Variant report

Variant	esv1798404
Chromosome Location	chr1:152472839-152587113
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:811)
CpG islands
(count:1713)
Chromatin interactive
region (count:22)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:811 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:152497800-152498135	HepG2	liver:	n/a	n/a
2	ATF2	chr1:152549641-152550036	GM12878	blood:	n/a	n/a
3	ATF2	chr1:152537532-152538062	GM12878	blood:	n/a	n/a
4	ATF3	chr1:152474035-152474592	A549	lung:	n/a	n/a
5	ATF3	chr1:152474023-152474647	A549	lung:	n/a	n/a
6	BACH1	chr1:152555244-152555264	K562	blood:	n/a	chr1:152555246-152555260
7	BATF	chr1:152537564-152537953	GM12878	blood:	n/a	n/a
8	BATF	chr1:152537583-152537985	GM12878	blood:	n/a	n/a
9	BATF	chr1:152549615-152549949	GM12878	blood:	n/a	n/a
10	BATF	chr1:152549573-152550008	GM12878	blood:	n/a	n/a
11	BCL3	chr1:152474009-152474620	A549	lung:	n/a	n/a
12	BCL3	chr1:152474020-152474727	A549	lung:	n/a	n/a
13	BHLHE40	chr1:152516435-152516557	K562	blood:	n/a	n/a
14	CEBPB	chr1:152535518-152535885	HepG2	liver:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
15	CEBPB	chr1:152535595-152535869	Hela-S3	cervix:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
16	CEBPB	chr1:152474042-152474652	A549	lung:	n/a	n/a
17	CEBPB	chr1:152474022-152474518	A549	lung:	n/a	n/a
18	CEBPB	chr1:152475333-152475515	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:152475323-152475483	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:152479431-152479933	A549	lung:	n/a	n/a
21	CEBPB	chr1:152479524-152479857	A549	lung:	n/a	n/a
22	CEBPB	chr1:152569565-152569765	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:152546403-152546497	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:152497637-152498096	HepG2	liver:	n/a	chr1:152497788-152497801
25	CEBPB	chr1:152535544-152535899	A549	lung:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
26	CEBPB	chr1:152497663-152498081	HepG2	liver:	n/a	chr1:152497788-152497801
27	CEBPB	chr1:152475046-152475605	A549	lung:	n/a	n/a
28	CEBPB	chr1:152497742-152497999	HepG2	liver:	n/a	chr1:152497788-152497801
29	CEBPB	chr1:152497662-152498094	A549	lung:	n/a	chr1:152497788-152497801
30	CEBPB	chr1:152474105-152474582	A549	lung:	n/a	n/a
31	CEBPB	chr1:152497790-152497957	K562	blood:	n/a	n/a
32	CEBPB	chr1:152497676-152498092	A549	lung:	n/a	chr1:152497788-152497801
33	CEBPB	chr1:152497570-152498264	A549	lung:	n/a	chr1:152497788-152497801
34	CEBPB	chr1:152535552-152535869	IMR90	lung:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
35	CEBPB	chr1:152493307-152493610	A549	lung:	n/a	chr1:152493595-152493607
36	CHD2	chr1:152482065-152482147	GM12878	blood:	n/a	n/a
37	CREB1	chr1:152489620-152489967	A549	lung:	n/a	n/a
38	CREB1	chr1:152474140-152474501	A549	lung:	n/a	n/a
39	CREB1	chr1:152474169-152474534	A549	lung:	n/a	n/a
40	CTCF	chr1:152516480-152516630	HMF	breast:	n/a	n/a
41	CTCF	chr1:152557900-152558050	GM12873	blood:	n/a	n/a
42	CTCF	chr1:152505920-152506070	HL-60	blood:	n/a	chr1:152505986-152506007
43	CTCF	chr1:152552800-152552950	NHEK	skin:	n/a	chr1:152552927-152552936 chr1:152552921-152552939
44	CTCF	chr1:152558167-152558328	K562	blood:	n/a	n/a
45	CTCF	chr1:152516540-152516690	HFF	foreskin:	n/a	n/a
46	CTCF	chr1:152516385-152516581	LNCaP	prostate:	n/a	n/a
47	CTCF	chr1:152505876-152506129	GM19238	blood:	n/a	chr1:152505986-152506007
48	CTCF	chr1:152516400-152516550	HEK293	kidney:	n/a	n/a
49	CTCF	chr1:152505880-152506030	GM12868	blood:	n/a	chr1:152505986-152506007
50	CTCF	chr1:152516351-152516598	T-47D	breast:	n/a	n/a

(count:1713 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152506842-152506892	PANC-1	pancreas:	n/a
2	chr1:152486609-152486659	HCPEpiC	choroid plexus:	n/a
3	chr1:152486609-152486659	HMEC	breast:	n/a
4	chr1:152538380-152538430	HRE	kidney:	n/a
5	chr1:152506886-152506936	SK-N-MC	brain:	n/a
6	chr1:152506842-152506892	PANC-1	pancreas:	n/a
7	chr1:152486609-152486659	HCPEpiC	choroid plexus:	n/a
8	chr1:152486609-152486659	HMEC	breast:	n/a
9	chr1:152538380-152538430	HRE	kidney:	n/a
10	chr1:152506886-152506936	SK-N-MC	brain:	n/a
11	chr1:152552175-152552225	AG04450	lung:	fetal
12	chr1:152486477-152486527	GM12892	blood:	n/a
13	chr1:152487844-152487894	BJ	skin:	n/a
14	chr1:152486609-152486659	NHDF-neo	bronchial:	n/a
15	chr1:152538857-152538907	AG04449	skin:	fetal
16	chr1:152483204-152483254	MCF-7	breast:	n/a
17	chr1:152538380-152538430	HepG2	liver:	n/a
18	chr1:152486477-152486527	MCF-7	breast:	n/a
19	chr1:152538380-152538430	PFSK-1	brain:	n/a
20	chr1:152488262-152488312	PFSK-1	brain:	n/a
21	chr1:152506886-152506936	HRCEpiC	kidney:	n/a
22	chr1:152487856-152487906	HIPEpiC	eye:	n/a
23	chr1:152488262-152488312	SKMC	muscle:	n/a
24	chr1:152538857-152538907	AG09309	skin:	n/a
25	chr1:152538888-152538938	NH-A	brain:	n/a
26	chr1:152506842-152506892	GM12892	blood:	n/a
27	chr1:152506922-152506972	SK-N-SH	brain:	n/a
28	chr1:152552175-152552225	GM12891	blood:	n/a
29	chr1:152552175-152552225	HUVEC	blood vessel:	n/a
30	chr1:152506886-152506936	HepG2	liver:	n/a
31	chr1:152488368-152488418	NT2-D1	testis:	n/a
32	chr1:152538380-152538430	SK-N-SH	brain:	n/a
33	chr1:152484386-152484436	CMK	blood:	n/a
34	chr1:152486950-152487000	MCF10A-Er-Src	breast:	n/a
35	chr1:152487909-152487959	U87	brain:	n/a
36	chr1:152552175-152552225	AoSMC	blood vessel:	n/a
37	chr1:152538380-152538430	U87	brain:	n/a
38	chr1:152506922-152506972	GM12891	blood:	n/a
39	chr1:152538857-152538907	ovcar-3	ovarian:	n/a
40	chr1:152552494-152552544	HEK293	kidney:	embryo
41	chr1:152490870-152490920	HCT-116	colon:	n/a
42	chr1:152488000-152488050	T-47D	breast:	n/a
43	chr1:152553244-152553294	HCF	heart:	n/a
44	chr1:152487909-152487959	HEK293	kidney:	embryo
45	chr1:152552494-152552544	BJ	skin:	n/a
46	chr1:152487909-152487959	GM12891	blood:	n/a
47	chr1:152552494-152552544	HepG2	liver:	n/a
48	chr1:152484386-152484436	HRE	kidney:	n/a
49	chr1:152506886-152506936	PANC-1	pancreas:	n/a
50	chr1:152483675-152483725	GM12878	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:152508160..152510844-chr1:152518388..152520386,2	K562	blood:
2	chr1:152467226..152468092-chr1:152505547..152506816,7	MCF-7	breast:
3	chr1:152580545..152582523-chr1:152584809..152586590,2	K562	blood:
4	chr1:152485897..152487871-chr1:152488735..152491342,2	MCF-7	breast:
5	chr1:152494849..152497210-chr1:152499471..152502246,2	MCF-7	breast:
6	chr1:152508160..152510844-chr1:152518388..152520386,2	K562	blood:
7	chr1:152486736..152490871-chr1:152492622..152496834,3	MCF-7	breast:
8	chr1:152507658..152510511-chr1:152512542..152515138,2	MCF-7	breast:
9	chr1:152485543..152488216-chr1:152489949..152493363,3	MCF-7	breast:
10	chr1:152494849..152497210-chr1:152499471..152502246,2	MCF-7	breast:
11	chr1:152433729..152434269-chr1:152505524..152506462,2	MCF-7	breast:
12	chr1:152469492..152471247-chr1:152505473..152506875,7	K562	blood:
13	chr1:152475128..152477150-chr1:152479048..152480719,2	MCF-7	breast:
14	chr1:152433975..152434768-chr1:152504695..152505339,2	MCF-7	breast:
15	chr1:152475128..152477150-chr1:152479048..152480719,2	MCF-7	breast:
16	chr1:152467377..152468575-chr1:152505519..152506463,7	MCF-7	breast:
17	chr1:152478290..152479934-chr1:152485097..152487214,2	MCF-7	breast:
18	chr1:152458591..152459582-chr1:152505807..152506392,3	MCF-7	breast:
19	chr1:152507658..152510511-chr1:152512542..152515138,2	MCF-7	breast:
20	chr1:152512266..152512767-chr16:8754919..8755481,3	MCF-7	breast:
21	chr1:152469001..152470435-chr1:152505453..152506443,13	MCF-7	breast:
22	chr1:152469495..152470816-chr1:152505489..152506516,11	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRCT1-2	chr1:152502924-152503231	expReg_chr1_17005_+
2	lnc-CRCT1-1	chr1:152493390-152493750	expReg_chr1_16986_+
3	lnc-LCE5A-4	chr1:152480695-152481126	expReg_chr1_16977_+

No data

Variant related genes	Relation type
LCE3C	TF binding region
LCE3E	TF binding region
LCE3B	TF binding region
LCE3D	TF binding region
CRCT1	TF binding region
LCE5A	TF binding region
LCE3C	CpG island
LCE3E	CpG island
LCE3B	CpG island
LCE3D	CpG island
CRCT1	CpG island
LCE5A	CpG island
ENSG00000187238	chromatin interactions
ENSG00000169509	chromatin interactions

Extended variants
information (count: 2506 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554323420	chr1:152472848-152472849	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187020534	chr1:152472882-152472883	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542436760	chr1:152472895-152472896	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572483180	chr1:152472913-152472914	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6662563	chr1:152472927-152472928	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs558233618	chr1:152472966-152472967	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576297990	chr1:152472976-152472977	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544929922	chr1:152472981-152472982	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564945492	chr1:152472983-152472984	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560830359	chr1:152472989-152472990	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541159639	chr1:152473079-152473080	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143228081	chr1:152473080-152473081	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529784810	chr1:152473144-152473145	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2004180	chr1:152473234-152473235	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs1984725	chr1:152473262-152473263	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs146678106	chr1:152473266-152473267	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551783351	chr1:152473292-152473293	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79412372	chr1:152473337-152473338	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533911936	chr1:152473358-152473359	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553722829	chr1:152473363-152473364	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567437455	chr1:152473364-152473365	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543752659	chr1:152473372-152473373	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377368265	chr1:152473442-152473443	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556329180	chr1:152473450-152473451	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189985448	chr1:152473491-152473492	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74128242	chr1:152473514-152473515	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs558553685	chr1:152473519-152473520	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181105075	chr1:152473552-152473553	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369812473	chr1:152473606-152473607	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377542223	chr1:152473613-152473614	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573856620	chr1:152473621-152473622	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374993626	chr1:152473625-152473626	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541047301	chr1:152473731-152473732	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185600241	chr1:152473795-152473796	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560832030	chr1:152473814-152473815	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs189674680	chr1:152473832-152473833	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183028952	chr1:152473882-152473883	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs188589677	chr1:152473904-152473905	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs115890775	chr1:152473943-152473944	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs552080249	chr1:152473953-152473954	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs565259900	chr1:152473993-152473994	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs540901258	chr1:152474023-152474024	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs547397594	chr1:152474031-152474032	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs546314602	chr1:152474070-152474071	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs370425558	chr1:152474126-152474127	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs536801934	chr1:152474151-152474152	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs549999623	chr1:152474177-152474178	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs144541122	chr1:152474184-152474185	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs35693064	chr1:152474207-152474208	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs192327384	chr1:152474209-152474210	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
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
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
Follicular lymphoma	18703704	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
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	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
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152470000-152473800	Enhancers	A549	lung
2	chr1:152471000-152474600	Weak transcription	Esophagus	oesophagus
3	chr1:152471400-152478800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:152473200-152474800	Enhancers	Fetal Intestine Large	intestine
5	chr1:152473200-152480600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:152473600-152476200	Enhancers	Placenta	Placenta
7	chr1:152473600-152480200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:152473800-152475000	Enhancers	NHEK	skin
9	chr1:152473800-152475800	Flanking Active TSS	A549	lung
10	chr1:152473800-152478400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:152473800-152480600	Enhancers	HMEC	breast
12	chr1:152474000-152475400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:152474200-152474600	Enhancers	HepG2	liver
14	chr1:152474200-152475000	Enhancers	Osteobl	bone
15	chr1:152474600-152475200	Enhancers	Esophagus	oesophagus
16	chr1:152474600-152475200	Enhancers	NHDF-Ad	bronchial
17	chr1:152474800-152475800	Weak transcription	Fetal Intestine Large	intestine
18	chr1:152475000-152475400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr1:152475000-152475400	Flanking Active TSS	NHEK	skin
20	chr1:152475200-152477200	Weak transcription	Esophagus	oesophagus
21	chr1:152475400-152480600	Enhancers	NHEK	skin
22	chr1:152475800-152476400	Enhancers	A549	lung
23	chr1:152475800-152479600	Enhancers	Fetal Intestine Large	intestine
24	chr1:152476200-152477600	Weak transcription	Placenta	Placenta
25	chr1:152476400-152482400	Weak transcription	A549	lung
26	chr1:152477000-152477200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr1:152477200-152478000	Enhancers	Esophagus	oesophagus
28	chr1:152477200-152478400	Enhancers	Fetal Intestine Small	intestine
29	chr1:152477600-152477800	Enhancers	Placenta	Placenta
30	chr1:152478000-152479400	Weak transcription	Esophagus	oesophagus
31	chr1:152478400-152478800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:152478400-152479000	Weak transcription	Fetal Intestine Small	intestine
33	chr1:152478800-152480400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:152479000-152479200	Enhancers	Fetal Intestine Small	intestine
35	chr1:152479200-152479400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
36	chr1:152479400-152479600	Enhancers	Esophagus	oesophagus
37	chr1:152479800-152480000	Enhancers	Liver	Liver
38	chr1:152480600-152486600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:152482000-152484600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr1:152483600-152485800	Weak transcription	A549	lung
41	chr1:152485000-152485200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
42	chr1:152485800-152486200	Enhancers	A549	lung
43	chr1:152486200-152486400	Bivalent/Poised TSS	Esophagus	oesophagus
44	chr1:152486200-152487000	Weak transcription	A549	lung
45	chr1:152486400-152486600	Weak transcription	NHEK	skin
46	chr1:152486400-152487000	Active TSS	Esophagus	oesophagus
47	chr1:152486400-152487200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:152486400-152487600	Enhancers	HMEC	breast
49	chr1:152486600-152486800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:152486600-152487600	Enhancers	NHEK	skin

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