Variant report

Variant	esv1793797
Chromosome Location	chr8:48955683-48992093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48989035-48989075	K562	blood:	n/a	n/a
2	ARID3A	chr8:48987503-48987712	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48986390-48986586	HepG2	liver:	n/a	n/a
4	ATF1	chr8:48975614-48975808	K562	blood:	n/a	n/a
5	ATF3	chr8:48987856-48987995	K562	blood:	n/a	chr8:48987957-48987966
6	ATF3	chr8:48988882-48989250	K562	blood:	n/a	n/a
7	BACH1	chr8:48988916-48989245	K562	blood:	n/a	n/a
8	BHLHE40	chr8:48987771-48988161	HepG2	liver:	n/a	chr8:48987957-48987966 chr8:48987955-48987968 chr8:48987956-48987965 chr8:48987957-48987966 chr8:48987958-48987967 chr8:48987951-48987972
9	BHLHE40	chr8:48987775-48988051	K562	blood:	n/a	chr8:48987957-48987966 chr8:48987955-48987968 chr8:48987956-48987965 chr8:48987957-48987966 chr8:48987958-48987967 chr8:48987951-48987972
10	CBX3	chr8:48988915-48989393	K562	blood:	n/a	n/a
11	CEBPB	chr8:48988761-48989262	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:48988891-48989038	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:48981714-48981906	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr8:48987402-48988232	IMR90	lung:	n/a	n/a
15	CEBPB	chr8:48984543-48984581	A549	lung:	n/a	n/a
16	CEBPB	chr8:48979594-48979929	A549	lung:	n/a	n/a
17	CEBPB	chr8:48988789-48989066	K562	blood:	n/a	n/a
18	CEBPB	chr8:48986670-48986991	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:48987369-48987570	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:48988840-48989134	A549	lung:	n/a	n/a
21	CEBPB	chr8:48982549-48982607	A549	lung:	n/a	n/a
22	CEBPB	chr8:48957785-48958040	IMR90	lung:	n/a	n/a
23	CTCF	chr8:48958734-48958806	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:48989080-48989230	HMF	breast:	n/a	n/a
25	CTCF	chr8:48965220-48965370	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr8:48984180-48984186	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:48958725-48958798	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:48989080-48989230	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr8:48984055-48984287	K562	blood:	n/a	n/a
30	CTCF	chr8:48984056-48984252	K562	blood:	n/a	n/a
31	CTCF	chr8:48990593-48990646	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr8:48958741-48958781	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:48962960-48963110	A549	lung:	n/a	n/a
34	CTCF	chr8:48967340-48967490	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr8:48984060-48984210	HMF	breast:	n/a	n/a
36	CTCF	chr8:48984191-48984204	MCF-7	breast:	n/a	n/a
37	E2F4	chr8:48975437-48975577	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr8:48987950-48988116	MCF10A-Er-Src	breast:	n/a	n/a
39	EP300	chr8:48989028-48989201	K562	blood:	n/a	n/a
40	FOS	chr8:48986819-48986910	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr8:48987375-48988086	MCF10A-Er-Src	breast:	n/a	chr8:48987588-48987600 chr8:48987589-48987599 chr8:48987590-48987597 chr8:48987589-48987599 chr8:48987590-48987598 chr8:48987589-48987599 chr8:48987895-48987906 chr8:48987897-48987905 chr8:48987590-48987598 chr8:48987589-48987599
42	FOS	chr8:48987457-48988115	MCF10A-Er-Src	breast:	n/a	chr8:48987588-48987600 chr8:48987589-48987599 chr8:48987590-48987597 chr8:48987589-48987599 chr8:48987590-48987598 chr8:48987589-48987599 chr8:48987895-48987906 chr8:48987897-48987905 chr8:48987590-48987598 chr8:48987589-48987599
43	FOS	chr8:48978307-48978488	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr8:48988958-48989225	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr8:48989006-48989242	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr8:48986902-48986905	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:48988911-48989240	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr8:48986889-48986975	MCF10A-Er-Src	breast:	n/a	chr8:48986920-48986930
49	FOS	chr8:48988916-48989225	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:48987423-48988115	MCF10A-Er-Src	breast:	n/a	chr8:48987588-48987600 chr8:48987589-48987599 chr8:48987590-48987597 chr8:48987589-48987599 chr8:48987590-48987598 chr8:48987589-48987599 chr8:48987895-48987906 chr8:48987897-48987905 chr8:48987590-48987598 chr8:48987589-48987599

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48986813-48986863	RPTEC	kidney:	n/a
2	chr8:48973636-48973686	SK-N-MC	brain:	n/a
3	chr8:48986813-48986863	RPTEC	kidney:	n/a
4	chr8:48973636-48973686	SK-N-MC	brain:	n/a
5	chr8:48986813-48986863	GM12878	blood:	n/a
6	chr8:48973636-48973686	HEK293	kidney:	embryo
7	chr8:48973636-48973686	SKMC	muscle:	n/a
8	chr8:48986813-48986863	GM12891	blood:	n/a
9	chr8:48973636-48973686	GM12891	blood:	n/a
10	chr8:48986813-48986863	MCF-7	breast:	n/a
11	chr8:48973636-48973686	ovcar-3	ovarian:	n/a
12	chr8:48986813-48986863	SAEC	small airway:	n/a
13	chr8:48986813-48986863	IMR90	lung:	fetal
14	chr8:48973636-48973686	NB4	blood:	n/a
15	chr8:48986813-48986863	ECC-1	luminal epithelium:	n/a
16	chr8:48986813-48986863	ProgFib	skin:	n/a
17	chr8:48986813-48986863	NH-A	brain:	n/a
18	chr8:48986813-48986863	HIPEpiC	eye:	n/a
19	chr8:48986813-48986863	MCF10A-Er-Src	breast:	n/a
20	chr8:48986813-48986863	HEK293	kidney:	embryo
21	chr8:48986813-48986863	HPAEpiC	pulmonary alveolar:	n/a
22	chr8:48986813-48986863	AoSMC	blood vessel:	n/a
23	chr8:48973636-48973686	RPTEC	kidney:	n/a
24	chr8:48986813-48986863	HCM	heart:	n/a
25	chr8:48986813-48986863	HRE	kidney:	n/a
26	chr8:48986813-48986863	T-47D	breast:	n/a
27	chr8:48973636-48973686	SK-N-SH	brain:	n/a
28	chr8:48986813-48986863	AG04449	skin:	fetal
29	chr8:48986813-48986863	GM12892	blood:	n/a
30	chr8:48973636-48973686	AG04450	lung:	fetal
31	chr8:48986813-48986863	ovcar-3	ovarian:	n/a
32	chr8:48986813-48986863	NB4	blood:	n/a
33	chr8:48973636-48973686	IMR90	lung:	fetal
34	chr8:48986813-48986863	SKMC	muscle:	n/a
35	chr8:48973636-48973686	K562	blood:	n/a
36	chr8:48973636-48973686	SK-N-SH_RA	brain:	n/a
37	chr8:48986813-48986863	AG09309	skin:	n/a
38	chr8:48973636-48973686	AG09319	gingival:	n/a
39	chr8:48973636-48973686	MCF-7	breast:	n/a
40	chr8:48986813-48986863	LNCaP	prostate:	n/a
41	chr8:48986813-48986863	Jurkat	blood:	n/a
42	chr8:48986813-48986863	SK-N-SH_RA	brain:	n/a
43	chr8:48986813-48986863	HepG2	liver:	n/a
44	chr8:48973636-48973686	Jurkat	blood:	n/a
45	chr8:48973636-48973686	T-47D	breast:	n/a
46	chr8:48973636-48973686	SAEC	small airway:	n/a
47	chr8:48973636-48973686	PFSK-1	brain:	n/a
48	chr8:48986813-48986863	PrEC	prostate:	n/a
49	chr8:48986813-48986863	GM06990	blood:	n/a
50	chr8:48986813-48986863	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:48984328..48988098-chr8:48992508..48996504,3	K562	blood:
2	chr8:48871660..48873986-chr8:48986184..48988577,2	MCF-7	breast:
3	chr8:48982765..48984545-chr8:48987553..48989325,2	K562	blood:
4	chr8:48957775..48961134-chr8:48963246..48966717,4	K562	blood:
5	chr8:48957180..48959047-chr8:48960507..48962710,2	K562	blood:
6	chr8:48965207..48966957-chr8:48986549..48988912,2	K562	blood:
7	chr8:48953429..48954984-chr8:48960210..48961992,2	K562	blood:
8	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
9	chr8:48965207..48966957-chr8:48986549..48988912,2	K562	blood:
10	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
11	chr8:48970388..48974071-chr8:48975063..48978866,4	K562	blood:
12	chr8:48957775..48961134-chr8:48963246..48966717,4	K562	blood:
13	chr8:48955264..48957497-chr8:48959787..48961410,2	K562	blood:
14	chr8:48982765..48984545-chr8:48987553..48989325,2	K562	blood:
15	chr8:48987869..48989634-chr8:48998371..48999991,2	MCF-7	breast:
16	chr8:48871629..48874079-chr8:48980802..48983659,2	MCF-7	breast:
17	chr8:48970388..48974071-chr8:48975063..48978866,4	K562	blood:

Variant related genes	Relation type
UBE2V2	TF binding region
UBE2V2	CpG island
ENSG00000169139	chromatin interactions
ENSG00000253729	chromatin interactions
ENSG00000104738	chromatin interactions

Extended variants
information (count: 1274 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1274 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11557776	chr8:48955683-48955684	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563336717	chr8:48955717-48955718	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12680284	chr8:48955783-48955784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575736014	chr8:48955793-48955794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370713340	chr8:48955910-48955911	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568994851	chr8:48955924-48955925	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531424331	chr8:48955945-48955946	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542674289	chr8:48955978-48955979	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550902649	chr8:48956013-48956014	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150449063	chr8:48956018-48956019	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs45480301	chr8:48956039-48956040	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs543402454	chr8:48956075-48956076	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78005154	chr8:48956083-48956084	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569219748	chr8:48956104-48956105	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145361672	chr8:48956114-48956115	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535851488	chr8:48956119-48956120	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529159662	chr8:48956128-48956129	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188826532	chr8:48956176-48956177	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375735305	chr8:48956230-48956231	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149207832	chr8:48956243-48956244	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548817130	chr8:48956322-48956323	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181257048	chr8:48956325-48956326	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs45566233	chr8:48956342-48956343	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537152739	chr8:48956347-48956348	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185319223	chr8:48956349-48956350	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567286145	chr8:48956393-48956394	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189680882	chr8:48956402-48956403	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552983364	chr8:48956427-48956428	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs45466795	chr8:48956463-48956464	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11426371	chr8:48956486-48956487	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75271624	chr8:48956487-48956488	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397977831	chr8:48956500-48956501	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115969204	chr8:48956537-48956538	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182178951	chr8:48956546-48956547	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187258265	chr8:48956559-48956560	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191892069	chr8:48956566-48956567	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370002238	chr8:48956571-48956572	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557131397	chr8:48956598-48956599	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575302063	chr8:48956634-48956635	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143395140	chr8:48956684-48956685	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs137882197	chr8:48956693-48956694	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572983298	chr8:48956700-48956701	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549316347	chr8:48956703-48956704	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540256492	chr8:48956711-48956712	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565131041	chr8:48956723-48956724	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532880390	chr8:48956732-48956733	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183800447	chr8:48956735-48956736	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187339469	chr8:48956808-48956809	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367797488	chr8:48956823-48956824	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs45613433	chr8:48956852-48956853	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
22q11 deletion syndrome	20357662	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:970 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48921600-48956000	Weak transcription	Esophagus	oesophagus
2	chr8:48921600-48957400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:48921800-48957400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:48921800-48957400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr8:48921800-48957400	Weak transcription	Stomach Mucosa	stomach
6	chr8:48921800-48960600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr8:48921800-48966800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:48922000-48957600	Weak transcription	Colonic Mucosa	Colon
9	chr8:48922400-48957800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr8:48922400-48958000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:48922400-48975400	Weak transcription	Fetal Brain Male	brain
12	chr8:48922600-48955800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr8:48922600-48956200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr8:48922600-48956200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr8:48922600-48956600	Weak transcription	Brain Anterior Caudate	brain
16	chr8:48922600-48956800	Weak transcription	NHLF	lung
17	chr8:48922600-48957800	Weak transcription	HUVEC	blood vessel
18	chr8:48925000-48957600	Weak transcription	HSMMtube	muscle
19	chr8:48932800-48957200	Weak transcription	Spleen	Spleen
20	chr8:48933000-48956000	Weak transcription	Right Ventricle	heart
21	chr8:48933000-48956600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:48933000-48956800	Weak transcription	Gastric	stomach
23	chr8:48933200-48956000	Weak transcription	Fetal Kidney	kidney
24	chr8:48933200-48956200	Weak transcription	Brain Angular Gyrus	brain
25	chr8:48933400-48955800	Weak transcription	HMEC	breast
26	chr8:48933400-48956000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr8:48934600-48956600	Weak transcription	Ovary	ovary
28	chr8:48934800-48955800	Weak transcription	Fetal Brain Female	brain
29	chr8:48934800-48956000	Weak transcription	HSMM	muscle
30	chr8:48935000-48956000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr8:48935000-48956000	Weak transcription	Lung	lung
32	chr8:48935000-48957000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr8:48935000-48957400	Weak transcription	NHEK	skin
34	chr8:48935200-48956000	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr8:48935200-48963000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr8:48935400-48956000	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr8:48935400-48956000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr8:48935400-48956000	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr8:48935400-48956000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr8:48935400-48956800	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr8:48935600-48956000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:48935600-48956000	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr8:48935600-48956200	Weak transcription	NHDF-Ad	bronchial
44	chr8:48936000-48956000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr8:48936000-48956000	Weak transcription	Left Ventricle	heart
46	chr8:48936200-48956200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr8:48936800-48956200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr8:48937600-48955800	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr8:48937800-48957400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr8:48938200-48956000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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