Variant report

Variant	esv1802186
Chromosome Location	chr5:37310765-37354259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:246)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:37349046-37349675	HepG2	liver:	n/a	n/a
2	CEBPB	chr5:37332403-37332643	K562	blood:	n/a	n/a
3	CEBPB	chr5:37310503-37310843	Hela-S3	cervix:	n/a	chr5:37310662-37310673
4	CEBPB	chr5:37310538-37310821	K562	blood:	n/a	chr5:37310662-37310673
5	CEBPB	chr5:37319208-37319518	IMR90	lung:	n/a	chr5:37319373-37319384
6	CEBPB	chr5:37319216-37319459	HepG2	liver:	n/a	chr5:37319373-37319384
7	CEBPB	chr5:37319215-37319515	A549	lung:	n/a	chr5:37319373-37319384
8	CEBPB	chr5:37310517-37310821	HepG2	liver:	n/a	chr5:37310662-37310673
9	CEBPB	chr5:37319098-37319509	K562	blood:	n/a	chr5:37319373-37319384
10	CEBPB	chr5:37332485-37332638	A549	lung:	n/a	n/a
11	CEBPB	chr5:37349333-37349648	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:37310532-37310827	IMR90	lung:	n/a	chr5:37310662-37310673
13	CEBPB	chr5:37332437-37332631	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:37323944-37324079	K562	blood:	n/a	n/a
15	CTCF	chr5:37345865-37345870	MCF-7	breast:	n/a	n/a
16	CTCF	chr5:37316160-37316310	HL-60	blood:	n/a	n/a
17	CTCF	chr5:37345874-37346009	MCF-7	breast:	n/a	n/a
18	CTCF	chr5:37345840-37345990	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr5:37325554-37325605	LNCaP	prostate:	n/a	n/a
20	CTCF	chr5:37353557-37353588	GM20000	blood:	n/a	n/a
21	CTCF	chr5:37345872-37345985	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:37345901-37345970	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:37352902-37352915	K562	blood:	n/a	n/a
24	CTCF	chr5:37345840-37345990	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr5:37340433-37340469	Lung_OC	lung:	n/a	n/a
26	CTCF	chr5:37345895-37345967	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:37338673-37338760	GM10248	blood:	n/a	n/a
28	CTCF	chr5:37315723-37315775	GM13976	blood:	n/a	n/a
29	CTCF	chr5:37325606-37325679	LNCaP	prostate:	n/a	n/a
30	E2F4	chr5:37312158-37312612	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr5:37318105-37318227	GM12878	blood:	n/a	n/a
32	EP300	chr5:37349203-37349626	HepG2	liver:	n/a	chr5:37349399-37349409 chr5:37349362-37349376 chr5:37349364-37349378
33	EP300	chr5:37349298-37349585	HepG2	liver:	n/a	chr5:37349399-37349409 chr5:37349362-37349376 chr5:37349364-37349378
34	EP300	chr5:37349139-37349717	HepG2	liver:	n/a	chr5:37349399-37349409 chr5:37349362-37349376 chr5:37349364-37349378
35	FAM48A	chr5:37324427-37324462	GM12878	blood:	n/a	n/a
36	FOXA1	chr5:37349248-37349636	HepG2	liver:	n/a	n/a
37	FOXA1	chr5:37349047-37349815	HepG2	liver:	n/a	n/a
38	FOXA1	chr5:37349156-37349741	HepG2	liver:	n/a	n/a
39	FOXA1	chr5:37327624-37327954	T-47D	breast:	n/a	n/a
40	FOXA1	chr5:37349047-37349772	HepG2	liver:	n/a	n/a
41	FOXA1	chr5:37327635-37327958	T-47D	breast:	n/a	n/a
42	FOXA2	chr5:37348786-37350114	HepG2	liver:	n/a	chr5:37349942-37349954
43	FOXA2	chr5:37348973-37349644	HepG2	liver:	n/a	n/a
44	GATA3	chr5:37327703-37328125	T-47D	breast:	n/a	n/a
45	GATA3	chr5:37327743-37327924	T-47D	breast:	n/a	n/a
46	HDAC2	chr5:37349236-37349601	HepG2	liver:	n/a	chr5:37349365-37349379 chr5:37349364-37349378 chr5:37349363-37349377 chr5:37349367-37349381 chr5:37349400-37349409 chr5:37349366-37349380 chr5:37349371-37349385 chr5:37349361-37349375 chr5:37349372-37349386
47	HDAC2	chr5:37349196-37349625	HepG2	liver:	n/a	chr5:37349365-37349379 chr5:37349364-37349378 chr5:37349363-37349377 chr5:37349367-37349381 chr5:37349400-37349409 chr5:37349366-37349380 chr5:37349371-37349385 chr5:37349361-37349375 chr5:37349372-37349386
48	HEY1	chr5:37349442-37349609	HepG2	liver:	n/a	n/a
49	HNF4A	chr5:37349300-37349573	HepG2	liver:	n/a	n/a
50	HNF4A	chr5:37349220-37349622	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37322183-37322233	GM19239	blood:	n/a
2	chr5:37322183-37322233	PFSK-1	brain:	n/a
3	chr5:37322183-37322233	NT2-D1	testis:	n/a
4	chr5:37322183-37322233	HUVEC	blood vessel:	n/a
5	chr5:37322183-37322233	SK-N-SH	brain:	n/a
6	chr5:37322183-37322233	T-47D	breast:	n/a
7	chr5:37322183-37322233	MCF-7	breast:	n/a
8	chr5:37322183-37322233	SK-N-MC	brain:	n/a
9	chr5:37322183-37322233	BJ	skin:	n/a
10	chr5:37322183-37322233	ECC-1	luminal epithelium:	n/a
11	chr5:37322183-37322233	Jurkat	blood:	n/a
12	chr5:37322183-37322233	MCF10A-Er-Src	breast:	n/a
13	chr5:37322183-37322233	ProgFib	skin:	n/a
14	chr5:37322183-37322233	NH-A	brain:	n/a
15	chr5:37322183-37322233	HCM	heart:	n/a
16	chr5:37322183-37322233	PrEC	prostate:	n/a
17	chr5:37322183-37322233	PANC-1	pancreas:	n/a
18	chr5:37322183-37322233	HCF	heart:	n/a
19	chr5:37322183-37322233	SK-N-SH_RA	brain:	n/a
20	chr5:37322183-37322233	NHDF-neo	bronchial:	n/a
21	chr5:37322183-37322233	AG10803	skin:	n/a
22	chr5:37322183-37322233	NB4	blood:	n/a
23	chr5:37322183-37322233	HRCEpiC	kidney:	n/a
24	chr5:37322183-37322233	ovcar-3	ovarian:	n/a
25	chr5:37322183-37322233	HRPEpiC	eye:	n/a
26	chr5:37322183-37322233	AoSMC	blood vessel:	n/a
27	chr5:37322183-37322233	CMK	blood:	n/a
28	chr5:37322183-37322233	HL-60	blood:	n/a
29	chr5:37322183-37322233	AG09319	gingival:	n/a
30	chr5:37322183-37322233	GM06990	blood:	n/a
31	chr5:37322183-37322233	K562	blood:	n/a
32	chr5:37322183-37322233	IMR90	lung:	fetal
33	chr5:37322183-37322233	GM12892	blood:	n/a
34	chr5:37322183-37322233	LNCaP	prostate:	n/a
35	chr5:37322183-37322233	Caco-2	colon:	n/a
36	chr5:37322183-37322233	Hela-S3	cervix:	n/a
37	chr5:37322183-37322233	GM12891	blood:	n/a
38	chr5:37322183-37322233	RPTEC	kidney:	n/a
39	chr5:37322183-37322233	HMEC	breast:	n/a
40	chr5:37322183-37322233	SKMC	muscle:	n/a
41	chr5:37322183-37322233	AG04450	lung:	fetal
42	chr5:37322183-37322233	BE2_C	brain:	n/a
43	chr5:37322183-37322233	HEEpiC	esophagus:	n/a
44	chr5:37322183-37322233	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:37322183-37322233	HIPEpiC	eye:	n/a
46	chr5:37322183-37322233	U87	brain:	n/a
47	chr5:37322183-37322233	HepG2	liver:	n/a
48	chr5:37322183-37322233	HCT-116	colon:	n/a
49	chr5:37322183-37322233	HRE	kidney:	n/a
50	chr5:37322183-37322233	SAEC	small airway:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:37326722..37329430-chr5:37348015..37351389,3	K562	blood:
2	chr5:37353747..37356748-chr5:37369994..37371965,3	K562	blood:
3	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
4	chr5:37329127..37329843-chr5:37340391..37341109,2	Hela-S3	cervix:
5	chr5:37341224..37342807-chr5:37371137..37373027,2	K562	blood:
6	chr5:37348597..37351209-chr5:37351351..37353763,2	K562	blood:
7	chr5:37313041..37316016-chr5:37316235..37320190,3	K562	blood:
8	chr5:37329127..37329843-chr5:37340391..37341109,2	Hela-S3	cervix:
9	chr5:37308340..37310527-chr5:37313095..37315302,2	K562	blood:
10	chr5:37326836..37328413-chr5:37330631..37332181,2	K562	blood:
11	chr5:37326722..37329430-chr5:37348015..37351389,3	K562	blood:
12	chr5:37343556..37345615-chr5:37366480..37369895,3	K562	blood:
13	chr5:37299270..37301087-chr5:37332798..37335148,2	K562	blood:
14	chr5:37296733..37298868-chr5:37344772..37346341,2	K562	blood:
15	chr5:37341337..37344195-chr5:37360002..37362809,2	K562	blood:
16	chr5:37351031..37353005-chr5:37354563..37356913,2	K562	blood:
17	chr5:37313041..37316016-chr5:37316235..37319015,2	K562	blood:
18	chr5:37313041..37316016-chr5:37316235..37319015,2	K562	blood:
19	chr15:94515130..94515844-chr5:37350902..37351467,2	MCF-7	breast:
20	chr5:37318176..37320415-chr5:37333622..37336534,2	K562	blood:
21	chr5:37313041..37316016-chr5:37316235..37320190,3	K562	blood:
22	chr5:37290610..37293343-chr5:37317784..37320761,2	K562	blood:
23	chr5:37318176..37320415-chr5:37333622..37336534,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf42-5	chr5:37324306-37324596	expReg_chr5_1217_-

No data

Variant related genes	Relation type
RNU7-75P	TF binding region
NUP155	TF binding region
RNU7-75P	CpG island
NUP155	CpG island
ENSG00000113569	chromatin interactions
ENSG00000251880	chromatin interactions

Extended variants
information (count: 1746 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1746 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs53429	chr5:37310765-37310766	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543310944	chr5:37310769-37310770	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187295468	chr5:37310790-37310791	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs151221761	chr5:37310803-37310804	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371605296	chr5:37310854-37310855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576529066	chr5:37310873-37310874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189642967	chr5:37310962-37310963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112259074	chr5:37311011-37311012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533386581	chr5:37311016-37311017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181448582	chr5:37311067-37311068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570111051	chr5:37311082-37311083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531283006	chr5:37311272-37311273	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs537754003	chr5:37311315-37311316	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs147465971	chr5:37311427-37311428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371634079	chr5:37311523-37311524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543946202	chr5:37311547-37311548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139107738	chr5:37311565-37311566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535067524	chr5:37311618-37311619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553479080	chr5:37311704-37311705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571831299	chr5:37311763-37311764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572101157	chr5:37311766-37311767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545547254	chr5:37311869-37311870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539080546	chr5:37311873-37311874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546281815	chr5:37311874-37311875	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553095588	chr5:37311877-37311878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199635972	chr5:37311879-37311880	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566278429	chr5:37311909-37311910	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs557940421	chr5:37311924-37311925	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs576108223	chr5:37311932-37311933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186132245	chr5:37312021-37312022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148476041	chr5:37312033-37312034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574113665	chr5:37312043-37312044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190108232	chr5:37312048-37312049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79262117	chr5:37312124-37312125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59842820	chr5:37312144-37312145	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs551539665	chr5:37312196-37312197	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs56369431	chr5:37312213-37312214	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs531005948	chr5:37312224-37312225	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs549303979	chr5:37312310-37312311	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs555727536	chr5:37312371-37312372	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs183369774	chr5:37312458-37312459	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs34968825	chr5:37312473-37312474	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs78623834	chr5:37312483-37312484	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs397997403	chr5:37312484-37312485	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs534959527	chr5:37312492-37312493	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs186485939	chr5:37312544-37312545	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs150591639	chr5:37312556-37312557	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs539522362	chr5:37312573-37312574	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs115623442	chr5:37312662-37312663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139544649	chr5:37312708-37312709	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Autism	22549408	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37288200-37320000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:37289000-37369200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:37289800-37323600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:37294400-37310800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:37296400-37365400	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr5:37296400-37369000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr5:37296600-37318600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr5:37296800-37311000	Strong transcription	H9 Cell Line	embryonic stem cell
9	chr5:37296800-37316600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr5:37296800-37316800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr5:37296800-37318400	Strong transcription	Fetal Muscle Trunk	muscle
12	chr5:37296800-37320200	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr5:37296800-37321600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr5:37296800-37353200	Strong transcription	Fetal Thymus	thymus
15	chr5:37296800-37358400	Strong transcription	Placenta	Placenta
16	chr5:37296800-37358600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr5:37296800-37358600	Strong transcription	Liver	Liver
18	chr5:37296800-37359000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr5:37296800-37359800	Strong transcription	HUES48 Cell Line	embryonic stem cell
20	chr5:37296800-37359800	Strong transcription	Fetal Intestine Large	intestine
21	chr5:37296800-37360000	Strong transcription	Adipose Nuclei	Adipose
22	chr5:37296800-37364600	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr5:37296800-37364600	Strong transcription	Dnd41	blood
24	chr5:37296800-37365600	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr5:37297000-37310800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:37297000-37310800	Strong transcription	A549	lung
27	chr5:37297000-37316800	Strong transcription	Primary T cells from cord blood	blood
28	chr5:37297000-37329600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr5:37297000-37333200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr5:37297000-37364200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr5:37297000-37365400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:37297200-37317800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:37297200-37330600	Strong transcription	Skeletal Muscle Female	skeletal muscle
34	chr5:37297200-37358800	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr5:37297400-37316000	Strong transcription	HUVEC	blood vessel
36	chr5:37297400-37318200	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr5:37297400-37334400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr5:37297400-37364600	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr5:37297800-37324800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:37297800-37359800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr5:37298600-37314200	Strong transcription	HepG2	liver
42	chr5:37298600-37316600	Strong transcription	Primary hematopoietic stem cells	blood
43	chr5:37298600-37337800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:37299600-37329400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr5:37302200-37311800	Weak transcription	Pancreas	Pancrea
46	chr5:37304000-37312800	Weak transcription	Psoas Muscle	Psoas
47	chr5:37305200-37327600	Weak transcription	Fetal Heart	heart
48	chr5:37305400-37315200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr5:37305600-37312400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr5:37305600-37312400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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