Variant report

Variant	esv3420807
Chromosome Location	chr14:105764707-105769605
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:507)
CpG islands
(count:732)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:507 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105767190-105767604	HepG2	liver:	n/a	n/a
2	BACH1	chr14:105766424-105767645	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr14:105766850-105767395	GM12878	blood:	n/a	n/a
4	BHLHE40	chr14:105766686-105767711	HepG2	liver:	n/a	chr14:105766760-105766776
5	BHLHE40	chr14:105766831-105767705	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:105767201-105767636	K562	blood:	n/a	n/a
7	BHLHE40	chr14:105767853-105768215	K562	blood:	n/a	n/a
8	BHLHE40	chr14:105767913-105768111	GM12878	blood:	n/a	n/a
9	BRCA1	chr14:105766891-105767604	HepG2	liver:	n/a	n/a
10	BRCA1	chr14:105766891-105767649	GM12878	blood:	n/a	n/a
11	BRCA1	chr14:105766843-105767916	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr14:105766891-105767298	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr14:105767897-105768155	K562	blood:	n/a	n/a
14	CBX3	chr14:105767136-105767735	K562	blood:	n/a	n/a
15	CBX3	chr14:105765911-105766270	K562	blood:	n/a	n/a
16	CBX3	chr14:105765920-105766209	K562	blood:	n/a	n/a
17	CCNT2	chr14:105766686-105768120	K562	blood:	n/a	chr14:105767659-105767668
18	CEBPB	chr14:105764715-105764938	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:105767004-105767243	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr14:105767925-105768011	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPD	chr14:105767067-105768002	HepG2	liver:	n/a	n/a
22	CEBPD	chr14:105767696-105767995	HepG2	liver:	n/a	n/a
23	CHD1	chr14:105766745-105767279	GM12878	blood:	n/a	n/a
24	CHD2	chr14:105766568-105766594	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr14:105766846-105767883	GM12878	blood:	n/a	n/a
26	CHD2	chr14:105766674-105767676	K562	blood:	n/a	n/a
27	CHD2	chr14:105766863-105767699	HepG2	liver:	n/a	n/a
28	CHD2	chr14:105766730-105768109	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr14:105766829-105767941	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr14:105767934-105767980	K562	blood:	n/a	n/a
31	CREB1	chr14:105767136-105768126	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr14:105766729-105768188	A549	lung:	n/a	n/a
33	CREB1	chr14:105766855-105767666	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr14:105767300-105767450	GM12868	blood:	n/a	n/a
35	CTCF	chr14:105767856-105768013	GM12878	blood:	n/a	chr14:105767899-105767912 chr14:105767899-105767908
36	CTCF	chr14:105766640-105766790	GM12873	blood:	n/a	chr14:105766762-105766775
37	CTCF	chr14:105766240-105766390	GM12873	blood:	n/a	n/a
38	CTCF	chr14:105767241-105767328	GM19238	blood:	n/a	n/a
39	CTCF	chr14:105767840-105767990	HUVEC	blood vessel:	n/a	chr14:105767899-105767912 chr14:105767899-105767908
40	CTCF	chr14:105767900-105768050	SAEC	small airway:	n/a	n/a
41	CTCF	chr14:105767283-105767411	GM12878	blood:	n/a	n/a
42	CTCF	chr14:105767180-105767330	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr14:105766826-105766952	GM19239	blood:	n/a	n/a
44	CTCF	chr14:105767840-105767990	GM12870	blood:	n/a	chr14:105767899-105767912 chr14:105767899-105767908
45	CTCF	chr14:105767195-105767414	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr14:105767873-105767956	K562	blood:	n/a	chr14:105767899-105767912 chr14:105767899-105767908
47	CTCF	chr14:105767220-105767370	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr14:105767260-105767410	AG04449	skin:	n/a	n/a
49	CTCF	chr14:105767268-105767337	GM12891	blood:	n/a	n/a
50	CTCF	chr14:105767180-105767330	HMEC	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	chr14:105768109-105768159	K562	blood:	n/a
2	chr14:105766991-105767041	A549	lung:	n/a
3	chr14:105766987-105767037	HPAEpiC	pulmonary alveolar:	n/a
4	chr14:105766987-105767037	AG04449	skin:	fetal
5	chr14:105767399-105767449	BJ	skin:	n/a
6	chr14:105767391-105767441	HCM	heart:	n/a
7	chr14:105766991-105767041	HNPCEpiC	eye:	n/a
8	chr14:105766346-105766396	Hepatocyte	liver:	n/a
9	chr14:105767882-105767932	HCT-116	colon:	n/a
10	chr14:105767399-105767449	HCT-116	colon:	n/a
11	chr14:105767520-105767570	MCF-7	breast:	n/a
12	chr14:105767399-105767449	BE2_C	brain:	n/a
13	chr14:105767882-105767932	PANC-1	pancreas:	n/a
14	chr14:105767639-105767689	HCF	heart:	n/a
15	chr14:105767391-105767441	AG09319	gingival:	n/a
16	chr14:105767391-105767441	Hepatocyte	liver:	n/a
17	chr14:105767391-105767441	PrEC	prostate:	n/a
18	chr14:105767882-105767932	GM12892	blood:	n/a
19	chr14:105768109-105768159	PANC-1	pancreas:	n/a
20	chr14:105767399-105767449	GM06990	blood:	n/a
21	chr14:105766987-105767037	HRE	kidney:	n/a
22	chr14:105767457-105767507	HepG2	liver:	n/a
23	chr14:105767399-105767449	HL-60	blood:	n/a
24	chr14:105767639-105767689	Jurkat	blood:	n/a
25	chr14:105767366-105767416	GM06990	blood:	n/a
26	chr14:105767399-105767449	SK-N-MC	brain:	n/a
27	chr14:105767409-105767459	HRE	kidney:	n/a
28	chr14:105767366-105767416	HUVEC	blood vessel:	n/a
29	chr14:105767882-105767932	HNPCEpiC	eye:	n/a
30	chr14:105767366-105767416	GM12891	blood:	n/a
31	chr14:105767639-105767689	MCF-7	breast:	n/a
32	chr14:105766991-105767041	AG09309	skin:	n/a
33	chr14:105767520-105767570	HNPCEpiC	eye:	n/a
34	chr14:105767409-105767459	Hepatocyte	liver:	n/a
35	chr14:105767457-105767507	PFSK-1	brain:	n/a
36	chr14:105767457-105767507	PrEC	prostate:	n/a
37	chr14:105766346-105766396	SK-N-MC	brain:	n/a
38	chr14:105767639-105767689	H1-hESC	embryonic stem cell:	embryo
39	chr14:105767520-105767570	HRE	kidney:	n/a
40	chr14:105766987-105767037	CMK	blood:	n/a
41	chr14:105766991-105767041	LNCaP	prostate:	n/a
42	chr14:105767639-105767689	AG04450	lung:	fetal
43	chr14:105767391-105767441	HRPEpiC	eye:	n/a
44	chr14:105767882-105767932	HEK293	kidney:	embryo
45	chr14:105767520-105767570	HCPEpiC	choroid plexus:	n/a
46	chr14:105767882-105767932	SAEC	small airway:	n/a
47	chr14:105767409-105767459	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:105767520-105767570	RPTEC	kidney:	n/a
49	chr14:105768109-105768159	GM19239	blood:	n/a
50	chr14:105768109-105768159	HCT-116	colon:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105765913..105767563-chr14:105954548..105956473,2	MCF-7	breast:
2	chr14:105757386..105760349-chr14:105763067..105764806,2	K562	blood:
3	chr14:105765347..105769450-chr14:105769470..105773842,3	K562	blood:
4	chr14:105760458..105762689-chr14:105764878..105766519,2	K562	blood:
5	chr14:105765347..105769263-chr14:105769470..105773685,4	K562	blood:
6	chr14:105767766..105768456-chr14:105800435..105801361,2	MCF-7	breast:
7	chr14:105265110..105267765-chr14:105766806..105769681,2	K562	blood:
8	chr14:105443928..105445902-chr14:105765680..105767557,2	MCF-7	breast:
9	chr14:105764841..105767262-chr14:105768886..105771341,2	MCF-7	breast:
10	chr14:105713902..105716022-chr14:105768956..105770763,2	MCF-7	breast:
11	chr14:105766401..105768254-chr14:105864654..105866501,3	MCF-7	breast:
12	chr14:23540375..23540895-chr14:105767305..105768183,2	HCT-116	colon:
13	chr14:105766164..105768024-chr14:105938486..105941026,2	MCF-7	breast:
14	chr14:105768384..105770510-chr14:105839259..105840826,2	MCF-7	breast:
15	chr14:105766490..105767158-chr17:41465540..41466173,2	Hela-S3	cervix:
16	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
17	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
18	chr14:105766778..105767468-chr16:88717407..88718073,2	Hela-S3	cervix:
19	chr14:105766350..105771356-chr14:105955110..105959126,6	MCF-7	breast:
20	chr1:144533618..144534203-chr14:105766994..105767831,2	Hela-S3	cervix:
21	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:

No data

Variant related genes	Relation type
PACS2	TF binding region
BRF1	TF binding region
PACS2	CpG island
BRF1	CpG island
ENSG00000179364	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000051523	chromatin interactions
ENSG00000257341	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000182809	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000100813	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 142 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:142 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587730912	chr14:105764739-105764740	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs587626499	chr14:105764764-105764765	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs370386255	chr14:105764767-105764768	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs150667876	chr14:105764768-105764769	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs370607916	chr14:105764787-105764788	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587636260	chr14:105764805-105764806	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs189748315	chr14:105764827-105764828	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs139217949	chr14:105764886-105764887	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs587637248	chr14:105764908-105764909	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs143127609	chr14:105764910-105764911	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs587617255	chr14:105764912-105764913	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs587675193	chr14:105764915-105764916	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs372692761	chr14:105764920-105764921	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs200842116	chr14:105764928-105764929	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs587662830	chr14:105764949-105764950	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs587764719	chr14:105764957-105764958	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs147479956	chr14:105765084-105765085	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs183063532	chr14:105765141-105765142	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587673665	chr14:105765185-105765186	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139903344	chr14:105765224-105765225	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587626609	chr14:105765230-105765231	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149983399	chr14:105765233-105765234	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10149942	chr14:105765256-105765257	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs587736596	chr14:105765352-105765353	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs587628848	chr14:105765367-105765368	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs187163417	chr14:105765403-105765404	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs587690086	chr14:105765410-105765411	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs112614447	chr14:105765417-105765418	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs192462037	chr14:105765427-105765428	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs10129522	chr14:105765440-105765441	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs183356581	chr14:105765445-105765446	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs386781136	chr14:105765457-105765458	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs10129527	chr14:105765459-105765460	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs144061492	chr14:105765502-105765503	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs72711563	chr14:105765522-105765523	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs188754597	chr14:105765601-105765602	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs191668480	chr14:105765632-105765633	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs370076031	chr14:105765662-105765663	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs376899851	chr14:105765671-105765672	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs587673219	chr14:105765679-105765680	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs182720861	chr14:105765683-105765684	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs146447556	chr14:105765731-105765732	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs75600103	chr14:105765764-105765765	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs61996223	chr14:105765813-105765814	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs587732298	chr14:105765879-105765880	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs186624077	chr14:105765931-105765932	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs587661680	chr14:105765975-105765976	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs587745442	chr14:105766064-105766065	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs150090391	chr14:105766104-105766105	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs371159407	chr14:105766147-105766148	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105715800-105766000	Weak transcription	Fetal Kidney	kidney
2	chr14:105739800-105765800	Weak transcription	NHEK	skin
3	chr14:105742200-105765600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr14:105742200-105765800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr14:105744600-105766000	Weak transcription	HSMMtube	muscle
6	chr14:105747000-105765600	Weak transcription	Colonic Mucosa	Colon
7	chr14:105747000-105766000	Weak transcription	Aorta	Aorta
8	chr14:105747200-105765600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr14:105748200-105765800	Weak transcription	HMEC	breast
10	chr14:105748600-105765800	Weak transcription	A549	lung
11	chr14:105749600-105766200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:105750800-105764800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:105753400-105766200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr14:105755800-105765600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:105759600-105766000	Weak transcription	Small Intestine	intestine
16	chr14:105759800-105765800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr14:105760000-105765800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr14:105760200-105765600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr14:105760800-105765400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr14:105760800-105765600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr14:105760800-105765800	Weak transcription	Psoas Muscle	Psoas
22	chr14:105760800-105765800	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr14:105760800-105766000	Weak transcription	HSMM	muscle
24	chr14:105760800-105766200	Weak transcription	Esophagus	oesophagus
25	chr14:105761000-105764800	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr14:105761000-105765400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr14:105761000-105765600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr14:105761000-105765600	Weak transcription	Liver	Liver
29	chr14:105761000-105765800	Weak transcription	Fetal Brain Male	brain
30	chr14:105761000-105765800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr14:105761000-105765800	Weak transcription	NH-A	brain
32	chr14:105761000-105766000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr14:105761000-105766000	Weak transcription	Gastric	stomach
34	chr14:105761000-105766200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr14:105761200-105765000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr14:105761200-105765600	Weak transcription	Fetal Brain Female	brain
37	chr14:105761200-105765600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr14:105761200-105765600	Weak transcription	Osteobl	bone
39	chr14:105761200-105765800	Weak transcription	Rectal Smooth Muscle	rectum
40	chr14:105761400-105765400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr14:105761400-105765800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr14:105761400-105765800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr14:105761400-105765800	Weak transcription	Brain Angular Gyrus	brain
44	chr14:105761400-105765800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr14:105761400-105765800	Weak transcription	Fetal Lung	lung
46	chr14:105761600-105765200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:105761600-105765200	Weak transcription	Brain Hippocampus Middle	brain
48	chr14:105761600-105765400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr14:105761600-105765600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr14:105761600-105765600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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