Variant report

Variant	esv2757759
Chromosome Location	chr1:166491879-166650985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:523)
CpG islands
(count:184)
Chromatin interactive
region (count:76)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:166646325-166646391	K562	blood:	n/a	n/a
2	ARID3A	chr1:166644310-166644741	K562	blood:	n/a	n/a
3	ARID3A	chr1:166567973-166568032	K562	blood:	n/a	n/a
4	ARID3A	chr1:166549726-166549735	K562	blood:	n/a	n/a
5	ARID3A	chr1:166602064-166602242	K562	blood:	n/a	n/a
6	ARID3A	chr1:166554164-166554757	K562	blood:	n/a	n/a
7	ARID3A	chr1:166555984-166555985	K562	blood:	n/a	n/a
8	ATF1	chr1:166549456-166549773	K562	blood:	n/a	n/a
9	ATF1	chr1:166554199-166554710	K562	blood:	n/a	n/a
10	ATF1	chr1:166530687-166530718	K562	blood:	n/a	n/a
11	BACH1	chr1:166583164-166583219	K562	blood:	n/a	n/a
12	BACH1	chr1:166644490-166644770	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:166585471-166585771	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr1:166644444-166644854	K562	blood:	n/a	n/a
15	BACH1	chr1:166585472-166585825	K562	blood:	n/a	n/a
16	BACH1	chr1:166554084-166554626	K562	blood:	n/a	n/a
17	BHLHE40	chr1:166644447-166644705	K562	blood:	n/a	n/a
18	BHLHE40	chr1:166554131-166554801	K562	blood:	n/a	n/a
19	BHLHE40	chr1:166548205-166548329	K562	blood:	n/a	n/a
20	BHLHE40	chr1:166607011-166607102	K562	blood:	n/a	n/a
21	BRCA1	chr1:166619952-166620065	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr1:166630060-166630198	GM12878	blood:	n/a	n/a
23	CBX3	chr1:166554065-166554902	K562	blood:	n/a	n/a
24	CBX3	chr1:166644363-166644828	K562	blood:	n/a	n/a
25	CBX3	chr1:166525579-166525895	K562	blood:	n/a	n/a
26	CBX3	chr1:166525520-166525829	K562	blood:	n/a	n/a
27	CBX3	chr1:166500999-166501356	K562	blood:	n/a	n/a
28	CBX3	chr1:166554160-166554714	K562	blood:	n/a	n/a
29	CBX3	chr1:166505601-166505971	K562	blood:	n/a	n/a
30	CCNT2	chr1:166554158-166554688	K562	blood:	n/a	n/a
31	CEBPB	chr1:166572326-166572939	MCF-7	breast:	n/a	chr1:166572450-166572463 chr1:166572452-166572463 chr1:166572452-166572463
32	CEBPB	chr1:166551307-166551346	K562	blood:	n/a	n/a
33	CEBPB	chr1:166570981-166571218	K562	blood:	n/a	n/a
34	CEBPB	chr1:166589724-166589993	K562	blood:	n/a	n/a
35	CEBPB	chr1:166497618-166497854	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:166554114-166554825	K562	blood:	n/a	n/a
37	CEBPB	chr1:166497724-166497840	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:166521965-166522147	K562	blood:	n/a	chr1:166522076-166522087
39	CEBPB	chr1:166521991-166522172	HepG2	liver:	n/a	chr1:166522076-166522087
40	CEBPB	chr1:166603123-166603255	K562	blood:	n/a	n/a
41	CEBPB	chr1:166497614-166497843	K562	blood:	n/a	n/a
42	CEBPB	chr1:166650765-166651013	K562	blood:	n/a	n/a
43	CEBPB	chr1:166554118-166554758	K562	blood:	n/a	n/a
44	CEBPB	chr1:166572416-166572866	MCF-7	breast:	n/a	chr1:166572450-166572463 chr1:166572452-166572463 chr1:166572452-166572463
45	CEBPB	chr1:166531518-166531646	A549	lung:	n/a	n/a
46	CEBPB	chr1:166584502-166584549	K562	blood:	n/a	n/a
47	CEBPB	chr1:166587229-166587284	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:166554389-166554670	K562	blood:	n/a	n/a
49	CEBPB	chr1:166599694-166599894	K562	blood:	n/a	n/a
50	CEBPD	chr1:166595921-166596400	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:166572716-166572766	MCF10A-Er-Src	breast:	n/a
2	chr1:166572716-166572766	MCF10A-Er-Src	breast:	n/a
3	chr1:166590947-166590997	HAEpiC	amniotic membrane:	n/a
4	chr1:166590947-166590997	LNCaP	prostate:	n/a
5	chr1:166590947-166590997	Jurkat	blood:	n/a
6	chr1:166590947-166590997	HEK293	kidney:	embryo
7	chr1:166572716-166572766	GM06990	blood:	n/a
8	chr1:166571691-166571741	BJ	skin:	n/a
9	chr1:166572716-166572766	SK-N-SH_RA	brain:	n/a
10	chr1:166590947-166590997	H1-hESC	embryonic stem cell:	embryo
11	chr1:166590947-166590997	SAEC	small airway:	n/a
12	chr1:166590947-166590997	HEEpiC	esophagus:	n/a
13	chr1:166572716-166572766	AG10803	skin:	n/a
14	chr1:166572716-166572766	HUVEC	blood vessel:	n/a
15	chr1:166590947-166590997	HRCEpiC	kidney:	n/a
16	chr1:166590947-166590997	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:166590947-166590997	HCM	heart:	n/a
18	chr1:166590947-166590997	HRE	kidney:	n/a
19	chr1:166571691-166571741	HAEpiC	amniotic membrane:	n/a
20	chr1:166572716-166572766	HAEpiC	amniotic membrane:	n/a
21	chr1:166590947-166590997	GM12878	blood:	n/a
22	chr1:166571691-166571741	NH-A	brain:	n/a
23	chr1:166572716-166572766	ECC-1	luminal epithelium:	n/a
24	chr1:166590947-166590997	ProgFib	skin:	n/a
25	chr1:166571691-166571741	HIPEpiC	eye:	n/a
26	chr1:166590947-166590997	HCF	heart:	n/a
27	chr1:166590947-166590997	K562	blood:	n/a
28	chr1:166571691-166571741	ProgFib	skin:	n/a
29	chr1:166590947-166590997	AG09319	gingival:	n/a
30	chr1:166590947-166590997	HNPCEpiC	eye:	n/a
31	chr1:166571691-166571741	Hepatocyte	liver:	n/a
32	chr1:166590947-166590997	AG04450	lung:	fetal
33	chr1:166590947-166590997	HUVEC	blood vessel:	n/a
34	chr1:166571691-166571741	Jurkat	blood:	n/a
35	chr1:166590947-166590997	SK-N-SH_RA	brain:	n/a
36	chr1:166571691-166571741	HRCEpiC	kidney:	n/a
37	chr1:166590947-166590997	ECC-1	luminal epithelium:	n/a
38	chr1:166572716-166572766	PrEC	prostate:	n/a
39	chr1:166572716-166572766	NHDF-neo	bronchial:	n/a
40	chr1:166590947-166590997	HMEC	breast:	n/a
41	chr1:166571691-166571741	HEEpiC	esophagus:	n/a
42	chr1:166572716-166572766	GM12892	blood:	n/a
43	chr1:166590947-166590997	GM12891	blood:	n/a
44	chr1:166572716-166572766	IMR90	lung:	fetal
45	chr1:166572716-166572766	HCM	heart:	n/a
46	chr1:166571691-166571741	Hela-S3	cervix:	n/a
47	chr1:166572716-166572766	HRE	kidney:	n/a
48	chr1:166571691-166571741	AG10803	skin:	n/a
49	chr1:166571691-166571741	HMEC	breast:	n/a
50	chr1:166572716-166572766	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr1:166541145..166543068-chr1:166552578..166555523,2	K562	blood:
2	chr1:166534937..166537659-chr1:166540902..166543509,2	K562	blood:
3	chr1:166559872..166561580-chr1:166564185..166567051,2	K562	blood:
4	chr1:166548285..166550394-chr1:166561795..166564014,2	K562	blood:
5	chr1:166503141..166505252-chr1:166506106..166508917,2	K562	blood:
6	chr1:166592488..166594055-chr1:166594735..166596268,2	K562	blood:
7	chr1:166606674..166608700-chr1:166627422..166629735,2	MCF-7	breast:
8	chr1:166642691..166644852-chr1:166657176..166659778,2	K562	blood:
9	chr1:166584740..166586661-chr1:166593653..166596420,2	K562	blood:
10	chr1:166491898..166494773-chr1:166503780..166506607,2	K562	blood:
11	chr1:166598376..166600400-chr1:166600678..166602405,2	K562	blood:
12	chr1:166630170..166632723-chr1:166642991..166645828,4	K562	blood:
13	chr1:166598318..166601316-chr1:166603442..166605798,2	K562	blood:
14	chr1:166548285..166550394-chr1:166561795..166564014,2	K562	blood:
15	chr1:166589682..166592157-chr1:166593940..166597259,3	K562	blood:
16	chr1:166545251..166548120-chr6:140575352..140577699,2	MCF-7	breast:
17	chr1:166526359..166528969-chr1:166551076..166553291,2	K562	blood:
18	chr1:166546817..166549594-chr1:166554279..166555815,3	K562	blood:
19	chr1:166646941..166649899-chr1:166808639..166811427,2	MCF-7	breast:
20	chr1:166589682..166592157-chr1:166593940..166597259,3	K562	blood:
21	chr1:166528353..166531255-chr1:166533541..166536612,3	K562	blood:
22	chr1:166433876..166435453-chr1:166541076..166543354,2	K562	blood:
23	chr1:166519753..166521489-chr1:166523362..166525642,2	K562	blood:
24	chr1:166553441..166555941-chr1:166692722..166694602,2	K562	blood:
25	chr1:166598296..166600144-chr1:166632730..166634319,2	K562	blood:
26	chr1:166630331..166631963-chr1:166643323..166644976,2	K562	blood:
27	chr1:166599816..166602307-chr1:166602461..166604942,2	K562	blood:
28	chr1:166555656..166557626-chr1:166807250..166809697,2	K562	blood:
29	chr1:166525439..166528045-chr1:166531507..166534045,2	K562	blood:
30	chr1:166638681..166640540-chr1:166682933..166685041,2	MCF-7	breast:
31	chr1:166606674..166608700-chr1:166627422..166629735,2	MCF-7	breast:
32	chr1:166507154..166509777-chr1:166808647..166811411,2	K562	blood:
33	chr1:166592488..166594055-chr1:166594735..166596268,2	K562	blood:
34	chr1:166566883..166568406-chr1:166568618..166571458,2	MCF-7	breast:
35	chr1:166552002..166554385-chr1:166564291..166566907,2	K562	blood:
36	chr1:166541145..166543068-chr1:166552578..166555523,2	K562	blood:
37	chr1:166598376..166600400-chr1:166600678..166602405,2	K562	blood:
38	chr1:166552621..166555359-chr1:166806304..166809167,2	K562	blood:
39	chr1:166624773..166627702-chr1:166632092..166634558,2	K562	blood:
40	chr1:166649321..166652229-chr1:166657244..166659747,3	K562	blood:
41	chr1:166559872..166561580-chr1:166564185..166567051,2	K562	blood:
42	chr1:166598318..166601316-chr1:166603442..166605798,2	K562	blood:
43	chr1:166630170..166632723-chr1:166642991..166645828,4	K562	blood:
44	chr1:166538818..166541010-chr1:166552416..166555173,2	K562	blood:
45	chr1:166557976..166561372-chr1:166563125..166565685,3	K562	blood:
46	chr1:166582556..166584274-chr1:166807960..166809715,2	MCF-7	breast:
47	chr1:166640499..166644852-chr1:166656070..166659050,4	K562	blood:
48	chr1:166525448..166527938-chr1:166528907..166531054,2	K562	blood:
49	chr1:166503141..166505252-chr1:166506106..166508917,2	K562	blood:
50	chr1:166519753..166521489-chr1:166523362..166525642,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TADA1-2	chr1:166643101-166643136	NONHSAT007366
2	lnc-TADA1-2	chr1:166637345-166637392	NONHSAT007366
3	lnc-TADA1-2	chr1:166637901-166638205	NONHSAT007366
4	lnc-TADA1-2	chr1:166648655-166648798	NONHSAT007365
5	lnc-TADA1-2	chr1:166636691-166638205	NONHSAT007365

No data

Variant related genes	Relation type
FMO9P	TF binding region
FMO10P	TF binding region
FMO8P	TF binding region
FMO9P	CpG island
FMO10P	CpG island
FMO8P	CpG island
ENSG00000238087	chromatin interactions
ENSG00000143157	chromatin interactions
ENSG00000234984	chromatin interactions

Extended variants
information (count: 3286 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3286 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555919338	chr1:166494834-166494835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557328547	chr1:166494856-166494857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576471751	chr1:166494874-166494875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10918501	chr1:166494900-166494901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs269682	chr1:166494904-166494905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562382219	chr1:166494910-166494911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190511771	chr1:166494911-166494912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201302103	chr1:166494940-166494941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147016660	chr1:166494997-166494998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs137887859	chr1:166495016-166495017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141999781	chr1:166495033-166495034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs10918502	chr1:166495077-166495078	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs181423683	chr1:166495137-166495138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145866286	chr1:166495152-166495153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527973182	chr1:166495187-166495188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs55777642	chr1:166495293-166495294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573665581	chr1:166495347-166495348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148208337	chr1:166495385-166495386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149535053	chr1:166495395-166495396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs67241036	chr1:166495399-166495400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368080703	chr1:166496403-166496404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113002076	chr1:166496493-166496494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376371217	chr1:166496506-166496507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371845542	chr1:166496544-166496545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190899467	chr1:166496550-166496551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544396366	chr1:166496556-166496557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146403825	chr1:166496582-166496583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs183138981	chr1:166496583-166496584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4657568	chr1:166496594-166496595	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs559850547	chr1:166496596-166496597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555370264	chr1:166496619-166496620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528805795	chr1:166496644-166496645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551754901	chr1:166496671-166496672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs565559299	chr1:166496676-166496677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567511834	chr1:166496677-166496678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187429475	chr1:166496686-166496687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144237766	chr1:166496735-166496736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34405988	chr1:166496752-166496753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4656504	chr1:166496788-166496789	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs567461904	chr1:166496798-166496799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565709615	chr1:166496804-166496805	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs144238125	chr1:166496850-166496851	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs556367495	chr1:166496894-166496895	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs148734400	chr1:166496954-166496955	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs193077500	chr1:166496994-166496995	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs539006011	chr1:166496995-166496996	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs558605190	chr1:166497033-166497034	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs577941587	chr1:166497041-166497042	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs545110416	chr1:166497046-166497047	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs557367094	chr1:166497053-166497054	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
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
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
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166494800-166495400	Enhancers	Liver	Liver
2	chr1:166496400-166496800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr1:166496400-166497000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr1:166496400-166498200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr1:166496600-166496800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr1:166496600-166497000	Enhancers	H1 Cell Line	embryonic stem cell
7	chr1:166496600-166498400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr1:166496800-166497000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr1:166496800-166497200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr1:166496800-166497600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr1:166496800-166498000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:166497000-166497200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr1:166497000-166497400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr1:166497200-166497600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr1:166497200-166498400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr1:166497400-166498400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr1:166497600-166498200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr1:166498200-166498400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:166498400-166500200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr1:166498400-166500800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr1:166499800-166500400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr1:166500000-166500200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
23	chr1:166505600-166507200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:166513800-166514200	Enhancers	K562	blood
25	chr1:166542000-166543200	Enhancers	K562	blood
26	chr1:166543200-166544600	Weak transcription	K562	blood
27	chr1:166547200-166549400	Weak transcription	K562	blood
28	chr1:166549400-166550200	Enhancers	K562	blood
29	chr1:166550200-166552400	Weak transcription	K562	blood
30	chr1:166552400-166554600	Enhancers	K562	blood
31	chr1:166553800-166554800	Enhancers	Fetal Heart	heart
32	chr1:166554200-166554400	Enhancers	Left Ventricle	heart
33	chr1:166554200-166554800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:166554400-166555000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:166554600-166555400	Flanking Active TSS	K562	blood
36	chr1:166555400-166556000	Enhancers	K562	blood
37	chr1:166556000-166559400	Weak transcription	K562	blood
38	chr1:166557400-166559000	Enhancers	Hela-S3	cervix
39	chr1:166559400-166559800	Enhancers	K562	blood
40	chr1:166559800-166569800	Weak transcription	K562	blood
41	chr1:166569800-166571400	Enhancers	K562	blood
42	chr1:166571000-166571200	Enhancers	HMEC	breast
43	chr1:166571400-166572400	Weak transcription	HMEC	breast
44	chr1:166571400-166574400	Weak transcription	K562	blood
45	chr1:166572400-166572800	Enhancers	HMEC	breast
46	chr1:166572800-166573000	Enhancers	Left Ventricle	heart
47	chr1:166574400-166575200	Enhancers	Fetal Heart	heart
48	chr1:166574400-166575400	Enhancers	K562	blood
49	chr1:166575000-166575400	Enhancers	Left Ventricle	heart
50	chr1:166575200-166578400	Weak transcription	Fetal Heart	heart

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