Variant report

Variant	esv3358208
Chromosome Location	chr6:82677282-82700658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:62)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:82689928-82690137	K562	blood:	n/a	n/a
2	ARID3A	chr6:82698304-82698419	K562	blood:	n/a	n/a
3	BHLHE40	chr6:82689229-82689286	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:82679601-82679821	K562	blood:	n/a	n/a
5	BHLHE40	chr6:82700369-82700387	K562	blood:	n/a	n/a
6	CEBPB	chr6:82691577-82691970	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr6:82698033-82698143	A549	lung:	n/a	chr6:82698039-82698056
8	CEBPB	chr6:82698688-82698933	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:82697917-82698131	IMR90	lung:	n/a	chr6:82698039-82698056
10	CEBPB	chr6:82697221-82697306	K562	blood:	n/a	n/a
11	CEBPB	chr6:82694954-82695199	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:82697177-82697399	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr6:82697220-82697387	A549	lung:	n/a	n/a
14	CHD2	chr6:82679760-82679959	K562	blood:	n/a	n/a
15	CREB1	chr6:82687929-82688344	GM12878	blood:	n/a	n/a
16	CTCF	chr6:82690020-82690170	AG10803	skin:	n/a	n/a
17	CTCF	chr6:82690046-82690157	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr6:82689980-82690130	RPTEC	kidney:	n/a	n/a
19	CTCF	chr6:82690020-82690170	BE2_C	brain:	n/a	n/a
20	CTCF	chr6:82690040-82690190	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr6:82690020-82690170	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr6:82690094-82690148	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr6:82689980-82690130	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr6:82689917-82690250	HCT-116	colon:	n/a	n/a
25	CTCF	chr6:82690060-82690210	HVMF	connective:	n/a	n/a
26	CTCF	chr6:82690036-82690190	K562	blood:	n/a	n/a
27	CTCF	chr6:82690000-82690150	AG10803	skin:	n/a	n/a
28	CTCF	chr6:82690062-82690179	LNCaP	prostate:	n/a	n/a
29	CTCF	chr6:82689980-82690130	HMF	breast:	n/a	n/a
30	CTCF	chr6:82690061-82690177	Pancreas_OC	pancreas:	n/a	n/a
31	CTCF	chr6:82690008-82690199	Medullo	brain:	n/a	n/a
32	CTCF	chr6:82691680-82691830	HMF	breast:	n/a	n/a
33	CTCF	chr6:82690023-82690177	A549	lung:	n/a	n/a
34	CTCF	chr6:82689977-82690160	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:82690040-82690190	HMF	breast:	n/a	n/a
36	CTCF	chr6:82689980-82690130	HVMF	connective:	n/a	n/a
37	CTCF	chr6:82689960-82690254	GM12878	blood:	n/a	n/a
38	CTCF	chr6:82690020-82690170	AG04449	skin:	n/a	n/a
39	CTCF	chr6:82690092-82690143	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr6:82689960-82690110	HCM	heart:	n/a	n/a
41	CTCF	chr6:82690040-82690190	HMEC	breast:	n/a	n/a
42	CTCF	chr6:82697774-82697789	K562	blood:	n/a	n/a
43	CTCF	chr6:82689900-82690050	RPTEC	kidney:	n/a	n/a
44	CTCF	chr6:82690006-82690140	A549	lung:	n/a	n/a
45	CTCF	chr6:82689927-82690248	IMR90	lung:	n/a	n/a
46	CTCF	chr6:82689899-82690283	A549	lung:	n/a	n/a
47	CTCF	chr6:82689953-82690267	K562	blood:	n/a	n/a
48	CTCF	chr6:82690040-82690190	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr6:82682818-82682895	GM13976	blood:	n/a	n/a
50	CTCF	chr6:82690053-82690172	LNCaP	prostate:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:82693821-82693871	HRE	kidney:	n/a
2	chr6:82693821-82693871	HRE	kidney:	n/a
3	chr6:82693821-82693871	HCF	heart:	n/a
4	chr6:82693821-82693871	RPTEC	kidney:	n/a
5	chr6:82693821-82693871	H1-hESC	embryonic stem cell:	embryo
6	chr6:82693821-82693871	AG04449	skin:	fetal
7	chr6:82693821-82693871	GM12878	blood:	n/a
8	chr6:82693821-82693871	NHBE	bronchial:	n/a
9	chr6:82693821-82693871	HAEpiC	amniotic membrane:	n/a
10	chr6:82693821-82693871	A549	lung:	n/a
11	chr6:82693821-82693871	BJ	skin:	n/a
12	chr6:82693821-82693871	AG04450	lung:	fetal
13	chr6:82693821-82693871	NH-A	brain:	n/a
14	chr6:82693821-82693871	HL-60	blood:	n/a
15	chr6:82693821-82693871	HCM	heart:	n/a
16	chr6:82693821-82693871	SK-N-SH	brain:	n/a
17	chr6:82693821-82693871	PFSK-1	brain:	n/a
18	chr6:82693821-82693871	ProgFib	skin:	n/a
19	chr6:82693821-82693871	MCF-7	breast:	n/a
20	chr6:82693821-82693871	HUVEC	blood vessel:	n/a
21	chr6:82693821-82693871	BE2_C	brain:	n/a
22	chr6:82693821-82693871	AG10803	skin:	n/a
23	chr6:82693821-82693871	NHDF-neo	bronchial:	n/a
24	chr6:82693821-82693871	SK-N-MC	brain:	n/a
25	chr6:82693821-82693871	MCF10A-Er-Src	breast:	n/a
26	chr6:82693821-82693871	GM12891	blood:	n/a
27	chr6:82693821-82693871	U87	brain:	n/a
28	chr6:82693821-82693871	NB4	blood:	n/a
29	chr6:82693821-82693871	CMK	blood:	n/a
30	chr6:82693821-82693871	HMEC	breast:	n/a
31	chr6:82693821-82693871	LNCaP	prostate:	n/a
32	chr6:82693821-82693871	HEEpiC	esophagus:	n/a
33	chr6:82693821-82693871	K562	blood:	n/a
34	chr6:82693821-82693871	SAEC	small airway:	n/a
35	chr6:82693821-82693871	AG09319	gingival:	n/a
36	chr6:82693821-82693871	Hepatocyte	liver:	n/a
37	chr6:82693821-82693871	Caco-2	colon:	n/a
38	chr6:82693821-82693871	IMR90	lung:	fetal
39	chr6:82693821-82693871	PANC-1	pancreas:	n/a
40	chr6:82693821-82693871	Jurkat	blood:	n/a
41	chr6:82693821-82693871	SK-N-SH_RA	brain:	n/a
42	chr6:82693821-82693871	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:82693821-82693871	HEK293	kidney:	embryo
44	chr6:82693821-82693871	AG09309	skin:	n/a
45	chr6:82693821-82693871	AoSMC	blood vessel:	n/a
46	chr6:82693821-82693871	T-47D	breast:	n/a
47	chr6:82693821-82693871	HRCEpiC	kidney:	n/a
48	chr6:82693821-82693871	HIPEpiC	eye:	n/a
49	chr6:82693821-82693871	GM06990	blood:	n/a
50	chr6:82693821-82693871	Hela-S3	cervix:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:82686817..82689739-chr6:82701513..82703111,2	MCF-7	breast:
2	chr6:82689854..82690591-chr6:82750428..82751055,2	MCF-7	breast:
3	chr6:82460171..82464074-chr6:82688065..82691180,4	MCF-7	breast:
4	chr6:82452704..82454911-chr6:82688444..82690552,2	MCF-7	breast:
5	chr6:82460208..82464483-chr6:82686357..82690775,7	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM46A-4	chr6:82699865-82699916	NONHSAT113755
2	lnc-IBTK-1	chr6:82679170-82679256	ENSG00000260574.1
3	lnc-FAM46A-4	chr6:82695293-82695337	l_3212_chr6:82612007-82704793_liver
4	lnc-FAM46A-4	chr6:82695293-82695337	NONHSAT113755

No data

Variant related genes	Relation type
ENSG00000260574	TF binding region
ENSG00000260574	CpG island
ENSG00000112773	chromatin interactions

Extended variants
information (count: 776 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541477811	chr6:82677287-82677288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147183472	chr6:82677320-82677321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62425446	chr6:82677357-82677358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562551466	chr6:82677364-82677365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185576999	chr6:82677372-82677373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115871859	chr6:82677378-82677379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568369287	chr6:82677411-82677412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539858342	chr6:82677455-82677456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527558200	chr6:82677473-82677474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138963248	chr6:82677482-82677483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375859504	chr6:82677485-82677486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs150730292	chr6:82677527-82677528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559591831	chr6:82677572-82677573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569292100	chr6:82677579-82677580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116242388	chr6:82677584-82677585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139024280	chr6:82677682-82677683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190484530	chr6:82677688-82677689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182070806	chr6:82677707-82677708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578181507	chr6:82677715-82677716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554372724	chr6:82677722-82677723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141098591	chr6:82677726-82677727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71866400	chr6:82677737-82677738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs398002103	chr6:82677750-82677751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79661169	chr6:82677752-82677753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545924948	chr6:82677754-82677755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562453205	chr6:82677761-82677762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200357020	chr6:82677776-82677777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201309585	chr6:82677780-82677781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561636384	chr6:82677805-82677806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527621473	chr6:82677869-82677870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371378338	chr6:82677891-82677892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547369714	chr6:82677902-82677903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116124452	chr6:82677922-82677923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532989334	chr6:82678029-82678030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186283436	chr6:82678106-82678107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569030967	chr6:82678126-82678127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149866997	chr6:82678130-82678131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188990780	chr6:82678149-82678150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181386948	chr6:82678180-82678181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534268693	chr6:82678199-82678200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554161031	chr6:82678221-82678222	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs185570609	chr6:82678370-82678371	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs114484948	chr6:82678371-82678372	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs373021462	chr6:82678374-82678375	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs190864742	chr6:82678388-82678389	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs75264203	chr6:82678421-82678422	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs182615759	chr6:82678426-82678427	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs12194197	chr6:82678465-82678466	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs540978369	chr6:82678544-82678545	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs369726516	chr6:82678577-82678578	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
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
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82672600-82677800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr6:82677800-82678200	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr6:82678000-82678600	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr6:82678200-82679000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr6:82678200-82680000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr6:82678400-82678600	Enhancers	Esophagus	oesophagus
7	chr6:82678600-82679000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr6:82678600-82679200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr6:82679000-82680000	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr6:82679000-82680000	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr6:82679200-82679400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:82679400-82679600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:82679400-82679600	Active TSS	HUES64 Cell Line	embryonic stem cell
14	chr6:82679400-82680000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:82679400-82680000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr6:82679400-82680200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr6:82679400-82680200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:82679400-82680200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:82679400-82680400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr6:82679400-82680400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:82679600-82679800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr6:82679600-82680000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:82679600-82680000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:82679600-82680000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr6:82679600-82680000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr6:82679600-82680000	Enhancers	K562	blood
27	chr6:82679600-82680200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr6:82679800-82680000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:82679800-82680400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr6:82680000-82680400	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr6:82680000-82680400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr6:82684000-82691200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr6:82687000-82687400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr6:82687000-82687400	Enhancers	NHDF-Ad	bronchial
35	chr6:82687000-82688000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:82687400-82690800	Weak transcription	NHDF-Ad	bronchial
37	chr6:82688000-82690800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:82690600-82691200	Enhancers	NHLF	lung
39	chr6:82690800-82691200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr6:82690800-82691400	Enhancers	NHDF-Ad	bronchial
41	chr6:82690800-82691800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr6:82690800-82691800	Enhancers	Placenta Amnion	Placenta Amnion
43	chr6:82690800-82692000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:82690800-82692400	Enhancers	HUVEC	blood vessel
45	chr6:82691000-82691200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr6:82691000-82691200	Enhancers	Osteobl	bone
47	chr6:82691000-82692200	Enhancers	Hela-S3	cervix
48	chr6:82691200-82691400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:82691200-82691400	Enhancers	GM12878-XiMat	blood
50	chr6:82691200-82691400	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links