Variant report

Variant	nsv441729
Chromosome Location	chr1:193661018-193710376
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	ATF2	chr1:193710341-193710777	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr1:193676268-193677032	A549	lung:	n/a	n/a
3	ATF3	chr1:193669965-193670500	A549	lung:	n/a	n/a
4	ATF3	chr1:193669993-193670545	A549	lung:	n/a	n/a
5	BACH1	chr1:193666327-193666598	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:193678732-193679039	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:193670131-193670393	GM12878	blood:	n/a	chr1:193670216-193670227 chr1:193670315-193670325 chr1:193670319-193670329
8	BCL3	chr1:193676283-193677081	A549	lung:	n/a	n/a
9	BCL3	chr1:193669863-193670456	A549	lung:	n/a	chr1:193670216-193670225
10	BCL3	chr1:193675791-193677268	A549	lung:	n/a	n/a
11	BRCA1	chr1:193698698-193699470	Hela-S3	cervix:	n/a	chr1:193699005-193699012
12	BRCA1	chr1:193676416-193677134	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:193698681-193699641	Hela-S3	cervix:	n/a	chr1:193699268-193699279
14	CEBPB	chr1:193674991-193675370	A549	lung:	n/a	chr1:193675155-193675166
15	CEBPB	chr1:193674494-193674976	A549	lung:	n/a	n/a
16	CEBPB	chr1:193703282-193703531	HepG2	liver:	n/a	chr1:193703393-193703404
17	CEBPB	chr1:193676374-193676727	HepG2	liver:	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
18	CEBPB	chr1:193674723-193674905	K562	blood:	n/a	n/a
19	CEBPB	chr1:193672866-193673033	Hela-S3	cervix:	n/a	chr1:193673020-193673033 chr1:193673022-193673033 chr1:193673020-193673033 chr1:193673022-193673033
20	CEBPB	chr1:193699029-193699628	A549	lung:	n/a	chr1:193699268-193699279
21	CEBPB	chr1:193669924-193670477	A549	lung:	n/a	n/a
22	CEBPB	chr1:193676350-193676774	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
23	CEBPB	chr1:193675044-193675257	H1-hESC	embryonic stem cell:	n/a	chr1:193675155-193675166
24	CEBPB	chr1:193674620-193675351	A549	lung:	n/a	chr1:193675155-193675166
25	CEBPB	chr1:193676071-193677191	Hela-S3	cervix:	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
26	CEBPB	chr1:193674567-193674928	A549	lung:	n/a	n/a
27	CEBPB	chr1:193699183-193699433	MCF-7	breast:	n/a	chr1:193699268-193699279
28	CEBPB	chr1:193699110-193699457	HepG2	liver:	n/a	chr1:193699268-193699279
29	CEBPB	chr1:193678847-193679096	A549	lung:	n/a	chr1:193679043-193679054
30	CEBPB	chr1:193678737-193679155	Hela-S3	cervix:	n/a	chr1:193679043-193679054
31	CEBPB	chr1:193676352-193677115	IMR90	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
32	CEBPB	chr1:193675974-193676147	A549	lung:	n/a	n/a
33	CEBPB	chr1:193695894-193696197	IMR90	lung:	n/a	n/a
34	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
35	CEBPB	chr1:193699094-193699474	A549	lung:	n/a	chr1:193699268-193699279
36	CEBPB	chr1:193675934-193677342	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
37	CEBPB	chr1:193674572-193675345	Hela-S3	cervix:	n/a	chr1:193675155-193675166
38	CEBPB	chr1:193674665-193675308	HepG2	liver:	n/a	chr1:193675155-193675166
39	CEBPB	chr1:193699089-193699516	A549	lung:	n/a	chr1:193699268-193699279
40	CEBPB	chr1:193678790-193679123	ECC-1	luminal epithelium:	n/a	chr1:193679043-193679054
41	CEBPB	chr1:193678796-193679122	ECC-1	luminal epithelium:	n/a	chr1:193679043-193679054
42	CEBPB	chr1:193678766-193679147	A549	lung:	n/a	chr1:193679043-193679054
43	CEBPB	chr1:193676394-193676726	K562	blood:	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
44	CEBPB	chr1:193677016-193677090	A549	lung:	n/a	n/a
45	CEBPB	chr1:193699108-193699363	H1-hESC	embryonic stem cell:	n/a	chr1:193699268-193699279
46	CEBPB	chr1:193698986-193699504	IMR90	lung:	n/a	chr1:193699268-193699279
47	CEBPB	chr1:193674600-193675346	IMR90	lung:	n/a	chr1:193675155-193675166
48	CHD2	chr1:193666450-193666523	Hela-S3	cervix:	n/a	n/a
49	CREB1	chr1:193676710-193676927	A549	lung:	n/a	n/a
50	CTCF	chr1:193677360-193677510	AG04449	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:193710042-193710092	HIPEpiC	eye:	n/a
2	chr1:193710042-193710092	ovcar-3	ovarian:	n/a
3	chr1:193710042-193710092	LNCaP	prostate:	n/a
4	chr1:193710042-193710092	SKMC	muscle:	n/a
5	chr1:193710042-193710092	AG04449	skin:	fetal
6	chr1:193710042-193710092	HCT-116	colon:	n/a
7	chr1:193710042-193710092	Jurkat	blood:	n/a
8	chr1:193710042-193710092	HepG2	liver:	n/a
9	chr1:193710042-193710092	T-47D	breast:	n/a
10	chr1:193710042-193710092	NHBE	bronchial:	n/a
11	chr1:193710042-193710092	HCM	heart:	n/a
12	chr1:193710042-193710092	HEK293	kidney:	embryo
13	chr1:193710042-193710092	HCPEpiC	choroid plexus:	n/a
14	chr1:193710042-193710092	GM12892	blood:	n/a
15	chr1:193710042-193710092	ECC-1	luminal epithelium:	n/a
16	chr1:193710042-193710092	SK-N-MC	brain:	n/a
17	chr1:193710042-193710092	IMR90	lung:	fetal
18	chr1:193710042-193710092	GM19239	blood:	n/a
19	chr1:193710042-193710092	AG10803	skin:	n/a
20	chr1:193710042-193710092	Caco-2	colon:	n/a
21	chr1:193710042-193710092	NH-A	brain:	n/a
22	chr1:193710042-193710092	BE2_C	brain:	n/a
23	chr1:193710042-193710092	HRE	kidney:	n/a
24	chr1:193710042-193710092	NHDF-neo	bronchial:	n/a
25	chr1:193710042-193710092	HL-60	blood:	n/a
26	chr1:193710042-193710092	CMK	blood:	n/a
27	chr1:193710042-193710092	HEEpiC	esophagus:	n/a
28	chr1:193710042-193710092	PrEC	prostate:	n/a
29	chr1:193710042-193710092	AG09309	skin:	n/a
30	chr1:193710042-193710092	K562	blood:	n/a
31	chr1:193710042-193710092	HCF	heart:	n/a
32	chr1:193710042-193710092	H1-hESC	embryonic stem cell:	embryo
33	chr1:193710042-193710092	HUVEC	blood vessel:	n/a
34	chr1:193710042-193710092	HNPCEpiC	eye:	n/a
35	chr1:193710042-193710092	MCF-7	breast:	n/a
36	chr1:193710042-193710092	NB4	blood:	n/a
37	chr1:193710042-193710092	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:193710042-193710092	MCF10A-Er-Src	breast:	n/a
39	chr1:193710042-193710092	HRPEpiC	eye:	n/a
40	chr1:193710042-193710092	Hepatocyte	liver:	n/a
41	chr1:193710042-193710092	ProgFib	skin:	n/a
42	chr1:193710042-193710092	GM12891	blood:	n/a
43	chr1:193710042-193710092	AG09319	gingival:	n/a
44	chr1:193710042-193710092	Hela-S3	cervix:	n/a
45	chr1:193710042-193710092	SK-N-SH	brain:	n/a
46	chr1:193710042-193710092	HRCEpiC	kidney:	n/a
47	chr1:193710042-193710092	AG04450	lung:	fetal
48	chr1:193710042-193710092	GM06990	blood:	n/a
49	chr1:193710042-193710092	A549	lung:	n/a
50	chr1:193710042-193710092	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:193678450..193681158-chr1:193682285..193685229,2	K562	blood:
2	chr1:193678450..193681158-chr1:193682285..193685229,2	K562	blood:
3	chr1:193705634..193708384-chr1:193710266..193712838,2	MCF-7	breast:
4	chr1:193681603..193683732-chr11:100996114..100998464,2	MCF-7	breast:
5	chr1:193705634..193708384-chr1:193710266..193712838,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDC73-2	chr1:193695962-193696313	XLOC_000509
2	lnc-CDC73-2	chr1:193695962-193696165	ENSG00000226640.2
3	lnc-CDC73-2	chr1:193694731-193694815	ENSG00000226640.2
4	lnc-CDC73-2	chr1:193694731-193694815	XLOC_000509

Variant related genes	Relation type
ENSG00000252241	TF binding region
ENSG00000237011	TF binding region
ENSG00000252241	CpG island
ENSG00000237011	CpG island

Extended variants
information (count: 987 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113254814	chr1:193661018-193661019	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs367566347	chr1:193661068-193661069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142077259	chr1:193661100-193661101	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs374980082	chr1:193661128-193661129	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566555297	chr1:193661183-193661184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs143652379	chr1:193661226-193661227	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs558830079	chr1:193661244-193661245	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs569017717	chr1:193661340-193661341	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs538048916	chr1:193661346-193661347	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs72728964	chr1:193661380-193661381	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs189266984	chr1:193661409-193661410	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs540365823	chr1:193661421-193661422	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs367614090	chr1:193661451-193661452	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs186115696	chr1:193661723-193661724	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs552242864	chr1:193661730-193661731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs569233497	chr1:193661748-193661749	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs55950830	chr1:193661772-193661773	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs61395568	chr1:193661778-193661779	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs74472149	chr1:193661779-193661780	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs200586017	chr1:193661780-193661781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs554890759	chr1:193661802-193661803	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs568292334	chr1:193661803-193661804	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs533949155	chr1:193661808-193661809	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs6694730	chr1:193661860-193661861	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs7547559	chr1:193661878-193661879	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs539514400	chr1:193661879-193661880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs555925073	chr1:193661907-193661908	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs564076278	chr1:193661942-193661943	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs79625122	chr1:193661947-193661948	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs544531008	chr1:193661950-193661951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs561217650	chr1:193661956-193661957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs183374109	chr1:193662011-193662012	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571907798	chr1:193662024-193662025	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs540388370	chr1:193662026-193662027	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs75931111	chr1:193664220-193664221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541370057	chr1:193664240-193664241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564232781	chr1:193664255-193664256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533298349	chr1:193664331-193664332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543347820	chr1:193664349-193664350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192907372	chr1:193664400-193664401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554091831	chr1:193664614-193664615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184714101	chr1:193664667-193664668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373815472	chr1:193664721-193664722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188599613	chr1:193664820-193664821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17376643	chr1:193664824-193664825	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs180733911	chr1:193664881-193664882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1339315	chr1:193664898-193664899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs201318660	chr1:193664905-193664906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183543064	chr1:193664922-193664923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149705223	chr1:193664969-193664970	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193664200-193664400	Enhancers	Brain Germinal Matrix	brain
2	chr1:193664600-193665000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:193665000-193665200	Enhancers	Brain Germinal Matrix	brain
4	chr1:193665600-193665800	Active TSS	A549	lung
5	chr1:193665800-193666000	Enhancers	A549	lung
6	chr1:193666000-193666200	Flanking Active TSS	A549	lung
7	chr1:193666000-193666600	Enhancers	Hela-S3	cervix
8	chr1:193666200-193666600	Enhancers	NHEK	skin
9	chr1:193666200-193667800	Enhancers	A549	lung
10	chr1:193666400-193667200	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr1:193666600-193669800	Weak transcription	Hela-S3	cervix
12	chr1:193666600-193669800	Weak transcription	NHEK	skin
13	chr1:193667800-193669000	Weak transcription	A549	lung
14	chr1:193669000-193669800	Enhancers	A549	lung
15	chr1:193669000-193673400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:193669200-193671400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr1:193669400-193670000	Enhancers	Right Atrium	heart
18	chr1:193669600-193670000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:193669600-193670600	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr1:193669600-193671400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:193669800-193670000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:193669800-193670200	Flanking Active TSS	A549	lung
23	chr1:193669800-193670600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:193669800-193670600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:193669800-193670800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:193669800-193670800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr1:193669800-193670800	Enhancers	NH-A	brain
28	chr1:193669800-193670800	Enhancers	NHEK	skin
29	chr1:193669800-193671200	Enhancers	HMEC	breast
30	chr1:193669800-193671400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:193669800-193671400	Enhancers	Hela-S3	cervix
32	chr1:193669800-193671600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:193669800-193672200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:193670000-193670600	Enhancers	HUVEC	blood vessel
35	chr1:193670000-193671400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr1:193670200-193670600	Active TSS	A549	lung
37	chr1:193670200-193671400	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr1:193670200-193674800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr1:193670600-193670800	Flanking Active TSS	A549	lung
40	chr1:193670600-193671000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr1:193670600-193674400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:193670600-193674600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:193670800-193672000	Enhancers	A549	lung
44	chr1:193670800-193674600	Weak transcription	NHEK	skin
45	chr1:193671000-193671200	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr1:193671200-193673800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr1:193671200-193674400	Weak transcription	HMEC	breast
48	chr1:193671400-193674600	Weak transcription	Hela-S3	cervix
49	chr1:193671400-193676000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:193671600-193672200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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