Variant report

Variant	nsv981766
Chromosome Location	chr7:5263064-5269294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:916)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:5269288-5271056	GM12878	blood:	n/a	n/a
2	CCNT2	chr7:5267871-5267978	K562	blood:	n/a	n/a
3	EGR1	chr7:5266331-5266676	H1-hESC	embryonic stem cell:	n/a	n/a
4	HMGN3	chr7:5266967-5267027	K562	blood:	n/a	n/a
5	MTA3	chr7:5269126-5273517	GM12878	blood:	n/a	n/a
6	NFIC	chr7:5269275-5272280	GM12878	blood:	n/a	n/a
7	PML	chr7:5269170-5272433	GM12878	blood:	n/a	n/a
8	POLR2A	chr7:5269202-5269404	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:5266485-5266626	K562	blood:	n/a	n/a
10	POLR2A	chr7:5263554-5263555	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:5267075-5267206	K562	blood:	n/a	n/a
12	POLR2A	chr7:5267323-5267470	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr7:5265870-5266045	GM12878	blood:	n/a	n/a
14	POLR2A	chr7:5266559-5266634	K562	blood:	n/a	n/a
15	POLR2A	chr7:5262895-5263349	GM12878	blood:	n/a	n/a
16	POLR2A	chr7:5269197-5269394	K562	blood:	n/a	n/a
17	POLR2A	chr7:5263168-5263366	GM12878	blood:	n/a	n/a
18	POLR2A	chr7:5266890-5266906	K562	blood:	n/a	n/a
19	POLR2A	chr7:5262931-5263179	K562	blood:	n/a	n/a
20	POLR2A	chr7:5269241-5269452	HepG2	liver:	n/a	n/a
21	POLR2A	chr7:5267278-5267451	K562	blood:	n/a	n/a
22	POLR2A	chr7:5266400-5266971	GM12878	blood:	n/a	n/a
23	POLR2A	chr7:5262533-5263600	MCF-7	breast:	n/a	n/a
24	POLR2A	chr7:5266423-5267642	K562	blood:	n/a	n/a
25	POLR2A	chr7:5264565-5264588	K562	blood:	n/a	n/a
26	POLR2A	chr7:5267587-5267594	MCF-7	breast:	n/a	n/a
27	POLR2A	chr7:5265456-5265476	MCF-7	breast:	n/a	n/a
28	POLR2A	chr7:5263412-5263450	MCF-7	breast:	n/a	n/a
29	POLR2A	chr7:5263355-5263452	HepG2	liver:	n/a	n/a
30	POLR2A	chr7:5266665-5266676	GM12878	blood:	n/a	n/a
31	POLR2A	chr7:5263322-5263345	HepG2	liver:	n/a	n/a
32	POLR2A	chr7:5269115-5269148	K562	blood:	n/a	n/a
33	POLR2A	chr7:5266995-5267143	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr7:5269156-5269370	MCF-7	breast:	n/a	n/a
35	POLR2A	chr7:5263141-5263527	K562	blood:	n/a	n/a
36	POLR2A	chr7:5266441-5266696	K562	blood:	n/a	n/a
37	POLR2A	chr7:5265654-5265839	GM12878	blood:	n/a	n/a
38	POLR2A	chr7:5269155-5269177	K562	blood:	n/a	n/a
39	POLR2A	chr7:5263217-5263361	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr7:5267891-5268262	K562	blood:	n/a	n/a
41	POLR2A	chr7:5265586-5266046	GM12878	blood:	n/a	n/a
42	POLR2A	chr7:5263068-5263343	MCF-7	breast:	n/a	n/a
43	POLR2A	chr7:5268039-5268646	GM12878	blood:	n/a	n/a
44	RUNX3	chr7:5269090-5271175	GM12878	blood:	n/a	chr7:5270409-5270424
45	SPI1	chr7:5269052-5270028	GM12878	blood:	n/a	n/a
46	YY1	chr7:5269271-5269973	GM12878	blood:	n/a	n/a
47	ZNF384	chr7:5269255-5272135	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5263854-5263904	PrEC	prostate:	n/a
2	chr7:5263854-5263904	PrEC	prostate:	n/a
3	chr7:5265722-5265772	T-47D	breast:	n/a
4	chr7:5269290-5269340	HRCEpiC	kidney:	n/a
5	chr7:5267686-5267736	BE2_C	brain:	n/a
6	chr7:5269290-5269340	Caco-2	colon:	n/a
7	chr7:5269161-5269211	Hela-S3	cervix:	n/a
8	chr7:5267896-5267946	GM12892	blood:	n/a
9	chr7:5269245-5269295	GM12892	blood:	n/a
10	chr7:5265865-5265915	SKMC	muscle:	n/a
11	chr7:5269245-5269295	GM19239	blood:	n/a
12	chr7:5267896-5267946	A549	lung:	n/a
13	chr7:5265623-5265673	HEK293	kidney:	embryo
14	chr7:5267686-5267736	AoSMC	blood vessel:	n/a
15	chr7:5267248-5267298	ovcar-3	ovarian:	n/a
16	chr7:5265623-5265673	HNPCEpiC	eye:	n/a
17	chr7:5267686-5267736	AG10803	skin:	n/a
18	chr7:5267896-5267946	HNPCEpiC	eye:	n/a
19	chr7:5269245-5269295	HNPCEpiC	eye:	n/a
20	chr7:5269290-5269340	AG09319	gingival:	n/a
21	chr7:5267686-5267736	HCF	heart:	n/a
22	chr7:5267994-5268044	AG09319	gingival:	n/a
23	chr7:5263854-5263904	HIPEpiC	eye:	n/a
24	chr7:5267896-5267946	HRPEpiC	eye:	n/a
25	chr7:5267110-5267160	SK-N-SH	brain:	n/a
26	chr7:5263854-5263904	NHBE	bronchial:	n/a
27	chr7:5266987-5267037	LNCaP	prostate:	n/a
28	chr7:5267749-5267799	Jurkat	blood:	n/a
29	chr7:5267994-5268044	U87	brain:	n/a
30	chr7:5267110-5267160	NB4	blood:	n/a
31	chr7:5267994-5268044	HEK293	kidney:	embryo
32	chr7:5269290-5269340	LNCaP	prostate:	n/a
33	chr7:5267749-5267799	GM06990	blood:	n/a
34	chr7:5265722-5265772	HEEpiC	esophagus:	n/a
35	chr7:5267248-5267298	GM12878	blood:	n/a
36	chr7:5267896-5267946	HCT-116	colon:	n/a
37	chr7:5269290-5269340	BJ	skin:	n/a
38	chr7:5267360-5267410	HCF	heart:	n/a
39	chr7:5269245-5269295	ovcar-3	ovarian:	n/a
40	chr7:5267248-5267298	MCF10A-Er-Src	breast:	n/a
41	chr7:5263854-5263904	NHDF-neo	bronchial:	n/a
42	chr7:5266987-5267037	HEEpiC	esophagus:	n/a
43	chr7:5265865-5265915	NT2-D1	testis:	n/a
44	chr7:5269245-5269295	T-47D	breast:	n/a
45	chr7:5269245-5269295	Hela-S3	cervix:	n/a
46	chr7:5267110-5267160	NHDF-neo	bronchial:	n/a
47	chr7:5267994-5268044	Hela-S3	cervix:	n/a
48	chr7:5269161-5269211	CMK	blood:	n/a
49	chr7:5265722-5265772	SAEC	small airway:	n/a
50	chr7:5269161-5269211	HIPEpiC	eye:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5256828..5260008-chr7:5263402..5265413,3	MCF-7	breast:
2	chr7:5265071..5268278-chr7:5269035..5271038,3	K562	blood:
3	chr7:5269235..5271608-chr7:5527076..5528752,3	MCF-7	breast:
4	chr7:5261463..5263943-chr7:5264334..5266476,2	MCF-7	breast:
5	chr7:5261238..5265959-chr7:5267428..5270937,4	K562	blood:
6	chr7:5261169..5263977-chr7:5465004..5466955,3	MCF-7	breast:
7	chr7:5261238..5263855-chr7:5267428..5269480,3	K562	blood:
8	chr7:5265071..5268278-chr7:5269035..5271038,3	K562	blood:
9	chr7:5260514..5264813-chr7:5463021..5466900,4	MCF-7	breast:
10	chr7:5263156..5265370-chr7:5467254..5468780,2	MCF-7	breast:
11	chr7:5261238..5265959-chr7:5267428..5270937,4	K562	blood:

No data

Variant related genes	Relation type
WIPI2	TF binding region
WIPI2	CpG island
ENSG00000273084	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000182095	chromatin interactions
ENSG00000157954	chromatin interactions
ENSG00000234432	chromatin interactions

Extended variants
information (count: 424 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564603868	chr7:5263101-5263102	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs531816780	chr7:5263107-5263108	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs544039765	chr7:5263122-5263123	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs577834822	chr7:5263154-5263155	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs13223581	chr7:5263194-5263195	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs191277595	chr7:5263219-5263220	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs547775480	chr7:5263226-5263227	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs370415899	chr7:5263232-5263233	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs147675080	chr7:5263245-5263246	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs142430680	chr7:5263249-5263250	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs114844265	chr7:5263261-5263262	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs182599552	chr7:5263262-5263263	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs537546467	chr7:5263273-5263274	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs556364226	chr7:5263307-5263308	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs115592056	chr7:5263311-5263312	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs576621768	chr7:5263323-5263324	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs35981530	chr7:5263325-5263326	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs535590322	chr7:5263326-5263327	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs553803839	chr7:5263331-5263332	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs572354764	chr7:5263337-5263338	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs114083464	chr7:5263352-5263353	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs558178796	chr7:5263388-5263389	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs576649555	chr7:5263420-5263421	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs543928046	chr7:5263435-5263436	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs562113685	chr7:5263450-5263451	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs367647995	chr7:5263460-5263461	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs113706273	chr7:5263483-5263484	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs529482566	chr7:5263487-5263488	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs574062937	chr7:5263504-5263505	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs559657006	chr7:5263510-5263511	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs533426805	chr7:5263528-5263529	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs187865188	chr7:5263543-5263544	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs570105416	chr7:5263544-5263545	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs150221356	chr7:5263548-5263549	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs544683984	chr7:5263549-5263550	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs549614784	chr7:5263581-5263582	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs568120903	chr7:5263598-5263599	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs75913586	chr7:5263601-5263602	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs553910446	chr7:5263605-5263606	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs559814477	chr7:5263729-5263730	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs138558775	chr7:5263753-5263754	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs539734028	chr7:5263754-5263755	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs193144806	chr7:5263780-5263781	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs576506491	chr7:5263801-5263802	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs372803994	chr7:5263819-5263820	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs55698647	chr7:5263828-5263829	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184862275	chr7:5263854-5263855	Weak transcription Strong transcription Enhancers	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs117560844	chr7:5263855-5263856	Weak transcription Strong transcription Enhancers	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs545278429	chr7:5263894-5263895	Weak transcription Strong transcription Enhancers	CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs541293755	chr7:5263910-5263911	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21525872	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5231400-5279800	Weak transcription	Fetal Brain Male	brain
2	chr7:5231800-5273400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:5234000-5274800	Weak transcription	Stomach Mucosa	stomach
4	chr7:5237400-5272600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr7:5237400-5273400	Strong transcription	Dnd41	blood
6	chr7:5239000-5267800	Strong transcription	Fetal Intestine Large	intestine
7	chr7:5239000-5270800	Strong transcription	Placenta	Placenta
8	chr7:5241000-5265600	Weak transcription	Psoas Muscle	Psoas
9	chr7:5246400-5271400	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr7:5247800-5270000	Strong transcription	Primary T cells from cord blood	blood
11	chr7:5248400-5273200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:5248800-5267800	Strong transcription	Thymus	Thymus
13	chr7:5248800-5270600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:5248800-5272000	Strong transcription	Rectal Mucosa Donor 29	rectum
15	chr7:5248800-5272200	Strong transcription	Fetal Muscle Leg	muscle
16	chr7:5248800-5272400	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr7:5249000-5269200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr7:5249000-5269200	Strong transcription	Duodenum Mucosa	Duodenum
19	chr7:5249000-5269600	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr7:5249000-5269800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr7:5249000-5271200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr7:5249000-5272600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr7:5249000-5272800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:5249000-5272800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr7:5249000-5273000	Strong transcription	Muscle Satellite Cultured Cells	--
26	chr7:5249000-5273200	Strong transcription	Fetal Muscle Trunk	muscle
27	chr7:5249000-5273600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr7:5249000-5273600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr7:5249200-5269400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:5249200-5271800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:5249200-5272200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr7:5249200-5272400	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:5249200-5272600	Strong transcription	Osteobl	bone
34	chr7:5249200-5272800	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:5249200-5273000	Strong transcription	Stomach Smooth Muscle	stomach
36	chr7:5249200-5273400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:5249200-5273400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr7:5249200-5273400	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr7:5249200-5273400	Strong transcription	Fetal Stomach	stomach
40	chr7:5249200-5273400	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr7:5249200-5273600	Strong transcription	Fetal Intestine Small	intestine
42	chr7:5249400-5272400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr7:5249600-5272800	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr7:5249600-5273400	Strong transcription	Right Ventricle	heart
45	chr7:5249800-5273600	Strong transcription	Fetal Brain Female	brain
46	chr7:5250000-5270000	Strong transcription	Brain Hippocampus Middle	brain
47	chr7:5250000-5270200	Strong transcription	Esophagus	oesophagus
48	chr7:5250200-5269000	Strong transcription	Spleen	Spleen
49	chr7:5250200-5272200	Strong transcription	Ovary	ovary
50	chr7:5250200-5272400	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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