Variant report

Variant	nsv878139
Chromosome Location	chr3:195058837-195158031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:445)
CpG islands
(count:184)
Chromatin interactive
region (count:67)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195073888-195074208	K562	blood:	n/a	n/a
2	ATF1	chr3:195146585-195147032	K562	blood:	n/a	n/a
3	ATF1	chr3:195073832-195074099	K562	blood:	n/a	n/a
4	ATF1	chr3:195118576-195118596	K562	blood:	n/a	n/a
5	ATF3	chr3:195073748-195074155	K562	blood:	n/a	n/a
6	BHLHE40	chr3:195114767-195115120	GM12878	blood:	n/a	n/a
7	BRCA1	chr3:195102403-195103241	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr3:195073920-195073950	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:195134115-195134473	A549	lung:	n/a	n/a
10	CEBPB	chr3:195142195-195142415	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:195117516-195117880	K562	blood:	n/a	n/a
12	CEBPB	chr3:195086963-195087317	HepG2	liver:	n/a	chr3:195087145-195087156
13	CEBPB	chr3:195134110-195134480	K562	blood:	n/a	n/a
14	CEBPB	chr3:195106354-195106618	A549	lung:	n/a	n/a
15	CEBPB	chr3:195134135-195134369	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:195073775-195074333	K562	blood:	n/a	chr3:195074161-195074172
17	CEBPB	chr3:195106347-195106743	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:195142168-195142509	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:195106302-195106726	A549	lung:	n/a	n/a
20	CEBPB	chr3:195086924-195087310	MCF-7	breast:	n/a	chr3:195087145-195087156
21	CEBPB	chr3:195134103-195134474	K562	blood:	n/a	n/a
22	CEBPB	chr3:195106321-195106707	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:195106262-195106744	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr3:195073672-195074349	HCT-116	colon:	n/a	chr3:195074161-195074172
25	CEBPB	chr3:195073820-195074079	K562	blood:	n/a	n/a
26	CEBPB	chr3:195102357-195102734	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:195086996-195087275	A549	lung:	n/a	chr3:195087145-195087156
28	CEBPB	chr3:195134115-195134423	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:195105475-195105662	HepG2	liver:	n/a	chr3:195105587-195105600 chr3:195105588-195105599
30	CEBPB	chr3:195073740-195074319	K562	blood:	n/a	chr3:195074161-195074172
31	CEBPB	chr3:195133956-195134439	MCF-7	breast:	n/a	chr3:195134040-195134053
32	CEBPB	chr3:195134080-195134538	MCF-7	breast:	n/a	n/a
33	CEBPB	chr3:195105592-195106014	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:195117387-195117882	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:195106346-195106695	MCF-7	breast:	n/a	n/a
36	CEBPB	chr3:195073856-195074333	HepG2	liver:	n/a	chr3:195074161-195074172
37	CEBPB	chr3:195116091-195116306	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:195073641-195074396	HCT-116	colon:	n/a	chr3:195074161-195074172
39	CEBPB	chr3:195106290-195106782	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:195073819-195074352	ECC-1	luminal epithelium:	n/a	chr3:195074161-195074172
41	CEBPB	chr3:195137594-195137784	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:195146731-195146822	K562	blood:	n/a	n/a
43	CEBPB	chr3:195106239-195106724	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr3:195106372-195106684	HepG2	liver:	n/a	n/a
45	CEBPB	chr3:195086977-195087306	Hela-S3	cervix:	n/a	chr3:195087145-195087156
46	CEBPB	chr3:195134221-195134401	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:195133940-195134434	IMR90	lung:	n/a	chr3:195134040-195134053
48	CEBPB	chr3:195073818-195074330	A549	lung:	n/a	chr3:195074161-195074172
49	CEBPB	chr3:195073814-195074248	H1-hESC	embryonic stem cell:	n/a	chr3:195074161-195074172
50	CEBPB	chr3:195086978-195087308	IMR90	lung:	n/a	chr3:195087145-195087156

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195077618-195077668	K562	blood:	n/a
2	chr3:195077618-195077668	K562	blood:	n/a
3	chr3:195102265-195102315	AG04450	lung:	fetal
4	chr3:195102265-195102315	Jurkat	blood:	n/a
5	chr3:195077618-195077668	ovcar-3	ovarian:	n/a
6	chr3:195087778-195087828	NB4	blood:	n/a
7	chr3:195087778-195087828	AG09319	gingival:	n/a
8	chr3:195102265-195102315	A549	lung:	n/a
9	chr3:195087778-195087828	HepG2	liver:	n/a
10	chr3:195102265-195102315	SAEC	small airway:	n/a
11	chr3:195087778-195087828	AG04449	skin:	fetal
12	chr3:195087778-195087828	AoSMC	blood vessel:	n/a
13	chr3:195102265-195102315	GM12878	blood:	n/a
14	chr3:195102265-195102315	HCPEpiC	choroid plexus:	n/a
15	chr3:195087778-195087828	GM19239	blood:	n/a
16	chr3:195087778-195087828	BE2_C	brain:	n/a
17	chr3:195087778-195087828	PrEC	prostate:	n/a
18	chr3:195087778-195087828	SAEC	small airway:	n/a
19	chr3:195102265-195102315	AG09309	skin:	n/a
20	chr3:195102265-195102315	ECC-1	luminal epithelium:	n/a
21	chr3:195077618-195077668	Hepatocyte	liver:	n/a
22	chr3:195102265-195102315	ovcar-3	ovarian:	n/a
23	chr3:195087778-195087828	LNCaP	prostate:	n/a
24	chr3:195087778-195087828	HCPEpiC	choroid plexus:	n/a
25	chr3:195077618-195077668	PFSK-1	brain:	n/a
26	chr3:195102265-195102315	AG09319	gingival:	n/a
27	chr3:195087778-195087828	HMEC	breast:	n/a
28	chr3:195077618-195077668	HCT-116	colon:	n/a
29	chr3:195087778-195087828	PANC-1	pancreas:	n/a
30	chr3:195077618-195077668	ECC-1	luminal epithelium:	n/a
31	chr3:195077618-195077668	MCF10A-Er-Src	breast:	n/a
32	chr3:195077618-195077668	HRE	kidney:	n/a
33	chr3:195102265-195102315	ProgFib	skin:	n/a
34	chr3:195102265-195102315	K562	blood:	n/a
35	chr3:195077618-195077668	HUVEC	blood vessel:	n/a
36	chr3:195087778-195087828	HIPEpiC	eye:	n/a
37	chr3:195102265-195102315	HRPEpiC	eye:	n/a
38	chr3:195077618-195077668	HCM	heart:	n/a
39	chr3:195087778-195087828	ECC-1	luminal epithelium:	n/a
40	chr3:195087778-195087828	MCF-7	breast:	n/a
41	chr3:195102265-195102315	IMR90	lung:	fetal
42	chr3:195077618-195077668	LNCaP	prostate:	n/a
43	chr3:195087778-195087828	MCF10A-Er-Src	breast:	n/a
44	chr3:195087778-195087828	SK-N-SH_RA	brain:	n/a
45	chr3:195087778-195087828	H1-hESC	embryonic stem cell:	embryo
46	chr3:195102265-195102315	CMK	blood:	n/a
47	chr3:195102265-195102315	HAEpiC	amniotic membrane:	n/a
48	chr3:195087778-195087828	AG04450	lung:	fetal
49	chr3:195102265-195102315	HCT-116	colon:	n/a
50	chr3:195087778-195087828	BJ	skin:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:195086495..195088641-chr3:195116660..195118594,2	K562	blood:
2	chr3:195152582..195154526-chr3:195161625..195163780,3	K562	blood:
3	chr3:195100963..195103104-chr3:195112352..195114705,2	MCF-7	breast:
4	chr3:195078115..195080618-chr3:195098644..195100393,2	K562	blood:
5	chr3:195112021..195114913-chr3:195121737..195123934,2	K562	blood:
6	chr3:195097533..195099212-chr3:195100181..195102038,2	MCF-7	breast:
7	chr3:195152779..195154771-chr3:195162258..195164678,3	MCF-7	breast:
8	chr3:195137707..195139591-chr3:195140470..195142903,2	MCF-7	breast:
9	chr3:195150893..195158887-chr3:195161492..195167356,11	K562	blood:
10	chr3:195115819..195117385-chr3:195118245..195120989,2	K562	blood:
11	chr3:195107747..195110594-chr3:195131187..195133391,2	MCF-7	breast:
12	chr3:195055975..195058560-chr3:195058914..195061074,2	K562	blood:
13	chr3:195151499..195154250-chr3:195155188..195159496,5	K562	blood:
14	chr3:195106101..195107795-chr3:195127208..195129590,2	MCF-7	breast:
15	chr3:195097533..195099212-chr3:195100181..195102038,2	MCF-7	breast:
16	chr3:195114422..195115970-chr3:195117512..195119641,2	MCF-7	breast:
17	chr3:195137797..195139503-chr3:195140426..195142233,2	K562	blood:
18	chr3:195155869..195158783-chr3:195162200..195163849,3	MCF-7	breast:
19	chr3:195069594..195071491-chr3:195086274..195088422,2	K562	blood:
20	chr3:195112021..195114749-chr3:195120473..195123237,3	K562	blood:
21	chr3:195137797..195139503-chr3:195140426..195142233,2	K562	blood:
22	chr3:195118569..195121497-chr3:195125322..195127616,3	K562	blood:
23	chr3:195140418..195142726-chr3:195147960..195149688,2	K562	blood:
24	chr3:195107747..195110594-chr3:195131187..195133391,2	MCF-7	breast:
25	chr3:195106649..195108609-chr3:195109731..195111728,2	K562	blood:
26	chr3:195145480..195148513-chr3:195161599..195165057,3	K562	blood:
27	chr3:195073143..195075655-chr3:195078501..195080208,2	K562	blood:
28	chr3:195139843..195142071-chr3:195162223..195164874,2	MCF-7	breast:
29	chr3:195086495..195088641-chr3:195116660..195118594,2	K562	blood:
30	chr3:195115819..195117385-chr3:195118245..195120989,2	K562	blood:
31	chr3:195149095..195152124-chr3:195158783..195163534,4	MCF-7	breast:
32	chr3:195073143..195075655-chr3:195078501..195080208,2	K562	blood:
33	chr3:195106101..195107795-chr3:195127208..195129590,2	MCF-7	breast:
34	chr3:195058126..195060411-chr3:195174177..195176241,2	K562	blood:
35	chr3:195140758..195142761-chr3:195162316..195165010,2	MCF-7	breast:
36	chr3:195138714..195141452-chr3:195144940..195147582,4	K562	blood:
37	chr3:195112021..195114913-chr3:195121737..195123934,2	K562	blood:
38	chr3:195081898..195084336-chr3:195160220..195162508,2	K562	blood:
39	chr3:195140418..195142726-chr3:195147960..195149688,2	K562	blood:
40	chr3:195078115..195080618-chr3:195098644..195100393,2	K562	blood:
41	chr3:195147386..195148942-chr3:195155792..195158079,2	MCF-7	breast:
42	chr3:195068888..195071135-chr3:195078131..195080514,2	MCF-7	breast:
43	chr3:195139973..195142726-chr3:195146764..195149688,2	K562	blood:
44	chr3:195112021..195114749-chr3:195120473..195123237,3	K562	blood:
45	chr3:195147386..195148942-chr3:195155792..195158079,2	MCF-7	breast:
46	chr3:195109170..195110798-chr3:195111996..195115917,3	K562	blood:
47	chr3:195106649..195108609-chr3:195109731..195111728,2	K562	blood:
48	chr3:195151499..195154250-chr3:195155188..195159496,5	K562	blood:
49	chr3:195127749..195130256-chr3:195162538..195164102,2	K562	blood:
50	chr3:195145080..195147347-chr3:195150908..195152978,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACAP2-1	chr3:195157857-195159161	refGeneNc_4303_NR_033944
2	lnc-MUC20-11	chr3:195070393-195070759	NONHSAT094153

No data

Variant related genes	Relation type
ACAP2	TF binding region
ENSG00000227433	TF binding region
ENSG00000207368	TF binding region
ACAP2	CpG island
ENSG00000227433	CpG island
ENSG00000207368	CpG island
ENSG00000227433	chromatin interactions
ENSG00000173950	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000207368	chromatin interactions

Extended variants
information (count: 3780 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3780 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9288744	chr3:195058837-195058838	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537832984	chr3:195058938-195058939	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs138477357	chr3:195058958-195058959	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs550134470	chr3:195058984-195058985	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559275074	chr3:195058998-195058999	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532576836	chr3:195059003-195059004	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568339744	chr3:195059077-195059078	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs73206692	chr3:195059112-195059113	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs553699759	chr3:195059154-195059155	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563942453	chr3:195059158-195059159	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs545655019	chr3:195059166-195059167	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11920942	chr3:195059210-195059211	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs115448740	chr3:195059278-195059279	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs576067043	chr3:195059279-195059280	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143997649	chr3:195059284-195059285	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7618499	chr3:195059315-195059316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs150940658	chr3:195059345-195059346	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574268993	chr3:195059385-195059386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541672740	chr3:195059501-195059502	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532933196	chr3:195059523-195059524	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs12488562	chr3:195059550-195059551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533570127	chr3:195059624-195059625	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs202033055	chr3:195059627-195059628	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374533874	chr3:195059648-195059649	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192098585	chr3:195059682-195059683	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs564156142	chr3:195059690-195059691	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs368637232	chr3:195059700-195059701	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs531363325	chr3:195059809-195059810	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs552581608	chr3:195059812-195059813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs371798863	chr3:195059852-195059853	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs184978628	chr3:195059870-195059871	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546302317	chr3:195059915-195059916	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372930541	chr3:195059939-195059940	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs189364261	chr3:195059985-195059986	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs529183040	chr3:195060068-195060069	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547622010	chr3:195060128-195060129	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs4677828	chr3:195060129-195060130	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs539608891	chr3:195060159-195060160	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs113717605	chr3:195060217-195060218	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs201981169	chr3:195060265-195060266	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs4677829	chr3:195060266-195060267	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs569838691	chr3:195060294-195060295	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs34320588	chr3:195060299-195060300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs4677830	chr3:195060343-195060344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs75876701	chr3:195060360-195060361	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs567485295	chr3:195060415-195060416	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs536017911	chr3:195060417-195060418	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs73890782	chr3:195060447-195060448	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553621295	chr3:195060458-195060459	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs78340680	chr3:195060473-195060474	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2036 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194992600-195090000	Weak transcription	Aorta	Aorta
2	chr3:194993000-195076000	Weak transcription	Fetal Heart	heart
3	chr3:195004000-195066600	Weak transcription	Small Intestine	intestine
4	chr3:195010000-195061000	Weak transcription	Fetal Kidney	kidney
5	chr3:195010000-195076400	Weak transcription	Brain Angular Gyrus	brain
6	chr3:195022600-195073400	Weak transcription	HMEC	breast
7	chr3:195022800-195073400	Weak transcription	NHEK	skin
8	chr3:195034800-195076800	Weak transcription	Psoas Muscle	Psoas
9	chr3:195040400-195062600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr3:195040400-195064800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr3:195040400-195066000	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr3:195040400-195076400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr3:195040400-195076600	Weak transcription	Brain Anterior Caudate	brain
14	chr3:195040400-195079400	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr3:195040400-195108400	Weak transcription	Colonic Mucosa	Colon
16	chr3:195040600-195059000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr3:195040600-195111200	Weak transcription	Fetal Brain Male	brain
18	chr3:195040800-195071200	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr3:195040800-195072800	Weak transcription	K562	blood
20	chr3:195040800-195073200	Weak transcription	Pancreas	Pancrea
21	chr3:195040800-195076400	Weak transcription	Brain Hippocampus Middle	brain
22	chr3:195041000-195062600	Weak transcription	Brain Germinal Matrix	brain
23	chr3:195041000-195065400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr3:195041000-195066400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:195041000-195067200	Weak transcription	Brain Substantia Nigra	brain
26	chr3:195041000-195077000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr3:195041000-195131200	Weak transcription	Gastric	stomach
28	chr3:195041200-195077200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr3:195041400-195064800	Strong transcription	Primary B cells from cord blood	blood
30	chr3:195041400-195076800	Weak transcription	Rectal Smooth Muscle	rectum
31	chr3:195041600-195061200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr3:195041600-195062200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr3:195041600-195071600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr3:195041600-195073600	Weak transcription	NHLF	lung
35	chr3:195041600-195077800	Weak transcription	Fetal Brain Female	brain
36	chr3:195042200-195062400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr3:195045800-195065200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:195048200-195059000	Weak transcription	Hela-S3	cervix
39	chr3:195048200-195061200	Weak transcription	NHDF-Ad	bronchial
40	chr3:195048800-195076800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr3:195049600-195106000	Weak transcription	HUVEC	blood vessel
42	chr3:195050400-195062600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr3:195051800-195073800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr3:195051800-195077000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr3:195052000-195060800	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr3:195052000-195061800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:195052000-195062400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr3:195052000-195071400	Weak transcription	HepG2	liver
49	chr3:195052000-195076400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr3:195052200-195060800	Weak transcription	Rectal Mucosa Donor 29	rectum

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