Variant report

Variant	nsv879873
Chromosome Location	chr4:124528452-124590869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:714)
CpG islands
(count:244)
Chromatin interactive
region (count:30)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:124580402-124581271	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:124582329-124582671	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:124582321-124582641	K562	blood:	n/a	n/a
4	ARID3A	chr4:124541093-124541471	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:124570740-124571648	HepG2	liver:	n/a	n/a
6	ATF3	chr4:124590284-124590714	K562	blood:	n/a	n/a
7	BATF	chr4:124546159-124546499	GM12878	blood:	n/a	chr4:124546339-124546350
8	BCL11A	chr4:124570328-124570744	GM12878	blood:	n/a	chr4:124570644-124570653
9	BCL11A	chr4:124528269-124528489	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:124570413-124570743	GM12878	blood:	n/a	chr4:124570644-124570653
11	BHLHE40	chr4:124570879-124571458	HepG2	liver:	n/a	n/a
12	BHLHE40	chr4:124535512-124535535	K562	blood:	n/a	n/a
13	BHLHE40	chr4:124570383-124570766	GM12878	blood:	n/a	n/a
14	CBX3	chr4:124577670-124578150	K562	blood:	n/a	n/a
15	CEBPB	chr4:124549542-124549770	H1-hESC	embryonic stem cell:	n/a	chr4:124549636-124549649 chr4:124549636-124549647
16	CEBPB	chr4:124574481-124574659	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:124574508-124574726	A549	lung:	n/a	chr4:124574662-124574671 chr4:124574660-124574673 chr4:124574660-124574671
18	CEBPB	chr4:124570893-124571074	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:124566412-124566622	K562	blood:	n/a	n/a
20	CEBPB	chr4:124570780-124571308	IMR90	lung:	n/a	chr4:124570798-124570815 chr4:124570799-124570812
21	CEBPB	chr4:124541338-124541559	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:124570823-124571802	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:124561342-124561768	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:124549479-124549789	IMR90	lung:	n/a	chr4:124549636-124549649 chr4:124549636-124549647
25	CEBPB	chr4:124549500-124549788	K562	blood:	n/a	chr4:124549636-124549649 chr4:124549636-124549647
26	CEBPB	chr4:124566378-124566585	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:124578193-124578433	A549	lung:	n/a	chr4:124578263-124578274
28	CEBPB	chr4:124578249-124578282	H1-hESC	embryonic stem cell:	n/a	chr4:124578263-124578274
29	CEBPB	chr4:124549454-124549820	HepG2	liver:	n/a	chr4:124549636-124549649 chr4:124549636-124549647
30	CEBPB	chr4:124549534-124549721	HepG2	liver:	n/a	chr4:124549636-124549649 chr4:124549636-124549647
31	CEBPB	chr4:124549514-124549802	A549	lung:	n/a	chr4:124549636-124549649 chr4:124549636-124549647
32	CEBPB	chr4:124578197-124578381	HepG2	liver:	n/a	chr4:124578263-124578274
33	CEBPB	chr4:124561498-124561689	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:124570802-124571231	A549	lung:	n/a	n/a
35	CEBPB	chr4:124578158-124578435	IMR90	lung:	n/a	chr4:124578263-124578274
36	CEBPB	chr4:124574493-124574804	HepG2	liver:	n/a	chr4:124574662-124574671 chr4:124574660-124574673 chr4:124574660-124574671
37	CEBPB	chr4:124578212-124578289	K562	blood:	n/a	chr4:124578263-124578274
38	CEBPB	chr4:124561453-124561684	A549	lung:	n/a	n/a
39	CEBPB	chr4:124539857-124540378	HepG2	liver:	n/a	chr4:124540258-124540269
40	CEBPB	chr4:124588629-124589378	IMR90	lung:	n/a	n/a
41	CEBPD	chr4:124590368-124590791	K562	blood:	n/a	n/a
42	CEBPD	chr4:124590388-124590618	K562	blood:	n/a	n/a
43	CHD2	chr4:124570406-124570761	GM12878	blood:	n/a	n/a
44	CTCF	chr4:124581058-124581201	GM10248	blood:	n/a	n/a
45	CTCF	chr4:124580869-124581337	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:124582400-124582550	HPAF	blood vessel:	n/a	chr4:124582461-124582482 chr4:124582467-124582483 chr4:124582466-124582484
47	CTCF	chr4:124582360-124582510	NHLF	lung:	n/a	chr4:124582461-124582482 chr4:124582467-124582483 chr4:124582466-124582484
48	CTCF	chr4:124543920-124544070	HCFaa	heart:	n/a	chr4:124543937-124543955 chr4:124543943-124543952
49	CTCF	chr4:124582400-124582550	HMF	breast:	n/a	chr4:124582461-124582482 chr4:124582467-124582483 chr4:124582466-124582484
50	CTCF	chr4:124580917-124581315	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:124571385-124571435	NB4	blood:	n/a
2	chr4:124534980-124535030	SKMC	muscle:	n/a
3	chr4:124572578-124572628	AG09319	gingival:	n/a
4	chr4:124534980-124535030	HUVEC	blood vessel:	n/a
5	chr4:124572578-124572628	ovcar-3	ovarian:	n/a
6	chr4:124534980-124535030	HRCEpiC	kidney:	n/a
7	chr4:124571385-124571435	HNPCEpiC	eye:	n/a
8	chr4:124534980-124535030	HepG2	liver:	n/a
9	chr4:124552897-124552947	Caco-2	colon:	n/a
10	chr4:124572578-124572628	SK-N-SH	brain:	n/a
11	chr4:124571385-124571435	GM12891	blood:	n/a
12	chr4:124552897-124552947	BE2_C	brain:	n/a
13	chr4:124572578-124572628	LNCaP	prostate:	n/a
14	chr4:124552897-124552947	AG09309	skin:	n/a
15	chr4:124572578-124572628	ECC-1	luminal epithelium:	n/a
16	chr4:124534980-124535030	IMR90	lung:	fetal
17	chr4:124534980-124535030	HAEpiC	amniotic membrane:	n/a
18	chr4:124571385-124571435	PrEC	prostate:	n/a
19	chr4:124534980-124535030	NB4	blood:	n/a
20	chr4:124572578-124572628	HCF	heart:	n/a
21	chr4:124534980-124535030	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:124534980-124535030	HL-60	blood:	n/a
23	chr4:124534980-124535030	Caco-2	colon:	n/a
24	chr4:124572578-124572628	Hepatocyte	liver:	n/a
25	chr4:124534980-124535030	U87	brain:	n/a
26	chr4:124571385-124571435	HL-60	blood:	n/a
27	chr4:124552897-124552947	U87	brain:	n/a
28	chr4:124572578-124572628	CMK	blood:	n/a
29	chr4:124534980-124535030	AG04449	skin:	fetal
30	chr4:124572578-124572628	GM19239	blood:	n/a
31	chr4:124534980-124535030	T-47D	breast:	n/a
32	chr4:124534980-124535030	HRE	kidney:	n/a
33	chr4:124571385-124571435	ECC-1	luminal epithelium:	n/a
34	chr4:124534980-124535030	PANC-1	pancreas:	n/a
35	chr4:124534980-124535030	HNPCEpiC	eye:	n/a
36	chr4:124534980-124535030	ECC-1	luminal epithelium:	n/a
37	chr4:124534980-124535030	GM12892	blood:	n/a
38	chr4:124572578-124572628	PrEC	prostate:	n/a
39	chr4:124572578-124572628	BJ	skin:	n/a
40	chr4:124572578-124572628	MCF-7	breast:	n/a
41	chr4:124552897-124552947	GM12891	blood:	n/a
42	chr4:124572578-124572628	ProgFib	skin:	n/a
43	chr4:124572578-124572628	GM12878	blood:	n/a
44	chr4:124572578-124572628	AG04449	skin:	fetal
45	chr4:124552897-124552947	PrEC	prostate:	n/a
46	chr4:124571385-124571435	MCF10A-Er-Src	breast:	n/a
47	chr4:124534980-124535030	BJ	skin:	n/a
48	chr4:124552897-124552947	SK-N-SH_RA	brain:	n/a
49	chr4:124552897-124552947	Hela-S3	cervix:	n/a
50	chr4:124534980-124535030	GM12878	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:124531065..124533065-chr4:124540303..124542494,2	MCF-7	breast:
2	chr4:124312099..124312874-chr4:124581927..124582437,2	MCF-7	breast:
3	chr4:124485427..124486524-chr4:124580578..124581744,8	MCF-7	breast:
4	chr4:124485623..124486524-chr4:124581998..124582924,2	MCF-7	breast:
5	chr4:124531898..124534337-chr4:124538687..124541460,2	K562	blood:
6	chr4:124521015..124523686-chr4:124532382..124534861,2	K562	blood:
7	chr4:124485658..124486578-chr4:124582431..124582959,2	K562	blood:
8	chr4:124530387..124532739-chr4:124537619..124539406,2	MCF-7	breast:
9	chr4:124531898..124534337-chr4:124538687..124541460,2	K562	blood:
10	chr4:124537300..124539042-chr4:124539831..124541822,2	K562	blood:
11	chr4:124521275..124523709-chr4:124536062..124537682,2	K562	blood:
12	chr4:124271449..124272025-chr4:124580652..124581509,3	MCF-7	breast:
13	chr4:124584154..124586562-chr4:124589727..124591476,2	K562	blood:
14	chr4:124311817..124312603-chr4:124581045..124581823,2	MCF-7	breast:
15	chr4:124587417..124589691-chr4:124590873..124592860,2	K562	blood:
16	chr4:124539235..124541836-chr4:124543531..124545537,2	MCF-7	breast:
17	chr4:124530387..124532739-chr4:124537619..124539406,2	MCF-7	breast:
18	chr4:124048317..124048943-chr4:124580795..124581655,2	MCF-7	breast:
19	chr4:124584154..124586562-chr4:124589727..124591476,2	K562	blood:
20	chr4:124311726..124312447-chr4:124543869..124544380,2	MCF-7	breast:
21	chr4:124582206..124582930-chr4:125183080..125184000,2	MCF-7	breast:
22	chr4:124539235..124541836-chr4:124543531..124545537,2	MCF-7	breast:
23	chr4:124531065..124533065-chr4:124540303..124542494,2	MCF-7	breast:
24	chr4:124537300..124539042-chr4:124539831..124541822,2	K562	blood:
25	chr4:124590521..124592638-chr4:124596281..124598290,3	K562	blood:
26	chr4:124048111..124048748-chr4:124582168..124582901,2	MCF-7	breast:
27	chr4:124048090..124049080-chr4:124581973..124582933,2	K562	blood:
28	chr4:124271082..124272019-chr4:124580612..124581573,2	MCF-7	breast:
29	chr4:124319981..124321573-chr4:124580466..124582446,2	MCF-7	breast:
30	chr4:124317878..124321716-chr4:124581134..124584700,4	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRY1-2	chr4:124571422-124571487	ENSG00000249464
2	lnc-SPRY1-2	chr4:124582908-124589223	NONHSAT098196
3	lnc-SPRY1-2	chr4:124560706-124560877	NONHSAT098194
4	lnc-SPRY1-4	chr4:124561437-124561699	NONHSAT098193
5	lnc-SPRY1-2	chr4:124571390-124571503	NONHSAT098195
6	lnc-SPRY1-2	chr4:124571446-124571487	ENSG00000249464
7	lnc-SPRY1-2	chr4:124573942-124574057	ENSG00000249464
8	lnc-SPRY1-2	chr4:124573942-124574057	ENSG00000249464
9	lnc-SPRY1-2	chr4:124582908-124582990	NONHSAT098194
10	lnc-SPRY1-2	chr4:124573942-124574057	NONHSAT098196
11	lnc-SPRY1-2	chr4:124582908-124582988	ENSG00000249464
12	lnc-SPRY1-2	chr4:124582908-124582988	ENSG00000249464
13	lnc-SPRY1-4	chr4:124542635-124542643	NONHSAT098193
14	lnc-SPRY1-2	chr4:124573942-124574057	ENSG00000249464
15	lnc-SPRY1-2	chr4:124571422-124571487	NONHSAT098196
16	lnc-SPRY1-2	chr4:124582908-124582988	NONHSAT098199
17	lnc-SPRY1-2	chr4:124573942-124574057	NONHSAT098195
18	lnc-SPRY1-2	chr4:124582908-124582988	NONHSAT098195
19	lnc-SPRY1-2	chr4:124571446-124571484	ENSG00000249464
20	lnc-SPRY1-2	chr4:124573942-124574057	NONHSAT098194
21	lnc-SPRY1-2	chr4:124573940-124574057	NONHSAT098199
22	lnc-SPRY1-2	chr4:124582908-124587987	ENSG00000249464
23	lnc-SPRY1-2	chr4:124580689-124580994	NONHSAT098194
24	lnc-SPRY1-2	chr4:124571147-124571487	NONHSAT098194

No data

Variant related genes	Relation type
LINC01091	TF binding region
LINC01091	CpG island
ENSG00000164056	chromatin interactions
SCD	miRNA target sites
GLB1L3	miRNA target sites
ARL2BP	miRNA target sites
DAND5	miRNA target sites
DUSP3	miRNA target sites
FRAT2	miRNA target sites
EGR1	miRNA target sites
C5orf24	miRNA target sites
E2F7	miRNA target sites

Extended variants
information (count: 2227 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2227 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs752500	chr4:124528452-124528453	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566189490	chr4:124528509-124528510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75240104	chr4:124528525-124528526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534650419	chr4:124528552-124528553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528579123	chr4:124528554-124528555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183321560	chr4:124528612-124528613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142792699	chr4:124528616-124528617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs112293864	chr4:124528649-124528650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376516520	chr4:124528658-124528659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371599616	chr4:124528659-124528660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79455791	chr4:124528698-124528699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556688965	chr4:124528737-124528738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1425422	chr4:124528798-124528799	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs386679195	chr4:124528799-124528800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs59386442	chr4:124528801-124528802	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs76207013	chr4:124528844-124528845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188012769	chr4:124528865-124528866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560957909	chr4:124528883-124528884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536584007	chr4:124528892-124528893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192110778	chr4:124528901-124528902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543337844	chr4:124528984-124528985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563466013	chr4:124529005-124529006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533485727	chr4:124529029-124529030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549340169	chr4:124529030-124529031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532232383	chr4:124529033-124529034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371041466	chr4:124529035-124529036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552137464	chr4:124529057-124529058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184372105	chr4:124529065-124529066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189987121	chr4:124529079-124529080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369634625	chr4:124529084-124529085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528201980	chr4:124529115-124529116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200531039	chr4:124529141-124529142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78064163	chr4:124529146-124529147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150780119	chr4:124529149-124529150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550241380	chr4:124529171-124529172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145992583	chr4:124529208-124529209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192852465	chr4:124529228-124529229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538464687	chr4:124529281-124529282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538912108	chr4:124529298-124529299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373382360	chr4:124529315-124529316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184834674	chr4:124529349-124529350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572169069	chr4:124529404-124529405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534798222	chr4:124529419-124529420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554517317	chr4:124529443-124529444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558219881	chr4:124529451-124529452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189391775	chr4:124529460-124529461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180941626	chr4:124529517-124529518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80319212	chr4:124529555-124529556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs58840370	chr4:124529573-124529574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs370483940	chr4:124529620-124529621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124524800-124529400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:124527400-124529000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr4:124527400-124529400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr4:124527600-124528600	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr4:124527600-124528800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr4:124527600-124529000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:124527600-124529200	Enhancers	Primary T cells from cord blood	blood
8	chr4:124527600-124529400	Enhancers	Primary hematopoietic stem cells	blood
9	chr4:124527600-124529400	Enhancers	Fetal Thymus	thymus
10	chr4:124527600-124529600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr4:124527800-124528600	Enhancers	GM12878-XiMat	blood
12	chr4:124527800-124528800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr4:124527800-124529200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr4:124528000-124528600	Enhancers	Primary B cells from peripheral blood	blood
15	chr4:124528000-124528600	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr4:124528000-124528600	Enhancers	Dnd41	blood
17	chr4:124528000-124528800	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr4:124528000-124528800	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr4:124528000-124529400	Enhancers	Primary T cells fromperipheralblood	blood
20	chr4:124528200-124528600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr4:124528200-124528600	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr4:124528200-124528800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:124528400-124529200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr4:124528600-124538400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr4:124529400-124536000	Weak transcription	Primary hematopoietic stem cells	blood
26	chr4:124529400-124537000	Weak transcription	Fetal Thymus	thymus
27	chr4:124533600-124534600	Enhancers	Fetal Stomach	stomach
28	chr4:124533600-124539400	Enhancers	Colon Smooth Muscle	Colon
29	chr4:124533800-124534000	Enhancers	Stomach Smooth Muscle	stomach
30	chr4:124533800-124535400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr4:124534000-124534600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr4:124534200-124534400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:124534200-124535000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:124534400-124534800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:124534400-124535200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr4:124534400-124535200	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:124534600-124534800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr4:124534600-124534800	Enhancers	Stomach Smooth Muscle	stomach
39	chr4:124534600-124535000	Weak transcription	Fetal Stomach	stomach
40	chr4:124534600-124535400	Enhancers	Hela-S3	cervix
41	chr4:124534800-124535400	Enhancers	Rectal Smooth Muscle	rectum
42	chr4:124534800-124537400	Weak transcription	Stomach Smooth Muscle	stomach
43	chr4:124535000-124535200	Enhancers	Fetal Stomach	stomach
44	chr4:124535000-124536600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr4:124535200-124535400	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr4:124535200-124535800	Enhancers	K562	blood
47	chr4:124535200-124537200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr4:124535200-124537800	Weak transcription	Fetal Stomach	stomach
49	chr4:124535400-124536400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr4:124535400-124538000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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