Variant report

Variant	nsv882387
Chromosome Location	chr5:94001476-94071404
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:690)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:94006338-94006365	K562	blood:	n/a	n/a
2	ATF2	chr5:94038400-94038840	GM12878	blood:	n/a	n/a
3	ATF2	chr5:94038328-94039039	GM12878	blood:	n/a	n/a
4	ATF2	chr5:94036156-94036763	GM12878	blood:	n/a	n/a
5	ATF2	chr5:94036162-94036723	GM12878	blood:	n/a	n/a
6	BATF	chr5:94036276-94036715	GM12878	blood:	n/a	chr5:94036517-94036527 chr5:94036516-94036527 chr5:94036535-94036544
7	BATF	chr5:94036308-94036624	GM12878	blood:	n/a	chr5:94036517-94036527 chr5:94036516-94036527 chr5:94036535-94036544
8	BATF	chr5:94038520-94038857	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:94036253-94036654	GM12878	blood:	n/a	chr5:94036542-94036551
10	BCL3	chr5:94036250-94036754	GM12878	blood:	n/a	chr5:94036542-94036551
11	BCL3	chr5:94038409-94038857	GM12878	blood:	n/a	chr5:94038823-94038832 chr5:94038545-94038554
12	BCLAF1	chr5:94036217-94036699	GM12878	blood:	n/a	chr5:94036542-94036551
13	BHLHE40	chr5:94038685-94038712	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:94035310-94035333	GM12878	blood:	n/a	n/a
15	BRCA1	chr5:94035035-94035831	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr5:94027542-94030061	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr5:94033548-94034368	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr5:94031845-94032115	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr5:94022887-94023113	Hela-S3	cervix:	n/a	chr5:94022976-94022987
20	CEBPB	chr5:94027719-94027977	K562	blood:	n/a	n/a
21	CEBPB	chr5:94027659-94028047	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:94022493-94022502	K562	blood:	n/a	n/a
23	CEBPB	chr5:94057618-94057776	A549	lung:	n/a	chr5:94057655-94057664 chr5:94057653-94057666 chr5:94057653-94057666 chr5:94057655-94057666
24	CEBPB	chr5:94022420-94022587	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr5:94027658-94028071	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr5:94068183-94068526	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:94027634-94029534	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:94022960-94023044	HepG2	liver:	n/a	chr5:94022976-94022987
29	CEBPB	chr5:94043155-94043405	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:94066590-94066904	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:94027671-94028029	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr5:94031822-94032136	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:94035173-94035621	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:94033733-94034500	Hela-S3	cervix:	n/a	chr5:94033762-94033775 chr5:94034131-94034144
35	CEBPB	chr5:94007096-94007750	Hela-S3	cervix:	n/a	chr5:94007245-94007258
36	CHD1	chr5:94038638-94038836	GM12878	blood:	n/a	n/a
37	CHD2	chr5:94027728-94028025	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr5:94033925-94034297	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr5:94029092-94029491	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr5:94038596-94038972	GM12878	blood:	n/a	n/a
41	CTCF	chr5:94028815-94029072	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr5:94041560-94041710	AG10803	skin:	n/a	n/a
43	CTCF	chr5:94052896-94052912	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr5:94028940-94029090	AG04450	lung:	n/a	n/a
45	CTCF	chr5:94021820-94021970	AG09319	gingival:	n/a	n/a
46	CTCF	chr5:94028746-94029111	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:94028920-94029070	AG09309	skin:	n/a	n/a
48	CTCF	chr5:94028860-94029010	HFF	foreskin:	n/a	n/a
49	CTCF	chr5:94028900-94029050	AG09309	skin:	n/a	n/a
50	CTCF	chr5:94028840-94028990	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:94027853-94027903	LNCaP	prostate:	n/a
2	chr5:94027853-94027903	GM12891	blood:	n/a
3	chr5:94027853-94027903	HMEC	breast:	n/a
4	chr5:94027853-94027903	BE2_C	brain:	n/a
5	chr5:94027853-94027903	Caco-2	colon:	n/a
6	chr5:94027853-94027903	AG09319	gingival:	n/a
7	chr5:94027853-94027903	AG09309	skin:	n/a
8	chr5:94027853-94027903	HUVEC	blood vessel:	n/a
9	chr5:94027853-94027903	MCF-7	breast:	n/a
10	chr5:94027853-94027903	HRPEpiC	eye:	n/a
11	chr5:94027853-94027903	HNPCEpiC	eye:	n/a
12	chr5:94027853-94027903	H1-hESC	embryonic stem cell:	embryo
13	chr5:94027853-94027903	SK-N-SH	brain:	n/a
14	chr5:94027853-94027903	Jurkat	blood:	n/a
15	chr5:94027853-94027903	HRCEpiC	kidney:	n/a
16	chr5:94027853-94027903	HCT-116	colon:	n/a
17	chr5:94027853-94027903	PFSK-1	brain:	n/a
18	chr5:94027853-94027903	NB4	blood:	n/a
19	chr5:94027853-94027903	SKMC	muscle:	n/a
20	chr5:94027853-94027903	AG10803	skin:	n/a
21	chr5:94027853-94027903	Hela-S3	cervix:	n/a
22	chr5:94027853-94027903	RPTEC	kidney:	n/a
23	chr5:94027853-94027903	AG04449	skin:	fetal
24	chr5:94027853-94027903	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:94027853-94027903	HRE	kidney:	n/a
26	chr5:94027853-94027903	SK-N-MC	brain:	n/a
27	chr5:94027853-94027903	AoSMC	blood vessel:	n/a
28	chr5:94027853-94027903	T-47D	breast:	n/a
29	chr5:94027853-94027903	HEEpiC	esophagus:	n/a
30	chr5:94027853-94027903	GM19239	blood:	n/a
31	chr5:94027853-94027903	IMR90	lung:	fetal
32	chr5:94027853-94027903	ECC-1	luminal epithelium:	n/a
33	chr5:94027853-94027903	HAEpiC	amniotic membrane:	n/a
34	chr5:94027853-94027903	HCM	heart:	n/a
35	chr5:94027853-94027903	GM12892	blood:	n/a
36	chr5:94027853-94027903	ProgFib	skin:	n/a
37	chr5:94027853-94027903	HCPEpiC	choroid plexus:	n/a
38	chr5:94027853-94027903	HIPEpiC	eye:	n/a
39	chr5:94027853-94027903	K562	blood:	n/a
40	chr5:94027853-94027903	NT2-D1	testis:	n/a
41	chr5:94027853-94027903	NH-A	brain:	n/a
42	chr5:94027853-94027903	A549	lung:	n/a
43	chr5:94027853-94027903	PANC-1	pancreas:	n/a
44	chr5:94027853-94027903	NHDF-neo	bronchial:	n/a
45	chr5:94027853-94027903	HepG2	liver:	n/a
46	chr5:94027853-94027903	Hepatocyte	liver:	n/a
47	chr5:94027853-94027903	BJ	skin:	n/a
48	chr5:94027853-94027903	MCF10A-Er-Src	breast:	n/a
49	chr5:94027853-94027903	U87	brain:	n/a
50	chr5:94027853-94027903	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:94068767..94070522-chr5:94072255..94073798,2	K562	blood:
2	chr5:94014366..94016114-chr5:94021219..94023742,2	K562	blood:
3	chr5:94013156..94016114-chr5:94021219..94023049,2	K562	blood:
4	chr5:94014544..94016348-chr5:94016679..94018757,2	K562	blood:
5	chr5:93860650..93861258-chr5:94028313..94029309,3	MCF-7	breast:
6	chr5:93958271..93960232-chr5:94030096..94032055,2	K562	blood:
7	chr11:6135989..6136489-chr5:94069519..94070020,2	NB4	blood:
8	chr5:94041697..94043970-chr5:94047357..94049354,2	K562	blood:
9	chr10:73608596..73609197-chr5:94047132..94048080,2	Hela-S3	cervix:
10	chr5:94041697..94043970-chr5:94047357..94049354,2	K562	blood:
11	chr5:93951256..93953174-chr5:94050678..94052441,2	K562	blood:
12	chr5:94014544..94016348-chr5:94016679..94018757,2	K562	blood:
13	chr5:93948705..93949988-chr5:94028528..94029361,5	MCF-7	breast:
14	chr5:94014366..94016114-chr5:94021219..94023742,2	K562	blood:
15	chr5:94020834..94023576-chr5:94026554..94028869,2	K562	blood:
16	chr5:94034610..94036248-chr5:94045168..94047165,2	K562	blood:
17	chr1:67390712..67391423-chr5:94061472..94061972,2	NB4	blood:
18	chr2:32581417..32582344-chr5:94051301..94052090,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD32-3	chr5:94027891-94027961	NONHSAT102831
2	lnc-ANKRD32-3	chr5:94043930-94043994	NONHSAT102831
3	lnc-KIAA0825-2	chr5:94043230-94043272	NONHSAT102832
4	lnc-KIAA0825-2	chr5:94044217-94046398	NONHSAT102832

No data

Variant related genes	Relation type
MCTP1	TF binding region
ANKRD32	TF binding region
MCTP1	CpG island
ANKRD32	CpG island
ENSG00000175471	chromatin interactions
ENSG00000115760	chromatin interactions
ENSG00000133302	chromatin interactions

Extended variants
information (count: 2412 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2412 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10051931	chr5:94001476-94001477	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566162993	chr5:94001477-94001478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115288968	chr5:94001509-94001510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs60087029	chr5:94001585-94001586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534843033	chr5:94001611-94001612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377358342	chr5:94001640-94001641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200577425	chr5:94001654-94001655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191863782	chr5:94001655-94001656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546479117	chr5:94001661-94001662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542764514	chr5:94001673-94001674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556088362	chr5:94001725-94001726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs557979949	chr5:94001735-94001736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576281956	chr5:94001751-94001752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545362018	chr5:94001779-94001780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183728416	chr5:94001787-94001788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527314529	chr5:94001788-94001789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541051161	chr5:94001862-94001863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561004456	chr5:94001883-94001884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529761017	chr5:94001898-94001899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1549180	chr5:94002048-94002049	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs569399556	chr5:94002075-94002076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531876756	chr5:94002081-94002082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188303735	chr5:94002095-94002096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192962259	chr5:94002100-94002101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202082815	chr5:94002120-94002121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184175685	chr5:94002167-94002168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553757257	chr5:94002204-94002205	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186955804	chr5:94002258-94002259	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117055379	chr5:94002282-94002283	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556918080	chr5:94002283-94002284	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7705424	chr5:94002299-94002300	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs141742791	chr5:94002376-94002377	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112016147	chr5:94002381-94002382	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545300351	chr5:94002443-94002444	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558865245	chr5:94002463-94002464	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542721608	chr5:94002482-94002483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113068471	chr5:94002570-94002571	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560727877	chr5:94002577-94002578	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529796383	chr5:94002642-94002643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34215806	chr5:94002658-94002659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139753077	chr5:94002721-94002722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568851647	chr5:94002730-94002731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs563084158	chr5:94002773-94002774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201119682	chr5:94002775-94002776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531760271	chr5:94002863-94002864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191473208	chr5:94002869-94002870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571566056	chr5:94002878-94002879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527979008	chr5:94002893-94002894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144753959	chr5:94002908-94002909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183616878	chr5:94002911-94002912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:910 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:93955800-94027600	Weak transcription	NH-A	brain
2	chr5:93969400-94008400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr5:93973800-94004200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr5:93975600-94012000	Weak transcription	Aorta	Aorta
5	chr5:93976800-94025000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr5:93981000-94012000	Weak transcription	Left Ventricle	heart
7	chr5:93990600-94008200	Weak transcription	Colon Smooth Muscle	Colon
8	chr5:93991200-94049000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:93994200-94010200	Weak transcription	NHEK	skin
10	chr5:93994200-94012000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr5:93994200-94030800	Weak transcription	Right Ventricle	heart
12	chr5:93994200-94047200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr5:93994400-94006200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr5:93994400-94012000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:93994400-94022600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr5:93994400-94025400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr5:93994400-94027600	Weak transcription	Liver	Liver
18	chr5:93994400-94027600	Weak transcription	NHDF-Ad	bronchial
19	chr5:93994400-94029000	Weak transcription	Brain Hippocampus Middle	brain
20	chr5:93994400-94048800	Weak transcription	Small Intestine	intestine
21	chr5:93994600-94007400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:93994600-94026600	Weak transcription	Fetal Kidney	kidney
23	chr5:93994600-94029200	Weak transcription	Brain Anterior Caudate	brain
24	chr5:93994600-94032200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr5:93995400-94012000	Weak transcription	HepG2	liver
26	chr5:93995400-94024800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr5:93995600-94009600	Weak transcription	Fetal Brain Female	brain
28	chr5:93995600-94024400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:93995600-94033000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr5:93995600-94050400	Weak transcription	Esophagus	oesophagus
31	chr5:93995800-94003000	Weak transcription	A549	lung
32	chr5:93995800-94003200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:93995800-94004600	Strong transcription	Fetal Thymus	thymus
34	chr5:93995800-94010600	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr5:93995800-94012000	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr5:93995800-94012000	Weak transcription	HSMM	muscle
37	chr5:93996000-94024000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr5:93996000-94027600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr5:93996000-94036000	Weak transcription	GM12878-XiMat	blood
40	chr5:93996200-94007400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:93996200-94026600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr5:93996200-94029800	Weak transcription	Ovary	ovary
43	chr5:93996400-94001600	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr5:93996400-94008000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr5:93996400-94012000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:93996600-94003400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr5:93996600-94012000	Weak transcription	Fetal Muscle Trunk	muscle
48	chr5:93996600-94019200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr5:93996600-94023000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr5:93996600-94027800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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