Variant report

Variant	nsv960025
Chromosome Location	chr16:71763047-71765882
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:33)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:33 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr16:71763320-71763470	GM12866	blood:	n/a	n/a
2	IRF1	chr16:71763439-71763440	K562	blood:	n/a	n/a
3	MAFF	chr16:71764658-71764903	HepG2	liver:	n/a	chr16:71764756-71764774
4	MAFF	chr16:71764622-71764822	K562	blood:	n/a	chr16:71764756-71764774
5	MAFK	chr16:71764587-71764929	HepG2	liver:	n/a	chr16:71764757-71764772
6	MAFK	chr16:71764636-71764880	IMR90	lung:	n/a	chr16:71764757-71764772
7	MAFK	chr16:71764600-71764811	HepG2	liver:	n/a	chr16:71764757-71764772
8	MAFK	chr16:71764698-71764796	K562	blood:	n/a	chr16:71764757-71764772
9	POLR2A	chr16:71765812-71766068	K562	blood:	n/a	n/a
10	POLR2A	chr16:71763536-71764821	K562	blood:	n/a	n/a
11	POLR2A	chr16:71764233-71764405	MCF-7	breast:	n/a	n/a
12	POLR2A	chr16:71764525-71764867	K562	blood:	n/a	n/a
13	POLR2A	chr16:71764409-71764418	MCF-7	breast:	n/a	n/a
14	POLR2A	chr16:71763941-71764438	K562	blood:	n/a	n/a
15	POLR2A	chr16:71765027-71766628	K562	blood:	n/a	n/a
16	POLR2A	chr16:71765232-71766093	HepG2	liver:	n/a	n/a
17	POLR2A	chr16:71764235-71764429	HepG2	liver:	n/a	n/a
18	POLR2A	chr16:71765222-71765235	MCF-7	breast:	n/a	n/a
19	POLR2A	chr16:71763848-71763856	HepG2	liver:	n/a	n/a
20	POLR2A	chr16:71765085-71765337	K562	blood:	n/a	n/a
21	POLR2A	chr16:71764517-71764556	MCF-7	breast:	n/a	n/a
22	POLR2A	chr16:71760198-71763288	K562	blood:	n/a	n/a
23	POLR2A	chr16:71764225-71764320	HepG2	liver:	n/a	n/a
24	POLR2A	chr16:71763653-71763696	A549	lung:	n/a	n/a
25	POLR2A	chr16:71764566-71764655	MCF-7	breast:	n/a	n/a
26	POLR2A	chr16:71763503-71763660	GM12878	blood:	n/a	n/a
27	POLR2A	chr16:71764496-71764512	MCF-7	breast:	n/a	n/a
28	POLR2A	chr16:71764010-71764172	MCF-7	breast:	n/a	n/a
29	POLR2A	chr16:71764549-71764752	HepG2	liver:	n/a	n/a
30	POLR2A	chr16:71764436-71764487	MCF-7	breast:	n/a	n/a
31	POLR2A	chr16:71764272-71764425	GM12878	blood:	n/a	n/a
32	POLR2A	chr16:71765842-71765973	HepG2	liver:	n/a	n/a
33	POLR2A	chr16:71765049-71765138	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71763859-71763909	GM12878	blood:	n/a
2	chr16:71763859-71763909	AG10803	skin:	n/a
3	chr16:71763859-71763909	RPTEC	kidney:	n/a
4	chr16:71763859-71763909	NT2-D1	testis:	n/a
5	chr16:71763859-71763909	Caco-2	colon:	n/a
6	chr16:71763859-71763909	HCF	heart:	n/a
7	chr16:71763859-71763909	HEK293	kidney:	embryo
8	chr16:71763859-71763909	Hepatocyte	liver:	n/a
9	chr16:71763859-71763909	ProgFib	skin:	n/a
10	chr16:71763859-71763909	SKMC	muscle:	n/a
11	chr16:71763859-71763909	SK-N-SH_RA	brain:	n/a
12	chr16:71763859-71763909	HMEC	breast:	n/a
13	chr16:71763859-71763909	AG04450	lung:	fetal
14	chr16:71763859-71763909	HAEpiC	amniotic membrane:	n/a
15	chr16:71763859-71763909	AG09319	gingival:	n/a
16	chr16:71763859-71763909	GM06990	blood:	n/a
17	chr16:71763859-71763909	LNCaP	prostate:	n/a
18	chr16:71763859-71763909	Jurkat	blood:	n/a
19	chr16:71763859-71763909	ECC-1	luminal epithelium:	n/a
20	chr16:71763859-71763909	PrEC	prostate:	n/a
21	chr16:71763859-71763909	MCF10A-Er-Src	breast:	n/a
22	chr16:71763859-71763909	PFSK-1	brain:	n/a
23	chr16:71763859-71763909	AG04449	skin:	fetal
24	chr16:71763859-71763909	HepG2	liver:	n/a
25	chr16:71763859-71763909	HUVEC	blood vessel:	n/a
26	chr16:71763859-71763909	NHBE	bronchial:	n/a
27	chr16:71763859-71763909	AG09309	skin:	n/a
28	chr16:71763859-71763909	HL-60	blood:	n/a
29	chr16:71763859-71763909	SK-N-SH	brain:	n/a
30	chr16:71763859-71763909	IMR90	lung:	fetal
31	chr16:71763859-71763909	GM12891	blood:	n/a
32	chr16:71763859-71763909	MCF-7	breast:	n/a
33	chr16:71763859-71763909	K562	blood:	n/a
34	chr16:71763859-71763909	SK-N-MC	brain:	n/a
35	chr16:71763859-71763909	NHDF-neo	bronchial:	n/a
36	chr16:71763859-71763909	HEEpiC	esophagus:	n/a
37	chr16:71763859-71763909	HNPCEpiC	eye:	n/a
38	chr16:71763859-71763909	BJ	skin:	n/a
39	chr16:71763859-71763909	NB4	blood:	n/a
40	chr16:71763859-71763909	HIPEpiC	eye:	n/a
41	chr16:71763859-71763909	HCPEpiC	choroid plexus:	n/a
42	chr16:71763859-71763909	ovcar-3	ovarian:	n/a
43	chr16:71763859-71763909	CMK	blood:	n/a
44	chr16:71763859-71763909	SAEC	small airway:	n/a
45	chr16:71763859-71763909	GM12892	blood:	n/a
46	chr16:71763859-71763909	A549	lung:	n/a
47	chr16:71763859-71763909	HCT-116	colon:	n/a
48	chr16:71763859-71763909	PANC-1	pancreas:	n/a
49	chr16:71763859-71763909	Hela-S3	cervix:	n/a
50	chr16:71763859-71763909	HCM	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:71763234..71765356-chr16:71767095..71769996,2	K562	blood:
2	chr16:71761696..71764343-chr16:71777022..71779148,2	MCF-7	breast:
3	chr16:71755935..71758052-chr16:71761285..71763420,2	MCF-7	breast:
4	chr16:71765255..71767670-chr16:71768064..71770223,3	MCF-7	breast:
5	chr16:71755440..71760927-chr16:71762234..71766346,5	K562	blood:
6	chr16:71762201..71765356-chr16:71767095..71769996,3	K562	blood:
7	chr16:71760858..71762927-chr16:71764626..71767390,2	MCF-7	breast:
8	chr16:71756413..71761113-chr16:71764688..71769079,7	K562	blood:
9	chr16:71756698..71758936-chr16:71764476..71768117,3	MCF-7	breast:
10	chr16:71755880..71759578-chr16:71759607..71764621,8	MCF-7	breast:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	AP1G1	hsa-miR-145-5p	chr16:71765846-71765839
2	AP1G1	hsa-miR-145-5p	chr16:71765840-71765860
3	AP1G1	hsa-miR-145-5p	chr16:71763515-71763537
4	AP1G1	hsa-miR-145-5p	chr16:71765228-71765250

Variant related genes	Relation type
PHLPP2	TF binding region
PHLPP2	CpG island
ENSG00000166747	chromatin interactions
ENSG00000260612	chromatin interactions
ENSG00000040199	chromatin interactions
ENSG00000261513	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561082669	chr16:71763059-71763060	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs567566257	chr16:71763061-71763062	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs201592122	chr16:71763062-71763063	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs529350029	chr16:71763085-71763086	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs547580721	chr16:71763121-71763122	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs557088452	chr16:71763135-71763136	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs559913824	chr16:71763136-71763137	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs533933000	chr16:71763246-71763247	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs376878493	chr16:71763281-71763282	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs554147781	chr16:71763303-71763304	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs372592612	chr16:71763335-71763336	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs77169995	chr16:71763354-71763355	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs376107390	chr16:71763355-71763356	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs62053140	chr16:71763356-71763357	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs186147354	chr16:71763630-71763631	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs539443670	chr16:71763647-71763648	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs551393482	chr16:71763665-71763666	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs569990186	chr16:71763687-71763688	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs146039009	chr16:71763688-71763689	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs555503988	chr16:71763699-71763700	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs190126559	chr16:71763711-71763712	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs140023246	chr16:71763712-71763713	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs76621365	chr16:71763779-71763780	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs577708252	chr16:71763817-71763818	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs544657851	chr16:71763826-71763827	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs182774018	chr16:71763833-71763834	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs186018491	chr16:71763887-71763888	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs542953796	chr16:71763979-71763980	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs571298667	chr16:71763982-71763983	Weak transcription Genic enhancers Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs111991984	chr16:71764057-71764058	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs561020317	chr16:71764058-71764059	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs190940597	chr16:71764111-71764112	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs143635575	chr16:71764128-71764129	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs546816143	chr16:71764150-71764151	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs559579789	chr16:71764158-71764159	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs561833390	chr16:71764173-71764174	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs568991320	chr16:71764176-71764177	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs56197651	chr16:71764198-71764199	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs575496425	chr16:71764203-71764204	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs75970052	chr16:71764207-71764208	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs551330343	chr16:71764214-71764215	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs569728309	chr16:71764307-71764308	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs151251378	chr16:71764363-71764364	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs564164518	chr16:71764380-71764381	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs74576731	chr16:71764390-71764391	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs113831755	chr16:71764415-71764416	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs184036267	chr16:71764416-71764417	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs150015997	chr16:71764423-71764424	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs571226927	chr16:71764510-71764511	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs376097642	chr16:71764527-71764528	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Neuroblastoma	18923524	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71758200-71765200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr16:71758200-71766200	Weak transcription	Gastric	stomach
3	chr16:71758400-71763200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr16:71758400-71763400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr16:71758400-71763400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr16:71758400-71763600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr16:71758400-71763800	Weak transcription	Fetal Stomach	stomach
8	chr16:71758400-71763800	Weak transcription	NHDF-Ad	bronchial
9	chr16:71758400-71764000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr16:71758400-71764000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr16:71758400-71764000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr16:71758400-71764200	Weak transcription	HSMM	muscle
13	chr16:71758400-71764200	Weak transcription	HSMMtube	muscle
14	chr16:71758400-71764200	Weak transcription	NH-A	brain
15	chr16:71758400-71764400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr16:71758400-71764400	Weak transcription	Brain Angular Gyrus	brain
17	chr16:71758400-71764400	Weak transcription	Brain Germinal Matrix	brain
18	chr16:71758400-71764400	Weak transcription	Left Ventricle	heart
19	chr16:71758400-71764800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr16:71758400-71765400	Weak transcription	Fetal Brain Female	brain
21	chr16:71758400-71765600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr16:71758400-71765600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr16:71758400-71765600	Weak transcription	Brain Substantia Nigra	brain
24	chr16:71758400-71765600	Weak transcription	Fetal Brain Male	brain
25	chr16:71758400-71765600	Weak transcription	Fetal Lung	lung
26	chr16:71758400-71765600	Weak transcription	Pancreas	Pancrea
27	chr16:71758400-71765600	Weak transcription	Spleen	Spleen
28	chr16:71758400-71765800	Weak transcription	Right Ventricle	heart
29	chr16:71758400-71766200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr16:71758400-71766200	Weak transcription	Psoas Muscle	Psoas
31	chr16:71758400-71766400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr16:71758400-71766400	Weak transcription	Esophagus	oesophagus
33	chr16:71758400-71766400	Weak transcription	Right Atrium	heart
34	chr16:71758400-71771000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr16:71758600-71763200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr16:71758600-71763200	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr16:71758600-71763400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr16:71758600-71763600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr16:71758600-71763600	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr16:71758600-71763600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr16:71758600-71763600	Weak transcription	Placenta	Placenta
42	chr16:71758600-71763600	Weak transcription	Osteobl	bone
43	chr16:71758600-71763800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr16:71758600-71764000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr16:71758600-71764000	Weak transcription	Primary T cells from cord blood	blood
46	chr16:71758600-71764000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr16:71758600-71764000	Weak transcription	Fetal Muscle Leg	muscle
48	chr16:71758600-71764000	Weak transcription	Fetal Thymus	thymus
49	chr16:71758600-71764000	Weak transcription	NHLF	lung
50	chr16:71758600-71764200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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