Variant report

Variant	nsv4551
Chromosome Location	chr4:152582617-152627367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:337)
CpG islands
(count:427)
Chromatin interactive
region (count:29)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:152592808-152593277	K562	blood:	n/a	n/a
2	ATF1	chr4:152592763-152593282	K562	blood:	n/a	n/a
3	ATF2	chr4:152595894-152596329	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:152592879-152593183	K562	blood:	n/a	n/a
5	BHLHE40	chr4:152592581-152593340	K562	blood:	n/a	n/a
6	BHLHE40	chr4:152595156-152595356	K562	blood:	n/a	n/a
7	CBX3	chr4:152592913-152593368	K562	blood:	n/a	n/a
8	CCNT2	chr4:152592673-152593311	K562	blood:	n/a	n/a
9	CEBPB	chr4:152603153-152603380	HepG2	liver:	n/a	n/a
10	CEBPB	chr4:152626514-152626823	K562	blood:	n/a	n/a
11	CEBPB	chr4:152615226-152615372	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:152622898-152623068	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:152622844-152623169	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:152591231-152591519	IMR90	lung:	n/a	n/a
15	CEBPD	chr4:152592630-152593371	K562	blood:	n/a	n/a
16	CEBPD	chr4:152592717-152593273	K562	blood:	n/a	n/a
17	CHD2	chr4:152608514-152608624	Hela-S3	cervix:	n/a	n/a
18	CREB1	chr4:152592611-152593453	K562	blood:	n/a	n/a
19	CTCF	chr4:152595940-152596090	BJ	skin:	n/a	n/a
20	CTCF	chr4:152595980-152596130	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr4:152595940-152596090	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr4:152614080-152614230	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr4:152614120-152614270	SAEC	small airway:	n/a	n/a
24	CTCF	chr4:152596580-152596730	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:152595940-152596090	NHLF	lung:	n/a	n/a
26	CTCF	chr4:152595900-152596050	HPF	lung:	n/a	n/a
27	CTCF	chr4:152610560-152610710	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr4:152595920-152596070	AG10803	skin:	n/a	n/a
29	CTCF	chr4:152595940-152596090	AG04449	skin:	n/a	n/a
30	CTCF	chr4:152595900-152596050	BE2_C	brain:	n/a	n/a
31	CTCF	chr4:152595960-152596110	HRE	kidney:	n/a	n/a
32	CTCF	chr4:152595920-152596070	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr4:152595920-152596070	BJ	skin:	n/a	n/a
34	CTCF	chr4:152595986-152596076	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr4:152596240-152596390	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr4:152595920-152596070	NHEK	skin:	n/a	n/a
37	CTCF	chr4:152592960-152593110	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr4:152596020-152596170	HCFaa	heart:	n/a	n/a
39	CTCF	chr4:152595960-152596110	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr4:152595900-152596050	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr4:152595900-152596050	HAc	cerebellar:	n/a	n/a
42	CTCF	chr4:152595960-152596110	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr4:152595960-152596110	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr4:152595940-152596090	AG10803	skin:	n/a	n/a
45	CTCF	chr4:152614120-152614270	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr4:152595960-152596110	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr4:152595960-152596110	HMEC	breast:	n/a	n/a
48	CTCF	chr4:152595920-152596070	AG04450	lung:	n/a	n/a
49	CTCF	chr4:152595900-152596050	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr4:152601960-152602110	GM12873	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:152589780-152589830	MCF10A-Er-Src	breast:	n/a
2	chr4:152592088-152592138	Hepatocyte	liver:	n/a
3	chr4:152597659-152597709	HRE	kidney:	n/a
4	chr4:152622536-152622586	GM19239	blood:	n/a
5	chr4:152589780-152589830	ECC-1	luminal epithelium:	n/a
6	chr4:152611527-152611577	Hepatocyte	liver:	n/a
7	chr4:152594952-152595002	HRE	kidney:	n/a
8	chr4:152594952-152595002	BE2_C	brain:	n/a
9	chr4:152594952-152595002	AG04450	lung:	fetal
10	chr4:152597659-152597709	AG09309	skin:	n/a
11	chr4:152611527-152611577	HUVEC	blood vessel:	n/a
12	chr4:152597659-152597709	AG04449	skin:	fetal
13	chr4:152611527-152611577	NB4	blood:	n/a
14	chr4:152594952-152595002	PrEC	prostate:	n/a
15	chr4:152589780-152589830	HRPEpiC	eye:	n/a
16	chr4:152592088-152592138	NHDF-neo	bronchial:	n/a
17	chr4:152592088-152592138	HNPCEpiC	eye:	n/a
18	chr4:152592088-152592138	SK-N-SH	brain:	n/a
19	chr4:152611527-152611577	RPTEC	kidney:	n/a
20	chr4:152592088-152592138	GM06990	blood:	n/a
21	chr4:152594952-152595002	HepG2	liver:	n/a
22	chr4:152597659-152597709	HCPEpiC	choroid plexus:	n/a
23	chr4:152584522-152584572	K562	blood:	n/a
24	chr4:152611527-152611577	SK-N-SH	brain:	n/a
25	chr4:152594952-152595002	ovcar-3	ovarian:	n/a
26	chr4:152622536-152622586	HIPEpiC	eye:	n/a
27	chr4:152597659-152597709	ECC-1	luminal epithelium:	n/a
28	chr4:152597659-152597709	SK-N-SH_RA	brain:	n/a
29	chr4:152611527-152611577	HCF	heart:	n/a
30	chr4:152622536-152622586	U87	brain:	n/a
31	chr4:152594952-152595002	SK-N-SH_RA	brain:	n/a
32	chr4:152592088-152592138	K562	blood:	n/a
33	chr4:152584522-152584572	H1-hESC	embryonic stem cell:	embryo
34	chr4:152592088-152592138	MCF10A-Er-Src	breast:	n/a
35	chr4:152584522-152584572	PANC-1	pancreas:	n/a
36	chr4:152584522-152584572	CMK	blood:	n/a
37	chr4:152589780-152589830	AG04449	skin:	fetal
38	chr4:152611527-152611577	AG04450	lung:	fetal
39	chr4:152622536-152622586	AG04450	lung:	fetal
40	chr4:152611527-152611577	NHBE	bronchial:	n/a
41	chr4:152589780-152589830	MCF-7	breast:	n/a
42	chr4:152622536-152622586	AG09309	skin:	n/a
43	chr4:152589780-152589830	NHDF-neo	bronchial:	n/a
44	chr4:152592088-152592138	HRE	kidney:	n/a
45	chr4:152594952-152595002	HNPCEpiC	eye:	n/a
46	chr4:152594952-152595002	SAEC	small airway:	n/a
47	chr4:152584522-152584572	ovcar-3	ovarian:	n/a
48	chr4:152611527-152611577	HepG2	liver:	n/a
49	chr4:152594952-152595002	NHBE	bronchial:	n/a
50	chr4:152594952-152595002	HRPEpiC	eye:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:152591570..152594728-chr4:152597153..152600543,3	MCF-7	breast:
2	chr3:64199202..64201470-chr4:152590503..152592987,2	MCF-7	breast:
3	chr4:152620191..152622280-chr4:152625003..152626689,2	K562	blood:
4	chr4:152592436..152594592-chr4:152638948..152641316,2	K562	blood:
5	chr4:152625421..152627707-chr4:152631872..152634146,2	K562	blood:
6	chr4:152593842..152596396-chr4:152600528..152602296,2	K562	blood:
7	chr16:4938802..4939631-chr4:152626739..152627404,2	MCF-7	breast:
8	chr4:152592922..152594503-chr4:152596609..152598897,2	K562	blood:
9	chr1:151965185..151965907-chr4:152610057..152611037,2	MCF-7	breast:
10	chr4:152608557..152610201-chr4:152614503..152616789,2	MCF-7	breast:
11	chr4:152604003..152606698-chr4:152611125..152613319,2	K562	blood:
12	chr4:152609052..152613001-chr4:152620763..152623852,3	MCF-7	breast:
13	chr4:152618513..152621111-chr4:152621997..152624940,2	MCF-7	breast:
14	chr4:152586811..152588784-chr4:152594944..152597793,2	MCF-7	breast:
15	chr4:152601188..152603111-chr4:152604045..152605768,2	MCF-7	breast:
16	chr4:152566191..152568403-chr4:152585457..152588104,2	K562	blood:
17	chr4:152591570..152594728-chr4:152597153..152600543,3	MCF-7	breast:
18	chr4:152597649..152600627-chr4:152664446..152666064,2	K562	blood:
19	chr4:152587087..152588949-chr4:152600852..152602863,2	K562	blood:
20	chr4:152610620..152612985-chr4:152613774..152616542,2	K562	blood:
21	chr4:152620191..152622280-chr4:152625003..152626689,2	K562	blood:
22	chr4:152586811..152588784-chr4:152594944..152597793,2	MCF-7	breast:
23	chr4:152601188..152603111-chr4:152604045..152605768,2	MCF-7	breast:
24	chr4:152618119..152619775-chr4:152630360..152632137,2	MCF-7	breast:
25	chr4:152625613..152627805-chr4:152644194..152646023,2	MCF-7	breast:
26	chr4:152608557..152610201-chr4:152614503..152616789,2	MCF-7	breast:
27	chr4:152609295..152612120-chr4:152614699..152616542,2	K562	blood:
28	chr4:152609052..152613001-chr4:152620763..152623852,3	MCF-7	breast:
29	chr4:152609295..152612120-chr4:152614699..152616542,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM160A1-1	chr4:152591103-152591639	XLOC_003734
2	lnc-FAM160A1-1	chr4:152588607-152590955	XLOC_003734
3	lnc-FAM160A1-2	chr4:152598452-152598583	ENSG00000251455.1
4	lnc-FAM160A1-2	chr4:152595635-152597712	ENSG00000251455.1
5	lnc-FAM160A1-1	chr4:152588376-152588467	XLOC_003734
6	lnc-FAM160A1-2	chr4:152598691-152599045	ENSG00000251455.1
7	lnc-FAM160A1-1	chr4:152591443-152591654	XLOC_003734

No data

Variant related genes	Relation type
ENSG00000251603	TF binding region
PET112	TF binding region
ENSG00000251455	TF binding region
ENSG00000251603	CpG island
PET112	CpG island
ENSG00000251455	CpG island
ENSG00000059691	chromatin interactions
ENSG00000251455	chromatin interactions
ENSG00000251603	chromatin interactions
KBTBD3	miRNA target sites
GTF2H1	miRNA target sites

Extended variants
information (count: 1639 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1639 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182591067	chr4:152582763-152582764	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554378491	chr4:152582778-152582779	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572525664	chr4:152582798-152582799	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546522563	chr4:152582827-152582828	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564431413	chr4:152582909-152582910	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531987722	chr4:152582924-152582925	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543756924	chr4:152582954-152582955	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185617449	chr4:152582955-152582956	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529705894	chr4:152583014-152583015	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115669675	chr4:152583078-152583079	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566690064	chr4:152583091-152583092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189690120	chr4:152583098-152583099	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183003513	chr4:152583133-152583134	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140609354	chr4:152583158-152583159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527515410	chr4:152583175-152583176	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375552801	chr4:152583206-152583207	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556569639	chr4:152583311-152583312	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552165113	chr4:152583353-152583354	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568585992	chr4:152583452-152583453	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144339271	chr4:152583526-152583527	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368512636	chr4:152583531-152583532	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532541897	chr4:152583557-152583558	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572639729	chr4:152583573-152583574	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17027764	chr4:152583606-152583607	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558029909	chr4:152583673-152583674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576298466	chr4:152583717-152583718	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75005416	chr4:152583764-152583765	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562180697	chr4:152583768-152583769	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377034800	chr4:152583780-152583781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541957794	chr4:152583790-152583791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559984530	chr4:152583793-152583794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116517919	chr4:152583837-152583838	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374404250	chr4:152583867-152583868	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11378262	chr4:152583907-152583908	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397805273	chr4:152583923-152583924	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145936774	chr4:152584172-152584173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552040277	chr4:152584223-152584224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371855370	chr4:152584240-152584241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113290908	chr4:152584287-152584288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141363756	chr4:152584399-152584400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143352750	chr4:152584456-152584457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550077424	chr4:152584478-152584479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs540898001	chr4:152584480-152584481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569327418	chr4:152584491-152584492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535471266	chr4:152584492-152584493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547878467	chr4:152584522-152584523	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs565991021	chr4:152584531-152584532	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs540043555	chr4:152584599-152584600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536371663	chr4:152584708-152584709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557894385	chr4:152584758-152584759	Weak transcription Strong transcription	n/a	n/a	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
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intellectual disability	22102821	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1324 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152563800-152625200	Weak transcription	Hela-S3	cervix
2	chr4:152564200-152595200	Weak transcription	Aorta	Aorta
3	chr4:152567400-152608600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:152567800-152609000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr4:152571200-152584200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:152571200-152584200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:152571600-152583600	Weak transcription	Ovary	ovary
8	chr4:152571600-152595000	Weak transcription	HepG2	liver
9	chr4:152574400-152582800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr4:152577200-152585000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr4:152578400-152595200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr4:152579000-152583400	Weak transcription	Duodenum Mucosa	Duodenum
13	chr4:152579200-152584000	Weak transcription	Colonic Mucosa	Colon
14	chr4:152579200-152597400	Weak transcription	Liver	Liver
15	chr4:152579600-152583200	Weak transcription	Esophagus	oesophagus
16	chr4:152579600-152584400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:152579600-152585000	Weak transcription	Gastric	stomach
18	chr4:152579600-152587600	Weak transcription	NHEK	skin
19	chr4:152579600-152592200	Weak transcription	Right Ventricle	heart
20	chr4:152579800-152583400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr4:152579800-152584000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr4:152579800-152585000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:152579800-152592800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:152580000-152595200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:152580200-152583200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:152580200-152583800	Weak transcription	HMEC	breast
27	chr4:152580200-152596000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr4:152580400-152583200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:152580400-152583200	Weak transcription	Pancreas	Pancrea
30	chr4:152580800-152583200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr4:152580800-152583400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr4:152580800-152595800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr4:152580800-152596800	Weak transcription	Primary T cells from cord blood	blood
34	chr4:152581000-152583400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr4:152581000-152592000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr4:152581200-152583200	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr4:152581200-152587600	Weak transcription	Dnd41	blood
38	chr4:152581200-152602800	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr4:152581200-152608400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr4:152581400-152582800	Weak transcription	Fetal Brain Female	brain
41	chr4:152581400-152583000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:152581400-152583400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr4:152581400-152583400	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr4:152581400-152584400	Weak transcription	Left Ventricle	heart
45	chr4:152581400-152585000	Weak transcription	Fetal Thymus	thymus
46	chr4:152581400-152585000	Weak transcription	HSMMtube	muscle
47	chr4:152581400-152587600	Weak transcription	Fetal Muscle Leg	muscle
48	chr4:152581600-152583800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr4:152581600-152595000	Weak transcription	Stomach Smooth Muscle	stomach
50	chr4:152581800-152583200	Weak transcription	Fetal Intestine Large	intestine

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