Variant report

Variant	nsv966270
Chromosome Location	chr4:56215138-56221281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr4:56219322-56219862	K562	blood:	n/a	n/a
2	CEBPB	chr4:56217108-56217457	IMR90	lung:	n/a	chr4:56217295-56217306
3	CEBPB	chr4:56218108-56218339	A549	lung:	n/a	n/a
4	CEBPB	chr4:56218152-56218304	K562	blood:	n/a	n/a
5	CEBPB	chr4:56217032-56217486	Hela-S3	cervix:	n/a	chr4:56217295-56217306
6	CEBPB	chr4:56218088-56218419	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr4:56218071-56218437	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:56218109-56218343	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:56217208-56217416	K562	blood:	n/a	chr4:56217295-56217306
10	CEBPB	chr4:56217101-56217446	MCF-7	breast:	n/a	chr4:56217295-56217306
11	CEBPB	chr4:56217263-56217385	HepG2	liver:	n/a	chr4:56217295-56217306
12	E2F4	chr4:56217145-56217177	MCF10A-Er-Src	breast:	n/a	n/a
13	EGR1	chr4:56217075-56217273	K562	blood:	n/a	n/a
14	EGR1	chr4:56216882-56217469	HCT-116	colon:	n/a	n/a
15	EGR1	chr4:56217006-56217254	K562	blood:	n/a	n/a
16	EP300	chr4:56217139-56217339	Hela-S3	cervix:	n/a	n/a
17	FOS	chr4:56217044-56217394	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr4:56218222-56218274	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr4:56217036-56217408	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr4:56218095-56218295	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr4:56218089-56218310	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr4:56217035-56217407	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr4:56217036-56217407	MCF10A-Er-Src	breast:	n/a	n/a
24	GTF2F1	chr4:56217137-56217337	Hela-S3	cervix:	n/a	n/a
25	JUND	chr4:56217148-56217248	K562	blood:	n/a	n/a
26	KAP1	chr4:56220754-56221195	HEK293	kidney:	n/a	n/a
27	MAFF	chr4:56219491-56219691	HepG2	liver:	n/a	chr4:56219574-56219592
28	MAFK	chr4:56219489-56219671	IMR90	lung:	n/a	n/a
29	MAX	chr4:56217112-56217409	Hela-S3	cervix:	n/a	n/a
30	MYC	chr4:56218069-56218270	MCF10A-Er-Src	breast:	n/a	n/a
31	MYC	chr4:56217067-56217373	MCF10A-Er-Src	breast:	n/a	n/a
32	MYC	chr4:56217072-56217407	MCF10A-Er-Src	breast:	n/a	n/a
33	NFYA	chr4:56219292-56219730	K562	blood:	n/a	chr4:56219547-56219565 chr4:56219572-56219590 chr4:56219596-56219614
34	NFYB	chr4:56219266-56219744	GM12878	blood:	n/a	chr4:56219617-56219632 chr4:56219544-56219559 chr4:56219593-56219608 chr4:56219569-56219584
35	NFYB	chr4:56219309-56219735	Hela-S3	cervix:	n/a	chr4:56219617-56219632 chr4:56219544-56219559 chr4:56219593-56219608 chr4:56219569-56219584
36	NFYB	chr4:56219279-56219749	K562	blood:	n/a	chr4:56219617-56219632 chr4:56219544-56219559 chr4:56219593-56219608 chr4:56219569-56219584
37	POLR2A	chr4:56214596-56215155	U87	brain:	n/a	n/a
38	POLR2A	chr4:56220871-56221013	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr4:56216213-56216216	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr4:56217131-56217289	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr4:56215196-56215402	HepG2	liver:	n/a	n/a
42	SETDB1	chr4:56220846-56221147	U2OS	brain:	n/a	n/a
43	SP1	chr4:56219351-56219745	K562	blood:	n/a	n/a
44	SP1	chr4:56219378-56219640	GM12878	blood:	n/a	n/a
45	STAT3	chr4:56217115-56217315	MCF10A-Er-Src	breast:	n/a	n/a
46	STAT3	chr4:56217112-56217315	MCF10A-Er-Src	breast:	n/a	n/a
47	STAT3	chr4:56217199-56217351	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr4:56217075-56217256	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr4:56218999-56219133	MCF10A-Er-Src	breast:	n/a	n/a
50	TCF7L2	chr4:56217113-56217309	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56215882-56215932	HRCEpiC	kidney:	n/a
2	chr4:56215882-56215932	SK-N-SH	brain:	n/a
3	chr4:56215882-56215932	A549	lung:	n/a
4	chr4:56215882-56215932	NHBE	bronchial:	n/a
5	chr4:56215882-56215932	HRE	kidney:	n/a
6	chr4:56215882-56215932	Caco-2	colon:	n/a
7	chr4:56215882-56215932	SK-N-SH_RA	brain:	n/a
8	chr4:56215882-56215932	T-47D	breast:	n/a
9	chr4:56215882-56215932	AG04449	skin:	fetal
10	chr4:56215882-56215932	MCF-7	breast:	n/a
11	chr4:56215882-56215932	H1-hESC	embryonic stem cell:	embryo
12	chr4:56215882-56215932	NHDF-neo	bronchial:	n/a
13	chr4:56215882-56215932	Jurkat	blood:	n/a
14	chr4:56215882-56215932	HIPEpiC	eye:	n/a
15	chr4:56215882-56215932	HRPEpiC	eye:	n/a
16	chr4:56215882-56215932	HCM	heart:	n/a
17	chr4:56215882-56215932	RPTEC	kidney:	n/a
18	chr4:56215882-56215932	HEEpiC	esophagus:	n/a
19	chr4:56215882-56215932	HCPEpiC	choroid plexus:	n/a
20	chr4:56215882-56215932	SAEC	small airway:	n/a
21	chr4:56215882-56215932	ProgFib	skin:	n/a
22	chr4:56215882-56215932	GM19239	blood:	n/a
23	chr4:56215882-56215932	HL-60	blood:	n/a
24	chr4:56215882-56215932	PANC-1	pancreas:	n/a
25	chr4:56215882-56215932	BE2_C	brain:	n/a
26	chr4:56215882-56215932	HNPCEpiC	eye:	n/a
27	chr4:56215882-56215932	ECC-1	luminal epithelium:	n/a
28	chr4:56215882-56215932	AoSMC	blood vessel:	n/a
29	chr4:56215882-56215932	SKMC	muscle:	n/a
30	chr4:56215882-56215932	LNCaP	prostate:	n/a
31	chr4:56215882-56215932	GM12892	blood:	n/a
32	chr4:56215882-56215932	Hela-S3	cervix:	n/a
33	chr4:56215882-56215932	AG10803	skin:	n/a
34	chr4:56215882-56215932	HPAEpiC	pulmonary alveolar:	n/a
35	chr4:56215882-56215932	MCF10A-Er-Src	breast:	n/a
36	chr4:56215882-56215932	AG09319	gingival:	n/a
37	chr4:56215882-56215932	Hepatocyte	liver:	n/a
38	chr4:56215882-56215932	GM12891	blood:	n/a
39	chr4:56215882-56215932	IMR90	lung:	fetal
40	chr4:56215882-56215932	U87	brain:	n/a
41	chr4:56215882-56215932	PFSK-1	brain:	n/a
42	chr4:56215882-56215932	GM12878	blood:	n/a
43	chr4:56215882-56215932	PrEC	prostate:	n/a
44	chr4:56215882-56215932	GM06990	blood:	n/a
45	chr4:56215882-56215932	BJ	skin:	n/a
46	chr4:56215882-56215932	HAEpiC	amniotic membrane:	n/a
47	chr4:56215882-56215932	HEK293	kidney:	embryo
48	chr4:56215882-56215932	ovcar-3	ovarian:	n/a
49	chr4:56215882-56215932	NT2-D1	testis:	n/a
50	chr4:56215882-56215932	HCF	heart:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:56221079..56223378-chr4:56272404..56274272,2	MCF-7	breast:
2	chr4:56211096..56216124-chr4:56256262..56265067,20	K562	blood:
3	chr4:56209954..56216628-chr4:56219638..56226284,12	MCF-7	breast:
4	chr4:56216631..56219493-chr4:56263836..56266245,2	K562	blood:
5	chr4:56216631..56219343-chr4:56262936..56265336,2	K562	blood:
6	chr4:56220332..56223664-chr4:56260663..56265029,5	K562	blood:
7	chr4:56212201..56215605-chr4:56218401..56220453,4	MCF-7	breast:
8	chr4:56211148..56230966-chr4:56256626..56269458,54	MCF-7	breast:
9	chr4:56210683..56216526-chr4:56216680..56221548,10	K562	blood:
10	chr4:56211281..56215987-chr4:56257992..56268538,18	K562	blood:
11	chr4:56211498..56213604-chr4:56215998..56219144,5	MCF-7	breast:
12	chr4:56211242..56218739-chr4:56258356..56267013,28	MCF-7	breast:
13	chr4:56212201..56215605-chr4:56218401..56220453,4	MCF-7	breast:
14	chr4:56209954..56216628-chr4:56219638..56226284,12	MCF-7	breast:
15	chr4:56210683..56216526-chr4:56216680..56221548,10	K562	blood:
16	chr4:56213251..56215609-chr4:56227634..56229656,2	MCF-7	breast:

No data

Variant related genes	Relation type
FCF1P8	TF binding region
SRD5A3	TF binding region
FCF1P8	CpG island
SRD5A3	CpG island
ENSG00000134851	chromatin interactions
ENSG00000251111	chromatin interactions
ENSG00000249700	chromatin interactions
ENSG00000128039	chromatin interactions

Extended variants
information (count: 305 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:305 , 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	rs564589707	chr4:56215174-56215175	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs192111721	chr4:56215194-56215195	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs550467306	chr4:56215203-56215204	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs567436526	chr4:56215211-56215212	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs376032967	chr4:56215226-56215227	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs536181831	chr4:56215233-56215234	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs546911268	chr4:56215241-56215242	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs566091460	chr4:56215251-56215252	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs375338788	chr4:56215255-56215256	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs7673512	chr4:56215266-56215267	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs558307402	chr4:56215302-56215303	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs144812649	chr4:56215347-56215348	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs537539137	chr4:56215364-56215365	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs557300745	chr4:56215414-56215415	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs138650626	chr4:56215428-56215429	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs112597458	chr4:56215450-56215451	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs141900592	chr4:56215615-56215616	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs572508784	chr4:56215619-56215620	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs544575761	chr4:56215620-56215621	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs374777556	chr4:56215626-56215627	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs11133373	chr4:56215631-56215632	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs188507886	chr4:56215652-56215653	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs550625627	chr4:56215655-56215656	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs560968708	chr4:56215700-56215701	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs561134776	chr4:56215702-56215703	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs74781033	chr4:56215703-56215704	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs55786762	chr4:56215715-56215716	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs62305111	chr4:56215718-56215719	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs145549875	chr4:56215756-56215757	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs555290579	chr4:56215767-56215768	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs533041443	chr4:56215792-56215793	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs6814943	chr4:56215796-56215797	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs138065325	chr4:56215842-56215843	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs566424511	chr4:56215953-56215954	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs369677238	chr4:56215968-56215969	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs191532427	chr4:56216024-56216025	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs184003218	chr4:56216042-56216043	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs62305112	chr4:56216060-56216061	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573743936	chr4:56216092-56216093	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs28408145	chr4:56216093-56216094	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs376405438	chr4:56216148-56216149	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs531719097	chr4:56216152-56216153	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs377374013	chr4:56216155-56216156	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs553272367	chr4:56216173-56216174	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs546837471	chr4:56216272-56216273	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs545279265	chr4:56216274-56216275	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs149458035	chr4:56216350-56216351	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs191255953	chr4:56216404-56216405	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs184547377	chr4:56216406-56216407	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs560994177	chr4:56216461-56216462	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	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
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56213200-56219000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr4:56213200-56230000	Weak transcription	Fetal Kidney	kidney
3	chr4:56213400-56215200	Enhancers	Fetal Lung	lung
4	chr4:56213400-56215200	Enhancers	Stomach Mucosa	stomach
5	chr4:56213400-56215200	Enhancers	NHDF-Ad	bronchial
6	chr4:56213400-56215200	Enhancers	Osteobl	bone
7	chr4:56213400-56215400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:56213400-56217000	Weak transcription	Fetal Stomach	stomach
9	chr4:56213400-56217200	Weak transcription	Lung	lung
10	chr4:56213400-56223800	Weak transcription	Fetal Heart	heart
11	chr4:56213400-56225400	Weak transcription	Spleen	Spleen
12	chr4:56213400-56233600	Weak transcription	Fetal Intestine Large	intestine
13	chr4:56213600-56215200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:56213600-56215200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:56213600-56219200	Weak transcription	Primary T cells from cord blood	blood
16	chr4:56213600-56221600	Weak transcription	HMEC	breast
17	chr4:56213600-56223000	Weak transcription	Esophagus	oesophagus
18	chr4:56213600-56223000	Weak transcription	HSMM	muscle
19	chr4:56213600-56224000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:56213600-56225600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr4:56213600-56229200	Weak transcription	Fetal Intestine Small	intestine
22	chr4:56213600-56230200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr4:56213600-56230200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:56213600-56242600	Weak transcription	Gastric	stomach
25	chr4:56213800-56217800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:56213800-56218600	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr4:56213800-56221600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:56213800-56223000	Weak transcription	Stomach Smooth Muscle	stomach
29	chr4:56213800-56225200	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr4:56213800-56225600	Weak transcription	Left Ventricle	heart
31	chr4:56213800-56227000	Weak transcription	Placenta	Placenta
32	chr4:56213800-56229800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr4:56213800-56229800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr4:56213800-56229800	Weak transcription	Fetal Muscle Trunk	muscle
35	chr4:56213800-56231800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr4:56213800-56233600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr4:56213800-56239000	Weak transcription	Brain Germinal Matrix	brain
38	chr4:56213800-56251400	Weak transcription	Pancreas	Pancrea
39	chr4:56214000-56215200	Enhancers	Brain Hippocampus Middle	brain
40	chr4:56214000-56215200	Enhancers	Hela-S3	cervix
41	chr4:56214000-56215200	Enhancers	NHLF	lung
42	chr4:56214000-56217400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr4:56214000-56223400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr4:56214000-56224600	Weak transcription	Primary B cells from peripheral blood	blood
45	chr4:56214000-56225600	Weak transcription	Fetal Muscle Leg	muscle
46	chr4:56214000-56229800	Weak transcription	Liver	Liver
47	chr4:56214000-56229800	Weak transcription	Fetal Thymus	thymus
48	chr4:56214000-56229800	Weak transcription	Thymus	Thymus
49	chr4:56214000-56230200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr4:56214000-56231000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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