Variant report

Variant	nsv884438
Chromosome Location	chr6:31742590-31751832
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:603)
CpG islands
(count:4093)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31744791-31745248	K562	blood:	n/a	n/a
2	ARID3A	chr6:31744950-31745207	HepG2	liver:	n/a	n/a
3	ATF1	chr6:31744739-31745294	K562	blood:	n/a	chr6:31744920-31744934
4	ATF2	chr6:31744662-31745294	GM12878	blood:	n/a	chr6:31744920-31744934
5	ATF2	chr6:31744593-31745360	GM12878	blood:	n/a	chr6:31744920-31744934
6	ATF3	chr6:31744570-31745542	K562	blood:	n/a	n/a
7	ATF3	chr6:31744657-31745504	K562	blood:	n/a	n/a
8	BACH1	chr6:31748097-31748139	K562	blood:	n/a	n/a
9	BACH1	chr6:31744775-31745310	K562	blood:	n/a	chr6:31745135-31745149
10	BATF	chr6:31744874-31745274	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:31744806-31745124	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:31744747-31745233	GM12878	blood:	n/a	n/a
13	BCL3	chr6:31744559-31745342	A549	lung:	n/a	n/a
14	BCL3	chr6:31744523-31745345	GM12878	blood:	n/a	n/a
15	BCL3	chr6:31744638-31745342	A549	lung:	n/a	n/a
16	BCL3	chr6:31744547-31745467	K562	blood:	n/a	n/a
17	BCLAF1	chr6:31744631-31745448	K562	blood:	n/a	n/a
18	BCLAF1	chr6:31744624-31745537	K562	blood:	n/a	n/a
19	BCLAF1	chr6:31744638-31745283	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:31744727-31745294	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:31744706-31745227	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:31744537-31745627	K562	blood:	n/a	n/a
23	BHLHE40	chr6:31744836-31745249	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:31743765-31744030	HepG2	liver:	n/a	n/a
25	BRCA1	chr6:31743138-31743170	HepG2	liver:	n/a	n/a
26	BRCA1	chr6:31744980-31745128	HepG2	liver:	n/a	n/a
27	BRCA1	chr6:31744767-31745359	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr6:31744655-31745413	K562	blood:	n/a	n/a
29	CBX3	chr6:31744203-31746270	K562	blood:	n/a	n/a
30	CCNT2	chr6:31744509-31745393	K562	blood:	n/a	chr6:31744819-31744828
31	CEBPB	chr6:31744698-31745355	GM12878	blood:	n/a	n/a
32	CEBPB	chr6:31744809-31745176	K562	blood:	n/a	n/a
33	CEBPB	chr6:31744758-31745483	K562	blood:	n/a	n/a
34	CEBPB	chr6:31742973-31743033	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:31744906-31745115	GM12878	blood:	n/a	n/a
36	CEBPB	chr6:31744914-31745375	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr6:31745430-31745585	K562	blood:	n/a	n/a
38	CEBPD	chr6:31744488-31745413	K562	blood:	n/a	n/a
39	CEBPD	chr6:31744644-31745408	HepG2	liver:	n/a	n/a
40	CHD2	chr6:31744738-31745219	GM12878	blood:	n/a	n/a
41	CHD2	chr6:31749637-31749926	K562	blood:	n/a	chr6:31749785-31749795
42	CHD2	chr6:31743828-31746134	K562	blood:	n/a	n/a
43	CHD2	chr6:31744467-31745392	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr6:31744723-31745243	HepG2	liver:	n/a	n/a
45	CREB1	chr6:31744702-31745220	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr6:31744494-31745318	GM12878	blood:	n/a	n/a
47	CREB1	chr6:31744433-31745520	HepG2	liver:	n/a	n/a
48	CREB1	chr6:31744487-31745354	HepG2	liver:	n/a	n/a
49	CREB1	chr6:31744727-31745266	A549	lung:	n/a	n/a
50	CTCF	chr6:31745480-31745630	GM12873	blood:	n/a	n/a

(count:4093 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31743928-31743978	HNPCEpiC	eye:	n/a
2	chr6:31743961-31744011	GM12892	blood:	n/a
3	chr6:31745821-31745871	BJ	skin:	n/a
4	chr6:31745181-31745231	RPTEC	kidney:	n/a
5	chr6:31743986-31744036	Jurkat	blood:	n/a
6	chr6:31746874-31746924	HUVEC	blood vessel:	n/a
7	chr6:31743928-31743978	HNPCEpiC	eye:	n/a
8	chr6:31743961-31744011	GM12892	blood:	n/a
9	chr6:31745821-31745871	BJ	skin:	n/a
10	chr6:31745181-31745231	RPTEC	kidney:	n/a
11	chr6:31743986-31744036	Jurkat	blood:	n/a
12	chr6:31746874-31746924	HUVEC	blood vessel:	n/a
13	chr6:31747257-31747307	GM19239	blood:	n/a
14	chr6:31744545-31744595	PFSK-1	brain:	n/a
15	chr6:31744398-31744448	AG04450	lung:	fetal
16	chr6:31745137-31745187	Hela-S3	cervix:	n/a
17	chr6:31744545-31744595	HRCEpiC	kidney:	n/a
18	chr6:31744391-31744441	PrEC	prostate:	n/a
19	chr6:31747250-31747300	A549	lung:	n/a
20	chr6:31747257-31747307	PFSK-1	brain:	n/a
21	chr6:31744628-31744678	HCT-116	colon:	n/a
22	chr6:31747237-31747287	IMR90	lung:	fetal
23	chr6:31744339-31744389	HCF	heart:	n/a
24	chr6:31747893-31747943	BE2_C	brain:	n/a
25	chr6:31750174-31750224	Caco-2	colon:	n/a
26	chr6:31748762-31748812	PANC-1	pancreas:	n/a
27	chr6:31749307-31749357	AG04449	skin:	fetal
28	chr6:31747133-31747183	LNCaP	prostate:	n/a
29	chr6:31744391-31744441	SK-N-MC	brain:	n/a
30	chr6:31746919-31746969	NT2-D1	testis:	n/a
31	chr6:31744962-31745012	LNCaP	prostate:	n/a
32	chr6:31746874-31746924	NHDF-neo	bronchial:	n/a
33	chr6:31744816-31744866	HEK293	kidney:	embryo
34	chr6:31744735-31744785	HL-60	blood:	n/a
35	chr6:31746941-31746991	IMR90	lung:	fetal
36	chr6:31750165-31750215	PrEC	prostate:	n/a
37	chr6:31747041-31747091	Hela-S3	cervix:	n/a
38	chr6:31743986-31744036	HL-60	blood:	n/a
39	chr6:31744391-31744441	MCF-7	breast:	n/a
40	chr6:31746832-31746882	K562	blood:	n/a
41	chr6:31747433-31747483	GM06990	blood:	n/a
42	chr6:31750141-31750191	HNPCEpiC	eye:	n/a
43	chr6:31745821-31745871	AG09319	gingival:	n/a
44	chr6:31743986-31744036	IMR90	lung:	fetal
45	chr6:31743769-31743819	HRE	kidney:	n/a
46	chr6:31747133-31747183	HL-60	blood:	n/a
47	chr6:31750138-31750188	PANC-1	pancreas:	n/a
48	chr6:31747269-31747319	CMK	blood:	n/a
49	chr6:31747010-31747060	AoSMC	blood vessel:	n/a
50	chr6:31744831-31744881	SK-N-SH_RA	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31740985..31743056-chr6:31795621..31797863,3	MCF-7	breast:
2	chr6:31743287..31747076-chr6:31793437..31796925,5	MCF-7	breast:
3	chr6:31742944..31744994-chr6:31869511..31871431,2	K562	blood:
4	chr6:31701475..31705916-chr6:31741171..31744372,4	MCF-7	breast:
5	chr6:31740931..31743197-chr6:31865687..31868469,2	MCF-7	breast:
6	chr6:31747450..31751295-chr6:31800640..31804723,4	MCF-7	breast:
7	chr6:31743176..31746587-chr6:31939802..31942689,4	K562	blood:
8	chr6:31632664..31635327-chr6:31741807..31745187,4	MCF-7	breast:
9	chr6:31642643..31644341-chr6:31742570..31744549,2	MCF-7	breast:
10	chr6:31737503..31739335-chr6:31742183..31744187,2	MCF-7	breast:
11	chr6:31745758..31747408-chr6:31800818..31802986,2	MCF-7	breast:
12	chr6:31735011..31745595-chr6:31798203..31806127,22	MCF-7	breast:
13	chr6:31742555..31745004-chr6:31773789..31777145,5	MCF-7	breast:
14	chr6:31743326..31746438-chr6:31828635..31833007,4	K562	blood:
15	chr6:31502088..31504001-chr6:31743213..31745224,2	MCF-7	breast:
16	chr6:31710678..31714958-chr6:31739473..31744061,4	MCF-7	breast:
17	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
18	chr6:31750326..31751829-chr6:31829443..31831754,2	MCF-7	breast:
19	chr6:31620739..31623442-chr6:31750369..31752880,2	MCF-7	breast:
20	chr11:64545106..64547042-chr6:31742109..31744042,2	MCF-7	breast:
21	chr6:31732922..31735851-chr6:31748037..31750099,2	MCF-7	breast:
22	chr6:31742934..31744615-chr6:31773250..31774889,2	MCF-7	breast:
23	chr6:31739355..31742514-chr6:31742775..31744985,3	MCF-7	breast:
24	chr6:31745070..31746845-chr6:31830028..31832915,2	MCF-7	breast:
25	chr6:31697592..31699245-chr6:31742808..31745377,2	MCF-7	breast:
26	chr6:31696116..31699055-chr6:31743914..31747307,3	MCF-7	breast:
27	chr6:31741163..31742824-chr6:31743275..31745395,3	MCF-7	breast:
28	chr6:31508578..31511041-chr6:31743489..31745514,2	K562	blood:
29	chr6:31743107..31747994-chr6:31781956..31785553,7	MCF-7	breast:
30	chr6:31742931..31744824-chr6:31926408..31928564,2	K562	blood:
31	chr6:31741149..31744902-chr6:31760858..31763694,5	MCF-7	breast:
32	chr6:31668602..31672513-chr6:31741310..31744822,4	MCF-7	breast:
33	chr6:31748274..31750464-chr6:31829000..31831442,2	MCF-7	breast:
34	chr6:31507944..31511146-chr6:31743964..31746169,3	K562	blood:
35	chr6:31508667..31511581-chr6:31742885..31745171,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000201555	TF binding region
VWA7	TF binding region
VARS	TF binding region
ENSG00000201555	CpG island
VWA7	CpG island
VARS	CpG island
ENSG00000201823	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000213719	chromatin interactions
ENSG00000269038	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000234006	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000265236	chromatin interactions
ENSG00000198563	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000204396	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000235663	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000204387	chromatin interactions
ENSG00000204410	chromatin interactions
ENSG00000204427	chromatin interactions
ENSG00000266776	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000204356	chromatin interactions
ENSG00000263020	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000204392	chromatin interactions
ENSG00000201754	chromatin interactions
ENSG00000204351	chromatin interactions
ENSG00000204444	chromatin interactions

Extended variants
information (count: 400 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs707928	chr6:31742590-31742591	Weak transcription Enhancers	TF binding region Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561615875	chr6:31742598-31742599	Weak transcription Enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
3	rs534239431	chr6:31742625-31742626	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs555497709	chr6:31742646-31742647	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
5	rs377298727	chr6:31742668-31742669	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
6	rs566802814	chr6:31742737-31742738	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
7	rs187073840	chr6:31742834-31742835	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
8	rs191555121	chr6:31742850-31742851	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
9	rs531917702	chr6:31742868-31742869	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
10	rs146595626	chr6:31742969-31742970	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
11	rs557056009	chr6:31743017-31743018	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
12	rs141434721	chr6:31743043-31743044	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
13	rs145136302	chr6:31743054-31743055	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
14	rs564092760	chr6:31743056-31743057	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
15	rs573140478	chr6:31743091-31743092	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
16	rs200089800	chr6:31743113-31743114	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
17	rs386699247	chr6:31743125-31743126	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
18	rs543762163	chr6:31743154-31743155	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
19	rs182789677	chr6:31743161-31743162	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
20	rs150095936	chr6:31743171-31743172	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
21	rs529144337	chr6:31743185-31743186	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
22	rs550783130	chr6:31743215-31743216	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
23	rs137907827	chr6:31743221-31743222	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
24	rs547517070	chr6:31743242-31743243	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
25	rs371203464	chr6:31743244-31743245	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
26	rs551721348	chr6:31743296-31743297	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
27	rs566539103	chr6:31743300-31743301	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
28	rs114713279	chr6:31743303-31743304	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
29	rs549310215	chr6:31743310-31743311	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	28 gene(s)	Overlapped CNVs	n/a
30	rs376090934	chr6:31743365-31743366	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
31	rs567510201	chr6:31743396-31743397	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
32	rs538464347	chr6:31743408-31743409	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
33	rs556757673	chr6:31743438-31743439	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
34	rs149454781	chr6:31743466-31743467	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
35	rs539175367	chr6:31743468-31743469	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
36	rs557744873	chr6:31743485-31743486	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
37	rs572923866	chr6:31743524-31743525	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
38	rs143097356	chr6:31743540-31743541	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
39	rs112112388	chr6:31743560-31743561	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
40	rs565527329	chr6:31743608-31743609	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
41	rs573734505	chr6:31743614-31743615	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
42	rs544368403	chr6:31743625-31743626	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
43	rs562559508	chr6:31743635-31743636	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
44	rs533427427	chr6:31743652-31743653	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
45	rs201107143	chr6:31743722-31743723	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
46	rs374059063	chr6:31743723-31743724	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
47	rs201940200	chr6:31743724-31743725	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
48	rs367544616	chr6:31743727-31743728	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
49	rs199885626	chr6:31743736-31743737	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a
50	rs527718367	chr6:31743756-31743757	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	30 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

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
Lung cancer	18438408	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
Ovarian cancer	21781307	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
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	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
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31716600-31744000	Weak transcription	GM12878-XiMat	blood
2	chr6:31729200-31742800	Weak transcription	A549	lung
3	chr6:31731400-31744400	Weak transcription	Left Ventricle	heart
4	chr6:31731600-31743400	Weak transcription	Lung	lung
5	chr6:31731800-31743600	Weak transcription	Right Ventricle	heart
6	chr6:31731800-31749600	Weak transcription	HUVEC	blood vessel
7	chr6:31732600-31745000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:31732800-31744400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:31734400-31742800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:31734400-31743400	Weak transcription	Right Atrium	heart
11	chr6:31734600-31743600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr6:31734600-31744200	Weak transcription	Brain Anterior Caudate	brain
13	chr6:31734600-31744200	Weak transcription	NH-A	brain
14	chr6:31734600-31744600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:31734600-31744600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr6:31734600-31745200	Weak transcription	Brain Germinal Matrix	brain
17	chr6:31734600-31745400	Weak transcription	Fetal Brain Female	brain
18	chr6:31734600-31746600	Weak transcription	Brain Angular Gyrus	brain
19	chr6:31734800-31745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr6:31735400-31742800	Weak transcription	Fetal Intestine Large	intestine
21	chr6:31737200-31744200	Weak transcription	Fetal Stomach	stomach
22	chr6:31737400-31744400	Weak transcription	Fetal Muscle Leg	muscle
23	chr6:31737400-31744600	Enhancers	Primary T cells fromperipheralblood	blood
24	chr6:31738000-31742600	Weak transcription	Fetal Intestine Small	intestine
25	chr6:31738000-31742800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:31738000-31742800	Weak transcription	Colonic Mucosa	Colon
27	chr6:31738000-31742800	Weak transcription	Gastric	stomach
28	chr6:31738000-31743400	Weak transcription	Pancreas	Pancrea
29	chr6:31738000-31744200	Weak transcription	Primary B cells from cord blood	blood
30	chr6:31738800-31745800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr6:31739000-31743000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr6:31739400-31742800	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr6:31739400-31742800	Weak transcription	NHEK	skin
34	chr6:31739800-31746000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr6:31740200-31744800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:31740400-31744200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr6:31740400-31744600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:31740800-31743800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:31741000-31742800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr6:31741000-31742800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr6:31741000-31743800	Weak transcription	Primary B cells from peripheral blood	blood
42	chr6:31741000-31744400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:31741000-31744400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr6:31741000-31744400	Weak transcription	Brain Hippocampus Middle	brain
45	chr6:31741000-31744800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr6:31741000-31745600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr6:31741200-31742800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr6:31741200-31742800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr6:31741200-31742800	Weak transcription	Esophagus	oesophagus
50	chr6:31741200-31742800	Weak transcription	HepG2	liver

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