Variant report

Variant	nsv1004706
Chromosome Location	chr4:75014770-75121643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1851)
CpG islands
(count:856)
Chromatin interactive
region (count:133)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1851 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:75054958-75055346	K562	blood:	n/a	n/a
2	ARID3A	chr4:75023522-75023797	K562	blood:	n/a	n/a
3	ARID3A	chr4:75023113-75023972	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:75056779-75057213	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:75073507-75073514	K562	blood:	n/a	n/a
6	ARID3A	chr4:75096789-75096882	K562	blood:	n/a	n/a
7	ARID3A	chr4:75021212-75021262	K562	blood:	n/a	n/a
8	ARID3A	chr4:75067522-75068289	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:75071960-75072316	K562	blood:	n/a	n/a
10	ARID3A	chr4:75054987-75055584	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:75040243-75040439	K562	blood:	n/a	n/a
12	ARID3A	chr4:75020661-75020892	K562	blood:	n/a	n/a
13	ATF1	chr4:75071874-75072276	K562	blood:	n/a	n/a
14	ATF2	chr4:75062780-75063229	GM12878	blood:	n/a	n/a
15	ATF2	chr4:75071823-75072691	GM12878	blood:	n/a	n/a
16	ATF2	chr4:75023507-75023908	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr4:75094472-75094740	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr4:75071810-75072598	GM12878	blood:	n/a	n/a
19	ATF2	chr4:75023487-75023984	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr4:75023411-75023934	A549	lung:	n/a	chr4:75023646-75023655
21	ATF3	chr4:75071871-75072182	K562	blood:	n/a	n/a
22	ATF3	chr4:75071934-75072120	K562	blood:	n/a	n/a
23	ATF3	chr4:75103285-75103754	HCT-116	colon:	n/a	n/a
24	BACH1	chr4:75024015-75024094	K562	blood:	n/a	n/a
25	BACH1	chr4:75023391-75024314	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr4:75096679-75096780	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr4:75096739-75096863	K562	blood:	n/a	n/a
28	BACH1	chr4:75073601-75073728	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr4:75023754-75023768	K562	blood:	n/a	n/a
30	BACH1	chr4:75083263-75083307	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr4:75033917-75034237	GM12878	blood:	n/a	chr4:75034110-75034121
32	BCL11A	chr4:75023629-75024004	GM12878	blood:	n/a	n/a
33	BCL3	chr4:75023426-75024022	A549	lung:	n/a	chr4:75024006-75024019
34	BCL3	chr4:75023580-75024083	GM12878	blood:	n/a	chr4:75024006-75024019 chr4:75024013-75024026
35	BCL3	chr4:75067689-75068196	A549	lung:	n/a	n/a
36	BCLAF1	chr4:75071883-75072576	GM12878	blood:	n/a	chr4:75072403-75072412
37	BCLAF1	chr4:75023212-75023918	K562	blood:	n/a	n/a
38	BCLAF1	chr4:75094377-75094758	GM12878	blood:	n/a	n/a
39	BCLAF1	chr4:75023311-75024008	K562	blood:	n/a	n/a
40	BCLAF1	chr4:75023379-75024367	GM12878	blood:	n/a	chr4:75024006-75024019 chr4:75024013-75024026
41	BHLHE40	chr4:75054991-75055336	GM12878	blood:	n/a	n/a
42	BHLHE40	chr4:75056850-75057158	HepG2	liver:	n/a	n/a
43	BHLHE40	chr4:75023059-75024321	HepG2	liver:	n/a	chr4:75023644-75023660 chr4:75024010-75024026 chr4:75024026-75024042 chr4:75024005-75024021
44	BHLHE40	chr4:75073753-75073963	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:75071969-75072571	GM12878	blood:	n/a	n/a
46	BHLHE40	chr4:75023367-75024606	GM12878	blood:	n/a	chr4:75023644-75023660 chr4:75024010-75024026 chr4:75024026-75024042 chr4:75024005-75024021
47	BHLHE40	chr4:75046503-75046529	K562	blood:	n/a	n/a
48	BHLHE40	chr4:75067754-75068280	HepG2	liver:	n/a	n/a
49	BHLHE40	chr4:75071760-75072313	K562	blood:	n/a	n/a
50	BHLHE40	chr4:75023054-75024314	K562	blood:	n/a	chr4:75023644-75023660 chr4:75024010-75024026 chr4:75024026-75024042 chr4:75024005-75024021

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:75023746-75023796	MCF-7	breast:	n/a
2	chr4:75023849-75023899	Caco-2	colon:	n/a
3	chr4:75023746-75023796	MCF-7	breast:	n/a
4	chr4:75023849-75023899	Caco-2	colon:	n/a
5	chr4:75023649-75023699	HCPEpiC	choroid plexus:	n/a
6	chr4:75023606-75023656	HAEpiC	amniotic membrane:	n/a
7	chr4:75024153-75024203	CMK	blood:	n/a
8	chr4:75023664-75023714	PFSK-1	brain:	n/a
9	chr4:75024153-75024203	GM19239	blood:	n/a
10	chr4:75023849-75023899	HNPCEpiC	eye:	n/a
11	chr4:75024153-75024203	HRPEpiC	eye:	n/a
12	chr4:75023219-75023269	ECC-1	luminal epithelium:	n/a
13	chr4:75023746-75023796	Hepatocyte	liver:	n/a
14	chr4:75023540-75023590	HRE	kidney:	n/a
15	chr4:75023649-75023699	SK-N-MC	brain:	n/a
16	chr4:75023629-75023679	ovcar-3	ovarian:	n/a
17	chr4:75023540-75023590	HNPCEpiC	eye:	n/a
18	chr4:75023851-75023901	GM12891	blood:	n/a
19	chr4:75023746-75023796	ECC-1	luminal epithelium:	n/a
20	chr4:75023746-75023796	U87	brain:	n/a
21	chr4:75023649-75023699	AG10803	skin:	n/a
22	chr4:75023851-75023901	HUVEC	blood vessel:	n/a
23	chr4:75023664-75023714	MCF10A-Er-Src	breast:	n/a
24	chr4:75023219-75023269	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:75023664-75023714	T-47D	breast:	n/a
26	chr4:75024153-75024203	NB4	blood:	n/a
27	chr4:75023849-75023899	U87	brain:	n/a
28	chr4:75023658-75023708	HCF	heart:	n/a
29	chr4:75023219-75023269	A549	lung:	n/a
30	chr4:75026843-75026893	Hepatocyte	liver:	n/a
31	chr4:75023719-75023769	LNCaP	prostate:	n/a
32	chr4:75024153-75024203	GM12891	blood:	n/a
33	chr4:75023649-75023699	PFSK-1	brain:	n/a
34	chr4:75023746-75023796	SKMC	muscle:	n/a
35	chr4:75023719-75023769	GM12892	blood:	n/a
36	chr4:75023849-75023899	HIPEpiC	eye:	n/a
37	chr4:75026843-75026893	BJ	skin:	n/a
38	chr4:75023851-75023901	SK-N-SH	brain:	n/a
39	chr4:75023540-75023590	GM12891	blood:	n/a
40	chr4:75023849-75023899	HRPEpiC	eye:	n/a
41	chr4:75023746-75023796	MCF10A-Er-Src	breast:	n/a
42	chr4:75023664-75023714	HIPEpiC	eye:	n/a
43	chr4:75023851-75023901	HepG2	liver:	n/a
44	chr4:75023629-75023679	NH-A	brain:	n/a
45	chr4:75023606-75023656	NB4	blood:	n/a
46	chr4:75023658-75023708	NH-A	brain:	n/a
47	chr4:75023851-75023901	GM06990	blood:	n/a
48	chr4:75023629-75023679	HMEC	breast:	n/a
49	chr4:75023649-75023699	ovcar-3	ovarian:	n/a
50	chr4:75023629-75023679	NB4	blood:	n/a

(count:133 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:75116462..75118101-chr4:75154963..75157104,2	K562	blood:
2	chr4:75031722..75034011-chr4:75130972..75132629,2	MCF-7	breast:
3	chr4:74527976..74529636-chr4:75025474..75027779,2	K562	blood:
4	chr4:75022870..75024459-chr4:75044858..75046610,2	MCF-7	breast:
5	chr4:74964506..74967065-chr4:75022087..75025561,3	K562	blood:
6	chr4:74976042..74977879-chr4:75018790..75020773,2	K562	blood:
7	chr4:75085650..75087545-chr4:75089867..75092462,3	K562	blood:
8	chr4:75097927..75100406-chr4:75102183..75105181,2	K562	blood:
9	chr4:75081253..75083346-chr4:75120623..75122127,2	K562	blood:
10	chr4:75021911..75023462-chr4:75229589..75232447,2	K562	blood:
11	chr4:75017734..75019236-chr4:75035314..75037734,2	K562	blood:
12	chr4:75054721..75055635-chr4:75094051..75095124,3	K562	blood:
13	chr4:75000738..75003533-chr4:75021528..75023491,2	K562	blood:
14	chr4:75051671..75055178-chr4:75229398..75232382,3	K562	blood:
15	chr4:75018443..75019977-chr4:75023297..75025270,2	MCF-7	breast:
16	chr4:74563928..74566862-chr4:75033357..75036869,3	K562	blood:
17	chr4:74962104..74964124-chr4:75017131..75019515,2	K562	blood:
18	chr4:75055396..75057559-chr4:75092904..75094536,2	K562	blood:
19	chr4:75030705..75032456-chr4:75033958..75036294,2	MCF-7	breast:
20	chr4:75023724..75025558-chr4:75028455..75031389,3	MCF-7	breast:
21	chr4:75023432..75024127-chr7:115891562..115892062,2	NB4	blood:
22	chr4:75090793..75093494-chr4:75193558..75196089,2	K562	blood:
23	chr4:75022878..75025928-chr4:75031708..75034530,3	MCF-7	breast:
24	chr4:74920487..74923421-chr4:75023614..75026198,3	K562	blood:
25	chr4:75039914..75042879-chr4:75059516..75061047,2	K562	blood:
26	chr4:75072066..75073934-chr4:75080235..75082986,2	K562	blood:
27	chr4:75054779..75055639-chr4:75595986..75596945,2	K562	blood:
28	chr4:74998740..75001079-chr4:75031773..75033857,2	K562	blood:
29	chr4:75014766..75017413-chr4:75021945..75024735,2	MCF-7	breast:
30	chr4:75054721..75055635-chr4:75094051..75095124,3	K562	blood:
31	chr4:75065926..75067463-chr4:75070226..75071957,2	K562	blood:
32	chr4:74513203..74514864-chr4:75031720..75034502,2	K562	blood:
33	chr4:75055479..75057780-chr4:75061856..75063799,2	K562	blood:
34	chr4:75065926..75067463-chr4:75070226..75071957,2	K562	blood:
35	chr4:75030705..75032456-chr4:75033958..75036294,2	MCF-7	breast:
36	chr4:75071138..75073600-chr4:75079457..75081137,2	MCF-7	breast:
37	chr4:75028000..75030668-chr4:75031442..75033767,3	MCF-7	breast:
38	chr15:25139573..25141078-chr4:75029307..75031542,2	K562	blood:
39	chr4:74917982..74919932-chr4:75041196..75043826,2	K562	blood:
40	chr4:75024221..75026156-chr4:75163622..75165985,2	K562	blood:
41	chr4:75094355..75095090-chr4:75547966..75548494,2	K562	blood:
42	chr4:75032536..75034809-chr4:75036870..75039307,2	MCF-7	breast:
43	chr4:75011353..75013399-chr4:75014178..75017069,2	K562	blood:
44	chr4:75023556..75025318-chr4:75054789..75057123,2	MCF-7	breast:
45	chr1:45196394..45197102-chr4:75023670..75024212,2	Hela-S3	cervix:
46	chr4:75023499..75025641-chr4:75097703..75100691,2	K562	blood:
47	chr4:75018655..75021289-chr4:75023791..75025452,2	MCF-7	breast:
48	chr4:75030845..75032521-chr4:75038666..75041397,2	MCF-7	breast:
49	chr4:75055396..75057559-chr4:75092904..75094536,2	K562	blood:
50	chr4:75010641..75013526-chr4:75028499..75030027,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPGN-4	chr4:75025772-75027969	NONHSAT096885
2	lnc-EPGN-4	chr4:75025772-75026231	NONHSAT096883
3	lnc-EPGN-4	chr4:75025772-75026487	NONHSAT096884
4	lnc-EPGN-4	chr4:75025772-75025805	NONHSAT096886
5	lnc-EPGN-4	chr4:75023892-75023998	NONHSAT096886
6	lnc-EPGN-4	chr4:75023829-75023998	NONHSAT096885
7	lnc-EPGN-4	chr4:75027497-75027823	NONHSAT096886

No data

Variant related genes	Relation type
ENSG00000269559	TF binding region
MTHFD2L	TF binding region
ENSG00000269559	CpG island
MTHFD2L	CpG island
ENSG00000200169	chromatin interactions
ENSG00000124882	chromatin interactions
ENSG00000047932	chromatin interactions
ENSG00000163738	chromatin interactions
ENSG00000132466	chromatin interactions
ENSG00000248848	chromatin interactions
ENSG00000269559	chromatin interactions
ENSG00000135269	chromatin interactions
ENSG00000177764	chromatin interactions
ENSG00000165905	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000182585	chromatin interactions
ENSG00000081041	chromatin interactions

Extended variants
information (count: 3864 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3864 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555728	chr4:75014770-75014771	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537540344	chr4:75014810-75014811	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs576392981	chr4:75014826-75014827	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs145102512	chr4:75014850-75014851	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561897148	chr4:75014851-75014852	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs146886104	chr4:75014856-75014857	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs542275758	chr4:75014928-75014929	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192204636	chr4:75014934-75014935	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs527632649	chr4:75014939-75014940	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs552143263	chr4:75015119-75015120	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564474909	chr4:75015139-75015140	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs531862343	chr4:75015165-75015166	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs550128532	chr4:75015190-75015191	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs140713821	chr4:75015242-75015243	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs145659425	chr4:75015244-75015245	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535205113	chr4:75015274-75015275	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs73827550	chr4:75015325-75015326	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs565774978	chr4:75015338-75015339	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532483545	chr4:75015343-75015344	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs539483507	chr4:75015371-75015372	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs552177583	chr4:75015402-75015403	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557773409	chr4:75015406-75015407	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs148075662	chr4:75015418-75015419	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574273593	chr4:75015429-75015430	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs55946357	chr4:75015433-75015434	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs537315548	chr4:75015444-75015445	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs72854826	chr4:75015458-75015459	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs573740208	chr4:75015462-75015463	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs541961127	chr4:75015464-75015465	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs183915162	chr4:75015504-75015505	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs572191644	chr4:75015507-75015508	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375148400	chr4:75015556-75015557	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545820184	chr4:75015569-75015570	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564110709	chr4:75015573-75015574	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs531896907	chr4:75015621-75015622	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs476893	chr4:75015633-75015634	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554261540	chr4:75015660-75015661	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs7660423	chr4:75015750-75015751	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs529534633	chr4:75015772-75015773	Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547668712	chr4:75015870-75015871	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs565817862	chr4:75015893-75015894	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs140990795	chr4:75015894-75015895	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551420417	chr4:75015897-75015898	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565124857	chr4:75015929-75015930	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs531683	chr4:75015939-75015940	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs150211654	chr4:75015946-75015947	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs117992577	chr4:75015959-75015960	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs11942036	chr4:75016059-75016060	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs111599863	chr4:75016132-75016133	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs369021806	chr4:75016160-75016161	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Renal cell carcinoma	20952505	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1597 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75011800-75022000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:75013200-75023200	Weak transcription	Psoas Muscle	Psoas
3	chr4:75013800-75014800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:75014000-75022000	Weak transcription	HMEC	breast
5	chr4:75014400-75022200	Weak transcription	NHEK	skin
6	chr4:75014800-75016000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:75015400-75015800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:75015800-75022600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:75016000-75016600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:75016600-75016800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:75016800-75018200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:75018200-75018400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:75018200-75019000	Enhancers	Fetal Brain Male	brain
14	chr4:75018200-75019200	Enhancers	Fetal Lung	lung
15	chr4:75018400-75018800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:75018400-75019000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr4:75018400-75019000	Enhancers	Colon Smooth Muscle	Colon
18	chr4:75018600-75019000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr4:75018800-75019000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:75018800-75019000	Enhancers	NHDF-Ad	bronchial
21	chr4:75019000-75019400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:75019000-75022600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr4:75019000-75022800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:75019000-75023000	Weak transcription	Colon Smooth Muscle	Colon
25	chr4:75019000-75023000	Weak transcription	Fetal Brain Male	brain
26	chr4:75019400-75021200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:75020400-75021400	Enhancers	K562	blood
28	chr4:75021200-75022200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:75021400-75021800	Weak transcription	K562	blood
30	chr4:75021800-75022000	Enhancers	K562	blood
31	chr4:75021800-75022600	Enhancers	HUVEC	blood vessel
32	chr4:75021800-75023000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:75021800-75023000	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr4:75022000-75022200	Enhancers	Colonic Mucosa	Colon
35	chr4:75022000-75022600	Flanking Active TSS	K562	blood
36	chr4:75022000-75022600	Enhancers	NHLF	lung
37	chr4:75022000-75022800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:75022000-75022800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr4:75022000-75022800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:75022000-75022800	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr4:75022000-75022800	Enhancers	Hela-S3	cervix
42	chr4:75022000-75022800	Enhancers	HMEC	breast
43	chr4:75022000-75022800	Enhancers	NHDF-Ad	bronchial
44	chr4:75022200-75022400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:75022200-75022400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:75022200-75022600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr4:75022200-75022600	Enhancers	NHEK	skin
48	chr4:75022200-75022800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr4:75022200-75022800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:75022200-75022800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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