Variant report

Variant	nsv1034844
Chromosome Location	chr5:16854341-16903100
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:970)
CpG islands
(count:611)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:970 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16881196-16881719	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:16894441-16894999	HepG2	liver:	n/a	n/a
3	ATF1	chr5:16894707-16894929	K562	blood:	n/a	n/a
4	ATF3	chr5:16894304-16895066	A549	lung:	n/a	n/a
5	ATF3	chr5:16897335-16897941	A549	lung:	n/a	n/a
6	ATF3	chr5:16897237-16897998	A549	lung:	n/a	n/a
7	BACH1	chr5:16867057-16867228	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr5:16896948-16898127	A549	lung:	n/a	n/a
9	BCL3	chr5:16894028-16895258	A549	lung:	n/a	n/a
10	BCL3	chr5:16897232-16898332	A549	lung:	n/a	n/a
11	BCL3	chr5:16894074-16895296	A549	lung:	n/a	n/a
12	BCL3	chr5:16889595-16890222	A549	lung:	n/a	chr5:16890042-16890049
13	BRCA1	chr5:16894296-16895117	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr5:16886452-16886811	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr5:16889668-16890524	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr5:16889723-16890599	HCT-116	colon:	n/a	n/a
17	CCNT2	chr5:16858190-16858390	K562	blood:	n/a	n/a
18	CEBPB	chr5:16888610-16889119	A549	lung:	n/a	n/a
19	CEBPB	chr5:16871067-16871416	MCF-7	breast:	n/a	chr5:16871204-16871215
20	CEBPB	chr5:16899272-16899563	A549	lung:	n/a	n/a
21	CEBPB	chr5:16870341-16870873	A549	lung:	n/a	n/a
22	CEBPB	chr5:16886443-16886833	A549	lung:	n/a	n/a
23	CEBPB	chr5:16889687-16890697	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:16854638-16854829	HepG2	liver:	n/a	chr5:16854744-16854755
25	CEBPB	chr5:16871016-16871390	A549	lung:	n/a	chr5:16871204-16871215
26	CEBPB	chr5:16881151-16881677	HepG2	liver:	n/a	chr5:16881331-16881342 chr5:16881332-16881343 chr5:16881331-16881344
27	CEBPB	chr5:16888734-16889252	A549	lung:	n/a	n/a
28	CEBPB	chr5:16894162-16895075	A549	lung:	n/a	n/a
29	CEBPB	chr5:16871085-16871404	ECC-1	luminal epithelium:	n/a	chr5:16871204-16871215
30	CEBPB	chr5:16897243-16898133	A549	lung:	n/a	n/a
31	CEBPB	chr5:16889755-16890748	A549	lung:	n/a	n/a
32	CEBPB	chr5:16881193-16881479	Hela-S3	cervix:	n/a	chr5:16881331-16881342 chr5:16881332-16881343 chr5:16881331-16881344
33	CEBPB	chr5:16855090-16855180	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:16881254-16881349	H1-hESC	embryonic stem cell:	n/a	chr5:16881331-16881342 chr5:16881332-16881343 chr5:16881331-16881344
35	CEBPB	chr5:16888737-16889149	A549	lung:	n/a	n/a
36	CEBPB	chr5:16871025-16871372	ECC-1	luminal epithelium:	n/a	chr5:16871204-16871215
37	CEBPB	chr5:16894394-16895131	A549	lung:	n/a	n/a
38	CEBPB	chr5:16854617-16855206	IMR90	lung:	n/a	chr5:16854744-16854755
39	CEBPB	chr5:16886518-16886718	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:16888778-16889171	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:16856657-16856987	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:16856697-16857048	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr5:16897372-16898164	A549	lung:	n/a	n/a
44	CEBPB	chr5:16894331-16894927	A549	lung:	n/a	n/a
45	CEBPB	chr5:16890376-16890684	A549	lung:	n/a	n/a
46	CEBPB	chr5:16854608-16855236	A549	lung:	n/a	chr5:16854744-16854755
47	CEBPB	chr5:16871071-16871274	K562	blood:	n/a	chr5:16871204-16871215
48	CEBPB	chr5:16886231-16886925	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr5:16877966-16878213	HepG2	liver:	n/a	n/a
50	CEBPB	chr5:16886389-16886908	IMR90	lung:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16901400-16901450	AoSMC	blood vessel:	n/a
2	chr5:16901400-16901450	AoSMC	blood vessel:	n/a
3	chr5:16857119-16857169	SKMC	muscle:	n/a
4	chr5:16854566-16854616	HMEC	breast:	n/a
5	chr5:16854566-16854616	GM06990	blood:	n/a
6	chr5:16857119-16857169	NHDF-neo	bronchial:	n/a
7	chr5:16881431-16881481	PrEC	prostate:	n/a
8	chr5:16864447-16864497	NHDF-neo	bronchial:	n/a
9	chr5:16854566-16854616	GM12892	blood:	n/a
10	chr5:16864447-16864497	NB4	blood:	n/a
11	chr5:16902633-16902683	AG09319	gingival:	n/a
12	chr5:16881431-16881481	ovcar-3	ovarian:	n/a
13	chr5:16881431-16881481	AoSMC	blood vessel:	n/a
14	chr5:16886424-16886474	SK-N-SH	brain:	n/a
15	chr5:16901400-16901450	HL-60	blood:	n/a
16	chr5:16867064-16867114	ovcar-3	ovarian:	n/a
17	chr5:16881431-16881481	HCPEpiC	choroid plexus:	n/a
18	chr5:16881431-16881481	HRE	kidney:	n/a
19	chr5:16864447-16864497	AG04450	lung:	fetal
20	chr5:16857119-16857169	Jurkat	blood:	n/a
21	chr5:16902573-16902623	CMK	blood:	n/a
22	chr5:16854566-16854616	Jurkat	blood:	n/a
23	chr5:16902573-16902623	T-47D	breast:	n/a
24	chr5:16886424-16886474	K562	blood:	n/a
25	chr5:16886424-16886474	GM06990	blood:	n/a
26	chr5:16902573-16902623	SKMC	muscle:	n/a
27	chr5:16881431-16881481	SK-N-MC	brain:	n/a
28	chr5:16867064-16867114	AoSMC	blood vessel:	n/a
29	chr5:16881431-16881481	AG10803	skin:	n/a
30	chr5:16902633-16902683	HRPEpiC	eye:	n/a
31	chr5:16901400-16901450	ProgFib	skin:	n/a
32	chr5:16857119-16857169	MCF-7	breast:	n/a
33	chr5:16864447-16864497	GM12878	blood:	n/a
34	chr5:16895511-16895561	HCPEpiC	choroid plexus:	n/a
35	chr5:16864447-16864497	HRE	kidney:	n/a
36	chr5:16854566-16854616	HUVEC	blood vessel:	n/a
37	chr5:16886424-16886474	NHBE	bronchial:	n/a
38	chr5:16857119-16857169	HRE	kidney:	n/a
39	chr5:16867064-16867114	AG04450	lung:	fetal
40	chr5:16864447-16864497	PrEC	prostate:	n/a
41	chr5:16895511-16895561	IMR90	lung:	fetal
42	chr5:16895511-16895561	AG04449	skin:	fetal
43	chr5:16895511-16895561	NB4	blood:	n/a
44	chr5:16854566-16854616	PANC-1	pancreas:	n/a
45	chr5:16902573-16902623	GM19239	blood:	n/a
46	chr5:16901400-16901450	PrEC	prostate:	n/a
47	chr5:16867064-16867114	HEK293	kidney:	embryo
48	chr5:16854566-16854616	AG09309	skin:	n/a
49	chr5:16902573-16902623	Jurkat	blood:	n/a
50	chr5:16895511-16895561	HPAEpiC	pulmonary alveolar:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:16855463..16857293-chr5:16859556..16861090,2	MCF-7	breast:
2	chr5:16876341..16879051-chr5:16898950..16901260,2	MCF-7	breast:
3	chr5:16893313..16896141-chr5:16935202..16937655,2	MCF-7	breast:
4	chr5:16876341..16879051-chr5:16898950..16901260,2	MCF-7	breast:
5	chr5:16883385..16886348-chr5:16888269..16889832,2	MCF-7	breast:
6	chr5:16866302..16868236-chr5:16870431..16873276,2	K562	blood:
7	chr5:16892933..16897070-chr5:16897498..16901971,5	MCF-7	breast:
8	chr5:16860814..16863771-chr5:16866048..16868636,3	MCF-7	breast:
9	chr5:16877490..16879580-chr5:16883776..16886386,2	MCF-7	breast:
10	chr5:16877490..16879580-chr5:16883776..16886386,2	MCF-7	breast:
11	chr5:16882313..16886357-chr5:16933451..16937299,4	MCF-7	breast:
12	chr5:16848554..16850179-chr5:16855617..16858396,2	K562	blood:
13	chr5:16866302..16868236-chr5:16870431..16873276,2	K562	blood:
14	chr5:16870568..16873401-chr5:16875593..16878423,2	K562	blood:
15	chr5:16863229..16863788-chr8:22102048..22102609,2	Hela-S3	cervix:
16	chr5:16852586..16854370-chr5:16854403..16855984,2	K562	blood:
17	chr5:16850266..16851821-chr5:16858055..16860279,2	MCF-7	breast:
18	chr5:16875713..16877407-chr5:16911491..16914086,2	MCF-7	breast:
19	chr5:16860814..16863771-chr5:16866048..16868636,3	MCF-7	breast:
20	chr5:16870568..16873401-chr5:16875593..16878423,2	K562	blood:
21	chr5:16899974..16902321-chr5:16904564..16907062,3	MCF-7	breast:
22	chr5:16854713..16857141-chr5:16861779..16864325,2	MCF-7	breast:
23	chr5:16855463..16857293-chr5:16859556..16861090,2	MCF-7	breast:
24	chr5:16883385..16886348-chr5:16888269..16889832,2	MCF-7	breast:
25	chr5:16827134..16829688-chr5:16861859..16863470,2	MCF-7	breast:
26	chr5:16895872..16898424-chr5:16934812..16936470,2	MCF-7	breast:
27	chr5:16889896..16891500-chr5:16935094..16936823,3	MCF-7	breast:
28	chr5:16854713..16857141-chr5:16861779..16864325,2	MCF-7	breast:
29	chr5:16892933..16897070-chr5:16897498..16901971,5	MCF-7	breast:
30	chr5:16894491..16896403-chr5:16903844..16905936,2	MCF-7	breast:
31	chr5:16893446..16895051-chr5:16936085..16937930,2	MCF-7	breast:
32	chr5:16883490..16885617-chr5:17011887..17014186,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000243538	TF binding region
ENSG00000243538	CpG island
ENSG00000208037	chromatin interactions
ENSG00000253093	chromatin interactions
ENSG00000145555	chromatin interactions

Extended variants
information (count: 2192 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2192 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375940472	chr5:16854411-16854412	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs191137649	chr5:16854476-16854477	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560031085	chr5:16854539-16854540	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs150435440	chr5:16854566-16854567	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551784262	chr5:16854584-16854585	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs76886326	chr5:16854641-16854642	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141910846	chr5:16854681-16854682	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548094379	chr5:16854694-16854695	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542621967	chr5:16854698-16854699	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11133865	chr5:16854705-16854706	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs569439007	chr5:16854721-16854722	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs531534698	chr5:16854732-16854733	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550093716	chr5:16854830-16854831	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149571674	chr5:16854836-16854837	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs145553706	chr5:16854863-16854864	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138170038	chr5:16854865-16854866	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2625204	chr5:16854916-16854917	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559007012	chr5:16854943-16854944	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs182634133	chr5:16854957-16854958	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs538139338	chr5:16854963-16854964	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547516305	chr5:16854968-16854969	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187715557	chr5:16854970-16854971	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs541693253	chr5:16854971-16854972	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2560859	chr5:16854973-16854974	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs71582462	chr5:16854986-16854987	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2560858	chr5:16854994-16854995	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs79547489	chr5:16855000-16855001	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531164432	chr5:16855002-16855003	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549355106	chr5:16855006-16855007	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563071050	chr5:16855027-16855028	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs148251762	chr5:16855035-16855036	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374161481	chr5:16855036-16855037	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs78282908	chr5:16855042-16855043	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2625205	chr5:16855060-16855061	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs191797442	chr5:16855074-16855075	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs184159937	chr5:16855099-16855100	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78511667	chr5:16855116-16855117	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538285154	chr5:16855119-16855120	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561731686	chr5:16855141-16855142	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556506937	chr5:16855153-16855154	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572481291	chr5:16855155-16855156	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568291981	chr5:16855156-16855157	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139024275	chr5:16855175-16855176	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553703534	chr5:16855199-16855200	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75896684	chr5:16855202-16855203	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116272090	chr5:16855206-16855207	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187661787	chr5:16855221-16855222	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs75257357	chr5:16855282-16855283	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543076175	chr5:16855314-16855315	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192101909	chr5:16855381-16855382	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1849 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16820800-16855200	Weak transcription	HSMM	muscle
2	chr5:16829400-16855800	Weak transcription	Fetal Intestine Small	intestine
3	chr5:16832400-16855000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:16839000-16855800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:16839000-16864600	Weak transcription	Fetal Brain Female	brain
6	chr5:16841800-16855600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr5:16842400-16862800	Weak transcription	Stomach Mucosa	stomach
8	chr5:16842600-16855200	Weak transcription	HUVEC	blood vessel
9	chr5:16842600-16855600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr5:16843400-16855000	Weak transcription	Lung	lung
11	chr5:16844400-16855600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:16844800-16855600	Weak transcription	NHEK	skin
13	chr5:16845600-16857000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:16846800-16855600	Weak transcription	Gastric	stomach
15	chr5:16846800-16856200	Weak transcription	HMEC	breast
16	chr5:16847000-16855000	Weak transcription	Pancreas	Pancrea
17	chr5:16847000-16855600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:16847800-16856000	Weak transcription	Fetal Thymus	thymus
19	chr5:16848800-16855800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:16850000-16855800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr5:16850400-16855600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr5:16851200-16854400	Genic enhancers	A549	lung
23	chr5:16852200-16856400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:16852400-16858200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr5:16852800-16855200	Weak transcription	Fetal Kidney	kidney
26	chr5:16852800-16855600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr5:16853000-16854600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:16853000-16855000	Weak transcription	NHLF	lung
29	chr5:16853000-16855200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:16853000-16855400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr5:16853000-16855400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:16853000-16855400	Weak transcription	Fetal Lung	lung
33	chr5:16853000-16855800	Weak transcription	NH-A	brain
34	chr5:16853000-16856800	Weak transcription	Placenta	Placenta
35	chr5:16853000-16860600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:16853200-16855000	Weak transcription	Fetal Stomach	stomach
37	chr5:16853200-16855200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:16853200-16855200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr5:16853200-16855200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:16853200-16855400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:16853200-16855600	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr5:16853200-16856600	Weak transcription	Osteobl	bone
43	chr5:16853200-16857400	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr5:16853400-16857000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr5:16853600-16854400	Enhancers	Fetal Muscle Leg	muscle
46	chr5:16853600-16858000	Enhancers	HSMMtube	muscle
47	chr5:16853800-16855600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr5:16854000-16855000	Weak transcription	NHDF-Ad	bronchial
49	chr5:16854000-16855200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr5:16854000-16855400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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