Variant report

Variant	esv275340
Chromosome Location	chr6:142620405-142624568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:509)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:142622007-142622355	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:142622792-142623208	HepG2	liver:	n/a	n/a
3	BACH1	chr6:142623058-142623526	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr6:142623448-142623997	A549	lung:	n/a	n/a
5	BHLHE40	chr6:142623027-142623096	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:142622903-142623128	A549	lung:	n/a	n/a
7	BHLHE40	chr6:142622596-142623525	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:142622886-142623212	HepG2	liver:	n/a	n/a
9	BRCA1	chr6:142624419-142624420	HepG2	liver:	n/a	n/a
10	CEBPB	chr6:142623330-142623924	MCF-7	breast:	n/a	n/a
11	CEBPB	chr6:142621828-142622670	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr6:142623558-142623752	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:142623378-142623916	A549	lung:	n/a	n/a
14	CEBPB	chr6:142623355-142624034	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr6:142623352-142623949	MCF-7	breast:	n/a	n/a
16	CEBPB	chr6:142620241-142620568	HepG2	liver:	n/a	chr6:142620377-142620388
17	CEBPB	chr6:142623515-142623822	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:142620271-142620509	A549	lung:	n/a	chr6:142620377-142620388
19	CEBPD	chr6:142622710-142623479	HepG2	liver:	n/a	n/a
20	CHD1	chr6:142623193-142623360	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr6:142622865-142623557	HepG2	liver:	n/a	chr6:142623094-142623104 chr6:142623109-142623119
22	CHD2	chr6:142623269-142623304	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr6:142621589-142622479	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr6:142623095-142623499	Hela-S3	cervix:	n/a	chr6:142623109-142623119
25	CREB1	chr6:142622491-142622742	A549	lung:	n/a	n/a
26	CREB1	chr6:142622905-142623287	A549	lung:	n/a	n/a
27	CTBP2	chr6:142622565-142623525	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr6:142622980-142623130	GM12870	blood:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
29	CTCF	chr6:142623040-142623081	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr6:142624340-142624490	HepG2	liver:	n/a	n/a
31	CTCF	chr6:142623060-142623210	GM12867	blood:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
32	CTCF	chr6:142622980-142623130	HMEC	breast:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
33	CTCF	chr6:142622865-142623132	T-47D	breast:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
34	CTCF	chr6:142622954-142623186	A549	lung:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
35	CTCF	chr6:142622842-142623212	HepG2	liver:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
36	CTCF	chr6:142623000-142623150	GM12865	blood:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
37	CTCF	chr6:142622960-142623110	GM12869	blood:	n/a	chr6:142623096-142623109
38	CTCF	chr6:142623006-142623133	Medullo	brain:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
39	CTCF	chr6:142622900-142623050	GM12868	blood:	n/a	n/a
40	CTCF	chr6:142622160-142622310	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr6:142623013-142623048	GM19239	blood:	n/a	n/a
42	CTCF	chr6:142623540-142623690	HRE	kidney:	n/a	n/a
43	CTCF	chr6:142622900-142623050	HVMF	connective:	n/a	n/a
44	CTCF	chr6:142622960-142623218	IMR90	lung:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
45	CTCF	chr6:142623020-142623170	GM12867	blood:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
46	CTCF	chr6:142622933-142623286	MCF-7	breast:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
47	CTCF	chr6:142624060-142624210	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:142623000-142623150	GM12866	blood:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
49	CTCF	chr6:142623000-142623150	AG09319	gingival:	n/a	chr6:142623096-142623109 chr6:142623100-142623113
50	CTCF	chr6:142622700-142622850	HUVEC	blood vessel:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:142623767-142623817	HIPEpiC	eye:	n/a
2	chr6:142623767-142623817	HIPEpiC	eye:	n/a
3	chr6:142622808-142622858	NH-A	brain:	n/a
4	chr6:142622903-142622953	Jurkat	blood:	n/a
5	chr6:142622903-142622953	HCM	heart:	n/a
6	chr6:142622808-142622858	K562	blood:	n/a
7	chr6:142623433-142623483	A549	lung:	n/a
8	chr6:142622808-142622858	HCPEpiC	choroid plexus:	n/a
9	chr6:142622808-142622858	SAEC	small airway:	n/a
10	chr6:142622903-142622953	SK-N-SH_RA	brain:	n/a
11	chr6:142622897-142622947	HEK293	kidney:	embryo
12	chr6:142622515-142622565	Caco-2	colon:	n/a
13	chr6:142622918-142622968	HL-60	blood:	n/a
14	chr6:142622903-142622953	RPTEC	kidney:	n/a
15	chr6:142622897-142622947	HCM	heart:	n/a
16	chr6:142622515-142622565	HIPEpiC	eye:	n/a
17	chr6:142622808-142622858	NHBE	bronchial:	n/a
18	chr6:142623433-142623483	HNPCEpiC	eye:	n/a
19	chr6:142622903-142622953	GM19239	blood:	n/a
20	chr6:142622903-142622953	HepG2	liver:	n/a
21	chr6:142622515-142622565	Hepatocyte	liver:	n/a
22	chr6:142622918-142622968	NH-A	brain:	n/a
23	chr6:142623767-142623817	A549	lung:	n/a
24	chr6:142622918-142622968	HNPCEpiC	eye:	n/a
25	chr6:142623767-142623817	NHBE	bronchial:	n/a
26	chr6:142622918-142622968	PFSK-1	brain:	n/a
27	chr6:142622808-142622858	AoSMC	blood vessel:	n/a
28	chr6:142622515-142622565	GM12891	blood:	n/a
29	chr6:142622808-142622858	ProgFib	skin:	n/a
30	chr6:142622920-142622970	SK-N-MC	brain:	n/a
31	chr6:142622920-142622970	RPTEC	kidney:	n/a
32	chr6:142622897-142622947	HepG2	liver:	n/a
33	chr6:142622920-142622970	ProgFib	skin:	n/a
34	chr6:142622918-142622968	Hepatocyte	liver:	n/a
35	chr6:142622918-142622968	K562	blood:	n/a
36	chr6:142622920-142622970	GM19239	blood:	n/a
37	chr6:142622918-142622968	LNCaP	prostate:	n/a
38	chr6:142622918-142622968	MCF10A-Er-Src	breast:	n/a
39	chr6:142623767-142623817	SAEC	small airway:	n/a
40	chr6:142622515-142622565	AG04449	skin:	fetal
41	chr6:142622515-142622565	HRE	kidney:	n/a
42	chr6:142622918-142622968	HRE	kidney:	n/a
43	chr6:142623433-142623483	SAEC	small airway:	n/a
44	chr6:142623767-142623817	SK-N-SH_RA	brain:	n/a
45	chr6:142622897-142622947	BJ	skin:	n/a
46	chr6:142622808-142622858	HCT-116	colon:	n/a
47	chr6:142623767-142623817	HRE	kidney:	n/a
48	chr6:142622903-142622953	HCPEpiC	choroid plexus:	n/a
49	chr6:142622897-142622947	HMEC	breast:	n/a
50	chr6:142622515-142622565	NH-A	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:142619918..142621591-chr6:142650811..142653503,2	MCF-7	breast:
2	chr6:142614542..142616316-chr6:142618256..142620564,2	K562	blood:
3	chr6:142616393..142621187-chr6:142621251..142624872,10	MCF-7	breast:
4	chr6:142624206..142626464-chr6:143264928..143267518,2	MCF-7	breast:
5	chr6:142624220..142625771-chr6:142695392..142697022,2	MCF-7	breast:
6	chr6:142619429..142621317-chr6:142736367..142738692,2	MCF-7	breast:
7	chr6:142622193..142623879-chr6:143265828..143267526,2	MCF-7	breast:
8	chr6:142616863..142618821-chr6:142620050..142622053,2	K562	blood:
9	chr5:43121611..43122180-chr6:142622739..142623312,2	Hela-S3	cervix:
10	chr6:142617568..142620556-chr6:142699575..142701431,2	MCF-7	breast:
11	chr6:142624264..142626987-chr6:142649609..142652476,2	MCF-7	breast:
12	chr6:142546061..142548979-chr6:142618829..142620603,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMBR-4	chr6:142622234-142622462	NONHSAT115309

No data

Variant related genes	Relation type
GPR126	TF binding region
GPR126	CpG island
ENSG00000112414	chromatin interactions
ENSG00000010818	chromatin interactions
ENSG00000172262	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6920468	chr6:142620405-142620406	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562587915	chr6:142620412-142620413	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs543151173	chr6:142620446-142620447	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs551607680	chr6:142620449-142620450	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560437800	chr6:142620460-142620461	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs527576722	chr6:142620465-142620466	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs549043638	chr6:142620475-142620476	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562570825	chr6:142620515-142620516	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs180998369	chr6:142620545-142620546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs144563419	chr6:142620548-142620549	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs545305774	chr6:142620574-142620575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs6905012	chr6:142620605-142620606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs527900779	chr6:142620610-142620611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370753827	chr6:142620746-142620747	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs118035676	chr6:142620783-142620784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201304093	chr6:142620798-142620799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs66680673	chr6:142620799-142620800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146496468	chr6:142620801-142620802	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs75091025	chr6:142620802-142620803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs71021660	chr6:142620803-142620804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs75493750	chr6:142620804-142620805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150272128	chr6:142620864-142620865	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs187060296	chr6:142620885-142620886	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs569010647	chr6:142620886-142620887	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs374771528	chr6:142620960-142620961	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs73576312	chr6:142620990-142620991	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs73576315	chr6:142621104-142621105	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs377021244	chr6:142621161-142621162	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549057547	chr6:142621166-142621167	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs192342121	chr6:142621186-142621187	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555809013	chr6:142621200-142621201	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573546951	chr6:142621247-142621248	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371177166	chr6:142621260-142621261	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs1418204	chr6:142621279-142621280	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556247126	chr6:142621290-142621291	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs6926685	chr6:142621321-142621322	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs6906368	chr6:142621339-142621340	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs76261296	chr6:142621359-142621360	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs75003080	chr6:142621360-142621361	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs560281717	chr6:142621373-142621374	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs370765656	chr6:142621374-142621375	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs6906539	chr6:142621411-142621412	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs571540611	chr6:142621414-142621415	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs149262020	chr6:142621415-142621416	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs58345825	chr6:142621437-142621438	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550555003	chr6:142621461-142621462	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs553720017	chr6:142621467-142621468	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs9496327	chr6:142621472-142621473	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs10688438	chr6:142621491-142621492	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs185822966	chr6:142621512-142621513	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
Colorectal cancer	16272173	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Burkitt''s lymphoma	19759907	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142616400-142621800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr6:142618200-142621800	Enhancers	HMEC	breast
3	chr6:142618400-142620600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:142618400-142621600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:142618400-142621600	Enhancers	NHEK	skin
6	chr6:142618600-142620600	Enhancers	HSMM	muscle
7	chr6:142618600-142621800	Weak transcription	Stomach Mucosa	stomach
8	chr6:142618800-142621800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:142618800-142622000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:142619200-142622200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:142619400-142621800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:142619400-142622000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:142619400-142622000	Enhancers	Placenta	Placenta
14	chr6:142619600-142620800	Enhancers	A549	lung
15	chr6:142619600-142621400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:142619600-142621600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:142619600-142621600	Weak transcription	Fetal Lung	lung
18	chr6:142619600-142622200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr6:142619600-142622200	Weak transcription	NHDF-Ad	bronchial
20	chr6:142619800-142621600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:142619800-142621800	Weak transcription	Fetal Heart	heart
22	chr6:142619800-142622000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:142619800-142622000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr6:142619800-142622000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:142619800-142622000	Weak transcription	NH-A	brain
26	chr6:142620000-142621800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:142620000-142621800	Weak transcription	Osteobl	bone
28	chr6:142620000-142622000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:142620000-142622200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:142620400-142621400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr6:142620400-142621400	Weak transcription	HUVEC	blood vessel
32	chr6:142620400-142621600	Enhancers	HepG2	liver
33	chr6:142620400-142621800	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr6:142620400-142621800	Weak transcription	NHLF	lung
35	chr6:142620400-142622000	Weak transcription	HSMMtube	muscle
36	chr6:142620400-142622200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:142620600-142621800	Weak transcription	HSMM	muscle
38	chr6:142620600-142622200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:142620800-142621200	Weak transcription	A549	lung
40	chr6:142621200-142621400	Enhancers	Hela-S3	cervix
41	chr6:142621200-142621600	Enhancers	Liver	Liver
42	chr6:142621200-142621600	Enhancers	A549	lung
43	chr6:142621400-142621600	Enhancers	HUVEC	blood vessel
44	chr6:142621400-142621800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr6:142621400-142622000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:142621400-142622000	Enhancers	Duodenum Mucosa	Duodenum
47	chr6:142621400-142622400	Flanking Active TSS	Hela-S3	cervix
48	chr6:142621600-142621800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:142621600-142621800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr6:142621600-142621800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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