Variant report

Variant	esv2761905
Chromosome Location	chr16:47524718-47586347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:688)
CpG islands
(count:245)
Chromatin interactive
region (count:39)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:688 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47538556-47538932	K562	blood:	n/a	n/a
2	ARID3A	chr16:47572269-47572803	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:47554148-47554743	K562	blood:	n/a	n/a
4	ARID3A	chr16:47526816-47527197	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47556945-47557537	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:47524403-47524722	K562	blood:	n/a	n/a
7	ARID3A	chr16:47526802-47527555	K562	blood:	n/a	n/a
8	ARID3A	chr16:47533067-47533932	HepG2	liver:	n/a	n/a
9	ATF1	chr16:47526819-47527180	K562	blood:	n/a	n/a
10	ATF1	chr16:47554214-47554593	K562	blood:	n/a	n/a
11	ATF2	chr16:47526273-47527368	GM12878	blood:	n/a	n/a
12	ATF2	chr16:47557169-47557724	GM12878	blood:	n/a	n/a
13	BACH1	chr16:47538552-47539389	K562	blood:	n/a	n/a
14	BATF	chr16:47526497-47527241	GM12878	blood:	n/a	n/a
15	BATF	chr16:47578156-47578439	GM12878	blood:	n/a	chr16:47578328-47578339
16	BATF	chr16:47526905-47527207	GM12878	blood:	n/a	n/a
17	BATF	chr16:47557294-47557576	GM12878	blood:	n/a	n/a
18	BCL11A	chr16:47526997-47527170	GM12878	blood:	n/a	n/a
19	BCLAF1	chr16:47557124-47557699	GM12878	blood:	n/a	n/a
20	BCLAF1	chr16:47526772-47527197	GM12878	blood:	n/a	n/a
21	BCLAF1	chr16:47527369-47528206	GM12878	blood:	n/a	n/a
22	BCLAF1	chr16:47526602-47527343	GM12878	blood:	n/a	n/a
23	BCLAF1	chr16:47557227-47557669	GM12878	blood:	n/a	n/a
24	BHLHE40	chr16:47554232-47554517	K562	blood:	n/a	n/a
25	BHLHE40	chr16:47526734-47528010	GM12878	blood:	n/a	n/a
26	BHLHE40	chr16:47525159-47525206	GM12878	blood:	n/a	n/a
27	BHLHE40	chr16:47526878-47527248	K562	blood:	n/a	n/a
28	BHLHE40	chr16:47538513-47539390	K562	blood:	n/a	n/a
29	BRCA1	chr16:47527049-47527051	HepG2	liver:	n/a	n/a
30	BRCA1	chr16:47538554-47539389	HepG2	liver:	n/a	n/a
31	BRCA1	chr16:47538553-47539390	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr16:47526736-47527233	K562	blood:	n/a	n/a
33	CBX3	chr16:47573687-47574266	K562	blood:	n/a	n/a
34	CBX3	chr16:47573711-47574221	K562	blood:	n/a	n/a
35	CBX3	chr16:47524314-47524743	K562	blood:	n/a	n/a
36	CBX3	chr16:47524405-47524761	K562	blood:	n/a	n/a
37	CCNT2	chr16:47553908-47554471	K562	blood:	n/a	n/a
38	CCNT2	chr16:47538514-47539391	K562	blood:	n/a	chr16:47539304-47539313
39	CEBPB	chr16:47543331-47543493	H1-hESC	embryonic stem cell:	n/a	chr16:47543398-47543409
40	CEBPB	chr16:47526890-47527162	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:47533546-47533802	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:47540907-47541035	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:47538513-47539385	K562	blood:	n/a	n/a
44	CEBPB	chr16:47543295-47543533	IMR90	lung:	n/a	chr16:47543398-47543409
45	CEBPB	chr16:47554161-47554656	K562	blood:	n/a	n/a
46	CEBPB	chr16:47534355-47534596	HepG2	liver:	n/a	chr16:47534479-47534490
47	CEBPB	chr16:47538513-47539379	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:47554100-47554655	K562	blood:	n/a	n/a
49	CEBPB	chr16:47543297-47543497	A549	lung:	n/a	chr16:47543398-47543409
50	CEBPB	chr16:47536409-47536596	H1-hESC	embryonic stem cell:	n/a	chr16:47536513-47536526 chr16:47536515-47536526

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47539166-47539216	K562	blood:	n/a
2	chr16:47539166-47539216	K562	blood:	n/a
3	chr16:47539166-47539216	NH-A	brain:	n/a
4	chr16:47539166-47539216	HEK293	kidney:	embryo
5	chr16:47539137-47539187	MCF10A-Er-Src	breast:	n/a
6	chr16:47527034-47527084	GM06990	blood:	n/a
7	chr16:47527034-47527084	HCT-116	colon:	n/a
8	chr16:47527034-47527084	PFSK-1	brain:	n/a
9	chr16:47539203-47539253	K562	blood:	n/a
10	chr16:47539166-47539216	BJ	skin:	n/a
11	chr16:47539166-47539216	T-47D	breast:	n/a
12	chr16:47539166-47539216	ProgFib	skin:	n/a
13	chr16:47539166-47539216	PrEC	prostate:	n/a
14	chr16:47539137-47539187	BJ	skin:	n/a
15	chr16:47539203-47539253	Caco-2	colon:	n/a
16	chr16:47539203-47539253	HEEpiC	esophagus:	n/a
17	chr16:47539137-47539187	CMK	blood:	n/a
18	chr16:47539166-47539216	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:47539137-47539187	GM06990	blood:	n/a
20	chr16:47539137-47539187	NT2-D1	testis:	n/a
21	chr16:47539203-47539253	AG04449	skin:	fetal
22	chr16:47539166-47539216	BE2_C	brain:	n/a
23	chr16:47527034-47527084	PrEC	prostate:	n/a
24	chr16:47539166-47539216	AG04450	lung:	fetal
25	chr16:47539137-47539187	HRE	kidney:	n/a
26	chr16:47527034-47527084	Hela-S3	cervix:	n/a
27	chr16:47539203-47539253	HCT-116	colon:	n/a
28	chr16:47539203-47539253	BJ	skin:	n/a
29	chr16:47539166-47539216	MCF-7	breast:	n/a
30	chr16:47539166-47539216	HUVEC	blood vessel:	n/a
31	chr16:47539166-47539216	HCPEpiC	choroid plexus:	n/a
32	chr16:47527034-47527084	RPTEC	kidney:	n/a
33	chr16:47527034-47527084	ECC-1	luminal epithelium:	n/a
34	chr16:47527034-47527084	SK-N-MC	brain:	n/a
35	chr16:47527034-47527084	SAEC	small airway:	n/a
36	chr16:47539166-47539216	NT2-D1	testis:	n/a
37	chr16:47527034-47527084	AoSMC	blood vessel:	n/a
38	chr16:47539203-47539253	Hepatocyte	liver:	n/a
39	chr16:47527034-47527084	SK-N-SH	brain:	n/a
40	chr16:47539203-47539253	LNCaP	prostate:	n/a
41	chr16:47539203-47539253	NHBE	bronchial:	n/a
42	chr16:47539137-47539187	HEK293	kidney:	embryo
43	chr16:47527034-47527084	SKMC	muscle:	n/a
44	chr16:47539166-47539216	AG10803	skin:	n/a
45	chr16:47539203-47539253	NB4	blood:	n/a
46	chr16:47527034-47527084	BE2_C	brain:	n/a
47	chr16:47539203-47539253	AG09319	gingival:	n/a
48	chr16:47539203-47539253	HCM	heart:	n/a
49	chr16:47539137-47539187	ovcar-3	ovarian:	n/a
50	chr16:47539137-47539187	LNCaP	prostate:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:47502808..47504633-chr16:47527127..47529319,2	K562	blood:
2	chr16:47548754..47550733-chr16:47554531..47556036,2	MCF-7	breast:
3	chr16:47530496..47533304-chr16:47537314..47539255,2	K562	blood:
4	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
5	chr16:47530496..47533304-chr16:47537314..47539416,3	K562	blood:
6	chr16:47538608..47539209-chr19:24184105..24184774,2	MCF-7	breast:
7	chr16:47541164..47545156-chr16:47546024..47549793,5	K562	blood:
8	chr16:47494533..47496670-chr16:47528896..47531498,2	MCF-7	breast:
9	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
10	chr16:47481523..47483741-chr16:47529384..47531603,2	K562	blood:
11	chr16:47541164..47545156-chr16:47546024..47549793,5	K562	blood:
12	chr16:47315203..47316940-chr16:47529898..47531487,2	K562	blood:
13	chr16:47521997..47524877-chr16:47525537..47527944,2	K562	blood:
14	chr16:47525470..47528929-chr16:47529310..47531688,3	K562	blood:
15	chr16:47495155..47497057-chr16:47571448..47573039,2	K562	blood:
16	chr16:47538608..47539232-chr19:24184323..24185236,2	MCF-7	breast:
17	chr16:47517170..47520211-chr16:47526974..47528925,3	K562	blood:
18	chr16:47542191..47545156-chr16:47546024..47549181,3	K562	blood:
19	chr16:47560964..47562749-chr16:47565268..47567477,2	K562	blood:
20	chr16:47527728..47529779-chr16:47631706..47633843,2	K562	blood:
21	chr16:47497354..47500127-chr16:47526363..47529187,2	K562	blood:
22	chr16:47502099..47504584-chr16:47526951..47528627,3	K562	blood:
23	chr16:47502629..47504464-chr16:47550187..47553009,2	K562	blood:
24	chr16:47493908..47496119-chr16:47525530..47527640,2	K562	blood:
25	chr16:47516457..47520432-chr16:47524851..47526977,4	K562	blood:
26	chr16:47521997..47524877-chr16:47525537..47527944,2	K562	blood:
27	chr16:47560964..47562749-chr16:47565268..47567477,2	K562	blood:
28	chr16:47535504..47537200-chr16:47537688..47539463,2	K562	blood:
29	chr16:47538624..47539255-chr19:24184251..24185320,3	MCF-7	breast:
30	chr16:47542191..47545156-chr16:47546024..47549181,3	K562	blood:
31	chr16:47493923..47496746-chr16:47529006..47531243,3	K562	blood:
32	chr16:47548754..47550733-chr16:47554531..47556036,2	MCF-7	breast:
33	chr16:47533842..47536233-chr16:47541991..47544849,2	K562	blood:
34	chr16:47493569..47497883-chr16:47557067..47559084,4	K562	blood:
35	chr16:47538608..47539204-chr19:24184110..24185018,4	MCF-7	breast:
36	chr16:47525470..47528929-chr16:47529310..47531688,3	K562	blood:
37	chr16:47538686..47539206-chr5:50081215..50081735,2	MCF-7	breast:
38	chr16:47530496..47533304-chr16:47537314..47539255,2	K562	blood:
39	chr16:47533842..47536233-chr16:47541991..47544849,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPT2-4	chr16:47563387-47563827	ENSG00000262038.1
2	lnc-GPT2-4	chr16:47563101-47563152	NONHSAT142298
3	lnc-GPT2-4	chr16:47563101-47563152	ENSG00000262038.1
4	lnc-GPT2-4	chr16:47563386-47563827	NONHSAT142298

No data

Variant related genes	Relation type
ENSG00000262038	TF binding region
PHKB	TF binding region
RNA5SP425	TF binding region
ENSG00000262038	CpG island
PHKB	CpG island
RNA5SP425	CpG island
ENSG00000129636	chromatin interactions
ENSG00000222268	chromatin interactions
ENSG00000259918	chromatin interactions
ENSG00000102893	chromatin interactions

Extended variants
information (count: 2003 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560150420	chr16:47524718-47524719	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs535733390	chr16:47524741-47524742	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368377772	chr16:47524808-47524809	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192601878	chr16:47524816-47524817	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552102185	chr16:47524884-47524885	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184468647	chr16:47524906-47524907	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537712277	chr16:47524928-47524929	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140764697	chr16:47524998-47524999	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557937440	chr16:47525066-47525067	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557162712	chr16:47525072-47525073	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535569676	chr16:47525074-47525075	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149773760	chr16:47525115-47525116	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565724569	chr16:47525138-47525139	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544526425	chr16:47525139-47525140	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539430765	chr16:47525165-47525166	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145729204	chr16:47525169-47525170	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113277668	chr16:47525170-47525171	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143199525	chr16:47525185-47525186	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190053527	chr16:47525208-47525209	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs568111747	chr16:47525217-47525218	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs181181521	chr16:47525238-47525239	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs186360781	chr16:47525255-47525256	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs573211486	chr16:47525264-47525265	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs527722569	chr16:47525356-47525357	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs189297881	chr16:47525382-47525383	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs564108812	chr16:47525400-47525401	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs531647437	chr16:47525410-47525411	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs549789151	chr16:47525437-47525438	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs568272804	chr16:47525457-47525458	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs529073580	chr16:47525477-47525478	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs547555253	chr16:47525488-47525489	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs146751375	chr16:47525519-47525520	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539493116	chr16:47525615-47525616	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540227784	chr16:47525668-47525669	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs145421695	chr16:47525719-47525720	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557808219	chr16:47525750-47525751	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs137941443	chr16:47525759-47525760	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs555716343	chr16:47525764-47525765	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs574671363	chr16:47525884-47525885	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs538564573	chr16:47525998-47525999	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542142529	chr16:47526003-47526004	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575025260	chr16:47526021-47526022	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs142499521	chr16:47526087-47526088	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs150113663	chr16:47526106-47526107	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs138398824	chr16:47526174-47526175	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs35535144	chr16:47526275-47526276	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs149241372	chr16:47526280-47526281	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs35118601	chr16:47526291-47526292	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs530115726	chr16:47526294-47526295	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs564171932	chr16:47526513-47526514	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Prostate cancer	22341455	CNVD

Chromatin state (count:2043 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47496200-47526400	Weak transcription	Pancreas	Pancrea
2	chr16:47496200-47532000	Weak transcription	Ovary	ovary
3	chr16:47496200-47538400	Weak transcription	NH-A	brain
4	chr16:47498200-47527800	Weak transcription	Small Intestine	intestine
5	chr16:47498400-47526000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr16:47498800-47526400	Weak transcription	Esophagus	oesophagus
7	chr16:47499000-47526400	Weak transcription	Fetal Stomach	stomach
8	chr16:47502400-47533200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr16:47504600-47526400	Weak transcription	Aorta	Aorta
10	chr16:47511800-47526600	Weak transcription	NHLF	lung
11	chr16:47513200-47526000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr16:47516000-47526400	Weak transcription	Right Ventricle	heart
13	chr16:47518800-47531600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr16:47519400-47527200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr16:47520400-47525800	ZNF genes & repeats	Primary B cells from cord blood	blood
16	chr16:47521000-47536400	Weak transcription	HSMMtube	muscle
17	chr16:47521400-47526200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
18	chr16:47521400-47527000	ZNF genes & repeats	Liver	Liver
19	chr16:47521600-47525200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
20	chr16:47521600-47525400	ZNF genes & repeats	Primary B cells from peripheral blood	blood
21	chr16:47521600-47526200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr16:47521800-47525600	Weak transcription	HepG2	liver
23	chr16:47523000-47525600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr16:47523200-47525200	Enhancers	GM12878-XiMat	blood
25	chr16:47523400-47525400	ZNF genes & repeats	Fetal Lung	lung
26	chr16:47523600-47524800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr16:47523600-47525400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr16:47523600-47526000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr16:47524000-47526000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr16:47524200-47525000	Weak transcription	Fetal Kidney	kidney
31	chr16:47524400-47524800	ZNF genes & repeats	Left Ventricle	heart
32	chr16:47524400-47525200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr16:47524400-47525200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr16:47524400-47525200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr16:47524400-47525200	ZNF genes & repeats	Psoas Muscle	Psoas
36	chr16:47524400-47525400	ZNF genes & repeats	K562	blood
37	chr16:47524400-47525600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
38	chr16:47524400-47526000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr16:47524600-47525000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr16:47524600-47525400	ZNF genes & repeats	Fetal Heart	heart
41	chr16:47524600-47526200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
42	chr16:47524600-47526400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr16:47524600-47545800	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr16:47524800-47525800	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
45	chr16:47524800-47526000	Weak transcription	Left Ventricle	heart
46	chr16:47524800-47526400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr16:47524800-47526400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr16:47525200-47525400	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr16:47525200-47525400	Weak transcription	Fetal Kidney	kidney
50	chr16:47525200-47525600	Weak transcription	Monocytes-CD14+_RO01746	blood

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