Variant report

Variant	nsv518747
Chromosome Location	chr14:36787226-36809926
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	ARID3A	chr14:36789827-36789998	K562	blood:	n/a	n/a
2	ARID3A	chr14:36789353-36790203	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:36787931-36788470	HepG2	liver:	n/a	n/a
4	ATF1	chr14:36789684-36790159	K562	blood:	n/a	n/a
5	ATF2	chr14:36789725-36790108	GM12878	blood:	n/a	n/a
6	ATF2	chr14:36789693-36790117	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr14:36789612-36790132	GM12878	blood:	n/a	n/a
8	ATF3	chr14:36789736-36790012	K562	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
9	ATF3	chr14:36789354-36790107	HepG2	liver:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
10	ATF3	chr14:36789765-36789985	GM12878	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
11	ATF3	chr14:36789635-36790064	H1-hESC	embryonic stem cell:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
12	BCL3	chr14:36789549-36790347	A549	lung:	n/a	n/a
13	BHLHE40	chr14:36789595-36790169	K562	blood:	n/a	n/a
14	BRCA1	chr14:36788746-36788783	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr14:36789033-36790188	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:36789668-36790245	HepG2	liver:	n/a	n/a
17	CBX3	chr14:36789680-36790403	K562	blood:	n/a	n/a
18	CCNT2	chr14:36789394-36790044	K562	blood:	n/a	chr14:36789846-36789855
19	CEBPB	chr14:36798107-36798380	HepG2	liver:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
20	CEBPB	chr14:36791061-36791224	K562	blood:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
21	CEBPB	chr14:36791032-36791270	A549	lung:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
22	CEBPB	chr14:36789331-36790233	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr14:36789706-36790106	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:36789584-36790156	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:36798092-36798403	K562	blood:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
26	CEBPB	chr14:36789730-36790173	K562	blood:	n/a	n/a
27	CEBPB	chr14:36789455-36790200	HepG2	liver:	n/a	n/a
28	CEBPB	chr14:36798124-36798432	Hela-S3	cervix:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
29	CEBPB	chr14:36798093-36798434	A549	lung:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
30	CEBPB	chr14:36789653-36790109	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:36789718-36790083	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:36790993-36791264	HepG2	liver:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
33	CEBPB	chr14:36798076-36798444	HepG2	liver:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
34	CEBPB	chr14:36789746-36790117	K562	blood:	n/a	n/a
35	CEBPB	chr14:36789602-36790208	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:36789699-36790108	A549	lung:	n/a	n/a
37	CEBPB	chr14:36805980-36806101	HepG2	liver:	n/a	chr14:36806038-36806049
38	CEBPB	chr14:36796560-36796920	HepG2	liver:	n/a	n/a
39	CEBPB	chr14:36789563-36790259	GM12878	blood:	n/a	n/a
40	CEBPB	chr14:36796572-36796924	A549	lung:	n/a	n/a
41	CEBPB	chr14:36796651-36796792	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr14:36798118-36798425	IMR90	lung:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
43	CEBPB	chr14:36796555-36796909	IMR90	lung:	n/a	n/a
44	CEBPB	chr14:36789686-36790191	IMR90	lung:	n/a	n/a
45	CEBPD	chr14:36789659-36790120	HepG2	liver:	n/a	n/a
46	CEBPD	chr14:36789365-36790221	HepG2	liver:	n/a	n/a
47	CHD1	chr14:36789033-36789753	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr14:36789343-36790242	HepG2	liver:	n/a	n/a
49	CHD2	chr14:36789393-36790207	GM12878	blood:	n/a	n/a
50	CHD2	chr14:36789183-36790156	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36790242-36790292	NB4	blood:	n/a
2	chr14:36789985-36790035	H1-hESC	embryonic stem cell:	embryo
3	chr14:36789488-36789538	HL-60	blood:	n/a
4	chr14:36790242-36790292	NB4	blood:	n/a
5	chr14:36789985-36790035	H1-hESC	embryonic stem cell:	embryo
6	chr14:36789488-36789538	HL-60	blood:	n/a
7	chr14:36789488-36789538	ECC-1	luminal epithelium:	n/a
8	chr14:36789985-36790035	NT2-D1	testis:	n/a
9	chr14:36790242-36790292	SKMC	muscle:	n/a
10	chr14:36789810-36789860	AG10803	skin:	n/a
11	chr14:36789810-36789860	NB4	blood:	n/a
12	chr14:36789810-36789860	HPAEpiC	pulmonary alveolar:	n/a
13	chr14:36789985-36790035	HMEC	breast:	n/a
14	chr14:36789488-36789538	NHDF-neo	bronchial:	n/a
15	chr14:36789886-36789936	ProgFib	skin:	n/a
16	chr14:36789691-36789741	ProgFib	skin:	n/a
17	chr14:36789810-36789860	Hepatocyte	liver:	n/a
18	chr14:36789985-36790035	AG09309	skin:	n/a
19	chr14:36789810-36789860	NH-A	brain:	n/a
20	chr14:36789886-36789936	HRPEpiC	eye:	n/a
21	chr14:36789691-36789741	SAEC	small airway:	n/a
22	chr14:36789810-36789860	ProgFib	skin:	n/a
23	chr14:36789886-36789936	Jurkat	blood:	n/a
24	chr14:36789691-36789741	PFSK-1	brain:	n/a
25	chr14:36789985-36790035	PFSK-1	brain:	n/a
26	chr14:36789985-36790035	HCM	heart:	n/a
27	chr14:36789810-36789860	HEEpiC	esophagus:	n/a
28	chr14:36789886-36789936	PFSK-1	brain:	n/a
29	chr14:36789886-36789936	NHBE	bronchial:	n/a
30	chr14:36789488-36789538	Hela-S3	cervix:	n/a
31	chr14:36789488-36789538	HCPEpiC	choroid plexus:	n/a
32	chr14:36789691-36789741	K562	blood:	n/a
33	chr14:36789691-36789741	HAEpiC	amniotic membrane:	n/a
34	chr14:36789691-36789741	SK-N-SH_RA	brain:	n/a
35	chr14:36789691-36789741	SK-N-SH	brain:	n/a
36	chr14:36789810-36789860	HIPEpiC	eye:	n/a
37	chr14:36790242-36790292	Caco-2	colon:	n/a
38	chr14:36789985-36790035	IMR90	lung:	fetal
39	chr14:36789985-36790035	AG04449	skin:	fetal
40	chr14:36790242-36790292	AG09319	gingival:	n/a
41	chr14:36789810-36789860	SK-N-MC	brain:	n/a
42	chr14:36789488-36789538	PFSK-1	brain:	n/a
43	chr14:36789985-36790035	K562	blood:	n/a
44	chr14:36789488-36789538	Caco-2	colon:	n/a
45	chr14:36789886-36789936	HNPCEpiC	eye:	n/a
46	chr14:36789691-36789741	IMR90	lung:	fetal
47	chr14:36790242-36790292	AG04450	lung:	fetal
48	chr14:36789488-36789538	SKMC	muscle:	n/a
49	chr14:36790242-36790292	NT2-D1	testis:	n/a
50	chr14:36789886-36789936	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
2	chr14:36538483..36541249-chr14:36788541..36791272,2	MCF-7	breast:
3	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
4	chr14:36780690..36783423-chr14:36785409..36787697,2	K562	blood:
5	chr14:36781444..36784031-chr14:36790836..36792756,2	K562	blood:
6	chr14:36789374..36789875-chr8:119123638..119124514,2	Hela-S3	cervix:
7	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
8	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
9	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
10	chr14:36784989..36787450-chr14:36787865..36790918,4	K562	blood:
11	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
12	chr14:36787110..36790093-chr14:36792032..36793692,2	K562	blood:
13	chr14:36788593..36791761-chr14:36792192..36795536,3	K562	blood:
14	chr14:36780477..36782487-chr14:36786743..36788959,2	MCF-7	breast:
15	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:

Variant related genes	Relation type
MBIP	TF binding region
MBIP	CpG island
ENSG00000182197	chromatin interactions
ENSG00000257585	chromatin interactions
ENSG00000151332	chromatin interactions

Extended variants
information (count: 304 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3805354	chr14:36787226-36787227	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3805353	chr14:36787313-36787314	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs190019090	chr14:36787362-36787363	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs575854516	chr14:36787441-36787442	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs370712670	chr14:36787472-36787473	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536591711	chr14:36787492-36787493	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs3805352	chr14:36787516-36787517	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs79855793	chr14:36787537-36787538	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs545371235	chr14:36787594-36787595	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565100522	chr14:36787613-36787614	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs180881230	chr14:36787692-36787693	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs185768938	chr14:36787723-36787724	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs564336815	chr14:36787756-36787757	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572914726	chr14:36787783-36787784	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs540540769	chr14:36787851-36787852	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs61994980	chr14:36787898-36787899	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs150638498	chr14:36787934-36787935	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs569190022	chr14:36788018-36788019	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs549033393	chr14:36788033-36788034	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs3850260	chr14:36788085-36788086	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs531470376	chr14:36788101-36788102	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543847812	chr14:36788115-36788116	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs75495968	chr14:36788146-36788147	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562143903	chr14:36788176-36788177	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs4636811	chr14:36788186-36788187	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs192333896	chr14:36788229-36788230	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547083541	chr14:36788267-36788268	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145207008	chr14:36788313-36788314	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs567568661	chr14:36788354-36788355	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536833949	chr14:36788367-36788368	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs532895550	chr14:36788380-36788381	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs556612951	chr14:36788439-36788440	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570344839	chr14:36788458-36788459	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs183711072	chr14:36788481-36788482	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs538916405	chr14:36788558-36788559	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs188752302	chr14:36788623-36788624	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs190407909	chr14:36788676-36788677	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs377616153	chr14:36788728-36788729	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs75031154	chr14:36788759-36788760	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs555628810	chr14:36788777-36788778	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs182650023	chr14:36788891-36788892	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs573913416	chr14:36788895-36788896	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs3792688	chr14:36788896-36788897	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528651577	chr14:36788948-36788949	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs562512928	chr14:36788987-36788988	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs531639457	chr14:36789010-36789011	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs118170965	chr14:36789021-36789022	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564581199	chr14:36789037-36789038	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs186972895	chr14:36789065-36789066	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149347213	chr14:36789072-36789073	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36765400-36788800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:36766600-36788000	Weak transcription	Fetal Heart	heart
3	chr14:36767400-36789200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:36767400-36789200	Weak transcription	Spleen	Spleen
5	chr14:36772600-36788800	Weak transcription	Stomach Mucosa	stomach
6	chr14:36773400-36789200	Weak transcription	Esophagus	oesophagus
7	chr14:36779200-36788600	Weak transcription	Fetal Intestine Small	intestine
8	chr14:36779400-36789000	Weak transcription	Colonic Mucosa	Colon
9	chr14:36780400-36788800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr14:36780400-36789200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:36780400-36789200	Weak transcription	Small Intestine	intestine
12	chr14:36780600-36788400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:36780600-36788400	Weak transcription	Brain Cingulate Gyrus	brain
14	chr14:36780600-36788400	Weak transcription	Fetal Stomach	stomach
15	chr14:36780600-36788600	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr14:36780600-36788600	Weak transcription	Colon Smooth Muscle	Colon
17	chr14:36780600-36789200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr14:36780800-36787400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr14:36780800-36788000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr14:36780800-36788000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr14:36780800-36788400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:36780800-36788400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr14:36780800-36788600	Weak transcription	Thymus	Thymus
24	chr14:36781000-36787400	Weak transcription	Primary T cells from cord blood	blood
25	chr14:36781000-36787400	Weak transcription	HSMM	muscle
26	chr14:36781000-36787800	Weak transcription	NHDF-Ad	bronchial
27	chr14:36781000-36787800	Weak transcription	NHLF	lung
28	chr14:36781000-36788000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr14:36781000-36788000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:36781000-36788000	Weak transcription	Fetal Brain Male	brain
31	chr14:36781000-36788400	Weak transcription	Fetal Kidney	kidney
32	chr14:36781000-36788400	Weak transcription	Fetal Muscle Leg	muscle
33	chr14:36781000-36788400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr14:36781000-36788600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr14:36781000-36788600	Weak transcription	Aorta	Aorta
36	chr14:36781000-36788600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr14:36781000-36788600	Weak transcription	Ovary	ovary
38	chr14:36781000-36788600	Weak transcription	Psoas Muscle	Psoas
39	chr14:36781000-36788600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr14:36781000-36788600	Weak transcription	HSMMtube	muscle
41	chr14:36781000-36788800	Weak transcription	Right Ventricle	heart
42	chr14:36781000-36789000	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr14:36781000-36789200	Weak transcription	Gastric	stomach
44	chr14:36781000-36789200	Weak transcription	Left Ventricle	heart
45	chr14:36781000-36789200	Weak transcription	Lung	lung
46	chr14:36781000-36789200	Weak transcription	Pancreas	Pancrea
47	chr14:36781200-36788400	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr14:36781200-36788600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr14:36781200-36788600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr14:36783000-36788200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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