Variant report

Variant	nsv1014231
Chromosome Location	chr1:76781140-76880630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	CBX3	chr1:76796545-76797128	HCT-116	colon:	n/a	n/a
3	CCNT2	chr1:76877130-76877206	K562	blood:	n/a	n/a
4	CEBPB	chr1:76785035-76785336	A549	lung:	n/a	chr1:76785133-76785144
5	CEBPB	chr1:76831025-76831218	HepG2	liver:	n/a	chr1:76831106-76831117
6	CEBPB	chr1:76784975-76785274	IMR90	lung:	n/a	chr1:76785133-76785144
7	CEBPB	chr1:76831038-76831227	A549	lung:	n/a	chr1:76831106-76831117
8	CEBPB	chr1:76802670-76803012	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr1:76796637-76797003	A549	lung:	n/a	n/a
10	CEBPB	chr1:76796692-76797006	MCF-7	breast:	n/a	n/a
11	CEBPB	chr1:76784987-76785293	HepG2	liver:	n/a	chr1:76785133-76785144
12	CEBPB	chr1:76802772-76802992	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr1:76802693-76803049	IMR90	lung:	n/a	n/a
14	CEBPB	chr1:76796607-76797014	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:76802794-76803000	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:76796720-76796870	NHLF	lung:	n/a	n/a
17	CTCF	chr1:76867614-76867647	LNCaP	prostate:	n/a	n/a
18	CTCF	chr1:76796800-76796950	SAEC	small airway:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
19	CTCF	chr1:76796763-76796941	SK-N-SH_RA	brain:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
20	CTCF	chr1:76796820-76796970	HA-sp	spinal cord:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
21	CTCF	chr1:76811680-76811830	BE2_C	brain:	n/a	n/a
22	CTCF	chr1:76796607-76797004	K562	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
23	CTCF	chr1:76796560-76797083	GM12878	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
24	CTCF	chr1:76796760-76796910	RPTEC	kidney:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
25	CTCF	chr1:76796800-76796950	GM12866	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
26	CTCF	chr1:76796742-76796971	NHEK	skin:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
27	CTCF	chr1:76796760-76796910	HRE	kidney:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
28	CTCF	chr1:76811700-76811850	AG10803	skin:	n/a	n/a
29	CTCF	chr1:76802620-76802770	GM12865	blood:	n/a	n/a
30	CTCF	chr1:76807461-76807494	GM13977	blood:	n/a	n/a
31	CTCF	chr1:76796739-76796956	Fibrobl	skin:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
32	CTCF	chr1:76796740-76796890	BE2_C	brain:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885
33	CTCF	chr1:76796960-76797110	A549	lung:	n/a	n/a
34	CTCF	chr1:76796780-76796930	GM12878	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
35	CTCF	chr1:76796820-76796970	HPAF	blood vessel:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
36	CTCF	chr1:76796725-76797002	Lung_OC	lung:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
37	CTCF	chr1:76811680-76811830	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr1:76796760-76796910	HEK293	kidney:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
39	CTCF	chr1:76796780-76796930	Hela-S3	cervix:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
40	CTCF	chr1:76811660-76811810	AG04450	lung:	n/a	n/a
41	CTCF	chr1:76796802-76796908	MCF-7	breast:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
42	CTCF	chr1:76796740-76796890	GM12866	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885
43	CTCF	chr1:76796820-76796970	HepG2	liver:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
44	CTCF	chr1:76796704-76796958	A549	lung:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
45	CTCF	chr1:76796780-76796930	HCFaa	heart:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
46	CTCF	chr1:76796729-76796991	LNCaP	prostate:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
47	CTCF	chr1:76796758-76796948	A549	lung:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
48	CTCF	chr1:76787223-76787315	Spleen_OC	spleen:	n/a	chr1:76787307-76787315
49	CTCF	chr1:76796820-76796970	GM12870	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
50	CTCF	chr1:76787272-76787304	GM19239	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76840032-76840082	SAEC	small airway:	n/a
2	chr1:76840032-76840082	SK-N-MC	brain:	n/a
3	chr1:76782984-76783034	SK-N-MC	brain:	n/a
4	chr1:76817670-76817720	IMR90	lung:	fetal
5	chr1:76817670-76817720	NH-A	brain:	n/a
6	chr1:76782984-76783034	H1-hESC	embryonic stem cell:	embryo
7	chr1:76817670-76817720	HCPEpiC	choroid plexus:	n/a
8	chr1:76817670-76817720	SK-N-MC	brain:	n/a
9	chr1:76840032-76840082	HAEpiC	amniotic membrane:	n/a
10	chr1:76840032-76840082	AoSMC	blood vessel:	n/a
11	chr1:76840032-76840082	GM19239	blood:	n/a
12	chr1:76840032-76840082	GM12892	blood:	n/a
13	chr1:76840032-76840082	T-47D	breast:	n/a
14	chr1:76782984-76783034	PrEC	prostate:	n/a
15	chr1:76817670-76817720	AoSMC	blood vessel:	n/a
16	chr1:76782984-76783034	NH-A	brain:	n/a
17	chr1:76782984-76783034	ECC-1	luminal epithelium:	n/a
18	chr1:76817670-76817720	HUVEC	blood vessel:	n/a
19	chr1:76817670-76817720	AG04450	lung:	fetal
20	chr1:76840032-76840082	NHBE	bronchial:	n/a
21	chr1:76817670-76817720	HCF	heart:	n/a
22	chr1:76782984-76783034	Caco-2	colon:	n/a
23	chr1:76840032-76840082	CMK	blood:	n/a
24	chr1:76840032-76840082	AG04450	lung:	fetal
25	chr1:76817670-76817720	NT2-D1	testis:	n/a
26	chr1:76840032-76840082	PrEC	prostate:	n/a
27	chr1:76817670-76817720	HCM	heart:	n/a
28	chr1:76782984-76783034	NHDF-neo	bronchial:	n/a
29	chr1:76817670-76817720	GM12891	blood:	n/a
30	chr1:76840032-76840082	SKMC	muscle:	n/a
31	chr1:76817670-76817720	H1-hESC	embryonic stem cell:	embryo
32	chr1:76840032-76840082	HNPCEpiC	eye:	n/a
33	chr1:76817670-76817720	Caco-2	colon:	n/a
34	chr1:76817670-76817720	MCF-7	breast:	n/a
35	chr1:76840032-76840082	HIPEpiC	eye:	n/a
36	chr1:76840032-76840082	HUVEC	blood vessel:	n/a
37	chr1:76782984-76783034	MCF-7	breast:	n/a
38	chr1:76817670-76817720	HRCEpiC	kidney:	n/a
39	chr1:76817670-76817720	SAEC	small airway:	n/a
40	chr1:76817670-76817720	SKMC	muscle:	n/a
41	chr1:76782984-76783034	NHBE	bronchial:	n/a
42	chr1:76840032-76840082	HepG2	liver:	n/a
43	chr1:76840032-76840082	NT2-D1	testis:	n/a
44	chr1:76817670-76817720	AG04449	skin:	fetal
45	chr1:76840032-76840082	Hela-S3	cervix:	n/a
46	chr1:76840032-76840082	Hepatocyte	liver:	n/a
47	chr1:76817670-76817720	A549	lung:	n/a
48	chr1:76840032-76840082	MCF10A-Er-Src	breast:	n/a
49	chr1:76782984-76783034	HRPEpiC	eye:	n/a
50	chr1:76782984-76783034	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:76796406..76797312-chr1:77366615..77367452,3	MCF-7	breast:
2	chr1:76813366..76816327-chr1:76818310..76820003,2	K562	blood:
3	chr1:76871350..76874295-chr1:76994896..76997570,2	K562	blood:
4	chr1:76880275..76881877-chr1:76884344..76886565,2	K562	blood:
5	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
6	chr1:76373718..76374271-chr1:76796370..76797302,2	MCF-7	breast:
7	chr1:76796476..76797352-chr1:77609351..77609861,2	K562	blood:
8	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
9	chr1:76796389..76797022-chr1:77608917..77609894,2	MCF-7	breast:
10	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
11	chr1:76796528..76797295-chr1:77206308..77207068,2	MCF-7	breast:
12	chr1:76620098..76620620-chr1:76796654..76797328,2	MCF-7	breast:
13	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:
14	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
15	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:
16	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
17	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
18	chr1:76796470..76797076-chr1:77591559..77592349,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB17-2	chr1:76819268-76819931	NONHSAT004012

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

Extended variants
information (count: 3293 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3293 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11809814	chr1:76781140-76781141	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538218698	chr1:76781144-76781145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185524327	chr1:76781167-76781168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575486940	chr1:76781169-76781170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147749569	chr1:76781178-76781179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548805842	chr1:76781200-76781201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573037212	chr1:76781204-76781205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533203681	chr1:76781224-76781225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540451723	chr1:76781304-76781305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112501755	chr1:76781318-76781319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189260430	chr1:76781337-76781338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142598172	chr1:76781352-76781353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146772210	chr1:76781354-76781355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372023287	chr1:76781453-76781454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529692534	chr1:76781454-76781455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548558018	chr1:76781497-76781498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3904686	chr1:76781576-76781577	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs566795952	chr1:76781616-76781617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372975129	chr1:76781638-76781639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535355841	chr1:76781664-76781665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527849917	chr1:76781688-76781689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149103058	chr1:76781753-76781754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552382470	chr1:76781756-76781757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570598670	chr1:76781777-76781778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61771477	chr1:76781778-76781779	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs556519194	chr1:76781782-76781783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs77753671	chr1:76781784-76781785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs61771478	chr1:76781808-76781809	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs11162120	chr1:76781823-76781824	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs573198099	chr1:76781837-76781838	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs117032117	chr1:76781932-76781933	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs139241887	chr1:76781935-76781936	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs557876017	chr1:76781938-76781939	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs149070716	chr1:76781944-76781945	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs181526924	chr1:76781964-76781965	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs562612299	chr1:76781983-76781984	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs529623799	chr1:76781994-76781995	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs375783312	chr1:76781996-76781997	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs78695323	chr1:76782026-76782027	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs185828520	chr1:76782047-76782048	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs143071972	chr1:76782048-76782049	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs570758609	chr1:76782131-76782132	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs554050291	chr1:76782148-76782149	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs148201915	chr1:76782155-76782156	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs549968839	chr1:76782186-76782187	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs188737415	chr1:76782198-76782199	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs535454978	chr1:76782199-76782200	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs141163701	chr1:76782251-76782252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566760933	chr1:76782267-76782268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534126406	chr1:76782305-76782306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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	21293372	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76755800-76783000	Weak transcription	Fetal Lung	lung
2	chr1:76774200-76796400	Weak transcription	Fetal Stomach	stomach
3	chr1:76775400-76796400	Weak transcription	Brain Substantia Nigra	brain
4	chr1:76778000-76782000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:76778400-76783400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr1:76779800-76782800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:76779800-76784000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:76780200-76784000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:76780200-76813800	Weak transcription	Primary B cells from cord blood	blood
10	chr1:76780600-76781600	Enhancers	Fetal Heart	heart
11	chr1:76780600-76783000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr1:76780600-76784000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:76780600-76817200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:76781600-76783400	Weak transcription	Fetal Heart	heart
15	chr1:76781800-76782200	ZNF genes & repeats	Fetal Kidney	kidney
16	chr1:76782200-76792800	Weak transcription	Fetal Kidney	kidney
17	chr1:76782800-76783600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:76783000-76783400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr1:76783000-76783600	Enhancers	Fetal Lung	lung
20	chr1:76783400-76783600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr1:76783400-76783600	Enhancers	Fetal Heart	heart
22	chr1:76783400-76784200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:76783600-76784600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr1:76783600-76792000	Weak transcription	Fetal Lung	lung
25	chr1:76783600-76802600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:76784000-76784800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr1:76784000-76784800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:76784000-76784800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:76784000-76784800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr1:76784200-76788400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:76784800-76787200	Weak transcription	HUVEC	blood vessel
32	chr1:76786800-76787200	Enhancers	Fetal Thymus	thymus
33	chr1:76787200-76791200	Weak transcription	Fetal Thymus	thymus
34	chr1:76790800-76792200	Enhancers	Primary T cells from cord blood	blood
35	chr1:76791200-76792000	Enhancers	Thymus	Thymus
36	chr1:76791200-76792200	Enhancers	Fetal Thymus	thymus
37	chr1:76792000-76792200	Enhancers	Fetal Lung	lung
38	chr1:76792000-76794000	Weak transcription	Thymus	Thymus
39	chr1:76792200-76794000	Weak transcription	Fetal Thymus	thymus
40	chr1:76792200-76794400	Weak transcription	Primary T cells from cord blood	blood
41	chr1:76794000-76794800	Enhancers	Thymus	Thymus
42	chr1:76794000-76795000	Enhancers	Fetal Thymus	thymus
43	chr1:76794200-76795000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr1:76794400-76794800	Enhancers	Primary T cells from cord blood	blood
45	chr1:76794800-76797000	Weak transcription	Primary T cells from cord blood	blood
46	chr1:76796400-76796800	Enhancers	Brain Substantia Nigra	brain
47	chr1:76796400-76797200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr1:76796400-76797200	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr1:76796400-76797200	Enhancers	Fetal Heart	heart
50	chr1:76796400-76797400	Enhancers	Fetal Stomach	stomach

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