Variant report

Variant	esv2761654
Chromosome Location	chr1:146750270-146809156
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:300)
CpG islands
(count:245)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:146758781-146759150	IMR90	lung:	n/a	chr1:146758970-146758981
2	CEBPB	chr1:146792919-146793071	A549	lung:	n/a	n/a
3	CEBPB	chr1:146756494-146756708	HepG2	liver:	n/a	chr1:146756597-146756608
4	CEBPB	chr1:146776093-146776292	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:146774059-146774335	K562	blood:	n/a	chr1:146774175-146774186
6	CEBPB	chr1:146774158-146774237	H1-hESC	embryonic stem cell:	n/a	chr1:146774175-146774186
7	CEBPB	chr1:146774017-146774358	HepG2	liver:	n/a	chr1:146774175-146774186
8	CEBPB	chr1:146774019-146774307	A549	lung:	n/a	chr1:146774175-146774186
9	CEBPB	chr1:146774011-146774354	IMR90	lung:	n/a	chr1:146774175-146774186
10	CEBPB	chr1:146801401-146801445	A549	lung:	n/a	n/a
11	CEBPB	chr1:146758822-146759113	K562	blood:	n/a	chr1:146758970-146758981
12	CEBPB	chr1:146758798-146759137	HepG2	liver:	n/a	chr1:146758970-146758981
13	CEBPB	chr1:146763673-146764967	IMR90	lung:	n/a	n/a
14	CHD1	chr1:146808199-146808588	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr1:146808807-146809266	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr1:146773328-146773534	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr1:146774219-146774483	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr1:146776706-146776779	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr1:146775472-146775477	HepG2	liver:	n/a	n/a
20	CHD2	chr1:146786721-146786945	K562	blood:	n/a	n/a
21	CTCF	chr1:146764200-146764350	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr1:146800420-146800525	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr1:146764280-146764430	HPF	lung:	n/a	n/a
24	CTCF	chr1:146764300-146764450	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr1:146761980-146762130	GM12864	blood:	n/a	n/a
26	CTCF	chr1:146788688-146788979	GM12878	blood:	n/a	n/a
27	CTCF	chr1:146764280-146764430	HCFaa	heart:	n/a	n/a
28	CTCF	chr1:146764140-146764290	HMF	breast:	n/a	n/a
29	CTCF	chr1:146764180-146764330	AG04450	lung:	n/a	n/a
30	CTCF	chr1:146764300-146764450	AG04450	lung:	n/a	n/a
31	CTCF	chr1:146764240-146764390	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr1:146787957-146788052	ProgFib	skin:	n/a	n/a
33	CTCF	chr1:146769555-146769589	LNCaP	prostate:	n/a	n/a
34	CTCF	chr1:146764220-146764370	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr1:146764020-146764310	HVMF	connective:	n/a	n/a
36	CTCF	chr1:146800183-146800279	LNCaP	prostate:	n/a	n/a
37	CTCF	chr1:146790263-146790293	Kidney_OC	kidney:	n/a	n/a
38	E2F4	chr1:146763753-146764054	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr1:146766466-146766570	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr1:146774743-146775019	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F6	chr1:146769610-146770152	H1-hESC	embryonic stem cell:	n/a	n/a
42	E2F6	chr1:146773282-146773628	H1-hESC	embryonic stem cell:	n/a	n/a
43	E2F6	chr1:146770564-146770735	K562	blood:	n/a	n/a
44	E2F6	chr1:146770387-146771093	H1-hESC	embryonic stem cell:	n/a	n/a
45	E2F6	chr1:146772133-146772728	H1-hESC	embryonic stem cell:	n/a	n/a
46	E2F6	chr1:146771218-146771596	H1-hESC	embryonic stem cell:	n/a	n/a
47	ELK1	chr1:146774473-146774542	GM12878	blood:	n/a	n/a
48	EP300	chr1:146808705-146809121	H1-hESC	embryonic stem cell:	n/a	n/a
49	EP300	chr1:146772289-146772295	GM12878	blood:	n/a	n/a
50	EP300	chr1:146808814-146809203	H1-hESC	embryonic stem cell:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146752298-146752348	NHBE	bronchial:	n/a
2	chr1:146752298-146752348	NHBE	bronchial:	n/a
3	chr1:146752023-146752073	SKMC	muscle:	n/a
4	chr1:146763914-146763964	HIPEpiC	eye:	n/a
5	chr1:146763914-146763964	H1-hESC	embryonic stem cell:	embryo
6	chr1:146752298-146752348	HEEpiC	esophagus:	n/a
7	chr1:146763914-146763964	NB4	blood:	n/a
8	chr1:146752298-146752348	AG04450	lung:	fetal
9	chr1:146763914-146763964	ProgFib	skin:	n/a
10	chr1:146752298-146752348	Hela-S3	cervix:	n/a
11	chr1:146807706-146807756	LNCaP	prostate:	n/a
12	chr1:146752023-146752073	HMEC	breast:	n/a
13	chr1:146752298-146752348	CMK	blood:	n/a
14	chr1:146752023-146752073	SK-N-MC	brain:	n/a
15	chr1:146752298-146752348	SK-N-SH	brain:	n/a
16	chr1:146752023-146752073	H1-hESC	embryonic stem cell:	embryo
17	chr1:146752298-146752348	T-47D	breast:	n/a
18	chr1:146752023-146752073	Hela-S3	cervix:	n/a
19	chr1:146807706-146807756	IMR90	lung:	fetal
20	chr1:146807706-146807756	AoSMC	blood vessel:	n/a
21	chr1:146752298-146752348	HCM	heart:	n/a
22	chr1:146807706-146807756	U87	brain:	n/a
23	chr1:146763914-146763964	Hela-S3	cervix:	n/a
24	chr1:146807706-146807756	HRPEpiC	eye:	n/a
25	chr1:146807706-146807756	SK-N-SH_RA	brain:	n/a
26	chr1:146807706-146807756	ovcar-3	ovarian:	n/a
27	chr1:146807706-146807756	HCPEpiC	choroid plexus:	n/a
28	chr1:146752023-146752073	AG09309	skin:	n/a
29	chr1:146763914-146763964	K562	blood:	n/a
30	chr1:146752298-146752348	BJ	skin:	n/a
31	chr1:146763914-146763964	NHDF-neo	bronchial:	n/a
32	chr1:146763914-146763964	SK-N-SH	brain:	n/a
33	chr1:146752298-146752348	GM12892	blood:	n/a
34	chr1:146752023-146752073	AG04450	lung:	fetal
35	chr1:146763914-146763964	AG09309	skin:	n/a
36	chr1:146763914-146763964	PANC-1	pancreas:	n/a
37	chr1:146752023-146752073	SK-N-SH	brain:	n/a
38	chr1:146807706-146807756	NT2-D1	testis:	n/a
39	chr1:146752298-146752348	SKMC	muscle:	n/a
40	chr1:146807706-146807756	Hepatocyte	liver:	n/a
41	chr1:146752298-146752348	HMEC	breast:	n/a
42	chr1:146752298-146752348	SAEC	small airway:	n/a
43	chr1:146752298-146752348	HIPEpiC	eye:	n/a
44	chr1:146752023-146752073	ECC-1	luminal epithelium:	n/a
45	chr1:146752298-146752348	LNCaP	prostate:	n/a
46	chr1:146752298-146752348	HRCEpiC	kidney:	n/a
47	chr1:146752298-146752348	H1-hESC	embryonic stem cell:	embryo
48	chr1:146752023-146752073	HCM	heart:	n/a
49	chr1:146807706-146807756	HRE	kidney:	n/a
50	chr1:146807706-146807756	GM06990	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
2	chr1:146753383..146755303-chr1:146758053..146759646,2	K562	blood:
3	chr1:146763180..146767980-chr1:146768468..146771849,4	MCF-7	breast:
4	chr1:146763180..146767980-chr1:146768468..146771849,4	MCF-7	breast:
5	chr1:146763219..146764772-chr1:146768463..146770035,2	MCF-7	breast:
6	chr1:146745634..146748931-chr1:146749215..146752140,3	K562	blood:
7	chr1:146746583..146748653-chr1:146752642..146755229,2	MCF-7	breast:
8	chr1:146753383..146755303-chr1:146758053..146759646,2	K562	blood:
9	chr1:146755140..146757255-chr1:146757615..146760362,2	MCF-7	breast:
10	chr1:146806520..146809758-chr1:146812607..146814433,3	K562	blood:
11	chr1:146752819..146753526-chr3:188313999..188314743,2	MCF-7	breast:
12	chr1:146763219..146764772-chr1:146768463..146770035,2	MCF-7	breast:
13	chr1:146751820..146755719-chr1:146756537..146760852,5	K562	blood:
14	chr1:146755140..146757255-chr1:146757615..146760362,2	MCF-7	breast:
15	chr1:146799000..146801299-chr1:146802761..146804812,2	K562	blood:
16	chr1:146749992..146752586-chr1:146753605..146755540,2	K562	blood:
17	chr1:146749992..146752586-chr1:146753605..146755540,2	K562	blood:
18	chr1:146751820..146755719-chr1:146756537..146760852,5	K562	blood:
19	chr1:146746161..146747922-chr1:146749349..146752441,4	MCF-7	breast:
20	chr1:146785986..146788702-chr1:146789697..146791855,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHD1L-1	chr1:146767170-146767458	NONHSAT006031

No data

Variant related genes	Relation type
ENSG00000213226	TF binding region
ENSG00000213226	CpG island
ENSG00000213226	chromatin interactions

Extended variants
information (count: 1793 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:1793 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12403141	chr1:146750270-146750271	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587674826	chr1:146750287-146750288	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191208908	chr1:146750303-146750304	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183463233	chr1:146750316-146750317	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12404113	chr1:146750343-146750344	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs587701635	chr1:146750369-146750370	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587608158	chr1:146750396-146750397	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370878753	chr1:146750454-146750455	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587663432	chr1:146750519-146750520	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587738913	chr1:146750532-146750533	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373915904	chr1:146750535-146750536	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587665765	chr1:146750563-146750564	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138439903	chr1:146750583-146750584	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587627019	chr1:146750604-146750605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587690465	chr1:146750606-146750607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587769738	chr1:146750610-146750611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79833764	chr1:146750677-146750678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587719658	chr1:146750683-146750684	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587772513	chr1:146750706-146750707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6683839	chr1:146750727-146750728	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs187945843	chr1:146750774-146750775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587753014	chr1:146750827-146750828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142949899	chr1:146750830-146750831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587708668	chr1:146750871-146750872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs193189157	chr1:146750880-146750881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185091254	chr1:146750932-146750933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187976887	chr1:146750976-146750977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587597107	chr1:146751028-146751029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587677981	chr1:146751067-146751068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375457516	chr1:146751083-146751084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587612186	chr1:146751104-146751105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587661921	chr1:146751108-146751109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs6694347	chr1:146751140-146751141	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs587639658	chr1:146751165-146751166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587721256	chr1:146751202-146751203	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372211356	chr1:146751226-146751227	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs80290435	chr1:146751253-146751254	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192401631	chr1:146751270-146751271	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10793656	chr1:146751272-146751273	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs74121885	chr1:146751333-146751334	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs587681787	chr1:146751353-146751354	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150702709	chr1:146751392-146751393	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17360443	chr1:146751410-146751411	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs376964935	chr1:146751414-146751415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587724645	chr1:146751418-146751419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587602513	chr1:146751441-146751442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587651238	chr1:146751479-146751480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587714691	chr1:146751486-146751487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587603969	chr1:146751489-146751490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587664863	chr1:146751521-146751522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:157)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	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
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	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
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	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
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	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
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Pancreatic cancer	17952125	CNVD
Lung squamous cell carcinoma	20842114	CNVD

Chromatin state (count:810 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146715800-146756800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:146717200-146751000	Weak transcription	Gastric	stomach
3	chr1:146719400-146757600	Weak transcription	Stomach Mucosa	stomach
4	chr1:146722800-146769800	Strong transcription	Dnd41	blood
5	chr1:146723800-146761200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:146723800-146763200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr1:146724200-146769800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr1:146726600-146769600	Strong transcription	Primary T helper cells PMA-I stimulated	--
9	chr1:146727000-146770000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:146727200-146754200	Strong transcription	Fetal Intestine Large	intestine
11	chr1:146727200-146762200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:146727200-146767800	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:146727200-146770200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr1:146727400-146767800	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:146727400-146767800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr1:146728200-146770800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr1:146729400-146769800	Strong transcription	Primary T cells from cord blood	blood
18	chr1:146730200-146755800	Weak transcription	Fetal Heart	heart
19	chr1:146732800-146750600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr1:146733000-146770600	Strong transcription	HepG2	liver
21	chr1:146733200-146762600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:146733600-146763000	Strong transcription	Primary B cells from cord blood	blood
23	chr1:146735400-146752000	Strong transcription	GM12878-XiMat	blood
24	chr1:146735600-146768600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr1:146735800-146769000	Strong transcription	Fetal Thymus	thymus
26	chr1:146736400-146770200	Strong transcription	Rectal Mucosa Donor 29	rectum
27	chr1:146740800-146751200	Weak transcription	Pancreas	Pancrea
28	chr1:146740800-146757000	Weak transcription	Brain Germinal Matrix	brain
29	chr1:146741000-146764800	Weak transcription	Fetal Brain Male	brain
30	chr1:146742400-146767800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr1:146742600-146754400	Strong transcription	Fetal Muscle Leg	muscle
32	chr1:146745200-146769400	Strong transcription	Fetal Muscle Trunk	muscle
33	chr1:146745600-146759200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:146745600-146764200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr1:146745600-146766400	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr1:146745600-146768200	Strong transcription	K562	blood
37	chr1:146745800-146766200	Strong transcription	A549	lung
38	chr1:146746000-146753000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr1:146746000-146754200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:146746000-146754600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:146746000-146756800	Weak transcription	Colon Smooth Muscle	Colon
42	chr1:146746000-146761800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:146746000-146763400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:146746000-146769400	Strong transcription	Hela-S3	cervix
45	chr1:146746200-146752800	Strong transcription	NH-A	brain
46	chr1:146746200-146753400	Strong transcription	Thymus	Thymus
47	chr1:146746200-146754000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:146746200-146754000	Strong transcription	HSMM	muscle
49	chr1:146746200-146754200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr1:146746200-146754200	Strong transcription	Brain Hippocampus Middle	brain

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