Variant report

Variant	nsv878720
Chromosome Location	chr4:16222046-16242215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:646)
CpG islands
(count:611)
Chromatin interactive
region (count:33)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:646 , 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	chr4:16230039-16230251	K562	blood:	n/a	n/a
2	ARID3A	chr4:16233262-16233723	K562	blood:	n/a	n/a
3	ARID3A	chr4:16224569-16225248	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:16226793-16227076	K562	blood:	n/a	n/a
5	ATF1	chr4:16239412-16239661	K562	blood:	n/a	n/a
6	ATF1	chr4:16228090-16228399	K562	blood:	n/a	chr4:16228224-16228238
7	ATF1	chr4:16239975-16240288	K562	blood:	n/a	n/a
8	ATF2	chr4:16226676-16227202	GM12878	blood:	n/a	n/a
9	ATF3	chr4:16228128-16228317	HepG2	liver:	n/a	chr4:16228228-16228238
10	ATF3	chr4:16228068-16228394	K562	blood:	n/a	chr4:16228228-16228238
11	BACH1	chr4:16233261-16233515	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr4:16227939-16228356	K562	blood:	n/a	n/a
13	BHLHE40	chr4:16228815-16228945	K562	blood:	n/a	chr4:16228815-16228831
14	BHLHE40	chr4:16239453-16239590	K562	blood:	n/a	n/a
15	BHLHE40	chr4:16239935-16240424	K562	blood:	n/a	n/a
16	BHLHE40	chr4:16227317-16227722	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:16227421-16227688	K562	blood:	n/a	n/a
18	BHLHE40	chr4:16228156-16228409	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:16228685-16228864	Hela-S3	cervix:	n/a	n/a
20	CCNT2	chr4:16227278-16229113	K562	blood:	n/a	chr4:16227795-16227804 chr4:16228813-16228822 chr4:16228154-16228163
21	CEBPB	chr4:16231287-16231559	H1-hESC	embryonic stem cell:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
22	CEBPB	chr4:16224644-16224883	HepG2	liver:	n/a	chr4:16224731-16224742
23	CEBPB	chr4:16224567-16225149	HepG2	liver:	n/a	chr4:16224731-16224742
24	CEBPB	chr4:16231254-16231592	A549	lung:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
25	CEBPB	chr4:16231235-16231605	IMR90	lung:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
26	CEBPB	chr4:16239404-16239649	K562	blood:	n/a	n/a
27	CEBPB	chr4:16239406-16239590	K562	blood:	n/a	n/a
28	CEBPB	chr4:16231245-16231592	HepG2	liver:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
29	CEBPB	chr4:16231225-16231606	K562	blood:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
30	CEBPB	chr4:16226759-16227141	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr4:16226750-16227074	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:16228680-16228981	Hela-S3	cervix:	n/a	chr4:16228866-16228878
33	CEBPB	chr4:16226766-16227087	K562	blood:	n/a	n/a
34	CEBPB	chr4:16227469-16228056	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr4:16224430-16224973	HepG2	liver:	n/a	chr4:16224731-16224742
36	CEBPB	chr4:16237790-16238006	IMR90	lung:	n/a	n/a
37	CEBPB	chr4:16237771-16237950	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:16231302-16231579	Hela-S3	cervix:	n/a	chr4:16231420-16231431 chr4:16231420-16231433 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231422-16231431 chr4:16231356-16231367 chr4:16231354-16231367
39	CEBPD	chr4:16228183-16228571	HepG2	liver:	n/a	n/a
40	CEBPD	chr4:16224685-16224885	HepG2	liver:	n/a	n/a
41	CHD1	chr4:16228347-16228624	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr4:16229420-16229538	GM12878	blood:	n/a	n/a
43	CHD1	chr4:16228876-16228963	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr4:16226879-16227693	GM12878	blood:	n/a	n/a
45	CHD1	chr4:16227900-16229043	GM12878	blood:	n/a	chr4:16228147-16228157 chr4:16228152-16228162
46	CHD2	chr4:16228217-16228364	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr4:16228838-16229221	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr4:16228679-16228806	GM12878	blood:	n/a	n/a
49	CHD2	chr4:16228211-16228411	GM12878	blood:	n/a	n/a
50	CHD2	chr4:16227493-16227564	K562	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:16228633-16228683	CMK	blood:	n/a
2	chr4:16228633-16228683	CMK	blood:	n/a
3	chr4:16230109-16230159	GM12892	blood:	n/a
4	chr4:16227813-16227863	GM12878	blood:	n/a
5	chr4:16225910-16225960	SK-N-SH_RA	brain:	n/a
6	chr4:16228885-16228935	Hela-S3	cervix:	n/a
7	chr4:16228633-16228683	AG04449	skin:	fetal
8	chr4:16229123-16229173	HEK293	kidney:	embryo
9	chr4:16228633-16228683	HAEpiC	amniotic membrane:	n/a
10	chr4:16225910-16225960	HepG2	liver:	n/a
11	chr4:16228633-16228683	GM12878	blood:	n/a
12	chr4:16230109-16230159	SK-N-MC	brain:	n/a
13	chr4:16228633-16228683	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:16227539-16227589	Hela-S3	cervix:	n/a
15	chr4:16228633-16228683	ECC-1	luminal epithelium:	n/a
16	chr4:16228633-16228683	T-47D	breast:	n/a
17	chr4:16230109-16230159	AG09319	gingival:	n/a
18	chr4:16229123-16229173	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:16228885-16228935	AG04449	skin:	fetal
20	chr4:16228633-16228683	SKMC	muscle:	n/a
21	chr4:16228647-16228697	HepG2	liver:	n/a
22	chr4:16227813-16227863	PrEC	prostate:	n/a
23	chr4:16227539-16227589	Caco-2	colon:	n/a
24	chr4:16227813-16227863	HCF	heart:	n/a
25	chr4:16228885-16228935	SKMC	muscle:	n/a
26	chr4:16228062-16228112	HRPEpiC	eye:	n/a
27	chr4:16228633-16228683	SK-N-MC	brain:	n/a
28	chr4:16227813-16227863	SKMC	muscle:	n/a
29	chr4:16228885-16228935	ovcar-3	ovarian:	n/a
30	chr4:16228885-16228935	HMEC	breast:	n/a
31	chr4:16228885-16228935	HCPEpiC	choroid plexus:	n/a
32	chr4:16228885-16228935	SK-N-SH_RA	brain:	n/a
33	chr4:16227813-16227863	HCPEpiC	choroid plexus:	n/a
34	chr4:16228885-16228935	NB4	blood:	n/a
35	chr4:16229123-16229173	AG09319	gingival:	n/a
36	chr4:16228633-16228683	Caco-2	colon:	n/a
37	chr4:16228885-16228935	U87	brain:	n/a
38	chr4:16227539-16227589	H1-hESC	embryonic stem cell:	embryo
39	chr4:16228633-16228683	H1-hESC	embryonic stem cell:	embryo
40	chr4:16228633-16228683	HRCEpiC	kidney:	n/a
41	chr4:16228062-16228112	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:16225910-16225960	GM12891	blood:	n/a
43	chr4:16225910-16225960	AG04450	lung:	fetal
44	chr4:16227539-16227589	HepG2	liver:	n/a
45	chr4:16227539-16227589	T-47D	breast:	n/a
46	chr4:16230109-16230159	AG10803	skin:	n/a
47	chr4:16228633-16228683	NH-A	brain:	n/a
48	chr4:16225910-16225960	HRE	kidney:	n/a
49	chr4:16230109-16230159	A549	lung:	n/a
50	chr4:16227539-16227589	HIPEpiC	eye:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:16227416..16229454-chr4:16230827..16235422,5	MCF-7	breast:
2	chr4:16210098..16212174-chr4:16220610..16223093,2	K562	blood:
3	chr4:16227890..16229761-chr4:17577650..17579806,2	MCF-7	breast:
4	chr4:16221619..16226314-chr4:16226369..16230057,8	MCF-7	breast:
5	chr4:16219652..16222405-chr4:16247960..16249931,2	K562	blood:
6	chr4:16238904..16240455-chr4:16240677..16243574,2	MCF-7	breast:
7	chr4:16230488..16232179-chr4:16234227..16236390,2	MCF-7	breast:
8	chr4:16225599..16229737-chr4:16237110..16241898,6	MCF-7	breast:
9	chr4:16233218..16235689-chr4:16242386..16245204,2	MCF-7	breast:
10	chr4:16051882..16054680-chr4:16233913..16235649,2	MCF-7	breast:
11	chr4:16230488..16232179-chr4:16234227..16236390,2	MCF-7	breast:
12	chr4:16239179..16242051-chr4:16245019..16247959,3	K562	blood:
13	chr4:15681714..15684664-chr4:16226494..16229781,3	K562	blood:
14	chr4:16238904..16240455-chr4:16240677..16243574,2	MCF-7	breast:
15	chr4:16234324..16237129-chr4:16262058..16264893,2	K562	blood:
16	chr4:16215439..16216101-chr4:16232860..16233690,2	K562	blood:
17	chr4:16219972..16222393-chr4:16236561..16239245,2	K562	blood:
18	chr4:16212529..16219737-chr4:16225844..16229602,8	MCF-7	breast:
19	chr4:15002785..15006911-chr4:16226901..16230678,5	K562	blood:
20	chr4:16230982..16233844-chr4:16235259..16238422,3	MCF-7	breast:
21	chr4:16230982..16233844-chr4:16235259..16238422,3	MCF-7	breast:
22	chr4:15976147..15979142-chr4:16221984..16223628,2	MCF-7	breast:
23	chr4:16219520..16223580-chr4:16226468..16229712,6	MCF-7	breast:
24	chr4:16208002..16209532-chr4:16222968..16225755,2	MCF-7	breast:
25	chr17:59476916..59479068-chr4:16227271..16228837,2	MCF-7	breast:
26	chr4:16207884..16210057-chr4:16223808..16226102,2	K562	blood:
27	chr4:16219972..16222393-chr4:16236561..16239245,2	K562	blood:
28	chr4:16216932..16218804-chr4:16227245..16229857,2	MCF-7	breast:
29	chr4:16228310..16230197-chr4:16235714..16237466,2	MCF-7	breast:
30	chr4:16235269..16243012-chr4:16245014..16252154,9	K562	blood:
31	chr4:16214985..16216532-chr4:16224088..16226157,2	K562	blood:
32	chr4:16226523..16228832-chr4:16238449..16240604,2	MCF-7	breast:
33	chr21:33104183..33104701-chr4:16227636..16228281,2	Hela-S3	cervix:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD38-2	chr4:16228630-16228800	ENSG00000263327.1
2	lnc-CD38-2	chr4:16228286-16230207	ENSG00000263327.2
3	lnc-CD38-2	chr4:16240394-16240494	ENSG00000225917
4	lnc-CD38-2	chr4:16240394-16240494	ENSG00000263327.1
5	lnc-CD38-2	chr4:16228308-16228800	ENSG00000263327.1
6	lnc-CD38-2	chr4:16228668-16228800	ENSG00000263327.1
7	lnc-CD38-2	chr4:16228286-16228800	NONHSAT095674
8	lnc-CD38-2	chr4:16240394-16240494	ENSG00000263327.1
9	lnc-CD38-2	chr4:16228286-16228800	ENSG00000225917
10	lnc-CD38-2	chr4:16240394-16240494	ENSG00000263327.1
11	lnc-CD38-2	chr4:16240394-16240494	NONHSAT095674
12	lnc-CD38-2	chr4:16240212-16240494	NONHSAT095679

No data

Variant related genes	Relation type
TAPT1-AS1	TF binding region
TAPT1	TF binding region
TAPT1-AS1	CpG island
TAPT1	CpG island
ENSG00000237765	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000247624	chromatin interactions
ENSG00000118564	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000156304	chromatin interactions
ENSG00000002549	chromatin interactions
ENSG00000263327	chromatin interactions
ENSG00000169762	chromatin interactions
ENSG00000267280	chromatin interactions
PDGFRA	miRNA target sites

Extended variants
information (count: 703 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10007592	chr4:16222046-16222047	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563060585	chr4:16222051-16222052	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs529042069	chr4:16222079-16222080	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373975621	chr4:16222089-16222090	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs373989913	chr4:16222136-16222137	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs562593340	chr4:16222148-16222149	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs141715428	chr4:16222154-16222155	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377123158	chr4:16222229-16222230	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs199611358	chr4:16222244-16222245	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146247832	chr4:16222303-16222304	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570891993	chr4:16222304-16222305	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs12504884	chr4:16222365-16222366	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547143367	chr4:16222376-16222377	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs567377135	chr4:16222392-16222393	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs535629165	chr4:16222483-16222484	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs73130470	chr4:16222529-16222530	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs144068352	chr4:16222539-16222540	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs564205293	chr4:16222541-16222542	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538535169	chr4:16222545-16222546	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558515975	chr4:16222595-16222596	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs35879842	chr4:16222603-16222604	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs540643288	chr4:16222612-16222613	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs183706332	chr4:16222614-16222615	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368628884	chr4:16222638-16222639	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs574080798	chr4:16222649-16222650	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542796060	chr4:16222699-16222700	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs562702374	chr4:16222707-16222708	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs28757814	chr4:16222724-16222725	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs201796120	chr4:16222732-16222733	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs11414718	chr4:16222744-16222745	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373688157	chr4:16222754-16222755	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376634517	chr4:16222756-16222757	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs139441259	chr4:16222775-16222776	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564851670	chr4:16222777-16222778	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs527268949	chr4:16222807-16222808	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149666798	chr4:16222813-16222814	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs6810390	chr4:16222827-16222828	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs186974855	chr4:16222864-16222865	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs549655422	chr4:16222870-16222871	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs569449696	chr4:16222874-16222875	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs538473160	chr4:16222877-16222878	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs62288992	chr4:16222893-16222894	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569089529	chr4:16222899-16222900	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs571991785	chr4:16222936-16222937	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs538226875	chr4:16222997-16222998	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs6854115	chr4:16223028-16223029	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs80020499	chr4:16223131-16223132	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573998640	chr4:16223137-16223138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543087494	chr4:16223171-16223172	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372210746	chr4:16223230-16223231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1093 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16181200-16223800	Weak transcription	Fetal Brain Male	brain
2	chr4:16193000-16225800	Weak transcription	Colonic Mucosa	Colon
3	chr4:16193200-16225800	Weak transcription	Fetal Brain Female	brain
4	chr4:16198600-16222400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:16198800-16225600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:16198800-16226000	Weak transcription	NHEK	skin
7	chr4:16198800-16226400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:16204800-16226600	Weak transcription	NH-A	brain
9	chr4:16205200-16225600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:16207400-16223600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr4:16208400-16224400	Weak transcription	Stomach Smooth Muscle	stomach
12	chr4:16208400-16225200	Weak transcription	Fetal Kidney	kidney
13	chr4:16208400-16225800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:16208800-16225600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:16208800-16225600	Weak transcription	Esophagus	oesophagus
16	chr4:16208800-16225600	Weak transcription	Gastric	stomach
17	chr4:16208800-16225800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr4:16208800-16225800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:16208800-16227200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr4:16209000-16225600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr4:16209200-16223400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr4:16209200-16225600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr4:16209200-16225600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:16209400-16226200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:16209400-16226200	Weak transcription	HSMMtube	muscle
26	chr4:16210400-16225800	Weak transcription	Brain Germinal Matrix	brain
27	chr4:16212200-16226000	Weak transcription	NHDF-Ad	bronchial
28	chr4:16214000-16224400	Weak transcription	Brain Anterior Caudate	brain
29	chr4:16214200-16224200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:16214400-16226800	Weak transcription	Fetal Muscle Trunk	muscle
31	chr4:16214600-16222600	Weak transcription	Fetal Heart	heart
32	chr4:16214600-16224400	Weak transcription	Brain Angular Gyrus	brain
33	chr4:16214600-16225800	Weak transcription	Placenta	Placenta
34	chr4:16214800-16224200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr4:16214800-16225200	Weak transcription	Hela-S3	cervix
36	chr4:16214800-16225800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:16215000-16223600	Weak transcription	Brain Hippocampus Middle	brain
38	chr4:16215000-16224600	Weak transcription	Colon Smooth Muscle	Colon
39	chr4:16215000-16226000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:16215200-16223400	Weak transcription	Adipose Nuclei	Adipose
41	chr4:16215200-16225000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:16215600-16225600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:16215800-16223800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:16216200-16225600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:16216400-16223600	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr4:16216600-16224400	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr4:16216800-16225600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr4:16218600-16222600	Weak transcription	Left Ventricle	heart
49	chr4:16218600-16224400	Weak transcription	Small Intestine	intestine
50	chr4:16218600-16224400	Weak transcription	Spleen	Spleen

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