Variant report

Variant	nsv968922
Chromosome Location	chr5:68628679-68631659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:810)
CpG islands
(count:366)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:810 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:68627607-68628919	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:68630649-68630758	K562	blood:	n/a	n/a
3	ARID3A	chr5:68630670-68630907	HepG2	liver:	n/a	n/a
4	ATF2	chr5:68628381-68628936	GM12878	blood:	n/a	n/a
5	ATF3	chr5:68628324-68628912	HepG2	liver:	n/a	chr5:68628651-68628671
6	ATF3	chr5:68628381-68628875	GM12878	blood:	n/a	chr5:68628651-68628671
7	ATF3	chr5:68628493-68628780	K562	blood:	n/a	chr5:68628651-68628671
8	ATF3	chr5:68628467-68628717	GM12878	blood:	n/a	chr5:68628651-68628671
9	ATF3	chr5:68628432-68628788	HepG2	liver:	n/a	chr5:68628651-68628671
10	ATF3	chr5:68628323-68628880	A549	lung:	n/a	chr5:68628651-68628671
11	ATF3	chr5:68628438-68628795	K562	blood:	n/a	chr5:68628651-68628671
12	ATF3	chr5:68628515-68628798	H1-hESC	embryonic stem cell:	n/a	chr5:68628651-68628671
13	BACH1	chr5:68628514-68628851	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:68630600-68630910	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr5:68630708-68630887	K562	blood:	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	chr5:68628395-68628834	HepG2	liver:	n/a	chr5:68628621-68628637
21	BHLHE40	chr5:68628430-68628941	GM12878	blood:	n/a	chr5:68628621-68628637
22	BHLHE40	chr5:68630683-68630877	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:68630632-68630932	K562	blood:	n/a	n/a
24	BHLHE40	chr5:68628468-68628887	K562	blood:	n/a	chr5:68628621-68628637
25	BRCA1	chr5:68628379-68628829	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:68630688-68630879	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:68630505-68630979	K562	blood:	n/a	n/a
28	CBX3	chr5:68628408-68629095	K562	blood:	n/a	n/a
29	CCNT2	chr5:68628430-68628816	K562	blood:	n/a	n/a
30	CEBPB	chr5:68628425-68628875	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:68630596-68630874	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr5:68628514-68629072	GM12878	blood:	n/a	n/a
33	CEBPD	chr5:68628424-68628900	HepG2	liver:	n/a	n/a
34	CHD1	chr5:68628030-68628959	GM12878	blood:	n/a	n/a
35	CHD1	chr5:68630681-68630922	GM12878	blood:	n/a	n/a
36	CHD2	chr5:68628376-68628764	HepG2	liver:	n/a	n/a
37	CHD2	chr5:68628558-68628953	K562	blood:	n/a	n/a
38	CHD2	chr5:68630658-68630919	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr5:68630703-68630873	GM12878	blood:	n/a	n/a
40	CHD2	chr5:68630618-68630916	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr5:68628432-68628882	GM12878	blood:	n/a	n/a
42	CHD2	chr5:68628354-68628920	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr5:68630566-68631014	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr5:68630565-68630948	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr5:68628320-68628926	A549	lung:	n/a	n/a
46	CTCF	chr5:68630700-68630850	GM12872	blood:	n/a	chr5:68630764-68630782 chr5:68630773-68630786
47	CTCF	chr5:68630680-68630830	HL-60	blood:	n/a	chr5:68630764-68630782 chr5:68630773-68630786
48	CTCF	chr5:68630643-68630930	MCF-7	breast:	n/a	chr5:68630764-68630782 chr5:68630773-68630786
49	CTCF	chr5:68630640-68630790	HVMF	connective:	n/a	chr5:68630764-68630782 chr5:68630773-68630786
50	CTCF	chr5:68630667-68630891	LNCaP	prostate:	n/a	chr5:68630764-68630782 chr5:68630773-68630786

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68628738-68628788	AoSMC	blood vessel:	n/a
2	chr5:68628738-68628788	HCT-116	colon:	n/a
3	chr5:68630796-68630846	MCF10A-Er-Src	breast:	n/a
4	chr5:68630832-68630882	LNCaP	prostate:	n/a
5	chr5:68630832-68630882	Hela-S3	cervix:	n/a
6	chr5:68630796-68630846	HepG2	liver:	n/a
7	chr5:68630832-68630882	PANC-1	pancreas:	n/a
8	chr5:68630898-68630948	Hela-S3	cervix:	n/a
9	chr5:68628738-68628788	HL-60	blood:	n/a
10	chr5:68628738-68628788	RPTEC	kidney:	n/a
11	chr5:68630898-68630948	GM12892	blood:	n/a
12	chr5:68630832-68630882	RPTEC	kidney:	n/a
13	chr5:68630832-68630882	NT2-D1	testis:	n/a
14	chr5:68629714-68629764	CMK	blood:	n/a
15	chr5:68630832-68630882	U87	brain:	n/a
16	chr5:68629755-68629805	U87	brain:	n/a
17	chr5:68630832-68630882	SK-N-SH_RA	brain:	n/a
18	chr5:68629755-68629805	PANC-1	pancreas:	n/a
19	chr5:68629755-68629805	AG09319	gingival:	n/a
20	chr5:68630898-68630948	AoSMC	blood vessel:	n/a
21	chr5:68630898-68630948	HCPEpiC	choroid plexus:	n/a
22	chr5:68629714-68629764	NT2-D1	testis:	n/a
23	chr5:68628738-68628788	GM19239	blood:	n/a
24	chr5:68628738-68628788	AG04449	skin:	fetal
25	chr5:68630898-68630948	PrEC	prostate:	n/a
26	chr5:68628738-68628788	SK-N-SH_RA	brain:	n/a
27	chr5:68629755-68629805	Hepatocyte	liver:	n/a
28	chr5:68629714-68629764	HRE	kidney:	n/a
29	chr5:68630898-68630948	Hepatocyte	liver:	n/a
30	chr5:68629714-68629764	K562	blood:	n/a
31	chr5:68628738-68628788	LNCaP	prostate:	n/a
32	chr5:68630796-68630846	U87	brain:	n/a
33	chr5:68629755-68629805	HPAEpiC	pulmonary alveolar:	n/a
34	chr5:68629714-68629764	BE2_C	brain:	n/a
35	chr5:68630832-68630882	HEEpiC	esophagus:	n/a
36	chr5:68629755-68629805	LNCaP	prostate:	n/a
37	chr5:68630898-68630948	HAEpiC	amniotic membrane:	n/a
38	chr5:68630832-68630882	HRCEpiC	kidney:	n/a
39	chr5:68629755-68629805	NHDF-neo	bronchial:	n/a
40	chr5:68629755-68629805	HRPEpiC	eye:	n/a
41	chr5:68630898-68630948	PFSK-1	brain:	n/a
42	chr5:68628738-68628788	HAEpiC	amniotic membrane:	n/a
43	chr5:68629714-68629764	AoSMC	blood vessel:	n/a
44	chr5:68630796-68630846	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:68629755-68629805	IMR90	lung:	fetal
46	chr5:68630832-68630882	K562	blood:	n/a
47	chr5:68630796-68630846	Hela-S3	cervix:	n/a
48	chr5:68629714-68629764	HL-60	blood:	n/a
49	chr5:68628738-68628788	HIPEpiC	eye:	n/a
50	chr5:68629714-68629764	Jurkat	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:68513358..68515252-chr5:68629266..68631706,2	K562	blood:
2	chr5:68606839..68610803-chr5:68625940..68628885,4	MCF-7	breast:
3	chr5:68319705..68320603-chr5:68630318..68631248,3	K562	blood:
4	chr5:68628027..68630302-chr5:68663373..68666765,3	K562	blood:
5	chr5:68338368..68339599-chr5:68630334..68631582,4	K562	blood:
6	chr5:68626462..68633259-chr5:68656360..68665608,14	MCF-7	breast:
7	chr5:68628802..68630677-chr5:68662896..68664873,2	K562	blood:
8	chr5:68630799..68633457-chr5:68666139..68668390,2	K562	blood:
9	chr5:68388706..68391393-chr5:68627238..68631529,6	MCF-7	breast:
10	chr5:68626792..68633026-chr5:68660168..68667090,13	MCF-7	breast:
11	chr5:68529975..68532202-chr5:68627120..68629377,3	MCF-7	breast:
12	chr5:68485299..68487066-chr5:68626120..68629033,4	MCF-7	breast:
13	chr5:68389421..68390037-chr5:68630293..68631196,2	K562	blood:
14	chr5:68628511..68630857-chr5:68714273..68716319,2	MCF-7	breast:
15	chr5:68625780..68629489-chr5:68629805..68632060,4	MCF-7	breast:

No data

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

Extended variants
information (count: 95 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570674782	chr5:68628736-68628737	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs577230623	chr5:68628752-68628753	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs556407466	chr5:68628755-68628756	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs375120916	chr5:68628759-68628760	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs118178117	chr5:68628785-68628786	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs149469151	chr5:68628819-68628820	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs554133274	chr5:68628828-68628829	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs144130068	chr5:68628914-68628915	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs2083643	chr5:68628929-68628930	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs377635648	chr5:68628958-68628959	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs565099480	chr5:68629004-68629005	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs192543839	chr5:68629009-68629010	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs544380445	chr5:68629019-68629020	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs142791464	chr5:68629051-68629052	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs4473723	chr5:68629119-68629120	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs547881988	chr5:68629194-68629195	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs573392590	chr5:68629197-68629198	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs559680862	chr5:68629214-68629215	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs527991846	chr5:68629261-68629262	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs552423188	chr5:68629269-68629270	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs541761196	chr5:68629281-68629282	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs560146780	chr5:68629311-68629312	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs182577670	chr5:68629329-68629330	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs202060936	chr5:68629332-68629333	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs140775064	chr5:68629348-68629349	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs535896187	chr5:68629357-68629358	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs554217528	chr5:68629383-68629384	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs570543545	chr5:68629522-68629523	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs551927172	chr5:68629523-68629524	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs193139664	chr5:68629549-68629550	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs531469890	chr5:68629560-68629561	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs185228913	chr5:68629569-68629570	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs560054710	chr5:68629575-68629576	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs558927659	chr5:68629584-68629585	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs531260684	chr5:68629605-68629606	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs577201351	chr5:68629610-68629611	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs549883753	chr5:68629660-68629661	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs544128131	chr5:68629701-68629702	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs111568338	chr5:68629715-68629716	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs562659346	chr5:68629719-68629720	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs113005034	chr5:68629722-68629723	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs574459610	chr5:68629740-68629741	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs61730508	chr5:68629748-68629749	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs559737410	chr5:68629749-68629750	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs189054554	chr5:68629786-68629787	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs192196987	chr5:68629862-68629863	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs535435973	chr5:68629868-68629869	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs551737474	chr5:68630009-68630010	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs369868095	chr5:68630023-68630024	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs564481141	chr5:68630029-68630030	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	7 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:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68627000-68628800	Active TSS	Duodenum Mucosa	Duodenum
2	chr5:68627200-68628800	Active TSS	Colonic Mucosa	Colon
3	chr5:68627200-68629200	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr5:68627400-68628800	Active TSS	Fetal Intestine Small	intestine
5	chr5:68627400-68628800	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr5:68627400-68628800	Active TSS	Fetal Stomach	stomach
7	chr5:68627400-68628800	Flanking Active TSS	HMEC	breast
8	chr5:68627400-68629000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr5:68627400-68629000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
10	chr5:68627400-68629000	Flanking Active TSS	Adipose Nuclei	Adipose
11	chr5:68627400-68629000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr5:68627400-68629000	Flanking Active TSS	NHEK	skin
13	chr5:68627400-68629200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:68627600-68628800	Active TSS	Fetal Intestine Large	intestine
15	chr5:68627600-68628800	Active TSS	Stomach Mucosa	stomach
16	chr5:68627600-68629000	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr5:68627600-68629000	Active TSS	Fetal Kidney	kidney
18	chr5:68627600-68629000	Active TSS	Thymus	Thymus
19	chr5:68627600-68629200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:68627800-68628800	Active TSS	Liver	Liver
21	chr5:68627800-68628800	Active TSS	Fetal Brain Male	brain
22	chr5:68627800-68628800	Active TSS	Pancreas	Pancrea
23	chr5:68627800-68628800	Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr5:68627800-68628800	Active TSS	NHDF-Ad	bronchial
25	chr5:68627800-68628800	Active TSS	NHLF	lung
26	chr5:68627800-68628800	Active TSS	Osteobl	bone
27	chr5:68627800-68629000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
28	chr5:68627800-68629000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr5:68627800-68629000	Active TSS	Brain Hippocampus Middle	brain
30	chr5:68627800-68629000	Active TSS	Fetal Lung	lung
31	chr5:68627800-68629200	Active TSS	Rectal Mucosa Donor 31	rectum
32	chr5:68627800-68629200	Active TSS	Stomach Smooth Muscle	stomach
33	chr5:68628000-68628800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
34	chr5:68628000-68628800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
35	chr5:68628000-68628800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
36	chr5:68628000-68628800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:68628000-68628800	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr5:68628000-68628800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr5:68628000-68628800	Active TSS	Fetal Muscle Leg	muscle
40	chr5:68628000-68628800	Active TSS	K562	blood
41	chr5:68628000-68629000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr5:68628000-68629000	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr5:68628000-68629000	Active TSS	Psoas Muscle	Psoas
44	chr5:68628000-68629000	Flanking Active TSS	HUVEC	blood vessel
45	chr5:68628000-68629000	Flanking Active TSS	NH-A	brain
46	chr5:68628000-68629200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr5:68628000-68629200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr5:68628000-68629400	Active TSS	A549	lung
49	chr5:68628200-68628800	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr5:68628200-68628800	Active TSS	Cortex derived primary cultured neurospheres	brain

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