Variant report

Variant	nsv538304
Chromosome Location	chr6:73876795-73996828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1383)
CpG islands
(count:1532)
Chromatin interactive
region (count:62)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1383 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:73933935-73934276	K562	blood:	n/a	n/a
2	ARID3A	chr6:73995519-73996168	K562	blood:	n/a	n/a
3	ATF3	chr6:73933914-73934300	K562	blood:	n/a	n/a
4	BACH1	chr6:73908064-73908191	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr6:73886997-73887209	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:73890707-73891147	GM12878	blood:	n/a	n/a
7	BCLAF1	chr6:73972677-73973186	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:73933897-73934190	K562	blood:	n/a	n/a
9	BHLHE40	chr6:73972841-73973170	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:73933933-73934169	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:73973420-73973459	GM12878	blood:	n/a	n/a
12	CBX3	chr6:73933534-73934385	HCT-116	colon:	n/a	n/a
13	CBX3	chr6:73972842-73973188	K562	blood:	n/a	n/a
14	CCNT2	chr6:73972808-73973171	K562	blood:	n/a	n/a
15	CEBPB	chr6:73942971-73943171	HepG2	liver:	n/a	chr6:73943037-73943048
16	CEBPB	chr6:73996470-73996831	ECC-1	luminal epithelium:	n/a	chr6:73996669-73996680
17	CEBPB	chr6:73890822-73891158	K562	blood:	n/a	chr6:73891066-73891077 chr6:73891065-73891078
18	CEBPB	chr6:73996588-73996699	K562	blood:	n/a	chr6:73996669-73996680
19	CEBPB	chr6:73948065-73948270	A549	lung:	n/a	n/a
20	CEBPB	chr6:73944482-73944921	HCT-116	colon:	n/a	n/a
21	CEBPB	chr6:73890738-73891215	IMR90	lung:	n/a	chr6:73891066-73891077 chr6:73891065-73891078
22	CEBPB	chr6:73942951-73943183	A549	lung:	n/a	chr6:73943037-73943048
23	CEBPB	chr6:73948028-73948327	K562	blood:	n/a	n/a
24	CEBPB	chr6:73996508-73996846	H1-hESC	embryonic stem cell:	n/a	chr6:73996669-73996680
25	CEBPB	chr6:73912789-73913045	A549	lung:	n/a	chr6:73912900-73912911
26	CEBPB	chr6:73996470-73996893	A549	lung:	n/a	chr6:73996669-73996680
27	CEBPB	chr6:73996516-73996821	K562	blood:	n/a	chr6:73996669-73996680
28	CEBPB	chr6:73927466-73927741	MCF-7	breast:	n/a	chr6:73927593-73927604
29	CEBPB	chr6:73927447-73927732	H1-hESC	embryonic stem cell:	n/a	chr6:73927593-73927604
30	CEBPB	chr6:73944480-73944880	IMR90	lung:	n/a	n/a
31	CEBPB	chr6:73889864-73890415	IMR90	lung:	n/a	chr6:73890241-73890252 chr6:73890241-73890254
32	CEBPB	chr6:73996582-73996890	MCF-7	breast:	n/a	chr6:73996669-73996680
33	CEBPB	chr6:73935502-73935699	MCF-7	breast:	n/a	n/a
34	CEBPB	chr6:73945844-73946543	A549	lung:	n/a	n/a
35	CEBPB	chr6:73927419-73927762	HepG2	liver:	n/a	chr6:73927593-73927604
36	CEBPB	chr6:73996462-73996880	MCF-7	breast:	n/a	chr6:73996669-73996680
37	CEBPB	chr6:73920035-73920162	K562	blood:	n/a	n/a
38	CEBPB	chr6:73912720-73913098	IMR90	lung:	n/a	chr6:73912900-73912911
39	CEBPB	chr6:73996508-73996860	HepG2	liver:	n/a	chr6:73996669-73996680
40	CEBPB	chr6:73986272-73986444	K562	blood:	n/a	n/a
41	CEBPB	chr6:73930444-73930619	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:73912526-73913056	K562	blood:	n/a	chr6:73912900-73912911
43	CEBPB	chr6:73972089-73972743	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:73945770-73946272	A549	lung:	n/a	n/a
45	CEBPB	chr6:73927418-73927765	IMR90	lung:	n/a	chr6:73927593-73927604
46	CEBPB	chr6:73945845-73946426	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:73944448-73944896	A549	lung:	n/a	n/a
48	CEBPB	chr6:73944353-73944978	A549	lung:	n/a	n/a
49	CEBPB	chr6:73944396-73944917	HCT-116	colon:	n/a	n/a
50	CEBPB	chr6:73944525-73944854	A549	lung:	n/a	n/a

(count:1532 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:73973719-73973769	HAEpiC	amniotic membrane:	n/a
2	chr6:73976940-73976990	HUVEC	blood vessel:	n/a
3	chr6:73969316-73969366	HCF	heart:	n/a
4	chr6:73934576-73934626	BJ	skin:	n/a
5	chr6:73969316-73969366	HRE	kidney:	n/a
6	chr6:73973078-73973128	HCF	heart:	n/a
7	chr6:73972768-73972818	HUVEC	blood vessel:	n/a
8	chr6:73973719-73973769	HAEpiC	amniotic membrane:	n/a
9	chr6:73976940-73976990	HUVEC	blood vessel:	n/a
10	chr6:73969316-73969366	HCF	heart:	n/a
11	chr6:73934576-73934626	BJ	skin:	n/a
12	chr6:73969316-73969366	HRE	kidney:	n/a
13	chr6:73973078-73973128	HCF	heart:	n/a
14	chr6:73972768-73972818	HUVEC	blood vessel:	n/a
15	chr6:73973078-73973128	AoSMC	blood vessel:	n/a
16	chr6:73935200-73935250	ovcar-3	ovarian:	n/a
17	chr6:73951939-73951989	A549	lung:	n/a
18	chr6:73977747-73977797	HepG2	liver:	n/a
19	chr6:73935676-73935726	GM12878	blood:	n/a
20	chr6:73973128-73973178	HCT-116	colon:	n/a
21	chr6:73972768-73972818	RPTEC	kidney:	n/a
22	chr6:73972820-73972870	HAEpiC	amniotic membrane:	n/a
23	chr6:73934576-73934626	H1-hESC	embryonic stem cell:	embryo
24	chr6:73973128-73973178	HEK293	kidney:	embryo
25	chr6:73976940-73976990	CMK	blood:	n/a
26	chr6:73972768-73972818	IMR90	lung:	fetal
27	chr6:73935270-73935320	HIPEpiC	eye:	n/a
28	chr6:73935270-73935320	HMEC	breast:	n/a
29	chr6:73973719-73973769	U87	brain:	n/a
30	chr6:73972820-73972870	H1-hESC	embryonic stem cell:	embryo
31	chr6:73935584-73935634	PANC-1	pancreas:	n/a
32	chr6:73935125-73935175	ovcar-3	ovarian:	n/a
33	chr6:73935584-73935634	RPTEC	kidney:	n/a
34	chr6:73907779-73907829	ProgFib	skin:	n/a
35	chr6:73935676-73935726	AG04449	skin:	fetal
36	chr6:73951939-73951989	RPTEC	kidney:	n/a
37	chr6:73972820-73972870	HRCEpiC	kidney:	n/a
38	chr6:73915866-73915916	HAEpiC	amniotic membrane:	n/a
39	chr6:73951939-73951989	H1-hESC	embryonic stem cell:	embryo
40	chr6:73972820-73972870	SAEC	small airway:	n/a
41	chr6:73976940-73976990	BJ	skin:	n/a
42	chr6:73935200-73935250	HCPEpiC	choroid plexus:	n/a
43	chr6:73907779-73907829	T-47D	breast:	n/a
44	chr6:73951939-73951989	PrEC	prostate:	n/a
45	chr6:73973128-73973178	HRPEpiC	eye:	n/a
46	chr6:73973719-73973769	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:73973103-73973153	HIPEpiC	eye:	n/a
48	chr6:73972768-73972818	HRCEpiC	kidney:	n/a
49	chr6:73933428-73933478	AG09319	gingival:	n/a
50	chr6:73951145-73951195	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:73995073..73995767-chr6:74036342..74037050,3	MCF-7	breast:
2	6:73899586-73904758..6:74078047-74099067	H1-hESC	embryonic stem cell:	embryo
3	chr6:73966087..73967944-chr6:73968086..73969956,2	MCF-7	breast:
4	6:73859137-73881637..6:74062967-74076046	GM12878	blood:
5	chr6:73970435..73971985-chr6:73974301..73976161,2	K562	blood:
6	6:73927031-73938730..6:73958859-73968658	Hela-S3	cervix:
7	chr6:73995184..73996292-chr6:74036159..74036919,3	MCF-7	breast:
8	6:73958859-73968658..6:74099986-74112890	GM12878	blood:
9	chr6:73994505..73996535-chr6:74019862..74021469,2	MCF-7	breast:
10	chr6:73988362..73991724-chr6:73992246..73995569,3	K562	blood:
11	6:73958859-73968658..6:74062967-74076046	GM12878	blood:
12	6:73955774-73958859..6:74099986-74112890	Hela-S3	cervix:
13	chr6:73121810..73122595-chr6:73890813..73891425,2	MCF-7	breast:
14	6:73978150-73986643..6:74099986-74112890	H1-hESC	embryonic stem cell:	embryo
15	6:73955774-73958859..6:74078047-74099067	Hela-S3	cervix:
16	6:73955774-73958859..6:74062967-74076046	GM12878	blood:
17	chr6:73919854..73922252-chr6:73925613..73927312,3	K562	blood:
18	6:73955774-73958859..6:74160392-74184826	Hela-S3	cervix:
19	6:73978150-73986643..6:74062967-74076046	H1-hESC	embryonic stem cell:	embryo
20	chr6:73964825..73968569-chr6:73969711..73973887,5	K562	blood:
21	chr6:73961399..73963162-chr6:74019547..74021489,2	K562	blood:
22	chr6:73988362..73991724-chr6:73992246..73995569,3	K562	blood:
23	chr6:73891121..73892828-chr6:74034986..74037407,2	MCF-7	breast:
24	chr6:73946310..73949239-chr6:73949645..73951252,2	K562	blood:
25	chr6:73966087..73967944-chr6:73968086..73969956,2	MCF-7	breast:
26	6:73978150-73986643..6:74160392-74184826	K562	blood:
27	chr6:73946310..73949239-chr6:73949645..73951252,2	K562	blood:
28	6:73859137-73881637..6:73927031-73938730	Hela-S3	cervix:
29	6:73958859-73968658..6:74078047-74099067	GM12878	blood:
30	chr6:73887931..73890516-chr6:73893748..73896015,2	MCF-7	breast:
31	chr6:73917306..73919203-chr6:73947739..73949540,2	K562	blood:
32	chr6:73995392..73997640-chr6:74104378..74106290,2	MCF-7	breast:
33	chr6:73887931..73890516-chr6:73893748..73896015,2	MCF-7	breast:
34	chr6:73970435..73971985-chr6:73974301..73976161,2	K562	blood:
35	chr6:73121678..73122602-chr6:73890471..73891079,4	MCF-7	breast:
36	chr6:73890367..73891378-chr6:74036227..74036958,3	MCF-7	breast:
37	chr6:73844216..73844877-chr6:73890551..73891344,2	MCF-7	breast:
38	chr6:73917306..73919203-chr6:73947739..73949540,2	K562	blood:
39	chr6:73975435..73977276-chr6:73979825..73982235,2	K562	blood:
40	chr6:73326001..73326770-chr6:73890518..73891023,2	MCF-7	breast:
41	chr6:73962925..73964813-chr6:73974768..73977580,2	K562	blood:
42	6:73946090-73955774..6:74099986-74112890	K562	blood:
43	chr6:73969840..73972620-chr6:74018459..74020371,2	MCF-7	breast:
44	6:73927031-73938730..6:74000304-74012200	K562	blood:
45	chr6:73995175..73995795-chr6:74098478..74099056,2	MCF-7	breast:
46	chr6:73975435..73977276-chr6:73979825..73982235,2	K562	blood:
47	chr6:73996124..73998490-chr6:74004776..74007375,2	K562	blood:
48	6:73859137-73881637..6:74099986-74112890	GM12878	blood:
49	6:73946090-73955774..6:74062967-74076046	GM12878	blood:
50	chr6:73972686..73974360-chr6:74230027..74232988,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf221-2	chr6:73980169-73980250	NONHSAT113543
2	lnc-KHDC1-1	chr6:73985137-73985279	NONHSAT113547
3	lnc-C6orf221-2	chr6:73994344-73994457	NONHSAT113548
4	lnc-KHDC1-1	chr6:73983862-73984877	NONHSAT113544
5	lnc-KHDC1-1	chr6:73985132-73985279	NONHSAT113544
6	lnc-C6orf221-2	chr6:73973106-73973139	NONHSAT113540
7	lnc-KHDC1-1	chr6:73983862-73985279	NONHSAT113546
8	lnc-KHDC1-1	chr6:73984769-73984882	NONHSAT113547

No data

Variant related genes	Relation type
KHDC1	TF binding region
RPSAP41	TF binding region
KHDC1L	TF binding region
KHDC1P1	TF binding region
ENSG00000263378	TF binding region
ENSG00000229852	TF binding region
EIF3EP1	TF binding region
ENSG00000243501	TF binding region
KHDC1	CpG island
RPSAP41	CpG island
KHDC1L	CpG island
KHDC1P1	CpG island
ENSG00000263378	CpG island
ENSG00000229852	CpG island
EIF3EP1	CpG island
ENSG00000243501	CpG island
ENSG00000234882	chromatin interactions
ENSG00000229852	chromatin interactions
ENSG00000203909	chromatin interactions
ENSG00000207023	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000226840	chromatin interactions
ENSG00000203907	chromatin interactions
ENSG00000263378	chromatin interactions
ENSG00000135314	chromatin interactions
ENSG00000203908	chromatin interactions
ENSG00000164430	chromatin interactions
ENSG00000238464	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000231332	chromatin interactions
ENSG00000235174	chromatin interactions
ENSG00000224221	chromatin interactions
ENSG00000243501	chromatin interactions
ENSG00000256980	chromatin interactions
ENSG00000080007	chromatin interactions
ENSG00000234025	chromatin interactions
ENSG00000156508	chromatin interactions

Extended variants
information (count: 4619 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4619 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184249190	chr6:73876841-73876842	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs568925541	chr6:73876883-73876884	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs35598044	chr6:73876897-73876898	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs536495295	chr6:73876954-73876955	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs35020460	chr6:73876966-73876967	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs548355340	chr6:73876971-73876972	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs566858491	chr6:73877003-73877004	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs534237308	chr6:73877011-73877012	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs116644994	chr6:73877039-73877040	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs142300644	chr6:73877040-73877041	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs538198308	chr6:73877115-73877116	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs188863402	chr6:73877122-73877123	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs540302695	chr6:73877160-73877161	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs145917328	chr6:73877186-73877187	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs372364629	chr6:73877209-73877210	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs77753235	chr6:73877212-73877213	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs191828728	chr6:73877276-73877277	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs2882406	chr6:73877301-73877302	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs565128502	chr6:73877345-73877346	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs2350388	chr6:73877404-73877405	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550550125	chr6:73877405-73877406	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs2350387	chr6:73877424-73877425	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs529784086	chr6:73877449-73877450	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs376762362	chr6:73877506-73877507	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs547846857	chr6:73877580-73877581	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs561036243	chr6:73877587-73877588	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs570031149	chr6:73877608-73877609	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs183953686	chr6:73877627-73877628	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs552460395	chr6:73877658-73877659	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs539056745	chr6:73877710-73877711	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs114175282	chr6:73877793-73877794	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs7763514	chr6:73877796-73877797	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs189650401	chr6:73877803-73877804	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs568493366	chr6:73877805-73877806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs535966292	chr6:73877852-73877853	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs117121417	chr6:73877858-73877859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs533762611	chr6:73877876-73877877	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs555348412	chr6:73877921-73877922	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs55756283	chr6:73877964-73877965	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs138839949	chr6:73877976-73877977	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs558627736	chr6:73878015-73878016	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs577049035	chr6:73878023-73878024	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs543904864	chr6:73878034-73878035	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs562519229	chr6:73878079-73878080	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs529630103	chr6:73878095-73878096	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs551862435	chr6:73878126-73878127	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs373167062	chr6:73878188-73878189	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs143063103	chr6:73878200-73878201	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs180687445	chr6:73878238-73878239	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs552349390	chr6:73878244-73878245	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Malignant fibrous histiocytomas	21085701	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Breast cancer	20409316	CNVD
Developmental delay	21147756	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1291 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73846400-73879200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:73863600-73878000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:73867000-73884600	Weak transcription	Primary T cells from cord blood	blood
4	chr6:73867400-73880600	Weak transcription	Aorta	Aorta
5	chr6:73867600-73890400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:73867600-73890400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:73867800-73876800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:73869000-73904200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr6:73876400-73876800	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr6:73876400-73877200	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr6:73876400-73877800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:73876600-73878000	Strong transcription	Primary B cells from cord blood	blood
13	chr6:73876800-73877200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:73876800-73878000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr6:73876800-73879200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:73876800-73889800	Weak transcription	HSMM	muscle
17	chr6:73877000-73877200	Enhancers	Psoas Muscle	Psoas
18	chr6:73877200-73877600	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr6:73877200-73877800	Weak transcription	Psoas Muscle	Psoas
20	chr6:73877200-73878800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr6:73877200-73884200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:73877600-73878200	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr6:73877800-73878400	Enhancers	Psoas Muscle	Psoas
24	chr6:73877800-73884200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:73878000-73878600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr6:73878000-73885600	Weak transcription	Primary B cells from cord blood	blood
27	chr6:73878200-73878400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:73878200-73878400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr6:73878400-73879000	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr6:73878400-73890200	Weak transcription	Psoas Muscle	Psoas
31	chr6:73878600-73879000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:73878600-73879000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr6:73878800-73879600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr6:73878800-73880200	Enhancers	NHEK	skin
35	chr6:73879000-73879200	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr6:73879000-73879400	Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr6:73879000-73880000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:73879200-73879600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
39	chr6:73879200-73879600	Enhancers	Osteobl	bone
40	chr6:73879200-73879800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:73879200-73880200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:73879400-73879600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr6:73879400-73879600	Enhancers	HMEC	breast
44	chr6:73879600-73879800	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr6:73879600-73884400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr6:73879800-73890000	Weak transcription	HMEC	breast
47	chr6:73880200-73889600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:73883600-73885800	Weak transcription	GM12878-XiMat	blood
49	chr6:73884200-73885400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr6:73884200-73887600	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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