Variant report

Variant	esv1839224
Chromosome Location	chr6:131703293-131834119
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	ATF2	chr6:131831289-131831713	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:131831188-131831700	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr6:131831396-131831607	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr6:131831325-131831604	H1-hESC	embryonic stem cell:	n/a	chr6:131831389-131831402
5	BCL11A	chr6:131831258-131831623	GM12878	blood:	n/a	chr6:131831555-131831564
6	BCL11A	chr6:131831315-131831597	H1-hESC	embryonic stem cell:	n/a	chr6:131831555-131831564
7	BCL11A	chr6:131831326-131831594	H1-hESC	embryonic stem cell:	n/a	chr6:131831555-131831564
8	BCL11A	chr6:131831267-131831633	GM12878	blood:	n/a	chr6:131831555-131831564
9	BHLHE40	chr6:131792842-131792881	HepG2	liver:	n/a	n/a
10	BRCA1	chr6:131721187-131722017	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr6:131781353-131781389	HepG2	liver:	n/a	n/a
12	CBX3	chr6:131800091-131800425	K562	blood:	n/a	n/a
13	CBX3	chr6:131721613-131722328	HCT-116	colon:	n/a	n/a
14	CEBPB	chr6:131784246-131784554	IMR90	lung:	n/a	chr6:131784396-131784405 chr6:131784394-131784407 chr6:131784396-131784405 chr6:131784396-131784405 chr6:131784394-131784407
15	CEBPB	chr6:131713721-131714007	A549	lung:	n/a	chr6:131713872-131713883
16	CEBPB	chr6:131720759-131722017	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr6:131745278-131745432	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr6:131771485-131771730	Hela-S3	cervix:	n/a	chr6:131771594-131771603 chr6:131771593-131771604 chr6:131771592-131771603
19	CEBPB	chr6:131784215-131784587	HepG2	liver:	n/a	chr6:131784396-131784405 chr6:131784394-131784407 chr6:131784396-131784405 chr6:131784396-131784405 chr6:131784394-131784407
20	CEBPB	chr6:131721441-131721949	A549	lung:	n/a	n/a
21	CEBPB	chr6:131771672-131771679	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:131721591-131721844	A549	lung:	n/a	n/a
23	CEBPB	chr6:131790006-131790167	K562	blood:	n/a	chr6:131790065-131790076
24	CEBPB	chr6:131789965-131790244	HepG2	liver:	n/a	chr6:131790065-131790076
25	CEBPB	chr6:131713735-131713978	IMR90	lung:	n/a	chr6:131713872-131713883
26	CEBPB	chr6:131745829-131746142	K562	blood:	n/a	chr6:131745972-131745983 chr6:131745972-131745985
27	CEBPB	chr6:131789925-131790191	A549	lung:	n/a	chr6:131790065-131790076
28	CEBPB	chr6:131713756-131714008	HepG2	liver:	n/a	chr6:131713872-131713883
29	CEBPB	chr6:131708304-131708404	K562	blood:	n/a	n/a
30	CEBPB	chr6:131777745-131777946	HepG2	liver:	n/a	chr6:131777872-131777883
31	CEBPB	chr6:131777758-131777972	K562	blood:	n/a	chr6:131777872-131777883
32	CEBPB	chr6:131711535-131711716	K562	blood:	n/a	chr6:131711661-131711678
33	CEBPB	chr6:131791869-131792293	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr6:131831287-131831697	H1-hESC	embryonic stem cell:	n/a	chr6:131831499-131831510
35	CEBPB	chr6:131777753-131777953	K562	blood:	n/a	chr6:131777872-131777883
36	CEBPB	chr6:131713781-131713952	H1-hESC	embryonic stem cell:	n/a	chr6:131713872-131713883
37	CEBPB	chr6:131771470-131771742	HepG2	liver:	n/a	chr6:131771594-131771603 chr6:131771593-131771604 chr6:131771592-131771603
38	CEBPB	chr6:131771469-131771673	K562	blood:	n/a	chr6:131771594-131771603 chr6:131771593-131771604 chr6:131771592-131771603
39	CEBPB	chr6:131745841-131746092	IMR90	lung:	n/a	chr6:131745972-131745983 chr6:131745972-131745985
40	CEBPB	chr6:131745850-131746117	HepG2	liver:	n/a	chr6:131745972-131745983 chr6:131745972-131745985
41	CEBPB	chr6:131784284-131784561	A549	lung:	n/a	chr6:131784396-131784405 chr6:131784394-131784407 chr6:131784396-131784405 chr6:131784396-131784405 chr6:131784394-131784407
42	CEBPB	chr6:131831343-131831573	HepG2	liver:	n/a	chr6:131831499-131831510
43	CEBPB	chr6:131771450-131771686	IMR90	lung:	n/a	chr6:131771594-131771603 chr6:131771593-131771604 chr6:131771592-131771603
44	CEBPD	chr6:131829925-131830254	K562	blood:	n/a	n/a
45	CEBPD	chr6:131800016-131800541	K562	blood:	n/a	n/a
46	CHD1	chr6:131799016-131799018	GM12878	blood:	n/a	n/a
47	CHD2	chr6:131831223-131831666	GM12878	blood:	n/a	n/a
48	CHD2	chr6:131811796-131811817	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr6:131721568-131722002	Hela-S3	cervix:	n/a	n/a
50	CREB1	chr6:131831294-131831701	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:131831544-131831594	Hepatocyte	liver:	n/a
2	chr6:131745773-131745823	NHDF-neo	bronchial:	n/a
3	chr6:131781271-131781321	HAEpiC	amniotic membrane:	n/a
4	chr6:131722497-131722547	PFSK-1	brain:	n/a
5	chr6:131705123-131705173	GM19239	blood:	n/a
6	chr6:131705123-131705173	PrEC	prostate:	n/a
7	chr6:131745773-131745823	RPTEC	kidney:	n/a
8	chr6:131705123-131705173	HEEpiC	esophagus:	n/a
9	chr6:131781271-131781321	T-47D	breast:	n/a
10	chr6:131781271-131781321	GM12892	blood:	n/a
11	chr6:131745773-131745823	HCF	heart:	n/a
12	chr6:131722497-131722547	HRPEpiC	eye:	n/a
13	chr6:131722497-131722547	NHBE	bronchial:	n/a
14	chr6:131722497-131722547	HEK293	kidney:	embryo
15	chr6:131745773-131745823	HL-60	blood:	n/a
16	chr6:131745773-131745823	PANC-1	pancreas:	n/a
17	chr6:131705123-131705173	AG04450	lung:	fetal
18	chr6:131722497-131722547	H1-hESC	embryonic stem cell:	embryo
19	chr6:131705123-131705173	K562	blood:	n/a
20	chr6:131781271-131781321	GM12878	blood:	n/a
21	chr6:131781271-131781321	MCF-7	breast:	n/a
22	chr6:131831544-131831594	MCF-7	breast:	n/a
23	chr6:131745773-131745823	BE2_C	brain:	n/a
24	chr6:131831544-131831594	HIPEpiC	eye:	n/a
25	chr6:131781271-131781321	HIPEpiC	eye:	n/a
26	chr6:131705123-131705173	HL-60	blood:	n/a
27	chr6:131781271-131781321	HNPCEpiC	eye:	n/a
28	chr6:131745773-131745823	SKMC	muscle:	n/a
29	chr6:131705123-131705173	HCT-116	colon:	n/a
30	chr6:131781271-131781321	Hepatocyte	liver:	n/a
31	chr6:131722497-131722547	AG04449	skin:	fetal
32	chr6:131745773-131745823	LNCaP	prostate:	n/a
33	chr6:131781271-131781321	SK-N-MC	brain:	n/a
34	chr6:131705123-131705173	BJ	skin:	n/a
35	chr6:131831544-131831594	IMR90	lung:	fetal
36	chr6:131722497-131722547	NB4	blood:	n/a
37	chr6:131722497-131722547	Jurkat	blood:	n/a
38	chr6:131745773-131745823	AG09319	gingival:	n/a
39	chr6:131831544-131831594	NB4	blood:	n/a
40	chr6:131781271-131781321	LNCaP	prostate:	n/a
41	chr6:131722497-131722547	HUVEC	blood vessel:	n/a
42	chr6:131831544-131831594	GM12891	blood:	n/a
43	chr6:131745773-131745823	HIPEpiC	eye:	n/a
44	chr6:131705123-131705173	SK-N-MC	brain:	n/a
45	chr6:131831544-131831594	NT2-D1	testis:	n/a
46	chr6:131745773-131745823	HNPCEpiC	eye:	n/a
47	chr6:131745773-131745823	AG04449	skin:	fetal
48	chr6:131831544-131831594	HRCEpiC	kidney:	n/a
49	chr6:131705123-131705173	ProgFib	skin:	n/a
50	chr6:131781271-131781321	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:131778003..131780613-chr6:131780626..131782189,2	MCF-7	breast:
2	chr6:131193460..131194072-chr6:131780514..131781439,2	K562	blood:
3	chr6:131778003..131780613-chr6:131780626..131782189,2	MCF-7	breast:
4	chr6:131709683..131711909-chr6:131717715..131719994,2	MCF-7	breast:
5	chr6:131767630..131769730-chr6:131774382..131776098,2	K562	blood:
6	chr6:131709683..131711909-chr6:131717715..131719994,2	MCF-7	breast:
7	chr6:131767630..131769730-chr6:131774382..131776098,2	K562	blood:
8	chr6:131743564..131746106-chr6:131750332..131753297,3	MCF-7	breast:
9	chr6:131738927..131740867-chr6:131743230..131745826,2	K562	blood:
10	chr6:131614360..131616508-chr6:131705803..131707677,2	K562	blood:
11	chr6:131698297..131700688-chr6:131701676..131704606,3	K562	blood:
12	chr6:131743564..131746106-chr6:131750332..131753297,3	MCF-7	breast:
13	chr22:29194058..29196875-chr6:131816342..131819242,2	MCF-7	breast:
14	chr6:131789769..131792307-chr6:131792846..131795621,3	K562	blood:
15	chr6:131520599..131521909-chr6:131780880..131781727,4	MCF-7	breast:
16	chr6:131784710..131787393-chr6:131791820..131794235,2	K562	blood:
17	chr6:131715833..131718825-chr6:131734370..131736424,2	K562	blood:
18	chr6:131738927..131740867-chr6:131743230..131745826,2	K562	blood:
19	chr6:131731836..131734655-chr6:131749824..131752389,2	K562	blood:
20	chr6:131731836..131734655-chr6:131749824..131752389,2	K562	blood:
21	chr6:131784710..131787393-chr6:131791820..131794235,2	K562	blood:
22	chr6:131715833..131718825-chr6:131734370..131736424,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARG1-1	chr6:131830003-131830191	NONHSAT114918
2	lnc-ARG1-2	chr6:131826619-131826851	FPKM1_group_28441_transcript_1
3	lnc-ARG1-4	chr6:131790199-131790676	NONHSAT114917
4	lnc-ARG1-1	chr6:131828613-131828721	NONHSAT114918
5	lnc-ARG1-2	chr6:131826150-131826462	FPKM1_group_28441_transcript_1

Variant related genes	Relation type
RPL21P67	TF binding region
RPL21P67	CpG island
ENSG00000219776	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000118507	chromatin interactions
ENSG00000100219	chromatin interactions

Extended variants
information (count: 4694 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4694 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs942150	chr6:131703293-131703294	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7760448	chr6:131703328-131703329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562570512	chr6:131703329-131703330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529932172	chr6:131703376-131703377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190563546	chr6:131703419-131703420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548117888	chr6:131703433-131703434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181030078	chr6:131703440-131703441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527500089	chr6:131703441-131703442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374771649	chr6:131703452-131703453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570050287	chr6:131703453-131703454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552223389	chr6:131703516-131703517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144322022	chr6:131703521-131703522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558705066	chr6:131703557-131703558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147394212	chr6:131703560-131703561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570879025	chr6:131703579-131703580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs28420754	chr6:131703597-131703598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148456459	chr6:131703639-131703640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542795475	chr6:131703650-131703651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201037730	chr6:131703723-131703724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552744422	chr6:131703744-131703745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536938235	chr6:131703790-131703791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555312345	chr6:131703806-131703807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562211275	chr6:131703835-131703836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534144470	chr6:131703872-131703873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186065879	chr6:131703881-131703882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190593976	chr6:131703928-131703929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76578706	chr6:131703934-131703935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9492943	chr6:131703966-131703967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs142690658	chr6:131703977-131703978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541673621	chr6:131703978-131703979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560212627	chr6:131703985-131703986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527449873	chr6:131703993-131703994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs151021399	chr6:131704000-131704001	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs9492944	chr6:131704008-131704009	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs370996273	chr6:131704024-131704025	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs140439634	chr6:131704056-131704057	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs549943229	chr6:131704097-131704098	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs549338417	chr6:131704114-131704115	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs568020468	chr6:131704191-131704192	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs556800809	chr6:131704221-131704222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144219918	chr6:131704228-131704229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548121752	chr6:131704255-131704256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17060193	chr6:131704312-131704313	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs181306234	chr6:131704340-131704341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534535229	chr6:131704348-131704349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575470847	chr6:131704435-131704436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558880761	chr6:131704490-131704491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370550220	chr6:131704511-131704512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550822325	chr6:131704537-131704538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397976457	chr6:131704548-131704549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131687600-131705800	Weak transcription	Gastric	stomach
2	chr6:131689000-131705000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:131690000-131711200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr6:131690200-131704400	Weak transcription	Primary T cells from cord blood	blood
5	chr6:131700800-131706400	Enhancers	HSMMtube	muscle
6	chr6:131701600-131708800	Weak transcription	Osteobl	bone
7	chr6:131701800-131705200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:131701800-131712400	Enhancers	Fetal Brain Male	brain
9	chr6:131702000-131705000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:131702000-131705000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:131702000-131705400	Enhancers	Fetal Muscle Leg	muscle
12	chr6:131702000-131705800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr6:131702200-131704000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr6:131702400-131704000	Enhancers	Brain Angular Gyrus	brain
15	chr6:131702400-131705000	Enhancers	Fetal Lung	lung
16	chr6:131702400-131705200	Enhancers	Fetal Brain Female	brain
17	chr6:131702400-131705800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:131702600-131703400	Enhancers	Brain Cingulate Gyrus	brain
19	chr6:131702600-131703600	Weak transcription	Brain Germinal Matrix	brain
20	chr6:131702600-131704000	Enhancers	Fetal Stomach	stomach
21	chr6:131702600-131704200	Enhancers	Brain Hippocampus Middle	brain
22	chr6:131702600-131704200	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr6:131702600-131704800	Weak transcription	HSMM	muscle
24	chr6:131702800-131703400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr6:131702800-131704800	Weak transcription	NHDF-Ad	bronchial
26	chr6:131702800-131705400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:131703000-131703800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr6:131703000-131704000	Weak transcription	Spleen	Spleen
29	chr6:131703000-131704600	Enhancers	Psoas Muscle	Psoas
30	chr6:131703200-131703400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr6:131703200-131703400	Enhancers	Fetal Muscle Trunk	muscle
32	chr6:131703400-131704000	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr6:131703400-131704000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr6:131703400-131704600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr6:131703400-131705000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr6:131703600-131704200	Enhancers	Brain Germinal Matrix	brain
37	chr6:131703800-131704000	Enhancers	H9 Cell Line	embryonic stem cell
38	chr6:131703800-131704000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:131703800-131704200	Enhancers	Brain Anterior Caudate	brain
40	chr6:131703800-131704200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr6:131703800-131705200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr6:131703800-131705600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:131703800-131707000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:131704000-131704200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:131704000-131704200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr6:131704000-131704200	Enhancers	Fetal Muscle Trunk	muscle
47	chr6:131704000-131704200	Enhancers	Spleen	Spleen
48	chr6:131704000-131705000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:131704000-131705200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr6:131704000-131705600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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