Variant report

Variant	nsv601185
Chromosome Location	chr6:26455811-26465384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:733)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26457836-26458207	HepG2	liver:	n/a	n/a
2	ATF1	chr6:26457908-26458286	K562	blood:	n/a	n/a
3	BHLHE40	chr6:26457962-26458226	HepG2	liver:	n/a	n/a
4	BHLHE40	chr6:26457940-26458334	K562	blood:	n/a	n/a
5	BHLHE40	chr6:26458552-26458563	K562	blood:	n/a	n/a
6	BHLHE40	chr6:26457911-26458325	GM12878	blood:	n/a	n/a
7	BRCA1	chr6:26457937-26458234	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr6:26458311-26458434	HepG2	liver:	n/a	n/a
9	CBX3	chr6:26457315-26458711	K562	blood:	n/a	n/a
10	CCNT2	chr6:26458339-26458524	K562	blood:	n/a	n/a
11	CEBPB	chr6:26459274-26459575	IMR90	lung:	n/a	chr6:26459425-26459438 chr6:26459426-26459437
12	CEBPB	chr6:26459435-26459456	K562	blood:	n/a	n/a
13	CEBPB	chr6:26459312-26459525	HepG2	liver:	n/a	chr6:26459425-26459438 chr6:26459426-26459437
14	CHD1	chr6:26458251-26458394	GM12878	blood:	n/a	n/a
15	CHD2	chr6:26457716-26457960	HepG2	liver:	n/a	n/a
16	CHD2	chr6:26458294-26458429	HepG2	liver:	n/a	n/a
17	CHD2	chr6:26457972-26458276	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr6:26457951-26458277	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr6:26457968-26458571	GM12878	blood:	n/a	n/a
20	CREB1	chr6:26457583-26458682	HepG2	liver:	n/a	n/a
21	CREB1	chr6:26457694-26458460	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr6:26457620-26458568	K562	blood:	n/a	n/a
23	CREB1	chr6:26457960-26458253	A549	lung:	n/a	n/a
24	CREB1	chr6:26457850-26458339	A549	lung:	n/a	n/a
25	CREB1	chr6:26457759-26458372	ECC-1	luminal epithelium:	n/a	n/a
26	CREB1	chr6:26457695-26458664	GM12878	blood:	n/a	n/a
27	CREB1	chr6:26457710-26458627	GM12878	blood:	n/a	n/a
28	CREB1	chr6:26457902-26458347	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr6:26457844-26458354	ECC-1	luminal epithelium:	n/a	n/a
30	CTCF	chr6:26458342-26458517	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:26457800-26457950	HFF	foreskin:	n/a	n/a
32	CTCF	chr6:26457760-26457910	AG09319	gingival:	n/a	n/a
33	CTCF	chr6:26458280-26458430	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr6:26464778-26464933	GM19238	blood:	n/a	n/a
35	CTCF	chr6:26458260-26458410	GM06990	blood:	n/a	n/a
36	CTCF	chr6:26464820-26464970	GM12872	blood:	n/a	n/a
37	CTCF	chr6:26458260-26458410	HMF	breast:	n/a	n/a
38	CTCF	chr6:26458280-26458430	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr6:26458240-26458390	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr6:26458280-26458430	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr6:26458321-26458475	GM12892	blood:	n/a	n/a
42	CTCF	chr6:26458240-26458390	GM12864	blood:	n/a	n/a
43	CTCF	chr6:26458320-26458470	GM12872	blood:	n/a	n/a
44	CTCF	chr6:26458280-26458430	GM12871	blood:	n/a	n/a
45	CTCF	chr6:26464820-26464970	GM12866	blood:	n/a	n/a
46	CTCF	chr6:26457740-26457890	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr6:26458160-26458310	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr6:26464812-26464904	GM12878	blood:	n/a	n/a
49	CTCF	chr6:26458220-26458370	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr6:26458328-26458463	ProgFib	skin:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26457984-26458034	HCPEpiC	choroid plexus:	n/a
2	chr6:26457984-26458034	HCPEpiC	choroid plexus:	n/a
3	chr6:26458189-26458239	Jurkat	blood:	n/a
4	chr6:26458489-26458539	PrEC	prostate:	n/a
5	chr6:26457353-26457403	AG09309	skin:	n/a
6	chr6:26456230-26456280	PFSK-1	brain:	n/a
7	chr6:26456230-26456280	AG04449	skin:	fetal
8	chr6:26459986-26460036	AG09319	gingival:	n/a
9	chr6:26456230-26456280	NT2-D1	testis:	n/a
10	chr6:26458326-26458376	HEK293	kidney:	embryo
11	chr6:26459986-26460036	CMK	blood:	n/a
12	chr6:26458489-26458539	NT2-D1	testis:	n/a
13	chr6:26458189-26458239	SK-N-SH	brain:	n/a
14	chr6:26458213-26458263	AG04449	skin:	fetal
15	chr6:26458326-26458376	GM06990	blood:	n/a
16	chr6:26457984-26458034	NHBE	bronchial:	n/a
17	chr6:26457984-26458034	PANC-1	pancreas:	n/a
18	chr6:26458489-26458539	BJ	skin:	n/a
19	chr6:26458326-26458376	BJ	skin:	n/a
20	chr6:26457984-26458034	HRPEpiC	eye:	n/a
21	chr6:26458121-26458171	K562	blood:	n/a
22	chr6:26458489-26458539	HL-60	blood:	n/a
23	chr6:26459986-26460036	MCF10A-Er-Src	breast:	n/a
24	chr6:26457928-26457978	NH-A	brain:	n/a
25	chr6:26457928-26457978	AG10803	skin:	n/a
26	chr6:26458489-26458539	GM06990	blood:	n/a
27	chr6:26459986-26460036	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:26457353-26457403	HEK293	kidney:	embryo
29	chr6:26458489-26458539	LNCaP	prostate:	n/a
30	chr6:26458121-26458171	IMR90	lung:	fetal
31	chr6:26458326-26458376	HRPEpiC	eye:	n/a
32	chr6:26458093-26458143	SK-N-SH	brain:	n/a
33	chr6:26457984-26458034	H1-hESC	embryonic stem cell:	embryo
34	chr6:26457984-26458034	PrEC	prostate:	n/a
35	chr6:26459986-26460036	NB4	blood:	n/a
36	chr6:26456230-26456280	HRCEpiC	kidney:	n/a
37	chr6:26456230-26456280	HCPEpiC	choroid plexus:	n/a
38	chr6:26458326-26458376	AG09319	gingival:	n/a
39	chr6:26457353-26457403	BE2_C	brain:	n/a
40	chr6:26459986-26460036	Caco-2	colon:	n/a
41	chr6:26457928-26457978	SAEC	small airway:	n/a
42	chr6:26456230-26456280	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:26458121-26458171	H1-hESC	embryonic stem cell:	embryo
44	chr6:26458489-26458539	SAEC	small airway:	n/a
45	chr6:26458013-26458063	SK-N-MC	brain:	n/a
46	chr6:26457928-26457978	ProgFib	skin:	n/a
47	chr6:26457984-26458034	HRCEpiC	kidney:	n/a
48	chr6:26458013-26458063	SK-N-SH_RA	brain:	n/a
49	chr6:26458013-26458063	ovcar-3	ovarian:	n/a
50	chr6:26458489-26458539	SKMC	muscle:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26158231..26160273-chr6:26456660..26458707,2	K562	blood:
2	chr6:26456959..26459749-chr6:26461329..26463001,2	MCF-7	breast:
3	chr11:62609075..62609632-chr6:26457866..26458649,2	NB4	blood:
4	chr6:26449553..26453974-chr6:26454911..26459271,5	K562	blood:
5	chr6:26462941..26465022-chr6:26475685..26477185,2	K562	blood:
6	chr6:26457960..26461047-chr6:26519488..26522400,3	MCF-7	breast:
7	chr6:26419843..26421610-chr6:26453709..26456222,2	K562	blood:
8	chr6:26420361..26423136-chr6:26455979..26458036,3	MCF-7	breast:
9	chr6:26204619..26206615-chr6:26455801..26457917,2	K562	blood:

No data

Variant related genes	Relation type
BTN2A1	TF binding region
BTN2A1	CpG island
ENSG00000133316	chromatin interactions
ENSG00000228223	chromatin interactions
ENSG00000198518	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000112763	chromatin interactions
ENSG00000199289	chromatin interactions
ENSG00000124549	chromatin interactions
ENSG00000111801	chromatin interactions

Extended variants
information (count: 408 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs71544291	chr6:26455811-26455812	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35680819	chr6:26455814-26455815	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs376634317	chr6:26455823-26455824	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs531241507	chr6:26455829-26455830	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs562228902	chr6:26455875-26455876	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs189331524	chr6:26455880-26455881	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs534232437	chr6:26455907-26455908	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs182478448	chr6:26455924-26455925	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs185008564	chr6:26455927-26455928	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs190202110	chr6:26455962-26455963	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs551561804	chr6:26456062-26456063	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs9295690	chr6:26456069-26456070	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs36033628	chr6:26456074-26456075	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs551227318	chr6:26456133-26456134	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs567580003	chr6:26456163-26456164	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs536633852	chr6:26456253-26456254	Weak transcription Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs547156562	chr6:26456254-26456255	Weak transcription Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs566964879	chr6:26456276-26456277	Weak transcription Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs9348718	chr6:26456280-26456281	Weak transcription Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563361173	chr6:26456362-26456363	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs6456724	chr6:26456443-26456444	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs571430329	chr6:26456457-26456458	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs536975788	chr6:26456602-26456603	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs557207235	chr6:26456801-26456802	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs149830778	chr6:26456822-26456823	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs542607398	chr6:26456850-26456851	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs181894843	chr6:26456917-26456918	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs572613732	chr6:26456927-26456928	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs185376903	chr6:26456938-26456939	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs565160613	chr6:26457034-26457035	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs531111257	chr6:26457071-26457072	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs544611190	chr6:26457072-26457073	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs9358942	chr6:26457124-26457125	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs530085815	chr6:26457144-26457145	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs528367255	chr6:26457179-26457180	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs116381244	chr6:26457183-26457184	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs566828469	chr6:26457224-26457225	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs532666080	chr6:26457229-26457230	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs552674362	chr6:26457256-26457257	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs571389750	chr6:26457281-26457282	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs148555708	chr6:26457290-26457291	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs557023300	chr6:26457292-26457293	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs111371249	chr6:26457306-26457307	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs112884218	chr6:26457307-26457308	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs567557068	chr6:26457349-26457350	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs142884549	chr6:26457353-26457354	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs552566549	chr6:26457437-26457438	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs149511437	chr6:26457444-26457445	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs536420037	chr6:26457489-26457490	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs572478971	chr6:26457504-26457505	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	21569311	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:997 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26441200-26457000	Weak transcription	Brain Substantia Nigra	brain
2	chr6:26441200-26457600	Weak transcription	Pancreas	Pancrea
3	chr6:26441400-26457000	Weak transcription	Brain Anterior Caudate	brain
4	chr6:26441400-26457400	Weak transcription	Psoas Muscle	Psoas
5	chr6:26442200-26457400	Weak transcription	Fetal Kidney	kidney
6	chr6:26442400-26457400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:26442400-26457400	Weak transcription	Hela-S3	cervix
8	chr6:26442600-26457400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:26443000-26457400	Weak transcription	Stomach Mucosa	stomach
10	chr6:26445200-26457400	Weak transcription	Small Intestine	intestine
11	chr6:26446400-26457200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr6:26446400-26457400	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr6:26446400-26458200	Weak transcription	Gastric	stomach
14	chr6:26446600-26457000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr6:26448000-26457600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr6:26448400-26456800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr6:26449000-26457600	Weak transcription	Right Ventricle	heart
18	chr6:26449200-26457400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr6:26449400-26457400	Weak transcription	HUVEC	blood vessel
20	chr6:26449800-26456600	Weak transcription	Colon Smooth Muscle	Colon
21	chr6:26450000-26456800	Weak transcription	Esophagus	oesophagus
22	chr6:26450200-26457400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr6:26450400-26456800	Weak transcription	Aorta	Aorta
24	chr6:26450400-26457400	Weak transcription	Thymus	Thymus
25	chr6:26450600-26456800	Weak transcription	Left Ventricle	heart
26	chr6:26450600-26457400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr6:26450800-26457200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr6:26450800-26457400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr6:26450800-26457600	Weak transcription	Placenta	Placenta
30	chr6:26450800-26458200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr6:26451000-26457400	Weak transcription	Primary B cells from cord blood	blood
32	chr6:26451000-26457400	Weak transcription	Fetal Intestine Large	intestine
33	chr6:26451000-26457600	Weak transcription	Fetal Muscle Trunk	muscle
34	chr6:26451200-26456600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr6:26451400-26456800	Weak transcription	Dnd41	blood
36	chr6:26451400-26457400	Weak transcription	Fetal Lung	lung
37	chr6:26451400-26457600	Weak transcription	Ovary	ovary
38	chr6:26451800-26457600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr6:26452000-26456800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr6:26452000-26456800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr6:26452000-26457200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr6:26452000-26457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr6:26452000-26457400	Weak transcription	Adipose Nuclei	Adipose
44	chr6:26452000-26457400	Weak transcription	Liver	Liver
45	chr6:26452000-26457400	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr6:26452000-26457400	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr6:26452000-26457600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr6:26452000-26457600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr6:26452000-26457600	Weak transcription	Colonic Mucosa	Colon
50	chr6:26452000-26457600	Weak transcription	Sigmoid Colon	Sigmoid Colon

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