Variant report

Variant	nsv508402
Chromosome Location	chr6:34840961-34951288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1967)
CpG islands
(count:2138)
Chromatin interactive
region (count:144)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1967 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34856773-34857038	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34913180-34913516	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:34867597-34867797	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:34855719-34856923	K562	blood:	n/a	n/a
5	ARID3A	chr6:34921206-34922396	HepG2	liver:	n/a	n/a
6	ATF1	chr6:34950737-34951033	K562	blood:	n/a	n/a
7	ATF1	chr6:34921512-34921692	K562	blood:	n/a	n/a
8	ATF1	chr6:34855487-34856397	K562	blood:	n/a	chr6:34855838-34855852
9	ATF1	chr6:34856679-34857207	K562	blood:	n/a	n/a
10	ATF1	chr6:34874691-34874810	K562	blood:	n/a	n/a
11	ATF2	chr6:34855528-34856206	GM12878	blood:	n/a	chr6:34855838-34855852
12	ATF2	chr6:34855549-34856136	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
13	ATF2	chr6:34856545-34857022	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:34856633-34857098	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr6:34855474-34856393	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
16	ATF2	chr6:34855555-34856110	GM12878	blood:	n/a	chr6:34855838-34855852
17	ATF2	chr6:34880420-34880916	GM12878	blood:	n/a	n/a
18	ATF3	chr6:34855553-34856043	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
19	ATF3	chr6:34937401-34937669	K562	blood:	n/a	n/a
20	ATF3	chr6:34855626-34856017	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
21	ATF3	chr6:34869076-34869473	K562	blood:	n/a	n/a
22	ATF3	chr6:34855748-34855947	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
23	ATF3	chr6:34855595-34856148	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
24	ATF3	chr6:34855584-34856143	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
25	ATF3	chr6:34856802-34857214	K562	blood:	n/a	n/a
26	ATF3	chr6:34855564-34856045	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
27	ATF3	chr6:34869194-34869500	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr6:34855569-34856012	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
29	ATF3	chr6:34855565-34856126	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	chr6:34855575-34856023	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
32	BACH1	chr6:34937468-34937748	K562	blood:	n/a	chr6:34937563-34937577
33	BACH1	chr6:34842743-34842837	K562	blood:	n/a	n/a
34	BACH1	chr6:34856735-34857116	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr6:34880490-34880853	GM12878	blood:	n/a	chr6:34880751-34880760
36	BATF	chr6:34923346-34923637	GM12878	blood:	n/a	n/a
37	BATF	chr6:34880482-34880828	GM12878	blood:	n/a	chr6:34880751-34880760
38	BCL3	chr6:34890225-34890526	GM12878	blood:	n/a	n/a
39	BCL3	chr6:34855610-34855991	GM12878	blood:	n/a	n/a
40	BCLAF1	chr6:34855583-34856152	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:34880487-34880827	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:34855498-34856151	GM12878	blood:	n/a	n/a
43	BHLHE40	chr6:34856804-34857164	GM12878	blood:	n/a	chr6:34857134-34857150
44	BHLHE40	chr6:34880557-34880866	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:34855612-34856038	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:34906089-34906432	K562	blood:	n/a	chr6:34906255-34906264 chr6:34906253-34906262 chr6:34906248-34906269 chr6:34906254-34906263 chr6:34906254-34906263 chr6:34906252-34906265
47	BHLHE40	chr6:34921407-34921627	K562	blood:	n/a	n/a
48	BHLHE40	chr6:34921417-34921776	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:34856532-34857173	K562	blood:	n/a	chr6:34857134-34857150
50	BHLHE40	chr6:34950847-34950880	K562	blood:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34861541-34861591	GM12892	blood:	n/a
2	chr6:34855797-34855847	BJ	skin:	n/a
3	chr6:34856704-34856754	HCM	heart:	n/a
4	chr6:34861541-34861591	GM12892	blood:	n/a
5	chr6:34855797-34855847	BJ	skin:	n/a
6	chr6:34856704-34856754	HCM	heart:	n/a
7	chr6:34856897-34856947	ovcar-3	ovarian:	n/a
8	chr6:34855470-34855520	AG04450	lung:	fetal
9	chr6:34853620-34853670	HCT-116	colon:	n/a
10	chr6:34855470-34855520	PrEC	prostate:	n/a
11	chr6:34857281-34857331	HNPCEpiC	eye:	n/a
12	chr6:34856927-34856977	GM19239	blood:	n/a
13	chr6:34856217-34856267	GM12878	blood:	n/a
14	chr6:34941065-34941115	HAEpiC	amniotic membrane:	n/a
15	chr6:34855885-34855935	GM12878	blood:	n/a
16	chr6:34853620-34853670	GM06990	blood:	n/a
17	chr6:34858220-34858270	HRCEpiC	kidney:	n/a
18	chr6:34855834-34855884	PANC-1	pancreas:	n/a
19	chr6:34919755-34919805	HCT-116	colon:	n/a
20	chr6:34941065-34941115	AG09309	skin:	n/a
21	chr6:34856927-34856977	Hepatocyte	liver:	n/a
22	chr6:34853620-34853670	HCM	heart:	n/a
23	chr6:34857162-34857212	SKMC	muscle:	n/a
24	chr6:34846110-34846160	NHBE	bronchial:	n/a
25	chr6:34843579-34843629	IMR90	lung:	fetal
26	chr6:34846110-34846160	CMK	blood:	n/a
27	chr6:34855635-34855685	NT2-D1	testis:	n/a
28	chr6:34922135-34922185	AG10803	skin:	n/a
29	chr6:34861541-34861591	HRE	kidney:	n/a
30	chr6:34852903-34852953	T-47D	breast:	n/a
31	chr6:34857663-34857713	NHDF-neo	bronchial:	n/a
32	chr6:34856927-34856977	A549	lung:	n/a
33	chr6:34880181-34880231	HEEpiC	esophagus:	n/a
34	chr6:34919755-34919805	Hela-S3	cervix:	n/a
35	chr6:34857162-34857212	CMK	blood:	n/a
36	chr6:34856217-34856267	SK-N-SH_RA	brain:	n/a
37	chr6:34856217-34856267	ProgFib	skin:	n/a
38	chr6:34846110-34846160	GM19239	blood:	n/a
39	chr6:34853620-34853670	BJ	skin:	n/a
40	chr6:34856897-34856947	HRCEpiC	kidney:	n/a
41	chr6:34856217-34856267	HCM	heart:	n/a
42	chr6:34856158-34856208	LNCaP	prostate:	n/a
43	chr6:34857473-34857523	HRCEpiC	kidney:	n/a
44	chr6:34846110-34846160	HL-60	blood:	n/a
45	chr6:34855980-34856030	HNPCEpiC	eye:	n/a
46	chr6:34855839-34855889	NHBE	bronchial:	n/a
47	chr6:34856897-34856947	GM12892	blood:	n/a
48	chr6:34856135-34856185	LNCaP	prostate:	n/a
49	chr6:34949773-34949823	ECC-1	luminal epithelium:	n/a
50	chr6:34855887-34855937	Hela-S3	cervix:	n/a

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:34878922..34882866-chr6:34883896..34887915,4	MCF-7	breast:
2	chr6:27798350..27799895-chr6:34855095..34857385,2	K562	blood:
3	chr6:34856018..34858760-chr6:34873113..34875329,3	K562	blood:
4	chr6:34855008..34857070-chr6:34934227..34936137,2	K562	blood:
5	chr6:34878922..34882866-chr6:34883896..34887915,4	MCF-7	breast:
6	chr6:34203408..34205869-chr6:34858444..34860576,2	K562	blood:
7	chr6:34853843..34858855-chr6:34871881..34876120,6	MCF-7	breast:
8	chr6:34893290..34895416-chr6:34950224..34952119,2	K562	blood:
9	chr6:34858926..34861792-chr6:34939953..34942289,2	MCF-7	breast:
10	chr6:34847495..34849709-chr6:34854522..34857115,3	MCF-7	breast:
11	chr6:34858328..34861023-chr6:34902579..34904193,2	K562	blood:
12	chr6:34869119..34871903-chr6:34874576..34877464,3	K562	blood:
13	chr6:34884853..34887138-chr6:34887416..34892086,4	K562	blood:
14	chr6:34759044..34761512-chr6:34840299..34841904,2	K562	blood:
15	chr6:34825507..34827584-chr6:34840818..34842443,2	MCF-7	breast:
16	chr12:120729250..120730043-chr6:34855337..34856229,2	Hela-S3	cervix:
17	chr6:34887307..34889419-chr6:34914664..34917494,2	MCF-7	breast:
18	chr6:34856254..34858967-chr6:34891774..34893975,2	MCF-7	breast:
19	chr6:34865959..34867467-chr6:34869062..34871406,2	K562	blood:
20	chr6:34855279..34857793-chr6:34917331..34920271,2	MCF-7	breast:
21	chr6:34869119..34871903-chr6:34874576..34877464,3	K562	blood:
22	chr6:34879811..34884262-chr6:34884635..34888970,5	K562	blood:
23	chr6:34937846..34940693-chr6:34953607..34956913,3	K562	blood:
24	chr6:34904349..34905899-chr6:34908056..34909609,2	MCF-7	breast:
25	chr6:34888117..34890171-chr6:34891285..34893271,2	K562	blood:
26	chr6:34839566..34841617-chr6:34847259..34849427,2	MCF-7	breast:
27	chr6:34860202..34861936-chr6:34863788..34865891,2	MCF-7	breast:
28	chr6:34891713..34895604-chr6:34895784..34899746,4	K562	blood:
29	chr6:34938891..34940598-chr6:35202108..35204116,2	K562	blood:
30	chr6:34759735..34762098-chr6:34842642..34844653,2	K562	blood:
31	chr6:34392549..34394826-chr6:34874788..34877623,2	MCF-7	breast:
32	chr6:34844007..34846659-chr6:34861219..34864126,3	K562	blood:
33	chr6:34884853..34887138-chr6:34887416..34892086,4	K562	blood:
34	chr6:34843479..34847323-chr6:34849401..34853884,4	MCF-7	breast:
35	chr6:34834250..34837156-chr6:34851105..34853013,3	MCF-7	breast:
36	chr6:34835870..34838689-chr6:34843706..34845674,2	K562	blood:
37	chr6:34944340..34947621-chr6:34949271..34952410,3	MCF-7	breast:
38	chr6:34723520..34726444-chr6:34854512..34857469,3	MCF-7	breast:
39	chr6:34892877..34895013-chr6:34901039..34903046,2	K562	blood:
40	chr6:34842945..34852488-chr6:34852501..34858927,16	MCF-7	breast:
41	chr6:34893096..34895778-chr6:34897349..34899496,2	MCF-7	breast:
42	chr6:34893096..34895778-chr6:34897349..34899496,2	MCF-7	breast:
43	chr6:34858328..34861023-chr6:34902579..34904193,2	K562	blood:
44	chr6:34392840..34394590-chr6:34855825..34858514,2	K562	blood:
45	chr6:34940870..34943018-chr6:34943935..34946831,3	K562	blood:
46	chr6:34882380..34884739-chr6:34891230..34893297,2	MCF-7	breast:
47	chr6:34844007..34846659-chr6:34861219..34864126,3	K562	blood:
48	chr6:34857178..34858858-chr6:35234868..35237489,2	MCF-7	breast:
49	chr6:34875439..34878531-chr6:34883509..34886060,3	MCF-7	breast:
50	chr3:156534879..156535549-chr6:34855191..34855795,2	Hela-S3	cervix:

No data

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

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

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

Extended variants
information (count: 3788 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3788 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371825941	chr6:34840983-34840984	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs565006458	chr6:34841023-34841024	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs532209490	chr6:34841043-34841044	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs111254761	chr6:34841054-34841055	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs552904575	chr6:34841124-34841125	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs565490768	chr6:34841190-34841191	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs530009033	chr6:34841218-34841219	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs548238248	chr6:34841252-34841253	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs3800453	chr6:34841330-34841331	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs115498198	chr6:34841331-34841332	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs147688698	chr6:34841380-34841381	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs149142133	chr6:34841385-34841386	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs538700989	chr6:34841394-34841395	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs535546464	chr6:34841508-34841509	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs188055641	chr6:34841520-34841521	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs192862014	chr6:34841521-34841522	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs185190297	chr6:34841527-34841528	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs576658185	chr6:34841530-34841531	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs575680450	chr6:34841596-34841597	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs544779651	chr6:34841625-34841626	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs373670307	chr6:34841633-34841634	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs544044199	chr6:34841641-34841642	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs565449397	chr6:34841680-34841681	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs577013349	chr6:34841704-34841705	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs541084163	chr6:34841708-34841709	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs559398009	chr6:34841743-34841744	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs529687349	chr6:34841770-34841771	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs142257263	chr6:34841777-34841778	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs76919582	chr6:34841782-34841783	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs151327462	chr6:34841798-34841799	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs530688450	chr6:34841813-34841814	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs578237645	chr6:34841837-34841838	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs551957677	chr6:34841841-34841842	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs374304934	chr6:34841860-34841861	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs370274043	chr6:34841921-34841922	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534500499	chr6:34841985-34841986	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140583634	chr6:34842027-34842028	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs540936843	chr6:34842036-34842037	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145892653	chr6:34842048-34842049	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs536282434	chr6:34842087-34842088	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs377137983	chr6:34842101-34842102	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs559356688	chr6:34842140-34842141	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs374089785	chr6:34842142-34842143	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190086683	chr6:34842162-34842163	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs11969436	chr6:34842192-34842193	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs375128994	chr6:34842200-34842201	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs181698862	chr6:34842202-34842203	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs541618745	chr6:34842216-34842217	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs369638745	chr6:34842254-34842255	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574442019	chr6:34842261-34842262	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3057 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34779400-34841000	Weak transcription	NH-A	brain
2	chr6:34816800-34853600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:34817400-34851200	Strong transcription	Fetal Thymus	thymus
4	chr6:34818600-34853400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:34819000-34842600	Strong transcription	Fetal Intestine Small	intestine
6	chr6:34820200-34855000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:34821000-34854600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:34822800-34849400	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr6:34823000-34851600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr6:34825800-34847600	Weak transcription	NHDF-Ad	bronchial
11	chr6:34827600-34841200	Weak transcription	Stomach Mucosa	stomach
12	chr6:34830000-34855000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:34830800-34848400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr6:34831400-34849400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:34834400-34849000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:34834400-34851200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:34834400-34853600	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr6:34834600-34841600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:34834600-34843600	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr6:34834600-34843800	Strong transcription	K562	blood
21	chr6:34834600-34849800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr6:34834800-34850200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr6:34835000-34841400	Strong transcription	Brain Germinal Matrix	brain
24	chr6:34835000-34841800	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr6:34835000-34842800	Strong transcription	Fetal Stomach	stomach
26	chr6:34835000-34843200	Strong transcription	Fetal Intestine Large	intestine
27	chr6:34835000-34843200	Strong transcription	Lung	lung
28	chr6:34835000-34843600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:34835000-34843800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr6:34835000-34846000	Strong transcription	HepG2	liver
31	chr6:34835000-34848000	Strong transcription	Fetal Brain Female	brain
32	chr6:34835000-34848000	Strong transcription	Thymus	Thymus
33	chr6:34835000-34848200	Strong transcription	Fetal Muscle Trunk	muscle
34	chr6:34835000-34848200	Strong transcription	Fetal Muscle Leg	muscle
35	chr6:34835000-34849200	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr6:34835000-34849400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:34835000-34849400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:34835200-34848000	Strong transcription	Brain Inferior Temporal Lobe	brain
39	chr6:34835200-34848600	Strong transcription	Brain Cingulate Gyrus	brain
40	chr6:34835400-34841800	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr6:34835400-34849000	Strong transcription	Adipose Nuclei	Adipose
42	chr6:34835400-34849400	Strong transcription	Liver	Liver
43	chr6:34835600-34845400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr6:34835800-34841800	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr6:34835800-34847600	Weak transcription	A549	lung
46	chr6:34835800-34855200	Weak transcription	Small Intestine	intestine
47	chr6:34836400-34841800	Strong transcription	Primary B cells from peripheral blood	blood
48	chr6:34836600-34843400	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr6:34836600-34849200	Strong transcription	Dnd41	blood
50	chr6:34836800-34841200	Strong transcription	Gastric	stomach

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