Variant report

Variant	nsv885988
Chromosome Location	chr6:63615339-63830759
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	BATF	chr6:63824630-63824797	GM12878	blood:	n/a	n/a
4	BATF	chr6:63807248-63807450	GM12878	blood:	n/a	n/a
5	BATF	chr6:63824586-63824792	GM12878	blood:	n/a	n/a
6	BATF	chr6:63807210-63807411	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:63824585-63824882	GM12878	blood:	n/a	chr6:63824743-63824752
8	BCL11A	chr6:63807120-63807515	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:63684321-63684646	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:63807199-63807405	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:63806476-63806656	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:63807126-63807476	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:63631034-63631100	K562	blood:	n/a	n/a
14	BHLHE40	chr6:63806449-63806803	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:63684342-63684727	GM12878	blood:	n/a	n/a
16	CEBPB	chr6:63808146-63808432	A549	lung:	n/a	chr6:63808261-63808272 chr6:63808261-63808274 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808274 chr6:63808263-63808272
17	CEBPB	chr6:63738543-63738654	K562	blood:	n/a	chr6:63738589-63738600
18	CEBPB	chr6:63772020-63772183	HepG2	liver:	n/a	chr6:63772099-63772110
19	CEBPB	chr6:63738434-63738741	HepG2	liver:	n/a	chr6:63738589-63738600
20	CEBPB	chr6:63628508-63628689	H1-hESC	embryonic stem cell:	n/a	chr6:63628537-63628548
21	CEBPB	chr6:63686157-63686509	HepG2	liver:	n/a	chr6:63686330-63686341
22	CEBPB	chr6:63667638-63667757	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr6:63768494-63768848	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:63749108-63749358	HepG2	liver:	n/a	chr6:63749218-63749229 chr6:63749198-63749209
25	CEBPB	chr6:63749086-63749369	A549	lung:	n/a	chr6:63749218-63749229 chr6:63749198-63749209
26	CEBPB	chr6:63733591-63733961	Hela-S3	cervix:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
27	CEBPB	chr6:63628391-63628686	HepG2	liver:	n/a	chr6:63628537-63628548
28	CEBPB	chr6:63808099-63808450	HepG2	liver:	n/a	chr6:63808261-63808272 chr6:63808261-63808274 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808274 chr6:63808263-63808272
29	CEBPB	chr6:63686196-63686515	IMR90	lung:	n/a	chr6:63686330-63686341
30	CEBPB	chr6:63681197-63681507	HepG2	liver:	n/a	chr6:63681347-63681358
31	CEBPB	chr6:63738461-63738743	IMR90	lung:	n/a	chr6:63738589-63738600
32	CEBPB	chr6:63808130-63808451	IMR90	lung:	n/a	chr6:63808261-63808272 chr6:63808261-63808274 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808272 chr6:63808263-63808274 chr6:63808263-63808272
33	CEBPB	chr6:63733606-63733992	MCF-7	breast:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
34	CEBPB	chr6:63733609-63733862	HepG2	liver:	n/a	chr6:63733758-63733769 chr6:63733758-63733771 chr6:63733758-63733771 chr6:63733758-63733769 chr6:63733759-63733770
35	CEBPB	chr6:63749043-63749369	Hela-S3	cervix:	n/a	chr6:63749218-63749229 chr6:63749198-63749209
36	CEBPB	chr6:63764073-63764237	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr6:63776140-63776577	GM12878	blood:	n/a	n/a
38	CTCF	chr6:63776098-63776219	GM10266	blood:	n/a	chr6:63776156-63776165 chr6:63776155-63776176 chr6:63776153-63776171
39	CTCF	chr6:63789100-63789250	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:63776140-63776290	GM12870	blood:	n/a	chr6:63776156-63776165 chr6:63776155-63776176 chr6:63776153-63776171
41	CTCF	chr6:63789100-63789250	GM12865	blood:	n/a	n/a
42	CTCF	chr6:63789120-63789270	HepG2	liver:	n/a	n/a
43	CTCF	chr6:63789151-63789246	GM12878	blood:	n/a	n/a
44	CTCF	chr6:63776060-63776210	GM12868	blood:	n/a	chr6:63776156-63776165 chr6:63776155-63776176 chr6:63776153-63776171
45	CTCF	chr6:63694507-63694547	GM10266	blood:	n/a	n/a
46	CTCF	chr6:63789160-63789310	NB4	blood:	n/a	n/a
47	CTCF	chr6:63789080-63789230	RPTEC	kidney:	n/a	n/a
48	CTCF	chr6:63776060-63776210	HEK293	kidney:	n/a	chr6:63776156-63776165 chr6:63776155-63776176 chr6:63776153-63776171
49	CTCF	chr6:63776040-63776190	GM12878	blood:	n/a	chr6:63776156-63776165 chr6:63776155-63776176 chr6:63776153-63776171
50	CTCF	chr6:63793380-63793530	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63709255-63709305	HRCEpiC	kidney:	n/a
2	chr6:63709255-63709305	AG10803	skin:	n/a
3	chr6:63762988-63763038	GM06990	blood:	n/a
4	chr6:63762988-63763038	HCM	heart:	n/a
5	chr6:63709255-63709305	T-47D	breast:	n/a
6	chr6:63709255-63709305	HRPEpiC	eye:	n/a
7	chr6:63709255-63709305	IMR90	lung:	fetal
8	chr6:63709255-63709305	HMEC	breast:	n/a
9	chr6:63762988-63763038	GM12891	blood:	n/a
10	chr6:63762988-63763038	SK-N-SH	brain:	n/a
11	chr6:63709255-63709305	Caco-2	colon:	n/a
12	chr6:63762988-63763038	HCF	heart:	n/a
13	chr6:63762988-63763038	HMEC	breast:	n/a
14	chr6:63762988-63763038	ovcar-3	ovarian:	n/a
15	chr6:63762988-63763038	AG10803	skin:	n/a
16	chr6:63709255-63709305	AG09309	skin:	n/a
17	chr6:63709255-63709305	CMK	blood:	n/a
18	chr6:63709255-63709305	BJ	skin:	n/a
19	chr6:63709255-63709305	LNCaP	prostate:	n/a
20	chr6:63709255-63709305	HIPEpiC	eye:	n/a
21	chr6:63762988-63763038	LNCaP	prostate:	n/a
22	chr6:63709255-63709305	Jurkat	blood:	n/a
23	chr6:63709255-63709305	HCM	heart:	n/a
24	chr6:63709255-63709305	PFSK-1	brain:	n/a
25	chr6:63762988-63763038	BJ	skin:	n/a
26	chr6:63762988-63763038	HCPEpiC	choroid plexus:	n/a
27	chr6:63762988-63763038	SK-N-MC	brain:	n/a
28	chr6:63709255-63709305	BE2_C	brain:	n/a
29	chr6:63709255-63709305	ProgFib	skin:	n/a
30	chr6:63709255-63709305	HepG2	liver:	n/a
31	chr6:63762988-63763038	HRPEpiC	eye:	n/a
32	chr6:63709255-63709305	H1-hESC	embryonic stem cell:	embryo
33	chr6:63762988-63763038	HCT-116	colon:	n/a
34	chr6:63762988-63763038	PANC-1	pancreas:	n/a
35	chr6:63762988-63763038	ProgFib	skin:	n/a
36	chr6:63709255-63709305	SAEC	small airway:	n/a
37	chr6:63762988-63763038	AG09309	skin:	n/a
38	chr6:63709255-63709305	HL-60	blood:	n/a
39	chr6:63762988-63763038	RPTEC	kidney:	n/a
40	chr6:63709255-63709305	AoSMC	blood vessel:	n/a
41	chr6:63762988-63763038	AG04449	skin:	fetal
42	chr6:63709255-63709305	Hepatocyte	liver:	n/a
43	chr6:63709255-63709305	NH-A	brain:	n/a
44	chr6:63762988-63763038	T-47D	breast:	n/a
45	chr6:63762988-63763038	HAEpiC	amniotic membrane:	n/a
46	chr6:63762988-63763038	CMK	blood:	n/a
47	chr6:63709255-63709305	SK-N-MC	brain:	n/a
48	chr6:63762988-63763038	NHDF-neo	bronchial:	n/a
49	chr6:63709255-63709305	MCF10A-Er-Src	breast:	n/a
50	chr6:63709255-63709305	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:163654633..163655494-chr6:63642308..63642940,2	MCF-7	breast:
2	chr6:63726588..63729343-chr6:63730639..63732811,2	K562	blood:
3	chr6:63775743..63776456-chr6:63981994..63982859,3	MCF-7	breast:
4	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: 3394 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3394 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4605861	chr6:63615339-63615340	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576978948	chr6:63615340-63615341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540693869	chr6:63615372-63615373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559329552	chr6:63615380-63615381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145112469	chr6:63615382-63615383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186872230	chr6:63615412-63615413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs67676320	chr6:63615427-63615428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530626217	chr6:63615448-63615449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550227455	chr6:63615481-63615482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73501710	chr6:63615498-63615499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376713999	chr6:63615499-63615500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568595955	chr6:63615504-63615505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538774949	chr6:63615521-63615522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547556311	chr6:63615546-63615547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566105356	chr6:63615547-63615548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536247458	chr6:63615566-63615567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536073186	chr6:63615570-63615571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189789962	chr6:63615596-63615597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370263757	chr6:63615598-63615599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564727176	chr6:63615654-63615655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537659618	chr6:63615674-63615675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559168096	chr6:63615697-63615698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9360945	chr6:63615699-63615700	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs11758167	chr6:63615725-63615726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142083919	chr6:63615734-63615735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533804184	chr6:63615735-63615736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574423716	chr6:63615752-63615753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs68152715	chr6:63615782-63615783	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs182062046	chr6:63615838-63615839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370972690	chr6:63615842-63615843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530686268	chr6:63615865-63615866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552029220	chr6:63615919-63615920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142931580	chr6:63615934-63615935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538209236	chr6:63615947-63615948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563973646	chr6:63615981-63615982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528260966	chr6:63615983-63615984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184785475	chr6:63653025-63653026	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs546819349	chr6:63653051-63653052	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs373155403	chr6:63653066-63653067	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs189690838	chr6:63653072-63653073	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs530174408	chr6:63653078-63653079	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs548647794	chr6:63653096-63653097	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs6935156	chr6:63653114-63653115	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs181242341	chr6:63653115-63653116	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs552116519	chr6:63653129-63653130	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs186291685	chr6:63653145-63653146	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs576055186	chr6:63653170-63653171	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs534941763	chr6:63653174-63653175	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs562305027	chr6:63653218-63653219	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs553200764	chr6:63653244-63653245	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63614600-63615800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:63614800-63616000	Enhancers	Placenta	Placenta
3	chr6:63653000-63653400	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr6:63656600-63657000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:63681400-63681600	Enhancers	Fetal Intestine Small	intestine
6	chr6:63681400-63683000	Enhancers	Fetal Intestine Large	intestine
7	chr6:63681600-63682600	Weak transcription	Fetal Intestine Small	intestine
8	chr6:63682600-63683200	Enhancers	Fetal Intestine Small	intestine
9	chr6:63682600-63683400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:63683200-63683400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:63683400-63690600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:63690600-63690800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:63690600-63691000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:63699600-63703600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:63703400-63705000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr6:63703600-63704600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:63704000-63704600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:63707600-63709600	Enhancers	Fetal Heart	heart
19	chr6:63707800-63708400	Enhancers	Fetal Intestine Large	intestine
20	chr6:63707800-63708600	Enhancers	Fetal Intestine Small	intestine
21	chr6:63708000-63708200	Enhancers	HepG2	liver
22	chr6:63708200-63709200	Weak transcription	HepG2	liver
23	chr6:63708400-63709600	Weak transcription	Fetal Intestine Large	intestine
24	chr6:63708600-63709000	Weak transcription	Fetal Intestine Small	intestine
25	chr6:63708600-63710200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:63708600-63710200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr6:63708800-63709000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr6:63708800-63710000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:63708800-63710200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:63708800-63710200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:63708800-63710600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr6:63709000-63709600	Enhancers	Fetal Intestine Small	intestine
33	chr6:63709000-63709800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr6:63709000-63710000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:63709000-63710000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:63709000-63710000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr6:63709000-63710200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:63709000-63710200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr6:63709000-63710200	Enhancers	HMEC	breast
40	chr6:63709000-63710200	Enhancers	NHEK	skin
41	chr6:63709000-63710600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr6:63709000-63710600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr6:63709200-63709800	Enhancers	HepG2	liver
44	chr6:63709600-63710000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr6:63709600-63710000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:63709600-63710000	Flanking Active TSS	Fetal Heart	heart
47	chr6:63709600-63710000	Enhancers	Fetal Intestine Large	intestine
48	chr6:63709600-63710800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:63710000-63710400	Enhancers	Fetal Heart	heart
50	chr6:63710600-63720600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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