Variant report

Variant	esv3369132
Chromosome Location	chr6:73928387-73943734
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	chr6:73933935-73934276	K562	blood:	n/a	n/a
2	ATF3	chr6:73933914-73934300	K562	blood:	n/a	n/a
3	BHLHE40	chr6:73933933-73934169	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:73933897-73934190	K562	blood:	n/a	n/a
5	CBX3	chr6:73933534-73934385	HCT-116	colon:	n/a	n/a
6	CEBPB	chr6:73942972-73943173	K562	blood:	n/a	chr6:73943037-73943048
7	CEBPB	chr6:73942951-73943183	A549	lung:	n/a	chr6:73943037-73943048
8	CEBPB	chr6:73942971-73943171	HepG2	liver:	n/a	chr6:73943037-73943048
9	CEBPB	chr6:73938032-73938281	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:73942958-73943206	Hela-S3	cervix:	n/a	chr6:73943037-73943048
11	CEBPB	chr6:73938080-73938262	K562	blood:	n/a	n/a
12	CEBPB	chr6:73935502-73935699	MCF-7	breast:	n/a	n/a
13	CEBPB	chr6:73935544-73935626	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:73930444-73930619	IMR90	lung:	n/a	n/a
15	CTCF	chr6:73928784-73928825	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr6:73935477-73935585	MCF-7	breast:	n/a	n/a
17	CTCF	chr6:73935516-73935570	MCF-7	breast:	n/a	n/a
18	CTCF	chr6:73935518-73935543	MCF-7	breast:	n/a	n/a
19	CTCF	chr6:73935533-73935581	K562	blood:	n/a	n/a
20	CTCF	chr6:73937740-73937890	BJ	skin:	n/a	n/a
21	E2F4	chr6:73939678-73939736	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F6	chr6:73933915-73934068	K562	blood:	n/a	n/a
23	EBF1	chr6:73941696-73941921	GM12878	blood:	n/a	n/a
24	EBF1	chr6:73933932-73934314	GM12878	blood:	n/a	chr6:73934112-73934125 chr6:73934113-73934124
25	EBF1	chr6:73941973-73942085	GM12878	blood:	n/a	n/a
26	EBF1	chr6:73934005-73934242	GM12878	blood:	n/a	chr6:73934112-73934125 chr6:73934113-73934124
27	EGR1	chr6:73933841-73934325	HCT-116	colon:	n/a	n/a
28	EGR1	chr6:73933985-73934281	K562	blood:	n/a	n/a
29	EGR1	chr6:73933793-73934387	HCT-116	colon:	n/a	n/a
30	EGR1	chr6:73933933-73934259	K562	blood:	n/a	n/a
31	EP300	chr6:73933996-73934185	GM12878	blood:	n/a	n/a
32	EP300	chr6:73934020-73934220	K562	blood:	n/a	n/a
33	EP300	chr6:73934014-73934244	GM12878	blood:	n/a	n/a
34	EP300	chr6:73943298-73943765	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr6:73943420-73943702	SK-N-SH_RA	brain:	n/a	n/a
36	FOS	chr6:73930337-73930671	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:73930340-73930656	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:73933926-73934390	MCF10A-Er-Src	breast:	n/a	chr6:73934153-73934162 chr6:73934152-73934163
39	FOS	chr6:73933962-73934385	MCF10A-Er-Src	breast:	n/a	chr6:73934153-73934162 chr6:73934152-73934163
40	FOS	chr6:73930324-73930681	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr6:73941960-73942134	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr6:73930348-73930656	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr6:73941825-73942227	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr6:73933961-73934393	MCF10A-Er-Src	breast:	n/a	chr6:73934153-73934162 chr6:73934152-73934163
45	FOS	chr6:73933975-73934386	MCF10A-Er-Src	breast:	n/a	chr6:73934153-73934162 chr6:73934152-73934163
46	FOS	chr6:73941942-73942142	MCF10A-Er-Src	breast:	n/a	n/a
47	FOSL1	chr6:73933738-73934497	HCT-116	colon:	n/a	chr6:73934153-73934162 chr6:73934152-73934163 chr6:73934152-73934163
48	FOSL1	chr6:73934032-73934333	K562	blood:	n/a	chr6:73934153-73934162 chr6:73934152-73934163 chr6:73934152-73934163
49	FOSL1	chr6:73933867-73934297	K562	blood:	n/a	chr6:73934153-73934162 chr6:73934152-73934163 chr6:73934152-73934163
50	FOSL1	chr6:73933718-73934499	HCT-116	colon:	n/a	chr6:73934153-73934162 chr6:73934152-73934163 chr6:73934152-73934163

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:73935584-73935634	HepG2	liver:	n/a
2	chr6:73935125-73935175	ECC-1	luminal epithelium:	n/a
3	chr6:73933428-73933478	HL-60	blood:	n/a
4	chr6:73934576-73934626	ovcar-3	ovarian:	n/a
5	chr6:73935270-73935320	AoSMC	blood vessel:	n/a
6	chr6:73934576-73934626	MCF10A-Er-Src	breast:	n/a
7	chr6:73933428-73933478	HCT-116	colon:	n/a
8	chr6:73934576-73934626	HCF	heart:	n/a
9	chr6:73935676-73935726	ProgFib	skin:	n/a
10	chr6:73935584-73935634	HUVEC	blood vessel:	n/a
11	chr6:73935584-73935634	HRPEpiC	eye:	n/a
12	chr6:73935584-73935634	SK-N-SH_RA	brain:	n/a
13	chr6:73935584-73935634	AG04449	skin:	fetal
14	chr6:73935270-73935320	SK-N-MC	brain:	n/a
15	chr6:73935584-73935634	T-47D	breast:	n/a
16	chr6:73933428-73933478	ovcar-3	ovarian:	n/a
17	chr6:73935125-73935175	NHDF-neo	bronchial:	n/a
18	chr6:73935125-73935175	HRE	kidney:	n/a
19	chr6:73933428-73933478	MCF10A-Er-Src	breast:	n/a
20	chr6:73935270-73935320	H1-hESC	embryonic stem cell:	embryo
21	chr6:73935200-73935250	H1-hESC	embryonic stem cell:	embryo
22	chr6:73935200-73935250	HIPEpiC	eye:	n/a
23	chr6:73935270-73935320	MCF-7	breast:	n/a
24	chr6:73935584-73935634	HCPEpiC	choroid plexus:	n/a
25	chr6:73934576-73934626	NT2-D1	testis:	n/a
26	chr6:73934576-73934626	PANC-1	pancreas:	n/a
27	chr6:73934576-73934626	GM12892	blood:	n/a
28	chr6:73935676-73935726	Hela-S3	cervix:	n/a
29	chr6:73935125-73935175	HMEC	breast:	n/a
30	chr6:73935676-73935726	HRPEpiC	eye:	n/a
31	chr6:73935584-73935634	GM12878	blood:	n/a
32	chr6:73935676-73935726	HepG2	liver:	n/a
33	chr6:73933428-73933478	SK-N-SH	brain:	n/a
34	chr6:73935676-73935726	PFSK-1	brain:	n/a
35	chr6:73935125-73935175	SAEC	small airway:	n/a
36	chr6:73934576-73934626	AG04450	lung:	fetal
37	chr6:73934576-73934626	AG10803	skin:	n/a
38	chr6:73934576-73934626	HL-60	blood:	n/a
39	chr6:73934576-73934626	HCPEpiC	choroid plexus:	n/a
40	chr6:73934576-73934626	T-47D	breast:	n/a
41	chr6:73935270-73935320	SAEC	small airway:	n/a
42	chr6:73935676-73935726	HCF	heart:	n/a
43	chr6:73935200-73935250	NHDF-neo	bronchial:	n/a
44	chr6:73935676-73935726	GM06990	blood:	n/a
45	chr6:73935200-73935250	ovcar-3	ovarian:	n/a
46	chr6:73934576-73934626	NHBE	bronchial:	n/a
47	chr6:73935270-73935320	GM06990	blood:	n/a
48	chr6:73935125-73935175	GM12892	blood:	n/a
49	chr6:73935125-73935175	GM19239	blood:	n/a
50	chr6:73935676-73935726	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	6:73859137-73881637..6:73927031-73938730	Hela-S3	cervix:
2	6:73927031-73938730..6:74000304-74012200	K562	blood:

Variant related genes	Relation type
KHDC1L	TF binding region
KHDC1L	CpG island
ENSG00000234882	chromatin interactions
ENSG00000234025	chromatin interactions

Extended variants
information (count: 547 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185671239	chr6:73928398-73928399	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs530430756	chr6:73928408-73928409	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs548522176	chr6:73928456-73928457	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs12195294	chr6:73928490-73928491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534399847	chr6:73928552-73928553	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs377443403	chr6:73928621-73928622	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs546820845	chr6:73928663-73928664	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558244597	chr6:73928695-73928696	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs571746806	chr6:73928714-73928715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs189994979	chr6:73928781-73928782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs557380616	chr6:73928791-73928792	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs193032107	chr6:73928830-73928831	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536668000	chr6:73928854-73928855	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs554967436	chr6:73928958-73928959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs573407417	chr6:73928980-73928981	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184838798	chr6:73928986-73928987	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs189736010	chr6:73929018-73929019	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs199636503	chr6:73929023-73929024	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs6453656	chr6:73929068-73929069	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs547217436	chr6:73929070-73929071	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs556834914	chr6:73929139-73929140	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs181114263	chr6:73929142-73929143	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs12210358	chr6:73929154-73929155	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542504170	chr6:73929172-73929173	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7759143	chr6:73929194-73929195	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375493535	chr6:73929238-73929239	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546282153	chr6:73929251-73929252	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs571281151	chr6:73929268-73929269	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185216924	chr6:73929288-73929289	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs533269490	chr6:73929354-73929355	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs377676118	chr6:73929361-73929362	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs563550748	chr6:73929396-73929397	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs6453657	chr6:73929410-73929411	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs541001578	chr6:73929519-73929520	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569466648	chr6:73929578-73929579	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs7760136	chr6:73929582-73929583	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs555030111	chr6:73929591-73929592	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573271373	chr6:73929616-73929617	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs74351967	chr6:73929680-73929681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558790559	chr6:73929724-73929725	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577218704	chr6:73929727-73929728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs544895677	chr6:73929752-73929753	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543041259	chr6:73929797-73929798	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs557082436	chr6:73929807-73929808	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575479075	chr6:73929809-73929810	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs72942627	chr6:73929881-73929882	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs560593545	chr6:73929891-73929892	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs141308722	chr6:73930055-73930056	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539797185	chr6:73930107-73930108	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs527740424	chr6:73930149-73930150	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Malignant fibrous histiocytomas	21085701	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Breast cancer	20409316	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73916200-73933800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:73928000-73929000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:73931400-73933000	Weak transcription	Ovary	ovary
4	chr6:73931600-73933200	Weak transcription	Fetal Brain Female	brain
5	chr6:73932800-73935200	Weak transcription	Brain Substantia Nigra	brain
6	chr6:73932800-73935200	Weak transcription	Fetal Lung	lung
7	chr6:73933000-73934000	Strong transcription	Ovary	ovary
8	chr6:73933200-73933600	Strong transcription	Fetal Brain Female	brain
9	chr6:73933400-73934200	ZNF genes & repeats	Fetal Stomach	stomach
10	chr6:73933600-73934200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:73933600-73935000	Weak transcription	Fetal Brain Female	brain
12	chr6:73933800-73934000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:73933800-73934000	Enhancers	Spleen	Spleen
14	chr6:73933800-73934200	Flanking Active TSS	K562	blood
15	chr6:73933800-73935200	Enhancers	Placenta	Placenta
16	chr6:73934000-73934200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
17	chr6:73934000-73934400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:73934000-73972400	Weak transcription	Ovary	ovary
19	chr6:73934200-73941400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:73934200-73941600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr6:73938000-73938200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:73938200-73938600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:73938400-73941000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:73938600-73943000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:73941000-73941200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:73941000-73941800	Enhancers	Osteobl	bone
27	chr6:73941200-73942200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:73941400-73944000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:73941600-73941800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr6:73941600-73942200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr6:73941600-73947000	Enhancers	Muscle Satellite Cultured Cells	--
32	chr6:73941800-73942000	Enhancers	NHDF-Ad	bronchial
33	chr6:73941800-73943600	Weak transcription	Osteobl	bone
34	chr6:73942000-73943000	Weak transcription	NHDF-Ad	bronchial
35	chr6:73942200-73945200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:73942600-73942800	Enhancers	NHLF	lung
37	chr6:73942800-73943400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:73943000-73943200	Enhancers	NHDF-Ad	bronchial
39	chr6:73943000-73944000	Weak transcription	NHLF	lung
40	chr6:73943000-73944200	Enhancers	A549	lung
41	chr6:73943000-73944800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr6:73943000-73946600	Enhancers	Hela-S3	cervix
43	chr6:73943000-73946800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:73943200-73943600	Weak transcription	NHDF-Ad	bronchial
45	chr6:73943200-73945200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:73943400-73944400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:73943400-73944600	Enhancers	NHEK	skin
48	chr6:73943600-73944800	Enhancers	Osteobl	bone
49	chr6:73943600-73946800	Enhancers	NHDF-Ad	bronchial

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