Variant report

Variant	nsv1008636
Chromosome Location	chr3:17173415-17208267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:436)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:17193198-17193523	K562	blood:	n/a	n/a
2	ATF1	chr3:17185022-17185058	K562	blood:	n/a	n/a
3	ATF2	chr3:17192850-17193833	GM12878	blood:	n/a	n/a
4	ATF2	chr3:17192838-17193840	GM12878	blood:	n/a	n/a
5	ATF3	chr3:17193276-17193502	K562	blood:	n/a	n/a
6	BACH1	chr3:17182780-17182791	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:17185731-17185875	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:17186044-17186437	GM12878	blood:	n/a	chr3:17186265-17186276
9	BATF	chr3:17186052-17186441	GM12878	blood:	n/a	chr3:17186265-17186276
10	BATF	chr3:17192978-17193563	GM12878	blood:	n/a	n/a
11	BATF	chr3:17177887-17178128	GM12878	blood:	n/a	n/a
12	BATF	chr3:17177189-17177551	GM12878	blood:	n/a	chr3:17177514-17177522 chr3:17177351-17177362
13	BCL11A	chr3:17193101-17193405	GM12878	blood:	n/a	chr3:17193128-17193137
14	BCL11A	chr3:17192923-17193647	GM12878	blood:	n/a	chr3:17193563-17193572 chr3:17193128-17193137
15	BCL11A	chr3:17186134-17186361	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:17177753-17178189	GM12878	blood:	n/a	n/a
17	BCL3	chr3:17193017-17193515	GM12878	blood:	n/a	chr3:17193128-17193137
18	BCL3	chr3:17193002-17193570	GM12878	blood:	n/a	chr3:17193128-17193137
19	BCL3	chr3:17183231-17183463	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:17192880-17193846	GM12878	blood:	n/a	chr3:17193563-17193572 chr3:17193128-17193137
21	BCLAF1	chr3:17192937-17193678	GM12878	blood:	n/a	chr3:17193563-17193572 chr3:17193128-17193137
22	BHLHE40	chr3:17193157-17193583	K562	blood:	n/a	n/a
23	BHLHE40	chr3:17193040-17193756	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:17177913-17178117	GM12878	blood:	n/a	n/a
25	BRCA1	chr3:17193353-17193646	GM12878	blood:	n/a	n/a
26	CBX3	chr3:17194749-17194994	K562	blood:	n/a	n/a
27	CBX3	chr3:17193205-17193588	K562	blood:	n/a	n/a
28	CBX3	chr3:17194651-17195083	K562	blood:	n/a	n/a
29	CEBPB	chr3:17200121-17200133	HepG2	liver:	n/a	n/a
30	CEBPB	chr3:17174699-17174836	A549	lung:	n/a	n/a
31	CEBPB	chr3:17192934-17193772	GM12878	blood:	n/a	n/a
32	CEBPB	chr3:17190594-17190874	HepG2	liver:	n/a	chr3:17190732-17190743 chr3:17190681-17190694 chr3:17190681-17190692
33	CEBPB	chr3:17193129-17193458	GM12878	blood:	n/a	n/a
34	CEBPB	chr3:17190578-17190920	IMR90	lung:	n/a	chr3:17190732-17190743 chr3:17190681-17190694 chr3:17190681-17190692
35	CEBPB	chr3:17205571-17205683	A549	lung:	n/a	n/a
36	CEBPB	chr3:17174020-17174176	HepG2	liver:	n/a	n/a
37	CEBPB	chr3:17174736-17174813	Hela-S3	cervix:	n/a	n/a
38	CHD1	chr3:17193756-17193851	GM12878	blood:	n/a	n/a
39	CHD1	chr3:17193052-17193460	GM12878	blood:	n/a	n/a
40	CHD2	chr3:17193017-17193932	GM12878	blood:	n/a	n/a
41	CHD2	chr3:17187689-17187927	K562	blood:	n/a	n/a
42	CTCF	chr3:17182666-17182891	GM12878	blood:	n/a	chr3:17182827-17182840 chr3:17182772-17182785
43	CTCF	chr3:17182520-17182670	A549	lung:	n/a	n/a
44	CTCF	chr3:17207977-17208176	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:17208020-17208170	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr3:17182690-17182871	GM10266	blood:	n/a	chr3:17182827-17182840 chr3:17182772-17182785
47	CTCF	chr3:17193060-17193210	GM12874	blood:	n/a	n/a
48	CTCF	chr3:17182783-17182818	Gliobla	brain:	n/a	n/a
49	CTCF	chr3:17182697-17182923	GM19239	blood:	n/a	chr3:17182827-17182840 chr3:17182772-17182785
50	CTCF	chr3:17182620-17182870	GM12864	blood:	n/a	chr3:17182827-17182840 chr3:17182772-17182785

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:17186314-17186364	PrEC	prostate:	n/a
2	chr3:17199496-17199546	HEEpiC	esophagus:	n/a
3	chr3:17197201-17197251	HRCEpiC	kidney:	n/a
4	chr3:17198551-17198601	GM12878	blood:	n/a
5	chr3:17186314-17186364	ProgFib	skin:	n/a
6	chr3:17197201-17197251	LNCaP	prostate:	n/a
7	chr3:17186314-17186364	AG04449	skin:	fetal
8	chr3:17197201-17197251	NHDF-neo	bronchial:	n/a
9	chr3:17197201-17197251	BJ	skin:	n/a
10	chr3:17199496-17199546	ProgFib	skin:	n/a
11	chr3:17199496-17199546	PrEC	prostate:	n/a
12	chr3:17198551-17198601	HAEpiC	amniotic membrane:	n/a
13	chr3:17199496-17199546	LNCaP	prostate:	n/a
14	chr3:17199496-17199546	ovcar-3	ovarian:	n/a
15	chr3:17199496-17199546	GM12878	blood:	n/a
16	chr3:17197201-17197251	GM19239	blood:	n/a
17	chr3:17198551-17198601	Hepatocyte	liver:	n/a
18	chr3:17199496-17199546	RPTEC	kidney:	n/a
19	chr3:17199496-17199546	BE2_C	brain:	n/a
20	chr3:17198551-17198601	ovcar-3	ovarian:	n/a
21	chr3:17186314-17186364	HMEC	breast:	n/a
22	chr3:17198551-17198601	AG09309	skin:	n/a
23	chr3:17186314-17186364	IMR90	lung:	fetal
24	chr3:17198551-17198601	SKMC	muscle:	n/a
25	chr3:17197201-17197251	AG04449	skin:	fetal
26	chr3:17186314-17186364	NHDF-neo	bronchial:	n/a
27	chr3:17198551-17198601	H1-hESC	embryonic stem cell:	embryo
28	chr3:17197201-17197251	MCF-7	breast:	n/a
29	chr3:17197201-17197251	AG09309	skin:	n/a
30	chr3:17197201-17197251	GM06990	blood:	n/a
31	chr3:17198551-17198601	GM12892	blood:	n/a
32	chr3:17197201-17197251	K562	blood:	n/a
33	chr3:17197201-17197251	NB4	blood:	n/a
34	chr3:17186314-17186364	HCF	heart:	n/a
35	chr3:17186314-17186364	HUVEC	blood vessel:	n/a
36	chr3:17198551-17198601	Hela-S3	cervix:	n/a
37	chr3:17197201-17197251	HIPEpiC	eye:	n/a
38	chr3:17197201-17197251	AG04450	lung:	fetal
39	chr3:17186314-17186364	HRPEpiC	eye:	n/a
40	chr3:17186314-17186364	AG09319	gingival:	n/a
41	chr3:17199496-17199546	NT2-D1	testis:	n/a
42	chr3:17197201-17197251	HCF	heart:	n/a
43	chr3:17186314-17186364	SK-N-SH	brain:	n/a
44	chr3:17199496-17199546	GM12891	blood:	n/a
45	chr3:17197201-17197251	HRE	kidney:	n/a
46	chr3:17198551-17198601	HCT-116	colon:	n/a
47	chr3:17198551-17198601	PFSK-1	brain:	n/a
48	chr3:17197201-17197251	HUVEC	blood vessel:	n/a
49	chr3:17198551-17198601	HEEpiC	esophagus:	n/a
50	chr3:17198551-17198601	NH-A	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:17171292..17173683-chr3:17174933..17176639,2	K562	blood:
2	chr3:17178887..17181144-chr3:17183106..17184956,2	MCF-7	breast:
3	chr3:17207202..17210072-chr3:17213126..17214686,2	MCF-7	breast:
4	chr3:17201185..17202806-chr3:17204861..17206362,2	K562	blood:
5	chr3:17174104..17176952-chr3:17185696..17187536,2	K562	blood:
6	chr3:17191881..17194308-chr3:17196780..17198405,2	K562	blood:
7	chr3:17174445..17176364-chr3:17179658..17182370,2	K562	blood:
8	chr3:16642484..16643095-chr3:17182333..17182847,2	MCF-7	breast:
9	chr3:17203436..17206201-chr3:17208117..17210640,2	MCF-7	breast:
10	chr3:17195512..17197058-chr3:17200290..17201914,2	K562	blood:
11	chr3:17174445..17176364-chr3:17179658..17182370,2	K562	blood:
12	chr3:17178887..17181144-chr3:17183106..17184956,2	MCF-7	breast:
13	chr3:17171292..17173683-chr3:17174933..17176639,2	K562	blood:
14	chr3:17191881..17194308-chr3:17196780..17198405,2	K562	blood:
15	chr3:17195512..17197058-chr3:17200290..17201914,2	K562	blood:
16	chr3:17174104..17176952-chr3:17185696..17187536,2	K562	blood:
17	chr3:17201185..17202806-chr3:17204861..17206362,2	K562	blood:
18	chr3:17203436..17206201-chr3:17208117..17210640,2	MCF-7	breast:
19	chr3:16927733..16930698-chr3:17179176..17180713,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000252976	TF binding region
ENSG00000252976	CpG island

Extended variants
information (count: 1512 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1512 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4077616	chr3:17173415-17173416	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571937661	chr3:17173456-17173457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141616468	chr3:17173462-17173463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563391341	chr3:17173463-17173464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557572643	chr3:17173533-17173534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567774024	chr3:17173544-17173545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536795409	chr3:17173595-17173596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553126148	chr3:17173666-17173667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4077615	chr3:17173712-17173713	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs558244725	chr3:17173713-17173714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575540213	chr3:17173748-17173749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560566982	chr3:17173840-17173841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529440811	chr3:17173850-17173851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150521512	chr3:17173900-17173901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574316039	chr3:17173978-17173979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540007004	chr3:17173979-17173980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559455780	chr3:17174007-17174008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373141093	chr3:17174010-17174011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551409851	chr3:17174038-17174039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565127117	chr3:17174055-17174056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183017397	chr3:17174059-17174060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs117832586	chr3:17174060-17174061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567920293	chr3:17174072-17174073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117902938	chr3:17174104-17174105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138388157	chr3:17174112-17174113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149629145	chr3:17174165-17174166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187349667	chr3:17174199-17174200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112186149	chr3:17174232-17174233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558563072	chr3:17174237-17174238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549420776	chr3:17174265-17174266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575138114	chr3:17174266-17174267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147332245	chr3:17174293-17174294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563140396	chr3:17174337-17174338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554586163	chr3:17174354-17174355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192731034	chr3:17174381-17174382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540067270	chr3:17174418-17174419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376149655	chr3:17174441-17174442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs57320563	chr3:17174470-17174471	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs140887851	chr3:17174482-17174483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530541768	chr3:17174483-17174484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545180473	chr3:17174491-17174492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370333548	chr3:17174570-17174571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565334107	chr3:17174587-17174588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550470187	chr3:17174633-17174634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530832242	chr3:17174653-17174654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550623921	chr3:17174664-17174665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183141384	chr3:17174695-17174696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576820170	chr3:17174716-17174717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368752516	chr3:17174717-17174718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561601513	chr3:17174743-17174744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	21364760	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:17150200-17182600	Weak transcription	Aorta	Aorta
2	chr3:17158800-17175800	Weak transcription	Right Atrium	heart
3	chr3:17172200-17174400	Enhancers	Psoas Muscle	Psoas
4	chr3:17174000-17174200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:17174000-17174400	Enhancers	Dnd41	blood
6	chr3:17174000-17174400	Enhancers	GM12878-XiMat	blood
7	chr3:17174200-17180600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:17174600-17177200	Weak transcription	Fetal Heart	heart
9	chr3:17174800-17175400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:17174800-17175600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:17175000-17175200	Enhancers	Adipose Nuclei	Adipose
12	chr3:17175000-17175600	Active TSS	Osteobl	bone
13	chr3:17175200-17175600	Active TSS	Adipose Nuclei	Adipose
14	chr3:17175400-17175600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:17175600-17176200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr3:17175800-17176000	Genic enhancers	Right Atrium	heart
17	chr3:17176000-17176200	Enhancers	Right Atrium	heart
18	chr3:17176200-17177400	Weak transcription	Right Atrium	heart
19	chr3:17176200-17177600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr3:17177000-17180200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr3:17177200-17178400	Enhancers	Fetal Heart	heart
22	chr3:17177200-17178800	Enhancers	Right Ventricle	heart
23	chr3:17177400-17178400	Enhancers	Ovary	ovary
24	chr3:17177400-17178800	Enhancers	Left Ventricle	heart
25	chr3:17177400-17178800	Enhancers	Right Atrium	heart
26	chr3:17177600-17178000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr3:17177600-17178000	Enhancers	Fetal Muscle Trunk	muscle
28	chr3:17177600-17178400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr3:17177600-17178400	Bivalent Enhancer	Fetal Stomach	stomach
30	chr3:17177600-17178600	Enhancers	GM12878-XiMat	blood
31	chr3:17177600-17178800	Enhancers	Pancreas	Pancrea
32	chr3:17178000-17178400	Enhancers	Fetal Lung	lung
33	chr3:17178000-17180200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr3:17178200-17178400	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr3:17178400-17179000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr3:17178400-17181800	Weak transcription	Fetal Lung	lung
37	chr3:17178400-17183200	Weak transcription	Fetal Heart	heart
38	chr3:17178600-17178800	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr3:17178800-17180600	Weak transcription	Right Atrium	heart
40	chr3:17178800-17181000	Weak transcription	Left Ventricle	heart
41	chr3:17178800-17182800	Weak transcription	Right Ventricle	heart
42	chr3:17179000-17179400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr3:17179000-17179400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
44	chr3:17179400-17180600	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr3:17179400-17193000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr3:17180200-17180600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:17180400-17181200	Enhancers	Primary B cells from cord blood	blood
48	chr3:17180400-17181400	Enhancers	Primary B cells from peripheral blood	blood
49	chr3:17180400-17182000	Enhancers	Fetal Thymus	thymus
50	chr3:17180400-17182200	Enhancers	Skeletal Muscle Female	skeletal muscle

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