Variant report

Variant	nsv876599
Chromosome Location	chr3:20264950-20813009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2344)
CpG islands
(count:549)
Chromatin interactive
region (count:114)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2344 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20630843-20631125	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
3	ARID3A	chr3:20553373-20553610	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:20363620-20364094	K562	blood:	n/a	chr3:20363734-20363750
6	ARID3A	chr3:20722557-20722641	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:20361861-20362463	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:20267278-20267600	K562	blood:	n/a	n/a
9	ARID3A	chr3:20371522-20371864	K562	blood:	n/a	n/a
10	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
11	ARID3A	chr3:20362800-20363279	K562	blood:	n/a	n/a
12	ARID3A	chr3:20366598-20367214	K562	blood:	n/a	n/a
13	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
14	ARID3A	chr3:20368591-20368761	K562	blood:	n/a	n/a
15	ARID3A	chr3:20364750-20365312	K562	blood:	n/a	n/a
16	ATF1	chr3:20364790-20365451	K562	blood:	n/a	n/a
17	ATF1	chr3:20710817-20710996	K562	blood:	n/a	n/a
18	ATF1	chr3:20521702-20521870	K562	blood:	n/a	n/a
19	ATF1	chr3:20346503-20346616	K562	blood:	n/a	n/a
20	ATF1	chr3:20366606-20366910	K562	blood:	n/a	n/a
21	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr3:20288131-20288515	GM12878	blood:	n/a	n/a
23	ATF2	chr3:20288074-20288600	GM12878	blood:	n/a	n/a
24	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
25	BACH1	chr3:20699095-20699443	K562	blood:	n/a	n/a
26	BACH1	chr3:20535546-20535645	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
28	BACH1	chr3:20363669-20363903	K562	blood:	n/a	n/a
29	BACH1	chr3:20649604-20649855	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr3:20394371-20394578	K562	blood:	n/a	n/a
31	BACH1	chr3:20492146-20492486	K562	blood:	n/a	n/a
32	BACH1	chr3:20699083-20699427	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr3:20366536-20366578	K562	blood:	n/a	n/a
34	BACH1	chr3:20536253-20536368	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr3:20616608-20616882	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr3:20578833-20579051	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr3:20492139-20492474	H1-hESC	embryonic stem cell:	n/a	n/a
39	BATF	chr3:20277379-20277647	GM12878	blood:	n/a	n/a
40	BATF	chr3:20288183-20288438	GM12878	blood:	n/a	chr3:20288290-20288301
41	BATF	chr3:20277377-20277645	GM12878	blood:	n/a	n/a
42	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
43	BATF	chr3:20288158-20288422	GM12878	blood:	n/a	chr3:20288290-20288301
44	BCL11A	chr3:20288193-20288461	GM12878	blood:	n/a	n/a
45	BCL11A	chr3:20371437-20371693	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL11A	chr3:20288232-20288418	GM12878	blood:	n/a	n/a
47	BHLHE40	chr3:20371536-20371904	K562	blood:	n/a	n/a
48	BHLHE40	chr3:20306641-20306956	K562	blood:	n/a	n/a
49	BHLHE40	chr3:20355407-20355580	A549	lung:	n/a	n/a
50	BHLHE40	chr3:20394266-20394730	K562	blood:	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	chr3:20575513-20575563	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:20418856-20418906	PrEC	prostate:	n/a
3	chr3:20321584-20321634	Jurkat	blood:	n/a
4	chr3:20589671-20589721	GM19239	blood:	n/a
5	chr3:20575513-20575563	CMK	blood:	n/a
6	chr3:20448283-20448333	A549	lung:	n/a
7	chr3:20412342-20412392	PFSK-1	brain:	n/a
8	chr3:20589671-20589721	H1-hESC	embryonic stem cell:	embryo
9	chr3:20321584-20321634	BJ	skin:	n/a
10	chr3:20589760-20589810	PANC-1	pancreas:	n/a
11	chr3:20522301-20522351	HCT-116	colon:	n/a
12	chr3:20522301-20522351	HEEpiC	esophagus:	n/a
13	chr3:20522301-20522351	AG10803	skin:	n/a
14	chr3:20412342-20412392	AG04450	lung:	fetal
15	chr3:20412342-20412392	HL-60	blood:	n/a
16	chr3:20412342-20412392	HRPEpiC	eye:	n/a
17	chr3:20418856-20418906	ovcar-3	ovarian:	n/a
18	chr3:20575513-20575563	NHDF-neo	bronchial:	n/a
19	chr3:20371290-20371340	Hela-S3	cervix:	n/a
20	chr3:20522301-20522351	NH-A	brain:	n/a
21	chr3:20371290-20371340	GM12878	blood:	n/a
22	chr3:20589760-20589810	GM19239	blood:	n/a
23	chr3:20589671-20589721	HepG2	liver:	n/a
24	chr3:20589760-20589810	T-47D	breast:	n/a
25	chr3:20371290-20371340	CMK	blood:	n/a
26	chr3:20418856-20418906	HRCEpiC	kidney:	n/a
27	chr3:20418856-20418906	MCF-7	breast:	n/a
28	chr3:20418856-20418906	H1-hESC	embryonic stem cell:	embryo
29	chr3:20321584-20321634	BE2_C	brain:	n/a
30	chr3:20575513-20575563	GM12892	blood:	n/a
31	chr3:20321584-20321634	AG10803	skin:	n/a
32	chr3:20522301-20522351	HNPCEpiC	eye:	n/a
33	chr3:20522301-20522351	HRCEpiC	kidney:	n/a
34	chr3:20418856-20418906	NHBE	bronchial:	n/a
35	chr3:20412342-20412392	Jurkat	blood:	n/a
36	chr3:20412342-20412392	HCPEpiC	choroid plexus:	n/a
37	chr3:20321584-20321634	AoSMC	blood vessel:	n/a
38	chr3:20321584-20321634	HEEpiC	esophagus:	n/a
39	chr3:20412342-20412392	HIPEpiC	eye:	n/a
40	chr3:20589671-20589721	GM12892	blood:	n/a
41	chr3:20371290-20371340	T-47D	breast:	n/a
42	chr3:20575513-20575563	HRE	kidney:	n/a
43	chr3:20589760-20589810	CMK	blood:	n/a
44	chr3:20371290-20371340	HCM	heart:	n/a
45	chr3:20412342-20412392	SKMC	muscle:	n/a
46	chr3:20522301-20522351	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:20321584-20321634	Hela-S3	cervix:	n/a
48	chr3:20418856-20418906	U87	brain:	n/a
49	chr3:20321584-20321634	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:20418856-20418906	Jurkat	blood:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:20732321..20734802-chr3:20736101..20739228,3	K562	blood:
2	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
3	chr17:57920861..57923845-chr3:20581102..20583235,2	MCF-7	breast:
4	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
5	chr3:20618172..20620795-chr3:20622169..20624863,2	MCF-7	breast:
6	chr3:20363426..20365605-chr3:20367558..20369154,2	K562	blood:
7	chr3:20361855..20364563-chr3:20364654..20366618,2	K562	blood:
8	chr3:20801549..20804402-chr3:20814292..20816121,2	MCF-7	breast:
9	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
10	chr3:20687019..20688591-chr3:20688596..20691199,2	K562	blood:
11	chr3:20715510..20717921-chr7:148983239..148984740,2	MCF-7	breast:
12	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
13	chr3:20735218..20737625-chr3:20738921..20741166,2	MCF-7	breast:
14	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
15	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
16	chr3:20618172..20620795-chr3:20622169..20624863,2	MCF-7	breast:
17	chr3:20791529..20793078-chr3:20793887..20796565,3	K562	blood:
18	chr3:20358467..20362257-chr3:20366935..20370675,4	K562	blood:
19	chr3:20687019..20688591-chr3:20688596..20691199,2	K562	blood:
20	chr3:20791529..20793078-chr3:20793887..20796565,3	K562	blood:
21	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
22	chr3:20684159..20686441-chr3:20690637..20692411,2	K562	blood:
23	chr3:20684159..20686441-chr3:20690637..20692411,2	K562	blood:
24	chr3:20553071..20554107-chr3:20781207..20782086,3	MCF-7	breast:
25	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
26	chr17:56736117..56736939-chr3:20708807..20709685,2	MCF-7	breast:
27	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
28	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
29	chr3:20771996..20774877-chr3:20941229..20943055,2	K562	blood:
30	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
31	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
32	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
33	chr3:20269133..20272394-chr3:20272728..20275710,3	K562	blood:
34	chr3:20795079..20796913-chr3:20797062..20799579,3	MCF-7	breast:
35	chr3:20545213..20547317-chr3:20547570..20549760,2	K562	blood:
36	chr3:20746425..20748094-chr3:20975073..20978027,2	K562	blood:
37	chr3:20552973..20553911-chr3:20970672..20972125,8	MCF-7	breast:
38	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
39	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
40	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
41	chr3:20800581..20802290-chr3:20809522..20812257,2	K562	blood:
42	chr3:20514130..20516158-chr3:20517415..20519398,2	K562	blood:
43	chr3:20795079..20796913-chr3:20797062..20799579,3	MCF-7	breast:
44	chr3:20381636..20382451-chr3:20971371..20972187,4	MCF-7	breast:
45	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
46	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
47	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
48	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
49	chr3:20691277..20693337-chr3:20693426..20695477,2	MCF-7	breast:
50	chr3:20711400..20713632-chr3:20716289..20718523,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595
2	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
3	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622
4	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1
5	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
6	lnc-KAT2B-8	chr3:20755529-20756407	NONHSAT088630
7	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
8	lnc-KAT2B-8	chr3:20747491-20747580	NONHSAT088630
9	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595
10	lnc-KAT2B-6	chr3:20286533-20287951	NONHSAT088619
11	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
12	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
13	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595

No data

Variant related genes	Relation type
ENSG00000261734	TF binding region
RNU6-815P	TF binding region
RNU6-822P	TF binding region
ENSG00000231304	TF binding region
ENSG00000261734	CpG island
RNU6-815P	CpG island
RNU6-822P	CpG island
ENSG00000231304	CpG island
ENSG00000202077	chromatin interactions
ENSG00000252557	chromatin interactions
ENSG00000244560	chromatin interactions
ENSG00000206807	chromatin interactions

Extended variants
information (count: 13123 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:13123 , 50 per page) page: 1 2 3 4 5 6 7 ... 263

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs952466	chr3:20264950-20264951	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556437433	chr3:20264970-20264971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568355599	chr3:20264978-20264979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145626643	chr3:20264985-20264986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375726870	chr3:20264986-20264987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190057970	chr3:20265098-20265099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566825263	chr3:20265115-20265116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112263168	chr3:20265121-20265122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138157603	chr3:20265147-20265148	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554502776	chr3:20265152-20265153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149533778	chr3:20265177-20265178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2135936	chr3:20265248-20265249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187194862	chr3:20265263-20265264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532579205	chr3:20265272-20265273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541652410	chr3:20265288-20265289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17006762	chr3:20265289-20265290	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs527336709	chr3:20265345-20265346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549111433	chr3:20265357-20265358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191018753	chr3:20265377-20265378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531356002	chr3:20265379-20265380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182451890	chr3:20265390-20265391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556266936	chr3:20265472-20265473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571553433	chr3:20265485-20265486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79959735	chr3:20265493-20265494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185617847	chr3:20265505-20265506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144085397	chr3:20265545-20265546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115635567	chr3:20265559-20265560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111779334	chr3:20265581-20265582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542033063	chr3:20265615-20265616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576004216	chr3:20265637-20265638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537485857	chr3:20265665-20265666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75507184	chr3:20265670-20265671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577514863	chr3:20265702-20265703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77653538	chr3:20265703-20265704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114927338	chr3:20265748-20265749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575104409	chr3:20265770-20265771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61207556	chr3:20265812-20265813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371551237	chr3:20265906-20265907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560993833	chr3:20265913-20265914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531194439	chr3:20265979-20265980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147381974	chr3:20266032-20266033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561892442	chr3:20266052-20266053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74500624	chr3:20266149-20266150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532394186	chr3:20266156-20266157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547390775	chr3:20266380-20266381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115216156	chr3:20266465-20266466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2365799	chr3:20266516-20266517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548259454	chr3:20266539-20266540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190130708	chr3:20266602-20266603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534833415	chr3:20266645-20266646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20260200-20265000	Weak transcription	Fetal Stomach	stomach
2	chr3:20262600-20265600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:20262800-20265200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:20264000-20265000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:20264200-20265200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:20264200-20267600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr3:20264600-20265200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr3:20264800-20265200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:20264800-20265600	Enhancers	Adipose Nuclei	Adipose
10	chr3:20264800-20267000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:20265000-20265200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:20265000-20265400	Enhancers	Fetal Stomach	stomach
13	chr3:20265000-20265800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:20265000-20265800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr3:20265200-20267600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:20265800-20267200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:20267000-20268000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr3:20267200-20267800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr3:20267200-20269800	Enhancers	Liver	Liver
20	chr3:20267400-20267800	Enhancers	Brain Hippocampus Middle	brain
21	chr3:20267600-20267800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:20267600-20267800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr3:20267600-20267800	Enhancers	Fetal Brain Male	brain
24	chr3:20268000-20271400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr3:20269800-20270400	Flanking Active TSS	Liver	Liver
26	chr3:20270000-20270200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr3:20270400-20271800	Enhancers	Liver	Liver
28	chr3:20271400-20271600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr3:20271800-20272600	Flanking Active TSS	Liver	Liver
30	chr3:20272600-20276000	Enhancers	Liver	Liver
31	chr3:20273400-20273800	Enhancers	Fetal Intestine Large	intestine
32	chr3:20273600-20274600	Enhancers	Fetal Intestine Small	intestine
33	chr3:20273800-20275200	Weak transcription	Fetal Intestine Large	intestine
34	chr3:20274400-20277200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr3:20274600-20275000	Weak transcription	Fetal Intestine Small	intestine
36	chr3:20274600-20275400	Enhancers	Fetal Kidney	kidney
37	chr3:20274600-20275400	Enhancers	Fetal Lung	lung
38	chr3:20275000-20275600	Enhancers	Fetal Intestine Small	intestine
39	chr3:20275200-20275600	Enhancers	Fetal Intestine Large	intestine
40	chr3:20275600-20278000	Weak transcription	Fetal Intestine Large	intestine
41	chr3:20275600-20278000	Weak transcription	Fetal Intestine Small	intestine
42	chr3:20276000-20276600	Weak transcription	Liver	Liver
43	chr3:20276600-20278600	Enhancers	Liver	Liver
44	chr3:20276800-20277400	Enhancers	GM12878-XiMat	blood
45	chr3:20277200-20277400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr3:20278000-20278400	Enhancers	Fetal Intestine Small	intestine
47	chr3:20278000-20278600	Enhancers	Fetal Intestine Large	intestine
48	chr3:20278000-20278600	Enhancers	Stomach Mucosa	stomach
49	chr3:20278400-20282200	Weak transcription	Fetal Intestine Small	intestine
50	chr3:20278600-20282000	Weak transcription	Liver	Liver

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