Variant report

Variant	nsv1026121
Chromosome Location	chr6:34786887-34961360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2876)
CpG islands
(count:2323)
Chromatin interactive
region (count:207)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2876 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34867597-34867797	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34807829-34807953	K562	blood:	n/a	n/a
3	ARID3A	chr6:34954566-34954923	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:34954572-34954906	K562	blood:	n/a	n/a
5	ARID3A	chr6:34802936-34803203	K562	blood:	n/a	n/a
6	ARID3A	chr6:34855719-34856923	K562	blood:	n/a	n/a
7	ARID3A	chr6:34856773-34857038	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:34832879-34833479	K562	blood:	n/a	n/a
9	ARID3A	chr6:34913180-34913516	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:34921206-34922396	HepG2	liver:	n/a	n/a
11	ATF1	chr6:34921512-34921692	K562	blood:	n/a	n/a
12	ATF1	chr6:34874691-34874810	K562	blood:	n/a	n/a
13	ATF1	chr6:34832863-34833326	K562	blood:	n/a	n/a
14	ATF1	chr6:34803008-34803279	K562	blood:	n/a	n/a
15	ATF1	chr6:34856679-34857207	K562	blood:	n/a	n/a
16	ATF1	chr6:34950737-34951033	K562	blood:	n/a	n/a
17	ATF1	chr6:34855487-34856397	K562	blood:	n/a	chr6:34855838-34855852
18	ATF1	chr6:34827687-34828162	K562	blood:	n/a	n/a
19	ATF2	chr6:34880420-34880916	GM12878	blood:	n/a	n/a
20	ATF2	chr6:34855549-34856136	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
21	ATF2	chr6:34855474-34856393	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
22	ATF2	chr6:34856545-34857022	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr6:34856633-34857098	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:34855528-34856206	GM12878	blood:	n/a	chr6:34855838-34855852
25	ATF2	chr6:34855555-34856110	GM12878	blood:	n/a	chr6:34855838-34855852
26	ATF3	chr6:34869076-34869473	K562	blood:	n/a	n/a
27	ATF3	chr6:34855748-34855947	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
28	ATF3	chr6:34937401-34937669	K562	blood:	n/a	n/a
29	ATF3	chr6:34855564-34856045	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
30	ATF3	chr6:34855611-34856089	A549	lung:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
31	ATF3	chr6:34855569-34856012	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
32	ATF3	chr6:34855565-34856126	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
33	ATF3	chr6:34855575-34856023	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
34	ATF3	chr6:34856802-34857214	K562	blood:	n/a	n/a
35	ATF3	chr6:34855553-34856043	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
36	ATF3	chr6:34855595-34856148	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
37	ATF3	chr6:34869194-34869500	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF3	chr6:34855584-34856143	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
39	ATF3	chr6:34855626-34856017	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
40	BACH1	chr6:34842743-34842837	K562	blood:	n/a	n/a
41	BACH1	chr6:34787485-34787796	K562	blood:	n/a	n/a
42	BACH1	chr6:34807714-34807998	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr6:34856735-34857116	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr6:34807689-34808041	K562	blood:	n/a	n/a
45	BACH1	chr6:34937468-34937748	K562	blood:	n/a	chr6:34937563-34937577
46	BATF	chr6:34923346-34923637	GM12878	blood:	n/a	n/a
47	BATF	chr6:34880490-34880853	GM12878	blood:	n/a	chr6:34880751-34880760
48	BATF	chr6:34880482-34880828	GM12878	blood:	n/a	chr6:34880751-34880760
49	BCL3	chr6:34890225-34890526	GM12878	blood:	n/a	n/a
50	BCL3	chr6:34855610-34855991	GM12878	blood:	n/a	n/a

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34954867-34954917	A549	lung:	n/a
2	chr6:34858220-34858270	PFSK-1	brain:	n/a
3	chr6:34861541-34861591	AoSMC	blood vessel:	n/a
4	chr6:34857663-34857713	ECC-1	luminal epithelium:	n/a
5	chr6:34857473-34857523	ProgFib	skin:	n/a
6	chr6:34954867-34954917	A549	lung:	n/a
7	chr6:34858220-34858270	PFSK-1	brain:	n/a
8	chr6:34861541-34861591	AoSMC	blood vessel:	n/a
9	chr6:34857663-34857713	ECC-1	luminal epithelium:	n/a
10	chr6:34857473-34857523	ProgFib	skin:	n/a
11	chr6:34856920-34856970	Hepatocyte	liver:	n/a
12	chr6:34843579-34843629	A549	lung:	n/a
13	chr6:34861541-34861591	Caco-2	colon:	n/a
14	chr6:34856158-34856208	ECC-1	luminal epithelium:	n/a
15	chr6:34857162-34857212	HNPCEpiC	eye:	n/a
16	chr6:34855887-34855937	HRCEpiC	kidney:	n/a
17	chr6:34856135-34856185	AG04450	lung:	fetal
18	chr6:34857162-34857212	GM06990	blood:	n/a
19	chr6:34855834-34855884	HAEpiC	amniotic membrane:	n/a
20	chr6:34855797-34855847	AG09309	skin:	n/a
21	chr6:34857663-34857713	PFSK-1	brain:	n/a
22	chr6:34857281-34857331	SKMC	muscle:	n/a
23	chr6:34856158-34856208	NT2-D1	testis:	n/a
24	chr6:34861541-34861591	SK-N-SH	brain:	n/a
25	chr6:34922135-34922185	HEK293	kidney:	embryo
26	chr6:34949773-34949823	HRCEpiC	kidney:	n/a
27	chr6:34922135-34922185	HL-60	blood:	n/a
28	chr6:34855408-34855458	LNCaP	prostate:	n/a
29	chr6:34949773-34949823	HRPEpiC	eye:	n/a
30	chr6:34856704-34856754	A549	lung:	n/a
31	chr6:34843579-34843629	HCT-116	colon:	n/a
32	chr6:34855797-34855847	HEK293	kidney:	embryo
33	chr6:34857663-34857713	HNPCEpiC	eye:	n/a
34	chr6:34941065-34941115	PrEC	prostate:	n/a
35	chr6:34879081-34879131	GM12891	blood:	n/a
36	chr6:34856217-34856267	IMR90	lung:	fetal
37	chr6:34856897-34856947	Hepatocyte	liver:	n/a
38	chr6:34857018-34857068	ProgFib	skin:	n/a
39	chr6:34861541-34861591	H1-hESC	embryonic stem cell:	embryo
40	chr6:34895360-34895410	NB4	blood:	n/a
41	chr6:34856158-34856208	AG09319	gingival:	n/a
42	chr6:34855470-34855520	NT2-D1	testis:	n/a
43	chr6:34857281-34857331	HRCEpiC	kidney:	n/a
44	chr6:34954030-34954080	HAEpiC	amniotic membrane:	n/a
45	chr6:34949773-34949823	IMR90	lung:	fetal
46	chr6:34855797-34855847	NT2-D1	testis:	n/a
47	chr6:34858220-34858270	HUVEC	blood vessel:	n/a
48	chr6:34856158-34856208	BJ	skin:	n/a
49	chr6:34954030-34954080	PrEC	prostate:	n/a
50	chr6:34919755-34919805	HNPCEpiC	eye:	n/a

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:34875439..34878531-chr6:34883509..34886060,3	MCF-7	breast:
2	chr6:34914307..34916532-chr6:34932966..34936178,3	K562	blood:
3	chr6:34757536..34760018-chr6:34783052..34787037,5	K562	blood:
4	chr6:34803335..34805787-chr6:34806399..34809385,2	K562	blood:
5	chr6:34869119..34871903-chr6:34874576..34877464,3	K562	blood:
6	chr6:34855693..34857942-chr6:35191744..35194149,2	MCF-7	breast:
7	chr17:73285374..73286157-chr6:34855342..34855976,2	Hela-S3	cervix:
8	chr6:34927113..34929243-chr6:34940078..34941859,2	K562	blood:
9	chr6:34893290..34895416-chr6:34950224..34952119,2	K562	blood:
10	chr17:56708594..56709416-chr6:34855776..34856394,2	Hela-S3	cervix:
11	chr6:34947461..34949129-chr6:34952748..34955327,2	MCF-7	breast:
12	chr6:34949753..34950779-chr6:35107305..35108332,7	MCF-7	breast:
13	chr6:34947461..34949129-chr6:34952748..34955327,2	MCF-7	breast:
14	chr6:34786614..34789043-chr6:34809197..34812183,2	K562	blood:
15	chr6:34944340..34947621-chr6:34949271..34952410,3	MCF-7	breast:
16	chr6:34832033..34834649-chr6:34867129..34869415,2	K562	blood:
17	chr6:34953914..34956313-chr6:34963882..34965683,2	MCF-7	breast:
18	chr6:34854671..34856774-chr6:34870944..34872529,2	MCF-7	breast:
19	chr6:34852396..34857039-chr6:34885312..34888900,5	MCF-7	breast:
20	chr6:34951228..34953386-chr6:35100588..35103332,2	K562	blood:
21	chr6:34954072..34954818-chr6:35208589..35209528,2	MCF-7	breast:
22	chr6:34960537..34962092-chr6:34983517..34986049,2	K562	blood:
23	chr12:120729250..120730043-chr6:34855337..34856229,2	Hela-S3	cervix:
24	chr6:34854042..34857854-chr6:34876810..34882352,6	K562	blood:
25	chr6:34951497..34953140-chr6:35208526..35210483,2	K562	blood:
26	chr6:34869119..34871903-chr6:34874576..34877464,3	K562	blood:
27	chr6:34858328..34861023-chr6:34902579..34904193,2	K562	blood:
28	chr6:34866548..34869381-chr6:34871968..34873734,2	K562	blood:
29	chr6:34392840..34394590-chr6:34855825..34858514,2	K562	blood:
30	chr6:34828049..34830008-chr6:34830119..34831858,2	K562	blood:
31	chr6:34874014..34875640-chr6:34878716..34880730,2	K562	blood:
32	chr6:34834235..34837166-chr6:34838772..34840616,2	MCF-7	breast:
33	chr6:34803335..34805787-chr6:34806399..34809385,2	K562	blood:
34	chr6:34954285..34955179-chr6:35208270..35209520,3	K562	blood:
35	chr6:34865959..34867467-chr6:34869062..34871406,2	K562	blood:
36	chr6:34759201..34762395-chr6:34788232..34791970,5	MCF-7	breast:
37	chr6:34834250..34837156-chr6:34851105..34853013,3	MCF-7	breast:
38	chr6:34927133..34929611-chr6:34935086..34937533,2	K562	blood:
39	chr6:34837193..34840409-chr6:34855219..34858367,4	K562	blood:
40	chr6:34855314..34856910-chr6:35435686..35437650,2	MCF-7	breast:
41	chr6:34854986..34858344-chr6:35226281..35229493,3	K562	blood:
42	chr6:34392549..34394826-chr6:34874788..34877623,2	MCF-7	breast:
43	chr6:34948492..34951112-chr6:34954153..34956114,2	K562	blood:
44	chr6:34956071..34958018-chr6:34959188..34960981,2	K562	blood:
45	chr6:34831813..34834796-chr6:34855426..34858110,2	MCF-7	breast:
46	chr6:34954674..34955203-chr6:35172145..35173032,2	K562	blood:
47	chr6:34937846..34940693-chr6:34953607..34956913,3	K562	blood:
48	chr6:34854944..34856631-chr6:34874568..34876971,2	MCF-7	breast:
49	chr6:34952785..34956692-chr6:34957031..34961884,7	K562	blood:
50	chr6:34827930..34830077-chr6:34830559..34833296,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UHRF1BP1	hsa-let-7e-5p	chr6:34843708-34843714
2	UHRF1BP1	hsa-let-7e-5p	chr6:34825126-34825148

Variant related genes	Relation type
ENSG00000206717	TF binding region
ANKS1A	TF binding region
TAF11	TF binding region
ENSG00000206717	CpG island
ANKS1A	CpG island
TAF11	CpG island
ENSG00000124614	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000264241	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000272374	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000159733	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000125454	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000064999	chromatin interactions
ENSG00000197914	chromatin interactions
ENSG00000174197	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 6191 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:6191 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71538273	chr6:34786919-34786920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs183738840	chr6:34786924-34786925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs71002504	chr6:34786931-34786932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368944595	chr6:34786934-34786935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs546924407	chr6:34786971-34786972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs568358502	chr6:34787052-34787053	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs35016333	chr6:34787075-34787076	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs536182911	chr6:34787087-34787088	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs71567466	chr6:34787088-34787089	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs77108815	chr6:34787119-34787120	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs192508719	chr6:34787152-34787153	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs183096916	chr6:34787157-34787158	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs572929324	chr6:34787244-34787245	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs539949855	chr6:34787246-34787247	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs138548116	chr6:34787263-34787264	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573539815	chr6:34787289-34787290	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377562054	chr6:34787325-34787326	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs370787370	chr6:34787339-34787340	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs544521582	chr6:34787340-34787341	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs114804155	chr6:34787353-34787354	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs114536019	chr6:34787380-34787381	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs115175823	chr6:34787391-34787392	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs564240189	chr6:34787410-34787411	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs187736670	chr6:34787436-34787437	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564774378	chr6:34787465-34787466	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs546765311	chr6:34787474-34787475	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs568472520	chr6:34787523-34787524	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs115566179	chr6:34787537-34787538	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs551274545	chr6:34787555-34787556	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs191478525	chr6:34787641-34787642	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs79636624	chr6:34787645-34787646	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs184240590	chr6:34787657-34787658	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs144139200	chr6:34787725-34787726	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533921357	chr6:34787750-34787751	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147324670	chr6:34787787-34787788	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs1318609	chr6:34787811-34787812	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140946960	chr6:34787838-34787839	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs6921759	chr6:34787886-34787887	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs4333405	chr6:34787899-34787900	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556046696	chr6:34787912-34787913	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs189990161	chr6:34787917-34787918	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs199919119	chr6:34787953-34787954	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149820342	chr6:34787959-34787960	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2395604	chr6:34787976-34787977	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs572127831	chr6:34788120-34788121	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs539279314	chr6:34788200-34788201	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1018622	chr6:34788231-34788232	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs192575030	chr6:34788301-34788302	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs140290264	chr6:34788343-34788344	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140754798	chr6:34788346-34788347	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5007 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34761400-34787200	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:34761400-34789400	Weak transcription	Fetal Stomach	stomach
3	chr6:34761400-34789400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:34761400-34790800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr6:34762000-34788400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:34764000-34803800	Weak transcription	HSMM	muscle
7	chr6:34764600-34787400	Weak transcription	Liver	Liver
8	chr6:34772600-34789400	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr6:34773200-34791400	Weak transcription	Gastric	stomach
10	chr6:34775400-34787200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr6:34775400-34787200	Weak transcription	Right Ventricle	heart
12	chr6:34775400-34802400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:34776600-34789600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr6:34777800-34789000	Weak transcription	Primary T cells from cord blood	blood
15	chr6:34778600-34787200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr6:34779200-34797000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr6:34779200-34807400	Weak transcription	A549	lung
18	chr6:34779400-34787400	Weak transcription	HUVEC	blood vessel
19	chr6:34779400-34789400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:34779400-34789400	Weak transcription	Hela-S3	cervix
21	chr6:34779400-34796400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr6:34779400-34841000	Weak transcription	NH-A	brain
23	chr6:34779600-34791000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:34779600-34791400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:34779600-34796200	Weak transcription	NHEK	skin
26	chr6:34779800-34787400	Weak transcription	Left Ventricle	heart
27	chr6:34779800-34789400	Weak transcription	Fetal Intestine Small	intestine
28	chr6:34780400-34787200	Weak transcription	Right Atrium	heart
29	chr6:34780800-34794000	Weak transcription	Aorta	Aorta
30	chr6:34781000-34787200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr6:34781000-34790800	Weak transcription	Brain Angular Gyrus	brain
32	chr6:34781000-34797000	Weak transcription	Colon Smooth Muscle	Colon
33	chr6:34781200-34789400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr6:34781400-34790800	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr6:34781600-34787400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:34781600-34787400	Weak transcription	Brain Hippocampus Middle	brain
37	chr6:34781600-34787400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr6:34781600-34787600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr6:34781600-34788000	Weak transcription	HSMMtube	muscle
40	chr6:34781600-34791000	Weak transcription	Brain Anterior Caudate	brain
41	chr6:34781600-34791400	Weak transcription	Brain Substantia Nigra	brain
42	chr6:34781600-34824000	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr6:34781800-34790600	Weak transcription	Brain Germinal Matrix	brain
44	chr6:34782600-34789400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:34782800-34790800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:34783200-34807400	Weak transcription	Psoas Muscle	Psoas
47	chr6:34783400-34787400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:34784200-34789600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr6:34784400-34787200	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr6:34784400-34787200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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