Variant report

Variant	nsv885925
Chromosome Location	chr6:57369086-57414774
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:894)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:894 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:57392130-57392164	HepG2	liver:	n/a	n/a
2	ATF1	chr6:57388328-57388901	K562	blood:	n/a	n/a
3	ATF1	chr6:57386257-57386379	K562	blood:	n/a	n/a
4	ATF1	chr6:57414346-57414465	K562	blood:	n/a	n/a
5	BACH1	chr6:57408878-57409078	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:57388299-57388865	K562	blood:	n/a	n/a
7	BHLHE40	chr6:57396741-57396999	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:57395851-57396136	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:57375272-57375472	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:57412393-57412615	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:57381413-57381830	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr6:57390670-57390900	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:57382748-57382761	HepG2	liver:	n/a	n/a
14	BRCA1	chr6:57370484-57370781	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:57398324-57398744	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr6:57376252-57377005	K562	blood:	n/a	n/a
17	CEBPB	chr6:57399959-57400230	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:57372189-57372470	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr6:57380150-57380500	Hela-S3	cervix:	n/a	chr6:57380307-57380318
20	CEBPB	chr6:57388199-57388630	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:57380170-57380548	MCF-7	breast:	n/a	chr6:57380307-57380318
22	CEBPB	chr6:57398622-57398907	HepG2	liver:	n/a	chr6:57398752-57398763
23	CEBPB	chr6:57380157-57380496	IMR90	lung:	n/a	chr6:57380307-57380318
24	CEBPB	chr6:57398646-57398920	HepG2	liver:	n/a	chr6:57398752-57398763
25	CEBPB	chr6:57385025-57385073	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr6:57380194-57380517	H1-hESC	embryonic stem cell:	n/a	chr6:57380307-57380318
27	CEBPB	chr6:57388224-57388584	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:57380175-57380499	A549	lung:	n/a	chr6:57380307-57380318
29	CEBPB	chr6:57388107-57388603	MCF-7	breast:	n/a	n/a
30	CEBPB	chr6:57380130-57380666	MCF-7	breast:	n/a	chr6:57380307-57380318
31	CEBPB	chr6:57380136-57380500	HepG2	liver:	n/a	chr6:57380307-57380318
32	CEBPB	chr6:57370190-57370638	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:57380149-57380488	K562	blood:	n/a	chr6:57380307-57380318
34	CEBPB	chr6:57388182-57388630	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:57380198-57380376	HepG2	liver:	n/a	chr6:57380307-57380318
36	CEBPZ	chr6:57373943-57374053	HepG2	liver:	n/a	n/a
37	CHD2	chr6:57386201-57386211	GM12878	blood:	n/a	n/a
38	CTCF	chr6:57396748-57396973	LNCaP	prostate:	n/a	n/a
39	CTCF	chr6:57412341-57412589	A549	lung:	n/a	chr6:57412435-57412453 chr6:57412438-57412451 chr6:57412437-57412458
40	CTCF	chr6:57412320-57412470	GM12878	blood:	n/a	chr6:57412435-57412453 chr6:57412438-57412451 chr6:57412437-57412458
41	CTCF	chr6:57412400-57412550	GM12866	blood:	n/a	chr6:57412435-57412453 chr6:57412438-57412451 chr6:57412437-57412458
42	CTCF	chr6:57412100-57412250	HPF	lung:	n/a	n/a
43	CTCF	chr6:57396780-57396930	HAc	cerebellar:	n/a	n/a
44	CTCF	chr6:57369820-57369970	HCFaa	heart:	n/a	n/a
45	CTCF	chr6:57396658-57397070	GM12878	blood:	n/a	n/a
46	CTCF	chr6:57369820-57369970	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr6:57396780-57396930	HepG2	liver:	n/a	n/a
48	CTCF	chr6:57369860-57370010	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:57412300-57412450	HMF	breast:	n/a	n/a
50	CTCF	chr6:57412350-57412557	NHEK	skin:	n/a	chr6:57412435-57412453 chr6:57412438-57412451 chr6:57412437-57412458

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:57385844-57385894	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:57384347-57384397	BE2_C	brain:	n/a
3	chr6:57391815-57391865	ovcar-3	ovarian:	n/a
4	chr6:57391815-57391865	GM12878	blood:	n/a
5	chr6:57384347-57384397	HUVEC	blood vessel:	n/a
6	chr6:57384347-57384397	SK-N-SH_RA	brain:	n/a
7	chr6:57385844-57385894	ProgFib	skin:	n/a
8	chr6:57391815-57391865	HAEpiC	amniotic membrane:	n/a
9	chr6:57384347-57384397	HMEC	breast:	n/a
10	chr6:57391815-57391865	RPTEC	kidney:	n/a
11	chr6:57385844-57385894	HL-60	blood:	n/a
12	chr6:57385844-57385894	HAEpiC	amniotic membrane:	n/a
13	chr6:57385844-57385894	HIPEpiC	eye:	n/a
14	chr6:57391815-57391865	LNCaP	prostate:	n/a
15	chr6:57385844-57385894	HRCEpiC	kidney:	n/a
16	chr6:57391815-57391865	CMK	blood:	n/a
17	chr6:57391815-57391865	AG10803	skin:	n/a
18	chr6:57384347-57384397	Jurkat	blood:	n/a
19	chr6:57384347-57384397	HCPEpiC	choroid plexus:	n/a
20	chr6:57391815-57391865	BJ	skin:	n/a
21	chr6:57385844-57385894	H1-hESC	embryonic stem cell:	embryo
22	chr6:57385844-57385894	RPTEC	kidney:	n/a
23	chr6:57385844-57385894	A549	lung:	n/a
24	chr6:57384347-57384397	GM06990	blood:	n/a
25	chr6:57384347-57384397	PANC-1	pancreas:	n/a
26	chr6:57391815-57391865	U87	brain:	n/a
27	chr6:57384347-57384397	SK-N-MC	brain:	n/a
28	chr6:57385844-57385894	AoSMC	blood vessel:	n/a
29	chr6:57384347-57384397	NB4	blood:	n/a
30	chr6:57385844-57385894	CMK	blood:	n/a
31	chr6:57385844-57385894	IMR90	lung:	fetal
32	chr6:57385844-57385894	GM19239	blood:	n/a
33	chr6:57385844-57385894	HepG2	liver:	n/a
34	chr6:57385844-57385894	PrEC	prostate:	n/a
35	chr6:57391815-57391865	AoSMC	blood vessel:	n/a
36	chr6:57391815-57391865	NB4	blood:	n/a
37	chr6:57384347-57384397	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:57385844-57385894	HEK293	kidney:	embryo
39	chr6:57385844-57385894	Hepatocyte	liver:	n/a
40	chr6:57384347-57384397	NHDF-neo	bronchial:	n/a
41	chr6:57385844-57385894	SK-N-MC	brain:	n/a
42	chr6:57384347-57384397	T-47D	breast:	n/a
43	chr6:57385844-57385894	GM12892	blood:	n/a
44	chr6:57391815-57391865	SKMC	muscle:	n/a
45	chr6:57384347-57384397	RPTEC	kidney:	n/a
46	chr6:57384347-57384397	ovcar-3	ovarian:	n/a
47	chr6:57385844-57385894	HCPEpiC	choroid plexus:	n/a
48	chr6:57385844-57385894	PANC-1	pancreas:	n/a
49	chr6:57385844-57385894	Hela-S3	cervix:	n/a
50	chr6:57391815-57391865	HMEC	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
2	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
3	chr6:57232895..57235001-chr6:57373838..57375777,2	K562	blood:
4	chr6:57380965..57383908-chr6:57390419..57392004,2	K562	blood:
5	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
6	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
7	chr6:57393591..57395977-chr6:57407320..57409957,2	MCF-7	breast:
8	chr6:57393591..57395977-chr6:57407320..57409957,2	MCF-7	breast:
9	chr6:57413449..57416181-chr6:57416496..57418603,2	K562	blood:
10	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
11	chr6:57368098..57370585-chr6:57379961..57384432,3	K562	blood:
12	chr6:57370604..57372865-chr6:57373848..57376238,2	K562	blood:
13	chr6:57386101..57388103-chr6:57389445..57391300,2	K562	blood:
14	chr6:57405693..57407850-chr6:57408076..57409919,2	K562	blood:
15	chr6:57396857..57397774-chr9:95368803..95369303,2	MCF-7	breast:
16	chr6:57371365..57373576-chr6:57373848..57375922,2	K562	blood:
17	chr6:57394320..57396660-chr6:58286293..58287831,2	MCF-7	breast:

No data

Variant related genes	Relation type
PRIM2	TF binding region
PRIM2	CpG island
ENSG00000146143	chromatin interactions
ENSG00000215190	chromatin interactions

Extended variants
information (count: 2916 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2916 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1407092	chr6:57369086-57369087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569145694	chr6:57369106-57369107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73755549	chr6:57369123-57369124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539331863	chr6:57369129-57369130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558069759	chr6:57369190-57369191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35467661	chr6:57369232-57369233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs375308035	chr6:57369235-57369236	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs375828214	chr6:57369236-57369237	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534041667	chr6:57369272-57369273	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555397077	chr6:57369303-57369304	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs573803912	chr6:57369307-57369308	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs76342631	chr6:57369326-57369327	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs72877197	chr6:57369330-57369331	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs201532661	chr6:57369333-57369334	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201004022	chr6:57369335-57369336	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs79035428	chr6:57369340-57369341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138197808	chr6:57369344-57369345	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs111572279	chr6:57369358-57369359	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs74756203	chr6:57369365-57369366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs9367753	chr6:57369378-57369379	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs556158447	chr6:57369379-57369380	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs577989605	chr6:57369385-57369386	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs545360728	chr6:57369402-57369403	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs78093556	chr6:57369434-57369435	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs76625188	chr6:57369448-57369449	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs77660032	chr6:57369469-57369470	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs78647869	chr6:57369480-57369481	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs78828860	chr6:57369481-57369482	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs560879929	chr6:57369485-57369486	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs572543690	chr6:57369491-57369492	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs28441291	chr6:57369502-57369503	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs62400894	chr6:57369510-57369511	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs77701301	chr6:57369548-57369549	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs79105637	chr6:57369561-57369562	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs80326614	chr6:57369577-57369578	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs75003452	chr6:57369578-57369579	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs74777255	chr6:57369590-57369591	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs77147843	chr6:57369607-57369608	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs77766190	chr6:57369615-57369616	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs62400895	chr6:57369624-57369625	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs67817875	chr6:57369651-57369652	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs543207462	chr6:57369677-57369678	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs558870193	chr6:57369695-57369696	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs369017485	chr6:57369696-57369697	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs561733577	chr6:57369698-57369699	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs28492998	chr6:57369703-57369704	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs529020467	chr6:57369743-57369744	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs28713778	chr6:57369763-57369764	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs78109430	chr6:57369847-57369848	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs28447577	chr6:57369893-57369894	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57355600-57370000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:57357000-57370000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:57358800-57372000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:57362800-57369800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:57362800-57369800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:57365400-57369400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:57365600-57369600	Weak transcription	Colon Smooth Muscle	Colon
8	chr6:57365800-57369400	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:57366000-57369400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:57366000-57369400	Weak transcription	NHDF-Ad	bronchial
11	chr6:57366000-57369800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:57366000-57370000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:57366000-57370200	Weak transcription	Osteobl	bone
14	chr6:57366000-57371800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:57367400-57370000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr6:57367400-57371800	Weak transcription	Aorta	Aorta
17	chr6:57367600-57369800	Weak transcription	Psoas Muscle	Psoas
18	chr6:57369200-57370600	Enhancers	Dnd41	blood
19	chr6:57369400-57369800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:57369400-57370000	Enhancers	NHDF-Ad	bronchial
21	chr6:57369400-57370400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr6:57369400-57372600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr6:57369600-57370600	Enhancers	Colon Smooth Muscle	Colon
24	chr6:57369800-57370200	Active TSS	Psoas Muscle	Psoas
25	chr6:57369800-57370400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:57369800-57370800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:57369800-57370800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:57369800-57370800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:57369800-57370800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:57370000-57370200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:57370000-57370400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr6:57370000-57370400	Flanking Active TSS	NHDF-Ad	bronchial
33	chr6:57370000-57370600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr6:57370000-57370800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:57370200-57370400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr6:57370200-57370400	Enhancers	Osteobl	bone
37	chr6:57370200-57370600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr6:57370200-57370600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr6:57370400-57370800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:57370400-57370800	Enhancers	NHDF-Ad	bronchial
41	chr6:57370400-57374200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:57370400-57380200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr6:57370600-57370800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:57370600-57372000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr6:57370600-57372200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr6:57370800-57371000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:57370800-57371800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr6:57370800-57372000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr6:57370800-57372000	Weak transcription	NHDF-Ad	bronchial
50	chr6:57371600-57375400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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