Variant report

Variant	esv3372415
Chromosome Location	chr1:193612172-193988265
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:193658299-193658408	K562	blood:	n/a	n/a
2	ATF1	chr1:193659057-193659080	K562	blood:	n/a	n/a
3	ATF1	chr1:193655244-193655412	K562	blood:	n/a	n/a
4	ATF2	chr1:193710341-193710777	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr1:193669993-193670545	A549	lung:	n/a	n/a
6	ATF3	chr1:193669965-193670500	A549	lung:	n/a	n/a
7	ATF3	chr1:193676268-193677032	A549	lung:	n/a	n/a
8	BACH1	chr1:193712976-193713031	K562	blood:	n/a	n/a
9	BACH1	chr1:193678732-193679039	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:193666327-193666598	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr1:193670131-193670393	GM12878	blood:	n/a	chr1:193670216-193670227 chr1:193670315-193670325 chr1:193670319-193670329
12	BCL11A	chr1:193710422-193710666	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr1:193669863-193670456	A549	lung:	n/a	chr1:193670216-193670225
14	BCL3	chr1:193675791-193677268	A549	lung:	n/a	n/a
15	BCL3	chr1:193807855-193808192	GM12878	blood:	n/a	chr1:193808104-193808113
16	BCL3	chr1:193807901-193808162	GM12878	blood:	n/a	chr1:193808104-193808113
17	BCL3	chr1:193676283-193677081	A549	lung:	n/a	n/a
18	BHLHE40	chr1:193722598-193722750	HepG2	liver:	n/a	n/a
19	BRCA1	chr1:193940834-193941120	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr1:193676416-193677134	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:193698698-193699470	Hela-S3	cervix:	n/a	chr1:193699005-193699012
22	CBX3	chr1:193896733-193896986	K562	blood:	n/a	n/a
23	CBX3	chr1:193896727-193896966	K562	blood:	n/a	n/a
24	CBX3	chr1:193878451-193879027	HCT-116	colon:	n/a	n/a
25	CCNT2	chr1:193655208-193655421	K562	blood:	n/a	chr1:193655329-193655349
26	CEBPB	chr1:193676253-193677159	A549	lung:	n/a	chr1:193676544-193676553 chr1:193676544-193676553 chr1:193676542-193676555 chr1:193676544-193676553 chr1:193676543-193676554 chr1:193676542-193676553 chr1:193676544-193676553 chr1:193676542-193676555
27	CEBPB	chr1:193674620-193675351	A549	lung:	n/a	chr1:193675155-193675166
28	CEBPB	chr1:193926957-193927261	Hela-S3	cervix:	n/a	chr1:193927238-193927251 chr1:193927239-193927250 chr1:193927240-193927249 chr1:193927070-193927083 chr1:193927238-193927249
29	CEBPB	chr1:193921138-193921324	A549	lung:	n/a	chr1:193921183-193921196 chr1:193921183-193921194
30	CEBPB	chr1:193672866-193673033	Hela-S3	cervix:	n/a	chr1:193673020-193673033 chr1:193673022-193673033 chr1:193673020-193673033 chr1:193673022-193673033
31	CEBPB	chr1:193699029-193699628	A549	lung:	n/a	chr1:193699268-193699279
32	CEBPB	chr1:193618726-193619098	IMR90	lung:	n/a	chr1:193618903-193618914
33	CEBPB	chr1:193764019-193764408	HepG2	liver:	n/a	chr1:193764165-193764178 chr1:193764167-193764176 chr1:193764165-193764176 chr1:193764167-193764176 chr1:193764165-193764178 chr1:193764167-193764178 chr1:193764167-193764176 chr1:193764167-193764176
34	CEBPB	chr1:193965094-193965243	A549	lung:	n/a	chr1:193965175-193965186 chr1:193965197-193965206
35	CEBPB	chr1:193819521-193819727	IMR90	lung:	n/a	chr1:193819619-193819630
36	CEBPB	chr1:193964224-193964428	A549	lung:	n/a	chr1:193964336-193964347
37	CEBPB	chr1:193669924-193670477	A549	lung:	n/a	n/a
38	CEBPB	chr1:193674665-193675308	HepG2	liver:	n/a	chr1:193675155-193675166
39	CEBPB	chr1:193878649-193878867	A549	lung:	n/a	n/a
40	CEBPB	chr1:193618723-193619091	H1-hESC	embryonic stem cell:	n/a	chr1:193618903-193618914
41	CEBPB	chr1:193940784-193941172	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:193926986-193927326	HepG2	liver:	n/a	chr1:193927238-193927251 chr1:193927239-193927250 chr1:193927240-193927249 chr1:193927070-193927083 chr1:193927238-193927249
43	CEBPB	chr1:193678790-193679123	ECC-1	luminal epithelium:	n/a	chr1:193679043-193679054
44	CEBPB	chr1:193703282-193703531	HepG2	liver:	n/a	chr1:193703393-193703404
45	CEBPB	chr1:193639833-193640033	HepG2	liver:	n/a	chr1:193639865-193639876
46	CEBPB	chr1:193764029-193764448	A549	lung:	n/a	chr1:193764165-193764178 chr1:193764167-193764176 chr1:193764165-193764176 chr1:193764167-193764176 chr1:193764165-193764178 chr1:193764167-193764178 chr1:193764167-193764176 chr1:193764167-193764176
47	CEBPB	chr1:193964221-193964475	HepG2	liver:	n/a	chr1:193964336-193964347
48	CEBPB	chr1:193819612-193819641	HepG2	liver:	n/a	chr1:193819619-193819630
49	CEBPB	chr1:193699108-193699363	H1-hESC	embryonic stem cell:	n/a	chr1:193699268-193699279
50	CEBPB	chr1:193964177-193964488	IMR90	lung:	n/a	chr1:193964336-193964347

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:193888105-193888155	BJ	skin:	n/a
2	chr1:193899449-193899499	HAEpiC	amniotic membrane:	n/a
3	chr1:193899449-193899499	HL-60	blood:	n/a
4	chr1:193710042-193710092	ECC-1	luminal epithelium:	n/a
5	chr1:193722865-193722915	AG04449	skin:	fetal
6	chr1:193722865-193722915	HRE	kidney:	n/a
7	chr1:193710042-193710092	HMEC	breast:	n/a
8	chr1:193888105-193888155	Hepatocyte	liver:	n/a
9	chr1:193710042-193710092	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:193888105-193888155	ProgFib	skin:	n/a
11	chr1:193710042-193710092	HCF	heart:	n/a
12	chr1:193722865-193722915	HL-60	blood:	n/a
13	chr1:193722865-193722915	NT2-D1	testis:	n/a
14	chr1:193888105-193888155	CMK	blood:	n/a
15	chr1:193899449-193899499	SAEC	small airway:	n/a
16	chr1:193899449-193899499	PrEC	prostate:	n/a
17	chr1:193710042-193710092	HCM	heart:	n/a
18	chr1:193888105-193888155	SAEC	small airway:	n/a
19	chr1:193722865-193722915	SK-N-SH_RA	brain:	n/a
20	chr1:193722865-193722915	GM12878	blood:	n/a
21	chr1:193888105-193888155	Caco-2	colon:	n/a
22	chr1:193899449-193899499	HCM	heart:	n/a
23	chr1:193899449-193899499	GM12891	blood:	n/a
24	chr1:193722865-193722915	PrEC	prostate:	n/a
25	chr1:193888105-193888155	SK-N-MC	brain:	n/a
26	chr1:193888105-193888155	U87	brain:	n/a
27	chr1:193722865-193722915	AoSMC	blood vessel:	n/a
28	chr1:193888105-193888155	SK-N-SH_RA	brain:	n/a
29	chr1:193888105-193888155	AG10803	skin:	n/a
30	chr1:193899449-193899499	HIPEpiC	eye:	n/a
31	chr1:193722865-193722915	BJ	skin:	n/a
32	chr1:193899449-193899499	NT2-D1	testis:	n/a
33	chr1:193888105-193888155	HCM	heart:	n/a
34	chr1:193710042-193710092	Caco-2	colon:	n/a
35	chr1:193899449-193899499	A549	lung:	n/a
36	chr1:193899449-193899499	CMK	blood:	n/a
37	chr1:193899449-193899499	AG04449	skin:	fetal
38	chr1:193899449-193899499	HRE	kidney:	n/a
39	chr1:193888105-193888155	HMEC	breast:	n/a
40	chr1:193899449-193899499	PFSK-1	brain:	n/a
41	chr1:193899449-193899499	Hela-S3	cervix:	n/a
42	chr1:193722865-193722915	PFSK-1	brain:	n/a
43	chr1:193899449-193899499	K562	blood:	n/a
44	chr1:193710042-193710092	LNCaP	prostate:	n/a
45	chr1:193899449-193899499	HRPEpiC	eye:	n/a
46	chr1:193899449-193899499	HNPCEpiC	eye:	n/a
47	chr1:193710042-193710092	BJ	skin:	n/a
48	chr1:193710042-193710092	NT2-D1	testis:	n/a
49	chr1:193722865-193722915	HUVEC	blood vessel:	n/a
50	chr1:193888105-193888155	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:193937203..193939818-chr1:193949717..193951267,2	K562	blood:
2	chr1:193928408..193930045-chr1:193932568..193934210,2	K562	blood:
3	chr1:193849623..193852343-chr1:193862165..193864487,2	K562	blood:
4	chr1:193375633..193376607-chr1:193723998..193724709,3	MCF-7	breast:
5	chr1:193812672..193814763-chr1:193814995..193817305,2	K562	blood:
6	chr1:193812672..193814763-chr1:193814995..193817305,2	K562	blood:
7	chr1:193705634..193708384-chr1:193710266..193712838,2	MCF-7	breast:
8	chr1:193576779..193577361-chr1:193723828..193724666,2	MCF-7	breast:
9	chr1:193644387..193646892-chr1:193648522..193650062,2	K562	blood:
10	chr1:193900151..193902941-chr1:193904625..193907312,2	K562	blood:
11	chr1:193829339..193831147-chr1:193831522..193834388,2	K562	blood:
12	chr1:193705634..193708384-chr1:193710266..193712838,2	MCF-7	breast:
13	chr1:193937203..193939818-chr1:193949717..193951267,2	K562	blood:
14	chr1:193678450..193681158-chr1:193682285..193685229,2	K562	blood:
15	chr1:193681603..193683732-chr11:100996114..100998464,2	MCF-7	breast:
16	chr1:193678450..193681158-chr1:193682285..193685229,2	K562	blood:
17	chr1:193728373..193730698-chr1:193736583..193739356,2	K562	blood:
18	chr1:193829339..193831147-chr1:193831522..193834388,2	K562	blood:
19	chr1:193783087..193785437-chr20:56932856..56935635,2	MCF-7	breast:
20	chr1:193426910..193427495-chr1:193888652..193889585,2	MCF-7	breast:
21	chr1:193631362..193634280-chr1:193636657..193638784,2	MCF-7	breast:
22	chr1:193631362..193634280-chr1:193636657..193638784,2	MCF-7	breast:
23	chr1:193734313..193736355-chr1:193736436..193738491,2	K562	blood:
24	chr1:193715834..193718393-chr1:193725574..193727798,2	K562	blood:
25	chr1:193734313..193736355-chr1:193736436..193738491,2	K562	blood:
26	chr1:193928408..193930045-chr1:193932568..193934210,2	K562	blood:
27	chr1:193723167..193725389-chr1:193725651..193727623,2	MCF-7	breast:
28	chr1:193900151..193902941-chr1:193904625..193907312,2	K562	blood:
29	chr1:193644387..193646892-chr1:193648522..193650062,2	K562	blood:
30	chr1:193728373..193730698-chr1:193736583..193739356,2	K562	blood:
31	chr1:193849623..193852343-chr1:193862165..193864487,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC73-11	chr1:193879218-193879294	NONHSAT008577
2	lnc-CDC73-2	chr1:193694731-193694815	ENSG00000226640.2
3	lnc-CDC73-2	chr1:193695962-193696165	ENSG00000226640.2
4	lnc-CDC73-2	chr1:193695962-193696313	XLOC_000509
5	lnc-CDC73-10	chr1:193868417-193868763	NONHSAT008576
6	lnc-CDC73-2	chr1:193694731-193694815	XLOC_000509
7	lnc-CDC73-10	chr1:193855454-193855547	NONHSAT008576
8	lnc-CDC73-11	chr1:193894657-193894745	NONHSAT008577
9	lnc-B3GALT2-4	chr1:193919209-193919280	NONHSAT008578
10	lnc-B3GALT2-3	chr1:193725945-193726397	NONHSAT008575
11	lnc-CDC73-2	chr1:193648024-193648135	XLOC_000509
12	lnc-CDC73-2	chr1:193648024-193648135	ENSG00000226640.2
13	lnc-B3GALT2-4	chr1:193931035-193931268	NONHSAT008578
14	lnc-CDC73-11	chr1:193904029-193904142	NONHSAT008577

Variant related genes	Relation type
RPL23AP22	TF binding region
ENSG00000237011	TF binding region
ENSG00000252241	TF binding region
ENSG00000226640	TF binding region
RPL23AP22	CpG island
ENSG00000237011	CpG island
ENSG00000252241	CpG island
ENSG00000226640	CpG island
ENSG00000237213	chromatin interactions

Extended variants
information (count: 6617 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:6617 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572232700	chr1:193613806-193613807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs77073451	chr1:193613812-193613813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535257642	chr1:193613888-193613889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374219812	chr1:193613898-193613899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564335247	chr1:193613901-193613902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12064935	chr1:193613902-193613903	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs180879069	chr1:193613939-193613940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563643088	chr1:193613950-193613951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs186083221	chr1:193614003-193614004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139964708	chr1:193614014-193614015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7553889	chr1:193614049-193614050	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528210153	chr1:193614097-193614098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551415423	chr1:193614118-193614119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571158276	chr1:193614119-193614120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529451188	chr1:193614139-193614140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556671840	chr1:193614150-193614151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547729176	chr1:193614155-193614156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373209153	chr1:193614165-193614166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551272602	chr1:193614176-193614177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs555559791	chr1:193614219-193614220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192040412	chr1:193614222-193614223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs558280338	chr1:193614223-193614224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs578029159	chr1:193614224-193614225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543834881	chr1:193614260-193614261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563513286	chr1:193614273-193614274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529227187	chr1:193614298-193614299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542908913	chr1:193614321-193614322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559596805	chr1:193614324-193614325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528247383	chr1:193614361-193614362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183547050	chr1:193614365-193614366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7413068	chr1:193614366-193614367	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs370460783	chr1:193614375-193614376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10921397	chr1:193614412-193614413	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4495677	chr1:193614455-193614456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs116692464	chr1:193614464-193614465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557225416	chr1:193614466-193614467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143526983	chr1:193614478-193614479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555596502	chr1:193614482-193614483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186697523	chr1:193614483-193614484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535263472	chr1:193614489-193614490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76901630	chr1:193614563-193614564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192064156	chr1:193614604-193614605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs151195194	chr1:193614608-193614609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537613874	chr1:193614633-193614634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556423419	chr1:193614636-193614637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140253747	chr1:193614652-193614653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577817299	chr1:193614708-193614709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575446363	chr1:193614718-193614719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542945803	chr1:193614728-193614729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559730610	chr1:193614733-193614734	Enhancers	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
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	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
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193613800-193614600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:193614400-193614800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr1:193617800-193618400	Active TSS	Fetal Heart	heart
4	chr1:193619200-193620000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:193622000-193627400	Weak transcription	Fetal Brain Male	brain
6	chr1:193623600-193624000	Active TSS	Fetal Heart	heart
7	chr1:193623800-193624400	ZNF genes & repeats	Aorta	Aorta
8	chr1:193624000-193624200	Enhancers	Hela-S3	cervix
9	chr1:193624000-193624400	Enhancers	Colon Smooth Muscle	Colon
10	chr1:193624000-193624400	ZNF genes & repeats	Left Ventricle	heart
11	chr1:193624000-193627400	Weak transcription	Fetal Heart	heart
12	chr1:193624200-193624600	Flanking Active TSS	Hela-S3	cervix
13	chr1:193624200-193624800	Enhancers	HSMMtube	muscle
14	chr1:193624400-193624600	Enhancers	Small Intestine	intestine
15	chr1:193624400-193627200	Weak transcription	Colon Smooth Muscle	Colon
16	chr1:193624400-193628600	Weak transcription	Left Ventricle	heart
17	chr1:193624400-193629000	Weak transcription	Aorta	Aorta
18	chr1:193624600-193624800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr1:193624600-193624800	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr1:193624600-193625400	Enhancers	Hela-S3	cervix
21	chr1:193624600-193627400	Weak transcription	Small Intestine	intestine
22	chr1:193624800-193626000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr1:193624800-193629000	Weak transcription	HSMMtube	muscle
24	chr1:193625600-193625800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr1:193625800-193626800	Enhancers	Fetal Intestine Large	intestine
26	chr1:193626000-193627200	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr1:193626000-193635400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr1:193626200-193626400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:193626400-193627400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:193626600-193627000	Enhancers	Fetal Intestine Small	intestine
31	chr1:193627200-193628000	Enhancers	Colon Smooth Muscle	Colon
32	chr1:193627400-193627600	Enhancers	Small Intestine	intestine
33	chr1:193627400-193627800	Enhancers	Brain Cingulate Gyrus	brain
34	chr1:193627400-193628000	Enhancers	Stomach Smooth Muscle	stomach
35	chr1:193627400-193628400	Enhancers	Fetal Brain Male	brain
36	chr1:193627400-193628800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:193627400-193631000	Enhancers	Fetal Heart	heart
38	chr1:193627600-193628200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr1:193627600-193628200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr1:193627600-193628200	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr1:193628000-193629000	Weak transcription	Stomach Smooth Muscle	stomach
42	chr1:193628000-193630600	Weak transcription	Colon Smooth Muscle	Colon
43	chr1:193628600-193630200	Enhancers	Left Ventricle	heart
44	chr1:193629000-193629200	Enhancers	Aorta	Aorta
45	chr1:193629000-193629200	Enhancers	Stomach Smooth Muscle	stomach
46	chr1:193629000-193629200	Enhancers	HSMMtube	muscle
47	chr1:193629200-193629600	Weak transcription	Aorta	Aorta
48	chr1:193629600-193631000	Enhancers	Aorta	Aorta
49	chr1:193630200-193630600	Weak transcription	Left Ventricle	heart
50	chr1:193630600-193630800	Enhancers	Colon Smooth Muscle	Colon

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