Variant report

Variant	esv998220
Chromosome Location	chr6:81258085-81298829
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	BRCA1	chr6:81259042-81259178	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr6:81258297-81258625	IMR90	lung:	n/a	n/a
3	CEBPB	chr6:81283814-81284092	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:81258155-81258675	Hela-S3	cervix:	n/a	n/a
5	CHD2	chr6:81258222-81258577	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr6:81269810-81269849	H1-hESC	embryonic stem cell:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
7	CTCF	chr6:81290440-81290590	HPF	lung:	n/a	n/a
8	CTCF	chr6:81269800-81269950	HepG2	liver:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
9	CTCF	chr6:81269680-81269830	GM12870	blood:	n/a	chr6:81269821-81269830
10	CTCF	chr6:81269788-81269865	MCF-7	breast:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
11	CTCF	chr6:81269780-81269930	HEK293	kidney:	n/a	chr6:81269810-81269831 chr6:81269821-81269830
12	CTCF	chr6:81258375-81258422	Fibrobl	skin:	n/a	n/a
13	CTCF	chr6:81272958-81273253	GM12878	blood:	n/a	n/a
14	CTCF	chr6:81296493-81296551	K562	blood:	n/a	n/a
15	CTCF	chr6:81296515-81296546	ProgFib	skin:	n/a	n/a
16	CUX1	chr6:81258273-81258306	GM12878	blood:	n/a	n/a
17	EP300	chr6:81276274-81276343	GM12878	blood:	n/a	n/a
18	EP300	chr6:81257382-81258135	SK-N-SH	brain:	n/a	n/a
19	EP300	chr6:81260065-81260270	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr6:81258134-81258645	Hela-S3	cervix:	n/a	n/a
21	EP300	chr6:81275533-81275699	GM12878	blood:	n/a	n/a
22	ESR1	chr6:81260537-81260979	ECC-1	luminal epithelium:	n/a	chr6:81260739-81260754 chr6:81260761-81260776
23	ESR1	chr6:81260637-81260963	ECC-1	luminal epithelium:	n/a	chr6:81260739-81260754 chr6:81260761-81260776
24	FOS	chr6:81258163-81258652	MCF10A-Er-Src	breast:	n/a	chr6:81258233-81258243
25	FOS	chr6:81287611-81287762	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr6:81287562-81287818	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr6:81258237-81258642	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr6:81258171-81258666	MCF10A-Er-Src	breast:	n/a	chr6:81258233-81258243
29	FOS	chr6:81258153-81258691	MCF10A-Er-Src	breast:	n/a	chr6:81258233-81258243
30	FOS	chr6:81274152-81274265	MCF10A-Er-Src	breast:	n/a	chr6:81274216-81274228 chr6:81274217-81274226 chr6:81274218-81274225 chr6:81274218-81274227 chr6:81274217-81274227 chr6:81274218-81274226 chr6:81274232-81274241 chr6:81274219-81274230
31	FOXA1	chr6:81283057-81283344	HepG2	liver:	n/a	n/a
32	FOXA1	chr6:81263152-81263483	HepG2	liver:	n/a	n/a
33	FOXA2	chr6:81282864-81283514	A549	lung:	n/a	n/a
34	GATA3	chr6:81297613-81297813	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr6:81276466-81276760	SH-SY5Y	brain:	n/a	chr6:81276678-81276689
36	GATA3	chr6:81257332-81258155	SK-N-SH	brain:	n/a	n/a
37	GATA3	chr6:81288808-81288975	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr6:81257515-81258163	SK-N-SH	brain:	n/a	n/a
39	GATA3	chr6:81276353-81276920	SK-N-SH	brain:	n/a	chr6:81276678-81276689
40	IRF1	chr6:81274044-81274179	K562	blood:	n/a	n/a
41	JUN	chr6:81274114-81274349	HepG2	liver:	n/a	chr6:81274216-81274228 chr6:81274217-81274226 chr6:81274218-81274225 chr6:81274218-81274227 chr6:81274217-81274227 chr6:81274218-81274226 chr6:81274232-81274241 chr6:81274219-81274230
42	JUND	chr6:81257380-81258097	SK-N-SH	brain:	n/a	chr6:81257678-81257688 chr6:81257678-81257688 chr6:81257678-81257688
43	JUND	chr6:81274056-81274392	HepG2	liver:	n/a	chr6:81274216-81274228 chr6:81274217-81274226 chr6:81274218-81274225 chr6:81274218-81274227 chr6:81274217-81274227 chr6:81274218-81274226 chr6:81274232-81274241 chr6:81274216-81274227 chr6:81274219-81274230
44	JUND	chr6:81283122-81283245	HepG2	liver:	n/a	n/a
45	KAP1	chr6:81295985-81296357	HEK293	kidney:	n/a	n/a
46	MAFF	chr6:81264037-81264246	HepG2	liver:	n/a	n/a
47	MAFK	chr6:81265935-81266126	HepG2	liver:	n/a	n/a
48	MAFK	chr6:81288271-81288399	HepG2	liver:	n/a	chr6:81288322-81288333 chr6:81288321-81288332 chr6:81288320-81288334 chr6:81288317-81288332
49	MAFK	chr6:81264044-81264302	HepG2	liver:	n/a	n/a
50	MAFK	chr6:81264027-81264276	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:81259014-81259064	ovcar-3	ovarian:	n/a
2	chr6:81283368-81283418	AG04449	skin:	fetal
3	chr6:81283368-81283418	ProgFib	skin:	n/a
4	chr6:81283368-81283418	IMR90	lung:	fetal
5	chr6:81259014-81259064	HCM	heart:	n/a
6	chr6:81259014-81259064	BE2_C	brain:	n/a
7	chr6:81259014-81259064	PrEC	prostate:	n/a
8	chr6:81259014-81259064	BJ	skin:	n/a
9	chr6:81283368-81283418	ovcar-3	ovarian:	n/a
10	chr6:81259014-81259064	HL-60	blood:	n/a
11	chr6:81283368-81283418	HL-60	blood:	n/a
12	chr6:81283368-81283418	K562	blood:	n/a
13	chr6:81283368-81283418	PrEC	prostate:	n/a
14	chr6:81259014-81259064	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:81283368-81283418	GM06990	blood:	n/a
16	chr6:81283368-81283418	GM12892	blood:	n/a
17	chr6:81283368-81283418	NB4	blood:	n/a
18	chr6:81259014-81259064	H1-hESC	embryonic stem cell:	embryo
19	chr6:81259014-81259064	ProgFib	skin:	n/a
20	chr6:81259014-81259064	ECC-1	luminal epithelium:	n/a
21	chr6:81283368-81283418	HCPEpiC	choroid plexus:	n/a
22	chr6:81283368-81283418	HCM	heart:	n/a
23	chr6:81259014-81259064	HepG2	liver:	n/a
24	chr6:81259014-81259064	T-47D	breast:	n/a
25	chr6:81259014-81259064	GM12878	blood:	n/a
26	chr6:81259014-81259064	Caco-2	colon:	n/a
27	chr6:81283368-81283418	Caco-2	colon:	n/a
28	chr6:81259014-81259064	GM19239	blood:	n/a
29	chr6:81259014-81259064	HEEpiC	esophagus:	n/a
30	chr6:81259014-81259064	LNCaP	prostate:	n/a
31	chr6:81259014-81259064	HCT-116	colon:	n/a
32	chr6:81283368-81283418	Jurkat	blood:	n/a
33	chr6:81283368-81283418	CMK	blood:	n/a
34	chr6:81283368-81283418	HEEpiC	esophagus:	n/a
35	chr6:81259014-81259064	K562	blood:	n/a
36	chr6:81259014-81259064	HNPCEpiC	eye:	n/a
37	chr6:81283368-81283418	NT2-D1	testis:	n/a
38	chr6:81259014-81259064	HRCEpiC	kidney:	n/a
39	chr6:81283368-81283418	U87	brain:	n/a
40	chr6:81283368-81283418	ECC-1	luminal epithelium:	n/a
41	chr6:81259014-81259064	IMR90	lung:	fetal
42	chr6:81283368-81283418	PANC-1	pancreas:	n/a
43	chr6:81283368-81283418	HNPCEpiC	eye:	n/a
44	chr6:81259014-81259064	MCF10A-Er-Src	breast:	n/a
45	chr6:81259014-81259064	HIPEpiC	eye:	n/a
46	chr6:81259014-81259064	AG09309	skin:	n/a
47	chr6:81259014-81259064	AoSMC	blood vessel:	n/a
48	chr6:81259014-81259064	Jurkat	blood:	n/a
49	chr6:81259014-81259064	MCF-7	breast:	n/a
50	chr6:81283368-81283418	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:81254930..81257563-chr6:81262833..81265650,2	K562	blood:
2	chr6:81260471..81262004-chr6:81266433..81268034,2	MCF-7	breast:
3	chr6:81264062..81265646-chr6:81268549..81270670,2	MCF-7	breast:
4	chr6:81266263..81267805-chr6:81274227..81276426,2	MCF-7	breast:
5	chr6:81264062..81265646-chr6:81268549..81270670,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000216352	TF binding region
ENSG00000216352	CpG island
ENSG00000216352	chromatin interactions

Extended variants
information (count: 823 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565371493	chr6:81258108-81258109	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs116173375	chr6:81258110-81258111	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs376691003	chr6:81258111-81258112	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs539746502	chr6:81258138-81258139	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs192892782	chr6:81258146-81258147	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs561336209	chr6:81258168-81258169	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs558043553	chr6:81258215-81258216	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs140199141	chr6:81258241-81258242	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs367885063	chr6:81258243-81258244	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs199872828	chr6:81258244-81258245	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs530376190	chr6:81258275-81258276	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs140865287	chr6:81258276-81258277	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs114910830	chr6:81258305-81258306	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs569647522	chr6:81258313-81258314	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs144697896	chr6:81258327-81258328	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs145020580	chr6:81258328-81258329	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs536614606	chr6:81258336-81258337	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs72901988	chr6:81258347-81258348	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148654752	chr6:81258365-81258366	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs559138425	chr6:81258375-81258376	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs11964999	chr6:81258417-81258418	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs114072759	chr6:81258429-81258430	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs534047822	chr6:81258430-81258431	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs554107504	chr6:81258438-81258439	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs142230798	chr6:81258452-81258453	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs151208908	chr6:81258474-81258475	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs140397009	chr6:81258487-81258488	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs28405112	chr6:81258610-81258611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575656968	chr6:81258636-81258637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373293792	chr6:81258683-81258684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544387611	chr6:81258758-81258759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561484711	chr6:81258786-81258787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530227836	chr6:81258825-81258826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540464875	chr6:81258826-81258827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6936716	chr6:81258828-81258829	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs532695742	chr6:81258851-81258852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185440702	chr6:81258853-81258854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145296531	chr6:81258854-81258855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531397075	chr6:81258985-81258986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187901437	chr6:81258988-81258989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146416538	chr6:81259006-81259007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533741111	chr6:81259015-81259016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369961316	chr6:81259017-81259018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191686104	chr6:81259029-81259030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539757877	chr6:81259052-81259053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541012583	chr6:81259056-81259057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575551413	chr6:81259251-81259252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115316904	chr6:81259281-81259282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184246252	chr6:81259284-81259285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373815163	chr6:81259288-81259289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81251400-81259000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:81251800-81260600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:81256800-81259000	Enhancers	HMEC	breast
4	chr6:81256800-81259200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:81256800-81259200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:81257000-81259400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:81257400-81259000	Enhancers	NHEK	skin
8	chr6:81257600-81258400	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr6:81257600-81258400	Enhancers	Fetal Stomach	stomach
10	chr6:81257600-81258600	Enhancers	NH-A	brain
11	chr6:81257600-81259000	Enhancers	Hela-S3	cervix
12	chr6:81257600-81259200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:81257800-81258400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr6:81257800-81258400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr6:81257800-81258400	Flanking Active TSS	NHDF-Ad	bronchial
16	chr6:81257800-81258400	Flanking Active TSS	Osteobl	bone
17	chr6:81257800-81258600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:81257800-81258600	Flanking Active TSS	HSMMtube	muscle
19	chr6:81257800-81259400	Enhancers	Placenta Amnion	Placenta Amnion
20	chr6:81258000-81258200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:81258000-81258200	Enhancers	NHLF	lung
22	chr6:81258000-81258400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:81258000-81258400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:81258000-81258400	Flanking Active TSS	HSMM	muscle
25	chr6:81258000-81258600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:81258000-81259200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:81258200-81258400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr6:81258200-81258400	Flanking Active TSS	NHLF	lung
29	chr6:81258200-81258600	Enhancers	Fetal Lung	lung
30	chr6:81258400-81259000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:81258400-81259200	Enhancers	HSMM	muscle
32	chr6:81258400-81259600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:81258400-81259800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:81258400-81259800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:81258400-81259800	Enhancers	Osteobl	bone
36	chr6:81258400-81260200	Enhancers	NHLF	lung
37	chr6:81258400-81260400	Weak transcription	Fetal Stomach	stomach
38	chr6:81258400-81260800	Enhancers	NHDF-Ad	bronchial
39	chr6:81258600-81259200	Enhancers	HSMMtube	muscle
40	chr6:81258600-81259600	Weak transcription	Fetal Lung	lung
41	chr6:81258600-81261600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:81259000-81260600	Weak transcription	HMEC	breast
43	chr6:81259000-81262800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:81259200-81260600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:81259200-81260600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:81259200-81262800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr6:81259400-81260000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr6:81259600-81259800	Enhancers	Fetal Lung	lung
49	chr6:81260000-81260200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr6:81260400-81260800	Enhancers	Fetal Stomach	stomach

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