Variant report

Variant	nsv960007
Chromosome Location	chr16:48413351-48426696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:710)
CpG islands
(count:549)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:710 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:48417831-48418153	K562	blood:	n/a	n/a
2	ARID3A	chr16:48419894-48420137	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:48419130-48419530	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:48416816-48417494	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:48419367-48419551	K562	blood:	n/a	n/a
6	ARID3A	chr16:48417781-48418469	HepG2	liver:	n/a	n/a
7	ATF2	chr16:48417986-48418364	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr16:48419311-48419585	HepG2	liver:	n/a	chr16:48419332-48419341 chr16:48419408-48419417
9	ATF3	chr16:48416091-48416419	K562	blood:	n/a	n/a
10	BCL3	chr16:48419028-48419378	GM12878	blood:	n/a	chr16:48419327-48419340 chr16:48419361-48419370 chr16:48419359-48419372
11	BCL3	chr16:48419341-48419762	A549	lung:	n/a	chr16:48419710-48419723 chr16:48419361-48419370 chr16:48419359-48419372 chr16:48419712-48419725 chr16:48419715-48419724 chr16:48419712-48419721 chr16:48419623-48419636
12	BCLAF1	chr16:48419242-48419765	GM12878	blood:	n/a	chr16:48419710-48419723 chr16:48419327-48419340 chr16:48419361-48419370 chr16:48419359-48419372 chr16:48419712-48419725 chr16:48419715-48419724 chr16:48419712-48419721 chr16:48419623-48419636
13	BHLHE40	chr16:48418075-48419797	GM12878	blood:	n/a	chr16:48419664-48419680 chr16:48419620-48419636 chr16:48418657-48418673
14	BHLHE40	chr16:48417811-48420020	K562	blood:	n/a	chr16:48419664-48419680 chr16:48419620-48419636 chr16:48418657-48418673
15	BHLHE40	chr16:48425313-48425429	HepG2	liver:	n/a	n/a
16	BHLHE40	chr16:48418641-48418772	A549	lung:	n/a	chr16:48418657-48418673
17	BHLHE40	chr16:48417882-48419832	HepG2	liver:	n/a	chr16:48419664-48419680 chr16:48419620-48419636 chr16:48418657-48418673
18	BRCA1	chr16:48420000-48420095	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr16:48419498-48419895	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr16:48419426-48419579	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr16:48419858-48419902	HepG2	liver:	n/a	n/a
22	CCNT2	chr16:48418457-48419867	K562	blood:	n/a	chr16:48418561-48418570 chr16:48419837-48419846 chr16:48418924-48418933 chr16:48419408-48419417 chr16:48418929-48418938
23	CEBPB	chr16:48416846-48417046	IMR90	lung:	n/a	n/a
24	CEBPB	chr16:48425514-48425714	HepG2	liver:	n/a	chr16:48425646-48425657
25	CEBPB	chr16:48419310-48419610	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr16:48416723-48417103	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr16:48416697-48417178	A549	lung:	n/a	chr16:48416704-48416715
28	CEBPB	chr16:48417011-48417012	A549	lung:	n/a	n/a
29	CEBPB	chr16:48417601-48417897	IMR90	lung:	n/a	n/a
30	CEBPB	chr16:48416800-48417112	HepG2	liver:	n/a	n/a
31	CEBPB	chr16:48417577-48418047	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr16:48415170-48415476	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr16:48425594-48425698	HepG2	liver:	n/a	chr16:48425646-48425657
34	CEBPB	chr16:48418494-48418583	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr16:48415168-48415381	MCF-7	breast:	n/a	n/a
36	CEBPD	chr16:48419182-48419804	HepG2	liver:	n/a	n/a
37	CEBPD	chr16:48418771-48419821	HepG2	liver:	n/a	n/a
38	CEBPD	chr16:48418443-48418750	HepG2	liver:	n/a	n/a
39	CHD1	chr16:48418594-48418677	GM12878	blood:	n/a	n/a
40	CHD1	chr16:48418999-48419289	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr16:48418974-48419965	GM12878	blood:	n/a	chr16:48419623-48419633 chr16:48418977-48418984
42	CHD1	chr16:48419944-48420114	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr16:48418054-48418654	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr16:48418969-48419747	K562	blood:	n/a	chr16:48419623-48419633 chr16:48418977-48418984
45	CHD2	chr16:48419447-48419985	H1-hESC	embryonic stem cell:	n/a	chr16:48419623-48419633
46	CHD2	chr16:48418074-48418559	K562	blood:	n/a	n/a
47	CHD2	chr16:48419032-48419232	GM12878	blood:	n/a	n/a
48	CHD2	chr16:48419431-48419915	HepG2	liver:	n/a	chr16:48419623-48419633
49	CHD2	chr16:48417705-48418715	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr16:48418430-48418627	H1-hESC	embryonic stem cell:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:48418433-48418483	SAEC	small airway:	n/a
2	chr16:48418433-48418483	IMR90	lung:	fetal
3	chr16:48421602-48421652	HPAEpiC	pulmonary alveolar:	n/a
4	chr16:48421602-48421652	AG09309	skin:	n/a
5	chr16:48413428-48413478	GM06990	blood:	n/a
6	chr16:48413428-48413478	MCF-7	breast:	n/a
7	chr16:48419522-48419572	K562	blood:	n/a
8	chr16:48413428-48413478	MCF10A-Er-Src	breast:	n/a
9	chr16:48414920-48414970	HEK293	kidney:	embryo
10	chr16:48419522-48419572	NT2-D1	testis:	n/a
11	chr16:48419812-48419862	SK-N-SH_RA	brain:	n/a
12	chr16:48414920-48414970	NHDF-neo	bronchial:	n/a
13	chr16:48413428-48413478	AG04449	skin:	fetal
14	chr16:48418433-48418483	HCM	heart:	n/a
15	chr16:48421602-48421652	GM19239	blood:	n/a
16	chr16:48419541-48419591	SK-N-MC	brain:	n/a
17	chr16:48419812-48419862	HEEpiC	esophagus:	n/a
18	chr16:48414920-48414970	CMK	blood:	n/a
19	chr16:48419541-48419591	T-47D	breast:	n/a
20	chr16:48419541-48419591	HUVEC	blood vessel:	n/a
21	chr16:48413428-48413478	HUVEC	blood vessel:	n/a
22	chr16:48418433-48418483	H1-hESC	embryonic stem cell:	embryo
23	chr16:48422428-48422478	K562	blood:	n/a
24	chr16:48414920-48414970	IMR90	lung:	fetal
25	chr16:48422428-48422478	U87	brain:	n/a
26	chr16:48421602-48421652	ECC-1	luminal epithelium:	n/a
27	chr16:48414920-48414970	MCF10A-Er-Src	breast:	n/a
28	chr16:48421602-48421652	GM12878	blood:	n/a
29	chr16:48419541-48419591	GM12891	blood:	n/a
30	chr16:48413428-48413478	HMEC	breast:	n/a
31	chr16:48414920-48414970	AG10803	skin:	n/a
32	chr16:48413428-48413478	HAEpiC	amniotic membrane:	n/a
33	chr16:48422428-48422478	MCF-7	breast:	n/a
34	chr16:48419541-48419591	HAEpiC	amniotic membrane:	n/a
35	chr16:48414920-48414970	H1-hESC	embryonic stem cell:	embryo
36	chr16:48414920-48414970	HCT-116	colon:	n/a
37	chr16:48419541-48419591	MCF10A-Er-Src	breast:	n/a
38	chr16:48414920-48414970	HUVEC	blood vessel:	n/a
39	chr16:48419541-48419591	HL-60	blood:	n/a
40	chr16:48414920-48414970	T-47D	breast:	n/a
41	chr16:48422428-48422478	HCM	heart:	n/a
42	chr16:48419812-48419862	NH-A	brain:	n/a
43	chr16:48419522-48419572	Caco-2	colon:	n/a
44	chr16:48413428-48413478	ovcar-3	ovarian:	n/a
45	chr16:48421602-48421652	HRE	kidney:	n/a
46	chr16:48421602-48421652	CMK	blood:	n/a
47	chr16:48414920-48414970	AG04449	skin:	fetal
48	chr16:48419812-48419862	AG09309	skin:	n/a
49	chr16:48419541-48419591	HNPCEpiC	eye:	n/a
50	chr16:48414920-48414970	ProgFib	skin:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:47494716..47496450-chr16:48424502..48427404,2	K562	blood:
2	chr15:85291369..85292229-chr16:48418740..48419424,2	Hela-S3	cervix:
3	chr16:48419382..48420884-chr16:48422551..48425300,2	MCF-7	breast:
4	chr16:48416330..48420180-chr16:48420798..48424375,5	K562	blood:
5	chr16:48399845..48400801-chr16:48418367..48419048,2	Hela-S3	cervix:
6	chr16:48417608..48421302-chr16:48425063..48429266,6	K562	blood:
7	chr16:48419370..48419971-chr19:17515260..17516132,2	Hela-S3	cervix:
8	chr16:48422934..48425997-chr16:48426022..48428467,3	K562	blood:
9	chr16:48417747..48421302-chr16:48425164..48430136,6	K562	blood:
10	chr16:48416397..48419006-chr16:48635531..48637181,2	K562	blood:
11	chr12:57039442..57040047-chr16:48419364..48420064,2	Hela-S3	cervix:
12	chr16:48398562..48401765-chr16:48412536..48415889,3	MCF-7	breast:
13	chr16:48406348..48408797-chr16:48412397..48415717,4	MCF-7	breast:
14	chr16:2013351..2015357-chr16:48417776..48419360,2	MCF-7	breast:
15	chr16:48397931..48401931-chr16:48416758..48423536,12	MCF-7	breast:
16	chr16:48418015..48420544-chr16:48643775..48645908,3	MCF-7	breast:
17	chr16:48380431..48382791-chr16:48417861..48420626,2	K562	blood:
18	chr1:153508413..153509221-chr16:48418944..48419933,2	Hela-S3	cervix:
19	chr16:48411748..48415998-chr16:48416243..48420831,11	K562	blood:
20	chr16:48367808..48369426-chr16:48417936..48419640,2	MCF-7	breast:
21	chr16:48417747..48421302-chr16:48425164..48430136,6	K562	blood:
22	chr12:7261155..7261904-chr16:48418914..48419874,2	Hela-S3	cervix:
23	chr16:48277094..48279506-chr16:48417848..48419466,2	K562	blood:
24	chr16:48388703..48393705-chr16:48416034..48420195,6	K562	blood:
25	chr16:48419410..48421944-chr16:48545496..48547470,2	MCF-7	breast:
26	chr16:48398121..48402229-chr16:48414201..48420573,11	MCF-7	breast:
27	chr11:6502371..6503037-chr16:48419377..48420020,2	NB4	blood:
28	chr16:48388635..48393801-chr16:48416034..48420195,7	K562	blood:
29	chr16:48417608..48421302-chr16:48425063..48429266,6	K562	blood:
30	chr16:48396253..48404408-chr16:48411826..48421166,27	K562	blood:
31	chr10:35284036..35284536-chr16:48418817..48419320,2	NB4	blood:
32	chr16:48417956..48420702-chr16:48642244..48644303,3	K562	blood:
33	chr16:48418761..48419469-chr22:42228810..42229760,2	Hela-S3	cervix:
34	chr16:48418738..48419529-chr16:89626613..89627546,2	Hela-S3	cervix:
35	chr16:48422311..48424434-chr16:48426532..48428467,2	K562	blood:
36	chr16:48392029..48394915-chr16:48416777..48418892,2	MCF-7	breast:
37	chr16:48416330..48419738-chr16:48422315..48424375,4	K562	blood:
38	chr16:48417371..48420713-chr16:48642499..48645364,3	K562	blood:
39	chr1:212208566..212209259-chr16:48419035..48419960,2	Hela-S3	cervix:
40	chr16:48406174..48409195-chr16:48411058..48414705,6	K562	blood:
41	chr16:48419382..48420884-chr16:48422551..48425300,2	MCF-7	breast:
42	chr16:48411112..48415935-chr16:48417584..48420654,6	MCF-7	breast:
43	chr16:48419190..48419723-chr20:30194517..30195068,2	HCT-116	colon:

No data

Variant related genes	Relation type
SIAH1	TF binding region
SIAH1	CpG island
ENSG00000121270	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000102910	chromatin interactions
ENSG00000132254	chromatin interactions
ENSG00000205885	chromatin interactions
ENSG00000255513	chromatin interactions
ENSG00000166716	chromatin interactions
ENSG00000130303	chromatin interactions
ENSG00000196470	chromatin interactions
ENSG00000102921	chromatin interactions
ENSG00000143476	chromatin interactions
ENSG00000167526	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000102893	chromatin interactions
ENSG00000132286	chromatin interactions
ENSG00000139178	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000240793	chromatin interactions
ENSG00000143493	chromatin interactions
ENSG00000265264	chromatin interactions
ENSG00000198911	chromatin interactions
ENSG00000110955	chromatin interactions

Extended variants
information (count: 463 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140453321	chr16:48413373-48413374	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552460118	chr16:48413378-48413379	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569243587	chr16:48413395-48413396	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs150391715	chr16:48413401-48413402	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs574469206	chr16:48413459-48413460	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs138644954	chr16:48413469-48413470	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566933687	chr16:48413472-48413473	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535826322	chr16:48413503-48413504	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542097635	chr16:48413623-48413624	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73562076	chr16:48413631-48413632	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs35551812	chr16:48413710-48413711	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs572819256	chr16:48413729-48413730	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs538863476	chr16:48413730-48413731	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547651766	chr16:48413738-48413739	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs148901709	chr16:48413745-48413746	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs117742089	chr16:48413746-48413747	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575659282	chr16:48413800-48413801	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs74017948	chr16:48413806-48413807	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs529889782	chr16:48413811-48413812	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145658530	chr16:48413822-48413823	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138005869	chr16:48413878-48413879	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574887505	chr16:48413900-48413901	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs116319190	chr16:48413924-48413925	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560651181	chr16:48413934-48413935	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs111553017	chr16:48413938-48413939	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546404263	chr16:48413950-48413951	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs562733776	chr16:48414002-48414003	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531751301	chr16:48414032-48414033	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs62059414	chr16:48414048-48414049	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs568387251	chr16:48414116-48414117	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142533685	chr16:48414135-48414136	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs373999784	chr16:48414166-48414167	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145975140	chr16:48414191-48414192	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs57554936	chr16:48414201-48414202	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375806065	chr16:48414214-48414215	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs112352654	chr16:48414268-48414269	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536721245	chr16:48414269-48414270	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538353928	chr16:48414294-48414295	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558826335	chr16:48414316-48414317	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74417185	chr16:48414345-48414346	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200621608	chr16:48414362-48414363	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558144413	chr16:48414370-48414371	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111931690	chr16:48414374-48414375	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs78055790	chr16:48414375-48414376	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs375782400	chr16:48414383-48414384	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs58864824	chr16:48414384-48414385	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535523241	chr16:48414418-48414419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574610655	chr16:48414425-48414426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs377423013	chr16:48414426-48414427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181567267	chr16:48414455-48414456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
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
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
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Disease	22140031	CNVD
Non-syndromic sensorineural hearing loss	22140031	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:48400600-48417600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr16:48400800-48417800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:48403200-48415000	Enhancers	Adipose Nuclei	Adipose
4	chr16:48404800-48417200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr16:48406400-48416800	Enhancers	Liver	Liver
6	chr16:48406600-48417200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr16:48407000-48414400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr16:48407600-48413600	Weak transcription	Esophagus	oesophagus
9	chr16:48407800-48417200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr16:48408000-48415000	Weak transcription	Fetal Muscle Leg	muscle
11	chr16:48408000-48416600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr16:48408600-48413600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr16:48409000-48417000	Weak transcription	Fetal Kidney	kidney
14	chr16:48409000-48417200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr16:48409200-48416800	Weak transcription	NHDF-Ad	bronchial
16	chr16:48409200-48417000	Weak transcription	NHLF	lung
17	chr16:48409200-48417200	Weak transcription	NH-A	brain
18	chr16:48409200-48417200	Weak transcription	Osteobl	bone
19	chr16:48409400-48416800	Weak transcription	HUVEC	blood vessel
20	chr16:48409400-48417800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr16:48410400-48413600	Enhancers	NHEK	skin
22	chr16:48410400-48414400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr16:48410400-48417600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr16:48410600-48413800	Enhancers	Brain Germinal Matrix	brain
25	chr16:48410600-48414000	Enhancers	Primary hematopoietic stem cells	blood
26	chr16:48410600-48414200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr16:48410800-48413600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr16:48410800-48414400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr16:48411200-48413800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr16:48411400-48414000	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr16:48411400-48416200	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr16:48411600-48414800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr16:48411600-48415000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr16:48411600-48415000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr16:48411600-48416200	Enhancers	Placenta	Placenta
36	chr16:48411600-48416400	Weak transcription	HSMM	muscle
37	chr16:48411600-48417400	Enhancers	Primary B cells from cord blood	blood
38	chr16:48411800-48415200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr16:48411800-48417800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr16:48412000-48414000	Enhancers	Fetal Heart	heart
41	chr16:48412000-48414000	Weak transcription	Fetal Muscle Trunk	muscle
42	chr16:48412000-48414000	Enhancers	Right Atrium	heart
43	chr16:48412000-48414400	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr16:48412000-48416800	Enhancers	HepG2	liver
45	chr16:48412000-48417000	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr16:48412200-48413400	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr16:48412200-48413400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr16:48412200-48413400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr16:48412200-48413800	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr16:48412200-48413800	Enhancers	Brain Angular Gyrus	brain

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