Variant report

Variant	nsv819609
Chromosome Location	chr6:36700559-36708943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:183)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr6:36708312-36708547	GM12878	blood:	n/a	n/a
2	BHLHE40	chr6:36708418-36708433	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:36708380-36708460	K562	blood:	n/a	n/a
4	CEBPB	chr6:36701348-36701475	HepG2	liver:	n/a	chr6:36701405-36701416
5	CEBPB	chr6:36701325-36701540	A549	lung:	n/a	chr6:36701405-36701416
6	CEBPB	chr6:36702907-36703264	IMR90	lung:	n/a	n/a
7	CTCF	chr6:36703560-36703710	AG04449	skin:	n/a	n/a
8	CTCF	chr6:36703540-36703690	HUVEC	blood vessel:	n/a	n/a
9	CTCF	chr6:36702900-36703050	HPF	lung:	n/a	n/a
10	CTCF	chr6:36702860-36703010	NHDF-neo	bronchial:	n/a	n/a
11	CTCF	chr6:36702400-36702550	HEK293	kidney:	n/a	chr6:36702494-36702512 chr6:36702501-36702509
12	CTCF	chr6:36702799-36703127	GM12878	blood:	n/a	n/a
13	CTCF	chr6:36702860-36703010	RPTEC	kidney:	n/a	n/a
14	CTCF	chr6:36702860-36703010	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr6:36702920-36703070	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr6:36702660-36702810	GM12872	blood:	n/a	n/a
17	CTCF	chr6:36702859-36703060	GM19238	blood:	n/a	n/a
18	CTCF	chr6:36702560-36702710	GM12874	blood:	n/a	n/a
19	CTCF	chr6:36702940-36703090	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr6:36702940-36703090	GM12869	blood:	n/a	n/a
21	CTCF	chr6:36702940-36703090	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr6:36702880-36703030	GM12868	blood:	n/a	n/a
23	CTCF	chr6:36702904-36703044	K562	blood:	n/a	n/a
24	CTCF	chr6:36702984-36703015	K562	blood:	n/a	n/a
25	CTCF	chr6:36702860-36703010	GM12874	blood:	n/a	n/a
26	CTCF	chr6:36702860-36703010	BJ	skin:	n/a	n/a
27	CTCF	chr6:36702840-36702990	GM12875	blood:	n/a	n/a
28	CTCF	chr6:36702920-36703070	HVMF	connective:	n/a	n/a
29	CTCF	chr6:36703180-36703330	WI-38	lung:	n/a	n/a
30	CTCF	chr6:36702860-36703010	HCM	heart:	n/a	n/a
31	CTCF	chr6:36702900-36703050	AG09319	gingival:	n/a	n/a
32	CTCF	chr6:36702360-36702510	GM12873	blood:	n/a	chr6:36702501-36702509
33	CTCF	chr6:36702880-36703030	HL-60	blood:	n/a	n/a
34	CTCF	chr6:36702900-36703050	HCFaa	heart:	n/a	n/a
35	CTCF	chr6:36702820-36702970	GM12864	blood:	n/a	n/a
36	CTCF	chr6:36702960-36703110	GM12872	blood:	n/a	n/a
37	CTCF	chr6:36703640-36703790	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr6:36702880-36703030	NHEK	skin:	n/a	n/a
39	CTCF	chr6:36702900-36703050	SAEC	small airway:	n/a	n/a
40	CTCF	chr6:36702900-36703190	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr6:36702920-36703070	GM12875	blood:	n/a	n/a
42	CTCF	chr6:36702840-36702990	AG04450	lung:	n/a	n/a
43	CTCF	chr6:36702920-36703070	AG10803	skin:	n/a	n/a
44	CTCF	chr6:36703660-36703810	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr6:36702880-36703030	GM12864	blood:	n/a	n/a
46	CTCF	chr6:36703560-36703710	AG10803	skin:	n/a	n/a
47	CTCF	chr6:36702880-36703030	GM12872	blood:	n/a	n/a
48	CTCF	chr6:36702900-36703050	GM12871	blood:	n/a	n/a
49	CTCF	chr6:36703660-36703810	HCM	heart:	n/a	n/a
50	CTCF	chr6:36702887-36702888	Fibrobl	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:36703127-36703177	GM12892	blood:	n/a
2	chr6:36703127-36703177	NT2-D1	testis:	n/a
3	chr6:36703127-36703177	BE2_C	brain:	n/a
4	chr6:36703127-36703177	HPAEpiC	pulmonary alveolar:	n/a
5	chr6:36703127-36703177	HCPEpiC	choroid plexus:	n/a
6	chr6:36703127-36703177	HRPEpiC	eye:	n/a
7	chr6:36703127-36703177	HIPEpiC	eye:	n/a
8	chr6:36703127-36703177	T-47D	breast:	n/a
9	chr6:36703127-36703177	A549	lung:	n/a
10	chr6:36703127-36703177	GM12891	blood:	n/a
11	chr6:36703127-36703177	IMR90	lung:	fetal
12	chr6:36703127-36703177	K562	blood:	n/a
13	chr6:36703127-36703177	HEEpiC	esophagus:	n/a
14	chr6:36703127-36703177	AG09309	skin:	n/a
15	chr6:36703127-36703177	LNCaP	prostate:	n/a
16	chr6:36703127-36703177	PFSK-1	brain:	n/a
17	chr6:36703127-36703177	Jurkat	blood:	n/a
18	chr6:36703127-36703177	Caco-2	colon:	n/a
19	chr6:36703127-36703177	ECC-1	luminal epithelium:	n/a
20	chr6:36703127-36703177	HRE	kidney:	n/a
21	chr6:36703127-36703177	HEK293	kidney:	embryo
22	chr6:36703127-36703177	HRCEpiC	kidney:	n/a
23	chr6:36703127-36703177	HL-60	blood:	n/a
24	chr6:36703127-36703177	GM19239	blood:	n/a
25	chr6:36703127-36703177	NHDF-neo	bronchial:	n/a
26	chr6:36703127-36703177	PANC-1	pancreas:	n/a
27	chr6:36703127-36703177	HUVEC	blood vessel:	n/a
28	chr6:36703127-36703177	ProgFib	skin:	n/a
29	chr6:36703127-36703177	AG10803	skin:	n/a
30	chr6:36703127-36703177	U87	brain:	n/a
31	chr6:36703127-36703177	SAEC	small airway:	n/a
32	chr6:36703127-36703177	GM06990	blood:	n/a
33	chr6:36703127-36703177	HAEpiC	amniotic membrane:	n/a
34	chr6:36703127-36703177	H1-hESC	embryonic stem cell:	embryo
35	chr6:36703127-36703177	Hepatocyte	liver:	n/a
36	chr6:36703127-36703177	HMEC	breast:	n/a
37	chr6:36703127-36703177	MCF-7	breast:	n/a
38	chr6:36703127-36703177	AoSMC	blood vessel:	n/a
39	chr6:36703127-36703177	AG09319	gingival:	n/a
40	chr6:36703127-36703177	GM12878	blood:	n/a
41	chr6:36703127-36703177	MCF10A-Er-Src	breast:	n/a
42	chr6:36703127-36703177	NHBE	bronchial:	n/a
43	chr6:36703127-36703177	HepG2	liver:	n/a
44	chr6:36703127-36703177	HCF	heart:	n/a
45	chr6:36703127-36703177	AG04450	lung:	fetal
46	chr6:36703127-36703177	AG04449	skin:	fetal
47	chr6:36703127-36703177	BJ	skin:	n/a
48	chr6:36703127-36703177	SKMC	muscle:	n/a
49	chr6:36703127-36703177	SK-N-SH	brain:	n/a
50	chr6:36703127-36703177	NH-A	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36695657..36698030-chr6:36700581..36702478,2	K562	blood:
2	chr6:36583432..36585248-chr6:36700120..36704013,3	MCF-7	breast:
3	chr6:36561612..36564233-chr6:36698669..36701218,2	MCF-7	breast:
4	chr6:36708174..36711394-chr6:36720287..36721932,3	MCF-7	breast:
5	chr6:36706791..36710785-chr6:36712838..36716064,4	MCF-7	breast:
6	chr6:36706145..36708888-chr6:36709331..36711123,2	MCF-7	breast:
7	chr6:36692869..36694899-chr6:36700775..36703080,2	MCF-7	breast:
8	chr6:36588827..36591407-chr6:36708568..36710825,2	MCF-7	breast:
9	chr6:36705988..36708979-chr6:36709402..36712073,2	K562	blood:
10	chr6:36681851..36683948-chr6:36705203..36707828,2	K562	blood:
11	chr6:36561849..36563615-chr6:36700031..36702846,2	K562	blood:
12	chr6:36706267..36708533-chr6:36712946..36714916,2	K562	blood:
13	chr6:36646178..36648267-chr6:36708912..36712169,4	MCF-7	breast:
14	chr6:36708918..36710565-chr6:36712727..36715586,2	K562	blood:
15	chr6:36705103..36707775-chr6:36711430..36713266,2	MCF-7	breast:
16	chr6:36704975..36706910-chr6:36710272..36712382,2	MCF-7	breast:
17	chr6:36693621..36695483-chr6:36698291..36701067,2	MCF-7	breast:
18	chr6:36575587..36577672-chr6:36699166..36700977,3	MCF-7	breast:
19	chr6:36699118..36702234-chr6:36702324..36705046,3	K562	blood:
20	chr6:36708140..36710606-chr6:36718569..36720077,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000220349	TF binding region
ENSG00000220349	CpG island
ENSG00000255587	chromatin interactions
ENSG00000263894	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000124762	chromatin interactions
ENSG00000220349	chromatin interactions

Extended variants
information (count: 347 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2105905	chr6:36700587-36700588	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs185960837	chr6:36700602-36700603	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs3939037	chr6:36700603-36700604	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547794659	chr6:36700607-36700608	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs369738683	chr6:36700620-36700621	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374905374	chr6:36700634-36700635	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2105906	chr6:36700636-36700637	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531346896	chr6:36700722-36700723	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs534361092	chr6:36700733-36700734	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs143837468	chr6:36700768-36700769	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs562864665	chr6:36700771-36700772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs236460	chr6:36700833-36700834	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs145809741	chr6:36700861-36700862	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530566366	chr6:36700888-36700889	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs236459	chr6:36700899-36700900	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs557745513	chr6:36700901-36700902	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs117097482	chr6:36700906-36700907	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs61201423	chr6:36700937-36700938	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs371086495	chr6:36700946-36700947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371872446	chr6:36700947-36700948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539272243	chr6:36700960-36700961	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs530696572	chr6:36700999-36701000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs236458	chr6:36701008-36701009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs375717903	chr6:36701030-36701031	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs58569420	chr6:36701034-36701035	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190424849	chr6:36701086-36701087	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs149072421	chr6:36701091-36701092	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566775185	chr6:36701097-36701098	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542417406	chr6:36701114-36701115	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs561054073	chr6:36701128-36701129	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs575705705	chr6:36701144-36701145	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142117370	chr6:36701152-36701153	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs564577971	chr6:36701192-36701193	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201482281	chr6:36701211-36701212	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs114605304	chr6:36701214-36701215	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs151158020	chr6:36701227-36701228	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560582704	chr6:36701239-36701240	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs527899650	chr6:36701245-36701246	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs549279936	chr6:36701279-36701280	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567824194	chr6:36701317-36701318	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs538373454	chr6:36701371-36701372	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577767580	chr6:36701377-36701378	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs55861143	chr6:36701408-36701409	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs236457	chr6:36701427-36701428	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554045404	chr6:36701429-36701430	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs55806450	chr6:36701466-36701467	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549653176	chr6:36701483-36701484	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183998907	chr6:36701500-36701501	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557951809	chr6:36701501-36701502	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs536469872	chr6:36701514-36701515	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	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
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36688400-36702200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:36689200-36702400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:36690400-36702600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:36694000-36703000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:36695800-36702600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:36695800-36702800	Weak transcription	Gastric	stomach
7	chr6:36696000-36702600	Weak transcription	NHEK	skin
8	chr6:36696600-36702200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr6:36696800-36702200	Weak transcription	Lung	lung
10	chr6:36696800-36702200	Weak transcription	Spleen	Spleen
11	chr6:36696800-36702200	Weak transcription	NHLF	lung
12	chr6:36697000-36702200	Weak transcription	Primary B cells from cord blood	blood
13	chr6:36697200-36702400	Weak transcription	Adipose Nuclei	Adipose
14	chr6:36697200-36702400	Weak transcription	NHDF-Ad	bronchial
15	chr6:36697400-36702600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr6:36697600-36701400	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr6:36697600-36701400	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr6:36697600-36702600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:36697600-36702600	Weak transcription	HUVEC	blood vessel
20	chr6:36697800-36702400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:36698000-36701400	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr6:36699000-36702200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr6:36699200-36702200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:36699200-36703200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr6:36699200-36703400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:36699600-36702400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:36699800-36702200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:36700000-36702200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:36700200-36700800	Enhancers	Fetal Brain Male	brain
30	chr6:36700200-36700800	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr6:36700600-36702400	Weak transcription	Right Atrium	heart
32	chr6:36700800-36701200	Enhancers	Brain Hippocampus Middle	brain
33	chr6:36700800-36702200	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr6:36700800-36702400	Weak transcription	Fetal Brain Male	brain
35	chr6:36701200-36702400	Enhancers	Fetal Muscle Leg	muscle
36	chr6:36701200-36702400	Weak transcription	GM12878-XiMat	blood
37	chr6:36701400-36701600	Genic enhancers	Monocytes-CD14+_RO01746	blood
38	chr6:36701400-36702000	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr6:36701400-36702200	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr6:36701600-36702200	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr6:36702000-36702800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr6:36702000-36704000	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr6:36702200-36702400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:36702200-36702400	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr6:36702200-36702400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr6:36702200-36702600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:36702200-36702600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr6:36702200-36702600	Bivalent Enhancer	Fetal Stomach	stomach
49	chr6:36702200-36702600	Enhancers	NHLF	lung
50	chr6:36702200-36702800	Enhancers	Primary B cells from cord blood	blood

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