Variant report

Variant	nsv885990
Chromosome Location	chr6:63665146-63746291
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	BACH1	chr6:63732724-63732911	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr6:63684432-63684699	GM12878	blood:	n/a	chr6:63684554-63684562
3	BCL11A	chr6:63684321-63684646	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:63684342-63684727	GM12878	blood:	n/a	n/a
5	CEBPB	chr6:63738543-63738654	K562	blood:	n/a	chr6:63738589-63738600
6	CEBPB	chr6:63667638-63667757	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr6:63738434-63738741	HepG2	liver:	n/a	chr6:63738589-63738600
8	CEBPB	chr6:63686196-63686515	IMR90	lung:	n/a	chr6:63686330-63686341
9	CEBPB	chr6:63733609-63733862	HepG2	liver:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
10	CEBPB	chr6:63686157-63686509	HepG2	liver:	n/a	chr6:63686330-63686341
11	CEBPB	chr6:63733591-63733961	Hela-S3	cervix:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
12	CEBPB	chr6:63738461-63738743	IMR90	lung:	n/a	chr6:63738589-63738600
13	CEBPB	chr6:63681197-63681507	HepG2	liver:	n/a	chr6:63681347-63681358
14	CEBPB	chr6:63733606-63733992	MCF-7	breast:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
15	CTCF	chr6:63694536-63694569	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr6:63690000-63690150	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr6:63707582-63707659	GM13976	blood:	n/a	n/a
18	CTCF	chr6:63678020-63678170	GM12869	blood:	n/a	n/a
19	CTCF	chr6:63694507-63694547	GM10266	blood:	n/a	n/a
20	CTCF	chr6:63700540-63700690	HEK293	kidney:	n/a	n/a
21	CTCF	chr6:63687840-63687990	K562	blood:	n/a	n/a
22	CTCF	chr6:63716941-63717026	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr6:63700534-63700590	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr6:63674827-63674842	GM20000	blood:	n/a	n/a
25	CTCF	chr6:63689743-63689807	GM13976	blood:	n/a	n/a
26	CTCF	chr6:63700460-63700610	Hela-S3	cervix:	n/a	n/a
27	CUX1	chr6:63688939-63689197	GM12878	blood:	n/a	n/a
28	E2F4	chr6:63689550-63689750	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr6:63665201-63665399	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr6:63683669-63683873	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr6:63684377-63684745	GM12878	blood:	n/a	n/a
32	EBF1	chr6:63690818-63690882	GM12878	blood:	n/a	n/a
33	EBF1	chr6:63681994-63682733	GM12878	blood:	n/a	n/a
34	EBF1	chr6:63682987-63683158	GM12878	blood:	n/a	n/a
35	EP300	chr6:63684329-63684838	GM12878	blood:	n/a	n/a
36	EP300	chr6:63690005-63690360	GM12878	blood:	n/a	n/a
37	FOS	chr6:63709776-63710148	MCF10A-Er-Src	breast:	n/a	chr6:63709977-63709987 chr6:63709978-63709986
38	FOS	chr6:63686534-63686734	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr6:63709807-63710148	MCF10A-Er-Src	breast:	n/a	chr6:63709977-63709987 chr6:63709978-63709986
40	FOS	chr6:63686619-63686694	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr6:63686529-63686754	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr6:63709821-63710162	MCF10A-Er-Src	breast:	n/a	chr6:63709977-63709987 chr6:63709978-63709986
43	FOS	chr6:63709825-63710087	MCF10A-Er-Src	breast:	n/a	chr6:63709977-63709987 chr6:63709978-63709986
44	FOSL2	chr6:63709806-63710242	SK-N-SH	brain:	n/a	chr6:63709977-63709987 chr6:63709978-63709986
45	GATA2	chr6:63681337-63681633	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr6:63681264-63681639	MCF-7	breast:	n/a	n/a
47	GATA3	chr6:63709636-63710288	SK-N-SH	brain:	n/a	chr6:63709812-63709820
48	GATA3	chr6:63709633-63710239	SK-N-SH	brain:	n/a	chr6:63709812-63709820
49	GATA3	chr6:63688910-63689110	SH-SY5Y	brain:	n/a	chr6:63689067-63689076
50	GATA3	chr6:63705398-63705598	SH-SY5Y	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63709255-63709305	HCT-116	colon:	n/a
2	chr6:63709255-63709305	HRCEpiC	kidney:	n/a
3	chr6:63709255-63709305	CMK	blood:	n/a
4	chr6:63709255-63709305	AG04450	lung:	fetal
5	chr6:63709255-63709305	PrEC	prostate:	n/a
6	chr6:63709255-63709305	A549	lung:	n/a
7	chr6:63709255-63709305	Jurkat	blood:	n/a
8	chr6:63709255-63709305	HPAEpiC	pulmonary alveolar:	n/a
9	chr6:63709255-63709305	GM19239	blood:	n/a
10	chr6:63709255-63709305	HepG2	liver:	n/a
11	chr6:63709255-63709305	GM12892	blood:	n/a
12	chr6:63709255-63709305	ovcar-3	ovarian:	n/a
13	chr6:63709255-63709305	SAEC	small airway:	n/a
14	chr6:63709255-63709305	HIPEpiC	eye:	n/a
15	chr6:63709255-63709305	MCF10A-Er-Src	breast:	n/a
16	chr6:63709255-63709305	AG04449	skin:	fetal
17	chr6:63709255-63709305	MCF-7	breast:	n/a
18	chr6:63709255-63709305	ProgFib	skin:	n/a
19	chr6:63709255-63709305	H1-hESC	embryonic stem cell:	embryo
20	chr6:63709255-63709305	U87	brain:	n/a
21	chr6:63709255-63709305	NT2-D1	testis:	n/a
22	chr6:63709255-63709305	NH-A	brain:	n/a
23	chr6:63709255-63709305	SK-N-MC	brain:	n/a
24	chr6:63709255-63709305	PANC-1	pancreas:	n/a
25	chr6:63709255-63709305	HRE	kidney:	n/a
26	chr6:63709255-63709305	AG09309	skin:	n/a
27	chr6:63709255-63709305	ECC-1	luminal epithelium:	n/a
28	chr6:63709255-63709305	NB4	blood:	n/a
29	chr6:63709255-63709305	IMR90	lung:	fetal
30	chr6:63709255-63709305	Hela-S3	cervix:	n/a
31	chr6:63709255-63709305	T-47D	breast:	n/a
32	chr6:63709255-63709305	GM12891	blood:	n/a
33	chr6:63709255-63709305	HL-60	blood:	n/a
34	chr6:63709255-63709305	HCM	heart:	n/a
35	chr6:63709255-63709305	GM12878	blood:	n/a
36	chr6:63709255-63709305	SKMC	muscle:	n/a
37	chr6:63709255-63709305	PFSK-1	brain:	n/a
38	chr6:63709255-63709305	HMEC	breast:	n/a
39	chr6:63709255-63709305	HUVEC	blood vessel:	n/a
40	chr6:63709255-63709305	Caco-2	colon:	n/a
41	chr6:63709255-63709305	AoSMC	blood vessel:	n/a
42	chr6:63709255-63709305	Hepatocyte	liver:	n/a
43	chr6:63709255-63709305	RPTEC	kidney:	n/a
44	chr6:63709255-63709305	HCPEpiC	choroid plexus:	n/a
45	chr6:63709255-63709305	AG10803	skin:	n/a
46	chr6:63709255-63709305	SK-N-SH	brain:	n/a
47	chr6:63709255-63709305	LNCaP	prostate:	n/a
48	chr6:63709255-63709305	SK-N-SH_RA	brain:	n/a
49	chr6:63709255-63709305	BE2_C	brain:	n/a
50	chr6:63709255-63709305	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:63726588..63729343-chr6:63730639..63732811,2	K562	blood:
2	chr6:63726588..63729343-chr6:63730639..63732811,2	K562	blood:

Variant related genes	Relation type
ENSG00000266682	TF binding region
ENSG00000266682	CpG island

Extended variants
information (count: 2677 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2677 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551303884	chr6:63681520-63681521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569560865	chr6:63681530-63681531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138060720	chr6:63681540-63681541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558044687	chr6:63681556-63681557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143529739	chr6:63681583-63681584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533665550	chr6:63681585-63681586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538882043	chr6:63681616-63681617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573558273	chr6:63681621-63681622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192207960	chr6:63681667-63681668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145828227	chr6:63681681-63681682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184712525	chr6:63681701-63681702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138281137	chr6:63681822-63681823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370482338	chr6:63681836-63681837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560106691	chr6:63681843-63681844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114695979	chr6:63681890-63681891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572743812	chr6:63681902-63681903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149608011	chr6:63681928-63681929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535009360	chr6:63681951-63681952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73496834	chr6:63681956-63681957	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569597785	chr6:63681957-63681958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369443888	chr6:63681980-63681981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555203519	chr6:63682056-63682057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9447716	chr6:63682089-63682090	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs566973829	chr6:63682109-63682110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534355767	chr6:63682151-63682152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555213069	chr6:63682154-63682155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534496407	chr6:63682260-63682261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543809006	chr6:63682274-63682275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563797741	chr6:63682300-63682301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187564330	chr6:63682304-63682305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546518987	chr6:63682319-63682320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144407607	chr6:63682377-63682378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7738181	chr6:63682426-63682427	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs148793557	chr6:63682430-63682431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572158602	chr6:63682433-63682434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192451427	chr6:63682479-63682480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143582146	chr6:63682481-63682482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562085510	chr6:63682485-63682486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184500944	chr6:63682507-63682508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538699273	chr6:63682542-63682543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544648977	chr6:63682634-63682635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141991001	chr6:63682663-63682664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189899615	chr6:63682670-63682671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528595068	chr6:63682673-63682674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373893488	chr6:63682706-63682707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567112769	chr6:63682739-63682740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs367860440	chr6:63682746-63682747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577399272	chr6:63682768-63682769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551334424	chr6:63682769-63682770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557282917	chr6:63682905-63682906	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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
Ependymoma	16718352	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	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63681400-63681600	Enhancers	Fetal Intestine Small	intestine
2	chr6:63681400-63683000	Enhancers	Fetal Intestine Large	intestine
3	chr6:63681600-63682600	Weak transcription	Fetal Intestine Small	intestine
4	chr6:63682600-63683200	Enhancers	Fetal Intestine Small	intestine
5	chr6:63682600-63683400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:63683200-63683400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:63683400-63690600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr6:63690600-63690800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:63690600-63691000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:63699600-63703600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:63703400-63705000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr6:63703600-63704600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:63704000-63704600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr6:63707600-63709600	Enhancers	Fetal Heart	heart
15	chr6:63707800-63708400	Enhancers	Fetal Intestine Large	intestine
16	chr6:63707800-63708600	Enhancers	Fetal Intestine Small	intestine
17	chr6:63708000-63708200	Enhancers	HepG2	liver
18	chr6:63708200-63709200	Weak transcription	HepG2	liver
19	chr6:63708400-63709600	Weak transcription	Fetal Intestine Large	intestine
20	chr6:63708600-63709000	Weak transcription	Fetal Intestine Small	intestine
21	chr6:63708600-63710200	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr6:63708600-63710200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr6:63708800-63709000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr6:63708800-63710000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:63708800-63710200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:63708800-63710200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr6:63708800-63710600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:63709000-63709600	Enhancers	Fetal Intestine Small	intestine
29	chr6:63709000-63709800	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr6:63709000-63710000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:63709000-63710000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:63709000-63710000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:63709000-63710200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr6:63709000-63710200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:63709000-63710200	Enhancers	HMEC	breast
36	chr6:63709000-63710200	Enhancers	NHEK	skin
37	chr6:63709000-63710600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr6:63709000-63710600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr6:63709200-63709800	Enhancers	HepG2	liver
40	chr6:63709600-63710000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:63709600-63710000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:63709600-63710000	Flanking Active TSS	Fetal Heart	heart
43	chr6:63709600-63710000	Enhancers	Fetal Intestine Large	intestine
44	chr6:63709600-63710800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:63710000-63710400	Enhancers	Fetal Heart	heart
46	chr6:63710600-63720600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr6:63720400-63722600	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr6:63720600-63721600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr6:63720600-63722400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr6:63721200-63721800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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