Variant report

Variant	esv1804302
Chromosome Location	chr1:179315357-179333194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:183)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:179332575-179332913	K562	blood:	n/a	n/a
2	ATF1	chr1:179332419-179332755	K562	blood:	n/a	n/a
3	BHLHE40	chr1:179332521-179332721	K562	blood:	n/a	n/a
4	CCNT2	chr1:179319665-179319857	K562	blood:	n/a	n/a
5	CEBPB	chr1:179321177-179321297	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:179316805-179317072	A549	lung:	n/a	chr1:179316934-179316945
7	CEBPB	chr1:179329778-179330058	HepG2	liver:	n/a	chr1:179329888-179329901
8	CEBPB	chr1:179316773-179317064	IMR90	lung:	n/a	chr1:179316934-179316945
9	CEBPB	chr1:179316765-179317078	HepG2	liver:	n/a	chr1:179316934-179316945
10	CTCF	chr1:179327970-179328026	Lung_OC	lung:	n/a	n/a
11	E2F4	chr1:179325379-179325573	MCF10A-Er-Src	breast:	n/a	n/a
12	EP300	chr1:179332413-179332796	K562	blood:	n/a	n/a
13	FOS	chr1:179320526-179320711	MCF10A-Er-Src	breast:	n/a	chr1:179320598-179320607
14	FOS	chr1:179322829-179322913	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr1:179322805-179323074	MCF10A-Er-Src	breast:	n/a	n/a
16	FOSL2	chr1:179322702-179323199	SK-N-SH	brain:	n/a	n/a
17	FOSL2	chr1:179322690-179322963	HepG2	liver:	n/a	n/a
18	GATA2	chr1:179332443-179332967	HUVEC	blood vessel:	n/a	n/a
19	IRF1	chr1:179332206-179332336	K562	blood:	n/a	n/a
20	JUN	chr1:179317027-179317145	K562	blood:	n/a	n/a
21	JUND	chr1:179322774-179323075	K562	blood:	n/a	chr1:179322895-179322906
22	JUND	chr1:179322747-179323031	HepG2	liver:	n/a	chr1:179322895-179322906
23	JUND	chr1:179332429-179332803	K562	blood:	n/a	n/a
24	JUND	chr1:179322870-179323060	H1-hESC	embryonic stem cell:	n/a	chr1:179322895-179322906
25	MAFK	chr1:179332585-179332723	K562	blood:	n/a	n/a
26	MAX	chr1:179332569-179332802	K562	blood:	n/a	n/a
27	MAX	chr1:179317045-179317054	NB4	blood:	n/a	n/a
28	MAZ	chr1:179332508-179332725	K562	blood:	n/a	n/a
29	MXI1	chr1:179322739-179322880	GM12878	blood:	n/a	n/a
30	MYC	chr1:179317068-179317084	H1-hESC	embryonic stem cell:	n/a	n/a
31	MYC	chr1:179332290-179332626	K562	blood:	n/a	n/a
32	NFIC	chr1:179317038-179317727	ECC-1	luminal epithelium:	n/a	chr1:179317382-179317398 chr1:179317382-179317399
33	NFIC	chr1:179317179-179317666	SK-N-SH	brain:	n/a	chr1:179317382-179317398 chr1:179317382-179317399
34	NFIC	chr1:179317177-179317636	ECC-1	luminal epithelium:	n/a	chr1:179317382-179317398 chr1:179317382-179317399
35	NR2F2	chr1:179332430-179332775	K562	blood:	n/a	n/a
36	PBX3	chr1:179322772-179323202	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr1:179326845-179326890	HepG2	liver:	n/a	n/a
38	POLR2A	chr1:179332512-179332817	K562	blood:	n/a	n/a
39	POLR2A	chr1:179329086-179329302	HepG2	liver:	n/a	n/a
40	POLR2A	chr1:179323168-179323411	K562	blood:	n/a	n/a
41	POLR2A	chr1:179326891-179326943	HepG2	liver:	n/a	n/a
42	POLR2A	chr1:179315572-179315716	GM12878	blood:	n/a	n/a
43	POLR2A	chr1:179330444-179330568	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr1:179331037-179331459	K562	blood:	n/a	n/a
45	POLR2A	chr1:179327924-179328083	K562	blood:	n/a	n/a
46	POLR2A	chr1:179324262-179324814	K562	blood:	n/a	n/a
47	POLR2A	chr1:179329529-179329556	HepG2	liver:	n/a	n/a
48	POLR2A	chr1:179324271-179324305	A549	lung:	n/a	n/a
49	POLR2A	chr1:179329353-179329476	GM12878	blood:	n/a	n/a
50	POLR2A	chr1:179328666-179328733	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:179324199-179324249	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:179332148-179332198	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:179322762-179322812	H1-hESC	embryonic stem cell:	embryo
4	chr1:179324199-179324249	HCT-116	colon:	n/a
5	chr1:179322762-179322812	NB4	blood:	n/a
6	chr1:179324199-179324249	HepG2	liver:	n/a
7	chr1:179324199-179324249	RPTEC	kidney:	n/a
8	chr1:179324199-179324249	BJ	skin:	n/a
9	chr1:179324199-179324249	PFSK-1	brain:	n/a
10	chr1:179322762-179322812	Jurkat	blood:	n/a
11	chr1:179324199-179324249	SK-N-SH	brain:	n/a
12	chr1:179332148-179332198	GM19239	blood:	n/a
13	chr1:179322762-179322812	NT2-D1	testis:	n/a
14	chr1:179322762-179322812	HRPEpiC	eye:	n/a
15	chr1:179322762-179322812	HL-60	blood:	n/a
16	chr1:179322762-179322812	SK-N-MC	brain:	n/a
17	chr1:179322762-179322812	HEEpiC	esophagus:	n/a
18	chr1:179324199-179324249	SKMC	muscle:	n/a
19	chr1:179324199-179324249	PrEC	prostate:	n/a
20	chr1:179324199-179324249	SK-N-MC	brain:	n/a
21	chr1:179322762-179322812	Hepatocyte	liver:	n/a
22	chr1:179324199-179324249	CMK	blood:	n/a
23	chr1:179324199-179324249	Jurkat	blood:	n/a
24	chr1:179324199-179324249	NB4	blood:	n/a
25	chr1:179322762-179322812	ovcar-3	ovarian:	n/a
26	chr1:179324199-179324249	AG04450	lung:	fetal
27	chr1:179332148-179332198	GM12891	blood:	n/a
28	chr1:179324199-179324249	IMR90	lung:	fetal
29	chr1:179324199-179324249	NH-A	brain:	n/a
30	chr1:179332148-179332198	NT2-D1	testis:	n/a
31	chr1:179332148-179332198	AG09319	gingival:	n/a
32	chr1:179332148-179332198	SK-N-SH	brain:	n/a
33	chr1:179322762-179322812	HNPCEpiC	eye:	n/a
34	chr1:179324199-179324249	T-47D	breast:	n/a
35	chr1:179324199-179324249	HIPEpiC	eye:	n/a
36	chr1:179322762-179322812	U87	brain:	n/a
37	chr1:179324199-179324249	NT2-D1	testis:	n/a
38	chr1:179332148-179332198	Caco-2	colon:	n/a
39	chr1:179322762-179322812	NHDF-neo	bronchial:	n/a
40	chr1:179332148-179332198	HAEpiC	amniotic membrane:	n/a
41	chr1:179332148-179332198	K562	blood:	n/a
42	chr1:179332148-179332198	MCF-7	breast:	n/a
43	chr1:179324199-179324249	SAEC	small airway:	n/a
44	chr1:179324199-179324249	ECC-1	luminal epithelium:	n/a
45	chr1:179324199-179324249	H1-hESC	embryonic stem cell:	embryo
46	chr1:179324199-179324249	BE2_C	brain:	n/a
47	chr1:179322762-179322812	HCPEpiC	choroid plexus:	n/a
48	chr1:179324199-179324249	HUVEC	blood vessel:	n/a
49	chr1:179332148-179332198	RPTEC	kidney:	n/a
50	chr1:179322762-179322812	MCF10A-Er-Src	breast:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:179329907..179332888-chr1:179333300..179336235,2	MCF-7	breast:
2	chr1:179315802..179317742-chr1:179327309..179329268,2	K562	blood:
3	chr1:179049229..179051266-chr1:179328606..179330148,2	MCF-7	breast:
4	chr1:179048972..179052099-chr1:179331450..179336701,5	MCF-7	breast:
5	chr1:179311628..179313681-chr1:179315946..179318351,2	K562	blood:
6	chr1:179319158..179320695-chr1:179327831..179330357,2	K562	blood:
7	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
8	chr1:179316253..179318749-chr1:179321719..179323631,3	MCF-7	breast:
9	chr1:179317813..179320620-chr1:179325439..179328200,3	MCF-7	breast:
10	chr1:179330939..179332441-chr1:179334465..179336040,2	MCF-7	breast:
11	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:
12	chr1:179324764..179330437-chr1:179332106..179336685,6	K562	blood:
13	chr1:179050571..179052997-chr1:179322581..179325112,2	MCF-7	breast:
14	chr1:179321788..179324308-chr1:179333616..179335747,3	MCF-7	breast:
15	chr1:179303201..179305368-chr1:179327214..179329206,2	MCF-7	breast:
16	chr1:179319158..179320695-chr1:179327831..179330357,2	K562	blood:
17	chr1:179261912..179264467-chr1:179313942..179316618,2	MCF-7	breast:
18	chr1:179323629..179325492-chr1:179329945..179332466,2	MCF-7	breast:
19	chr1:179319218..179322738-chr1:179324103..179326545,3	K562	blood:
20	chr1:179316253..179318749-chr1:179321719..179323631,3	MCF-7	breast:
21	chr1:179319218..179322738-chr1:179324103..179326545,3	K562	blood:
22	chr1:179317813..179319571-chr1:179319821..179322785,2	K562	blood:
23	chr1:179315825..179319571-chr1:179319821..179322785,4	K562	blood:
24	chr1:179314011..179316743-chr1:179317198..179320043,2	K562	blood:
25	chr1:179325938..179328666-chr1:179330165..179332477,2	K562	blood:
26	chr1:179315802..179317742-chr1:179327309..179329268,2	K562	blood:
27	chr1:179314011..179316743-chr1:179317198..179320043,2	K562	blood:
28	chr1:179317813..179319571-chr1:179319821..179322785,2	K562	blood:
29	chr1:179315825..179319571-chr1:179319821..179322785,4	K562	blood:
30	chr1:179332952..179336574-chr1:179337996..179342859,7	MCF-7	breast:
31	chr1:179317813..179320620-chr1:179325439..179328200,3	MCF-7	breast:

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SOAT1	hsa-miR-215-5p	chr1:179323373-179323394
2	SOAT1	hsa-miR-192-5p	chr1:179323550-179323571
3	SOAT1	hsa-miR-192-5p	chr1:179323373-179323394
4	SOAT1	hsa-miR-215-5p	chr1:179323550-179323571
5	SOAT1	hsa-miR-192-5p	chr1:179322901-179322921
6	SOAT1	hsa-miR-215-5p	chr1:179322901-179322921

Variant related genes	Relation type
RN7SL374P	TF binding region
AXDND1	TF binding region
RN7SL374P	CpG island
AXDND1	CpG island
ENSG00000057252	chromatin interactions
ENSG00000263633	chromatin interactions
ENSG00000186283	chromatin interactions
ENSG00000162779	chromatin interactions

Extended variants
information (count: 714 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2152319	chr1:179315357-179315358	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370852720	chr1:179315361-179315362	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562716413	chr1:179315503-179315504	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531393410	chr1:179315545-179315546	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551684441	chr1:179315623-179315624	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs117692771	chr1:179315672-179315673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs547040776	chr1:179315718-179315719	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs533800481	chr1:179315727-179315728	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7518843	chr1:179315738-179315739	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs567026556	chr1:179315760-179315761	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs10913731	chr1:179315785-179315786	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs548581634	chr1:179315821-179315822	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs75564783	chr1:179315824-179315825	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182518549	chr1:179315837-179315838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs4421551	chr1:179315898-179315899	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs558446329	chr1:179315914-179315915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs578161881	chr1:179315917-179315918	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540629781	chr1:179315940-179315941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs61824390	chr1:179316038-179316039	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560478362	chr1:179316045-179316046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547184610	chr1:179316115-179316116	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34556778	chr1:179316125-179316126	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186478464	chr1:179316127-179316128	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565822942	chr1:179316131-179316132	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536104576	chr1:179316135-179316136	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554896875	chr1:179316175-179316176	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570001290	chr1:179316232-179316233	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189727888	chr1:179316238-179316239	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs531558889	chr1:179316262-179316263	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551255481	chr1:179316286-179316287	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565196311	chr1:179316296-179316297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs6425535	chr1:179316320-179316321	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs547288922	chr1:179316321-179316322	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537423279	chr1:179316343-179316344	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112547742	chr1:179316345-179316346	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs10913732	chr1:179316367-179316368	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs149824358	chr1:179316447-179316448	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569622028	chr1:179316449-179316450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538447949	chr1:179316466-179316467	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs375127277	chr1:179316492-179316493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564415417	chr1:179316499-179316500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs57499931	chr1:179316509-179316510	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs397944528	chr1:179316510-179316511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs578198230	chr1:179316511-179316512	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs534541922	chr1:179316532-179316533	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554493697	chr1:179316549-179316550	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376653418	chr1:179316558-179316559	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs34159787	chr1:179316637-179316638	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574113617	chr1:179316663-179316664	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543017354	chr1:179316686-179316687	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179264800-179334200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:179266400-179322800	Weak transcription	Small Intestine	intestine
3	chr1:179292400-179328000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:179293000-179322600	Weak transcription	Fetal Heart	heart
5	chr1:179294200-179324600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:179296800-179327800	Weak transcription	Colonic Mucosa	Colon
7	chr1:179297400-179321600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:179298600-179324200	Weak transcription	Thymus	Thymus
9	chr1:179299400-179316800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr1:179300400-179334600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:179300600-179322400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:179301800-179322800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr1:179303200-179324600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr1:179303400-179322600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:179304200-179316000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr1:179304200-179316600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:179304200-179320000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr1:179304200-179324400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:179304200-179324400	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr1:179304200-179324600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:179304200-179325200	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr1:179304400-179318400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr1:179304400-179324400	Strong transcription	Primary T helper cells PMA-I stimulated	--
24	chr1:179304600-179316000	Strong transcription	Hela-S3	cervix
25	chr1:179304600-179324200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr1:179305200-179315800	Weak transcription	Brain Germinal Matrix	brain
27	chr1:179305200-179327200	Weak transcription	Right Ventricle	heart
28	chr1:179305600-179334200	Weak transcription	Pancreas	Pancrea
29	chr1:179305800-179322600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr1:179306000-179321000	Strong transcription	Dnd41	blood
31	chr1:179306800-179324600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:179307200-179316800	Strong transcription	Adipose Nuclei	Adipose
33	chr1:179307400-179325800	Weak transcription	Esophagus	oesophagus
34	chr1:179307600-179322600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:179307600-179325200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:179307800-179322200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:179308000-179321000	Weak transcription	Fetal Brain Male	brain
38	chr1:179308000-179324400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:179308400-179316000	Strong transcription	Stomach Smooth Muscle	stomach
40	chr1:179308400-179322600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr1:179308600-179316000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr1:179308600-179316400	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr1:179308600-179318000	Strong transcription	Fetal Intestine Large	intestine
44	chr1:179308600-179322000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:179308800-179318000	Strong transcription	Fetal Muscle Leg	muscle
46	chr1:179308800-179320800	Strong transcription	Osteobl	bone
47	chr1:179309800-179326400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr1:179310000-179325200	Strong transcription	Primary T cells from cord blood	blood
49	chr1:179310200-179322000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:179310200-179323000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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