Variant report

Variant	nsv1023687
Chromosome Location	chr6:55868611-55940255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:451)
CpG islands
(count:184)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:55888699-55888722	HepG2	liver:	n/a	n/a
2	CBX3	chr6:55918563-55918866	HCT-116	colon:	n/a	n/a
3	CEBPB	chr6:55929954-55930109	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:55884808-55885065	A549	lung:	n/a	chr6:55884963-55884974
5	CEBPB	chr6:55905081-55905419	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr6:55929895-55930181	HepG2	liver:	n/a	n/a
7	CEBPB	chr6:55925803-55925911	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr6:55869280-55869543	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:55905099-55905433	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:55884800-55885126	HepG2	liver:	n/a	chr6:55884963-55884974
11	CEBPB	chr6:55884793-55885108	Hela-S3	cervix:	n/a	chr6:55884963-55884974
12	CEBPB	chr6:55929926-55930126	A549	lung:	n/a	n/a
13	CEBPB	chr6:55884861-55885013	H1-hESC	embryonic stem cell:	n/a	chr6:55884963-55884974
14	CEBPB	chr6:55884782-55885131	IMR90	lung:	n/a	chr6:55884963-55884974
15	CTCF	chr6:55886789-55887064	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr6:55918740-55918890	HCT-116	colon:	n/a	n/a
17	CTCF	chr6:55902480-55902630	AG04449	skin:	n/a	n/a
18	CTCF	chr6:55927880-55928030	NHLF	lung:	n/a	chr6:55927903-55927912
19	CTCF	chr6:55918651-55918811	LNCaP	prostate:	n/a	chr6:55918717-55918730
20	CTCF	chr6:55918700-55918850	MCF-7	breast:	n/a	chr6:55918717-55918730
21	CTCF	chr6:55918514-55918861	MCF-7	breast:	n/a	chr6:55918717-55918730
22	CTCF	chr6:55918700-55918850	BJ	skin:	n/a	chr6:55918717-55918730
23	CTCF	chr6:55918640-55918790	HRE	kidney:	n/a	chr6:55918717-55918730
24	CTCF	chr6:55918740-55918890	HCM	heart:	n/a	n/a
25	CTCF	chr6:55897440-55897590	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr6:55918700-55918850	HMF	breast:	n/a	chr6:55918717-55918730
27	CTCF	chr6:55902500-55902650	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr6:55886735-55887077	GM12878	blood:	n/a	n/a
29	CTCF	chr6:55918600-55918750	HA-sp	spinal cord:	n/a	chr6:55918717-55918730
30	CTCF	chr6:55902580-55902730	AG04449	skin:	n/a	n/a
31	CTCF	chr6:55886826-55887017	HepG2	liver:	n/a	n/a
32	CTCF	chr6:55918663-55918832	LNCaP	prostate:	n/a	chr6:55918717-55918730
33	CTCF	chr6:55918640-55918790	AG09319	gingival:	n/a	chr6:55918717-55918730
34	CTCF	chr6:55918660-55918810	HUVEC	blood vessel:	n/a	chr6:55918717-55918730
35	CTCF	chr6:55918620-55918770	GM12878	blood:	n/a	chr6:55918717-55918730
36	CTCF	chr6:55918680-55918830	GM12870	blood:	n/a	chr6:55918717-55918730
37	CTCF	chr6:55918557-55918851	GM12878	blood:	n/a	chr6:55918717-55918730
38	CTCF	chr6:55886860-55887010	NHLF	lung:	n/a	n/a
39	CTCF	chr6:55886837-55886998	Gliobla	brain:	n/a	n/a
40	CTCF	chr6:55918720-55918870	HFF-Myc	foreskin:	n/a	n/a
41	CTCF	chr6:55886820-55886970	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr6:55916560-55916710	GM12872	blood:	n/a	n/a
43	CTCF	chr6:55918700-55918850	BE2_C	brain:	n/a	chr6:55918717-55918730
44	CTCF	chr6:55918640-55918790	HepG2	liver:	n/a	chr6:55918717-55918730
45	CTCF	chr6:55918500-55918650	BE2_C	brain:	n/a	n/a
46	CTCF	chr6:55918700-55918850	GM12872	blood:	n/a	chr6:55918717-55918730
47	CTCF	chr6:55902520-55902670	HPF	lung:	n/a	n/a
48	CTCF	chr6:55886800-55886950	AG04449	skin:	n/a	n/a
49	CTCF	chr6:55918640-55918790	HUVEC	blood vessel:	n/a	chr6:55918717-55918730
50	CTCF	chr6:55902580-55902730	HMEC	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:55887782-55887832	T-47D	breast:	n/a
2	chr6:55887782-55887832	T-47D	breast:	n/a
3	chr6:55905409-55905459	HAEpiC	amniotic membrane:	n/a
4	chr6:55905409-55905459	GM12892	blood:	n/a
5	chr6:55905409-55905459	RPTEC	kidney:	n/a
6	chr6:55921912-55921962	U87	brain:	n/a
7	chr6:55887782-55887832	NHBE	bronchial:	n/a
8	chr6:55905409-55905459	HCM	heart:	n/a
9	chr6:55905409-55905459	GM12891	blood:	n/a
10	chr6:55905409-55905459	AG09319	gingival:	n/a
11	chr6:55887782-55887832	SK-N-SH	brain:	n/a
12	chr6:55921912-55921962	GM12891	blood:	n/a
13	chr6:55887782-55887832	SK-N-SH_RA	brain:	n/a
14	chr6:55887782-55887832	HEEpiC	esophagus:	n/a
15	chr6:55905409-55905459	AG04450	lung:	fetal
16	chr6:55887782-55887832	A549	lung:	n/a
17	chr6:55905409-55905459	HepG2	liver:	n/a
18	chr6:55905409-55905459	MCF10A-Er-Src	breast:	n/a
19	chr6:55887782-55887832	ECC-1	luminal epithelium:	n/a
20	chr6:55921912-55921962	GM12878	blood:	n/a
21	chr6:55921912-55921962	AG04450	lung:	fetal
22	chr6:55921912-55921962	ECC-1	luminal epithelium:	n/a
23	chr6:55921912-55921962	GM06990	blood:	n/a
24	chr6:55887782-55887832	HCM	heart:	n/a
25	chr6:55905409-55905459	LNCaP	prostate:	n/a
26	chr6:55905409-55905459	GM19239	blood:	n/a
27	chr6:55921912-55921962	HUVEC	blood vessel:	n/a
28	chr6:55887782-55887832	HEK293	kidney:	embryo
29	chr6:55887782-55887832	MCF10A-Er-Src	breast:	n/a
30	chr6:55905409-55905459	NB4	blood:	n/a
31	chr6:55905409-55905459	H1-hESC	embryonic stem cell:	embryo
32	chr6:55905409-55905459	AG10803	skin:	n/a
33	chr6:55921912-55921962	RPTEC	kidney:	n/a
34	chr6:55905409-55905459	HNPCEpiC	eye:	n/a
35	chr6:55887782-55887832	GM12878	blood:	n/a
36	chr6:55905409-55905459	BJ	skin:	n/a
37	chr6:55905409-55905459	GM06990	blood:	n/a
38	chr6:55887782-55887832	HAEpiC	amniotic membrane:	n/a
39	chr6:55887782-55887832	HRCEpiC	kidney:	n/a
40	chr6:55905409-55905459	Caco-2	colon:	n/a
41	chr6:55887782-55887832	NT2-D1	testis:	n/a
42	chr6:55887782-55887832	AG09309	skin:	n/a
43	chr6:55921912-55921962	PANC-1	pancreas:	n/a
44	chr6:55887782-55887832	PrEC	prostate:	n/a
45	chr6:55887782-55887832	CMK	blood:	n/a
46	chr6:55887782-55887832	Hepatocyte	liver:	n/a
47	chr6:55887782-55887832	Jurkat	blood:	n/a
48	chr6:55921912-55921962	H1-hESC	embryonic stem cell:	embryo
49	chr6:55921912-55921962	SK-N-SH	brain:	n/a
50	chr6:55921912-55921962	BE2_C	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:55886493..55887163-chr6:56155410..56156320,2	MCF-7	breast:
2	chr6:55865744..55868626-chr6:55870571..55872911,2	K562	blood:
3	chr6:55926997..55929020-chr6:55932279..55934927,2	MCF-7	breast:
4	chr6:55904181..55905774-chr6:55908809..55911144,2	MCF-7	breast:
5	chr6:55886589..55887225-chr6:56157105..56157760,2	MCF-7	breast:
6	chr6:55886603..55887384-chr6:55918244..55919071,2	MCF-7	breast:
7	chr6:55886603..55887384-chr6:55918244..55919071,2	MCF-7	breast:
8	chr6:55886745..55887604-chr6:56157130..56158002,2	MCF-7	breast:
9	chr6:55932576..55934705-chr6:55937943..55940116,3	K562	blood:
10	chr6:55904181..55905774-chr6:55908809..55911144,2	MCF-7	breast:
11	chr6:55926997..55929020-chr6:55932279..55934927,2	MCF-7	breast:
12	chr6:55932576..55934705-chr6:55937943..55940116,3	K562	blood:
13	chr6:55865744..55868626-chr6:55870571..55872911,2	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	COL21A1	hsa-miR-29c-3p	chr6:55922417-55922438
2	COL21A1	hsa-miR-29c-3p	chr6:55922423-55922417
3	COL21A1	hsa-miR-29c-3p	chr6:55921829-55921850

Variant related genes	Relation type
COL21A1	TF binding region
COL21A1	CpG island

Extended variants
information (count: 2159 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2159 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551617336	chr6:55868614-55868615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540614189	chr6:55868618-55868619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373923368	chr6:55868641-55868642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577901383	chr6:55868787-55868788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9464316	chr6:55868827-55868828	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs539356103	chr6:55868839-55868840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549712155	chr6:55868844-55868845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370352449	chr6:55868846-55868847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77306118	chr6:55868889-55868890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563772974	chr6:55868903-55868904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182416114	chr6:55868910-55868911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78798306	chr6:55868920-55868921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534673946	chr6:55868921-55868922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557468472	chr6:55868943-55868944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79609983	chr6:55868981-55868982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543430401	chr6:55869014-55869015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142506634	chr6:55869017-55869018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542747527	chr6:55869024-55869025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145871203	chr6:55869037-55869038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562439464	chr6:55869065-55869066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562230477	chr6:55869090-55869091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370884786	chr6:55869143-55869144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs35713344	chr6:55869175-55869176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527794032	chr6:55869183-55869184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs56136644	chr6:55869184-55869185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs564421161	chr6:55869287-55869288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533405533	chr6:55869303-55869304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549749246	chr6:55869336-55869337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138702305	chr6:55869381-55869382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535328913	chr6:55869407-55869408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34307889	chr6:55869415-55869416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536969076	chr6:55869419-55869420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548774674	chr6:55869424-55869425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565819027	chr6:55869430-55869431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9475496	chr6:55869441-55869442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534513009	chr6:55869446-55869447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140137642	chr6:55869459-55869460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs62406075	chr6:55869466-55869467	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111518393	chr6:55869467-55869468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556971547	chr6:55869588-55869589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548395394	chr6:55869625-55869626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576826336	chr6:55869642-55869643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2206678	chr6:55869665-55869666	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566682543	chr6:55869753-55869754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146327900	chr6:55869763-55869764	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10599089	chr6:55869766-55869767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555686353	chr6:55869797-55869798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115394558	chr6:55869828-55869829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138103820	chr6:55869853-55869854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62406076	chr6:55869855-55869856	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55867600-55868800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:55867600-55869200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:55867800-55869000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:55867800-55869000	Weak transcription	Osteobl	bone
5	chr6:55868000-55869000	Weak transcription	HSMM	muscle
6	chr6:55868800-55869600	Enhancers	HSMMtube	muscle
7	chr6:55868800-55870000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr6:55868800-55870800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr6:55869000-55869200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr6:55869000-55869400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:55869000-55869400	Enhancers	HMEC	breast
12	chr6:55869000-55869400	Enhancers	HSMM	muscle
13	chr6:55869000-55869600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:55869000-55869600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:55869000-55869600	Enhancers	Osteobl	bone
16	chr6:55869000-55870600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr6:55869200-55869800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:55869200-55869800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:55869200-55870200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr6:55869600-55874200	Weak transcription	Osteobl	bone
21	chr6:55869800-55870800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr6:55869800-55874600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:55870000-55871000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:55870200-55870400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr6:55870200-55871000	Enhancers	Primary hematopoietic stem cells	blood
26	chr6:55870400-55870600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr6:55870600-55870800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
28	chr6:55870800-55871200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr6:55874200-55874600	Enhancers	NHDF-Ad	bronchial
30	chr6:55874200-55875200	Enhancers	Osteobl	bone
31	chr6:55874800-55875000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:55886200-55887200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr6:55886400-55887000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr6:55886400-55887200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:55886400-55887200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr6:55886600-55887200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr6:55886600-55887400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:55886600-55887400	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr6:55886800-55887400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr6:55886800-55888000	Enhancers	HSMM	muscle
41	chr6:55887000-55887800	Enhancers	HSMMtube	muscle
42	chr6:55887200-55888400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr6:55887400-55888400	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr6:55887600-55887800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr6:55887600-55887800	Enhancers	Fetal Stomach	stomach
46	chr6:55887600-55887800	Enhancers	Osteobl	bone
47	chr6:55887600-55888400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:55887800-55890000	Weak transcription	Osteobl	bone
49	chr6:55887800-55891000	Weak transcription	Fetal Stomach	stomach
50	chr6:55888000-55889800	Weak transcription	Muscle Satellite Cultured Cells	--

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