Variant report

Variant	esv3447747
Chromosome Location	chr5:60217244-60241866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:610)
CpG islands
(count:979)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
2	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
3	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
4	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
5	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:60240684-60241301	GM12878	blood:	n/a	chr5:60241008-60241024
8	BHLHE40	chr5:60241820-60242140	K562	blood:	n/a	n/a
9	BHLHE40	chr5:60240872-60241581	K562	blood:	n/a	chr5:60241008-60241024
10	CBX3	chr5:60231541-60231761	K562	blood:	n/a	n/a
11	CBX3	chr5:60240930-60241613	K562	blood:	n/a	n/a
12	CCNT2	chr5:60241747-60241947	K562	blood:	n/a	n/a
13	CCNT2	chr5:60240705-60241024	K562	blood:	n/a	n/a
14	CEBPB	chr5:60240799-60241057	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:60241137-60241281	K562	blood:	n/a	n/a
16	CEBPB	chr5:60239556-60240203	HepG2	liver:	n/a	chr5:60239733-60239744
17	CEBPB	chr5:60239553-60239813	A549	lung:	n/a	chr5:60239733-60239744
18	CEBPB	chr5:60240711-60242121	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr5:60239558-60239890	IMR90	lung:	n/a	chr5:60239733-60239744
20	CEBPB	chr5:60236700-60237001	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:60239532-60239892	K562	blood:	n/a	chr5:60239733-60239744
22	CEBPB	chr5:60239540-60239884	Hela-S3	cervix:	n/a	chr5:60239733-60239744
23	CEBPB	chr5:60240741-60241412	IMR90	lung:	n/a	n/a
24	CEBPD	chr5:60240787-60241142	HepG2	liver:	n/a	n/a
25	CHD1	chr5:60241123-60241161	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr5:60240748-60240773	GM12878	blood:	n/a	n/a
27	CHD2	chr5:60240692-60241371	K562	blood:	n/a	n/a
28	CHD2	chr5:60240662-60241524	GM12878	blood:	n/a	n/a
29	CHD2	chr5:60241804-60241993	K562	blood:	n/a	n/a
30	CHD2	chr5:60240689-60241539	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr5:60241056-60241063	HepG2	liver:	n/a	n/a
32	CHD2	chr5:60240697-60241779	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr5:60241795-60241842	GM12878	blood:	n/a	n/a
34	CREB1	chr5:60240714-60241128	A549	lung:	n/a	n/a
35	CREB1	chr5:60241159-60241375	A549	lung:	n/a	n/a
36	CTCF	chr5:60225080-60225230	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr5:60224920-60225070	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr5:60224960-60225110	GM12871	blood:	n/a	n/a
39	CTCF	chr5:60224978-60225143	LNCaP	prostate:	n/a	n/a
40	CTCF	chr5:60224953-60225120	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr5:60224968-60225209	A549	lung:	n/a	n/a
42	CTCF	chr5:60224960-60225110	HFF	foreskin:	n/a	n/a
43	CTCF	chr5:60224883-60225159	A549	lung:	n/a	n/a
44	CTCF	chr5:60224940-60225090	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr5:60224980-60225130	AG10803	skin:	n/a	n/a
46	CTCF	chr5:60241080-60241088	ProgFib	skin:	n/a	n/a
47	CTCF	chr5:60225280-60225430	HPF	lung:	n/a	n/a
48	CTCF	chr5:60240960-60241110	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr5:60224940-60225090	GM12801	blood:	n/a	n/a
50	CTCF	chr5:60225000-60225150	HMF	breast:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60241424-60241474	AG04450	lung:	fetal
2	chr5:60241424-60241474	HRCEpiC	kidney:	n/a
3	chr5:60240938-60240988	IMR90	lung:	fetal
4	chr5:60241424-60241474	AG04450	lung:	fetal
5	chr5:60241424-60241474	HRCEpiC	kidney:	n/a
6	chr5:60240938-60240988	IMR90	lung:	fetal
7	chr5:60241428-60241478	HUVEC	blood vessel:	n/a
8	chr5:60241428-60241478	NHBE	bronchial:	n/a
9	chr5:60240952-60241002	IMR90	lung:	fetal
10	chr5:60241424-60241474	BJ	skin:	n/a
11	chr5:60240938-60240988	HUVEC	blood vessel:	n/a
12	chr5:60240926-60240976	ECC-1	luminal epithelium:	n/a
13	chr5:60240670-60240720	GM12878	blood:	n/a
14	chr5:60240670-60240720	HEK293	kidney:	embryo
15	chr5:60239580-60239630	BJ	skin:	n/a
16	chr5:60240926-60240976	HAEpiC	amniotic membrane:	n/a
17	chr5:60240568-60240618	SKMC	muscle:	n/a
18	chr5:60240926-60240976	SK-N-SH_RA	brain:	n/a
19	chr5:60241428-60241478	H1-hESC	embryonic stem cell:	embryo
20	chr5:60241019-60241069	GM12892	blood:	n/a
21	chr5:60241428-60241478	HCF	heart:	n/a
22	chr5:60240938-60240988	GM12891	blood:	n/a
23	chr5:60240870-60240920	A549	lung:	n/a
24	chr5:60241324-60241374	ECC-1	luminal epithelium:	n/a
25	chr5:60240838-60240888	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:60241636-60241686	GM12892	blood:	n/a
27	chr5:60241428-60241478	Caco-2	colon:	n/a
28	chr5:60241428-60241478	K562	blood:	n/a
29	chr5:60241424-60241474	GM12892	blood:	n/a
30	chr5:60241428-60241478	Hela-S3	cervix:	n/a
31	chr5:60241003-60241053	NH-A	brain:	n/a
32	chr5:60241428-60241478	Jurkat	blood:	n/a
33	chr5:60240952-60241002	AG09319	gingival:	n/a
34	chr5:60241019-60241069	GM19239	blood:	n/a
35	chr5:60241324-60241374	U87	brain:	n/a
36	chr5:60241636-60241686	AoSMC	blood vessel:	n/a
37	chr5:60240838-60240888	HRPEpiC	eye:	n/a
38	chr5:60241428-60241478	GM12878	blood:	n/a
39	chr5:60240870-60240920	HepG2	liver:	n/a
40	chr5:60240952-60241002	GM19239	blood:	n/a
41	chr5:60240568-60240618	HNPCEpiC	eye:	n/a
42	chr5:60240817-60240867	GM12878	blood:	n/a
43	chr5:60241019-60241069	U87	brain:	n/a
44	chr5:60241019-60241069	Hepatocyte	liver:	n/a
45	chr5:60240891-60240941	NH-A	brain:	n/a
46	chr5:60239580-60239630	SKMC	muscle:	n/a
47	chr5:60241428-60241478	HRCEpiC	kidney:	n/a
48	chr5:60240838-60240888	HepG2	liver:	n/a
49	chr5:60241003-60241053	HEEpiC	esophagus:	n/a
50	chr5:60240926-60240976	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:156698013..156698560-chr5:60240745..60241454,2	Hela-S3	cervix:
2	chr2:25194755..25195595-chr5:60240745..60241487,2	Hela-S3	cervix:
3	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
4	chr5:60234534..60237256-chr5:60239004..60241956,3	K562	blood:
5	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
6	chr5:59973247..59973801-chr5:60224508..60225118,3	K562	blood:
7	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
8	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
9	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:
10	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
11	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
12	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
13	chr5:60231929..60237280-chr5:60239098..60242865,6	MCF-7	breast:
14	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
15	chr5:10761355..10761920-chr5:60240758..60241387,2	NB4	blood:
16	chr5:60238903..60240533-chr5:60255101..60257245,2	K562	blood:
17	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
18	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
19	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
20	chr5:59995721..59997582-chr5:60231998..60233519,2	K562	blood:
21	chr5:60238110..60240722-chr5:60956482..60958434,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655

No data

Variant related genes	Relation type
NDUFAF2	TF binding region
ERCC8	TF binding region
NDUFAF2	CpG island
ERCC8	CpG island
ENSG00000143303	chromatin interactions
ENSG00000112977	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000224165	chromatin interactions

Extended variants
information (count: 908 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139195959	chr5:60217314-60217315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548380899	chr5:60217418-60217419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4647076	chr5:60217427-60217428	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs4647075	chr5:60217439-60217440	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs531019884	chr5:60217453-60217454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4647074	chr5:60217487-60217488	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570762468	chr5:60217511-60217512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186761116	chr5:60217560-60217561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553406463	chr5:60217616-60217617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375207363	chr5:60217621-60217622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs976080	chr5:60217651-60217652	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191143378	chr5:60217668-60217669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535680749	chr5:60217691-60217692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555526708	chr5:60217708-60217709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574238840	chr5:60217739-60217740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543117619	chr5:60217760-60217761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56015997	chr5:60217791-60217792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs56108456	chr5:60217799-60217800	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs556597415	chr5:60217822-60217823	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs376383083	chr5:60217836-60217837	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs371296308	chr5:60217879-60217880	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs369951599	chr5:60217885-60217886	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs146740678	chr5:60217906-60217907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56376749	chr5:60217919-60217920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372707555	chr5:60217922-60217923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528369656	chr5:60217952-60217953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200205429	chr5:60217964-60217965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140343389	chr5:60217981-60217982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530679736	chr5:60217982-60217983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551105507	chr5:60217983-60217984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201535238	chr5:60218010-60218011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539548460	chr5:60218016-60218017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533194792	chr5:60218040-60218041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183314166	chr5:60218054-60218055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187560776	chr5:60218064-60218065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546952821	chr5:60218084-60218085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567085979	chr5:60218166-60218167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79314404	chr5:60218225-60218226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143221570	chr5:60218251-60218252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147474400	chr5:60218285-60218286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538014812	chr5:60218327-60218328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556800134	chr5:60218405-60218406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76858571	chr5:60218419-60218420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367623962	chr5:60218608-60218609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552922148	chr5:60218629-60218630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76910838	chr5:60218670-60218671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542150700	chr5:60218745-60218746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561924860	chr5:60218767-60218768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192041599	chr5:60218836-60218837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544393002	chr5:60218837-60218838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
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
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60167800-60228200	Weak transcription	Psoas Muscle	Psoas
2	chr5:60175800-60239400	Weak transcription	NHEK	skin
3	chr5:60176400-60220400	Weak transcription	Esophagus	oesophagus
4	chr5:60177200-60239600	Weak transcription	HSMMtube	muscle
5	chr5:60177400-60232800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:60181000-60218800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr5:60181600-60230800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr5:60183400-60228000	Weak transcription	Small Intestine	intestine
9	chr5:60185600-60221200	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr5:60187600-60223800	Weak transcription	HUVEC	blood vessel
11	chr5:60187600-60239600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr5:60187800-60239600	Weak transcription	Brain Angular Gyrus	brain
13	chr5:60188000-60223400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr5:60189400-60240000	Weak transcription	Spleen	Spleen
15	chr5:60189600-60224000	Weak transcription	Osteobl	bone
16	chr5:60189600-60239600	Weak transcription	Right Ventricle	heart
17	chr5:60189600-60240000	Weak transcription	Pancreas	Pancrea
18	chr5:60189800-60223600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr5:60189800-60225000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr5:60189800-60225800	Weak transcription	Fetal Brain Female	brain
21	chr5:60190200-60224000	Weak transcription	Brain Germinal Matrix	brain
22	chr5:60191000-60227200	Weak transcription	Fetal Intestine Small	intestine
23	chr5:60191000-60232800	Weak transcription	Fetal Stomach	stomach
24	chr5:60193200-60227400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr5:60193200-60232800	Weak transcription	Lung	lung
26	chr5:60193200-60239800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr5:60194600-60222800	Weak transcription	HMEC	breast
28	chr5:60199600-60224400	Weak transcription	Brain Hippocampus Middle	brain
29	chr5:60201600-60229800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr5:60201800-60225600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr5:60202000-60223200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr5:60202000-60223400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr5:60202800-60223200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:60207600-60225400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr5:60209800-60218400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:60210200-60218000	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr5:60210200-60220600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:60210800-60223800	Weak transcription	Stomach Mucosa	stomach
39	chr5:60211000-60217400	Strong transcription	Dnd41	blood
40	chr5:60211600-60223200	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr5:60211800-60233400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr5:60212000-60223000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr5:60212200-60223000	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr5:60212400-60223200	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr5:60212800-60225200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr5:60213000-60239800	Weak transcription	Colonic Mucosa	Colon
47	chr5:60213200-60233000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr5:60213200-60233200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr5:60213400-60222800	Weak transcription	Fetal Intestine Large	intestine
50	chr5:60213400-60223200	Weak transcription	NH-A	brain

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