Variant report

Variant	nsv533785
Chromosome Location	chr4:129785683-129857992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:490)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:490 , 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	ATF2	chr4:129837905-129838481	GM12878	blood:	n/a	n/a
2	ATF2	chr4:129837715-129838462	GM12878	blood:	n/a	n/a
3	ATF2	chr4:129792908-129793330	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:129787441-129787873	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:129838788-129839413	GM12878	blood:	n/a	n/a
6	ATF2	chr4:129786523-129786934	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:129838782-129839408	GM12878	blood:	n/a	n/a
8	ATF2	chr4:129788328-129788944	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:129834181-129834816	GM12878	blood:	n/a	n/a
10	ATF2	chr4:129834221-129834957	GM12878	blood:	n/a	n/a
11	BACH1	chr4:129787497-129787679	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:129797317-129797325	K562	blood:	n/a	n/a
13	BATF	chr4:129837910-129838268	GM12878	blood:	n/a	n/a
14	BATF	chr4:129838922-129839343	GM12878	blood:	n/a	n/a
15	BATF	chr4:129827779-129828010	GM12878	blood:	n/a	chr4:129827877-129827888
16	BATF	chr4:129838911-129839317	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:129839033-129839295	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:129838977-129839324	GM12878	blood:	n/a	n/a
19	BCL3	chr4:129834324-129834632	GM12878	blood:	n/a	n/a
20	BCL3	chr4:129834252-129834735	GM12878	blood:	n/a	n/a
21	BCL3	chr4:129838908-129839307	GM12878	blood:	n/a	n/a
22	BCLAF1	chr4:129837719-129838296	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:129838883-129839358	GM12878	blood:	n/a	n/a
24	BCLAF1	chr4:129838854-129839425	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:129837821-129838334	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:129838002-129838412	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:129838803-129839362	GM12878	blood:	n/a	n/a
28	BRCA1	chr4:129846236-129846257	GM12878	blood:	n/a	n/a
29	BRCA1	chr4:129797349-129797464	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr4:129787527-129787528	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:129789900-129790268	IMR90	lung:	n/a	chr4:129790075-129790086 chr4:129790074-129790087 chr4:129790076-129790085
32	CEBPB	chr4:129801770-129802182	A549	lung:	n/a	chr4:129801978-129801989
33	CEBPB	chr4:129801795-129802172	HepG2	liver:	n/a	chr4:129801978-129801989
34	CEBPB	chr4:129800477-129800760	H1-hESC	embryonic stem cell:	n/a	chr4:129800629-129800640
35	CEBPB	chr4:129789889-129790274	MCF-7	breast:	n/a	chr4:129790075-129790086 chr4:129790074-129790087 chr4:129790076-129790085
36	CEBPB	chr4:129800457-129800812	K562	blood:	n/a	chr4:129800629-129800640
37	CEBPB	chr4:129801840-129802139	Hela-S3	cervix:	n/a	chr4:129801978-129801989
38	CEBPB	chr4:129800461-129800824	A549	lung:	n/a	chr4:129800629-129800640
39	CEBPB	chr4:129801764-129802160	K562	blood:	n/a	chr4:129801978-129801989
40	CEBPB	chr4:129829994-129830286	IMR90	lung:	n/a	chr4:129830178-129830189 chr4:129830129-129830142
41	CEBPB	chr4:129800556-129800805	Hela-S3	cervix:	n/a	chr4:129800629-129800640
42	CEBPB	chr4:129801797-129802171	IMR90	lung:	n/a	chr4:129801978-129801989
43	CEBPB	chr4:129801800-129802160	H1-hESC	embryonic stem cell:	n/a	chr4:129801978-129801989
44	CEBPB	chr4:129800453-129800816	HepG2	liver:	n/a	chr4:129800629-129800640
45	CEBPB	chr4:129801817-129802128	ECC-1	luminal epithelium:	n/a	chr4:129801978-129801989
46	CEBPB	chr4:129793423-129793432	K562	blood:	n/a	n/a
47	CEBPB	chr4:129793214-129793501	A549	lung:	n/a	n/a
48	CEBPB	chr4:129830009-129830338	HepG2	liver:	n/a	chr4:129830178-129830189 chr4:129830129-129830142
49	CEBPB	chr4:129790902-129790991	IMR90	lung:	n/a	n/a
50	CEBPB	chr4:129812446-129812519	H1-hESC	embryonic stem cell:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:129805520-129805570	T-47D	breast:	n/a
2	chr4:129793434-129793484	HUVEC	blood vessel:	n/a
3	chr4:129793434-129793484	HepG2	liver:	n/a
4	chr4:129805520-129805570	GM12891	blood:	n/a
5	chr4:129793434-129793484	HCPEpiC	choroid plexus:	n/a
6	chr4:129793434-129793484	K562	blood:	n/a
7	chr4:129793434-129793484	Hela-S3	cervix:	n/a
8	chr4:129805520-129805570	HepG2	liver:	n/a
9	chr4:129805520-129805570	Hela-S3	cervix:	n/a
10	chr4:129805520-129805570	BE2_C	brain:	n/a
11	chr4:129805520-129805570	H1-hESC	embryonic stem cell:	embryo
12	chr4:129793434-129793484	A549	lung:	n/a
13	chr4:129805520-129805570	SK-N-SH	brain:	n/a
14	chr4:129805520-129805570	HL-60	blood:	n/a
15	chr4:129805520-129805570	HRCEpiC	kidney:	n/a
16	chr4:129793434-129793484	HEEpiC	esophagus:	n/a
17	chr4:129793434-129793484	GM12878	blood:	n/a
18	chr4:129793434-129793484	Hepatocyte	liver:	n/a
19	chr4:129793434-129793484	GM06990	blood:	n/a
20	chr4:129805520-129805570	AG10803	skin:	n/a
21	chr4:129793434-129793484	SK-N-SH	brain:	n/a
22	chr4:129793434-129793484	T-47D	breast:	n/a
23	chr4:129805520-129805570	HCT-116	colon:	n/a
24	chr4:129793434-129793484	AG09319	gingival:	n/a
25	chr4:129805520-129805570	SK-N-SH_RA	brain:	n/a
26	chr4:129793434-129793484	HCT-116	colon:	n/a
27	chr4:129805520-129805570	GM12878	blood:	n/a
28	chr4:129793434-129793484	MCF10A-Er-Src	breast:	n/a
29	chr4:129793434-129793484	BE2_C	brain:	n/a
30	chr4:129805520-129805570	LNCaP	prostate:	n/a
31	chr4:129793434-129793484	PANC-1	pancreas:	n/a
32	chr4:129793434-129793484	Jurkat	blood:	n/a
33	chr4:129793434-129793484	NHDF-neo	bronchial:	n/a
34	chr4:129805520-129805570	GM12892	blood:	n/a
35	chr4:129805520-129805570	HCPEpiC	choroid plexus:	n/a
36	chr4:129805520-129805570	K562	blood:	n/a
37	chr4:129805520-129805570	ECC-1	luminal epithelium:	n/a
38	chr4:129793434-129793484	IMR90	lung:	fetal
39	chr4:129793434-129793484	HNPCEpiC	eye:	n/a
40	chr4:129805520-129805570	SKMC	muscle:	n/a
41	chr4:129793434-129793484	AG04449	skin:	fetal
42	chr4:129805520-129805570	NB4	blood:	n/a
43	chr4:129805520-129805570	Hepatocyte	liver:	n/a
44	chr4:129793434-129793484	ProgFib	skin:	n/a
45	chr4:129793434-129793484	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:129805520-129805570	PFSK-1	brain:	n/a
47	chr4:129793434-129793484	HIPEpiC	eye:	n/a
48	chr4:129793434-129793484	PrEC	prostate:	n/a
49	chr4:129793434-129793484	H1-hESC	embryonic stem cell:	embryo
50	chr4:129805520-129805570	U87	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:129483813..129486118-chr4:129786642..129788490,2	MCF-7	breast:
2	chr4:129770197..129772164-chr4:129783210..129785874,2	K562	blood:
3	chr4:129810865..129812723-chr4:129812841..129815400,2	K562	blood:
4	chr4:129834048..129836614-chr4:129837936..129840499,3	K562	blood:
5	chr4:129725702..129726480-chr4:129789353..129790148,2	MCF-7	breast:
6	chr4:129802100..129804907-chr4:129805391..129807043,2	K562	blood:
7	chr4:129729198..129732287-chr4:129784290..129787717,5	K562	blood:
8	chr4:129732016..129733966-chr4:129800387..129802773,2	K562	blood:
9	chr4:129810865..129812723-chr4:129812841..129815400,2	K562	blood:
10	chr4:129770901..129772590-chr4:129787099..129788677,2	K562	blood:
11	chr4:129796835..129799070-chr4:129823245..129825174,2	K562	blood:
12	chr4:129834245..129836614-chr4:129838172..129840499,2	K562	blood:
13	chr4:129731505..129733452-chr4:129799174..129801929,2	MCF-7	breast:
14	chr4:129802100..129804907-chr4:129805391..129807043,2	K562	blood:
15	chr4:129830344..129833253-chr4:129837741..129840090,2	K562	blood:
16	chr4:129834048..129836614-chr4:129837936..129840499,3	K562	blood:
17	chr4:129731039..129733137-chr4:129832126..129834778,3	K562	blood:
18	chr4:129731707..129733254-chr4:129789500..129791100,2	MCF-7	breast:
19	chr4:129787325..129790041-chr4:129799398..129801047,2	K562	blood:
20	chr4:129830344..129833253-chr4:129837741..129840090,2	K562	blood:
21	chr4:129784722..129788908-chr4:129789150..129792648,4	K562	blood:
22	chr4:129834245..129836614-chr4:129838172..129840499,2	K562	blood:
23	chr4:129784722..129788908-chr4:129789150..129792648,4	K562	blood:
24	chr4:129729294..129734540-chr4:129782960..129791658,9	K562	blood:
25	chr4:129796835..129799070-chr4:129823245..129825174,2	K562	blood:
26	chr4:129787325..129790041-chr4:129799398..129801047,2	K562	blood:
27	chr4:129798920..129801366-chr4:129805840..129808673,2	K562	blood:
28	chr4:129792576..129794412-chr4:129795148..129798091,2	MCF-7	breast:
29	chr4:129792576..129794412-chr4:129795148..129798091,2	MCF-7	breast:
30	chr4:129729755..129733795-chr4:129783264..129786218,5	MCF-7	breast:
31	chr4:129798920..129801366-chr4:129805840..129808673,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF17	hsa-miR-155-5p	chr4:129794674-129794681
2	PHF17	hsa-miR-124-3p	chr4:129796320-129796339
3	PHF17	hsa-miR-124-3p	chr4:129795562-129795568
4	PHF17	hsa-miR-21-5p	chr4:129794503-129794525
5	PHF17	hsa-miR-124-3p	chr4:129796332-129796338
6	PHF17	hsa-miR-124-3p	chr4:129795549-129795568
7	PHF17	hsa-miR-155-5p	chr4:129794659-129794681

Variant related genes	Relation type
SCLT1	TF binding region
SCLT1	CpG island
ENSG00000077684	chromatin interactions

Extended variants
information (count: 2457 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2457 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185327656	chr4:129785711-129785712	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541914606	chr4:129785742-129785743	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564394380	chr4:129785804-129785805	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577916224	chr4:129785814-129785815	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560152302	chr4:129785886-129785887	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs17013854	chr4:129785973-129785974	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs142997360	chr4:129785984-129785985	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564769444	chr4:129786064-129786065	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190084976	chr4:129786081-129786082	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146151975	chr4:129786095-129786096	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs570498628	chr4:129786184-129786185	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368220208	chr4:129786232-129786233	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181343121	chr4:129786253-129786254	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs529039398	chr4:129786272-129786273	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs149234261	chr4:129786314-129786315	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186865574	chr4:129786325-129786326	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144450322	chr4:129786353-129786354	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34436460	chr4:129786427-129786428	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs148421922	chr4:129786498-129786499	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569889948	chr4:129786535-129786536	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536855006	chr4:129786558-129786559	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs555186206	chr4:129786575-129786576	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs199554264	chr4:129786661-129786662	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs56657477	chr4:129786662-129786663	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573489911	chr4:129786735-129786736	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376617385	chr4:129786736-129786737	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs553824659	chr4:129786751-129786752	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs17013857	chr4:129786769-129786770	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs546140834	chr4:129786809-129786810	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs35757086	chr4:129786852-129786853	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564629433	chr4:129786867-129786868	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs142552659	chr4:129786870-129786871	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560301522	chr4:129787027-129787028	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs147598057	chr4:129787029-129787030	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs79867602	chr4:129787046-129787047	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191710832	chr4:129787100-129787101	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs572816494	chr4:129787122-129787123	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532797519	chr4:129787184-129787185	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184003387	chr4:129787196-129787197	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551309012	chr4:129787250-129787251	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569544212	chr4:129787296-129787297	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs537389922	chr4:129787319-129787320	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567587781	chr4:129787380-129787381	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs567149081	chr4:129787394-129787395	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187911574	chr4:129787400-129787401	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs140497765	chr4:129787456-129787457	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572457401	chr4:129787485-129787486	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539549099	chr4:129787494-129787495	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368321580	chr4:129787500-129787501	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114881192	chr4:129787527-129787528	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD

Chromatin state (count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129753600-129798600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:129753800-129795000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:129763000-129785800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
4	chr4:129763000-129787200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr4:129763600-129786600	Strong transcription	Fetal Intestine Large	intestine
6	chr4:129772600-129786000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
7	chr4:129773200-129794000	Strong transcription	K562	blood
8	chr4:129774000-129788600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr4:129776400-129796200	Strong transcription	Dnd41	blood
10	chr4:129779600-129809800	Weak transcription	Small Intestine	intestine
11	chr4:129779800-129793200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr4:129782200-129785800	Strong transcription	H1 Cell Line	embryonic stem cell
13	chr4:129782400-129786800	Strong transcription	Fetal Intestine Small	intestine
14	chr4:129782400-129787200	Weak transcription	Hela-S3	cervix
15	chr4:129782800-129786800	Strong transcription	Fetal Stomach	stomach
16	chr4:129783400-129789200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr4:129783400-129800600	Weak transcription	Fetal Kidney	kidney
18	chr4:129783600-129789600	Weak transcription	HMEC	breast
19	chr4:129784000-129788200	Weak transcription	Placenta	Placenta
20	chr4:129784000-129788600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:129784000-129789800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:129784200-129786000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr4:129784200-129786000	Weak transcription	HepG2	liver
24	chr4:129784200-129788400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:129784200-129788400	Weak transcription	Ovary	ovary
26	chr4:129784200-129790000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr4:129784200-129790800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:129784400-129786000	Weak transcription	Aorta	Aorta
29	chr4:129784400-129786200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
30	chr4:129784400-129786400	Strong transcription	Pancreas	Pancrea
31	chr4:129784400-129787400	Weak transcription	Right Atrium	heart
32	chr4:129784400-129788400	Weak transcription	Brain Germinal Matrix	brain
33	chr4:129784400-129792000	Weak transcription	Colonic Mucosa	Colon
34	chr4:129784400-129792600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr4:129784400-129799200	Weak transcription	Fetal Brain Male	brain
36	chr4:129784600-129785800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr4:129784600-129785800	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr4:129784600-129786000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:129784600-129786000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr4:129784600-129786000	Weak transcription	Gastric	stomach
41	chr4:129784600-129786000	Weak transcription	Left Ventricle	heart
42	chr4:129784600-129786200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:129784600-129786400	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr4:129784600-129787200	Strong transcription	A549	lung
45	chr4:129784600-129787600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr4:129784600-129788200	Weak transcription	Lung	lung
47	chr4:129784600-129789800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr4:129784600-129791000	Weak transcription	Esophagus	oesophagus
49	chr4:129784600-129791400	Weak transcription	Spleen	Spleen
50	chr4:129784600-129792600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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