Variant report

Variant	esv1799666
Chromosome Location	chr4:77119942-77129568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:77129295-77129859	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:77121987-77122317	HepG2	liver:	n/a	n/a
3	ATF2	chr4:77118690-77120437	GM12878	blood:	n/a	n/a
4	ATF2	chr4:77119476-77121237	GM12878	blood:	n/a	n/a
5	ATF2	chr4:77120499-77121437	GM12878	blood:	n/a	n/a
6	ATF3	chr4:77119844-77120054	K562	blood:	n/a	n/a
7	BATF	chr4:77119444-77120161	GM12878	blood:	n/a	n/a
8	BATF	chr4:77120716-77121142	GM12878	blood:	n/a	n/a
9	BATF	chr4:77119539-77120091	GM12878	blood:	n/a	n/a
10	BATF	chr4:77120757-77121122	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:77120770-77121107	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:77120708-77121133	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:77119532-77119995	GM12878	blood:	n/a	n/a
14	BCL3	chr4:77120735-77121183	GM12878	blood:	n/a	n/a
15	BCL3	chr4:77119561-77120118	GM12878	blood:	n/a	n/a
16	BCLAF1	chr4:77118972-77120365	GM12878	blood:	n/a	chr4:77120136-77120145
17	BCLAF1	chr4:77119138-77120169	GM12878	blood:	n/a	chr4:77120136-77120145
18	BCLAF1	chr4:77120683-77121214	GM12878	blood:	n/a	n/a
19	BCLAF1	chr4:77120532-77121349	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:77120674-77121459	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:77119158-77120267	K562	blood:	n/a	chr4:77119972-77119981 chr4:77119970-77119983 chr4:77119972-77119981
22	BHLHE40	chr4:77122039-77122387	HepG2	liver:	n/a	n/a
23	BHLHE40	chr4:77129567-77129906	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:77119061-77120469	GM12878	blood:	n/a	chr4:77119972-77119981 chr4:77119970-77119983 chr4:77119972-77119981
25	CBX3	chr4:77119595-77120123	K562	blood:	n/a	n/a
26	CEBPB	chr4:77129554-77129855	IMR90	lung:	n/a	chr4:77129589-77129597
27	CEBPB	chr4:77121839-77122414	HepG2	liver:	n/a	chr4:77122013-77122021
28	CEBPB	chr4:77120779-77121126	GM12878	blood:	n/a	n/a
29	CEBPB	chr4:77122083-77122390	K562	blood:	n/a	n/a
30	CEBPB	chr4:77127688-77128039	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:77129556-77129826	HepG2	liver:	n/a	chr4:77129589-77129597
32	CEBPB	chr4:77121965-77122421	HepG2	liver:	n/a	chr4:77122013-77122021
33	CEBPB	chr4:77122077-77122322	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr4:77122003-77122367	MCF-7	breast:	n/a	chr4:77122013-77122021
35	CEBPB	chr4:77122066-77122317	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:77121869-77122404	HepG2	liver:	n/a	chr4:77122013-77122021
37	CEBPB	chr4:77119465-77120312	GM12878	blood:	n/a	n/a
38	CEBPD	chr4:77122066-77122398	HepG2	liver:	n/a	n/a
39	CHD1	chr4:77119329-77121096	GM12878	blood:	n/a	n/a
40	CHD2	chr4:77119087-77120373	GM12878	blood:	n/a	n/a
41	CHD2	chr4:77122078-77122398	HepG2	liver:	n/a	n/a
42	CHD2	chr4:77120724-77121358	GM12878	blood:	n/a	chr4:77121265-77121272
43	CREB1	chr4:77119463-77120394	GM12878	blood:	n/a	n/a
44	CTCF	chr4:77120969-77121131	GM13977	blood:	n/a	chr4:77121041-77121059
45	CTCF	chr4:77120940-77121090	GM12875	blood:	n/a	chr4:77121041-77121059
46	CTCF	chr4:77120960-77121110	GM12872	blood:	n/a	chr4:77121041-77121059
47	CTCF	chr4:77120932-77121139	GM12892	blood:	n/a	chr4:77121041-77121059
48	CTCF	chr4:77121260-77121410	GM12864	blood:	n/a	n/a
49	CTCF	chr4:77120980-77121130	HRE	kidney:	n/a	chr4:77121041-77121059
50	CTCF	chr4:77120880-77121030	GM12869	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:77128252-77128302	AoSMC	blood vessel:	n/a
2	chr4:77128252-77128302	RPTEC	kidney:	n/a
3	chr4:77128252-77128302	NH-A	brain:	n/a
4	chr4:77128252-77128302	AG09319	gingival:	n/a
5	chr4:77128252-77128302	PANC-1	pancreas:	n/a
6	chr4:77128252-77128302	Hepatocyte	liver:	n/a
7	chr4:77128252-77128302	SKMC	muscle:	n/a
8	chr4:77128252-77128302	HMEC	breast:	n/a
9	chr4:77128252-77128302	HCF	heart:	n/a
10	chr4:77128252-77128302	U87	brain:	n/a
11	chr4:77128252-77128302	AG09309	skin:	n/a
12	chr4:77128252-77128302	PFSK-1	brain:	n/a
13	chr4:77128252-77128302	SAEC	small airway:	n/a
14	chr4:77128252-77128302	GM06990	blood:	n/a
15	chr4:77128252-77128302	NHDF-neo	bronchial:	n/a
16	chr4:77128252-77128302	SK-N-SH	brain:	n/a
17	chr4:77128252-77128302	SK-N-SH_RA	brain:	n/a
18	chr4:77128252-77128302	NHBE	bronchial:	n/a
19	chr4:77128252-77128302	HL-60	blood:	n/a
20	chr4:77128252-77128302	CMK	blood:	n/a
21	chr4:77128252-77128302	HUVEC	blood vessel:	n/a
22	chr4:77128252-77128302	HIPEpiC	eye:	n/a
23	chr4:77128252-77128302	HCM	heart:	n/a
24	chr4:77128252-77128302	SK-N-MC	brain:	n/a
25	chr4:77128252-77128302	Caco-2	colon:	n/a
26	chr4:77128252-77128302	HAEpiC	amniotic membrane:	n/a
27	chr4:77128252-77128302	HEEpiC	esophagus:	n/a
28	chr4:77128252-77128302	GM12892	blood:	n/a
29	chr4:77128252-77128302	GM12891	blood:	n/a
30	chr4:77128252-77128302	AG04449	skin:	fetal
31	chr4:77128252-77128302	BJ	skin:	n/a
32	chr4:77128252-77128302	HCT-116	colon:	n/a
33	chr4:77128252-77128302	MCF10A-Er-Src	breast:	n/a
34	chr4:77128252-77128302	IMR90	lung:	fetal
35	chr4:77128252-77128302	HEK293	kidney:	embryo
36	chr4:77128252-77128302	K562	blood:	n/a
37	chr4:77128252-77128302	A549	lung:	n/a
38	chr4:77128252-77128302	NB4	blood:	n/a
39	chr4:77128252-77128302	Hela-S3	cervix:	n/a
40	chr4:77128252-77128302	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:77128252-77128302	ECC-1	luminal epithelium:	n/a
42	chr4:77128252-77128302	HNPCEpiC	eye:	n/a
43	chr4:77128252-77128302	AG04450	lung:	fetal
44	chr4:77128252-77128302	NT2-D1	testis:	n/a
45	chr4:77128252-77128302	PrEC	prostate:	n/a
46	chr4:77128252-77128302	Jurkat	blood:	n/a
47	chr4:77128252-77128302	T-47D	breast:	n/a
48	chr4:77128252-77128302	ProgFib	skin:	n/a
49	chr4:77128252-77128302	GM19239	blood:	n/a
50	chr4:77128252-77128302	LNCaP	prostate:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:77122932..77125835-chr4:77128901..77130952,2	MCF-7	breast:
2	chr4:77119760..77123050-chr4:77133589..77135332,3	K562	blood:
3	chr4:77117716..77120024-chr4:77122804..77125775,4	K562	blood:
4	chr4:77122331..77124750-chr4:77227129..77228896,2	MCF-7	breast:
5	chr4:77114541..77118897-chr4:77119397..77123368,6	K562	blood:
6	chr4:77122932..77125835-chr4:77128901..77130952,2	MCF-7	breast:
7	chr4:77122190..77124913-chr4:77147273..77149332,2	K562	blood:
8	chr4:77118497..77121388-chr4:77227077..77230082,4	MCF-7	breast:
9	chr4:77117574..77120210-chr4:77127527..77130330,2	K562	blood:
10	chr4:77126443..77128731-chr4:77132915..77135566,2	MCF-7	breast:
11	chr4:77117574..77120210-chr4:77127527..77130330,2	K562	blood:
12	chr4:77118780..77124053-chr4:77134347..77137767,5	MCF-7	breast:
13	chr4:77122262..77124788-chr4:77127198..77129570,2	K562	blood:
14	chr4:77125230..77126946-chr4:77133828..77136459,2	MCF-7	breast:
15	chr4:77120877..77123601-chr4:77133534..77136298,3	MCF-7	breast:
16	chr4:77125920..77131688-chr4:77131770..77137672,14	K562	blood:
17	chr4:77122262..77124788-chr4:77127198..77129570,2	K562	blood:
18	chr4:77117716..77120024-chr4:77122804..77125775,4	K562	blood:
19	chr4:77115676..77118604-chr4:77122425..77126369,3	MCF-7	breast:
20	chr4:77118894..77122374-chr4:77129647..77132337,3	K562	blood:

No data

Variant related genes	Relation type
SCARB2	TF binding region
SCARB2	CpG island
ENSG00000138760	chromatin interactions
ENSG00000189157	chromatin interactions
ENSG00000118804	chromatin interactions

Extended variants
information (count: 335 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17001626	chr4:77119942-77119943	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550272968	chr4:77119971-77119972	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs17001627	chr4:77119974-77119975	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs201034693	chr4:77119993-77119994	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs201694442	chr4:77119994-77119995	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs111941261	chr4:77119995-77119996	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs368695668	chr4:77119996-77119997	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs73826392	chr4:77119998-77119999	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs529502096	chr4:77120017-77120018	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs549641521	chr4:77120018-77120019	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs114302114	chr4:77120026-77120027	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs552749570	chr4:77120027-77120028	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs535365864	chr4:77120033-77120034	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs114006102	chr4:77120034-77120035	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs570440025	chr4:77120035-77120036	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs11938219	chr4:77120036-77120037	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs536677253	chr4:77120128-77120129	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs13434713	chr4:77120189-77120190	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs576114335	chr4:77120307-77120308	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs149148331	chr4:77120329-77120330	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs535626771	chr4:77120345-77120346	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs11934628	chr4:77120369-77120370	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs181319146	chr4:77120405-77120406	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs370287952	chr4:77120450-77120451	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs77722996	chr4:77120483-77120484	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs184930827	chr4:77120497-77120498	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs115922145	chr4:77120545-77120546	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs1372410	chr4:77120546-77120547	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs529415481	chr4:77120562-77120563	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs543220457	chr4:77120688-77120689	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs560020384	chr4:77120697-77120698	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs189391864	chr4:77120709-77120710	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs150923560	chr4:77120721-77120722	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs552121769	chr4:77120761-77120762	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs115386249	chr4:77120764-77120765	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs62302997	chr4:77120769-77120770	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs532950532	chr4:77120821-77120822	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs549551305	chr4:77120830-77120831	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs17001633	chr4:77120873-77120874	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs370840933	chr4:77120897-77120898	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs17001636	chr4:77120898-77120899	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs78582124	chr4:77120915-77120916	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs372911286	chr4:77120977-77120978	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs565560118	chr4:77120987-77120988	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs144995498	chr4:77120993-77120994	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs75772188	chr4:77121016-77121017	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs577901350	chr4:77121019-77121020	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs543798409	chr4:77121021-77121022	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs375665127	chr4:77121152-77121153	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs149094066	chr4:77121203-77121204	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:77113200-77134000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:77113600-77134200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:77114200-77122400	Enhancers	Right Ventricle	heart
4	chr4:77114600-77121000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:77114600-77122000	Enhancers	HMEC	breast
6	chr4:77114800-77122800	Enhancers	Psoas Muscle	Psoas
7	chr4:77115200-77122200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:77115400-77122600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr4:77115600-77120800	Enhancers	Adipose Nuclei	Adipose
10	chr4:77116200-77122400	Enhancers	Pancreas	Pancrea
11	chr4:77116200-77122400	Enhancers	Right Atrium	heart
12	chr4:77116600-77122600	Enhancers	Fetal Thymus	thymus
13	chr4:77116800-77122200	Enhancers	Primary B cells from peripheral blood	blood
14	chr4:77117000-77120000	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr4:77117000-77122800	Enhancers	Small Intestine	intestine
16	chr4:77117000-77134000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:77117200-77121400	Enhancers	Spleen	Spleen
18	chr4:77117200-77129200	Enhancers	Liver	Liver
19	chr4:77117400-77122600	Enhancers	Thymus	Thymus
20	chr4:77117400-77132800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:77117600-77121000	Enhancers	Primary hematopoietic stem cells	blood
22	chr4:77117800-77120000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:77117800-77122200	Enhancers	NHDF-Ad	bronchial
24	chr4:77117800-77122400	Enhancers	Left Ventricle	heart
25	chr4:77117800-77122800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr4:77118000-77120400	Flanking Active TSS	Brain Cingulate Gyrus	brain
27	chr4:77118000-77120400	Flanking Active TSS	GM12878-XiMat	blood
28	chr4:77118000-77121400	Enhancers	Aorta	Aorta
29	chr4:77118000-77122000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr4:77118000-77122400	Enhancers	Fetal Heart	heart
31	chr4:77118200-77120200	Enhancers	Esophagus	oesophagus
32	chr4:77118200-77120400	Flanking Active TSS	Brain Anterior Caudate	brain
33	chr4:77118200-77121000	Enhancers	Primary B cells from cord blood	blood
34	chr4:77118200-77121600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr4:77118200-77122600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr4:77118400-77120400	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr4:77118400-77121800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr4:77118400-77122000	Enhancers	Primary T cells from cord blood	blood
39	chr4:77118600-77121000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr4:77118600-77121200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr4:77118600-77121200	Enhancers	Fetal Muscle Trunk	muscle
42	chr4:77118600-77121800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr4:77118600-77122400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr4:77118800-77120400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr4:77118800-77120800	Enhancers	Fetal Intestine Small	intestine
46	chr4:77118800-77120800	Weak transcription	Ovary	ovary
47	chr4:77118800-77121800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr4:77118800-77122000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
49	chr4:77118800-77122200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:77118800-77122400	Enhancers	Primary monocytes fromperipheralblood	blood

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