Variant report

Variant	nsv975792
Chromosome Location	chr10:5998348-6008505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:137)
CpG islands
(count:184)
Chromatin interactive
region (count:16)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:137 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr10:6002173-6002755	K562	blood:	n/a	n/a
2	BRCA1	chr10:6001335-6001580	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr10:6000645-6001055	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr10:6002349-6002801	K562	blood:	n/a	n/a
5	CCNT2	chr10:6002340-6002714	K562	blood:	n/a	n/a
6	CEBPB	chr10:5999951-6000383	IMR90	lung:	n/a	n/a
7	CEBPB	chr10:6000007-6000994	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:6001204-6001565	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr10:6001313-6001378	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr10:6004622-6004678	GM19239	blood:	n/a	n/a
11	CTCF	chr10:6001620-6001770	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr10:6001661-6001773	K562	blood:	n/a	n/a
13	CTCF	chr10:6001684-6001736	MCF-7	breast:	n/a	n/a
14	CTCF	chr10:6001595-6001824	HepG2	liver:	n/a	n/a
15	CTCF	chr10:6005209-6005344	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr10:6001688-6001754	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr10:6001684-6001768	MCF-7	breast:	n/a	n/a
18	CTCF	chr10:6005214-6005343	MCF-7	breast:	n/a	n/a
19	CTCF	chr10:6005140-6005290	HRE	kidney:	n/a	n/a
20	CTCF	chr10:6005160-6005310	AG04449	skin:	n/a	n/a
21	CTCF	chr10:6001647-6001803	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:6005240-6005390	AG04449	skin:	n/a	n/a
23	CTCF	chr10:6001660-6001810	HepG2	liver:	n/a	n/a
24	CTCF	chr10:6005180-6005330	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr10:6005260-6005410	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr10:6005237-6005328	MCF-7	breast:	n/a	n/a
27	CTCF	chr10:6005250-6005282	MCF-7	breast:	n/a	n/a
28	CTCF	chr10:6005180-6005330	HepG2	liver:	n/a	n/a
29	CTCF	chr10:6001596-6001908	HepG2	liver:	n/a	n/a
30	CTCF	chr10:6001627-6001816	HepG2	liver:	n/a	n/a
31	CTCF	chr10:6001697-6001756	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:6005239-6005296	K562	blood:	n/a	n/a
33	CTCF	chr10:6005180-6005330	Caco-2	colon:	n/a	n/a
34	CTCF	chr10:6005160-6005310	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr10:6005180-6005330	HEK293	kidney:	n/a	n/a
36	CTCF	chr10:6007100-6007250	GM12873	blood:	n/a	chr10:6007225-6007234
37	CTCF	chr10:6005230-6005313	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:6004622-6004634	GM12891	blood:	n/a	n/a
39	CTCF	chr10:6005200-6005350	AG04450	lung:	n/a	n/a
40	EGR1	chr10:6002210-6002551	K562	blood:	n/a	n/a
41	ELK1	chr10:6002003-6002020	Hela-S3	cervix:	n/a	n/a
42	EP300	chr10:6000676-6000876	K562	blood:	n/a	chr10:6000756-6000765 chr10:6000757-6000766
43	EP300	chr10:6001264-6001486	Hela-S3	cervix:	n/a	n/a
44	EP300	chr10:6000649-6000882	SK-N-SH_RA	brain:	n/a	chr10:6000756-6000765 chr10:6000757-6000766
45	EP300	chr10:6002309-6002698	K562	blood:	n/a	chr10:6002577-6002593
46	EP300	chr10:6000588-6001025	Hela-S3	cervix:	n/a	chr10:6000756-6000765 chr10:6000757-6000766
47	FOS	chr10:6000654-6000860	MCF10A-Er-Src	breast:	n/a	chr10:6000758-6000765 chr10:6000756-6000765 chr10:6000757-6000765 chr10:6000757-6000766
48	FOS	chr10:6000625-6000896	MCF10A-Er-Src	breast:	n/a	chr10:6000758-6000765 chr10:6000756-6000765 chr10:6000757-6000765 chr10:6000757-6000766
49	FOS	chr10:6000598-6000902	MCF10A-Er-Src	breast:	n/a	chr10:6000758-6000765 chr10:6000756-6000765 chr10:6000757-6000765 chr10:6000757-6000766
50	FOS	chr10:6000577-6000928	MCF10A-Er-Src	breast:	n/a	chr10:6000758-6000765 chr10:6000756-6000765 chr10:6000757-6000765 chr10:6000757-6000766

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:6003621-6003671	AG09309	skin:	n/a
2	chr10:6003621-6003671	AG09309	skin:	n/a
3	chr10:6003764-6003814	BE2_C	brain:	n/a
4	chr10:6003524-6003574	HNPCEpiC	eye:	n/a
5	chr10:6003764-6003814	PrEC	prostate:	n/a
6	chr10:6003524-6003574	RPTEC	kidney:	n/a
7	chr10:6003524-6003574	HEEpiC	esophagus:	n/a
8	chr10:6003764-6003814	HEEpiC	esophagus:	n/a
9	chr10:6003621-6003671	SK-N-SH_RA	brain:	n/a
10	chr10:6003524-6003574	A549	lung:	n/a
11	chr10:6003524-6003574	HCM	heart:	n/a
12	chr10:6003621-6003671	ProgFib	skin:	n/a
13	chr10:6003621-6003671	Jurkat	blood:	n/a
14	chr10:6003621-6003671	HPAEpiC	pulmonary alveolar:	n/a
15	chr10:6003621-6003671	HAEpiC	amniotic membrane:	n/a
16	chr10:6003524-6003574	HRPEpiC	eye:	n/a
17	chr10:6003524-6003574	HRCEpiC	kidney:	n/a
18	chr10:6003621-6003671	HRPEpiC	eye:	n/a
19	chr10:6003524-6003574	PrEC	prostate:	n/a
20	chr10:6003621-6003671	RPTEC	kidney:	n/a
21	chr10:6003764-6003814	NT2-D1	testis:	n/a
22	chr10:6003764-6003814	AG09309	skin:	n/a
23	chr10:6003764-6003814	IMR90	lung:	fetal
24	chr10:6003621-6003671	GM12891	blood:	n/a
25	chr10:6003621-6003671	U87	brain:	n/a
26	chr10:6003764-6003814	AG10803	skin:	n/a
27	chr10:6003621-6003671	HIPEpiC	eye:	n/a
28	chr10:6003621-6003671	Hela-S3	cervix:	n/a
29	chr10:6003524-6003574	GM19239	blood:	n/a
30	chr10:6003621-6003671	HEK293	kidney:	embryo
31	chr10:6003524-6003574	ProgFib	skin:	n/a
32	chr10:6003524-6003574	T-47D	breast:	n/a
33	chr10:6003764-6003814	A549	lung:	n/a
34	chr10:6003764-6003814	Jurkat	blood:	n/a
35	chr10:6003621-6003671	HEEpiC	esophagus:	n/a
36	chr10:6003621-6003671	MCF10A-Er-Src	breast:	n/a
37	chr10:6003764-6003814	BJ	skin:	n/a
38	chr10:6003621-6003671	ovcar-3	ovarian:	n/a
39	chr10:6003524-6003574	BE2_C	brain:	n/a
40	chr10:6003621-6003671	SK-N-SH	brain:	n/a
41	chr10:6003621-6003671	T-47D	breast:	n/a
42	chr10:6003764-6003814	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:6003621-6003671	CMK	blood:	n/a
44	chr10:6003764-6003814	NHDF-neo	bronchial:	n/a
45	chr10:6003621-6003671	BE2_C	brain:	n/a
46	chr10:6003764-6003814	GM19239	blood:	n/a
47	chr10:6003764-6003814	PFSK-1	brain:	n/a
48	chr10:6003764-6003814	PANC-1	pancreas:	n/a
49	chr10:6003764-6003814	SK-N-SH_RA	brain:	n/a
50	chr10:6003764-6003814	HRPEpiC	eye:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:6000182..6002722-chr10:6191709..6195207,3	K562	blood:
2	chr10:6000236..6003390-chr10:6003998..6007470,4	K562	blood:
3	chr10:5993943..5996506-chr10:5999317..6001462,2	K562	blood:
4	chr10:5996869..5999162-chr10:6018672..6020209,2	MCF-7	breast:
5	chr10:5996282..5998515-chr10:6007767..6010563,2	K562	blood:
6	chr10:6005970..6007574-chr10:6034228..6036383,2	MCF-7	breast:
7	chr10:5990354..5995622-chr10:5995920..5999201,5	K562	blood:
8	chr10:5993943..5996022-chr10:5999962..6001752,2	K562	blood:
9	chr10:5991870..5998426-chr10:6018061..6021300,7	MCF-7	breast:
10	chr10:5991363..5993211-chr10:5997425..5999174,2	MCF-7	breast:
11	chr10:6000236..6003390-chr10:6003998..6007470,4	K562	blood:
12	chr10:5999303..6003344-chr10:6003662..6007961,5	MCF-7	breast:
13	chr10:6001696..6002224-chr10:6018770..6019697,2	MCF-7	breast:
14	chr10:5993229..5995375-chr10:6003228..6005603,2	MCF-7	breast:
15	chr10:6003571..6011080-chr10:6014794..6021269,11	K562	blood:
16	chr10:5999303..6003344-chr10:6003662..6007961,5	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL15RA-2	chr10:6002330-6002530	NONHSAT011199
2	lnc-IL15RA-2	chr10:5998342-5998417	NONHSAT011199
3	lnc-IL15RA-2	chr10:5998342-5998417	NONHSAT011197
4	lnc-IL15RA-2	chr10:6002330-6002530	NONHSAT011197
5	lnc-IL15RA-2	chr10:6001717-6001749	NONHSAT011198
6	lnc-IL15RA-2	chr10:6001717-6001749	NONHSAT011197
7	lnc-IL15RA-2	chr10:6008108-6008302	NONHSAT011198
8	lnc-IL15RA-2	chr10:6002330-6002431	NONHSAT011198
9	lnc-IL15RA-2	chr10:6001717-6001749	NONHSAT011199
10	lnc-IL15RA-2	chr10:5998342-5998417	NONHSAT011198
11	lnc-IL15RA-2	chr10:6008108-6008302	NONHSAT011199

No data

Variant related genes	Relation type
IL15RA	TF binding region
IL15RA	CpG island
ENSG00000263628	chromatin interactions
ENSG00000134470	chromatin interactions

Extended variants
information (count: 506 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372279024	chr10:5998380-5998381	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs8177718	chr10:5998389-5998390	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs376266317	chr10:5998404-5998405	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs142602826	chr10:5998405-5998406	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs150111327	chr10:5998436-5998437	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138544981	chr10:5998456-5998457	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs535381902	chr10:5998489-5998490	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571677636	chr10:5998566-5998567	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184294734	chr10:5998575-5998576	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561204750	chr10:5998600-5998601	Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2296141	chr10:5998659-5998660	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs148818697	chr10:5998695-5998696	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs2296140	chr10:5998696-5998697	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs8177717	chr10:5998729-5998730	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545547679	chr10:5998744-5998745	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190016739	chr10:5998748-5998749	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372888647	chr10:5998781-5998782	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376412337	chr10:5998792-5998793	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559909819	chr10:5998823-5998824	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530082836	chr10:5998828-5998829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs8177716	chr10:5998834-5998835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs137927627	chr10:5998835-5998836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371341417	chr10:5998837-5998838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs112036632	chr10:5998852-5998853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537800004	chr10:5998879-5998880	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143692415	chr10:5998885-5998886	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115594091	chr10:5998895-5998896	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200765911	chr10:5998902-5998903	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374227695	chr10:5998921-5998922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs56183325	chr10:5998940-5998941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112667559	chr10:5998941-5998942	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538847339	chr10:5998982-5998983	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564124501	chr10:5999034-5999035	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553415386	chr10:5999037-5999038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372575911	chr10:5999080-5999081	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs571816998	chr10:5999168-5999169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138826463	chr10:5999178-5999179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554190260	chr10:5999216-5999217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576664565	chr10:5999298-5999299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181201240	chr10:5999312-5999313	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543795959	chr10:5999313-5999314	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141286468	chr10:5999315-5999316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs577339571	chr10:5999379-5999380	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541661096	chr10:5999399-5999400	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12256367	chr10:5999444-5999445	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs139745513	chr10:5999456-5999457	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs41294149	chr10:5999470-5999471	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs529246577	chr10:5999479-5999480	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs41294151	chr10:5999480-5999481	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs12247660	chr10:5999497-5999498	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5969600-6012000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr10:5971400-6013200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr10:5980000-6013200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr10:5980800-6017800	Weak transcription	Thymus	Thymus
5	chr10:5981000-6003600	Weak transcription	Primary T cells from cord blood	blood
6	chr10:5986200-6018600	Weak transcription	Aorta	Aorta
7	chr10:5987600-6018000	Weak transcription	Psoas Muscle	Psoas
8	chr10:5987800-6017800	Weak transcription	Fetal Thymus	thymus
9	chr10:5988000-6000800	Weak transcription	Colonic Mucosa	Colon
10	chr10:5988000-6001400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr10:5988200-5998600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr10:5988200-6001800	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr10:5988400-6001200	Weak transcription	Ovary	ovary
14	chr10:5988400-6001600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr10:5988600-6011800	Weak transcription	Colon Smooth Muscle	Colon
16	chr10:5989200-6001600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr10:5989400-6001200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr10:5991400-5999000	Weak transcription	Brain Hippocampus Middle	brain
19	chr10:5991400-6000800	Weak transcription	K562	blood
20	chr10:5991400-6004800	Weak transcription	Brain Anterior Caudate	brain
21	chr10:5993000-5999800	Weak transcription	HUVEC	blood vessel
22	chr10:5993200-6001600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr10:5993400-6000400	Weak transcription	NHLF	lung
24	chr10:5993600-6013200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:5994000-5998800	Strong transcription	Duodenum Mucosa	Duodenum
26	chr10:5994000-6011000	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr10:5994000-6012800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr10:5994200-5998400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr10:5994200-5999800	Weak transcription	Hela-S3	cervix
30	chr10:5994200-6012200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr10:5994200-6012800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr10:5994800-6001800	Weak transcription	Stomach Mucosa	stomach
33	chr10:5995000-5998400	Strong transcription	GM12878-XiMat	blood
34	chr10:5995000-6004600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr10:5995400-5998400	Weak transcription	Fetal Stomach	stomach
36	chr10:5995400-6000400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr10:5995400-6001600	Weak transcription	Fetal Intestine Large	intestine
38	chr10:5995400-6012400	Weak transcription	Small Intestine	intestine
39	chr10:5995600-6001200	Weak transcription	Gastric	stomach
40	chr10:5995600-6001600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr10:5995800-6000400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr10:5996000-6000000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr10:5996000-6000800	Weak transcription	Adipose Nuclei	Adipose
44	chr10:5996200-6000000	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr10:5997200-5999000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr10:5997400-5999000	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr10:5997600-5998800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr10:5997600-5998800	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr10:5997600-6007600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr10:5997800-5998600	Strong transcription	Left Ventricle	heart

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