Variant report

Variant	nsv519632
Chromosome Location	chr6:167615010-167627760
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	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
2	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
3	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
4	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
5	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:167626130-167626424	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:167617441-167617909	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:167617544-167617803	K562	blood:	n/a	n/a
9	BHLHE40	chr6:167626013-167626185	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:167617148-167617887	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:167617588-167617796	HepG2	liver:	n/a	n/a
12	BRCA1	chr6:167624418-167624607	HepG2	liver:	n/a	n/a
13	BRCA1	chr6:167625284-167625312	HepG2	liver:	n/a	n/a
14	CBX3	chr6:167617380-167617754	K562	blood:	n/a	n/a
15	CEBPB	chr6:167624471-167624762	HepG2	liver:	n/a	n/a
16	CHD2	chr6:167624353-167624597	HepG2	liver:	n/a	n/a
17	CREB1	chr6:167624142-167624971	HepG2	liver:	n/a	n/a
18	CTCF	chr6:167616940-167617090	HepG2	liver:	n/a	chr6:167617042-167617051
19	CTCF	chr6:167619506-167619579	GM20000	blood:	n/a	n/a
20	CTCF	chr6:167620960-167621110	GM12867	blood:	n/a	n/a
21	CTCF	chr6:167622475-167622650	H1-hESC	embryonic stem cell:	n/a	chr6:167622562-167622571
22	CTCF	chr6:167617479-167617527	GM20000	blood:	n/a	n/a
23	CTCF	chr6:167619497-167619503	GM20000	blood:	n/a	n/a
24	CTCF	chr6:167618860-167619010	HepG2	liver:	n/a	n/a
25	CTCF	chr6:167622540-167622690	HepG2	liver:	n/a	chr6:167622562-167622571
26	CTCF	chr6:167622520-167622670	HEK293	kidney:	n/a	chr6:167622562-167622571
27	CTCF	chr6:167616705-167616741	GM13976	blood:	n/a	n/a
28	CTCF	chr6:167625780-167625930	HEK293	kidney:	n/a	chr6:167625827-167625837 chr6:167625803-167625816
29	EBF1	chr6:167626039-167626328	GM12878	blood:	n/a	n/a
30	EP300	chr6:167626129-167626387	GM12878	blood:	n/a	n/a
31	EP300	chr6:167624439-167624771	HepG2	liver:	n/a	n/a
32	EP300	chr6:167617546-167617736	HepG2	liver:	n/a	chr6:167617578-167617587
33	EP300	chr6:167617327-167617821	HepG2	liver:	n/a	chr6:167617578-167617587
34	EP300	chr6:167617328-167617822	HepG2	liver:	n/a	chr6:167617578-167617587
35	EP300	chr6:167624368-167624933	HepG2	liver:	n/a	n/a
36	FOS	chr6:167617421-167617621	MCF10A-Er-Src	breast:	n/a	chr6:167617579-167617588 chr6:167617577-167617589 chr6:167617578-167617587
37	FOS	chr6:167617608-167617616	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:167617428-167617621	MCF10A-Er-Src	breast:	n/a	chr6:167617579-167617588 chr6:167617577-167617589 chr6:167617578-167617587
39	FOSL1	chr6:167617516-167617673	K562	blood:	n/a	chr6:167617579-167617588 chr6:167617577-167617589 chr6:167617577-167617588 chr6:167617578-167617587
40	FOSL1	chr6:167617401-167617717	K562	blood:	n/a	chr6:167617579-167617588 chr6:167617577-167617589 chr6:167617577-167617588 chr6:167617578-167617587
41	FOSL2	chr6:167616633-167617940	HepG2	liver:	n/a	chr6:167617579-167617588 chr6:167617576-167617587 chr6:167617577-167617589 chr6:167616700-167616709 chr6:167616882-167616890 chr6:167617578-167617587
42	FOSL2	chr6:167617156-167617979	HepG2	liver:	n/a	chr6:167617579-167617588 chr6:167617576-167617587 chr6:167617577-167617589 chr6:167617578-167617587
43	FOSL2	chr6:167617416-167617731	A549	lung:	n/a	chr6:167617579-167617588 chr6:167617576-167617587 chr6:167617577-167617589 chr6:167617578-167617587
44	FOSL2	chr6:167624110-167624945	HepG2	liver:	n/a	n/a
45	FOXA1	chr6:167624289-167624959	HepG2	liver:	n/a	n/a
46	FOXA1	chr6:167617294-167618000	HepG2	liver:	n/a	n/a
47	FOXA1	chr6:167624351-167624916	HepG2	liver:	n/a	n/a
48	FOXA1	chr6:167617291-167617836	HepG2	liver:	n/a	n/a
49	FOXA1	chr6:167617320-167617809	HepG2	liver:	n/a	n/a
50	FOXA1	chr6:167617337-167617714	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167623149-167623199	SKMC	muscle:	n/a
2	chr6:167622441-167622491	HCF	heart:	n/a
3	chr6:167623149-167623199	BJ	skin:	n/a
4	chr6:167622202-167622252	AG04449	skin:	fetal
5	chr6:167622441-167622491	MCF-7	breast:	n/a
6	chr6:167623149-167623199	HRCEpiC	kidney:	n/a
7	chr6:167617119-167617169	CMK	blood:	n/a
8	chr6:167622202-167622252	RPTEC	kidney:	n/a
9	chr6:167617119-167617169	HepG2	liver:	n/a
10	chr6:167617119-167617169	NB4	blood:	n/a
11	chr6:167617119-167617169	SK-N-SH_RA	brain:	n/a
12	chr6:167622202-167622252	BE2_C	brain:	n/a
13	chr6:167616968-167617018	NB4	blood:	n/a
14	chr6:167616968-167617018	HL-60	blood:	n/a
15	chr6:167622202-167622252	AG04450	lung:	fetal
16	chr6:167616968-167617018	A549	lung:	n/a
17	chr6:167622202-167622252	HRE	kidney:	n/a
18	chr6:167616968-167617018	PANC-1	pancreas:	n/a
19	chr6:167622441-167622491	HEEpiC	esophagus:	n/a
20	chr6:167623149-167623199	NHBE	bronchial:	n/a
21	chr6:167617119-167617169	HRPEpiC	eye:	n/a
22	chr6:167616968-167617018	Caco-2	colon:	n/a
23	chr6:167623149-167623199	HCM	heart:	n/a
24	chr6:167617119-167617169	NT2-D1	testis:	n/a
25	chr6:167623149-167623199	PrEC	prostate:	n/a
26	chr6:167622441-167622491	NT2-D1	testis:	n/a
27	chr6:167623149-167623199	HIPEpiC	eye:	n/a
28	chr6:167622202-167622252	SKMC	muscle:	n/a
29	chr6:167617119-167617169	IMR90	lung:	fetal
30	chr6:167622441-167622491	Caco-2	colon:	n/a
31	chr6:167616968-167617018	GM12891	blood:	n/a
32	chr6:167622441-167622491	HepG2	liver:	n/a
33	chr6:167622202-167622252	GM19239	blood:	n/a
34	chr6:167617119-167617169	HUVEC	blood vessel:	n/a
35	chr6:167623149-167623199	AG04449	skin:	fetal
36	chr6:167622202-167622252	K562	blood:	n/a
37	chr6:167623149-167623199	CMK	blood:	n/a
38	chr6:167616968-167617018	NH-A	brain:	n/a
39	chr6:167622202-167622252	NH-A	brain:	n/a
40	chr6:167616968-167617018	U87	brain:	n/a
41	chr6:167617119-167617169	K562	blood:	n/a
42	chr6:167623149-167623199	ProgFib	skin:	n/a
43	chr6:167616968-167617018	K562	blood:	n/a
44	chr6:167622441-167622491	NHDF-neo	bronchial:	n/a
45	chr6:167623149-167623199	H1-hESC	embryonic stem cell:	embryo
46	chr6:167622202-167622252	CMK	blood:	n/a
47	chr6:167623149-167623199	SK-N-MC	brain:	n/a
48	chr6:167622441-167622491	Hela-S3	cervix:	n/a
49	chr6:167617119-167617169	NHDF-neo	bronchial:	n/a
50	chr6:167622441-167622491	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
2	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
3	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
4	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:

Variant related genes	Relation type
ENSG00000216966	TF binding region
ENSG00000216966	CpG island
ENSG00000216966	chromatin interactions

Extended variants
information (count: 728 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2180713	chr6:167615010-167615011	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143098185	chr6:167615030-167615031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9459913	chr6:167615057-167615058	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs147458457	chr6:167615135-167615136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193187141	chr6:167615185-167615186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575102048	chr6:167615249-167615250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9457286	chr6:167615299-167615300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139233165	chr6:167615308-167615309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183328171	chr6:167615318-167615319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112405106	chr6:167615406-167615407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575290948	chr6:167615415-167615416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545918014	chr6:167615427-167615428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs386708557	chr6:167615428-167615429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145603541	chr6:167615439-167615440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573141212	chr6:167615441-167615442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs540652394	chr6:167615442-167615443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376066311	chr6:167615446-167615447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371797189	chr6:167615467-167615468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148476739	chr6:167615473-167615474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563477570	chr6:167615474-167615475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9459914	chr6:167615493-167615494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs552317202	chr6:167615502-167615503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187411298	chr6:167615504-167615505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9457287	chr6:167615508-167615509	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs546618719	chr6:167615528-167615529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144116697	chr6:167615572-167615573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535752521	chr6:167615606-167615607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557083154	chr6:167615611-167615612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569126555	chr6:167615612-167615613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567942367	chr6:167615679-167615680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539681593	chr6:167615716-167615717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191842869	chr6:167615732-167615733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9459915	chr6:167615739-167615740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113408283	chr6:167615740-167615741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9457288	chr6:167615743-167615744	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111910039	chr6:167615748-167615749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140955384	chr6:167615750-167615751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs55787520	chr6:167615775-167615776	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs184014089	chr6:167615776-167615777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563438047	chr6:167615827-167615828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530709110	chr6:167615855-167615856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557505931	chr6:167615889-167615890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564019941	chr6:167615905-167615906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373658163	chr6:167615932-167615933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547584471	chr6:167615940-167615941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199588031	chr6:167615941-167615942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546236136	chr6:167615946-167615947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568049414	chr6:167615947-167615948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529511679	chr6:167615956-167615957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75565077	chr6:167616008-167616009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167610600-167615400	Weak transcription	Fetal Brain Male	brain
2	chr6:167613000-167616600	Enhancers	Placenta Amnion	Placenta Amnion
3	chr6:167613800-167622200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:167614000-167615400	Enhancers	HepG2	liver
5	chr6:167614400-167623200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:167614800-167616400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:167615000-167616800	Weak transcription	Fetal Intestine Small	intestine
8	chr6:167615400-167616400	Weak transcription	HepG2	liver
9	chr6:167615400-167617400	Enhancers	Fetal Brain Male	brain
10	chr6:167615800-167616200	Enhancers	Fetal Lung	lung
11	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
12	chr6:167616400-167617000	Enhancers	HepG2	liver
13	chr6:167616400-167617400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:167616400-167617600	Enhancers	Rectal Smooth Muscle	rectum
15	chr6:167616600-167617200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr6:167616600-167617800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:167616600-167618400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr6:167616800-167617200	Enhancers	Stomach Smooth Muscle	stomach
19	chr6:167616800-167617400	Bivalent Enhancer	K562	blood
20	chr6:167616800-167617600	Enhancers	Fetal Intestine Small	intestine
21	chr6:167617000-167617400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr6:167617000-167617400	Enhancers	Liver	Liver
23	chr6:167617000-167617400	Enhancers	Fetal Heart	heart
24	chr6:167617000-167617400	Enhancers	Fetal Intestine Large	intestine
25	chr6:167617000-167617400	Enhancers	Lung	lung
26	chr6:167617000-167617400	Active TSS	A549	lung
27	chr6:167617000-167617400	Flanking Active TSS	HepG2	liver
28	chr6:167617000-167617400	Enhancers	NH-A	brain
29	chr6:167617200-167617400	Enhancers	Colon Smooth Muscle	Colon
30	chr6:167617200-167617400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
31	chr6:167617400-167618200	Weak transcription	NH-A	brain
32	chr6:167617400-167618600	Weak transcription	Fetal Brain Male	brain
33	chr6:167617400-167619000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:167617400-167620800	Enhancers	HepG2	liver
35	chr6:167617400-167622400	Weak transcription	Fetal Intestine Large	intestine
36	chr6:167617600-167618000	Weak transcription	Fetal Intestine Small	intestine
37	chr6:167617600-167618000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr6:167617600-167618200	Weak transcription	Colon Smooth Muscle	Colon
39	chr6:167618000-167619000	Enhancers	Fetal Intestine Small	intestine
40	chr6:167618000-167619000	Enhancers	Rectal Smooth Muscle	rectum
41	chr6:167618200-167618400	Enhancers	Colon Smooth Muscle	Colon
42	chr6:167618400-167618600	Enhancers	NH-A	brain
43	chr6:167618400-167619000	Enhancers	Placenta Amnion	Placenta Amnion
44	chr6:167618400-167624400	Weak transcription	Colon Smooth Muscle	Colon
45	chr6:167618600-167619200	Enhancers	Fetal Brain Male	brain
46	chr6:167619000-167619200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr6:167619000-167620200	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr6:167619000-167622400	Weak transcription	Fetal Intestine Small	intestine
49	chr6:167619000-167624200	Weak transcription	Rectal Smooth Muscle	rectum
50	chr6:167619200-167620200	Weak transcription	Fetal Brain Male	brain

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