Variant report

Variant	nsv998270
Chromosome Location	chr4:99063275-99120404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:731)
CpG islands
(count:549)
Chromatin interactive
region (count:21)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:99071668-99071877	K562	blood:	n/a	n/a
2	ARID3A	chr4:99071751-99071820	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:99064134-99064579	HepG2	liver:	n/a	n/a
4	ATF2	chr4:99064087-99064946	GM12878	blood:	n/a	n/a
5	BCLAF1	chr4:99064100-99064744	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:99064170-99064924	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:99064573-99064575	HepG2	liver:	n/a	n/a
8	BRCA1	chr4:99064062-99064976	Hela-S3	cervix:	n/a	chr4:99064951-99064958
9	CBX3	chr4:99114607-99114961	K562	blood:	n/a	n/a
10	CBX3	chr4:99114602-99115008	K562	blood:	n/a	n/a
11	CBX3	chr4:99114621-99114898	HCT-116	colon:	n/a	n/a
12	CEBPB	chr4:99070270-99070343	K562	blood:	n/a	chr4:99070321-99070332
13	CEBPB	chr4:99070074-99070490	ECC-1	luminal epithelium:	n/a	chr4:99070321-99070332
14	CEBPB	chr4:99070108-99070430	MCF-7	breast:	n/a	chr4:99070321-99070332
15	CEBPB	chr4:99063786-99064795	Hela-S3	cervix:	n/a	chr4:99064502-99064514
16	CEBPB	chr4:99070174-99070498	Hela-S3	cervix:	n/a	chr4:99070321-99070332
17	CEBPB	chr4:99063807-99064112	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:99074468-99074725	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:99070158-99070428	A549	lung:	n/a	chr4:99070321-99070332
20	CEBPB	chr4:99070209-99070452	HepG2	liver:	n/a	chr4:99070321-99070332
21	CEBPB	chr4:99063834-99064087	A549	lung:	n/a	n/a
22	CEBPB	chr4:99074467-99074741	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:99070093-99070455	ECC-1	luminal epithelium:	n/a	chr4:99070321-99070332
24	CHD2	chr4:99064447-99064821	HepG2	liver:	n/a	chr4:99064454-99064464
25	CHD2	chr4:99064186-99065138	Hela-S3	cervix:	n/a	chr4:99064454-99064464
26	CHD2	chr4:99087693-99087766	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr4:99064395-99065131	GM12878	blood:	n/a	chr4:99064454-99064464
28	CREB1	chr4:99103047-99103359	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr4:99064332-99064694	A549	lung:	n/a	n/a
30	CTCF	chr4:99094820-99094970	GM12873	blood:	n/a	n/a
31	CTCF	chr4:99072361-99072548	GM12878	blood:	n/a	chr4:99072468-99072489 chr4:99072489-99072502
32	CTCF	chr4:99064160-99064310	AG04449	skin:	n/a	n/a
33	CTCF	chr4:99064200-99064350	HRE	kidney:	n/a	n/a
34	CTCF	chr4:99071620-99071770	HCFaa	heart:	n/a	chr4:99071697-99071718 chr4:99071696-99071712 chr4:99071695-99071713 chr4:99071700-99071708
35	CTCF	chr4:99064200-99064350	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr4:99064360-99064510	A549	lung:	n/a	n/a
37	CTCF	chr4:99072436-99072470	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr4:99120400-99120550	RPTEC	kidney:	n/a	n/a
39	CTCF	chr4:99064240-99064390	GM12878	blood:	n/a	n/a
40	CTCF	chr4:99064180-99064330	Caco-2	colon:	n/a	n/a
41	CTCF	chr4:99072300-99072450	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr4:99064140-99064290	GM12870	blood:	n/a	n/a
43	CTCF	chr4:99064145-99064385	GM12878	blood:	n/a	n/a
44	CTCF	chr4:99064160-99064310	HVMF	connective:	n/a	n/a
45	CTCF	chr4:99064200-99064350	AG09319	gingival:	n/a	n/a
46	CTCF	chr4:99071650-99071768	Lung_OC	lung:	n/a	chr4:99071697-99071718 chr4:99071696-99071712 chr4:99071695-99071713 chr4:99071700-99071708
47	CTCF	chr4:99064140-99064290	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr4:99064140-99064290	HMEC	breast:	n/a	n/a
49	CTCF	chr4:99072384-99072543	MCF-7	breast:	n/a	chr4:99072468-99072489 chr4:99072489-99072502
50	CTCF	chr4:99064200-99064350	GM12873	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99064831-99064881	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:99064541-99064591	HRE	kidney:	n/a
3	chr4:99064459-99064509	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:99064322-99064372	NHBE	bronchial:	n/a
5	chr4:99064831-99064881	GM12892	blood:	n/a
6	chr4:99064459-99064509	MCF-7	breast:	n/a
7	chr4:99064541-99064591	K562	blood:	n/a
8	chr4:99064102-99064152	ProgFib	skin:	n/a
9	chr4:99064831-99064881	Hela-S3	cervix:	n/a
10	chr4:99064831-99064881	HEK293	kidney:	embryo
11	chr4:99064904-99064954	NHBE	bronchial:	n/a
12	chr4:99064459-99064509	AG04450	lung:	fetal
13	chr4:99064102-99064152	AG04450	lung:	fetal
14	chr4:99064603-99064653	GM12891	blood:	n/a
15	chr4:99064102-99064152	HCM	heart:	n/a
16	chr4:99064459-99064509	AG10803	skin:	n/a
17	chr4:99064322-99064372	HCT-116	colon:	n/a
18	chr4:99064573-99064623	GM19239	blood:	n/a
19	chr4:99064459-99064509	MCF10A-Er-Src	breast:	n/a
20	chr4:99064573-99064623	PrEC	prostate:	n/a
21	chr4:99064541-99064591	BE2_C	brain:	n/a
22	chr4:99064102-99064152	HL-60	blood:	n/a
23	chr4:99064831-99064881	MCF10A-Er-Src	breast:	n/a
24	chr4:99064459-99064509	HCF	heart:	n/a
25	chr4:99064459-99064509	BJ	skin:	n/a
26	chr4:99064573-99064623	HAEpiC	amniotic membrane:	n/a
27	chr4:99064541-99064591	PANC-1	pancreas:	n/a
28	chr4:99064459-99064509	IMR90	lung:	fetal
29	chr4:99064541-99064591	NH-A	brain:	n/a
30	chr4:99064459-99064509	NHDF-neo	bronchial:	n/a
31	chr4:99064102-99064152	HAEpiC	amniotic membrane:	n/a
32	chr4:99064831-99064881	CMK	blood:	n/a
33	chr4:99064541-99064591	HUVEC	blood vessel:	n/a
34	chr4:99064746-99064796	AG09309	skin:	n/a
35	chr4:99064459-99064509	Hela-S3	cervix:	n/a
36	chr4:99064541-99064591	SAEC	small airway:	n/a
37	chr4:99064603-99064653	T-47D	breast:	n/a
38	chr4:99064322-99064372	PFSK-1	brain:	n/a
39	chr4:99064904-99064954	A549	lung:	n/a
40	chr4:99064541-99064591	HepG2	liver:	n/a
41	chr4:99064603-99064653	SK-N-SH_RA	brain:	n/a
42	chr4:99064102-99064152	LNCaP	prostate:	n/a
43	chr4:99064603-99064653	Jurkat	blood:	n/a
44	chr4:99064322-99064372	AG04449	skin:	fetal
45	chr4:99064831-99064881	T-47D	breast:	n/a
46	chr4:99064102-99064152	HUVEC	blood vessel:	n/a
47	chr4:99064831-99064881	HNPCEpiC	eye:	n/a
48	chr4:99064746-99064796	SK-N-MC	brain:	n/a
49	chr4:99064573-99064623	GM12892	blood:	n/a
50	chr4:99064603-99064653	AG04449	skin:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:99076051..99077551-chr4:99180191..99182364,2	MCF-7	breast:
2	chr4:99062262..99068404-chr4:99178848..99183768,9	MCF-7	breast:
3	chr4:99064473..99066402-chr4:99398593..99401325,2	MCF-7	breast:
4	chr20:56285284..56287699-chr4:99065164..99066706,2	MCF-7	breast:
5	chr4:99071301..99072792-chr4:99120456..99121365,4	MCF-7	breast:
6	chr4:99077205..99079531-chr4:99181198..99183165,2	MCF-7	breast:
7	chr4:99105475..99108210-chr4:99112091..99113844,2	MCF-7	breast:
8	chr4:99071303..99072113-chr4:99388789..99389313,2	MCF-7	breast:
9	chr4:99083174..99085665-chr4:99180019..99182924,2	MCF-7	breast:
10	chr4:99069075..99071216-chr4:99181902..99184864,2	MCF-7	breast:
11	chr4:99072160..99072897-chr4:99308436..99309402,2	MCF-7	breast:
12	chr4:99092058..99095008-chr4:99098244..99101009,2	MCF-7	breast:
13	chr4:99086672..99088660-chr4:99180652..99182426,2	MCF-7	breast:
14	chr4:99120152..99122281-chr4:99124783..99127768,2	K562	blood:
15	chr4:99093723..99096153-chr4:99098147..99099856,2	K562	blood:
16	chr4:99037506..99039090-chr4:99060858..99063344,2	MCF-7	breast:
17	chr4:99105475..99108210-chr4:99112091..99113844,2	MCF-7	breast:
18	chr4:99066128..99069024-chr4:99180594..99183920,3	MCF-7	breast:
19	chr4:99118953..99122803-chr4:99123376..99126878,4	MCF-7	breast:
20	chr4:99063959..99066263-chr4:99181971..99183968,2	K562	blood:
21	chr4:99062833..99065837-chr4:99072029..99075529,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf37-1	chr4:99106282-99106355	XLOC_004020
2	lnc-RAP1GDS1-2	chr4:99067481-99067492	FPKM1_group_23748_transcript_1
3	lnc-RAP1GDS1-2	chr4:99064931-99065281	XLOC_003613
4	lnc-RAP1GDS1-2	chr4:99064930-99065281	FPKM1_group_23748_transcript_1
5	lnc-RAP1GDS1-2	chr4:99090441-99090451	XLOC_003613
6	lnc-RAP1GDS1-2	chr4:99064930-99065281	NONHSAT097482
7	lnc-C4orf37-1	chr4:99104226-99104923	XLOC_004020
8	lnc-RAP1GDS1-2	chr4:99090440-99090451	NONHSAT097482

No data

Variant related genes	Relation type
STPG2	TF binding region
ENSG00000200658	TF binding region
STPG2	CpG island
ENSG00000200658	CpG island
ENSG00000138698	chromatin interactions
ENSG00000214559	chromatin interactions
ENSG00000124225	chromatin interactions
ENSG00000200658	chromatin interactions
ENSG00000163116	chromatin interactions

Extended variants
information (count: 1552 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368196874	chr4:99063327-99063328	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs548577579	chr4:99063364-99063365	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs6828752	chr4:99063382-99063383	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs55898505	chr4:99063415-99063416	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374137850	chr4:99063439-99063440	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs187202767	chr4:99063441-99063442	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528938958	chr4:99063466-99063467	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs570909898	chr4:99063485-99063486	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538336665	chr4:99063492-99063493	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs556732393	chr4:99063527-99063528	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs192147248	chr4:99063558-99063559	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs536471666	chr4:99063571-99063572	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs184645825	chr4:99063582-99063583	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs573103798	chr4:99063583-99063584	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs190578002	chr4:99063625-99063626	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs138818993	chr4:99063672-99063673	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs576471522	chr4:99063676-99063677	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201192360	chr4:99063695-99063696	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543888469	chr4:99063718-99063719	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs201240028	chr4:99063719-99063720	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs200672068	chr4:99063878-99063879	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201413109	chr4:99063880-99063881	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs199803026	chr4:99063881-99063882	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs543865556	chr4:99063884-99063885	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562271699	chr4:99063908-99063909	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530202882	chr4:99063958-99063959	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548779037	chr4:99064028-99064029	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs560582796	chr4:99064031-99064032	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs527989798	chr4:99064130-99064131	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs552639238	chr4:99064140-99064141	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs199783032	chr4:99064143-99064144	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs538275116	chr4:99064161-99064162	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs550275178	chr4:99064174-99064175	Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs138596856	chr4:99064212-99064213	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201481567	chr4:99064218-99064219	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149258882	chr4:99064248-99064249	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs371275654	chr4:99064249-99064250	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs144452195	chr4:99064252-99064253	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs371618978	chr4:99064264-99064265	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs115261157	chr4:99064283-99064284	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs199501880	chr4:99064292-99064293	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562047974	chr4:99064298-99064299	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573002393	chr4:99064305-99064306	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs534085347	chr4:99064306-99064307	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142782230	chr4:99064310-99064311	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573387136	chr4:99064329-99064330	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370035773	chr4:99064337-99064338	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs4699605	chr4:99064379-99064380	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs113032368	chr4:99064395-99064396	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs555734986	chr4:99064434-99064435	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	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
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:534 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99056400-99063800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr4:99062400-99063600	Weak transcription	Fetal Intestine Small	intestine
3	chr4:99063000-99063400	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr4:99063000-99063600	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:99063000-99063600	Enhancers	NHEK	skin
6	chr4:99063200-99063400	Enhancers	HMEC	breast
7	chr4:99063200-99063600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr4:99063200-99063600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:99063200-99063600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:99063200-99063800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr4:99063200-99063800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr4:99063400-99063600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:99063400-99063600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:99063400-99063600	Enhancers	Liver	Liver
15	chr4:99063400-99063600	Flanking Active TSS	HMEC	breast
16	chr4:99063400-99063800	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr4:99063400-99063800	Enhancers	Brain Angular Gyrus	brain
18	chr4:99063400-99064800	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr4:99063400-99065200	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr4:99063400-99065600	Active TSS	Rectal Mucosa Donor 29	rectum
21	chr4:99063600-99063800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:99063600-99063800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:99063600-99063800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:99063600-99063800	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr4:99063600-99063800	Enhancers	Primary B cells from cord blood	blood
26	chr4:99063600-99063800	Enhancers	Primary T cells from cord blood	blood
27	chr4:99063600-99063800	Enhancers	Primary hematopoietic stem cells	blood
28	chr4:99063600-99063800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr4:99063600-99063800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr4:99063600-99063800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:99063600-99063800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:99063600-99063800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:99063600-99063800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:99063600-99063800	Enhancers	Adipose Nuclei	Adipose
35	chr4:99063600-99063800	Enhancers	Brain Anterior Caudate	brain
36	chr4:99063600-99063800	Active TSS	Brain Cingulate Gyrus	brain
37	chr4:99063600-99063800	Enhancers	Colon Smooth Muscle	Colon
38	chr4:99063600-99063800	Enhancers	Duodenum Mucosa	Duodenum
39	chr4:99063600-99063800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr4:99063600-99063800	Enhancers	Fetal Intestine Small	intestine
41	chr4:99063600-99063800	Enhancers	Fetal Thymus	thymus
42	chr4:99063600-99063800	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr4:99063600-99063800	Enhancers	Stomach Mucosa	stomach
44	chr4:99063600-99063800	Enhancers	Hela-S3	cervix
45	chr4:99063600-99063800	Enhancers	HUVEC	blood vessel
46	chr4:99063600-99063800	Enhancers	NH-A	brain
47	chr4:99063600-99064000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr4:99063600-99064000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr4:99063600-99064000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:99063600-99064000	Enhancers	Primary B cells from peripheral blood	blood

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