Variant report

Variant	nsv947730
Chromosome Location	chr10:5817688-5827238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:178)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:178 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CREB1	chr10:5817589-5817981	GM12878	blood:	n/a	chr10:5817787-5817800
2	CTCF	chr10:5818160-5818310	RPTEC	kidney:	n/a	n/a
3	CTCF	chr10:5818179-5818228	K562	blood:	n/a	n/a
4	CTCF	chr10:5818213-5818216	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr10:5818080-5818230	HMF	breast:	n/a	n/a
6	CTCF	chr10:5818120-5818270	HepG2	liver:	n/a	n/a
7	CTCF	chr10:5818120-5818270	SK-N-SH_RA	brain:	n/a	n/a
8	CTCF	chr10:5818120-5818270	HMEC	breast:	n/a	n/a
9	CTCF	chr10:5818140-5818290	Caco-2	colon:	n/a	n/a
10	CTCF	chr10:5818150-5818282	A549	lung:	n/a	n/a
11	CTCF	chr10:5818202-5818250	Fibrobl	skin:	n/a	n/a
12	CTCF	chr10:5818095-5818306	HepG2	liver:	n/a	n/a
13	CTCF	chr10:5818240-5818390	AG04450	lung:	n/a	n/a
14	CTCF	chr10:5818080-5818230	AG09319	gingival:	n/a	n/a
15	CTCF	chr10:5818160-5818310	MCF-7	breast:	n/a	n/a
16	CTCF	chr10:5818040-5818190	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr10:5818089-5818315	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr10:5817974-5818448	MCF-7	breast:	n/a	n/a
19	CTCF	chr10:5818100-5818250	HVMF	connective:	n/a	n/a
20	CTCF	chr10:5818089-5818310	MCF-7	breast:	n/a	n/a
21	CTCF	chr10:5818229-5818232	LNCaP	prostate:	n/a	n/a
22	CTCF	chr10:5818140-5818290	HRPEpiC	eye:	n/a	n/a
23	CTCF	chr10:5818160-5818310	HCM	heart:	n/a	n/a
24	CTCF	chr10:5818120-5818270	HVMF	connective:	n/a	n/a
25	CTCF	chr10:5823460-5823610	GM12866	blood:	n/a	n/a
26	CTCF	chr10:5818080-5818230	AG04449	skin:	n/a	n/a
27	CTCF	chr10:5818080-5818230	AG04450	lung:	n/a	n/a
28	CTCF	chr10:5818120-5818270	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr10:5817907-5817975	MCF-7	breast:	n/a	n/a
30	CTCF	chr10:5818060-5818210	HCT-116	colon:	n/a	n/a
31	CTCF	chr10:5818060-5818210	HRE	kidney:	n/a	n/a
32	CTCF	chr10:5818137-5818333	IMR90	lung:	n/a	n/a
33	CTCF	chr10:5818140-5818290	AG09319	gingival:	n/a	n/a
34	CTCF	chr10:5818140-5818290	HepG2	liver:	n/a	n/a
35	CTCF	chr10:5818100-5818250	AG10803	skin:	n/a	n/a
36	CTCF	chr10:5818160-5818310	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr10:5818180-5818330	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr10:5818160-5818310	HAc	cerebellar:	n/a	n/a
39	CTCF	chr10:5818160-5818310	K562	blood:	n/a	n/a
40	CTCF	chr10:5818080-5818230	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr10:5817808-5817878	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:5818120-5818270	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr10:5821780-5821930	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr10:5818080-5818230	HCM	heart:	n/a	n/a
45	CTCF	chr10:5821880-5822030	HepG2	liver:	n/a	n/a
46	CTCF	chr10:5821840-5821990	GM12867	blood:	n/a	n/a
47	CTCF	chr10:5818200-5818350	BE2_C	brain:	n/a	n/a
48	CTCF	chr10:5821860-5822010	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr10:5818020-5818170	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr10:5818140-5818290	HPAF	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5817943-5817993	SAEC	small airway:	n/a
2	chr10:5817943-5817993	SK-N-SH	brain:	n/a
3	chr10:5817943-5817993	NB4	blood:	n/a
4	chr10:5817943-5817993	HAEpiC	amniotic membrane:	n/a
5	chr10:5817943-5817993	IMR90	lung:	fetal
6	chr10:5817943-5817993	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:5817943-5817993	H1-hESC	embryonic stem cell:	embryo
8	chr10:5817943-5817993	HL-60	blood:	n/a
9	chr10:5817943-5817993	Hepatocyte	liver:	n/a
10	chr10:5817943-5817993	AG09319	gingival:	n/a
11	chr10:5817943-5817993	HRCEpiC	kidney:	n/a
12	chr10:5817943-5817993	U87	brain:	n/a
13	chr10:5817943-5817993	PANC-1	pancreas:	n/a
14	chr10:5817943-5817993	HCPEpiC	choroid plexus:	n/a
15	chr10:5817943-5817993	HMEC	breast:	n/a
16	chr10:5817943-5817993	HCT-116	colon:	n/a
17	chr10:5817943-5817993	NH-A	brain:	n/a
18	chr10:5817943-5817993	HRE	kidney:	n/a
19	chr10:5817943-5817993	ECC-1	luminal epithelium:	n/a
20	chr10:5817943-5817993	A549	lung:	n/a
21	chr10:5817943-5817993	BJ	skin:	n/a
22	chr10:5817943-5817993	HRPEpiC	eye:	n/a
23	chr10:5817943-5817993	AG10803	skin:	n/a
24	chr10:5817943-5817993	CMK	blood:	n/a
25	chr10:5817943-5817993	HCF	heart:	n/a
26	chr10:5817943-5817993	HepG2	liver:	n/a
27	chr10:5817943-5817993	Hela-S3	cervix:	n/a
28	chr10:5817943-5817993	NHDF-neo	bronchial:	n/a
29	chr10:5817943-5817993	GM12878	blood:	n/a
30	chr10:5817943-5817993	AG09309	skin:	n/a
31	chr10:5817943-5817993	K562	blood:	n/a
32	chr10:5817943-5817993	HNPCEpiC	eye:	n/a
33	chr10:5817943-5817993	SK-N-SH_RA	brain:	n/a
34	chr10:5817943-5817993	T-47D	breast:	n/a
35	chr10:5817943-5817993	AoSMC	blood vessel:	n/a
36	chr10:5817943-5817993	ovcar-3	ovarian:	n/a
37	chr10:5817943-5817993	SK-N-MC	brain:	n/a
38	chr10:5817943-5817993	AG04450	lung:	fetal
39	chr10:5817943-5817993	Jurkat	blood:	n/a
40	chr10:5817943-5817993	LNCaP	prostate:	n/a
41	chr10:5817943-5817993	PFSK-1	brain:	n/a
42	chr10:5817943-5817993	HEK293	kidney:	embryo
43	chr10:5817943-5817993	GM12892	blood:	n/a
44	chr10:5817943-5817993	BE2_C	brain:	n/a
45	chr10:5817943-5817993	ProgFib	skin:	n/a
46	chr10:5817943-5817993	NT2-D1	testis:	n/a
47	chr10:5817943-5817993	GM19239	blood:	n/a
48	chr10:5817943-5817993	AG04449	skin:	fetal
49	chr10:5817943-5817993	PrEC	prostate:	n/a
50	chr10:5817943-5817993	GM06990	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5822221..5824197-chr10:5834472..5837418,2	MCF-7	breast:
2	chr10:5815026..5819070-chr10:5852954..5857275,5	MCF-7	breast:
3	chr10:5814258..5816443-chr10:5818047..5819761,2	K562	blood:
4	chr10:5824368..5825931-chr10:5853511..5855472,2	MCF-7	breast:
5	chr10:5822061..5824683-chr10:5847855..5850406,3	K562	blood:
6	chr10:5816487..5819223-chr10:5854186..5856565,2	MCF-7	breast:
7	chr10:5819103..5820799-chr10:5833032..5835919,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM208B-3	chr10:5818034-5818821	NONHSAT011186

No data

Variant related genes	Relation type
NRBF2P5	TF binding region
NRBF2P5	CpG island
ENSG00000057608	chromatin interactions
ENSG00000272764	chromatin interactions

Extended variants
information (count: 419 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:419 , 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	rs142497333	chr10:5817718-5817719	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs537399937	chr10:5817732-5817733	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551546538	chr10:5817733-5817734	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs146772162	chr10:5817751-5817752	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs577258215	chr10:5817757-5817758	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs533732069	chr10:5817809-5817810	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs112101817	chr10:5817857-5817858	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs3924378	chr10:5817872-5817873	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554195951	chr10:5817926-5817927	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs572571550	chr10:5817932-5817933	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs189975311	chr10:5817935-5817936	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs35244699	chr10:5818000-5818001	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs80250441	chr10:5818014-5818015	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs576615705	chr10:5818017-5818018	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs182964682	chr10:5818073-5818074	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs565272593	chr10:5818075-5818076	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs528990832	chr10:5818123-5818124	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs35846123	chr10:5818155-5818156	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs551634242	chr10:5818169-5818170	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs77074885	chr10:5818239-5818240	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs117499020	chr10:5818240-5818241	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs573861698	chr10:5818242-5818243	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs548906433	chr10:5818246-5818247	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs10905159	chr10:5818268-5818269	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537537983	chr10:5818269-5818270	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs78662140	chr10:5818271-5818272	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs138449992	chr10:5818299-5818300	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs544359634	chr10:5818322-5818323	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs187294615	chr10:5818428-5818429	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs554411682	chr10:5818488-5818489	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs572660026	chr10:5818490-5818491	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs577457416	chr10:5818529-5818530	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs536808000	chr10:5818530-5818531	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs545097424	chr10:5818580-5818581	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs555199973	chr10:5818604-5818605	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs548496619	chr10:5818616-5818617	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs148861149	chr10:5818647-5818648	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs543921930	chr10:5818658-5818659	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs559124597	chr10:5818821-5818822	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs78168040	chr10:5818866-5818867	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs117036012	chr10:5818867-5818868	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs572222312	chr10:5818909-5818910	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs527586195	chr10:5818923-5818924	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143437698	chr10:5818924-5818925	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542979376	chr10:5818988-5818989	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560732649	chr10:5819003-5819004	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531430563	chr10:5819052-5819053	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549436551	chr10:5819088-5819089	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs564469581	chr10:5819090-5819091	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs532092111	chr10:5819094-5819095	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5762600-5843400	Strong transcription	Dnd41	blood
2	chr10:5762800-5843000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr10:5768000-5849400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:5781400-5818600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr10:5784800-5818000	Weak transcription	Stomach Mucosa	stomach
6	chr10:5788000-5818000	Strong transcription	Duodenum Mucosa	Duodenum
7	chr10:5795000-5817800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:5796000-5822400	Strong transcription	Fetal Intestine Large	intestine
9	chr10:5797200-5819000	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr10:5797400-5847400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr10:5797600-5817800	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr10:5797600-5817800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:5798000-5818200	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr10:5798000-5842800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr10:5798200-5843000	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr10:5798400-5817800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr10:5798400-5817800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr10:5798600-5817800	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr10:5798600-5818400	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr10:5798600-5820200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr10:5798600-5842800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr10:5798800-5817800	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr10:5804800-5818200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr10:5805000-5843200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr10:5805200-5819000	Strong transcription	GM12878-XiMat	blood
26	chr10:5805600-5818200	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr10:5806000-5818200	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr10:5806200-5817800	Strong transcription	Fetal Muscle Leg	muscle
29	chr10:5807400-5821800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr10:5808400-5817800	Strong transcription	Liver	Liver
31	chr10:5808400-5826400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr10:5808600-5817800	Weak transcription	Psoas Muscle	Psoas
33	chr10:5808800-5817800	Weak transcription	Fetal Brain Male	brain
34	chr10:5808800-5825800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr10:5809000-5824400	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr10:5810200-5817800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr10:5810400-5817800	Weak transcription	Aorta	Aorta
38	chr10:5810400-5818000	Weak transcription	Brain Angular Gyrus	brain
39	chr10:5810400-5818000	Weak transcription	Brain Anterior Caudate	brain
40	chr10:5810400-5824800	Weak transcription	Ovary	ovary
41	chr10:5810800-5817800	Weak transcription	Brain Substantia Nigra	brain
42	chr10:5811800-5824400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr10:5812000-5823800	Weak transcription	Fetal Kidney	kidney
44	chr10:5812000-5824000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr10:5812400-5821600	Weak transcription	Brain Germinal Matrix	brain
46	chr10:5813000-5817800	Strong transcription	HMEC	breast
47	chr10:5813000-5818600	Strong transcription	NHEK	skin
48	chr10:5813000-5818800	Strong transcription	HepG2	liver
49	chr10:5813000-5819200	Strong transcription	K562	blood
50	chr10:5813600-5818400	Strong transcription	Fetal Brain Female	brain

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