Variant report

Variant	nsv1013077
Chromosome Location	chr4:20599841-20732558
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:20692322-20692456	K562	blood:	n/a	n/a
2	ARID3A	chr4:20701873-20702300	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:20700015-20700842	K562	blood:	n/a	n/a
4	ARID3A	chr4:20701592-20701812	K562	blood:	n/a	n/a
5	ATF1	chr4:20701653-20702260	K562	blood:	n/a	chr4:20702025-20702039
6	ATF1	chr4:20700407-20700806	K562	blood:	n/a	n/a
7	ATF2	chr4:20701648-20702230	H1-hESC	embryonic stem cell:	n/a	chr4:20702025-20702039
8	ATF3	chr4:20700358-20700813	K562	blood:	n/a	n/a
9	ATF3	chr4:20701697-20702170	H1-hESC	embryonic stem cell:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
10	ATF3	chr4:20701711-20702195	HepG2	liver:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
11	ATF3	chr4:20701728-20702041	A549	lung:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
12	ATF3	chr4:20701734-20702174	GM12878	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
13	ATF3	chr4:20701701-20702121	K562	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
14	ATF3	chr4:20701812-20702063	GM12878	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
15	ATF3	chr4:20701739-20702217	K562	blood:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
16	ATF3	chr4:20701755-20702123	H1-hESC	embryonic stem cell:	n/a	chr4:20702026-20702037 chr4:20702029-20702039 chr4:20702028-20702039 chr4:20702026-20702039 chr4:20702028-20702048 chr4:20702025-20702040 chr4:20702029-20702037 chr4:20702029-20702036
17	BHLHE40	chr4:20701761-20702364	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:20701625-20702344	K562	blood:	n/a	n/a
19	BHLHE40	chr4:20688384-20688430	K562	blood:	n/a	n/a
20	BHLHE40	chr4:20701479-20702280	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:20627171-20627455	K562	blood:	n/a	n/a
22	BHLHE40	chr4:20726709-20727073	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:20686889-20687054	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:20700392-20700749	K562	blood:	n/a	n/a
25	BRCA1	chr4:20701812-20702075	HepG2	liver:	n/a	n/a
26	BRCA1	chr4:20686884-20687072	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr4:20701819-20702207	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr4:20701588-20702105	K562	blood:	n/a	n/a
29	CCNT2	chr4:20700385-20700870	K562	blood:	n/a	n/a
30	CCNT2	chr4:20701740-20702316	K562	blood:	n/a	n/a
31	CEBPB	chr4:20603233-20603464	HepG2	liver:	n/a	chr4:20603367-20603378
32	CEBPB	chr4:20622154-20622294	A549	lung:	n/a	chr4:20622207-20622216 chr4:20622205-20622218 chr4:20622205-20622216 chr4:20622207-20622216 chr4:20622207-20622216 chr4:20622207-20622216
33	CEBPB	chr4:20691553-20691591	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:20605245-20605908	IMR90	lung:	n/a	chr4:20605386-20605395 chr4:20605384-20605395 chr4:20605384-20605397 chr4:20605384-20605397 chr4:20605385-20605396
35	CEBPB	chr4:20702852-20703146	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:20605311-20605767	HepG2	liver:	n/a	chr4:20605386-20605395 chr4:20605384-20605395 chr4:20605384-20605397 chr4:20605384-20605397 chr4:20605385-20605396
37	CEBPB	chr4:20700088-20700367	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
38	CEBPB	chr4:20700039-20700408	HepG2	liver:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
39	CEBPB	chr4:20699967-20700805	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
40	CEBPB	chr4:20622069-20622353	K562	blood:	n/a	chr4:20622207-20622216 chr4:20622205-20622218 chr4:20622205-20622216 chr4:20622207-20622216 chr4:20622207-20622216 chr4:20622207-20622216
41	CEBPB	chr4:20699983-20700439	MCF-7	breast:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
42	CEBPB	chr4:20700054-20700411	IMR90	lung:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
43	CEBPB	chr4:20699982-20700715	K562	blood:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
44	CEBPB	chr4:20702839-20703100	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:20700053-20700351	H1-hESC	embryonic stem cell:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
46	CEBPB	chr4:20700057-20700382	A549	lung:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
47	CEBPB	chr4:20667757-20667982	HepG2	liver:	n/a	chr4:20667897-20667910
48	CEBPB	chr4:20622038-20622365	HepG2	liver:	n/a	chr4:20622207-20622216 chr4:20622205-20622218 chr4:20622205-20622216 chr4:20622207-20622216 chr4:20622207-20622216 chr4:20622207-20622216
49	CEBPB	chr4:20699992-20700456	MCF-7	breast:	n/a	chr4:20700220-20700231 chr4:20700218-20700229 chr4:20700218-20700231 chr4:20700218-20700231
50	CEBPB	chr4:20605210-20605920	Hela-S3	cervix:	n/a	chr4:20605386-20605395 chr4:20605384-20605395 chr4:20605384-20605397 chr4:20605384-20605397 chr4:20605385-20605396

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20701870-20701920	K562	blood:	n/a
2	chr4:20702182-20702232	IMR90	lung:	fetal
3	chr4:20729211-20729261	AoSMC	blood vessel:	n/a
4	chr4:20701990-20702040	LNCaP	prostate:	n/a
5	chr4:20698772-20698822	SKMC	muscle:	n/a
6	chr4:20660098-20660148	GM06990	blood:	n/a
7	chr4:20701925-20701975	IMR90	lung:	fetal
8	chr4:20701990-20702040	AG09309	skin:	n/a
9	chr4:20702377-20702427	H1-hESC	embryonic stem cell:	embryo
10	chr4:20701990-20702040	HRPEpiC	eye:	n/a
11	chr4:20702329-20702379	NHDF-neo	bronchial:	n/a
12	chr4:20660098-20660148	NHDF-neo	bronchial:	n/a
13	chr4:20698772-20698822	LNCaP	prostate:	n/a
14	chr4:20698772-20698822	HRE	kidney:	n/a
15	chr4:20702329-20702379	U87	brain:	n/a
16	chr4:20706485-20706535	ovcar-3	ovarian:	n/a
17	chr4:20704940-20704990	AG09319	gingival:	n/a
18	chr4:20701889-20701939	NB4	blood:	n/a
19	chr4:20701889-20701939	H1-hESC	embryonic stem cell:	embryo
20	chr4:20660098-20660148	H1-hESC	embryonic stem cell:	embryo
21	chr4:20702377-20702427	Hepatocyte	liver:	n/a
22	chr4:20701889-20701939	SK-N-SH	brain:	n/a
23	chr4:20701870-20701920	HUVEC	blood vessel:	n/a
24	chr4:20701889-20701939	NHBE	bronchial:	n/a
25	chr4:20701925-20701975	PANC-1	pancreas:	n/a
26	chr4:20701870-20701920	Hepatocyte	liver:	n/a
27	chr4:20702182-20702232	HAEpiC	amniotic membrane:	n/a
28	chr4:20701914-20701964	HNPCEpiC	eye:	n/a
29	chr4:20702329-20702379	AoSMC	blood vessel:	n/a
30	chr4:20704940-20704990	AG04449	skin:	fetal
31	chr4:20701990-20702040	U87	brain:	n/a
32	chr4:20702045-20702095	A549	lung:	n/a
33	chr4:20730493-20730543	AG10803	skin:	n/a
34	chr4:20704940-20704990	K562	blood:	n/a
35	chr4:20702377-20702427	HCM	heart:	n/a
36	chr4:20701575-20701625	HEK293	kidney:	embryo
37	chr4:20701925-20701975	T-47D	breast:	n/a
38	chr4:20706485-20706535	BE2_C	brain:	n/a
39	chr4:20701950-20702000	SAEC	small airway:	n/a
40	chr4:20701691-20701741	HRE	kidney:	n/a
41	chr4:20701990-20702040	MCF10A-Er-Src	breast:	n/a
42	chr4:20698772-20698822	NH-A	brain:	n/a
43	chr4:20702045-20702095	HAEpiC	amniotic membrane:	n/a
44	chr4:20701870-20701920	H1-hESC	embryonic stem cell:	embryo
45	chr4:20730493-20730543	A549	lung:	n/a
46	chr4:20702182-20702232	CMK	blood:	n/a
47	chr4:20702329-20702379	SKMC	muscle:	n/a
48	chr4:20702377-20702427	PrEC	prostate:	n/a
49	chr4:20660098-20660148	HRPEpiC	eye:	n/a
50	chr4:20702329-20702379	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20705332..20707768-chr4:20710083..20712545,3	K562	blood:
2	chr4:20702290..20703806-chr4:20728599..20731005,2	K562	blood:
3	chr4:20420524..20421239-chr4:20686532..20687103,2	K562	blood:
4	chr4:20693086..20698959-chr4:20699230..20704175,9	K562	blood:
5	chr4:20700229..20702940-chr4:20728046..20730028,2	MCF-7	breast:
6	chr4:20678463..20679308-chr6:4856088..4856696,2	MCF-7	breast:
7	chr4:20702272..20703966-chr4:20709575..20711144,2	MCF-7	breast:
8	chr4:20702290..20704847-chr4:20728043..20731005,3	K562	blood:
9	chr4:20673472..20675496-chr4:20701529..20703125,2	K562	blood:
10	chr4:20650338..20652484-chr4:20652879..20655131,2	K562	blood:
11	chr4:20700245..20702604-chr4:20707211..20709448,2	MCF-7	breast:
12	chr4:20647329..20649016-chr4:20649617..20652093,2	K562	blood:
13	chr4:20701257..20703146-chr4:20703451..20705273,2	MCF-7	breast:
14	chr4:20705332..20707768-chr4:20710083..20712545,3	K562	blood:
15	chr4:20701536..20702331-chr9:91933301..91933855,2	Hela-S3	cervix:
16	chr4:20702290..20704847-chr4:20728043..20731005,3	K562	blood:
17	chr4:20693086..20698959-chr4:20699230..20704175,9	K562	blood:
18	chr4:20702290..20703806-chr4:20728599..20731005,2	K562	blood:
19	chr4:20702272..20703966-chr4:20709575..20711144,2	MCF-7	breast:
20	chr4:20700439..20703043-chr4:20709421..20711457,2	MCF-7	breast:
21	chr4:20700439..20703043-chr4:20709421..20711457,2	MCF-7	breast:
22	chr4:20699912..20701731-chr4:20714831..20716673,2	K562	blood:
23	chr4:20647329..20649016-chr4:20649617..20652093,2	K562	blood:
24	chr4:20423749..20424719-chr4:20686427..20687473,4	K562	blood:
25	chr4:20700245..20702604-chr4:20707211..20709448,2	MCF-7	breast:
26	chr4:20699912..20701731-chr4:20714831..20716673,2	K562	blood:
27	chr4:20650338..20652484-chr4:20652879..20655131,2	K562	blood:
28	chr4:20424367..20425209-chr4:20686856..20687583,2	MCF-7	breast:
29	chr4:20702888..20705883-chr4:20707634..20710929,3	K562	blood:
30	chr4:20701205..20703695-chr4:20723209..20725454,2	MCF-7	breast:
31	chr4:20700788..20703573-chr4:20723140..20724857,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLIT2-2	chr4:20703764-20703844	NONHSAT095736
2	lnc-SLIT2-2	chr4:20702061-20702329	NONHSAT095736
3	lnc-SLIT2-2	chr4:20703381-20703507	NONHSAT095736
4	lnc-SLIT2-2	chr4:20704298-20704317	NONHSAT095736
5	lnc-SLIT2-3	chr4:20731428-20733259	NONHSAT095738

Variant related genes	Relation type
SLIT2	TF binding region
PACRGL	TF binding region
SLIT2	CpG island
PACRGL	CpG island
ENSG00000187742	chromatin interactions
ENSG00000163138	chromatin interactions

Extended variants
information (count: 5283 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5283 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377300122	chr4:20599850-20599851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531572803	chr4:20599851-20599852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374643163	chr4:20599860-20599861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547207452	chr4:20599909-20599910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149600791	chr4:20599918-20599919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142099148	chr4:20599944-20599945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144274723	chr4:20599947-20599948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200082920	chr4:20599991-20599992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201968832	chr4:20600045-20600046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73252501	chr4:20600109-20600110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187518143	chr4:20600143-20600144	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537758502	chr4:20600161-20600162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555901159	chr4:20600168-20600169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574181357	chr4:20600223-20600224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192440989	chr4:20600240-20600241	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185631361	chr4:20600244-20600245	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34388730	chr4:20600279-20600280	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577718978	chr4:20600292-20600293	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6820674	chr4:20600314-20600315	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563356444	chr4:20600351-20600352	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs151173273	chr4:20600407-20600408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549833680	chr4:20600415-20600416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376722667	chr4:20600420-20600421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56411745	chr4:20600421-20600422	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs529114743	chr4:20600547-20600548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79446815	chr4:20600559-20600560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570981361	chr4:20600570-20600571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6821757	chr4:20600572-20600573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547534404	chr4:20600589-20600590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565595022	chr4:20600643-20600644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539550043	chr4:20600665-20600666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551363296	chr4:20600670-20600671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs569692673	chr4:20600704-20600705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6826108	chr4:20600717-20600718	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs555821301	chr4:20600740-20600741	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553402927	chr4:20600741-20600742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564338105	chr4:20600791-20600792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573187058	chr4:20600793-20600794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73252502	chr4:20600819-20600820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77885582	chr4:20600823-20600824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140253914	chr4:20600831-20600832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545118112	chr4:20600862-20600863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150350308	chr4:20600885-20600886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113450345	chr4:20600895-20600896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200660715	chr4:20601044-20601045	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114915554	chr4:20601060-20601061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576310983	chr4:20601111-20601112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543689775	chr4:20601150-20601151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189311873	chr4:20601153-20601154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538886340	chr4:20601179-20601180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2221 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20536800-20618600	Weak transcription	Spleen	Spleen
2	chr4:20567000-20604000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:20567200-20605200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr4:20567200-20617000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr4:20578000-20617400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:20578200-20616800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:20578400-20610000	Weak transcription	Fetal Brain Male	brain
8	chr4:20579400-20605600	Weak transcription	Adipose Nuclei	Adipose
9	chr4:20584200-20600200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:20589200-20610600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:20589200-20620800	Weak transcription	Fetal Muscle Leg	muscle
12	chr4:20590000-20620400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr4:20590800-20618400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:20591400-20617000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr4:20591600-20605200	Weak transcription	NHEK	skin
16	chr4:20593000-20619000	Weak transcription	Placenta	Placenta
17	chr4:20594400-20619000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:20594600-20600000	Weak transcription	Colon Smooth Muscle	Colon
19	chr4:20594600-20601600	Strong transcription	Fetal Lung	lung
20	chr4:20594600-20602600	Weak transcription	Fetal Intestine Large	intestine
21	chr4:20594600-20605200	Weak transcription	NHLF	lung
22	chr4:20594800-20603800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:20594800-20620600	Weak transcription	Brain Cingulate Gyrus	brain
24	chr4:20595000-20605400	Strong transcription	NHDF-Ad	bronchial
25	chr4:20595600-20601600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:20595800-20604800	Weak transcription	Brain Anterior Caudate	brain
27	chr4:20596200-20600800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:20596400-20601600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:20596600-20600200	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr4:20596800-20605200	Weak transcription	HUVEC	blood vessel
31	chr4:20597200-20600800	Strong transcription	Osteobl	bone
32	chr4:20597800-20624600	Weak transcription	Brain Hippocampus Middle	brain
33	chr4:20598400-20605400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr4:20598400-20615000	Weak transcription	Fetal Stomach	stomach
35	chr4:20598600-20601000	Weak transcription	Brain Substantia Nigra	brain
36	chr4:20598600-20619200	Weak transcription	Ovary	ovary
37	chr4:20599200-20600600	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr4:20599200-20601400	Weak transcription	Lung	lung
39	chr4:20599600-20600400	Strong transcription	Fetal Kidney	kidney
40	chr4:20599800-20600400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:20599800-20600600	Strong transcription	Aorta	Aorta
42	chr4:20599800-20600800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr4:20600000-20600800	Strong transcription	Colon Smooth Muscle	Colon
44	chr4:20600200-20600400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:20600200-20600400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:20600200-20600800	Strong transcription	Placenta Amnion	Placenta Amnion
47	chr4:20600400-20602800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:20600400-20614800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:20600400-20619000	Weak transcription	Fetal Kidney	kidney
50	chr4:20600600-20601600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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