Variant report

Variant	nsv885812
Chromosome Location	chr6:36696904-36705684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:229)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:229 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:36701348-36701475	HepG2	liver:	n/a	chr6:36701405-36701416
2	CEBPB	chr6:36702907-36703264	IMR90	lung:	n/a	n/a
3	CEBPB	chr6:36701325-36701540	A549	lung:	n/a	chr6:36701405-36701416
4	CTCF	chr6:36702880-36703030	NHEK	skin:	n/a	n/a
5	CTCF	chr6:36699780-36699930	HEK293	kidney:	n/a	n/a
6	CTCF	chr6:36702860-36703010	HPF	lung:	n/a	n/a
7	CTCF	chr6:36699747-36699918	MCF-7	breast:	n/a	n/a
8	CTCF	chr6:36702800-36702950	NB4	blood:	n/a	n/a
9	CTCF	chr6:36702560-36702710	GM12874	blood:	n/a	n/a
10	CTCF	chr6:36702860-36703010	NHEK	skin:	n/a	n/a
11	CTCF	chr6:36702500-36702650	GM12865	blood:	n/a	chr6:36702501-36702509
12	CTCF	chr6:36702799-36703127	GM12878	blood:	n/a	n/a
13	CTCF	chr6:36702860-36703010	HVMF	connective:	n/a	n/a
14	CTCF	chr6:36702940-36703090	NHLF	lung:	n/a	n/a
15	CTCF	chr6:36699753-36699935	GM19240	blood:	n/a	n/a
16	CTCF	chr6:36699780-36699930	GM12873	blood:	n/a	n/a
17	CTCF	chr6:36699820-36699905	GM19239	blood:	n/a	n/a
18	CTCF	chr6:36702920-36703070	AG10803	skin:	n/a	n/a
19	CTCF	chr6:36703560-36703710	AG10803	skin:	n/a	n/a
20	CTCF	chr6:36702920-36703070	AG09319	gingival:	n/a	n/a
21	CTCF	chr6:36699763-36699902	A549	lung:	n/a	n/a
22	CTCF	chr6:36702920-36702984	GM13976	blood:	n/a	n/a
23	CTCF	chr6:36699740-36699890	HCT-116	colon:	n/a	n/a
24	CTCF	chr6:36702920-36703070	GM12875	blood:	n/a	n/a
25	CTCF	chr6:36703800-36703950	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr6:36702920-36703070	HMF	breast:	n/a	n/a
27	CTCF	chr6:36702860-36703010	HCM	heart:	n/a	n/a
28	CTCF	chr6:36699740-36699890	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr6:36702660-36702810	GM12872	blood:	n/a	n/a
30	CTCF	chr6:36702920-36703070	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr6:36703700-36703850	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr6:36702860-36703010	RPTEC	kidney:	n/a	n/a
33	CTCF	chr6:36703620-36703770	AG10803	skin:	n/a	n/a
34	CTCF	chr6:36702900-36703050	GM12878	blood:	n/a	n/a
35	CTCF	chr6:36699740-36699890	GM12874	blood:	n/a	n/a
36	CTCF	chr6:36703795-36703886	Lung_OC	lung:	n/a	n/a
37	CTCF	chr6:36699823-36699864	Medullo	brain:	n/a	n/a
38	CTCF	chr6:36702951-36703023	Gliobla	brain:	n/a	n/a
39	CTCF	chr6:36702880-36703030	GM12864	blood:	n/a	n/a
40	CTCF	chr6:36702904-36703044	K562	blood:	n/a	n/a
41	CTCF	chr6:36702820-36702970	HAc	cerebellar:	n/a	n/a
42	CTCF	chr6:36702840-36702990	AG04450	lung:	n/a	n/a
43	CTCF	chr6:36702800-36702950	HCM	heart:	n/a	n/a
44	CTCF	chr6:36702840-36702990	GM12875	blood:	n/a	n/a
45	CTCF	chr6:36702859-36703060	GM19238	blood:	n/a	n/a
46	CTCF	chr6:36703800-36703950	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr6:36703660-36703810	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr6:36699753-36699913	K562	blood:	n/a	n/a
49	CTCF	chr6:36702900-36703050	AG09319	gingival:	n/a	n/a
50	CTCF	chr6:36702893-36703008	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	K562	blood:	n/a
2	chr6:36703127-36703177	U87	brain:	n/a
3	chr6:36703127-36703177	AG04449	skin:	fetal
4	chr6:36703127-36703177	MCF-7	breast:	n/a
5	chr6:36703127-36703177	HCPEpiC	choroid plexus:	n/a
6	chr6:36703127-36703177	NT2-D1	testis:	n/a
7	chr6:36703127-36703177	BJ	skin:	n/a
8	chr6:36703127-36703177	LNCaP	prostate:	n/a
9	chr6:36703127-36703177	SK-N-SH_RA	brain:	n/a
10	chr6:36703127-36703177	HEEpiC	esophagus:	n/a
11	chr6:36703127-36703177	SK-N-MC	brain:	n/a
12	chr6:36703127-36703177	HCF	heart:	n/a
13	chr6:36703127-36703177	HIPEpiC	eye:	n/a
14	chr6:36703127-36703177	AG09319	gingival:	n/a
15	chr6:36703127-36703177	GM19239	blood:	n/a
16	chr6:36703127-36703177	AG09309	skin:	n/a
17	chr6:36703127-36703177	ECC-1	luminal epithelium:	n/a
18	chr6:36703127-36703177	Hela-S3	cervix:	n/a
19	chr6:36703127-36703177	SAEC	small airway:	n/a
20	chr6:36703127-36703177	HAEpiC	amniotic membrane:	n/a
21	chr6:36703127-36703177	NHDF-neo	bronchial:	n/a
22	chr6:36703127-36703177	GM12891	blood:	n/a
23	chr6:36703127-36703177	HNPCEpiC	eye:	n/a
24	chr6:36703127-36703177	ovcar-3	ovarian:	n/a
25	chr6:36703127-36703177	PANC-1	pancreas:	n/a
26	chr6:36703127-36703177	HepG2	liver:	n/a
27	chr6:36703127-36703177	GM12878	blood:	n/a
28	chr6:36703127-36703177	MCF10A-Er-Src	breast:	n/a
29	chr6:36703127-36703177	Hepatocyte	liver:	n/a
30	chr6:36703127-36703177	HCT-116	colon:	n/a
31	chr6:36703127-36703177	HRCEpiC	kidney:	n/a
32	chr6:36703127-36703177	Caco-2	colon:	n/a
33	chr6:36703127-36703177	HEK293	kidney:	embryo
34	chr6:36703127-36703177	AoSMC	blood vessel:	n/a
35	chr6:36703127-36703177	SK-N-SH	brain:	n/a
36	chr6:36703127-36703177	SKMC	muscle:	n/a
37	chr6:36703127-36703177	HCM	heart:	n/a
38	chr6:36703127-36703177	IMR90	lung:	fetal
39	chr6:36703127-36703177	GM12892	blood:	n/a
40	chr6:36703127-36703177	HMEC	breast:	n/a
41	chr6:36703127-36703177	Jurkat	blood:	n/a
42	chr6:36703127-36703177	RPTEC	kidney:	n/a
43	chr6:36703127-36703177	H1-hESC	embryonic stem cell:	embryo
44	chr6:36703127-36703177	AG10803	skin:	n/a
45	chr6:36703127-36703177	ProgFib	skin:	n/a
46	chr6:36703127-36703177	BE2_C	brain:	n/a
47	chr6:36703127-36703177	HL-60	blood:	n/a
48	chr6:36703127-36703177	HUVEC	blood vessel:	n/a
49	chr6:36703127-36703177	PrEC	prostate:	n/a
50	chr6:36703127-36703177	NHBE	bronchial:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36692637..36694151-chr6:36698641..36700541,2	MCF-7	breast:
2	chr6:36561849..36563615-chr6:36700031..36702846,2	K562	blood:
3	chr6:36645663..36650199-chr6:36694521..36699153,6	MCF-7	breast:
4	chr6:36689656..36693910-chr6:36696758..36700115,6	K562	blood:
5	chr6:36692869..36694899-chr6:36700775..36703080,2	MCF-7	breast:
6	chr6:36704975..36706910-chr6:36710272..36712382,2	MCF-7	breast:
7	chr6:36705103..36707775-chr6:36711430..36713266,2	MCF-7	breast:
8	chr6:36583432..36585248-chr6:36700120..36704013,3	MCF-7	breast:
9	chr6:36561612..36564233-chr6:36698669..36701218,2	MCF-7	breast:
10	chr6:36695657..36698030-chr6:36700581..36702478,2	K562	blood:
11	chr6:36699118..36702234-chr6:36702324..36705046,3	K562	blood:
12	chr6:36561511..36564084-chr6:36695779..36697652,2	K562	blood:
13	chr6:36681851..36683948-chr6:36705203..36707828,2	K562	blood:
14	chr6:36696414..36698487-chr6:36724998..36726714,2	MCF-7	breast:
15	chr6:36560896..36563675-chr6:36695597..36697920,2	MCF-7	breast:
16	chr6:36695657..36698030-chr6:36700581..36702478,2	K562	blood:
17	chr6:36693621..36695483-chr6:36698291..36701067,2	MCF-7	breast:
18	chr6:36575587..36577672-chr6:36699166..36700977,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000220349	TF binding region
ENSG00000220349	CpG island
ENSG00000112081	chromatin interactions
ENSG00000255587	chromatin interactions
ENSG00000124772	chromatin interactions
ENSG00000220349	chromatin interactions
ENSG00000124762	chromatin interactions

Extended variants
information (count: 389 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs236468	chr6:36696904-36696905	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536977904	chr6:36696963-36696964	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs369233778	chr6:36696969-36696970	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs554218885	chr6:36696982-36696983	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs558417318	chr6:36697060-36697061	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs570357346	chr6:36697062-36697063	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs534461565	chr6:36697101-36697102	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs567945836	chr6:36697154-36697155	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs552663151	chr6:36697173-36697174	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs236467	chr6:36697201-36697202	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs541833357	chr6:36697241-36697242	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs201113849	chr6:36697259-36697260	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs556712532	chr6:36697260-36697261	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201216327	chr6:36697263-36697264	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs187703357	chr6:36697293-36697294	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs565574898	chr6:36697297-36697298	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs192637645	chr6:36697331-36697332	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs541604199	chr6:36697345-36697346	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs140770232	chr6:36697353-36697354	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs377593408	chr6:36697369-36697370	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs200172612	chr6:36697413-36697414	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs530164277	chr6:36697415-36697416	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs184953963	chr6:36697417-36697418	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs574654014	chr6:36697426-36697427	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs569991103	chr6:36697451-36697452	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs530809157	chr6:36697456-36697457	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs553380363	chr6:36697473-36697474	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs236465	chr6:36697507-36697508	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs570375643	chr6:36697540-36697541	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs534526106	chr6:36697593-36697594	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs533531558	chr6:36697620-36697621	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs552724425	chr6:36697621-36697622	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138381865	chr6:36697648-36697649	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs535232585	chr6:36697673-36697674	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs236464	chr6:36697682-36697683	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs562179035	chr6:36697708-36697709	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs79628682	chr6:36697797-36697798	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs559308293	chr6:36697904-36697905	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs577585138	chr6:36697996-36697997	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs79122174	chr6:36698056-36698057	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559729549	chr6:36698058-36698059	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs530302675	chr6:36698085-36698086	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs236463	chr6:36698160-36698161	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs563752890	chr6:36698281-36698282	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs190201	chr6:36698285-36698286	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552120740	chr6:36698292-36698293	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374600244	chr6:36698293-36698294	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs386700198	chr6:36698294-36698295	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532052897	chr6:36698295-36698296	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs189805752	chr6:36698325-36698326	Enhancers Weak transcription Strong transcription	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:371 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr6:36692400-36697000	Enhancers	Primary B cells from cord blood	blood
5	chr6:36692600-36699000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:36694000-36703000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:36694400-36697000	Enhancers	HSMM	muscle
8	chr6:36694400-36697200	Enhancers	HSMMtube	muscle
9	chr6:36695000-36697200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr6:36695200-36697400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:36695400-36698800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr6:36695600-36697200	Enhancers	NHDF-Ad	bronchial
13	chr6:36695600-36697400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr6:36695800-36697200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr6:36695800-36698200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:36695800-36698800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:36695800-36702600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:36695800-36702800	Weak transcription	Gastric	stomach
19	chr6:36696000-36698200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:36696000-36702600	Weak transcription	NHEK	skin
21	chr6:36696200-36698400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr6:36696400-36697000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr6:36696400-36697200	Enhancers	Adipose Nuclei	Adipose
24	chr6:36696400-36697400	Enhancers	Fetal Muscle Leg	muscle
25	chr6:36696400-36697600	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr6:36696400-36697600	Enhancers	HUVEC	blood vessel
27	chr6:36696400-36697800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr6:36696400-36698000	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr6:36696600-36697000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:36696600-36697000	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr6:36696600-36697200	Enhancers	Placenta	Placenta
32	chr6:36696600-36697200	Enhancers	Osteobl	bone
33	chr6:36696600-36697600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:36696600-36702200	Weak transcription	Primary B cells from peripheral blood	blood
35	chr6:36696800-36697200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr6:36696800-36697800	Weak transcription	GM12878-XiMat	blood
37	chr6:36696800-36698200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr6:36696800-36698800	Weak transcription	Right Atrium	heart
39	chr6:36696800-36699400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr6:36696800-36700200	Weak transcription	Fetal Brain Male	brain
41	chr6:36696800-36702200	Weak transcription	Lung	lung
42	chr6:36696800-36702200	Weak transcription	Spleen	Spleen
43	chr6:36696800-36702200	Weak transcription	NHLF	lung
44	chr6:36697000-36697400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr6:36697000-36698800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr6:36697000-36702200	Weak transcription	Primary B cells from cord blood	blood
47	chr6:36697200-36697600	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr6:36697200-36702400	Weak transcription	Adipose Nuclei	Adipose
49	chr6:36697200-36702400	Weak transcription	NHDF-Ad	bronchial
50	chr6:36697400-36697600	Enhancers	Skeletal Muscle Female	skeletal muscle

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