Variant report

Variant	nsv882777
Chromosome Location	chr5:118870452-118981480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:519)
CpG islands
(count:794)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:519 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:118873197-118874032	GM12878	blood:	n/a	n/a
2	ATF2	chr5:118914677-118915033	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:118873223-118873968	GM12878	blood:	n/a	n/a
4	BATF	chr5:118873364-118873881	GM12878	blood:	n/a	n/a
5	BATF	chr5:118873272-118873908	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:118873461-118873945	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
7	BCL11A	chr5:118873315-118873926	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
8	BCL3	chr5:118873342-118873895	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
9	BCLAF1	chr5:118873277-118873927	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
10	BCLAF1	chr5:118873198-118873942	GM12878	blood:	n/a	chr5:118873665-118873674 chr5:118873666-118873675
11	BHLHE40	chr5:118873360-118873825	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:118967365-118967634	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:118905293-118905295	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr5:118914624-118915116	HCT-116	colon:	n/a	n/a
15	CEBPB	chr5:118950582-118950912	A549	lung:	n/a	chr5:118950732-118950743
16	CEBPB	chr5:118919578-118919777	IMR90	lung:	n/a	chr5:118919684-118919697 chr5:118919684-118919695
17	CEBPB	chr5:118881941-118881942	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr5:118950582-118950884	H1-hESC	embryonic stem cell:	n/a	chr5:118950732-118950743
19	CEBPB	chr5:118950660-118950968	A549	lung:	n/a	chr5:118950732-118950743 chr5:118950910-118950923
20	CEBPB	chr5:118950581-118950898	Hela-S3	cervix:	n/a	chr5:118950732-118950743
21	CEBPB	chr5:118873191-118873959	GM12878	blood:	n/a	n/a
22	CEBPB	chr5:118919582-118919782	HepG2	liver:	n/a	chr5:118919684-118919697 chr5:118919684-118919695
23	CEBPB	chr5:118950558-118950922	HepG2	liver:	n/a	chr5:118950732-118950743
24	CEBPB	chr5:118950598-118950884	K562	blood:	n/a	chr5:118950732-118950743
25	CEBPB	chr5:118950580-118950925	IMR90	lung:	n/a	chr5:118950732-118950743 chr5:118950910-118950923
26	CEBPB	chr5:118967986-118968181	HepG2	liver:	n/a	chr5:118968078-118968089 chr5:118968080-118968091 chr5:118968078-118968091 chr5:118968080-118968091 chr5:118968078-118968091 chr5:118968078-118968091
27	CEBPB	chr5:118881846-118881850	K562	blood:	n/a	n/a
28	CHD2	chr5:118919572-118919740	GM12878	blood:	n/a	n/a
29	CHD2	chr5:118873456-118873835	GM12878	blood:	n/a	n/a
30	CTCF	chr5:118914736-118914921	NHEK	skin:	n/a	n/a
31	CTCF	chr5:118918777-118918876	Gliobla	brain:	n/a	n/a
32	CTCF	chr5:118914800-118914950	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr5:118914760-118914910	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr5:118914660-118914810	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr5:118914750-118914851	GM12891	blood:	n/a	n/a
36	CTCF	chr5:118914680-118914830	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr5:118914603-118915143	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:118914780-118914930	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr5:118918742-118918903	K562	blood:	n/a	n/a
40	CTCF	chr5:118914720-118914870	GM12801	blood:	n/a	n/a
41	CTCF	chr5:118970849-118970909	MCF-7	breast:	n/a	chr5:118970869-118970878
42	CTCF	chr5:118914760-118914910	HCFaa	heart:	n/a	n/a
43	CTCF	chr5:118914716-118914914	GM19239	blood:	n/a	n/a
44	CTCF	chr5:118914800-118914950	AG09309	skin:	n/a	n/a
45	CTCF	chr5:118914703-118914939	IMR90	lung:	n/a	n/a
46	CTCF	chr5:118914760-118914910	GM12871	blood:	n/a	n/a
47	CTCF	chr5:118914660-118914810	HVMF	connective:	n/a	n/a
48	CTCF	chr5:118914660-118915025	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:118914680-118914830	GM12878	blood:	n/a	n/a
50	CTCF	chr5:118914900-118915050	NHDF-neo	bronchial:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118964760-118964810	GM06990	blood:	n/a
2	chr5:118964760-118964810	GM06990	blood:	n/a
3	chr5:118945798-118945848	HEEpiC	esophagus:	n/a
4	chr5:118945798-118945848	SKMC	muscle:	n/a
5	chr5:118943582-118943632	CMK	blood:	n/a
6	chr5:118971490-118971540	HCPEpiC	choroid plexus:	n/a
7	chr5:118964311-118964361	NH-A	brain:	n/a
8	chr5:118943582-118943632	A549	lung:	n/a
9	chr5:118965233-118965283	AG09309	skin:	n/a
10	chr5:118964760-118964810	Caco-2	colon:	n/a
11	chr5:118964311-118964361	HCM	heart:	n/a
12	chr5:118965202-118965252	MCF-7	breast:	n/a
13	chr5:118918353-118918403	NB4	blood:	n/a
14	chr5:118966450-118966500	HL-60	blood:	n/a
15	chr5:118966450-118966500	GM12891	blood:	n/a
16	chr5:118965199-118965249	Hela-S3	cervix:	n/a
17	chr5:118964330-118964380	SK-N-SH_RA	brain:	n/a
18	chr5:118965233-118965283	NH-A	brain:	n/a
19	chr5:118964311-118964361	PrEC	prostate:	n/a
20	chr5:118966450-118966500	HRPEpiC	eye:	n/a
21	chr5:118964330-118964380	Hela-S3	cervix:	n/a
22	chr5:118965347-118965397	HMEC	breast:	n/a
23	chr5:118943582-118943632	SAEC	small airway:	n/a
24	chr5:118945798-118945848	Hela-S3	cervix:	n/a
25	chr5:118965199-118965249	ovcar-3	ovarian:	n/a
26	chr5:118945798-118945848	SK-N-MC	brain:	n/a
27	chr5:118965347-118965397	BJ	skin:	n/a
28	chr5:118964760-118964810	SAEC	small airway:	n/a
29	chr5:118965233-118965283	SK-N-SH_RA	brain:	n/a
30	chr5:118965093-118965143	HCM	heart:	n/a
31	chr5:118965093-118965143	GM12892	blood:	n/a
32	chr5:118966450-118966500	GM06990	blood:	n/a
33	chr5:118965347-118965397	NHDF-neo	bronchial:	n/a
34	chr5:118965093-118965143	AG04449	skin:	fetal
35	chr5:118965202-118965252	HUVEC	blood vessel:	n/a
36	chr5:118965202-118965252	RPTEC	kidney:	n/a
37	chr5:118965347-118965397	GM12891	blood:	n/a
38	chr5:118965199-118965249	GM12892	blood:	n/a
39	chr5:118964311-118964361	AG09319	gingival:	n/a
40	chr5:118971490-118971540	AG09319	gingival:	n/a
41	chr5:118943582-118943632	HepG2	liver:	n/a
42	chr5:118943582-118943632	LNCaP	prostate:	n/a
43	chr5:118964330-118964380	Jurkat	blood:	n/a
44	chr5:118964760-118964810	Jurkat	blood:	n/a
45	chr5:118964760-118964810	SK-N-MC	brain:	n/a
46	chr5:118965233-118965283	HCPEpiC	choroid plexus:	n/a
47	chr5:118965347-118965397	CMK	blood:	n/a
48	chr5:118965347-118965397	HAEpiC	amniotic membrane:	n/a
49	chr5:118918353-118918403	GM12878	blood:	n/a
50	chr5:118966450-118966500	AG10803	skin:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:118872062..118874467-chr5:118875456..118877548,2	K562	blood:
2	chr5:118894936..118898702-chr5:118910373..118913198,3	K562	blood:
3	chr5:118894936..118898702-chr5:118910373..118913198,3	K562	blood:
4	chr5:118969350..118971172-chr5:118976054..118978224,2	K562	blood:
5	chr5:118804092..118805803-chr5:118943072..118945052,2	K562	blood:
6	chr5:118863717..118866521-chr5:118868164..118871056,3	K562	blood:
7	chr5:118973233..118975098-chr5:118976996..118979393,2	K562	blood:
8	chr5:118868196..118870095-chr5:118875556..118878228,2	K562	blood:
9	chr5:118891974..118894099-chr5:118898157..118900146,2	K562	blood:
10	chr5:118872062..118875418-chr5:118875456..118880778,4	K562	blood:
11	chr5:118914344..118915154-chr5:119079337..119079948,2	MCF-7	breast:
12	chr5:118969350..118971172-chr5:118976054..118978224,2	K562	blood:
13	chr17:59527418..59528358-chr5:118905430..118906391,2	MCF-7	breast:
14	chr5:118969123..118972666-chr5:118973811..118977554,4	K562	blood:
15	chr5:118894367..118897199-chr5:119080311..119081964,2	K562	blood:
16	chr5:118872062..118875418-chr5:118875456..118880778,4	K562	blood:
17	chr5:118969123..118972666-chr5:118973811..118977554,4	K562	blood:
18	chr5:118973233..118975098-chr5:118976996..118979393,2	K562	blood:
19	chr5:118891974..118894099-chr5:118898157..118900146,2	K562	blood:
20	chr5:118872062..118874467-chr5:118875456..118877548,2	K562	blood:
21	chr5:118866950..118868481-chr5:118871752..118873914,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-11	chr5:118890945-118891353	NONHSAT103440

No data

Variant related genes	Relation type
HSD17B4	TF binding region
FAM170A	TF binding region
FABP5P6	TF binding region
ENSG00000213663	TF binding region
ENSG00000239067	TF binding region
HSD17B4	CpG island
FAM170A	CpG island
FABP5P6	CpG island
ENSG00000213663	CpG island
ENSG00000239067	CpG island
ENSG00000239084	chromatin interactions

Extended variants
information (count: 2811 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2811 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3797372	chr5:118870452-118870453	Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72561788	chr5:118870493-118870494	Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553705475	chr5:118870524-118870525	Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182136787	chr5:118870548-118870549	Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72563763	chr5:118870549-118870550	Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7716785	chr5:118870581-118870582	Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs562182265	chr5:118870603-118870604	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186871272	chr5:118870622-118870623	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs33948978	chr5:118870662-118870663	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372300147	chr5:118870669-118870670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200386516	chr5:118870670-118870671	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190942670	chr5:118870703-118870704	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183518457	chr5:118870746-118870747	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575942890	chr5:118870756-118870757	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548925917	chr5:118870797-118870798	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563977840	chr5:118870832-118870833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139345287	chr5:118870843-118870844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567657080	chr5:118870898-118870899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188337851	chr5:118870925-118870926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs193200771	chr5:118870941-118870942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138017396	chr5:118870956-118870957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185183873	chr5:118871023-118871024	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs75499100	chr5:118871024-118871025	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs571487199	chr5:118871072-118871073	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs548726151	chr5:118871140-118871141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568913734	chr5:118871149-118871150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188102365	chr5:118871187-118871188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78347528	chr5:118871228-118871229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538831552	chr5:118871243-118871244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571104770	chr5:118871258-118871259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554048588	chr5:118871287-118871288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540046941	chr5:118871315-118871316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191751231	chr5:118871328-118871329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138422180	chr5:118871365-118871366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34379490	chr5:118871366-118871367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183529778	chr5:118871367-118871368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540219441	chr5:118871381-118871382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs397806569	chr5:118871382-118871383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397882330	chr5:118871386-118871387	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542182898	chr5:118871435-118871436	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555510874	chr5:118871453-118871454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575681030	chr5:118871456-118871457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368301450	chr5:118871469-118871470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544423151	chr5:118871482-118871483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188271259	chr5:118871484-118871485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577379743	chr5:118871536-118871537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370824891	chr5:118871580-118871581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181833979	chr5:118871616-118871617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536354102	chr5:118871636-118871637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143318807	chr5:118871648-118871649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118804200-118879600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr5:118832400-118878200	Weak transcription	NH-A	brain
3	chr5:118840200-118878400	Weak transcription	Psoas Muscle	Psoas
4	chr5:118841000-118880000	Weak transcription	Brain Germinal Matrix	brain
5	chr5:118841200-118880000	Weak transcription	A549	lung
6	chr5:118841400-118873200	Weak transcription	Fetal Brain Male	brain
7	chr5:118846800-118878200	Weak transcription	NHLF	lung
8	chr5:118847200-118873200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr5:118847200-118877800	Weak transcription	Small Intestine	intestine
10	chr5:118847200-118878200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr5:118847200-118879800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr5:118847400-118872000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:118847400-118873000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr5:118847400-118873200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr5:118847400-118873800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr5:118847400-118875800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr5:118847400-118876000	Weak transcription	Colonic Mucosa	Colon
18	chr5:118847400-118878200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr5:118847400-118879800	Weak transcription	HSMMtube	muscle
20	chr5:118847600-118873200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr5:118847600-118873400	Weak transcription	Fetal Muscle Leg	muscle
22	chr5:118847600-118873600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr5:118847600-118877600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr5:118847600-118878200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr5:118847600-118879800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr5:118851800-118876400	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr5:118852800-118878200	Weak transcription	Aorta	Aorta
28	chr5:118853000-118880200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr5:118853400-118878200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:118853400-118878200	Weak transcription	Esophagus	oesophagus
31	chr5:118853400-118878200	Weak transcription	Gastric	stomach
32	chr5:118854200-118875600	Weak transcription	Pancreas	Pancrea
33	chr5:118854400-118877600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr5:118854400-118878400	Weak transcription	Spleen	Spleen
35	chr5:118854400-118879600	Weak transcription	Fetal Kidney	kidney
36	chr5:118854400-118880600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:118854800-118875600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr5:118854800-118877600	Weak transcription	Fetal Intestine Small	intestine
39	chr5:118854800-118878200	Weak transcription	Thymus	Thymus
40	chr5:118855200-118873200	Weak transcription	Stomach Smooth Muscle	stomach
41	chr5:118855400-118874200	Weak transcription	Ovary	ovary
42	chr5:118855400-118875800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr5:118855400-118876400	Weak transcription	Lung	lung
44	chr5:118855600-118873200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr5:118855600-118878200	Weak transcription	Fetal Stomach	stomach
46	chr5:118856200-118872800	Weak transcription	Brain Hippocampus Middle	brain
47	chr5:118856200-118874200	Weak transcription	Left Ventricle	heart
48	chr5:118856200-118878400	Weak transcription	Right Ventricle	heart
49	chr5:118857200-118878200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:118860400-118876000	Weak transcription	Brain Substantia Nigra	brain

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