Variant report

Variant	nsv1067912
Chromosome Location	chr6:24521495-24523949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:24522471-24523064	GM12878	blood:	n/a	n/a
2	ATF2	chr6:24522483-24523007	GM12878	blood:	n/a	n/a
3	ATF3	chr6:24522744-24522938	K562	blood:	n/a	n/a
4	ATF3	chr6:24522654-24523097	GM12878	blood:	n/a	n/a
5	BACH1	chr6:24522747-24522954	K562	blood:	n/a	n/a
6	BATF	chr6:24522644-24523026	GM12878	blood:	n/a	chr6:24522818-24522828 chr6:24522813-24522824
7	BCL3	chr6:24522589-24522951	GM12878	blood:	n/a	n/a
8	BCLAF1	chr6:24522353-24523202	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:24522521-24523081	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:24522658-24523096	K562	blood:	n/a	n/a
11	BHLHE40	chr6:24521227-24521585	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:24522571-24523157	GM12878	blood:	n/a	n/a
13	CBX3	chr6:24522646-24523049	K562	blood:	n/a	n/a
14	CEBPB	chr6:24522506-24523293	GM12878	blood:	n/a	n/a
15	CTCF	chr6:24521246-24521506	GM12892	blood:	n/a	chr6:24521363-24521381
16	CTCF	chr6:24521235-24521507	ProgFib	skin:	n/a	chr6:24521363-24521381
17	CTCF	chr6:24521231-24521507	MCF-7	breast:	n/a	chr6:24521363-24521381
18	CTCF	chr6:24521169-24521582	K562	blood:	n/a	chr6:24521363-24521381
19	CTCF	chr6:24521182-24521523	K562	blood:	n/a	chr6:24521363-24521381
20	CTCF	chr6:24521380-24521530	A549	lung:	n/a	n/a
21	CTCF	chr6:24521262-24521503	GM13977	blood:	n/a	chr6:24521363-24521381
22	CTCF	chr6:24521240-24521511	MCF-7	breast:	n/a	chr6:24521363-24521381
23	CTCF	chr6:24521116-24521685	MCF-7	breast:	n/a	chr6:24521363-24521381
24	CTCF	chr6:24521173-24521574	GM12878	blood:	n/a	chr6:24521363-24521381
25	CTCF	chr6:24521030-24521705	HCT-116	colon:	n/a	chr6:24521363-24521381
26	CTCF	chr6:24521263-24521501	LNCaP	prostate:	n/a	chr6:24521363-24521381
27	CTCF	chr6:24521155-24521638	HCT-116	colon:	n/a	chr6:24521363-24521381
28	CTCF	chr6:24521253-24521497	NHEK	skin:	n/a	chr6:24521363-24521381
29	CTCF	chr6:24521191-24521625	MCF-7	breast:	n/a	chr6:24521363-24521381
30	CTCF	chr6:24521268-24521510	GM10266	blood:	n/a	chr6:24521363-24521381
31	CTCF	chr6:24521236-24521532	T-47D	breast:	n/a	chr6:24521363-24521381
32	CTCF	chr6:24521179-24521525	HepG2	liver:	n/a	chr6:24521363-24521381
33	CTCF	chr6:24521380-24521530	GM12870	blood:	n/a	n/a
34	CTCF	chr6:24521380-24521530	HAc	cerebellar:	n/a	n/a
35	CTCF	chr6:24521234-24521503	GM19240	blood:	n/a	chr6:24521363-24521381
36	CTCF	chr6:24521239-24521497	Hela-S3	cervix:	n/a	chr6:24521363-24521381
37	CTCF	chr6:24521181-24521570	IMR90	lung:	n/a	chr6:24521363-24521381
38	CTCF	chr6:24521236-24521514	A549	lung:	n/a	chr6:24521363-24521381
39	CTCF	chr6:24521254-24521510	HepG2	liver:	n/a	chr6:24521363-24521381
40	CTCF	chr6:24521223-24521511	MCF-7	breast:	n/a	chr6:24521363-24521381
41	CTCF	chr6:24521247-24521495	Spleen_OC	spleen:	n/a	chr6:24521363-24521381
42	CTCF	chr6:24521246-24521502	GM12891	blood:	n/a	chr6:24521363-24521381
43	CTCF	chr6:24521229-24521502	LNCaP	prostate:	n/a	chr6:24521363-24521381
44	CTCF	chr6:24521254-24521495	H1-hESC	embryonic stem cell:	n/a	chr6:24521363-24521381
45	CTCF	chr6:24521239-24521506	Fibrobl	skin:	n/a	chr6:24521363-24521381
46	CTCF	chr6:24521660-24521810	SAEC	small airway:	n/a	n/a
47	CTCF	chr6:24521122-24521560	H1-hESC	embryonic stem cell:	n/a	chr6:24521363-24521381
48	CTCF	chr6:24521185-24521576	H1-hESC	embryonic stem cell:	n/a	chr6:24521363-24521381
49	CTCF	chr6:24521232-24521515	GM19238	blood:	n/a	chr6:24521363-24521381
50	CTCF	chr6:24521042-24521656	A549	lung:	n/a	chr6:24521363-24521381

No.	Distal block	Cell Line	Cell type
1	chr6:24522066..24523918-chr6:24775174..24778168,2	K562	blood:
2	chr6:24431387..24432156-chr6:24520936..24521780,2	K562	blood:
3	chr6:24492633..24493385-chr6:24520875..24521776,3	MCF-7	breast:
4	chr6:24523679..24525395-chr6:24719900..24722362,3	K562	blood:
5	chr6:24521062..24521673-chr6:24695938..24696469,2	MCF-7	breast:
6	chr6:24430350..24432062-chr6:24520550..24521835,7	MCF-7	breast:
7	chr6:24282990..24283576-chr6:24521142..24521868,2	MCF-7	breast:
8	chr6:24494574..24495932-chr6:24520788..24521752,7	MCF-7	breast:
9	chr6:24430975..24431906-chr6:24520567..24521619,5	MCF-7	breast:
10	chr6:24282882..24283800-chr6:24521072..24521695,2	K562	blood:
11	chr6:24495374..24495964-chr6:24520682..24521498,2	MCF-7	breast:
12	chr6:24523679..24525342-chr6:24719900..24722320,2	K562	blood:
13	chr6:24523688..24526663-chr6:24667463..24669411,2	K562	blood:

Variant related genes	Relation type
ALDH5A1	TF binding region
ENSG00000112293	chromatin interactions
ENSG00000112294	chromatin interactions
ENSG00000112312	chromatin interactions
ENSG00000112308	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73728141	chr6:24521503-24521504	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146571827	chr6:24521517-24521518	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs370212422	chr6:24521545-24521546	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs555799286	chr6:24521550-24521551	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs569516382	chr6:24521588-24521589	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535241325	chr6:24521604-24521605	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs190065470	chr6:24521614-24521615	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs572283062	chr6:24521626-24521627	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs115584968	chr6:24521709-24521710	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs148287025	chr6:24521764-24521765	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs79257782	chr6:24521807-24521808	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115159610	chr6:24521864-24521865	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2322458	chr6:24521904-24521905	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs200472918	chr6:24522035-24522036	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542887895	chr6:24522058-24522059	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs71542679	chr6:24522086-24522087	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs201525909	chr6:24522107-24522108	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs2874798	chr6:24522109-24522110	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs2874797	chr6:24522110-24522111	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2328825	chr6:24522112-24522113	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs141440469	chr6:24522121-24522122	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544608854	chr6:24522173-24522174	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528829228	chr6:24522180-24522181	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs111427144	chr6:24522188-24522189	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs373097923	chr6:24522272-24522273	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184576292	chr6:24522365-24522366	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs532718679	chr6:24522366-24522367	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs549485167	chr6:24522372-24522373	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532041938	chr6:24522442-24522443	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375438647	chr6:24522468-24522469	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs569374149	chr6:24522478-24522479	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2251547	chr6:24522488-24522489	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs371460740	chr6:24522509-24522510	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139219754	chr6:24522512-24522513	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565859507	chr6:24522515-24522516	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs71555148	chr6:24522519-24522520	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534624043	chr6:24522526-24522527	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs142539958	chr6:24522550-24522551	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs565318946	chr6:24522582-24522583	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs373120350	chr6:24522599-24522600	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376086118	chr6:24522603-24522604	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545050860	chr6:24522610-24522611	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs76940868	chr6:24522624-24522625	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs79884160	chr6:24522628-24522629	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145991740	chr6:24522665-24522666	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188242852	chr6:24522683-24522684	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573346305	chr6:24522707-24522708	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs67848159	chr6:24522729-24522730	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201211514	chr6:24522732-24522733	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs61208485	chr6:24522760-24522761	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
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
Myelodysplastic syndrome	21251322	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
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	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
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	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
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
small cell lung cancer	20016488	CNVD
XY gonadal dysgenesis	20685758	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24496000-24534200	Weak transcription	Gastric	stomach
2	chr6:24496000-24538000	Weak transcription	Esophagus	oesophagus
3	chr6:24496200-24526400	Weak transcription	Right Atrium	heart
4	chr6:24496200-24527800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:24496200-24534200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:24496200-24535000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr6:24496200-24536200	Weak transcription	Psoas Muscle	Psoas
8	chr6:24496200-24583000	Weak transcription	Hela-S3	cervix
9	chr6:24496400-24532200	Weak transcription	Brain Germinal Matrix	brain
10	chr6:24496800-24522800	Weak transcription	Lung	lung
11	chr6:24496800-24532400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr6:24497000-24528200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr6:24497400-24522400	Weak transcription	K562	blood
14	chr6:24504200-24522600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:24504400-24534200	Weak transcription	Pancreas	Pancrea
16	chr6:24505400-24534000	Weak transcription	Brain Cingulate Gyrus	brain
17	chr6:24505800-24527800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr6:24505800-24530800	Weak transcription	Right Ventricle	heart
19	chr6:24505800-24534000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr6:24505800-24534000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr6:24506400-24530000	Weak transcription	Placenta	Placenta
22	chr6:24507400-24531400	Weak transcription	Fetal Lung	lung
23	chr6:24507600-24522800	Weak transcription	Fetal Kidney	kidney
24	chr6:24507600-24532400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr6:24507600-24532400	Weak transcription	Fetal Brain Female	brain
26	chr6:24507800-24532400	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr6:24507800-24536800	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr6:24507800-24539200	Weak transcription	Brain Hippocampus Middle	brain
29	chr6:24509400-24545800	Weak transcription	Small Intestine	intestine
30	chr6:24512200-24525000	Strong transcription	Fetal Intestine Small	intestine
31	chr6:24512400-24533000	Weak transcription	Brain Substantia Nigra	brain
32	chr6:24515000-24532200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr6:24516000-24522400	Weak transcription	Aorta	Aorta
34	chr6:24516000-24523600	Weak transcription	Duodenum Mucosa	Duodenum
35	chr6:24516000-24530800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr6:24516000-24531000	Weak transcription	Brain Anterior Caudate	brain
37	chr6:24516000-24534200	Weak transcription	Brain Angular Gyrus	brain
38	chr6:24516200-24527800	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr6:24516200-24532400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:24516400-24522600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr6:24517400-24532600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr6:24517600-24532200	Weak transcription	Left Ventricle	heart
43	chr6:24517800-24522800	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr6:24518200-24527400	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr6:24518200-24530800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:24518400-24522800	Weak transcription	Fetal Muscle Leg	muscle
47	chr6:24518600-24522400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:24518600-24531600	Weak transcription	Fetal Muscle Trunk	muscle
49	chr6:24518800-24522400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:24518800-24522600	Weak transcription	Adipose Nuclei	Adipose

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