Variant report

Variant	nsv600886
Chromosome Location	chr6:5426265-5511614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:839)
CpG islands
(count:488)
Chromatin interactive
region (count:34)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5466765-5467343	K562	blood:	n/a	n/a
2	ARID3A	chr6:5471245-5471536	K562	blood:	n/a	n/a
3	ATF2	chr6:5507200-5507833	GM12878	blood:	n/a	n/a
4	ATF2	chr6:5507116-5507755	GM12878	blood:	n/a	n/a
5	ATF2	chr6:5486408-5486752	GM12878	blood:	n/a	n/a
6	ATF2	chr6:5486322-5486870	GM12878	blood:	n/a	n/a
7	BACH1	chr6:5472378-5472661	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:5466733-5467034	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr6:5486359-5486772	GM12878	blood:	n/a	n/a
10	BATF	chr6:5486405-5486840	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:5486472-5486770	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:5439210-5439426	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr6:5486426-5486800	GM12878	blood:	n/a	n/a
14	BCLAF1	chr6:5486464-5486825	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:5507105-5507974	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:5507151-5507667	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:5486462-5486879	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:5475344-5475513	K562	blood:	n/a	n/a
19	BHLHE40	chr6:5507146-5507955	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:5486474-5486846	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:5471216-5471558	K562	blood:	n/a	n/a
22	BHLHE40	chr6:5467008-5467253	K562	blood:	n/a	n/a
23	BHLHE40	chr6:5502110-5502446	K562	blood:	n/a	n/a
24	CEBPB	chr6:5504423-5504635	H1-hESC	embryonic stem cell:	n/a	chr6:5504502-5504513
25	CEBPB	chr6:5452057-5452363	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:5504348-5504672	HepG2	liver:	n/a	chr6:5504502-5504513
27	CEBPB	chr6:5480453-5480620	HepG2	liver:	n/a	chr6:5480518-5480529
28	CEBPB	chr6:5439238-5439539	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:5504446-5504603	A549	lung:	n/a	chr6:5504502-5504513
30	CEBPB	chr6:5471248-5471547	HepG2	liver:	n/a	chr6:5471398-5471409
31	CEBPB	chr6:5471226-5471535	A549	lung:	n/a	chr6:5471398-5471409
32	CEBPB	chr6:5471235-5471578	A549	lung:	n/a	chr6:5471398-5471409
33	CEBPB	chr6:5504323-5504687	K562	blood:	n/a	chr6:5504502-5504513
34	CEBPB	chr6:5504334-5504662	IMR90	lung:	n/a	chr6:5504502-5504513
35	CEBPB	chr6:5468827-5469078	IMR90	lung:	n/a	chr6:5468912-5468923
36	CEBPB	chr6:5426867-5426988	HepG2	liver:	n/a	chr6:5426914-5426925
37	CEBPB	chr6:5472487-5472649	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr6:5471262-5471542	Hela-S3	cervix:	n/a	chr6:5471398-5471409
39	CEBPB	chr6:5471254-5471553	H1-hESC	embryonic stem cell:	n/a	chr6:5471398-5471409
40	CEBPB	chr6:5479007-5479143	K562	blood:	n/a	n/a
41	CEBPB	chr6:5471218-5471599	K562	blood:	n/a	chr6:5471398-5471409
42	CEBPB	chr6:5444631-5444694	K562	blood:	n/a	n/a
43	CEBPB	chr6:5471293-5471423	HepG2	liver:	n/a	chr6:5471398-5471409
44	CEBPB	chr6:5471266-5471607	MCF-7	breast:	n/a	chr6:5471398-5471409
45	CEBPB	chr6:5471200-5471522	K562	blood:	n/a	chr6:5471398-5471409
46	CEBPB	chr6:5474607-5474770	K562	blood:	n/a	n/a
47	CEBPZ	chr6:5471203-5471301	HepG2	liver:	n/a	n/a
48	CHD1	chr6:5486486-5486799	GM12878	blood:	n/a	n/a
49	CHD1	chr6:5507231-5507958	GM12878	blood:	n/a	n/a
50	CHD2	chr6:5507270-5507736	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5442953-5443003	A549	lung:	n/a
2	chr6:5439460-5439510	GM12891	blood:	n/a
3	chr6:5442953-5443003	SK-N-SH	brain:	n/a
4	chr6:5439460-5439510	HEEpiC	esophagus:	n/a
5	chr6:5510697-5510747	Hela-S3	cervix:	n/a
6	chr6:5442953-5443003	Hela-S3	cervix:	n/a
7	chr6:5442953-5443003	PANC-1	pancreas:	n/a
8	chr6:5442953-5443003	GM06990	blood:	n/a
9	chr6:5510748-5510798	NHBE	bronchial:	n/a
10	chr6:5472095-5472145	H1-hESC	embryonic stem cell:	embryo
11	chr6:5431669-5431719	NHDF-neo	bronchial:	n/a
12	chr6:5472095-5472145	HRCEpiC	kidney:	n/a
13	chr6:5510800-5510850	SK-N-MC	brain:	n/a
14	chr6:5431669-5431719	RPTEC	kidney:	n/a
15	chr6:5431669-5431719	HRCEpiC	kidney:	n/a
16	chr6:5510697-5510747	PrEC	prostate:	n/a
17	chr6:5510748-5510798	NB4	blood:	n/a
18	chr6:5442953-5443003	PrEC	prostate:	n/a
19	chr6:5463751-5463801	PrEC	prostate:	n/a
20	chr6:5510748-5510798	PrEC	prostate:	n/a
21	chr6:5439460-5439510	NH-A	brain:	n/a
22	chr6:5439460-5439510	IMR90	lung:	fetal
23	chr6:5439460-5439510	U87	brain:	n/a
24	chr6:5431669-5431719	GM12892	blood:	n/a
25	chr6:5439460-5439510	HIPEpiC	eye:	n/a
26	chr6:5472095-5472145	ovcar-3	ovarian:	n/a
27	chr6:5442953-5443003	AG04450	lung:	fetal
28	chr6:5510697-5510747	HMEC	breast:	n/a
29	chr6:5431669-5431719	BJ	skin:	n/a
30	chr6:5510697-5510747	T-47D	breast:	n/a
31	chr6:5510748-5510798	LNCaP	prostate:	n/a
32	chr6:5442953-5443003	Jurkat	blood:	n/a
33	chr6:5463751-5463801	HUVEC	blood vessel:	n/a
34	chr6:5463751-5463801	HepG2	liver:	n/a
35	chr6:5463751-5463801	HIPEpiC	eye:	n/a
36	chr6:5472095-5472145	HEK293	kidney:	embryo
37	chr6:5510800-5510850	SK-N-SH_RA	brain:	n/a
38	chr6:5442953-5443003	NHBE	bronchial:	n/a
39	chr6:5510800-5510850	AG09319	gingival:	n/a
40	chr6:5431669-5431719	ovcar-3	ovarian:	n/a
41	chr6:5510800-5510850	AG10803	skin:	n/a
42	chr6:5510748-5510798	Hepatocyte	liver:	n/a
43	chr6:5439460-5439510	HCF	heart:	n/a
44	chr6:5472095-5472145	HCT-116	colon:	n/a
45	chr6:5472095-5472145	BJ	skin:	n/a
46	chr6:5510748-5510798	PFSK-1	brain:	n/a
47	chr6:5510697-5510747	HEK293	kidney:	embryo
48	chr6:5442953-5443003	HL-60	blood:	n/a
49	chr6:5510800-5510850	MCF10A-Er-Src	breast:	n/a
50	chr6:5431669-5431719	HNPCEpiC	eye:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:5470498..5472871-chr6:6545581..6547972,2	MCF-7	breast:
2	chr6:5485806..5488225-chr6:5489962..5492920,2	K562	blood:
3	chr6:5478279..5480478-chr6:5483218..5485001,2	K562	blood:
4	chr6:5499395..5501300-chr6:5509807..5511478,2	K562	blood:
5	chr6:5438413..5441149-chr6:5444124..5446462,2	K562	blood:
6	chr6:5455034..5457596-chr6:5459159..5460952,3	K562	blood:
7	chr6:5469656..5471454-chr6:5488519..5490118,2	K562	blood:
8	chr6:5434559..5437034-chr6:5438817..5440512,2	MCF-7	breast:
9	chr6:5434559..5437034-chr6:5438817..5440512,2	MCF-7	breast:
10	chr6:5471400..5474244-chr6:6052015..6054966,2	MCF-7	breast:
11	chr6:5422015..5424265-chr6:5433420..5435571,2	K562	blood:
12	chr6:5499395..5501300-chr6:5509807..5511478,2	K562	blood:
13	chr6:5435025..5437230-chr6:5438877..5440438,2	MCF-7	breast:
14	chr6:5424951..5427870-chr6:5732837..5734922,2	MCF-7	breast:
15	chr6:5478279..5480478-chr6:5483218..5485001,2	K562	blood:
16	chr6:5431881..5436604-chr6:5436753..5441713,4	K562	blood:
17	chr6:5435025..5437230-chr6:5438877..5440438,2	MCF-7	breast:
18	chr6:5471377..5471902-chr6:5520001..5520569,2	MCF-7	breast:
19	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
20	chr6:5438413..5441149-chr6:5444124..5446462,2	K562	blood:
21	chr6:5471461..5471990-chr6:5766502..5767102,2	K562	blood:
22	chr6:5469656..5471454-chr6:5488519..5490118,2	K562	blood:
23	chr6:5470888..5471844-chr6:6131906..6132435,2	MCF-7	breast:
24	chr6:5451514..5453139-chr6:5455554..5457510,2	K562	blood:
25	chr6:5471238..5471818-chr6:5519987..5520960,2	K562	blood:
26	chr6:5485806..5488225-chr6:5489962..5492920,2	K562	blood:
27	chr6:5451514..5453139-chr6:5455554..5457510,2	K562	blood:
28	chr6:5473023..5474708-chr6:5475378..5477106,2	K562	blood:
29	chr6:5431424..5433341-chr6:5434266..5436505,3	K562	blood:
30	chr6:5455034..5457596-chr6:5459159..5460952,3	K562	blood:
31	chr6:5511127..5514739-chr6:5516626..5520619,5	K562	blood:
32	chr6:5431881..5436604-chr6:5436753..5441713,4	K562	blood:
33	chr6:5445214..5446148-chr7:141145714..141146573,2	MCF-7	breast:
34	chr6:5473023..5474708-chr6:5475378..5477106,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYRM4-3	chr6:5451916-5452990	ENSG00000269985.1
2	lnc-LYRM4-3	chr6:5458127-5458278	NONHSAT107520
3	lnc-LYRM4-3	chr6:5457093-5457261	NONHSAT107520
4	lnc-LYRM4-3	chr6:5458127-5458266	ENSG00000269985.1
5	lnc-LYRM4-3	chr6:5452701-5452990	ENSG00000269985.1
6	lnc-LYRM4-3	chr6:5458127-5458308	ENSG00000269985.1
7	lnc-PPP1R3G-7	chr6:5502505-5504640	NONHSAT107521
8	lnc-LYRM4-3	chr6:5457186-5457261	ENSG00000269985.1

No data

Variant related genes	Relation type
ENSG00000269985	TF binding region
ENSG00000269985	CpG island

Extended variants
information (count: 3569 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3569 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375162284	chr6:5426265-5426266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34304958	chr6:5426266-5426267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149190121	chr6:5426273-5426274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114481988	chr6:5426367-5426368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs57037759	chr6:5426385-5426386	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs149890112	chr6:5426416-5426417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs59478390	chr6:5426424-5426425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11752504	chr6:5426450-5426451	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs529193117	chr6:5426451-5426452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146767745	chr6:5426452-5426453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12153950	chr6:5426464-5426465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs573012800	chr6:5426489-5426490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139097879	chr6:5426528-5426529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567007410	chr6:5426565-5426566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527765817	chr6:5426578-5426579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114426555	chr6:5426596-5426597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376599472	chr6:5426598-5426599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141662514	chr6:5426619-5426620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147028718	chr6:5426633-5426634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550341210	chr6:5426638-5426639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186589789	chr6:5426640-5426641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571846337	chr6:5426641-5426642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368859049	chr6:5426672-5426673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190253919	chr6:5426714-5426715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138273633	chr6:5426793-5426794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570201745	chr6:5426817-5426818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182494787	chr6:5426820-5426821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9378423	chr6:5426826-5426827	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs114245580	chr6:5426837-5426838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141861097	chr6:5426843-5426844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188565959	chr6:5426850-5426851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116464361	chr6:5426864-5426865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533249620	chr6:5426868-5426869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555514474	chr6:5426875-5426876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2503831	chr6:5426895-5426896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs150797123	chr6:5426919-5426920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527803036	chr6:5426923-5426924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370927100	chr6:5427060-5427061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549419527	chr6:5427078-5427079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567769759	chr6:5427079-5427080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369877506	chr6:5427086-5427087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138088380	chr6:5427090-5427091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529915770	chr6:5427163-5427164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542653674	chr6:5427241-5427242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542099394	chr6:5427279-5427280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145663481	chr6:5427321-5427322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs193158757	chr6:5427335-5427336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552641697	chr6:5427348-5427349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs142126746	chr6:5427350-5427351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185016903	chr6:5427393-5427394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5374400-5431400	Weak transcription	Primary B cells from cord blood	blood
2	chr6:5395400-5431200	Weak transcription	Left Ventricle	heart
3	chr6:5399200-5440000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:5403200-5439800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:5403400-5445200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:5403600-5437600	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr6:5404800-5428200	Weak transcription	Lung	lung
8	chr6:5405200-5431000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:5405400-5439800	Weak transcription	Pancreas	Pancrea
10	chr6:5406600-5431400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr6:5407000-5431000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr6:5407400-5439600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr6:5408600-5431200	Weak transcription	Gastric	stomach
14	chr6:5410200-5431200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr6:5410400-5427600	Weak transcription	Thymus	Thymus
16	chr6:5411600-5431200	Weak transcription	HepG2	liver
17	chr6:5411600-5432800	Weak transcription	Fetal Muscle Leg	muscle
18	chr6:5412800-5431200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:5412800-5437000	Weak transcription	Ovary	ovary
20	chr6:5412800-5439400	Weak transcription	Spleen	Spleen
21	chr6:5413400-5431400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:5413400-5433200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:5413400-5435200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:5413400-5442800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:5417000-5440400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:5419000-5432800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:5420200-5436200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:5421200-5435400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr6:5421400-5432800	Weak transcription	Aorta	Aorta
30	chr6:5421600-5431200	Weak transcription	Fetal Intestine Large	intestine
31	chr6:5421600-5433000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:5421600-5433000	Weak transcription	Fetal Stomach	stomach
33	chr6:5421600-5455000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:5421600-5455400	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr6:5421600-5457400	Weak transcription	Fetal Intestine Small	intestine
36	chr6:5422600-5432800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:5422800-5444000	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr6:5423000-5427600	Weak transcription	GM12878-XiMat	blood
39	chr6:5423000-5431200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr6:5423000-5436200	Weak transcription	NHLF	lung
41	chr6:5424000-5435000	Weak transcription	Adipose Nuclei	Adipose
42	chr6:5424400-5440000	Weak transcription	Small Intestine	intestine
43	chr6:5424600-5428400	Enhancers	Fetal Thymus	thymus
44	chr6:5425000-5432800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr6:5425200-5435600	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr6:5425600-5427400	Enhancers	Dnd41	blood
47	chr6:5425800-5426400	Enhancers	Primary T cells from cord blood	blood
48	chr6:5425800-5426400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr6:5425800-5433200	Weak transcription	Brain Anterior Caudate	brain
50	chr6:5425800-5434000	Weak transcription	Rectal Smooth Muscle	rectum

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