Variant report

Variant	nsv946405
Chromosome Location	chr1:154179146-154180987
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:79)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:79 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MTA3	chr1:154178396-154179155	GM12878	blood:	n/a	n/a
2	POLR2A	chr1:154179911-154180047	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr1:154180810-154180987	HepG2	liver:	n/a	n/a
4	POLR2A	chr1:154179265-154179746	HepG2	liver:	n/a	n/a
5	POLR2A	chr1:154179157-154179855	PFSK-1	brain:	n/a	n/a
6	POLR2A	chr1:154180961-154180987	HUVEC	blood vessel:	n/a	n/a
7	POLR2A	chr1:154180718-154180912	GM12878	blood:	n/a	n/a
8	POLR2A	chr1:154179966-154180117	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr1:154179687-154179852	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr1:154178597-154179571	HepG2	liver:	n/a	n/a
11	POLR2A	chr1:154180613-154181008	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr1:154179240-154179676	PFSK-1	brain:	n/a	n/a
13	POLR2A	chr1:154180506-154181103	K562	blood:	n/a	n/a
14	POLR2A	chr1:154177962-154183356	HepG2	liver:	n/a	n/a
15	POLR2A	chr1:154180682-154180985	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr1:154178406-154179223	GM12892	blood:	n/a	n/a
17	POLR2A	chr1:154180661-154181079	MCF-7	breast:	n/a	n/a
18	POLR2A	chr1:154180616-154181143	GM12892	blood:	n/a	n/a
19	POLR2A	chr1:154178423-154179175	GM12891	blood:	n/a	n/a
20	POLR2A	chr1:154178394-154179174	K562	blood:	n/a	n/a
21	POLR2A	chr1:154179311-154179755	K562	blood:	n/a	n/a
22	POLR2A	chr1:154180631-154181230	K562	blood:	n/a	n/a
23	POLR2A	chr1:154179246-154179587	PANC-1	pancreas:	n/a	n/a
24	POLR2A	chr1:154179895-154180044	ProgFib	skin:	n/a	n/a
25	POLR2A	chr1:154179498-154179613	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr1:154178847-154179195	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr1:154177690-154179164	SK-N-MC	brain:	n/a	n/a
28	POLR2A	chr1:154178395-154179192	SK-N-SH	brain:	n/a	n/a
29	POLR2A	chr1:154179824-154179894	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr1:154180486-154181075	GM12878	blood:	n/a	n/a
31	POLR2A	chr1:154180968-154181119	GM12878	blood:	n/a	n/a
32	POLR2A	chr1:154178527-154179162	GM12891	blood:	n/a	n/a
33	POLR2A	chr1:154180847-154181182	A549	lung:	n/a	n/a
34	POLR2A	chr1:154180813-154180853	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr1:154180776-154180811	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr1:154179635-154179641	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr1:154177691-154180265	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr1:154180987-154181020	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr1:154178446-154179245	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr1:154178386-154179158	HCT-116	colon:	n/a	n/a
41	POLR2A	chr1:154180643-154180995	GM12891	blood:	n/a	n/a
42	POLR2A	chr1:154179821-154180280	HepG2	liver:	n/a	n/a
43	POLR2A	chr1:154179246-154179581	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr1:154178290-154179147	PFSK-1	brain:	n/a	n/a
45	POLR2A	chr1:154178394-154179163	MCF-7	breast:	n/a	n/a
46	POLR2A	chr1:154178371-154179191	U87	brain:	n/a	n/a
47	POLR2A	chr1:154178649-154179225	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr1:154179772-154180210	K562	blood:	n/a	n/a
49	POLR2A	chr1:154180052-154180251	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr1:154179671-154179742	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:154179861-154179911	HIPEpiC	eye:	n/a
2	chr1:154179996-154180046	K562	blood:	n/a
3	chr1:154179861-154179911	HepG2	liver:	n/a
4	chr1:154179856-154179906	A549	lung:	n/a
5	chr1:154179856-154179906	Hepatocyte	liver:	n/a
6	chr1:154179996-154180046	HepG2	liver:	n/a
7	chr1:154179996-154180046	Caco-2	colon:	n/a
8	chr1:154179996-154180046	SKMC	muscle:	n/a
9	chr1:154179996-154180046	AoSMC	blood vessel:	n/a
10	chr1:154179856-154179906	HUVEC	blood vessel:	n/a
11	chr1:154179996-154180046	SK-N-MC	brain:	n/a
12	chr1:154179856-154179906	H1-hESC	embryonic stem cell:	embryo
13	chr1:154179861-154179911	SK-N-SH_RA	brain:	n/a
14	chr1:154179861-154179911	MCF-7	breast:	n/a
15	chr1:154179856-154179906	BJ	skin:	n/a
16	chr1:154179861-154179911	U87	brain:	n/a
17	chr1:154179861-154179911	GM12892	blood:	n/a
18	chr1:154179996-154180046	NHBE	bronchial:	n/a
19	chr1:154179996-154180046	HEEpiC	esophagus:	n/a
20	chr1:154179861-154179911	PFSK-1	brain:	n/a
21	chr1:154179856-154179906	HEEpiC	esophagus:	n/a
22	chr1:154179861-154179911	ECC-1	luminal epithelium:	n/a
23	chr1:154179996-154180046	HCF	heart:	n/a
24	chr1:154179856-154179906	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:154179861-154179911	H1-hESC	embryonic stem cell:	embryo
26	chr1:154179996-154180046	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:154179996-154180046	GM12878	blood:	n/a
28	chr1:154179856-154179906	ProgFib	skin:	n/a
29	chr1:154179861-154179911	AG09319	gingival:	n/a
30	chr1:154179861-154179911	LNCaP	prostate:	n/a
31	chr1:154179856-154179906	CMK	blood:	n/a
32	chr1:154179996-154180046	SK-N-SH	brain:	n/a
33	chr1:154179861-154179911	AG09309	skin:	n/a
34	chr1:154179996-154180046	AG09309	skin:	n/a
35	chr1:154179856-154179906	HIPEpiC	eye:	n/a
36	chr1:154179856-154179906	Caco-2	colon:	n/a
37	chr1:154179861-154179911	HRCEpiC	kidney:	n/a
38	chr1:154179996-154180046	HRE	kidney:	n/a
39	chr1:154179996-154180046	PrEC	prostate:	n/a
40	chr1:154179861-154179911	IMR90	lung:	fetal
41	chr1:154179861-154179911	T-47D	breast:	n/a
42	chr1:154179996-154180046	HCM	heart:	n/a
43	chr1:154179856-154179906	HRPEpiC	eye:	n/a
44	chr1:154179996-154180046	SK-N-SH_RA	brain:	n/a
45	chr1:154179861-154179911	AG04449	skin:	fetal
46	chr1:154179861-154179911	HCM	heart:	n/a
47	chr1:154179856-154179906	GM12892	blood:	n/a
48	chr1:154179861-154179911	ProgFib	skin:	n/a
49	chr1:154179861-154179911	GM12878	blood:	n/a
50	chr1:154179861-154179911	HCT-116	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:154164207..154166951-chr1:154178142..154180976,3	K562	blood:
2	chr1:154178712..154180249-chr1:154186169..154187712,2	MCF-7	breast:
3	chr1:154164207..154166650-chr1:154177801..154180976,3	K562	blood:
4	chr1:154177747..154182716-chr1:154190412..154196946,9	K562	blood:
5	chr1:154179575..154184047-chr1:154184381..154189147,7	K562	blood:
6	chr1:154179244..154180954-chr1:154181456..154183378,2	K562	blood:
7	chr1:154152910..154155985-chr1:154176488..154179732,3	K562	blood:
8	chr1:154153345..154155827-chr1:154177952..154179974,2	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	C1orf43	hsa-miR-340-5p	chr1:154179230-154179248
2	C1orf43	hsa-miR-296-3p	chr1:154179752-154179773
3	C1orf43	hsa-miR-340-5p	chr1:154179236-154179229

Variant related genes	Relation type
C1orf189	TF binding region
C1orf189	CpG island
ENSG00000215938	chromatin interactions
ENSG00000143612	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000143569	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578114275	chr1:154179146-154179147	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs115866336	chr1:154179194-154179195	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs41315565	chr1:154179230-154179231	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region miRNA target site	6 gene(s)	Overlapped CNVs	n/a
4	rs114552165	chr1:154179289-154179290	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs565801042	chr1:154179294-154179295	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs11547687	chr1:154179485-154179486	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs1128829	chr1:154179556-154179557	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs376203360	chr1:154179624-154179625	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs182391693	chr1:154179628-154179629	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs528861348	chr1:154179649-154179650	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs6719	chr1:154179679-154179680	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs371507833	chr1:154179726-154179727	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs113836745	chr1:154179731-154179732	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs559448599	chr1:154179741-154179742	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs368962986	chr1:154179781-154179782	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs187831459	chr1:154179804-154179805	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs372265049	chr1:154179805-154179806	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs145273762	chr1:154179813-154179814	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs57651556	chr1:154179827-154179828	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs376331077	chr1:154179856-154179857	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs56900557	chr1:154179866-154179867	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs139844682	chr1:154179874-154179875	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs371479727	chr1:154179891-154179892	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs74538949	chr1:154179901-154179902	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs577581738	chr1:154179908-154179909	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs534655057	chr1:154179926-154179927	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs375042634	chr1:154179927-154179928	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs553061978	chr1:154179956-154179957	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs571707767	chr1:154179990-154179991	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs201312652	chr1:154179997-154179998	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs11555361	chr1:154180004-154180005	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs369497079	chr1:154180019-154180020	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs538914112	chr1:154180041-154180042	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs551487853	chr1:154180051-154180052	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs192687503	chr1:154180052-154180053	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs145364215	chr1:154180085-154180086	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs375236035	chr1:154180137-154180138	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs200974971	chr1:154180149-154180150	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs573686994	chr1:154180151-154180152	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs541016783	chr1:154180163-154180164	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs145214426	chr1:154180177-154180178	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs149159453	chr1:154180196-154180197	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs371835705	chr1:154180198-154180199	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs111579891	chr1:154180210-154180211	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs369816420	chr1:154180290-154180291	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs112347473	chr1:154180302-154180303	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs184825922	chr1:154180314-154180315	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs530589965	chr1:154180355-154180356	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs187626662	chr1:154180375-154180376	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs567185193	chr1:154180394-154180395	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	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
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154159000-154184400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:154172000-154180600	Weak transcription	Small Intestine	intestine
3	chr1:154172000-154184600	Weak transcription	Fetal Brain Male	brain
4	chr1:154172200-154184200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:154172200-154190000	Weak transcription	Fetal Heart	heart
6	chr1:154172400-154184600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr1:154172600-154179400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:154176400-154179800	Weak transcription	Right Ventricle	heart
9	chr1:154177000-154191000	Strong transcription	Fetal Stomach	stomach
10	chr1:154177000-154192000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:154177200-154180200	Strong transcription	Colon Smooth Muscle	Colon
12	chr1:154177200-154187200	Strong transcription	Brain Hippocampus Middle	brain
13	chr1:154177200-154187400	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr1:154177200-154187600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:154177200-154190200	Strong transcription	Primary T cells from cord blood	blood
16	chr1:154177400-154190400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr1:154177600-154181000	Strong transcription	Brain Cingulate Gyrus	brain
18	chr1:154177600-154184600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:154177600-154184800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:154177600-154187000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:154177600-154187000	Strong transcription	Adipose Nuclei	Adipose
22	chr1:154177600-154187000	Strong transcription	Fetal Brain Female	brain
23	chr1:154177600-154187200	Strong transcription	Sigmoid Colon	Sigmoid Colon
24	chr1:154177600-154187400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr1:154177600-154187400	Strong transcription	Fetal Thymus	thymus
26	chr1:154177600-154191400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:154177800-154180200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
28	chr1:154177800-154185600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:154177800-154185800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr1:154177800-154186000	Strong transcription	A549	lung
31	chr1:154177800-154186200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:154177800-154186800	Strong transcription	Liver	Liver
33	chr1:154177800-154187200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr1:154177800-154187200	Strong transcription	Primary monocytes fromperipheralblood	blood
35	chr1:154177800-154187200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr1:154177800-154187200	Strong transcription	Brain Substantia Nigra	brain
37	chr1:154177800-154187200	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr1:154177800-154187200	Strong transcription	Stomach Smooth Muscle	stomach
39	chr1:154177800-154187400	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr1:154177800-154187400	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr1:154177800-154187400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr1:154177800-154187400	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr1:154177800-154187400	Strong transcription	Fetal Intestine Large	intestine
44	chr1:154177800-154187600	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr1:154177800-154188000	Strong transcription	Fetal Muscle Trunk	muscle
46	chr1:154177800-154190400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:154177800-154190600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:154177800-154190600	Strong transcription	Fetal Intestine Small	intestine
49	chr1:154177800-154191000	Strong transcription	Fetal Muscle Leg	muscle
50	chr1:154177800-154191400	Strong transcription	Placenta	Placenta

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