Variant report

Variant	nsv918222
Chromosome Location	chr16:34739999-35076660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1031)
CpG islands
(count:2508)
Chromatin interactive
region (count:9)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1031 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
2	ATF1	chr16:34787094-34787358	K562	blood:	n/a	n/a
3	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
4	ATF2	chr16:34833744-34834198	GM12878	blood:	n/a	n/a
5	BATF	chr16:34795349-34795509	GM12878	blood:	n/a	chr16:34795453-34795464
6	BATF	chr16:34795249-34795638	GM12878	blood:	n/a	chr16:34795453-34795464
7	BATF	chr16:34796038-34796270	GM12878	blood:	n/a	chr16:34796152-34796163
8	BATF	chr16:34792970-34793204	GM12878	blood:	n/a	chr16:34793057-34793068 chr16:34793089-34793100
9	BATF	chr16:34796836-34797144	GM12878	blood:	n/a	chr16:34797014-34797025
10	BATF	chr16:34854854-34855022	GM12878	blood:	n/a	n/a
11	BATF	chr16:34894940-34895190	GM12878	blood:	n/a	chr16:34895069-34895080
12	BATF	chr16:34894892-34895125	GM12878	blood:	n/a	chr16:34895069-34895080
13	BCL11A	chr16:34833758-34834113	GM12878	blood:	n/a	n/a
14	BCL3	chr16:34833700-34834141	GM12878	blood:	n/a	n/a
15	BCL3	chr16:34894998-34895220	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:34833735-34834061	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34795575-34795581	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
19	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
20	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
21	BHLHE40	chr16:34796951-34797111	GM12878	blood:	n/a	n/a
22	BHLHE40	chr16:34836978-34836992	GM12878	blood:	n/a	n/a
23	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
24	CBX3	chr16:34825393-34825600	K562	blood:	n/a	n/a
25	CBX3	chr16:34849319-34849535	K562	blood:	n/a	n/a
26	CEBPB	chr16:34759185-34759725	HepG2	liver:	n/a	chr16:34759593-34759604 chr16:34759630-34759641 chr16:34759565-34759576
27	CEBPB	chr16:34799963-34800294	A549	lung:	n/a	chr16:34800131-34800142
28	CEBPB	chr16:34803835-34804176	A549	lung:	n/a	n/a
29	CEBPB	chr16:34793731-34794093	HepG2	liver:	n/a	chr16:34793909-34793920
30	CEBPB	chr16:34768026-34768406	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr16:34768107-34768405	K562	blood:	n/a	n/a
32	CEBPB	chr16:35047511-35047736	HepG2	liver:	n/a	chr16:35047601-35047612
33	CEBPB	chr16:34973700-34973888	HepG2	liver:	n/a	chr16:34973763-34973774
34	CEBPB	chr16:35044569-35044729	K562	blood:	n/a	n/a
35	CEBPB	chr16:34806329-34806484	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:34767984-34768445	A549	lung:	n/a	n/a
37	CEBPB	chr16:34801325-34801709	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:34805162-34805662	HepG2	liver:	n/a	n/a
39	CEBPB	chr16:34944785-34945077	IMR90	lung:	n/a	chr16:34944902-34944913
40	CEBPB	chr16:35044630-35044830	HepG2	liver:	n/a	chr16:35044752-35044763
41	CEBPB	chr16:34802242-34802862	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:34795854-34796102	IMR90	lung:	n/a	n/a
43	CEBPB	chr16:34797538-34797659	A549	lung:	n/a	n/a
44	CEBPB	chr16:34798691-34799607	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:35047591-35047687	A549	lung:	n/a	chr16:35047601-35047612
46	CEBPB	chr16:34805074-34805626	A549	lung:	n/a	n/a
47	CEBPB	chr16:34795741-34796123	A549	lung:	n/a	n/a
48	CEBPB	chr16:34944778-34945011	HepG2	liver:	n/a	chr16:34944902-34944913
49	CEBPB	chr16:34790370-34790445	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:34759219-34759383	MCF-7	breast:	n/a	n/a

(count:2508 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34983384-34983434	HEEpiC	esophagus:	n/a
2	chr16:34806416-34806466	Jurkat	blood:	n/a
3	chr16:34809677-34809727	ProgFib	skin:	n/a
4	chr16:34777881-34777931	HPAEpiC	pulmonary alveolar:	n/a
5	chr16:34807860-34807910	HRPEpiC	eye:	n/a
6	chr16:34812259-34812309	HPAEpiC	pulmonary alveolar:	n/a
7	chr16:34984121-34984171	HCPEpiC	choroid plexus:	n/a
8	chr16:34983384-34983434	HEEpiC	esophagus:	n/a
9	chr16:34806416-34806466	Jurkat	blood:	n/a
10	chr16:34809677-34809727	ProgFib	skin:	n/a
11	chr16:34777881-34777931	HPAEpiC	pulmonary alveolar:	n/a
12	chr16:34807860-34807910	HRPEpiC	eye:	n/a
13	chr16:34812259-34812309	HPAEpiC	pulmonary alveolar:	n/a
14	chr16:34984121-34984171	HCPEpiC	choroid plexus:	n/a
15	chr16:34808939-34808989	T-47D	breast:	n/a
16	chr16:34741966-34742016	T-47D	breast:	n/a
17	chr16:34740585-34740635	ECC-1	luminal epithelium:	n/a
18	chr16:34760531-34760581	PrEC	prostate:	n/a
19	chr16:34740585-34740635	PANC-1	pancreas:	n/a
20	chr16:34740934-34740984	GM12892	blood:	n/a
21	chr16:34740934-34740984	NT2-D1	testis:	n/a
22	chr16:34984121-34984171	ovcar-3	ovarian:	n/a
23	chr16:34741966-34742016	MCF-7	breast:	n/a
24	chr16:34806416-34806466	NB4	blood:	n/a
25	chr16:35030232-35030282	Jurkat	blood:	n/a
26	chr16:34848776-34848826	NHBE	bronchial:	n/a
27	chr16:34777881-34777931	Jurkat	blood:	n/a
28	chr16:34740520-34740570	HCT-116	colon:	n/a
29	chr16:34741251-34741301	AoSMC	blood vessel:	n/a
30	chr16:34808939-34808989	BJ	skin:	n/a
31	chr16:34979575-34979625	GM19239	blood:	n/a
32	chr16:34786998-34787048	Jurkat	blood:	n/a
33	chr16:34760531-34760581	HCM	heart:	n/a
34	chr16:34740520-34740570	Hela-S3	cervix:	n/a
35	chr16:34787597-34787647	PFSK-1	brain:	n/a
36	chr16:34741493-34741543	NHBE	bronchial:	n/a
37	chr16:35037569-35037619	GM12891	blood:	n/a
38	chr16:34807860-34807910	SK-N-MC	brain:	n/a
39	chr16:34979575-34979625	SK-N-SH	brain:	n/a
40	chr16:35029890-35029940	Hela-S3	cervix:	n/a
41	chr16:34979575-34979625	SAEC	small airway:	n/a
42	chr16:35026985-35027035	GM12891	blood:	n/a
43	chr16:34741966-34742016	AG04450	lung:	fetal
44	chr16:34809677-34809727	GM06990	blood:	n/a
45	chr16:34809256-34809306	NH-A	brain:	n/a
46	chr16:35029890-35029940	NB4	blood:	n/a
47	chr16:34809256-34809306	Hepatocyte	liver:	n/a
48	chr16:34807860-34807910	NHDF-neo	bronchial:	n/a
49	chr16:34740520-34740570	MCF10A-Er-Src	breast:	n/a
50	chr16:34777881-34777931	HUVEC	blood vessel:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:34815853..34816462-chr16:34876054..34876591,2	MCF-7	breast:
2	chr16:34815137..34816427-chr16:34875759..34876664,4	MCF-7	breast:
3	chr16:34799028..34799683-chr16:34875753..34876623,3	MCF-7	breast:
4	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
5	chr16:34815137..34816427-chr16:34875759..34876664,4	MCF-7	breast:
6	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:
7	chr16:34815853..34816462-chr16:34876054..34876591,2	MCF-7	breast:
8	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:
9	chr16:34799028..34799683-chr16:34875753..34876623,3	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-35	chr16:35071257-35072103	NONHSAT142246
2	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
3	lnc-CTD-2144E22.5.1-8	chr16:34874400-34874953	ENSG00000259791.1
4	lnc-LINC00273-30	chr16:34956639-34956900	NONHSAT142221
5	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
6	lnc-LINC00273-31	chr16:35036459-35037041	NONHSAT142244
7	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
8	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
9	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
10	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
11	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
12	lnc-CTD-2144E22.5.1-31	chr16:34758333-34758358	NONHSAT142207
13	lnc-CTD-2144E22.5.1-32	chr16:34782288-34783200	NONHSAT142214
14	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
15	lnc-LINC00273-9	chr16:35019940-35021258	ENSG00000260611.1
16	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204

No data

Variant related genes	Relation type
ENSG00000260134	TF binding region
RNA5SP417	TF binding region
ENSG00000260611	TF binding region
ENSG00000261122	TF binding region
RNA5SP409	TF binding region
ENSG00000260746	TF binding region
RNA5SP419	TF binding region
RNA5SP407	TF binding region
ENSG00000261733	TF binding region
ENSG00000260857	TF binding region
RNA5SP406	TF binding region
RNA5SP408	TF binding region
RNA5SP413	TF binding region
RNA5SP415	TF binding region
RNA5SP418	TF binding region
RNA5SP422	TF binding region
HMGN2P41	TF binding region
VN1R70P	TF binding region
ENSG00000261046	TF binding region
ENSG00000269622	TF binding region
ENSG00000260994	TF binding region
RNA5SP421	TF binding region
ENSG00000259791	TF binding region
RNA5SP416	TF binding region
RNA5SP410	TF binding region
ENSG00000260522	TF binding region
RNA5SP420	TF binding region
RNA5SP423	TF binding region
RARRES2P8	TF binding region
ENSG00000260134	CpG island
RNA5SP417	CpG island
ENSG00000260611	CpG island
ENSG00000261122	CpG island
RNA5SP409	CpG island
ENSG00000260746	CpG island
RNA5SP419	CpG island
RNA5SP407	CpG island
ENSG00000261733	CpG island
ENSG00000260857	CpG island
RNA5SP406	CpG island
RNA5SP408	CpG island
RNA5SP413	CpG island
RNA5SP415	CpG island
RNA5SP418	CpG island
RNA5SP422	CpG island
HMGN2P41	CpG island
VN1R70P	CpG island
ENSG00000261046	CpG island
ENSG00000269622	CpG island
ENSG00000260994	CpG island
RNA5SP421	CpG island
ENSG00000259791	CpG island
RNA5SP416	CpG island
RNA5SP410	CpG island
ENSG00000260522	CpG island
RNA5SP420	CpG island
RNA5SP423	CpG island
RARRES2P8	CpG island
ENSG00000137871	chromatin interactions
ZNF451	miRNA target sites
ZNF407	miRNA target sites

Extended variants
information (count: 7197 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:7197 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373854289	chr16:34740003-34740004	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs575655453	chr16:34740018-34740019	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs118109154	chr16:34740020-34740021	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs139218607	chr16:34740085-34740086	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs188616442	chr16:34740103-34740104	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs560799768	chr16:34740140-34740141	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
7	rs572950058	chr16:34740194-34740195	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
8	rs79310374	chr16:34740219-34740220	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
9	rs540291737	chr16:34740233-34740234	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs546266734	chr16:34740255-34740256	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs149925524	chr16:34740259-34740260	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs192720650	chr16:34740294-34740295	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs550861962	chr16:34740312-34740313	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs569109024	chr16:34740334-34740335	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs72812797	chr16:34740355-34740356	Active TSS ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs183772147	chr16:34740371-34740372	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs574041493	chr16:34740454-34740455	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
18	rs535078537	chr16:34740478-34740479	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs553097140	chr16:34740490-34740491	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
20	rs543920559	chr16:34740527-34740528	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs562835224	chr16:34740564-34740565	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs577584997	chr16:34740569-34740570	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs118035966	chr16:34740580-34740581	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs547582950	chr16:34740589-34740590	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs188842797	chr16:34740625-34740626	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs74015949	chr16:34740626-34740627	Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs542849179	chr16:34740648-34740649	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs551539091	chr16:34740668-34740669	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs111431837	chr16:34740759-34740760	Active TSS ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
30	rs181175848	chr16:34740840-34740841	Active TSS ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs528182384	chr16:34740874-34740875	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs546626752	chr16:34740875-34740876	Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs564891389	chr16:34740943-34740944	Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs560285463	chr16:34740948-34740949	Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs1684102	chr16:34740950-34740951	Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs1684101	chr16:34740956-34740957	Active TSS ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs550923202	chr16:34740976-34740977	Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs569170661	chr16:34740979-34740980	Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs536489846	chr16:34740981-34740982	Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs1668010	chr16:34740985-34740986	Active TSS ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs548094628	chr16:34741006-34741007	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs530986730	chr16:34741053-34741054	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs149057190	chr16:34741073-34741074	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs184657084	chr16:34741126-34741127	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs571339353	chr16:34741141-34741142	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs182959	chr16:34741171-34741172	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs1668009	chr16:34741183-34741184	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs557275149	chr16:34741242-34741243	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs575838668	chr16:34741257-34741258	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs17052151	chr16:34741262-34741263	Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Disorders of sex development	21048976	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Medulloblastoma	21163964	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34736800-34740000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr16:34740000-34741400	Active TSS	K562	blood
3	chr16:34740000-34741800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr16:34740000-34741800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
5	chr16:34740000-34742000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr16:34740000-34742000	Active TSS	Brain Anterior Caudate	brain
7	chr16:34740200-34741200	Active TSS	A549	lung
8	chr16:34740200-34741600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr16:34740200-34741800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr16:34740600-34741600	ZNF genes & repeats	Pancreas	Pancrea
11	chr16:34740800-34741400	ZNF genes & repeats	Brain Hippocampus Middle	brain
12	chr16:34740800-34741800	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr16:34741000-34741400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
14	chr16:34743600-34743800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr16:34743800-34745400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr16:34744800-34745200	Enhancers	NHEK	skin
17	chr16:34745000-34745600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr16:34745800-34746000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
19	chr16:34746400-34746800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr16:34747200-34748000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
21	chr16:34752600-34753000	Active TSS	Fetal Heart	heart
22	chr16:34758400-34758600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
23	chr16:34758400-34758800	Enhancers	Brain Hippocampus Middle	brain
24	chr16:34760200-34760600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
25	chr16:34762600-34763200	Active TSS	Primary T cells from cord blood	blood
26	chr16:34767000-34768000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr16:34767200-34767800	ZNF genes & repeats	Adipose Nuclei	Adipose
28	chr16:34767600-34767800	ZNF genes & repeats	Gastric	stomach
29	chr16:34767800-34768800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
30	chr16:34767800-34770800	Weak transcription	Gastric	stomach
31	chr16:34773200-34773800	Weak transcription	Gastric	stomach
32	chr16:34775000-34777600	Weak transcription	Gastric	stomach
33	chr16:34777600-34778600	ZNF genes & repeats	Gastric	stomach
34	chr16:34777800-34778400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
35	chr16:34787000-34788000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr16:34787200-34787600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr16:34790400-34793600	ZNF genes & repeats	Dnd41	blood
38	chr16:34792000-34792600	Active TSS	Fetal Heart	heart
39	chr16:34793400-34797800	Enhancers	NHEK	skin
40	chr16:34793600-34794800	Flanking Active TSS	Dnd41	blood
41	chr16:34793800-34794000	Enhancers	HMEC	breast
42	chr16:34794000-34796200	Weak transcription	HMEC	breast
43	chr16:34794800-34795800	Enhancers	Dnd41	blood
44	chr16:34795800-34796000	Flanking Active TSS	Dnd41	blood
45	chr16:34796000-34796800	Transcr. at gene 5' and 3'	Dnd41	blood
46	chr16:34796200-34796800	Enhancers	HMEC	breast
47	chr16:34796800-34797400	Genic enhancers	Dnd41	blood
48	chr16:34797400-34797800	ZNF genes & repeats	Dnd41	blood
49	chr16:34799200-34800000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr16:34799400-34800200	Enhancers	Esophagus	oesophagus

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