Variant report

Variant	nsv830463
Chromosome Location	chr5:119806643-119968825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:902)
CpG islands
(count:366)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:902 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:119808789-119808848	K562	blood:	n/a	n/a
2	ARID3A	chr5:119814969-119815009	K562	blood:	n/a	n/a
3	ARID3A	chr5:119845695-119846337	K562	blood:	n/a	n/a
4	ARID3A	chr5:119848349-119848986	K562	blood:	n/a	n/a
5	ARID3A	chr5:119853390-119853829	K562	blood:	n/a	n/a
6	ATF1	chr5:119848381-119848909	K562	blood:	n/a	n/a
7	ATF1	chr5:119899838-119899993	K562	blood:	n/a	n/a
8	ATF1	chr5:119853689-119853917	K562	blood:	n/a	n/a
9	ATF2	chr5:119847523-119848070	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr5:119848349-119848681	K562	blood:	n/a	n/a
11	BACH1	chr5:119959300-119959328	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr5:119845855-119845896	K562	blood:	n/a	n/a
13	BRCA1	chr5:119940521-119941137	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr5:119848317-119849007	K562	blood:	n/a	n/a
15	CCNT2	chr5:119868130-119868256	K562	blood:	n/a	n/a
16	CCNT2	chr5:119848506-119848843	K562	blood:	n/a	n/a
17	CCNT2	chr5:119891204-119891275	K562	blood:	n/a	n/a
18	CCNT2	chr5:119852471-119852671	K562	blood:	n/a	n/a
19	CCNT2	chr5:119845998-119846328	K562	blood:	n/a	chr5:119846139-119846159
20	CCNT2	chr5:119927724-119927859	K562	blood:	n/a	n/a
21	CEBPB	chr5:119842896-119844175	K562	blood:	n/a	chr5:119843056-119843069
22	CEBPB	chr5:119845852-119846353	K562	blood:	n/a	chr5:119846148-119846157
23	CEBPB	chr5:119864268-119864570	K562	blood:	n/a	chr5:119864549-119864562 chr5:119864549-119864562
24	CEBPB	chr5:119839825-119840125	H1-hESC	embryonic stem cell:	n/a	chr5:119839966-119839977
25	CEBPB	chr5:119940627-119940974	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:119950210-119950705	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:119936395-119936681	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:119945256-119945647	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:119843844-119844119	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:119951673-119952096	IMR90	lung:	n/a	chr5:119951865-119951878
31	CEBPB	chr5:119908492-119908611	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:119843853-119844133	K562	blood:	n/a	n/a
33	CEBPB	chr5:119937714-119938123	Hela-S3	cervix:	n/a	chr5:119937940-119937951
34	CEBPB	chr5:119937786-119938093	HepG2	liver:	n/a	chr5:119937940-119937951
35	CEBPB	chr5:119839786-119840142	IMR90	lung:	n/a	chr5:119839966-119839977
36	CEBPB	chr5:119854679-119855222	K562	blood:	n/a	n/a
37	CEBPB	chr5:119857154-119857355	IMR90	lung:	n/a	chr5:119857273-119857284
38	CEBPB	chr5:119854971-119855149	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:119937773-119938120	IMR90	lung:	n/a	chr5:119937940-119937951
40	CEBPB	chr5:119842879-119843193	K562	blood:	n/a	chr5:119843056-119843069
41	CEBPB	chr5:119959582-119960151	IMR90	lung:	n/a	chr5:119959754-119959765 chr5:119959754-119959767 chr5:119959754-119959767
42	CEBPB	chr5:119855022-119855176	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:119959643-119959893	Hela-S3	cervix:	n/a	chr5:119959754-119959765 chr5:119959754-119959767 chr5:119959754-119959767
44	CEBPB	chr5:119937761-119938116	K562	blood:	n/a	chr5:119937940-119937951
45	CEBPB	chr5:119839864-119840116	HepG2	liver:	n/a	chr5:119839966-119839977
46	CEBPB	chr5:119857162-119857394	HepG2	liver:	n/a	chr5:119857273-119857284
47	CEBPB	chr5:119936349-119936589	HepG2	liver:	n/a	n/a
48	CEBPB	chr5:119873912-119874713	IMR90	lung:	n/a	n/a
49	CEBPB	chr5:119935306-119935685	IMR90	lung:	n/a	n/a
50	CEBPB	chr5:119864238-119864636	IMR90	lung:	n/a	chr5:119864549-119864562 chr5:119864549-119864562

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:119852385-119852435	HMEC	breast:	n/a
2	chr5:119846291-119846341	HEK293	kidney:	embryo
3	chr5:119951527-119951577	HAEpiC	amniotic membrane:	n/a
4	chr5:119952679-119952729	GM19239	blood:	n/a
5	chr5:119864497-119864547	K562	blood:	n/a
6	chr5:119952679-119952729	MCF-7	breast:	n/a
7	chr5:119951527-119951577	SKMC	muscle:	n/a
8	chr5:119864497-119864547	HEEpiC	esophagus:	n/a
9	chr5:119942454-119942504	AG10803	skin:	n/a
10	chr5:119951527-119951577	PrEC	prostate:	n/a
11	chr5:119852385-119852435	LNCaP	prostate:	n/a
12	chr5:119864497-119864547	A549	lung:	n/a
13	chr5:119864497-119864547	MCF-7	breast:	n/a
14	chr5:119952679-119952729	PrEC	prostate:	n/a
15	chr5:119846291-119846341	ovcar-3	ovarian:	n/a
16	chr5:119951527-119951577	NHBE	bronchial:	n/a
17	chr5:119852385-119852435	HEEpiC	esophagus:	n/a
18	chr5:119852385-119852435	AG09309	skin:	n/a
19	chr5:119852385-119852435	AG10803	skin:	n/a
20	chr5:119942454-119942504	HUVEC	blood vessel:	n/a
21	chr5:119951527-119951577	T-47D	breast:	n/a
22	chr5:119942454-119942504	LNCaP	prostate:	n/a
23	chr5:119952679-119952729	K562	blood:	n/a
24	chr5:119846291-119846341	GM12891	blood:	n/a
25	chr5:119852385-119852435	U87	brain:	n/a
26	chr5:119951527-119951577	LNCaP	prostate:	n/a
27	chr5:119951527-119951577	ovcar-3	ovarian:	n/a
28	chr5:119951527-119951577	U87	brain:	n/a
29	chr5:119952679-119952729	AG04449	skin:	fetal
30	chr5:119846291-119846341	PANC-1	pancreas:	n/a
31	chr5:119846291-119846341	HCPEpiC	choroid plexus:	n/a
32	chr5:119864497-119864547	HCF	heart:	n/a
33	chr5:119952679-119952729	SK-N-SH	brain:	n/a
34	chr5:119942454-119942504	AG04450	lung:	fetal
35	chr5:119952679-119952729	GM12878	blood:	n/a
36	chr5:119846291-119846341	HRE	kidney:	n/a
37	chr5:119864497-119864547	HCM	heart:	n/a
38	chr5:119951527-119951577	A549	lung:	n/a
39	chr5:119951527-119951577	GM12891	blood:	n/a
40	chr5:119952679-119952729	HCF	heart:	n/a
41	chr5:119846291-119846341	SK-N-SH_RA	brain:	n/a
42	chr5:119864497-119864547	HL-60	blood:	n/a
43	chr5:119864497-119864547	PANC-1	pancreas:	n/a
44	chr5:119942454-119942504	HRE	kidney:	n/a
45	chr5:119864497-119864547	IMR90	lung:	fetal
46	chr5:119846291-119846341	Hepatocyte	liver:	n/a
47	chr5:119952679-119952729	GM12891	blood:	n/a
48	chr5:119852385-119852435	HRPEpiC	eye:	n/a
49	chr5:119846291-119846341	RPTEC	kidney:	n/a
50	chr5:119852385-119852435	H1-hESC	embryonic stem cell:	embryo

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:119847102..119848643-chr5:119877942..119880653,2	K562	blood:
2	chr5:119806492..119808449-chr5:119834650..119836281,2	K562	blood:
3	chr5:119848883..119851465-chr5:119858913..119862355,3	K562	blood:
4	chr5:119886756..119889709-chr5:119891670..119893322,2	K562	blood:
5	chr5:119859163..119862505-chr5:119863189..119865594,3	K562	blood:
6	chr5:119877678..119879721-chr5:119882058..119884163,2	K562	blood:
7	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
8	chr5:119798174..119800652-chr5:119851053..119853705,2	K562	blood:
9	chr5:119858416..119860878-chr5:119871767..119873808,2	K562	blood:
10	chr5:119808055..119810558-chr5:119818687..119821313,2	K562	blood:
11	chr5:119803768..119806455-chr5:119850808..119853040,2	K562	blood:
12	chr5:119851956..119853481-chr5:119862285..119864209,2	K562	blood:
13	chr5:119847102..119848643-chr5:119877942..119880653,2	K562	blood:
14	chr5:119808055..119810558-chr5:119818687..119821313,2	K562	blood:
15	chr5:119891736..119894093-chr5:119898854..119902222,3	K562	blood:
16	chr5:119851956..119853481-chr5:119862285..119864209,2	K562	blood:
17	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
18	chr5:119835822..119838149-chr5:119840873..119842800,2	K562	blood:
19	chr5:119814891..119816438-chr5:119818822..119820625,2	K562	blood:
20	chr5:119834205..119836736-chr5:119837818..119840539,3	K562	blood:
21	chr5:119899537..119902283-chr5:119906756..119908959,2	K562	blood:
22	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
23	chr5:119851956..119854339-chr5:119862015..119863785,2	K562	blood:
24	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
25	chr5:119849515..119851535-chr5:119903167..119905944,2	K562	blood:
26	chr5:119835822..119838149-chr5:119840873..119842800,2	K562	blood:
27	chr5:119802488..119804867-chr5:119844244..119845883,2	K562	blood:
28	chr5:119852641..119855403-chr5:119858663..119861465,3	K562	blood:
29	chr5:119852123..119854010-chr5:120038446..120041236,2	K562	blood:
30	chr5:119848832..119850459-chr5:119850972..119852496,2	K562	blood:
31	chr5:119851956..119854339-chr5:119862015..119863785,2	K562	blood:
32	chr5:119852641..119855403-chr5:119858663..119861465,3	K562	blood:
33	chr5:119848932..119850925-chr5:119866521..119868339,2	K562	blood:
34	chr5:119803768..119806715-chr5:119850808..119853246,2	K562	blood:
35	chr5:119889111..119891337-chr5:119901156..119903856,2	K562	blood:
36	chr5:119803768..119806715-chr5:119850808..119853246,2	K562	blood:
37	chr5:119899537..119902283-chr5:119906756..119908959,2	K562	blood:
38	chr5:119933357..119934903-chr5:119957823..119959697,2	K562	blood:
39	chr5:119859163..119862505-chr5:119863189..119865594,3	K562	blood:
40	chr5:119858416..119860878-chr5:119871767..119873808,2	K562	blood:
41	chr5:119906837..119908623-chr5:119910419..119912812,2	K562	blood:
42	chr5:119834205..119836736-chr5:119837818..119840539,3	K562	blood:
43	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
44	chr5:119866722..119869345-chr5:119872405..119873933,2	K562	blood:
45	chr5:119901221..119903356-chr5:119911285..119913616,2	K562	blood:
46	chr5:119877678..119879721-chr5:119882058..119884163,2	K562	blood:
47	chr5:119870688..119872446-chr5:119874411..119876714,2	K562	blood:
48	chr5:119797915..119802369-chr5:119845575..119850142,8	K562	blood:
49	chr5:119875090..119877798-chr5:119880363..119881947,2	K562	blood:
50	chr5:119848883..119851465-chr5:119858913..119862355,3	K562	blood:

No data

Variant related genes	Relation type
PRR16	TF binding region
PRR16	CpG island
ENSG00000184838	chromatin interactions

Extended variants
information (count: 6866 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6866 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191611865	chr5:119806719-119806720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs537590258	chr5:119806726-119806727	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562495553	chr5:119806780-119806781	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs145746970	chr5:119806803-119806804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544870574	chr5:119806833-119806834	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564744338	chr5:119806836-119806837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555821880	chr5:119806855-119806856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7715549	chr5:119806872-119806873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs547173164	chr5:119806873-119806874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140317196	chr5:119806889-119806890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566972653	chr5:119806900-119806901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138415499	chr5:119806911-119806912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538218124	chr5:119806923-119806924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560658359	chr5:119806927-119806928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs569220260	chr5:119806975-119806976	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs537777630	chr5:119807061-119807062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557651282	chr5:119807148-119807149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373515729	chr5:119807203-119807204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34667485	chr5:119807220-119807221	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573412689	chr5:119807269-119807270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540921010	chr5:119807298-119807299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs559585173	chr5:119807325-119807326	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533743328	chr5:119807327-119807328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543855323	chr5:119807360-119807361	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183614521	chr5:119807365-119807366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs11954044	chr5:119807396-119807397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs116332606	chr5:119807456-119807457	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536330640	chr5:119807473-119807474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144474394	chr5:119807483-119807484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148008538	chr5:119807552-119807553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544746745	chr5:119807557-119807558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544647526	chr5:119807574-119807575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564781110	chr5:119807618-119807619	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562943154	chr5:119807676-119807677	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532731719	chr5:119807688-119807689	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189507877	chr5:119807698-119807699	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560655978	chr5:119807748-119807749	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142107868	chr5:119807777-119807778	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs533381354	chr5:119807778-119807779	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549434019	chr5:119807806-119807807	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146374614	chr5:119807823-119807824	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531745521	chr5:119807845-119807846	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs551316026	chr5:119807890-119807891	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs139746710	chr5:119808042-119808043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs181820589	chr5:119808076-119808077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144557239	chr5:119808099-119808100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547224572	chr5:119808127-119808128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146056563	chr5:119808128-119808129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536034394	chr5:119808129-119808130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201460999	chr5:119808131-119808132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119801800-119809200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:119802400-119809600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr5:119802600-119808000	Weak transcription	HSMMtube	muscle
4	chr5:119802600-119808000	Weak transcription	NH-A	brain
5	chr5:119802800-119807400	Weak transcription	NHLF	lung
6	chr5:119802800-119809600	Weak transcription	Aorta	Aorta
7	chr5:119803000-119811800	Weak transcription	Fetal Heart	heart
8	chr5:119803800-119807600	Weak transcription	HSMM	muscle
9	chr5:119803800-119809200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:119804200-119806800	Weak transcription	Osteobl	bone
11	chr5:119804400-119807400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:119804400-119812000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:119804800-119807000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:119804800-119808000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:119806400-119806800	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr5:119806600-119809400	Enhancers	Muscle Satellite Cultured Cells	--
17	chr5:119806800-119808400	Enhancers	Osteobl	bone
18	chr5:119807000-119809000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr5:119807400-119808000	Enhancers	NHLF	lung
20	chr5:119807400-119810000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:119807600-119808000	Genic enhancers	HSMM	muscle
22	chr5:119808000-119808600	Enhancers	HSMM	muscle
23	chr5:119808000-119808600	Enhancers	NH-A	brain
24	chr5:119808000-119809200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:119808200-119808600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:119808400-119810400	Weak transcription	Osteobl	bone
27	chr5:119808600-119835800	Weak transcription	HSMM	muscle
28	chr5:119809000-119809800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr5:119809000-119814200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr5:119809200-119809800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:119809200-119810000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:119809400-119814200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr5:119809600-119810000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr5:119809600-119810200	Enhancers	Aorta	Aorta
35	chr5:119809800-119810600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr5:119809800-119816800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr5:119810000-119811800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr5:119810000-119814200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:119810000-119814400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr5:119810400-119812000	Enhancers	Osteobl	bone
41	chr5:119810600-119811000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:119811000-119813200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:119811200-119811400	Enhancers	Ovary	ovary
44	chr5:119811400-119813400	Weak transcription	Ovary	ovary
45	chr5:119811800-119812000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:119811800-119812200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr5:119811800-119812200	Enhancers	Fetal Heart	heart
48	chr5:119811800-119812400	Enhancers	K562	blood
49	chr5:119812000-119812200	Enhancers	Fetal Lung	lung
50	chr5:119812000-119812400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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