Variant report

Variant	nsv879502
Chromosome Location	chr4:79052851-79144309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79097596-79098142	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:79071452-79072261	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:79076142-79076168	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:79059293-79059927	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:79086728-79087416	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:79056594-79057947	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:79141036-79141685	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:79076727-79077341	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:79122109-79122522	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:79139434-79139814	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:79054793-79054935	HepG2	liver:	n/a	n/a
12	ATF1	chr4:79121235-79121392	K562	blood:	n/a	n/a
13	ATF1	chr4:79139582-79139790	K562	blood:	n/a	n/a
14	BACH1	chr4:79066195-79066538	H1-hESC	embryonic stem cell:	n/a	n/a
15	BHLHE40	chr4:79097581-79098214	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:79100452-79100644	GM12878	blood:	n/a	chr4:79100516-79100525 chr4:79100516-79100525 chr4:79100517-79100526 chr4:79100514-79100527
17	BHLHE40	chr4:79097626-79097968	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:79097712-79097922	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:79077692-79078066	HepG2	liver:	n/a	chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077872-79077883
20	CEBPB	chr4:79132890-79132972	K562	blood:	n/a	chr4:79132922-79132933
21	CEBPB	chr4:79057198-79057635	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:79139433-79139713	HepG2	liver:	n/a	chr4:79139607-79139618
23	CEBPB	chr4:79121226-79121605	HepG2	liver:	n/a	chr4:79121312-79121325
24	CEBPB	chr4:79077772-79077971	MCF-7	breast:	n/a	chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077872-79077883
25	CEBPB	chr4:79097699-79098020	A549	lung:	n/a	chr4:79097866-79097877
26	CEBPB	chr4:79077700-79078067	H1-hESC	embryonic stem cell:	n/a	chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077872-79077883
27	CEBPB	chr4:79097728-79097956	HepG2	liver:	n/a	chr4:79097866-79097877
28	CEBPB	chr4:79139578-79139759	H1-hESC	embryonic stem cell:	n/a	chr4:79139607-79139618
29	CEBPB	chr4:79077692-79078064	IMR90	lung:	n/a	chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077872-79077883
30	CEBPB	chr4:79128707-79129021	HepG2	liver:	n/a	chr4:79128871-79128882
31	CEBPB	chr4:79132786-79133065	HepG2	liver:	n/a	chr4:79132922-79132933
32	CEBPB	chr4:79139418-79139808	HepG2	liver:	n/a	chr4:79139607-79139618
33	CEBPB	chr4:79086929-79087362	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:79139499-79139697	HepG2	liver:	n/a	chr4:79139607-79139618
35	CEBPB	chr4:79132793-79133084	IMR90	lung:	n/a	chr4:79132922-79132933
36	CEBPB	chr4:79131971-79132152	HepG2	liver:	n/a	chr4:79132046-79132057 chr4:79132046-79132059 chr4:79132047-79132058 chr4:79132048-79132057
37	CEBPB	chr4:79059532-79059663	K562	blood:	n/a	chr4:79059642-79059655 chr4:79059642-79059653 chr4:79059643-79059654
38	CEBPB	chr4:79077699-79078044	K562	blood:	n/a	chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077872-79077883
39	CEBPB	chr4:79111859-79112039	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:79077766-79078051	Hela-S3	cervix:	n/a	chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077872-79077883
41	CEBPB	chr4:79124340-79124353	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:79097686-79098307	HepG2	liver:	n/a	chr4:79097866-79097877
43	CEBPB	chr4:79097563-79098106	A549	lung:	n/a	chr4:79097866-79097877
44	CEBPB	chr4:79077721-79078018	A549	lung:	n/a	chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077873-79077882 chr4:79077872-79077883
45	CEBPB	chr4:79059433-79059819	Hela-S3	cervix:	n/a	chr4:79059642-79059655 chr4:79059642-79059653 chr4:79059643-79059654
46	CEBPB	chr4:79056591-79056928	HepG2	liver:	n/a	chr4:79056647-79056658 chr4:79056647-79056658 chr4:79056762-79056773 chr4:79056645-79056658
47	CEBPB	chr4:79139449-79139792	Hela-S3	cervix:	n/a	chr4:79139607-79139618
48	CEBPB	chr4:79059360-79059815	HepG2	liver:	n/a	chr4:79059642-79059655 chr4:79059642-79059653 chr4:79059643-79059654
49	CEBPB	chr4:79097633-79098082	A549	lung:	n/a	chr4:79097866-79097877
50	CEBPB	chr4:79097438-79098246	Hela-S3	cervix:	n/a	chr4:79097866-79097877

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79077191-79077241	MCF-7	breast:	n/a
2	chr4:79126719-79126769	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:79077191-79077241	MCF-7	breast:	n/a
4	chr4:79126719-79126769	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:79103290-79103340	HCT-116	colon:	n/a
6	chr4:79103030-79103080	HNPCEpiC	eye:	n/a
7	chr4:79143682-79143732	SK-N-SH_RA	brain:	n/a
8	chr4:79077191-79077241	HCF	heart:	n/a
9	chr4:79102910-79102960	AG10803	skin:	n/a
10	chr4:79103030-79103080	GM19239	blood:	n/a
11	chr4:79057742-79057792	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:79096535-79096585	GM19239	blood:	n/a
13	chr4:79057742-79057792	Hepatocyte	liver:	n/a
14	chr4:79143682-79143732	NHBE	bronchial:	n/a
15	chr4:79103126-79103176	HRPEpiC	eye:	n/a
16	chr4:79138888-79138938	ECC-1	luminal epithelium:	n/a
17	chr4:79119852-79119902	HCT-116	colon:	n/a
18	chr4:79143682-79143732	NH-A	brain:	n/a
19	chr4:79103030-79103080	ECC-1	luminal epithelium:	n/a
20	chr4:79106308-79106358	SK-N-SH_RA	brain:	n/a
21	chr4:79102901-79102951	HMEC	breast:	n/a
22	chr4:79102901-79102951	AoSMC	blood vessel:	n/a
23	chr4:79119852-79119902	NB4	blood:	n/a
24	chr4:79103244-79103294	GM12891	blood:	n/a
25	chr4:79096535-79096585	Hepatocyte	liver:	n/a
26	chr4:79126719-79126769	HepG2	liver:	n/a
27	chr4:79103126-79103176	SK-N-MC	brain:	n/a
28	chr4:79083545-79083595	ECC-1	luminal epithelium:	n/a
29	chr4:79102707-79102757	HL-60	blood:	n/a
30	chr4:79103126-79103176	MCF10A-Er-Src	breast:	n/a
31	chr4:79091679-79091729	HepG2	liver:	n/a
32	chr4:79057742-79057792	SK-N-SH_RA	brain:	n/a
33	chr4:79102910-79102960	SK-N-SH	brain:	n/a
34	chr4:79103290-79103340	GM19239	blood:	n/a
35	chr4:79143682-79143732	CMK	blood:	n/a
36	chr4:79057742-79057792	NHBE	bronchial:	n/a
37	chr4:79126719-79126769	HCF	heart:	n/a
38	chr4:79103126-79103176	HL-60	blood:	n/a
39	chr4:79103126-79103176	HNPCEpiC	eye:	n/a
40	chr4:79126719-79126769	PFSK-1	brain:	n/a
41	chr4:79102707-79102757	NHDF-neo	bronchial:	n/a
42	chr4:79101988-79102038	HRCEpiC	kidney:	n/a
43	chr4:79103244-79103294	AoSMC	blood vessel:	n/a
44	chr4:79138888-79138938	SK-N-MC	brain:	n/a
45	chr4:79103126-79103176	NB4	blood:	n/a
46	chr4:79143682-79143732	PrEC	prostate:	n/a
47	chr4:79077191-79077241	GM12878	blood:	n/a
48	chr4:79126719-79126769	HMEC	breast:	n/a
49	chr4:79119852-79119902	LNCaP	prostate:	n/a
50	chr4:79101988-79102038	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:79104998..79106622-chr4:79109198..79111577,2	K562	blood:
2	chr4:79068664..79070445-chr4:79070622..79072179,2	MCF-7	breast:
3	chr4:78980297..78981139-chr4:79092342..79093264,2	MCF-7	breast:
4	chr4:79116297..79118632-chr4:79121339..79123057,2	K562	blood:
5	chr4:79093805..79095382-chr4:79119242..79121206,2	K562	blood:
6	chr4:79091323..79093499-chr4:79096107..79097895,2	MCF-7	breast:
7	chr4:79116297..79118632-chr4:79121339..79123057,2	K562	blood:
8	chr4:79085535..79087352-chr4:79088663..79090965,2	K562	blood:
9	chr4:79085535..79087352-chr4:79088663..79090965,2	K562	blood:
10	chr4:79097455..79099663-chr4:79105000..79107358,2	MCF-7	breast:
11	chr4:79068664..79070445-chr4:79070622..79072179,2	MCF-7	breast:
12	chr4:79080375..79082514-chr4:79085692..79087997,2	MCF-7	breast:
13	chr4:79080375..79082514-chr4:79085692..79087997,2	MCF-7	breast:
14	chr4:79093805..79095382-chr4:79119242..79121206,2	K562	blood:
15	chr4:79091323..79093499-chr4:79096107..79097895,2	MCF-7	breast:
16	chr4:79143866..79146531-chr4:79146925..79148583,2	K562	blood:
17	chr4:79082865..79083529-chr6:109330266..109331128,2	Hela-S3	cervix:
18	chr4:79097455..79099663-chr4:79105000..79107358,2	MCF-7	breast:

Variant related genes	Relation type
SERBP1P5	TF binding region
ENSG00000221183	TF binding region
SERBP1P5	CpG island
ENSG00000221183	CpG island
ENSG00000080546	chromatin interactions
ENSG00000221183	chromatin interactions

Extended variants
information (count: 3320 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3320 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2078481	chr4:79052851-79052852	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117345445	chr4:79052886-79052887	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs187088676	chr4:79052918-79052919	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs376760094	chr4:79053054-79053055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs371329694	chr4:79053069-79053070	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs7699120	chr4:79053078-79053079	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs76333019	chr4:79053080-79053081	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs77877857	chr4:79053110-79053111	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs541950706	chr4:79053145-79053146	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs565902843	chr4:79053147-79053148	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs190586713	chr4:79053154-79053155	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373767378	chr4:79053184-79053185	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs572452748	chr4:79053229-79053230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557921577	chr4:79053251-79053252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371400932	chr4:79053252-79053253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs578224150	chr4:79053325-79053326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181776865	chr4:79053337-79053338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532251657	chr4:79053363-79053364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375177074	chr4:79053367-79053368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545737952	chr4:79053371-79053372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58118093	chr4:79053555-79053556	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs531294915	chr4:79053559-79053560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557734444	chr4:79053589-79053590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114401966	chr4:79053602-79053603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568117190	chr4:79053611-79053612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186303382	chr4:79053670-79053671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547991837	chr4:79053723-79053724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571087024	chr4:79053754-79053755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540136322	chr4:79053758-79053759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201704116	chr4:79053784-79053785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143649986	chr4:79053803-79053804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145761969	chr4:79053833-79053834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148500076	chr4:79053898-79053899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34084426	chr4:79053909-79053910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555500806	chr4:79053912-79053913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577402959	chr4:79053930-79053931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530276195	chr4:79053980-79053981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372904255	chr4:79053982-79053983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142809459	chr4:79053986-79053987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112671180	chr4:79054005-79054006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576667054	chr4:79054007-79054008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370127859	chr4:79054010-79054011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35374567	chr4:79054026-79054027	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs542677815	chr4:79054045-79054046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562754833	chr4:79054051-79054052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559315415	chr4:79054060-79054061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140409486	chr4:79054071-79054072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376274833	chr4:79054074-79054075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146983368	chr4:79054122-79054123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs561560377	chr4:79054123-79054124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:884 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79047600-79057200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:79047600-79057400	Weak transcription	Pancreas	Pancrea
3	chr4:79050400-79056800	Enhancers	HepG2	liver
4	chr4:79050600-79053600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:79050600-79053800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:79051200-79053000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:79051200-79053600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr4:79051200-79053800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:79051200-79056400	Weak transcription	Fetal Intestine Large	intestine
10	chr4:79051200-79060200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:79051600-79056600	Weak transcription	Fetal Intestine Small	intestine
12	chr4:79051800-79053200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr4:79051800-79053800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:79052000-79053400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:79052000-79053400	Enhancers	HSMMtube	muscle
16	chr4:79052000-79053600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:79052200-79054000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:79052400-79053200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:79052400-79053400	Enhancers	NHDF-Ad	bronchial
20	chr4:79052400-79053600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:79052400-79053800	Enhancers	Fetal Heart	heart
22	chr4:79052600-79053000	Enhancers	Left Ventricle	heart
23	chr4:79052600-79053000	Enhancers	Psoas Muscle	Psoas
24	chr4:79052600-79053200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr4:79052600-79053200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr4:79052600-79053400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:79052800-79053000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:79052800-79053000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr4:79052800-79053000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr4:79052800-79053200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
31	chr4:79052800-79053200	Enhancers	HSMM	muscle
32	chr4:79052800-79053400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr4:79052800-79053400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr4:79052800-79054000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:79053000-79053200	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr4:79053000-79053400	Enhancers	Colon Smooth Muscle	Colon
37	chr4:79053000-79053800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr4:79053000-79056800	Weak transcription	Psoas Muscle	Psoas
39	chr4:79053200-79053400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr4:79053200-79053800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr4:79053200-79053800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr4:79053200-79056400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:79053200-79056600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr4:79053400-79056400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr4:79053400-79056600	Weak transcription	HSMMtube	muscle
46	chr4:79053400-79058600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:79053600-79053800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:79053800-79054000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr4:79053800-79054000	Enhancers	H9 Cell Line	embryonic stem cell
50	chr4:79053800-79056400	Weak transcription	Fetal Heart	heart

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