Variant report

Variant	nsv534168
Chromosome Location	chr1:76718950-77039352
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1077)
CpG islands
(count:732)
Chromatin interactive
region (count:34)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:76796829-76797028	K562	blood:	n/a	n/a
2	ATF3	chr1:76719813-76720341	HCT-116	colon:	n/a	n/a
3	BATF	chr1:76760142-76760428	GM12878	blood:	n/a	n/a
4	BATF	chr1:76960412-76960867	GM12878	blood:	n/a	n/a
5	BATF	chr1:76760090-76760529	GM12878	blood:	n/a	n/a
6	BATF	chr1:76736152-76736451	GM12878	blood:	n/a	n/a
7	BATF	chr1:76960469-76960865	GM12878	blood:	n/a	n/a
8	BATF	chr1:76736134-76736451	GM12878	blood:	n/a	n/a
9	BATF	chr1:76928925-76929273	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:76745095-76745436	HepG2	liver:	n/a	chr1:76745276-76745289 chr1:76745329-76745345 chr1:76745337-76745353 chr1:76745272-76745293 chr1:76745279-76745288
11	BHLHE40	chr1:76745098-76745399	K562	blood:	n/a	chr1:76745276-76745289 chr1:76745329-76745345 chr1:76745337-76745353 chr1:76745272-76745293 chr1:76745279-76745288
12	BHLHE40	chr1:76960390-76960674	GM12878	blood:	n/a	n/a
13	CBX3	chr1:76734775-76735330	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:76796545-76797128	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:76719758-76720796	HCT-116	colon:	n/a	chr1:76720185-76720196
16	CCNT2	chr1:76877130-76877206	K562	blood:	n/a	n/a
17	CEBPB	chr1:76724206-76724260	H1-hESC	embryonic stem cell:	n/a	chr1:76724228-76724241
18	CEBPB	chr1:76939345-76939527	A549	lung:	n/a	chr1:76939449-76939460
19	CEBPB	chr1:76773793-76774091	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr1:76972957-76973289	HepG2	liver:	n/a	chr1:76973039-76973050
21	CEBPB	chr1:76939324-76939541	IMR90	lung:	n/a	chr1:76939449-76939460
22	CEBPB	chr1:76891368-76891765	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:76931757-76931991	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:76972894-76973221	IMR90	lung:	n/a	chr1:76973039-76973050
25	CEBPB	chr1:76939402-76939598	HepG2	liver:	n/a	chr1:76939449-76939460
26	CEBPB	chr1:76728494-76728618	A549	lung:	n/a	chr1:76728550-76728561
27	CEBPB	chr1:76831038-76831227	A549	lung:	n/a	chr1:76831106-76831117
28	CEBPB	chr1:76946577-76946857	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:76773792-76774105	A549	lung:	n/a	n/a
30	CEBPB	chr1:76943523-76943705	HepG2	liver:	n/a	chr1:76943621-76943632
31	CEBPB	chr1:76773795-76774118	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:76939310-76939479	H1-hESC	embryonic stem cell:	n/a	chr1:76939449-76939460
33	CEBPB	chr1:76802693-76803049	IMR90	lung:	n/a	n/a
34	CEBPB	chr1:76785035-76785336	A549	lung:	n/a	chr1:76785133-76785144
35	CEBPB	chr1:76802772-76802992	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr1:76759472-76759571	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:76742636-76742920	HepG2	liver:	n/a	chr1:76742757-76742768
38	CEBPB	chr1:76784975-76785274	IMR90	lung:	n/a	chr1:76785133-76785144
39	CEBPB	chr1:76940656-76941010	IMR90	lung:	n/a	chr1:76940832-76940843 chr1:76940833-76940842 chr1:76940831-76940844 chr1:76940831-76940844 chr1:76940831-76940842
40	CEBPB	chr1:77028817-77029169	HepG2	liver:	n/a	chr1:77028992-77029003
41	CEBPB	chr1:76784987-76785293	HepG2	liver:	n/a	chr1:76785133-76785144
42	CEBPB	chr1:76940645-76940970	A549	lung:	n/a	chr1:76940832-76940843 chr1:76940833-76940842 chr1:76940831-76940844 chr1:76940831-76940844 chr1:76940831-76940842
43	CEBPB	chr1:76759368-76759663	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:76796637-76797003	A549	lung:	n/a	n/a
45	CEBPB	chr1:76831025-76831218	HepG2	liver:	n/a	chr1:76831106-76831117
46	CEBPB	chr1:76802670-76803012	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr1:76728414-76728705	HepG2	liver:	n/a	chr1:76728550-76728561
48	CEBPB	chr1:76940708-76940907	H1-hESC	embryonic stem cell:	n/a	chr1:76940832-76940843 chr1:76940833-76940842 chr1:76940831-76940844 chr1:76940831-76940844 chr1:76940831-76940842
49	CEBPB	chr1:76899228-76899474	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:76796692-76797006	MCF-7	breast:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76734569-76734619	NHDF-neo	bronchial:	n/a
2	chr1:77013304-77013354	Hepatocyte	liver:	n/a
3	chr1:76968506-76968556	HCT-116	colon:	n/a
4	chr1:76840032-76840082	SK-N-SH	brain:	n/a
5	chr1:76891398-76891448	AG04450	lung:	fetal
6	chr1:76761200-76761250	HEK293	kidney:	embryo
7	chr1:76840032-76840082	AoSMC	blood vessel:	n/a
8	chr1:76968506-76968556	RPTEC	kidney:	n/a
9	chr1:76899846-76899896	ECC-1	luminal epithelium:	n/a
10	chr1:76968506-76968556	NB4	blood:	n/a
11	chr1:76891398-76891448	HIPEpiC	eye:	n/a
12	chr1:76723043-76723093	MCF10A-Er-Src	breast:	n/a
13	chr1:76840032-76840082	AG04450	lung:	fetal
14	chr1:76968506-76968556	BJ	skin:	n/a
15	chr1:76817670-76817720	HCM	heart:	n/a
16	chr1:76891398-76891448	CMK	blood:	n/a
17	chr1:76891398-76891448	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:76723043-76723093	HEK293	kidney:	embryo
19	chr1:76899846-76899896	HIPEpiC	eye:	n/a
20	chr1:76891398-76891448	IMR90	lung:	fetal
21	chr1:76734569-76734619	BE2_C	brain:	n/a
22	chr1:76782984-76783034	MCF10A-Er-Src	breast:	n/a
23	chr1:76761200-76761250	AG10803	skin:	n/a
24	chr1:76840032-76840082	GM12891	blood:	n/a
25	chr1:76976572-76976622	HCPEpiC	choroid plexus:	n/a
26	chr1:76840032-76840082	HMEC	breast:	n/a
27	chr1:76723043-76723093	AG04450	lung:	fetal
28	chr1:76976572-76976622	AG09309	skin:	n/a
29	chr1:76968506-76968556	HEEpiC	esophagus:	n/a
30	chr1:76782984-76783034	GM06990	blood:	n/a
31	chr1:77013304-77013354	HNPCEpiC	eye:	n/a
32	chr1:76840032-76840082	K562	blood:	n/a
33	chr1:76782984-76783034	PANC-1	pancreas:	n/a
34	chr1:76891398-76891448	HCPEpiC	choroid plexus:	n/a
35	chr1:76899846-76899896	HUVEC	blood vessel:	n/a
36	chr1:76723043-76723093	GM12892	blood:	n/a
37	chr1:76817670-76817720	U87	brain:	n/a
38	chr1:76761200-76761250	HAEpiC	amniotic membrane:	n/a
39	chr1:76723043-76723093	GM12891	blood:	n/a
40	chr1:76734569-76734619	HRCEpiC	kidney:	n/a
41	chr1:76899846-76899896	AoSMC	blood vessel:	n/a
42	chr1:76976572-76976622	HRCEpiC	kidney:	n/a
43	chr1:76968506-76968556	SK-N-MC	brain:	n/a
44	chr1:76840032-76840082	AG09309	skin:	n/a
45	chr1:77013304-77013354	Hela-S3	cervix:	n/a
46	chr1:76891398-76891448	HAEpiC	amniotic membrane:	n/a
47	chr1:76734569-76734619	AG09309	skin:	n/a
48	chr1:76723043-76723093	SK-N-SH_RA	brain:	n/a
49	chr1:76817670-76817720	AG04450	lung:	fetal
50	chr1:76782984-76783034	HCM	heart:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
2	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
3	chr1:76758604..76761482-chr1:76764775..76767017,2	K562	blood:
4	chr1:76741759..76743474-chr1:76745342..76747848,2	K562	blood:
5	chr1:76796389..76797022-chr1:77608917..77609894,2	MCF-7	breast:
6	chr1:76796406..76797312-chr1:77366615..77367452,3	MCF-7	breast:
7	chr1:76373718..76374271-chr1:76796370..76797302,2	MCF-7	breast:
8	chr1:76741759..76743474-chr1:76745342..76747848,2	K562	blood:
9	chr1:76620098..76620620-chr1:76796654..76797328,2	MCF-7	breast:
10	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
11	chr1:76796528..76797295-chr1:77206308..77207068,2	MCF-7	breast:
12	chr1:76741346..76744130-chr1:76749152..76752097,2	K562	blood:
13	chr1:76885764..76887919-chr1:76891776..76893368,2	K562	blood:
14	chr1:76880275..76881877-chr1:76884344..76886565,2	K562	blood:
15	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
16	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:
17	chr1:76739718..76741247-chr1:76741551..76743104,2	K562	blood:
18	chr1:76880275..76881877-chr1:76884344..76886565,2	K562	blood:
19	chr1:76884483..76887341-chr1:76890524..76892236,2	MCF-7	breast:
20	chr1:76756888..76759692-chr1:76896597..76899350,2	K562	blood:
21	chr1:76871350..76874295-chr1:76994896..76997570,2	K562	blood:
22	chr1:76884483..76887341-chr1:76890524..76892236,2	MCF-7	breast:
23	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:
24	chr1:76813366..76816327-chr1:76818310..76820003,2	K562	blood:
25	chr1:76885764..76887919-chr1:76891776..76893368,2	K562	blood:
26	chr1:76758604..76761482-chr1:76764775..76767017,2	K562	blood:
27	chr1:76796476..76797352-chr1:77609351..77609861,2	K562	blood:
28	chr1:76796470..76797076-chr1:77591559..77592349,2	MCF-7	breast:
29	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
30	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
31	chr1:76741346..76744130-chr1:76749152..76752097,2	K562	blood:
32	chr1:76871350..76874295-chr1:76994896..76997570,2	K562	blood:
33	chr1:76756888..76759692-chr1:76896597..76899350,2	K562	blood:
34	chr1:76739718..76741247-chr1:76741551..76743104,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGK-4	chr1:77017263-77017540	NONHSAT004013
2	lnc-PIGK-4	chr1:76996553-76996677	NONHSAT004013
3	lnc-PIGK-4	chr1:76996397-76996441	NONHSAT004013
4	lnc-ASB17-2	chr1:76819268-76819931	NONHSAT004012

No data

Variant related genes	Relation type
ST6GALNAC3	TF binding region
ENSG00000223905	TF binding region
ST6GALNAC3	CpG island
ENSG00000223905	CpG island
ENSG00000223905	chromatin interactions

Extended variants
information (count: 10563 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:10563 , 50 per page) page: 1 2 3 4 5 6 7 ... 212

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369854695	chr1:76718975-76718976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566479954	chr1:76719023-76719024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79841811	chr1:76719077-76719078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551926015	chr1:76719082-76719083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113446466	chr1:76719091-76719092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538491240	chr1:76719131-76719132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555228342	chr1:76719183-76719184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568634016	chr1:76719272-76719273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192039028	chr1:76719329-76719330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140145307	chr1:76719330-76719331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572495401	chr1:76719333-76719334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557594965	chr1:76719339-76719340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539815018	chr1:76719353-76719354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557692157	chr1:76719381-76719382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576032194	chr1:76719412-76719413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373526542	chr1:76719473-76719474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534417870	chr1:76719474-76719475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544073875	chr1:76719481-76719482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562460060	chr1:76719493-76719494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183128167	chr1:76719512-76719513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376963714	chr1:76719570-76719571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536811	chr1:76719571-76719572	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs560182349	chr1:76719602-76719603	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs527355831	chr1:76719643-76719644	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552252078	chr1:76719777-76719778	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs545036055	chr1:76719778-76719779	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs564039788	chr1:76719789-76719790	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs531346078	chr1:76719793-76719794	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs522935	chr1:76719794-76719795	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs143812896	chr1:76719804-76719805	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs571844731	chr1:76719835-76719836	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs78080538	chr1:76719870-76719871	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs547716990	chr1:76719872-76719873	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs76128036	chr1:76719873-76719874	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs540704735	chr1:76719883-76719884	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557851696	chr1:76719887-76719888	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs560762738	chr1:76719902-76719903	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs187419680	chr1:76719922-76719923	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs575994159	chr1:76720001-76720002	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs537083203	chr1:76720003-76720004	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs191902643	chr1:76720036-76720037	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs150866878	chr1:76720042-76720043	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs184167047	chr1:76720069-76720070	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs370642697	chr1:76720119-76720120	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs574860493	chr1:76720132-76720133	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs545878525	chr1:76720178-76720179	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs564202550	chr1:76720227-76720228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs374345704	chr1:76720244-76720245	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs187905700	chr1:76720249-76720250	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs114091087	chr1:76720253-76720254	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1745 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76713400-76720200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr1:76713600-76719400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:76714000-76719400	Weak transcription	Fetal Thymus	thymus
4	chr1:76714000-76719800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:76714200-76719600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr1:76716400-76719400	Weak transcription	NHDF-Ad	bronchial
7	chr1:76716400-76719600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr1:76716400-76722000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:76716400-76723200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:76716600-76719800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr1:76716600-76723600	Weak transcription	Fetal Muscle Leg	muscle
12	chr1:76716800-76719600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:76716800-76719600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr1:76717000-76719000	Enhancers	Primary T cells from cord blood	blood
15	chr1:76717000-76719600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr1:76717200-76719000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr1:76717200-76719600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr1:76717200-76719600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr1:76717400-76720000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:76717600-76719400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:76717600-76722000	Weak transcription	Fetal Lung	lung
22	chr1:76718000-76719200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:76718000-76719800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:76718200-76719600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:76718200-76719800	Weak transcription	Brain Hippocampus Middle	brain
26	chr1:76718400-76719600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr1:76718600-76722000	Weak transcription	Small Intestine	intestine
28	chr1:76719000-76719400	Weak transcription	Primary T cells from cord blood	blood
29	chr1:76719000-76719600	Enhancers	HUVEC	blood vessel
30	chr1:76719000-76720600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr1:76719200-76721000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:76719400-76719600	Enhancers	Aorta	Aorta
33	chr1:76719400-76719600	Enhancers	Fetal Thymus	thymus
34	chr1:76719400-76720000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:76719400-76720000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:76719400-76720000	Enhancers	NHDF-Ad	bronchial
37	chr1:76719400-76722000	Enhancers	Primary T cells from cord blood	blood
38	chr1:76719600-76719800	Enhancers	Adipose Nuclei	Adipose
39	chr1:76719600-76720000	Enhancers	Brain Cingulate Gyrus	brain
40	chr1:76719600-76720000	Weak transcription	Fetal Thymus	thymus
41	chr1:76719600-76720200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr1:76719600-76720400	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:76719600-76720400	Flanking Active TSS	HUVEC	blood vessel
44	chr1:76719600-76720600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr1:76719600-76720600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr1:76719600-76720600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:76719600-76720800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr1:76719600-76720800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr1:76719600-76722000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr1:76719600-76727200	Weak transcription	Aorta	Aorta

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