Variant report

Variant	nsv933357
Chromosome Location	chr2:152526786-152591138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:339)
CpG islands
(count:367)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:152573493-152573660	K562	blood:	n/a	n/a
2	ATF1	chr2:152528794-152529106	K562	blood:	n/a	n/a
3	ATF1	chr2:152539857-152539920	K562	blood:	n/a	n/a
4	ATF1	chr2:152588093-152588268	K562	blood:	n/a	n/a
5	ATF2	chr2:152586663-152587049	GM12878	blood:	n/a	n/a
6	ATF2	chr2:152586528-152587117	GM12878	blood:	n/a	n/a
7	ATF3	chr2:152528751-152529119	K562	blood:	n/a	n/a
8	BACH1	chr2:152541263-152541270	K562	blood:	n/a	n/a
9	BACH1	chr2:152583492-152583526	K562	blood:	n/a	n/a
10	BACH1	chr2:152528510-152528513	K562	blood:	n/a	n/a
11	BATF	chr2:152526804-152527173	GM12878	blood:	n/a	n/a
12	BCL3	chr2:152526779-152527150	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:152528885-152529132	K562	blood:	n/a	n/a
14	BHLHE40	chr2:152525901-152527031	K562	blood:	n/a	n/a
15	CBX3	chr2:152561175-152561591	K562	blood:	n/a	n/a
16	CCNT2	chr2:152580463-152580593	K562	blood:	n/a	n/a
17	CCNT2	chr2:152589494-152589546	K562	blood:	n/a	n/a
18	CCNT2	chr2:152539414-152539447	K562	blood:	n/a	n/a
19	CEBPB	chr2:152542623-152542711	K562	blood:	n/a	n/a
20	CEBPB	chr2:152530184-152530368	K562	blood:	n/a	n/a
21	CEBPB	chr2:152548272-152548506	HepG2	liver:	n/a	chr2:152548401-152548412
22	CEBPB	chr2:152545276-152545484	K562	blood:	n/a	n/a
23	CEBPB	chr2:152528780-152529061	K562	blood:	n/a	chr2:152528948-152528959
24	CEBPB	chr2:152530176-152530383	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:152545302-152545496	K562	blood:	n/a	n/a
26	CEBPB	chr2:152527963-152528234	K562	blood:	n/a	n/a
27	CEBPB	chr2:152567587-152567854	HepG2	liver:	n/a	chr2:152567750-152567761
28	CEBPB	chr2:152528238-152528482	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr2:152554792-152554870	HepG2	liver:	n/a	chr2:152554826-152554837
30	CEBPB	chr2:152582808-152583106	HepG2	liver:	n/a	chr2:152582897-152582909 chr2:152582943-152582954
31	CEBPB	chr2:152561428-152561437	K562	blood:	n/a	n/a
32	CEBPB	chr2:152548336-152548467	K562	blood:	n/a	chr2:152548401-152548412
33	CEBPB	chr2:152528678-152529079	K562	blood:	n/a	chr2:152528948-152528959
34	CEBPB	chr2:152586497-152586789	K562	blood:	n/a	chr2:152586627-152586638
35	CEBPB	chr2:152528694-152529104	Hela-S3	cervix:	n/a	chr2:152528948-152528959
36	CEBPB	chr2:152566243-152566454	A549	lung:	n/a	n/a
37	CEBPB	chr2:152528779-152529083	A549	lung:	n/a	chr2:152528948-152528959
38	CEBPB	chr2:152574662-152574741	HepG2	liver:	n/a	chr2:152574728-152574739 chr2:152574728-152574739
39	CEBPB	chr2:152582870-152583115	K562	blood:	n/a	chr2:152582897-152582909 chr2:152582943-152582954
40	CEBPB	chr2:152566182-152566512	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:152586545-152586750	HepG2	liver:	n/a	chr2:152586627-152586638
42	CEBPB	chr2:152566370-152566371	K562	blood:	n/a	n/a
43	CEBPB	chr2:152528124-152528305	A549	lung:	n/a	n/a
44	CEBPB	chr2:152528742-152529089	K562	blood:	n/a	chr2:152528948-152528959
45	CEBPB	chr2:152528753-152529125	HepG2	liver:	n/a	chr2:152528948-152528959
46	CEBPB	chr2:152545203-152545539	K562	blood:	n/a	n/a
47	CEBPB	chr2:152528824-152529025	H1-hESC	embryonic stem cell:	n/a	chr2:152528948-152528959
48	CREB1	chr2:152586591-152587141	GM12878	blood:	n/a	n/a
49	CREB1	chr2:152586596-152587132	GM12878	blood:	n/a	n/a
50	CTCF	chr2:152585720-152585870	HCT-116	colon:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:152564724-152564774	HRE	kidney:	n/a
2	chr2:152564724-152564774	HRE	kidney:	n/a
3	chr2:152564480-152564530	IMR90	lung:	fetal
4	chr2:152527013-152527063	HNPCEpiC	eye:	n/a
5	chr2:152590396-152590446	SK-N-MC	brain:	n/a
6	chr2:152527013-152527063	HepG2	liver:	n/a
7	chr2:152585111-152585161	HEEpiC	esophagus:	n/a
8	chr2:152590736-152590786	HCM	heart:	n/a
9	chr2:152590396-152590446	Hela-S3	cervix:	n/a
10	chr2:152590736-152590786	MCF10A-Er-Src	breast:	n/a
11	chr2:152564480-152564530	SKMC	muscle:	n/a
12	chr2:152564480-152564530	A549	lung:	n/a
13	chr2:152564480-152564530	HCM	heart:	n/a
14	chr2:152590396-152590446	HUVEC	blood vessel:	n/a
15	chr2:152564480-152564530	HIPEpiC	eye:	n/a
16	chr2:152564480-152564530	SAEC	small airway:	n/a
17	chr2:152564480-152564530	HRPEpiC	eye:	n/a
18	chr2:152527013-152527063	SK-N-SH_RA	brain:	n/a
19	chr2:152564724-152564774	AG09319	gingival:	n/a
20	chr2:152564724-152564774	HRCEpiC	kidney:	n/a
21	chr2:152564480-152564530	GM19239	blood:	n/a
22	chr2:152527013-152527063	H1-hESC	embryonic stem cell:	embryo
23	chr2:152590396-152590446	HepG2	liver:	n/a
24	chr2:152590736-152590786	RPTEC	kidney:	n/a
25	chr2:152590736-152590786	SK-N-MC	brain:	n/a
26	chr2:152564724-152564774	T-47D	breast:	n/a
27	chr2:152527013-152527063	AG04449	skin:	fetal
28	chr2:152564480-152564530	AG04449	skin:	fetal
29	chr2:152585111-152585161	SKMC	muscle:	n/a
30	chr2:152564480-152564530	HCPEpiC	choroid plexus:	n/a
31	chr2:152527013-152527063	HPAEpiC	pulmonary alveolar:	n/a
32	chr2:152590396-152590446	PFSK-1	brain:	n/a
33	chr2:152585111-152585161	Caco-2	colon:	n/a
34	chr2:152590396-152590446	GM12878	blood:	n/a
35	chr2:152590396-152590446	GM12891	blood:	n/a
36	chr2:152590396-152590446	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:152564480-152564530	ECC-1	luminal epithelium:	n/a
38	chr2:152585111-152585161	AG09309	skin:	n/a
39	chr2:152527013-152527063	ECC-1	luminal epithelium:	n/a
40	chr2:152527013-152527063	GM12878	blood:	n/a
41	chr2:152527013-152527063	NT2-D1	testis:	n/a
42	chr2:152585111-152585161	HMEC	breast:	n/a
43	chr2:152527013-152527063	A549	lung:	n/a
44	chr2:152564724-152564774	MCF10A-Er-Src	breast:	n/a
45	chr2:152527013-152527063	NH-A	brain:	n/a
46	chr2:152585111-152585161	HRPEpiC	eye:	n/a
47	chr2:152527013-152527063	SK-N-MC	brain:	n/a
48	chr2:152585111-152585161	SK-N-SH_RA	brain:	n/a
49	chr2:152564724-152564774	Hela-S3	cervix:	n/a
50	chr2:152585111-152585161	SK-N-MC	brain:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:152531745..152533702-chr2:152613377..152614925,2	K562	blood:
2	chr2:152575377..152577212-chr2:152579516..152582033,2	MCF-7	breast:
3	chr2:152585426..152588067-chr2:152592929..152595399,2	K562	blood:
4	chr2:152530052..152532883-chr2:152536746..152539228,2	K562	blood:
5	chr2:152575377..152577212-chr2:152579516..152582033,2	MCF-7	breast:
6	chr2:152569897..152572373-chr2:152573121..152575260,2	K562	blood:
7	chr2:152539206..152543340-chr2:152544613..152549104,5	K562	blood:
8	chr2:152582502..152584750-chr2:152594668..152596852,2	MCF-7	breast:
9	chr2:152567546..152569440-chr2:152615206..152617035,2	K562	blood:
10	chr2:152547462..152550339-chr2:152552453..152555229,3	K562	blood:
11	chr2:152579209..152581480-chr2:152582486..152584522,2	K562	blood:
12	chr2:152559984..152561620-chr2:152568227..152570991,2	K562	blood:
13	chr2:152547960..152548861-chr2:152860870..152861751,2	MCF-7	breast:
14	chr2:152548118..152550339-chr2:152551774..152553953,2	K562	blood:
15	chr2:152567412..152569218-chr2:152573208..152575308,2	K562	blood:
16	chr2:152534290..152537088-chr2:152539247..152541650,3	K562	blood:
17	chr2:152534290..152537088-chr2:152539247..152541650,3	K562	blood:
18	chr2:152146753..152148649-chr2:152552733..152554484,2	MCF-7	breast:
19	chr2:152579209..152581480-chr2:152582486..152584522,2	K562	blood:
20	chr2:152567043..152569651-chr2:152580099..152581679,2	K562	blood:
21	chr2:152540559..152543086-chr2:152704244..152707063,2	K562	blood:
22	chr2:152504847..152507731-chr2:152567998..152569679,2	K562	blood:
23	chr2:152567043..152568747-chr2:152580099..152582937,2	K562	blood:
24	chr2:152530052..152532883-chr2:152536746..152539228,2	K562	blood:
25	chr2:152559984..152561620-chr2:152568227..152570991,2	K562	blood:
26	chr2:152526558..152529382-chr2:152543340..152545416,2	K562	blood:
27	chr2:152524660..152526249-chr2:152545100..152547655,2	K562	blood:
28	chr2:152542053..152544842-chr2:152548104..152550538,2	MCF-7	breast:
29	chr2:152567412..152569836-chr2:152573596..152575308,2	K562	blood:
30	chr2:152563836..152565601-chr2:152630541..152632941,2	K562	blood:
31	chr2:152567412..152569218-chr2:152573208..152575308,2	K562	blood:
32	chr2:152579209..152581619-chr2:152582308..152583986,2	K562	blood:
33	chr2:152542053..152544842-chr2:152548104..152550538,2	MCF-7	breast:
34	chr2:152524436..152526394-chr2:152528690..152531514,2	K562	blood:
35	chr2:152585502..152587063-chr2:152681615..152683144,2	K562	blood:
36	chr2:152520871..152523235-chr2:152540284..152542903,2	K562	blood:
37	chr2:152525703..152527793-chr2:152563733..152565410,2	K562	blood:
38	chr2:152569897..152572373-chr2:152573121..152575260,2	K562	blood:
39	chr2:152538686..152541160-chr2:152542416..152544904,3	K562	blood:
40	chr2:152567412..152569836-chr2:152573596..152575308,2	K562	blood:
41	chr2:152539206..152543340-chr2:152544613..152549104,5	K562	blood:
42	chr2:152524436..152527296-chr2:152527815..152531514,4	K562	blood:
43	chr2:152579209..152581619-chr2:152582308..152583986,2	K562	blood:
44	chr2:152567043..152569651-chr2:152580099..152581679,2	K562	blood:
45	chr2:152538686..152541160-chr2:152542416..152544904,3	K562	blood:
46	chr2:152561165..152563453-chr2:152587104..152589381,2	K562	blood:
47	chr2:152551667..152554419-chr2:152559897..152564145,4	K562	blood:
48	chr2:152547877..152548735-chr2:152644313..152645176,2	MCF-7	breast:
49	chr2:152552543..152554419-chr2:152559897..152564145,3	K562	blood:
50	chr2:152567043..152568747-chr2:152580099..152582937,2	K562	blood:

No data

Variant related genes	Relation type
NEB	TF binding region
NEB	CpG island
ENSG00000183091	chromatin interactions
ENSG00000162980	chromatin interactions

Extended variants
information (count: 2341 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:2341 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535864508	chr2:152526795-152526796	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148054269	chr2:152526856-152526857	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192599031	chr2:152526859-152526860	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78415336	chr2:152526873-152526874	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs78128680	chr2:152526881-152526882	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs184895840	chr2:152526928-152526929	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149933044	chr2:152526940-152526941	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs59941666	chr2:152526977-152526978	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs188208355	chr2:152526998-152526999	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112960449	chr2:152527005-152527006	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539298730	chr2:152527034-152527035	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576220399	chr2:152527050-152527051	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs80264058	chr2:152527114-152527115	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561297238	chr2:152527215-152527216	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77829631	chr2:152527274-152527275	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141807057	chr2:152527291-152527292	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540766586	chr2:152527354-152527355	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563821589	chr2:152527362-152527363	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533601461	chr2:152527375-152527376	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550078964	chr2:152527384-152527385	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570337448	chr2:152527412-152527413	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184716855	chr2:152527473-152527474	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370854178	chr2:152527480-152527481	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374044989	chr2:152527505-152527506	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs199793754	chr2:152527507-152527508	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112517981	chr2:152527536-152527537	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7426114	chr2:152527572-152527573	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs554984749	chr2:152527574-152527575	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs74482326	chr2:152527577-152527578	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368215104	chr2:152527579-152527580	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201545521	chr2:152527580-152527581	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374440932	chr2:152527606-152527607	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34577613	chr2:152527608-152527609	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs140558263	chr2:152527612-152527613	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371545317	chr2:152527618-152527619	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34800215	chr2:152527636-152527637	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368136951	chr2:152527645-152527646	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371542110	chr2:152527668-152527669	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs267598924	chr2:152527692-152527693	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200002537	chr2:152527701-152527702	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576286059	chr2:152527702-152527703	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541803470	chr2:152527706-152527707	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111241479	chr2:152527738-152527739	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35318345	chr2:152527748-152527749	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571741519	chr2:152527784-152527785	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558430454	chr2:152527808-152527809	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142728108	chr2:152527839-152527840	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563860284	chr2:152527930-152527931	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532854253	chr2:152528011-152528012	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs77567545	chr2:152528025-152528026	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	19156171	CNVD
Acute myeloid leukemia	18000384	CNVD
Autism	20808228	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152504400-152531600	Weak transcription	Primary B cells from cord blood	blood
2	chr2:152505200-152543600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:152511200-152531200	Strong transcription	Fetal Muscle Trunk	muscle
4	chr2:152511400-152531400	Strong transcription	Fetal Muscle Leg	muscle
5	chr2:152514600-152542800	Strong transcription	HSMMtube	muscle
6	chr2:152515400-152529000	Weak transcription	Aorta	Aorta
7	chr2:152520400-152528600	Weak transcription	Brain Anterior Caudate	brain
8	chr2:152521600-152537800	Weak transcription	Psoas Muscle	Psoas
9	chr2:152522600-152527400	Weak transcription	Spleen	Spleen
10	chr2:152525400-152527200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:152525400-152527400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr2:152525400-152530000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
13	chr2:152525600-152527200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr2:152525600-152527800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr2:152525600-152533000	Genic enhancers	Skeletal Muscle Female	skeletal muscle
16	chr2:152525800-152527200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:152525800-152527600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:152526000-152526800	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr2:152526000-152526800	Enhancers	NH-A	brain
20	chr2:152526000-152527000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:152526000-152527000	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr2:152526000-152527800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr2:152526000-152527800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr2:152526000-152527800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:152526200-152527400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr2:152526200-152527800	Enhancers	Fetal Heart	heart
27	chr2:152526200-152527800	Enhancers	Fetal Intestine Small	intestine
28	chr2:152526400-152527400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr2:152526400-152527400	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr2:152526400-152527400	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr2:152526400-152528000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:152526600-152527600	Enhancers	K562	blood
33	chr2:152527000-152527800	Enhancers	Right Atrium	heart
34	chr2:152527200-152536400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr2:152527400-152527600	Enhancers	Primary T cells fromperipheralblood	blood
36	chr2:152527400-152527600	Enhancers	Fetal Intestine Large	intestine
37	chr2:152527400-152527600	Enhancers	Spleen	Spleen
38	chr2:152527400-152529400	Enhancers	Fetal Lung	lung
39	chr2:152527400-152532800	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr2:152527600-152528600	Weak transcription	K562	blood
41	chr2:152527600-152529000	Weak transcription	Fetal Intestine Large	intestine
42	chr2:152527800-152532800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:152528600-152529000	Enhancers	Brain Anterior Caudate	brain
44	chr2:152528600-152529200	Enhancers	K562	blood
45	chr2:152529000-152529200	ZNF genes & repeats	Aorta	Aorta
46	chr2:152529000-152530000	Enhancers	Fetal Intestine Large	intestine
47	chr2:152529200-152550000	Weak transcription	Aorta	Aorta
48	chr2:152529600-152529800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr2:152530000-152531000	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr2:152531000-152531600	Genic enhancers	Skeletal Muscle Male	skeletal muscle

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