Variant report

Variant	nsv1018528
Chromosome Location	chr6:65706561-65900388
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:65877133-65877402	HepG2	liver:	n/a	chr6:65877288-65877299
2	CEBPB	chr6:65714814-65714999	A549	lung:	n/a	chr6:65714880-65714891
3	CEBPB	chr6:65867884-65868178	IMR90	lung:	n/a	chr6:65867989-65868002 chr6:65867991-65868000 chr6:65867991-65868002
4	CEBPB	chr6:65769840-65770057	HepG2	liver:	n/a	chr6:65769968-65769979
5	CEBPB	chr6:65714828-65715032	HepG2	liver:	n/a	chr6:65714880-65714891
6	CEBPB	chr6:65755777-65756072	A549	lung:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
7	CEBPB	chr6:65852457-65852466	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:65755724-65756051	K562	blood:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
9	CEBPB	chr6:65840033-65840285	HepG2	liver:	n/a	chr6:65840147-65840158
10	CEBPB	chr6:65895166-65895539	HepG2	liver:	n/a	chr6:65895346-65895357
11	CEBPB	chr6:65757460-65757715	HepG2	liver:	n/a	chr6:65757602-65757613
12	CEBPB	chr6:65895196-65895497	A549	lung:	n/a	chr6:65895346-65895357
13	CEBPB	chr6:65866932-65867276	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:65866986-65867268	A549	lung:	n/a	n/a
15	CEBPB	chr6:65866950-65867272	IMR90	lung:	n/a	n/a
16	CEBPB	chr6:65716700-65717039	HepG2	liver:	n/a	chr6:65716874-65716885
17	CEBPB	chr6:65867011-65867264	K562	blood:	n/a	n/a
18	CEBPB	chr6:65755716-65756078	HepG2	liver:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
19	CEBPB	chr6:65755738-65756070	IMR90	lung:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
20	CEBPB	chr6:65755702-65756077	Hela-S3	cervix:	n/a	chr6:65755859-65755870 chr6:65755888-65755899
21	CEBPB	chr6:65866943-65867264	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:65716699-65717038	H1-hESC	embryonic stem cell:	n/a	chr6:65716874-65716885
23	CHD2	chr6:65740417-65740502	HepG2	liver:	n/a	n/a
24	CTCF	chr6:65723620-65723770	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr6:65799702-65799745	GM13976	blood:	n/a	n/a
26	CTCF	chr6:65723598-65723621	GM19238	blood:	n/a	n/a
27	CTCF	chr6:65731488-65731566	Lung_OC	lung:	n/a	n/a
28	CTCF	chr6:65723540-65723690	GM12868	blood:	n/a	n/a
29	CTCF	chr6:65801215-65801258	GM13976	blood:	n/a	n/a
30	CTCF	chr6:65836720-65836870	GM12871	blood:	n/a	n/a
31	CTCF	chr6:65723460-65723610	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr6:65783645-65783977	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:65723540-65723690	HepG2	liver:	n/a	n/a
34	CTCF	chr6:65723520-65723670	GM12878	blood:	n/a	n/a
35	CTCF	chr6:65723440-65723590	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr6:65723460-65723610	GM12871	blood:	n/a	n/a
37	CTCF	chr6:65783716-65783806	LNCaP	prostate:	n/a	n/a
38	CTCF	chr6:65723540-65723690	GM12864	blood:	n/a	n/a
39	CTCF	chr6:65723463-65723778	GM12878	blood:	n/a	n/a
40	CTCF	chr6:65736512-65736545	GM13977	blood:	n/a	n/a
41	CTCF	chr6:65783872-65783874	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:65723560-65723710	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:65723540-65723690	GM12865	blood:	n/a	n/a
44	CTCF	chr6:65714320-65714470	HEK293	kidney:	n/a	n/a
45	CTCF	chr6:65723572-65723673	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:65723565-65723648	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr6:65731412-65731453	GM13976	blood:	n/a	n/a
48	CTCF	chr6:65723547-65723666	Gliobla	brain:	n/a	n/a
49	CTCF	chr6:65733640-65733676	Fibrobl	skin:	n/a	n/a
50	CTCF	chr6:65714280-65714430	HBMEC	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:65779514-65779564	HCPEpiC	choroid plexus:	n/a
2	chr6:65779514-65779564	ovcar-3	ovarian:	n/a
3	chr6:65779514-65779564	Hepatocyte	liver:	n/a
4	chr6:65779514-65779564	K562	blood:	n/a
5	chr6:65779514-65779564	HepG2	liver:	n/a
6	chr6:65779514-65779564	HNPCEpiC	eye:	n/a
7	chr6:65779514-65779564	NB4	blood:	n/a
8	chr6:65779514-65779564	HUVEC	blood vessel:	n/a
9	chr6:65779514-65779564	HEK293	kidney:	embryo
10	chr6:65779514-65779564	HRPEpiC	eye:	n/a
11	chr6:65779514-65779564	HMEC	breast:	n/a
12	chr6:65779514-65779564	AG04450	lung:	fetal
13	chr6:65779514-65779564	MCF-7	breast:	n/a
14	chr6:65779514-65779564	AG04449	skin:	fetal
15	chr6:65779514-65779564	BJ	skin:	n/a
16	chr6:65779514-65779564	PANC-1	pancreas:	n/a
17	chr6:65779514-65779564	GM19239	blood:	n/a
18	chr6:65779514-65779564	NT2-D1	testis:	n/a
19	chr6:65779514-65779564	RPTEC	kidney:	n/a
20	chr6:65779514-65779564	ECC-1	luminal epithelium:	n/a
21	chr6:65779514-65779564	IMR90	lung:	fetal
22	chr6:65779514-65779564	Caco-2	colon:	n/a
23	chr6:65779514-65779564	CMK	blood:	n/a
24	chr6:65779514-65779564	ProgFib	skin:	n/a
25	chr6:65779514-65779564	SK-N-SH	brain:	n/a
26	chr6:65779514-65779564	AG09309	skin:	n/a
27	chr6:65779514-65779564	SK-N-SH_RA	brain:	n/a
28	chr6:65779514-65779564	HCM	heart:	n/a
29	chr6:65779514-65779564	AG09319	gingival:	n/a
30	chr6:65779514-65779564	Jurkat	blood:	n/a
31	chr6:65779514-65779564	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:65779514-65779564	HCT-116	colon:	n/a
33	chr6:65779514-65779564	T-47D	breast:	n/a
34	chr6:65779514-65779564	HAEpiC	amniotic membrane:	n/a
35	chr6:65779514-65779564	SK-N-MC	brain:	n/a
36	chr6:65779514-65779564	HIPEpiC	eye:	n/a
37	chr6:65779514-65779564	A549	lung:	n/a
38	chr6:65779514-65779564	HRE	kidney:	n/a
39	chr6:65779514-65779564	AoSMC	blood vessel:	n/a
40	chr6:65779514-65779564	GM12878	blood:	n/a
41	chr6:65779514-65779564	NHDF-neo	bronchial:	n/a
42	chr6:65779514-65779564	AG10803	skin:	n/a
43	chr6:65779514-65779564	HL-60	blood:	n/a
44	chr6:65779514-65779564	NH-A	brain:	n/a
45	chr6:65779514-65779564	H1-hESC	embryonic stem cell:	embryo
46	chr6:65779514-65779564	LNCaP	prostate:	n/a
47	chr6:65779514-65779564	U87	brain:	n/a
48	chr6:65779514-65779564	HEEpiC	esophagus:	n/a
49	chr6:65779514-65779564	PrEC	prostate:	n/a
50	chr6:65779514-65779564	HCF	heart:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:62312608..62314638-chr6:65744579..65746564,2	MCF-7	breast:
2	chr6:65761200..65763394-chr6:65766854..65768992,2	K562	blood:
3	chr6:65821770..65824951-chr6:65826871..65829970,3	K562	blood:
4	chr6:65781439..65783033-chr6:65783370..65784893,2	MCF-7	breast:
5	chr6:65781439..65783033-chr6:65783370..65784893,2	MCF-7	breast:
6	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:
7	chr6:65778187..65780499-chr6:65782117..65784614,2	K562	blood:
8	chr6:65821523..65823761-chr6:65825584..65828218,2	MCF-7	breast:
9	chr6:65761200..65763394-chr6:65766854..65768992,2	K562	blood:
10	chr6:65879743..65881792-chr6:65884642..65887053,2	MCF-7	breast:
11	chr6:65821523..65823761-chr6:65825584..65828218,2	MCF-7	breast:
12	chr6:65778187..65780499-chr6:65782117..65784614,2	K562	blood:
13	chr6:65821770..65824951-chr6:65826871..65829970,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000256352	TF binding region
ENSG00000256352	CpG island
ENSG00000257058	chromatin interactions
ENSG00000124942	chromatin interactions

Extended variants
information (count: 2363 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2363 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78430676	chr6:65706563-65706564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546909940	chr6:65706576-65706577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566732687	chr6:65706581-65706582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs535892443	chr6:65706585-65706586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs9363310	chr6:65706605-65706606	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs575285311	chr6:65706621-65706622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537967594	chr6:65706624-65706625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188320323	chr6:65706656-65706657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139429852	chr6:65706717-65706718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142934743	chr6:65706730-65706731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554495213	chr6:65706761-65706762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9345583	chr6:65706775-65706776	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146137585	chr6:65706798-65706799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561531064	chr6:65706805-65706806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140073318	chr6:65706872-65706873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143652179	chr6:65706915-65706916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533192226	chr6:65706927-65706928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9363311	chr6:65706941-65706942	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs529025135	chr6:65706994-65706995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529174705	chr6:65707010-65707011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549327606	chr6:65707031-65707032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146816475	chr6:65707035-65707036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73765712	chr6:65707054-65707055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185554931	chr6:65707071-65707072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62416484	chr6:65707087-65707088	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534444311	chr6:65707108-65707109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115079179	chr6:65707123-65707124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574229001	chr6:65707155-65707156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542973760	chr6:65707165-65707166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376823015	chr6:65707206-65707207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575347982	chr6:65707215-65707216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190357926	chr6:65707283-65707284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564222990	chr6:65707296-65707297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376045129	chr6:65707311-65707312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533154524	chr6:65707382-65707383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540385421	chr6:65707392-65707393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183469696	chr6:65707404-65707405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187199454	chr6:65707455-65707456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78511049	chr6:65707465-65707466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201652272	chr6:65707500-65707501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191946856	chr6:65707544-65707545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531640725	chr6:65707575-65707576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9453148	chr6:65707577-65707578	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs370950248	chr6:65707633-65707634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184197085	chr6:65707639-65707640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554315246	chr6:65707654-65707655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567779767	chr6:65707680-65707681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368742065	chr6:65707704-65707705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115062003	chr6:65707716-65707717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556926587	chr6:65707720-65707721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Epilepsy	20502679	CNVD
Dyslexia	22102821	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:65706200-65707000	Enhancers	Pancreas	Pancrea
2	chr6:65706400-65707000	Enhancers	Fetal Heart	heart
3	chr6:65707000-65716000	Weak transcription	Pancreas	Pancrea
4	chr6:65707400-65707600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr6:65707600-65709400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:65708400-65712000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:65709200-65709800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr6:65709400-65709600	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr6:65709400-65709800	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr6:65709600-65709800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr6:65712000-65715000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:65716000-65716200	Enhancers	Pancreas	Pancrea
13	chr6:65716400-65716800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr6:65716400-65717000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr6:65716600-65717000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr6:65716600-65717000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:65730400-65731000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:65731000-65740200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr6:65738800-65743200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr6:65739800-65740200	Enhancers	Pancreas	Pancrea
21	chr6:65740200-65740400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:65740200-65740600	ZNF genes & repeats	Pancreas	Pancrea
23	chr6:65743200-65743400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:65767200-65767800	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr6:65767800-65768600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:65774800-65775000	Enhancers	Spleen	Spleen
27	chr6:65784800-65786400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr6:65785400-65786600	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr6:65785800-65786200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr6:65786600-65788400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr6:65788400-65788600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr6:65788600-65789000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:65789800-65791400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:65807800-65808200	Enhancers	Fetal Brain Female	brain
35	chr6:65808000-65808400	Enhancers	Fetal Brain Male	brain
36	chr6:65819600-65819800	Enhancers	Ovary	ovary
37	chr6:65820000-65820400	Enhancers	Fetal Kidney	kidney
38	chr6:65822600-65823600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:65822600-65823800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:65823400-65824000	Enhancers	HUVEC	blood vessel
41	chr6:65826400-65826800	Enhancers	Placenta Amnion	Placenta Amnion
42	chr6:65826800-65827200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:65826800-65827200	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr6:65827200-65827400	Enhancers	Placenta Amnion	Placenta Amnion
45	chr6:65827400-65828200	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr6:65828000-65828600	Enhancers	Fetal Lung	lung
47	chr6:65828200-65828600	Enhancers	Placenta Amnion	Placenta Amnion
48	chr6:65833200-65833800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr6:65833400-65833800	Enhancers	Fetal Lung	lung
50	chr6:65833400-65834000	Enhancers	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links