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28701139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28735013	0.94[AFR][1000 genomes]
rs9806067	1.00[AMR][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	esv3392700	chr14:34989406-35365530	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
2	nsv1041857	chr14:35084889-35417180	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
3	nsv1052162	chr14:35245349-35451187	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
4	nsv1053722	chr14:35257458-35465784	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35231200-35291800	Weak transcription	Fetal Brain Male	brain
2	chr14:35232600-35293200	Weak transcription	Fetal Kidney	kidney
3	chr14:35234200-35311600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr14:35252200-35301000	Weak transcription	Psoas Muscle	Psoas
5	chr14:35265000-35296000	Weak transcription	Colon Smooth Muscle	Colon
6	chr14:35267800-35292200	Weak transcription	Right Ventricle	heart
7	chr14:35269200-35298000	Weak transcription	Ovary	ovary
8	chr14:35269400-35322200	Weak transcription	Fetal Brain Female	brain
9	chr14:35269400-35341600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr14:35270400-35303400	Weak transcription	Stomach Mucosa	stomach
11	chr14:35271800-35291400	Weak transcription	Spleen	Spleen
12	chr14:35271800-35326400	Weak transcription	Esophagus	oesophagus
13	chr14:35272000-35296200	Weak transcription	Brain Germinal Matrix	brain
14	chr14:35272200-35291200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr14:35272400-35290800	Weak transcription	Fetal Stomach	stomach
16	chr14:35272400-35300200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr14:35272400-35333600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr14:35274200-35311800	Weak transcription	HSMMtube	muscle
19	chr14:35274400-35296400	Weak transcription	Aorta	Aorta
20	chr14:35274400-35303400	Weak transcription	Left Ventricle	heart
21	chr14:35274400-35312400	Weak transcription	Gastric	stomach
22	chr14:35274600-35293000	Weak transcription	Fetal Lung	lung
23	chr14:35274800-35290800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr14:35274800-35312400	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr14:35275200-35298000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr14:35276200-35307200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr14:35276200-35342400	Weak transcription	Pancreas	Pancrea
28	chr14:35276400-35291200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr14:35276400-35291600	Weak transcription	Thymus	Thymus
30	chr14:35276400-35297800	Weak transcription	Fetal Muscle Trunk	muscle
31	chr14:35276400-35329600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr14:35276400-35330000	Weak transcription	Colonic Mucosa	Colon
33	chr14:35276600-35291200	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr14:35276600-35320000	Weak transcription	Fetal Muscle Leg	muscle
35	chr14:35276800-35293000	Weak transcription	NHLF	lung
36	chr14:35276800-35293600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr14:35276800-35293600	Weak transcription	K562	blood
38	chr14:35277000-35300600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr14:35277000-35307200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr14:35277200-35322000	Weak transcription	Fetal Intestine Large	intestine
41	chr14:35280200-35291800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr14:35280200-35293000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr14:35280200-35294200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr14:35280200-35295800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr14:35280200-35295800	Weak transcription	NHDF-Ad	bronchial
46	chr14:35280400-35293800	Weak transcription	HUVEC	blood vessel
47	chr14:35282000-35300400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr14:35282200-35300000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr14:35282600-35291400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr14:35282600-35294200	Weak transcription	Adipose Nuclei	Adipose

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