Variant report

Variant	nsv522204
Chromosome Location	chr21:45220483-45246326
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1424)
CpG islands
(count:1161)
Chromatin interactive
region (count:95)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45230711-45230921	K562	blood:	n/a	n/a
2	ATF2	chr21:45225100-45225830	GM12878	blood:	n/a	n/a
3	ATF2	chr21:45230618-45231142	GM12878	blood:	n/a	n/a
4	ATF2	chr21:45225114-45226193	GM12878	blood:	n/a	n/a
5	ATF3	chr21:45230203-45230542	K562	blood:	n/a	n/a
6	ATF3	chr21:45230571-45230910	K562	blood:	n/a	n/a
7	BACH1	chr21:45230745-45230981	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr21:45230707-45230937	K562	blood:	n/a	n/a
9	BATF	chr21:45225357-45225722	GM12878	blood:	n/a	chr21:45225615-45225626
10	BATF	chr21:45230670-45230927	GM12878	blood:	n/a	n/a
11	BATF	chr21:45225275-45225906	GM12878	blood:	n/a	chr21:45225615-45225626
12	BCL11A	chr21:45225103-45225641	GM12878	blood:	n/a	n/a
13	BCL11A	chr21:45225037-45225741	GM12878	blood:	n/a	n/a
14	BCL11A	chr21:45230649-45230948	GM12878	blood:	n/a	n/a
15	BCL3	chr21:45246319-45246608	GM12878	blood:	n/a	n/a
16	BCL3	chr21:45225042-45225765	GM12878	blood:	n/a	n/a
17	BCL3	chr21:45246275-45246666	GM12878	blood:	n/a	n/a
18	BCL3	chr21:45224336-45224987	K562	blood:	n/a	n/a
19	BCLAF1	chr21:45225129-45225851	GM12878	blood:	n/a	n/a
20	BCLAF1	chr21:45230623-45231085	GM12878	blood:	n/a	n/a
21	BCLAF1	chr21:45230598-45231041	GM12878	blood:	n/a	n/a
22	BCLAF1	chr21:45225112-45225757	GM12878	blood:	n/a	n/a
23	BHLHE40	chr21:45244366-45244530	K562	blood:	n/a	n/a
24	BHLHE40	chr21:45230644-45231017	HepG2	liver:	n/a	n/a
25	BHLHE40	chr21:45230622-45231042	GM12878	blood:	n/a	n/a
26	BHLHE40	chr21:45225443-45225658	K562	blood:	n/a	n/a
27	BHLHE40	chr21:45238457-45238507	K562	blood:	n/a	n/a
28	BHLHE40	chr21:45230594-45231125	K562	blood:	n/a	n/a
29	BHLHE40	chr21:45225027-45226022	GM12878	blood:	n/a	n/a
30	BHLHE40	chr21:45232195-45232216	HepG2	liver:	n/a	n/a
31	BRCA1	chr21:45229336-45229354	GM12878	blood:	n/a	n/a
32	BRCA1	chr21:45230945-45231132	HepG2	liver:	n/a	n/a
33	CBX3	chr21:45230602-45231120	K562	blood:	n/a	n/a
34	CBX3	chr21:45244243-45244895	K562	blood:	n/a	n/a
35	CBX3	chr21:45230636-45230943	K562	blood:	n/a	n/a
36	CBX3	chr21:45245011-45245299	K562	blood:	n/a	n/a
37	CBX3	chr21:45230162-45230600	K562	blood:	n/a	n/a
38	CCNT2	chr21:45225192-45225351	K562	blood:	n/a	n/a
39	CCNT2	chr21:45244276-45244582	K562	blood:	n/a	n/a
40	CCNT2	chr21:45227861-45227949	K562	blood:	n/a	n/a
41	CCNT2	chr21:45230681-45231185	K562	blood:	n/a	n/a
42	CEBPB	chr21:45238100-45238206	K562	blood:	n/a	n/a
43	CEBPB	chr21:45225149-45225688	K562	blood:	n/a	n/a
44	CEBPB	chr21:45231961-45232205	IMR90	lung:	n/a	n/a
45	CEBPB	chr21:45230720-45230898	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr21:45231939-45232247	K562	blood:	n/a	n/a
47	CEBPB	chr21:45225392-45225699	GM12878	blood:	n/a	n/a
48	CEBPB	chr21:45225248-45225639	K562	blood:	n/a	n/a
49	CEBPB	chr21:45231968-45232168	HepG2	liver:	n/a	n/a
50	CEBPB	chr21:45231992-45232226	A549	lung:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45232595-45232645	PANC-1	pancreas:	n/a
2	chr21:45246252-45246302	GM19239	blood:	n/a
3	chr21:45232595-45232645	PANC-1	pancreas:	n/a
4	chr21:45246252-45246302	GM19239	blood:	n/a
5	chr21:45232587-45232637	A549	lung:	n/a
6	chr21:45243302-45243352	PANC-1	pancreas:	n/a
7	chr21:45222093-45222143	SK-N-SH_RA	brain:	n/a
8	chr21:45223723-45223773	AoSMC	blood vessel:	n/a
9	chr21:45246308-45246358	SK-N-MC	brain:	n/a
10	chr21:45232232-45232282	NB4	blood:	n/a
11	chr21:45246252-45246302	HNPCEpiC	eye:	n/a
12	chr21:45233662-45233712	A549	lung:	n/a
13	chr21:45233585-45233635	NHDF-neo	bronchial:	n/a
14	chr21:45223723-45223773	HL-60	blood:	n/a
15	chr21:45233662-45233712	BE2_C	brain:	n/a
16	chr21:45223723-45223773	RPTEC	kidney:	n/a
17	chr21:45232531-45232581	BE2_C	brain:	n/a
18	chr21:45233508-45233558	IMR90	lung:	fetal
19	chr21:45233508-45233558	T-47D	breast:	n/a
20	chr21:45232595-45232645	HEK293	kidney:	embryo
21	chr21:45233508-45233558	HCM	heart:	n/a
22	chr21:45246252-45246302	HIPEpiC	eye:	n/a
23	chr21:45223723-45223773	PFSK-1	brain:	n/a
24	chr21:45224678-45224728	NHDF-neo	bronchial:	n/a
25	chr21:45222093-45222143	NHDF-neo	bronchial:	n/a
26	chr21:45233585-45233635	SKMC	muscle:	n/a
27	chr21:45246164-45246214	SK-N-MC	brain:	n/a
28	chr21:45233662-45233712	NHBE	bronchial:	n/a
29	chr21:45246252-45246302	BE2_C	brain:	n/a
30	chr21:45232601-45232651	AoSMC	blood vessel:	n/a
31	chr21:45233585-45233635	HRPEpiC	eye:	n/a
32	chr21:45246308-45246358	PrEC	prostate:	n/a
33	chr21:45246164-45246214	H1-hESC	embryonic stem cell:	embryo
34	chr21:45233508-45233558	NB4	blood:	n/a
35	chr21:45232595-45232645	GM12878	blood:	n/a
36	chr21:45222093-45222143	HEK293	kidney:	embryo
37	chr21:45232601-45232651	ovcar-3	ovarian:	n/a
38	chr21:45223723-45223773	HAEpiC	amniotic membrane:	n/a
39	chr21:45246308-45246358	T-47D	breast:	n/a
40	chr21:45221122-45221172	HPAEpiC	pulmonary alveolar:	n/a
41	chr21:45233585-45233635	LNCaP	prostate:	n/a
42	chr21:45232587-45232637	ProgFib	skin:	n/a
43	chr21:45223524-45223574	RPTEC	kidney:	n/a
44	chr21:45222093-45222143	AoSMC	blood vessel:	n/a
45	chr21:45221122-45221172	LNCaP	prostate:	n/a
46	chr21:45223524-45223574	HEK293	kidney:	embryo
47	chr21:45232601-45232651	LNCaP	prostate:	n/a
48	chr21:45232587-45232637	HMEC	breast:	n/a
49	chr21:45223723-45223773	NT2-D1	testis:	n/a
50	chr21:45223524-45223574	ProgFib	skin:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:45226284..45237567-chr21:45281864..45289573,19	K562	blood:
2	chr21:45192905..45195528-chr21:45235425..45238416,2	MCF-7	breast:
3	chr21:45220210..45222300-chr21:45526707..45528465,2	MCF-7	breast:
4	chr21:45233368..45235252-chr21:45401269..45403414,2	MCF-7	breast:
5	chr21:45210899..45216228-chr21:45227595..45230862,5	MCF-7	breast:
6	chr21:45227701..45229997-chr21:45280310..45283557,3	K562	blood:
7	chr21:45228402..45230320-chr21:45526070..45527844,2	MCF-7	breast:
8	chr21:45230369..45231282-chr21:45395339..45396518,7	MCF-7	breast:
9	chr21:45240125..45242679-chr21:45283332..45285060,2	MCF-7	breast:
10	chr21:45238343..45240639-chr21:45244780..45247104,2	MCF-7	breast:
11	chr21:45231023..45235105-chr21:45244093..45247662,3	MCF-7	breast:
12	chr21:45244325..45246343-chr21:45341504..45344218,2	K562	blood:
13	chr21:45225967..45228845-chr21:45233717..45236389,2	MCF-7	breast:
14	chr21:45230381..45231220-chr21:45557530..45558478,3	MCF-7	breast:
15	chr21:45209190..45209944-chr21:45230362..45230868,2	K562	blood:
16	chr21:45209783..45212594-chr21:45222169..45224397,2	MCF-7	breast:
17	chr21:45227991..45230203-chr21:45396778..45398676,2	K562	blood:
18	chr21:45238343..45240639-chr21:45244780..45247104,2	MCF-7	breast:
19	chr21:45236743..45238556-chr21:45284722..45286345,2	MCF-7	breast:
20	chr21:45233461..45235454-chr21:45304310..45305936,2	K562	blood:
21	chr21:45224931..45227488-chr21:45343356..45345629,2	K562	blood:
22	chr21:45230413..45233240-chr21:45552025..45554993,2	MCF-7	breast:
23	chr21:45225840..45228634-chr21:45360679..45363193,2	K562	blood:
24	chr21:45233269..45236576-chr21:45283514..45285914,3	MCF-7	breast:
25	chr21:45217580..45220509-chr21:45224777..45226627,2	MCF-7	breast:
26	chr21:45231740..45232316-chr21:45358668..45359330,2	MCF-7	breast:
27	chr21:45226367..45233141-chr21:45284145..45288607,11	K562	blood:
28	chr21:45236395..45237208-chr21:45348998..45349676,2	MCF-7	breast:
29	chr21:45229004..45230702-chr21:45230841..45232657,2	MCF-7	breast:
30	chr21:45232650..45235289-chr21:45658982..45661573,2	MCF-7	breast:
31	chr21:45194765..45196421-chr21:45232951..45234586,2	MCF-7	breast:
32	chr21:45229749..45232080-chr21:45430603..45432486,2	K562	blood:
33	chr21:45224259..45226376-chr21:45393066..45395792,2	K562	blood:
34	chr21:45230328..45230908-chr21:45327950..45328510,2	MCF-7	breast:
35	chr21:45233511..45236046-chr21:45357246..45359137,3	K562	blood:
36	chr21:45156182..45158069-chr21:45230385..45232004,2	K562	blood:
37	chr21:45245397..45247406-chr21:45719221..45721877,2	K562	blood:
38	chr21:45230768..45231505-chr21:45337693..45338259,2	K562	blood:
39	chr21:45243436..45244800-chr21:45358660..45359547,3	K562	blood:
40	chr21:45225718..45228025-chr21:45244966..45246549,2	MCF-7	breast:
41	chr21:45233056..45235969-chr21:45284211..45286371,2	MCF-7	breast:
42	chr21:45228592..45232844-chr21:45283509..45286625,5	MCF-7	breast:
43	chr21:45238123..45243699-chr21:45249780..45254219,5	K562	blood:
44	chr21:45244798..45246785-chr21:45283892..45286070,2	MCF-7	breast:
45	chr21:45238190..45239894-chr21:45283911..45285576,2	MCF-7	breast:
46	chr21:45210395..45213335-chr21:45233315..45235867,2	MCF-7	breast:
47	chr21:45230354..45231265-chr21:45395061..45396060,7	K562	blood:
48	chr21:45230726..45231265-chr21:45368758..45369723,2	K562	blood:
49	chr21:45230951..45231574-chr21:45358755..45359268,2	MCF-7	breast:
50	chr21:45223265..45225321-chr21:45284150..45286190,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSTB-2	chr21:45243550-45243999	NONHSAT082461
2	lnc-CSTB-1	chr21:45230112-45230404	XLOC_014107
3	lnc-CSTB-1	chr21:45230467-45230480	XLOC_014107
4	lnc-PDXK-2	chr21:45221462-45221835	expReg_chr21_1734_+
5	lnc-CSTB-1	chr21:45225639-45226469	ENSG00000215458.4
6	lnc-CSTB-1	chr21:45230112-45230242	XLOC_014107
7	lnc-CSTB-1	chr21:45224585-45226469	XLOC_014107
8	lnc-CSTB-1	chr21:45225403-45226469	XLOC_014107
9	lnc-CSTB-1	chr21:45230112-45230341	NONHSAT082453
10	lnc-CSTB-1	chr21:45228682-45229235	XLOC_014107
11	lnc-CSTB-1	chr21:45229089-45229235	XLOC_014107
12	lnc-CSTB-1	chr21:45230112-45230378	XLOC_014107
13	lnc-CSTB-2	chr21:45244734-45244760	l_2228_chr21:45243513-45244760_testes
14	lnc-CSTB-2	chr21:45243514-45243999	l_2228_chr21:45243513-45244760_testes
15	lnc-CSTB-1	chr21:45230112-45230315	XLOC_014107
16	lnc-CSTB-1	chr21:45225641-45226469	XLOC_014107
17	lnc-CSTB-1	chr21:45220692-45223322	NONHSAT082453
18	lnc-CSTB-1	chr21:45230112-45230212	ENSG00000215458.4

No data

Variant related genes	Relation type
ENSG00000215458	TF binding region
ENSG00000215458	CpG island
ENSG00000160218	chromatin interactions
ENSG00000141959	chromatin interactions
ENSG00000241945	chromatin interactions
ENSG00000160223	chromatin interactions
ENSG00000160209	chromatin interactions
ENSG00000234030	chromatin interactions
ENSG00000199598	chromatin interactions
ENSG00000160214	chromatin interactions
ENSG00000252606	chromatin interactions
ENSG00000215458	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000160216	chromatin interactions
ENSG00000160221	chromatin interactions
PXDN	miRNA target sites
SMCR8	miRNA target sites

Extended variants
information (count: 1437 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1437 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs915770	chr21:45220483-45220484	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376330937	chr21:45220491-45220492	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368502608	chr21:45220511-45220512	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs73906620	chr21:45220512-45220513	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs370563345	chr21:45220529-45220530	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs554430091	chr21:45220551-45220552	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs731935	chr21:45220570-45220571	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs546373574	chr21:45220581-45220582	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs558020296	chr21:45220599-45220600	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs576546922	chr21:45220604-45220605	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs543876240	chr21:45220612-45220613	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs3216106	chr21:45220626-45220627	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs562172691	chr21:45220640-45220641	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs2329575	chr21:45220659-45220660	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs149818702	chr21:45220680-45220681	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541801631	chr21:45220691-45220692	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs374992641	chr21:45220694-45220695	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs368121544	chr21:45220704-45220705	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs560395660	chr21:45220705-45220706	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs201331848	chr21:45220712-45220713	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs200895005	chr21:45220728-45220729	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs552360721	chr21:45220771-45220772	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs192661788	chr21:45220775-45220776	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs371997224	chr21:45220776-45220777	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs199714273	chr21:45220777-45220778	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs114739249	chr21:45220786-45220787	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs2329576	chr21:45220787-45220788	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs535969042	chr21:45220809-45220810	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs535840216	chr21:45220839-45220840	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs547821265	chr21:45220852-45220853	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs146860814	chr21:45220881-45220882	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs183721433	chr21:45220900-45220901	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs572330031	chr21:45220953-45220954	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs558354171	chr21:45220979-45220980	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs140711499	chr21:45221014-45221015	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs373963641	chr21:45221035-45221036	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs555723571	chr21:45221036-45221037	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs111742469	chr21:45221037-45221038	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs563988937	chr21:45221068-45221069	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs537584360	chr21:45221069-45221070	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs563938706	chr21:45221084-45221085	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs555831888	chr21:45221114-45221115	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs574145571	chr21:45221140-45221141	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs541814920	chr21:45221141-45221142	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs146651167	chr21:45221184-45221185	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs371420498	chr21:45221234-45221235	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs188244694	chr21:45221263-45221264	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs371486171	chr21:45221266-45221267	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs148829610	chr21:45221272-45221273	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs143464249	chr21:45221276-45221277	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	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	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45210400-45221000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr21:45211000-45223200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr21:45211000-45224200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr21:45211000-45224200	Strong transcription	Osteobl	bone
5	chr21:45211000-45224800	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr21:45211000-45224800	Strong transcription	Brain Hippocampus Middle	brain
7	chr21:45211000-45224800	Strong transcription	Placenta	Placenta
8	chr21:45211000-45226200	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr21:45211000-45226200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr21:45211000-45226600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr21:45211000-45226600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr21:45211000-45229200	Strong transcription	Fetal Intestine Small	intestine
13	chr21:45211000-45230400	Weak transcription	Stomach Mucosa	stomach
14	chr21:45211000-45257200	Weak transcription	Right Atrium	heart
15	chr21:45211200-45221800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr21:45211200-45223400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr21:45211200-45224000	Strong transcription	Muscle Satellite Cultured Cells	--
18	chr21:45211200-45224400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
19	chr21:45211200-45224400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr21:45211200-45224400	Strong transcription	Brain Cingulate Gyrus	brain
21	chr21:45211200-45224600	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr21:45211200-45224600	Strong transcription	Skeletal Muscle Male	skeletal muscle
23	chr21:45211200-45224800	Strong transcription	H9 Cell Line	embryonic stem cell
24	chr21:45211200-45224800	Strong transcription	Ovary	ovary
25	chr21:45211200-45225000	Strong transcription	Right Ventricle	heart
26	chr21:45211200-45225200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr21:45211200-45226200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr21:45211200-45226400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr21:45211200-45226800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr21:45211200-45226800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr21:45211200-45226800	Strong transcription	Esophagus	oesophagus
32	chr21:45211200-45227000	Strong transcription	Primary T cells from cord blood	blood
33	chr21:45211200-45227200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr21:45211200-45227200	Strong transcription	NHEK	skin
35	chr21:45211200-45229400	Strong transcription	Fetal Stomach	stomach
36	chr21:45211200-45230600	Weak transcription	Fetal Brain Male	brain
37	chr21:45211400-45222000	Strong transcription	K562	blood
38	chr21:45211400-45223200	Strong transcription	Hela-S3	cervix
39	chr21:45211400-45224000	Strong transcription	HepG2	liver
40	chr21:45211400-45224200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr21:45211400-45224400	Strong transcription	Thymus	Thymus
42	chr21:45211400-45224600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
43	chr21:45211400-45224600	Strong transcription	Duodenum Mucosa	Duodenum
44	chr21:45211400-45224800	Strong transcription	Fetal Thymus	thymus
45	chr21:45211400-45225000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr21:45211400-45225800	Strong transcription	Fetal Intestine Large	intestine
47	chr21:45211400-45226200	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr21:45211400-45226200	Strong transcription	A549	lung
49	chr21:45211400-45226400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr21:45211400-45226400	Strong transcription	HUES64 Cell Line	embryonic stem cell

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