Variant report

Variant	esv3515528
Chromosome Location	chr5:68624487-68653938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:993)
CpG islands
(count:671)
Chromatin interactive
region (count:40)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:68630649-68630758	K562	blood:	n/a	n/a
2	ARID3A	chr5:68630670-68630907	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:68627607-68628919	HepG2	liver:	n/a	n/a
4	ATF2	chr5:68628381-68628936	GM12878	blood:	n/a	n/a
5	ATF3	chr5:68628467-68628717	GM12878	blood:	n/a	chr5:68628651-68628671
6	ATF3	chr5:68628515-68628798	H1-hESC	embryonic stem cell:	n/a	chr5:68628651-68628671
7	ATF3	chr5:68628381-68628875	GM12878	blood:	n/a	chr5:68628651-68628671
8	ATF3	chr5:68628323-68628880	A549	lung:	n/a	chr5:68628651-68628671
9	ATF3	chr5:68628438-68628795	K562	blood:	n/a	chr5:68628651-68628671
10	ATF3	chr5:68628324-68628912	HepG2	liver:	n/a	chr5:68628651-68628671
11	ATF3	chr5:68628432-68628788	HepG2	liver:	n/a	chr5:68628651-68628671
12	ATF3	chr5:68628493-68628780	K562	blood:	n/a	chr5:68628651-68628671
13	BACH1	chr5:68630708-68630887	K562	blood:	n/a	n/a
14	BACH1	chr5:68630600-68630910	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:68628514-68628851	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr5:68628431-68628863	GM12878	blood:	n/a	chr5:68628624-68628637
17	BCL3	chr5:68628522-68629005	A549	lung:	n/a	chr5:68628624-68628637
18	BCLAF1	chr5:68630554-68630902	GM12878	blood:	n/a	n/a
19	BCLAF1	chr5:68628290-68628878	GM12878	blood:	n/a	chr5:68628624-68628637 chr5:68628346-68628353
20	BHLHE40	chr5:68630683-68630877	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:68630632-68630932	K562	blood:	n/a	n/a
22	BHLHE40	chr5:68627456-68627662	K562	blood:	n/a	n/a
23	BHLHE40	chr5:68628430-68628941	GM12878	blood:	n/a	chr5:68628621-68628637
24	BHLHE40	chr5:68628395-68628834	HepG2	liver:	n/a	chr5:68628621-68628637
25	BHLHE40	chr5:68628468-68628887	K562	blood:	n/a	chr5:68628621-68628637
26	BRCA1	chr5:68628379-68628829	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr5:68630688-68630879	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr5:68628499-68628504	HepG2	liver:	n/a	n/a
29	CBX3	chr5:68630505-68630979	K562	blood:	n/a	n/a
30	CBX3	chr5:68628408-68629095	K562	blood:	n/a	n/a
31	CCNT2	chr5:68628430-68628816	K562	blood:	n/a	n/a
32	CEBPB	chr5:68642258-68642377	K562	blood:	n/a	n/a
33	CEBPB	chr5:68625877-68626222	MCF-7	breast:	n/a	n/a
34	CEBPB	chr5:68642204-68642374	A549	lung:	n/a	n/a
35	CEBPB	chr5:68630596-68630874	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr5:68642139-68642351	K562	blood:	n/a	n/a
37	CEBPB	chr5:68628425-68628875	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:68628514-68629072	GM12878	blood:	n/a	n/a
39	CEBPB	chr5:68635375-68635434	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPD	chr5:68628424-68628900	HepG2	liver:	n/a	n/a
41	CHD1	chr5:68630681-68630922	GM12878	blood:	n/a	n/a
42	CHD1	chr5:68628030-68628959	GM12878	blood:	n/a	n/a
43	CHD2	chr5:68627744-68628014	HepG2	liver:	n/a	n/a
44	CHD2	chr5:68630658-68630919	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr5:68628376-68628764	HepG2	liver:	n/a	n/a
46	CHD2	chr5:68628354-68628920	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr5:68628558-68628953	K562	blood:	n/a	n/a
48	CHD2	chr5:68630703-68630873	GM12878	blood:	n/a	n/a
49	CHD2	chr5:68628432-68628882	GM12878	blood:	n/a	n/a
50	CHD2	chr5:68630618-68630916	Hela-S3	cervix:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68626145-68626195	IMR90	lung:	fetal
2	chr5:68628618-68628668	HL-60	blood:	n/a
3	chr5:68629755-68629805	GM06990	blood:	n/a
4	chr5:68628431-68628481	NHBE	bronchial:	n/a
5	chr5:68630832-68630882	HNPCEpiC	eye:	n/a
6	chr5:68628545-68628595	K562	blood:	n/a
7	chr5:68628240-68628290	Caco-2	colon:	n/a
8	chr5:68630898-68630948	MCF10A-Er-Src	breast:	n/a
9	chr5:68628431-68628481	HNPCEpiC	eye:	n/a
10	chr5:68628738-68628788	AG04449	skin:	fetal
11	chr5:68626145-68626195	ProgFib	skin:	n/a
12	chr5:68630898-68630948	BE2_C	brain:	n/a
13	chr5:68628618-68628668	PFSK-1	brain:	n/a
14	chr5:68628545-68628595	NB4	blood:	n/a
15	chr5:68629714-68629764	HRPEpiC	eye:	n/a
16	chr5:68630898-68630948	NT2-D1	testis:	n/a
17	chr5:68626145-68626195	GM06990	blood:	n/a
18	chr5:68628431-68628481	HCF	heart:	n/a
19	chr5:68629755-68629805	AG04449	skin:	fetal
20	chr5:68629714-68629764	ProgFib	skin:	n/a
21	chr5:68630898-68630948	Hela-S3	cervix:	n/a
22	chr5:68630796-68630846	HEK293	kidney:	embryo
23	chr5:68628545-68628595	GM12878	blood:	n/a
24	chr5:68629755-68629805	HUVEC	blood vessel:	n/a
25	chr5:68628240-68628290	NB4	blood:	n/a
26	chr5:68630832-68630882	SAEC	small airway:	n/a
27	chr5:68628240-68628290	SK-N-SH_RA	brain:	n/a
28	chr5:68629755-68629805	BJ	skin:	n/a
29	chr5:68628240-68628290	A549	lung:	n/a
30	chr5:68630832-68630882	IMR90	lung:	fetal
31	chr5:68630796-68630846	BE2_C	brain:	n/a
32	chr5:68626145-68626195	GM12878	blood:	n/a
33	chr5:68628431-68628481	HEK293	kidney:	embryo
34	chr5:68628240-68628290	AG04450	lung:	fetal
35	chr5:68628618-68628668	Jurkat	blood:	n/a
36	chr5:68629755-68629805	SAEC	small airway:	n/a
37	chr5:68626145-68626195	Hela-S3	cervix:	n/a
38	chr5:68630898-68630948	HRCEpiC	kidney:	n/a
39	chr5:68628618-68628668	HPAEpiC	pulmonary alveolar:	n/a
40	chr5:68630832-68630882	AG04450	lung:	fetal
41	chr5:68628240-68628290	NHDF-neo	bronchial:	n/a
42	chr5:68628431-68628481	HRE	kidney:	n/a
43	chr5:68628240-68628290	HNPCEpiC	eye:	n/a
44	chr5:68629714-68629764	GM06990	blood:	n/a
45	chr5:68630898-68630948	Hepatocyte	liver:	n/a
46	chr5:68628738-68628788	HRPEpiC	eye:	n/a
47	chr5:68628618-68628668	HEEpiC	esophagus:	n/a
48	chr5:68628545-68628595	BE2_C	brain:	n/a
49	chr5:68628431-68628481	PANC-1	pancreas:	n/a
50	chr5:68626145-68626195	CMK	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:68625780..68629489-chr5:68629805..68632060,4	MCF-7	breast:
2	chr5:68623977..68626079-chr5:68626593..68628678,2	K562	blood:
3	chr5:68389421..68390037-chr5:68630293..68631196,2	K562	blood:
4	chr5:68633945..68635826-chr5:68665040..68666817,2	K562	blood:
5	chr5:68620531..68622041-chr5:68623429..68625161,2	MCF-7	breast:
6	chr5:68626462..68633259-chr5:68656360..68665608,14	MCF-7	breast:
7	chr5:68631692..68634148-chr5:68638657..68640415,2	K562	blood:
8	chr5:68388706..68391393-chr5:68627238..68631529,6	MCF-7	breast:
9	chr5:68627053..68629254-chr5:68650186..68651873,2	MCF-7	breast:
10	chr5:68628802..68630677-chr5:68662896..68664873,2	K562	blood:
11	chr5:68626208..68627882-chr5:68665634..68668081,2	MCF-7	breast:
12	chr5:68626762..68628383-chr5:68787111..68789288,2	MCF-7	breast:
13	chr5:68392072..68393994-chr5:68636820..68639072,2	K562	blood:
14	chr5:68606839..68610803-chr5:68625940..68628885,4	MCF-7	breast:
15	chr5:68630799..68633457-chr5:68666139..68668390,2	K562	blood:
16	chr5:68644789..68648896-chr5:68660361..68665573,5	K562	blood:
17	chr5:68628511..68630857-chr5:68714273..68716319,2	MCF-7	breast:
18	chr5:68513358..68515252-chr5:68629266..68631706,2	K562	blood:
19	chr5:68620241..68624836-chr5:68626144..68630926,8	MCF-7	breast:
20	chr5:68534808..68537076-chr5:68626446..68628069,2	MCF-7	breast:
21	chr5:68338368..68339599-chr5:68630334..68631582,4	K562	blood:
22	chr5:68625641..68627490-chr5:68628684..68631572,2	K562	blood:
23	chr5:68485299..68487066-chr5:68626120..68629033,4	MCF-7	breast:
24	chr5:68631692..68634148-chr5:68638657..68640415,2	K562	blood:
25	chr5:68649986..68652513-chr5:68664085..68665816,2	MCF-7	breast:
26	chr11:65186090..65188584-chr5:68640496..68642731,2	MCF-7	breast:
27	chr5:68651096..68653691-chr5:68653964..68655664,2	MCF-7	breast:
28	chr5:68619412..68621979-chr5:68645837..68648113,2	K562	blood:
29	chr5:68588146..68590724-chr5:68626782..68628489,2	MCF-7	breast:
30	chr5:68514182..68515689-chr5:68624413..68626099,2	MCF-7	breast:
31	chr5:68529975..68532202-chr5:68627120..68629377,3	MCF-7	breast:
32	chr5:68511595..68514121-chr5:68626401..68628217,2	MCF-7	breast:
33	chr5:68527870..68529921-chr5:68647388..68650083,2	K562	blood:
34	chr5:68642046..68643554-chr5:68664633..68666593,2	K562	blood:
35	chr5:68591369..68594137-chr5:68623717..68625664,2	MCF-7	breast:
36	chr5:68626792..68633026-chr5:68660168..68667090,13	MCF-7	breast:
37	chr5:68626738..68629576-chr5:68632937..68635065,2	MCF-7	breast:
38	chr5:68319705..68320603-chr5:68630318..68631248,3	K562	blood:
39	chr5:68637589..68639798-chr5:68660289..68662388,2	MCF-7	breast:
40	chr5:68628027..68630302-chr5:68663373..68666765,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAD17-2	chr5:68645763-68646272	NONHSAT101913

No data

Variant related genes	Relation type
CCDC125	TF binding region
CHCHD2P2	TF binding region
ENSG00000271045	TF binding region
CCDC125	CpG island
CHCHD2P2	CpG island
ENSG00000271045	CpG island
ENSG00000197822	chromatin interactions
ENSG00000134056	chromatin interactions
ENSG00000183323	chromatin interactions
ENSG00000085231	chromatin interactions
ENSG00000134058	chromatin interactions
ENSG00000152942	chromatin interactions
ENSG00000145740	chromatin interactions
ENSG00000152939	chromatin interactions
ENSG00000153044	chromatin interactions
ENSG00000215006	chromatin interactions
ENSG00000213830	chromatin interactions

Extended variants
information (count: 1007 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1007 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78628287	chr5:68624530-68624531	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs6865493	chr5:68624531-68624532	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs555086633	chr5:68624541-68624542	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573553436	chr5:68624548-68624549	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372850011	chr5:68624607-68624608	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs375274393	chr5:68624668-68624669	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs560124020	chr5:68624680-68624681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs6450033	chr5:68624744-68624745	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs190414155	chr5:68624751-68624752	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576811761	chr5:68624770-68624771	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563824746	chr5:68624777-68624778	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs62371691	chr5:68624781-68624782	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557691573	chr5:68624794-68624795	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs193012199	chr5:68624843-68624844	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372638805	chr5:68624854-68624855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185348485	chr5:68624872-68624873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374704925	chr5:68624899-68624900	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528512059	chr5:68624990-68624991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546660982	chr5:68625049-68625050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565686554	chr5:68625064-68625065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539303341	chr5:68625077-68625078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9791036	chr5:68625131-68625132	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs6866908	chr5:68625196-68625197	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs536768839	chr5:68625240-68625241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555468533	chr5:68625266-68625267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573640285	chr5:68625267-68625268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188500591	chr5:68625273-68625274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566606388	chr5:68625290-68625291	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552999632	chr5:68625293-68625294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372782487	chr5:68625300-68625301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535306741	chr5:68625326-68625327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs369594355	chr5:68625327-68625328	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs377361440	chr5:68625376-68625377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545675084	chr5:68625396-68625397	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181314426	chr5:68625400-68625401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370676840	chr5:68625444-68625445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10940218	chr5:68625460-68625461	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs377764909	chr5:68625473-68625474	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185005938	chr5:68625503-68625504	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs573339173	chr5:68625550-68625551	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs12188076	chr5:68625619-68625620	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs565226909	chr5:68625620-68625621	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533075706	chr5:68625656-68625657	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs551236289	chr5:68625709-68625710	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs569592396	chr5:68625718-68625719	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs12187268	chr5:68625786-68625787	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs548896437	chr5:68625796-68625797	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs567403446	chr5:68625850-68625851	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534373039	chr5:68625857-68625858	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs577605213	chr5:68625901-68625902	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	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
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
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	20729466	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
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68565600-68627400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr5:68576400-68627600	Weak transcription	Brain Substantia Nigra	brain
3	chr5:68576400-68627800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr5:68576600-68627800	Weak transcription	Brain Angular Gyrus	brain
5	chr5:68577400-68628200	Weak transcription	Small Intestine	intestine
6	chr5:68577600-68627400	Weak transcription	NHEK	skin
7	chr5:68577800-68626600	Weak transcription	A549	lung
8	chr5:68581600-68627600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:68581800-68626800	Weak transcription	Fetal Brain Female	brain
10	chr5:68581800-68627600	Weak transcription	Brain Anterior Caudate	brain
11	chr5:68591600-68627600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:68596000-68626800	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr5:68599600-68627800	Weak transcription	NH-A	brain
14	chr5:68601400-68627600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr5:68605600-68627400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr5:68606200-68625600	Weak transcription	Hela-S3	cervix
17	chr5:68609600-68627400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr5:68609600-68627600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:68609800-68627200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr5:68609800-68627400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr5:68609800-68627400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:68609800-68627400	Weak transcription	Esophagus	oesophagus
23	chr5:68609800-68627400	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr5:68609800-68627400	Weak transcription	GM12878-XiMat	blood
25	chr5:68609800-68627600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr5:68609800-68627600	Weak transcription	Fetal Thymus	thymus
27	chr5:68609800-68628200	Weak transcription	Right Ventricle	heart
28	chr5:68609800-68628400	Weak transcription	Lung	lung
29	chr5:68610000-68627400	Weak transcription	Dnd41	blood
30	chr5:68610400-68627600	Weak transcription	Primary B cells from peripheral blood	blood
31	chr5:68610600-68627800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr5:68611000-68628200	Weak transcription	Aorta	Aorta
33	chr5:68612400-68627400	Weak transcription	Adipose Nuclei	Adipose
34	chr5:68612800-68626600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr5:68613800-68627200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr5:68613800-68627400	Weak transcription	Primary B cells from cord blood	blood
37	chr5:68614200-68627400	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr5:68616200-68626600	Weak transcription	Colonic Mucosa	Colon
39	chr5:68616400-68627400	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr5:68616600-68628200	Weak transcription	Left Ventricle	heart
41	chr5:68616800-68627200	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr5:68617000-68627400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr5:68617000-68627600	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr5:68617400-68627400	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr5:68617600-68626400	Weak transcription	Liver	Liver
46	chr5:68618000-68627400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:68620800-68626400	Weak transcription	Stomach Mucosa	stomach
48	chr5:68621000-68628200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr5:68621400-68627600	Weak transcription	Primary T cells from cord blood	blood
50	chr5:68622000-68627400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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