Variant report

Variant	nsv834628
Chromosome Location	chr3:20265608-20424087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1064)
CpG islands
(count:245)
Chromatin interactive
region (count:61)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1064 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20364750-20365312	K562	blood:	n/a	n/a
2	ARID3A	chr3:20366598-20367214	K562	blood:	n/a	n/a
3	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:20368591-20368761	K562	blood:	n/a	n/a
5	ARID3A	chr3:20361861-20362463	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:20363620-20364094	K562	blood:	n/a	chr3:20363734-20363750
7	ARID3A	chr3:20267278-20267600	K562	blood:	n/a	n/a
8	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
9	ARID3A	chr3:20362800-20363279	K562	blood:	n/a	n/a
10	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
11	ARID3A	chr3:20371522-20371864	K562	blood:	n/a	n/a
12	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
13	ATF1	chr3:20346503-20346616	K562	blood:	n/a	n/a
14	ATF1	chr3:20364790-20365451	K562	blood:	n/a	n/a
15	ATF1	chr3:20366606-20366910	K562	blood:	n/a	n/a
16	ATF2	chr3:20288131-20288515	GM12878	blood:	n/a	n/a
17	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr3:20288074-20288600	GM12878	blood:	n/a	n/a
19	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
20	BACH1	chr3:20366536-20366578	K562	blood:	n/a	n/a
21	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr3:20363669-20363903	K562	blood:	n/a	n/a
23	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
24	BACH1	chr3:20394371-20394578	K562	blood:	n/a	n/a
25	BATF	chr3:20277379-20277647	GM12878	blood:	n/a	n/a
26	BATF	chr3:20288183-20288438	GM12878	blood:	n/a	chr3:20288290-20288301
27	BATF	chr3:20277377-20277645	GM12878	blood:	n/a	n/a
28	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
29	BATF	chr3:20288158-20288422	GM12878	blood:	n/a	chr3:20288290-20288301
30	BCL11A	chr3:20288232-20288418	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:20288193-20288461	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:20371437-20371693	H1-hESC	embryonic stem cell:	n/a	n/a
33	BHLHE40	chr3:20366210-20366396	K562	blood:	n/a	n/a
34	BHLHE40	chr3:20394266-20394730	K562	blood:	n/a	n/a
35	BHLHE40	chr3:20361903-20362390	HepG2	liver:	n/a	n/a
36	BHLHE40	chr3:20371536-20371904	K562	blood:	n/a	n/a
37	BHLHE40	chr3:20355407-20355580	A549	lung:	n/a	n/a
38	BHLHE40	chr3:20306641-20306956	K562	blood:	n/a	n/a
39	BHLHE40	chr3:20381816-20382255	K562	blood:	n/a	n/a
40	BHLHE40	chr3:20364697-20365365	K562	blood:	n/a	n/a
41	BRCA1	chr3:20381852-20382113	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr3:20364770-20365367	K562	blood:	n/a	n/a
43	CBX3	chr3:20324344-20324598	K562	blood:	n/a	n/a
44	CBX3	chr3:20347694-20347925	K562	blood:	n/a	n/a
45	CBX3	chr3:20324264-20324647	K562	blood:	n/a	n/a
46	CBX3	chr3:20394150-20394723	K562	blood:	n/a	chr3:20394644-20394655
47	CBX3	chr3:20346385-20346769	K562	blood:	n/a	n/a
48	CBX3	chr3:20347626-20347963	K562	blood:	n/a	n/a
49	CBX3	chr3:20366551-20367349	K562	blood:	n/a	n/a
50	CCNT2	chr3:20364768-20365575	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20321584-20321634	SAEC	small airway:	n/a
2	chr3:20321584-20321634	SAEC	small airway:	n/a
3	chr3:20371290-20371340	K562	blood:	n/a
4	chr3:20321584-20321634	AoSMC	blood vessel:	n/a
5	chr3:20418856-20418906	HL-60	blood:	n/a
6	chr3:20371290-20371340	HepG2	liver:	n/a
7	chr3:20371290-20371340	BE2_C	brain:	n/a
8	chr3:20418856-20418906	H1-hESC	embryonic stem cell:	embryo
9	chr3:20321584-20321634	GM19239	blood:	n/a
10	chr3:20371290-20371340	GM12892	blood:	n/a
11	chr3:20418856-20418906	SK-N-MC	brain:	n/a
12	chr3:20412342-20412392	GM06990	blood:	n/a
13	chr3:20321584-20321634	BJ	skin:	n/a
14	chr3:20371290-20371340	Caco-2	colon:	n/a
15	chr3:20412342-20412392	BJ	skin:	n/a
16	chr3:20321584-20321634	AG09309	skin:	n/a
17	chr3:20371290-20371340	HMEC	breast:	n/a
18	chr3:20371290-20371340	GM12878	blood:	n/a
19	chr3:20321584-20321634	Hepatocyte	liver:	n/a
20	chr3:20412342-20412392	HRCEpiC	kidney:	n/a
21	chr3:20321584-20321634	Jurkat	blood:	n/a
22	chr3:20321584-20321634	LNCaP	prostate:	n/a
23	chr3:20321584-20321634	HepG2	liver:	n/a
24	chr3:20371290-20371340	HRPEpiC	eye:	n/a
25	chr3:20371290-20371340	Jurkat	blood:	n/a
26	chr3:20418856-20418906	BJ	skin:	n/a
27	chr3:20371290-20371340	NB4	blood:	n/a
28	chr3:20412342-20412392	HCM	heart:	n/a
29	chr3:20412342-20412392	AG09309	skin:	n/a
30	chr3:20418856-20418906	HEEpiC	esophagus:	n/a
31	chr3:20418856-20418906	SAEC	small airway:	n/a
32	chr3:20321584-20321634	HEK293	kidney:	embryo
33	chr3:20418856-20418906	GM19239	blood:	n/a
34	chr3:20418856-20418906	AG09309	skin:	n/a
35	chr3:20412342-20412392	PANC-1	pancreas:	n/a
36	chr3:20371290-20371340	ProgFib	skin:	n/a
37	chr3:20371290-20371340	MCF-7	breast:	n/a
38	chr3:20418856-20418906	HEK293	kidney:	embryo
39	chr3:20371290-20371340	SK-N-SH_RA	brain:	n/a
40	chr3:20412342-20412392	NHBE	bronchial:	n/a
41	chr3:20418856-20418906	GM12878	blood:	n/a
42	chr3:20418856-20418906	HCT-116	colon:	n/a
43	chr3:20412342-20412392	NHDF-neo	bronchial:	n/a
44	chr3:20321584-20321634	SK-N-SH	brain:	n/a
45	chr3:20412342-20412392	Caco-2	colon:	n/a
46	chr3:20371290-20371340	HCF	heart:	n/a
47	chr3:20412342-20412392	Hepatocyte	liver:	n/a
48	chr3:20418856-20418906	Caco-2	colon:	n/a
49	chr3:20321584-20321634	HCPEpiC	choroid plexus:	n/a
50	chr3:20321584-20321634	AG04449	skin:	fetal

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
2	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
3	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
4	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
5	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
6	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
7	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
8	chr3:20365682..20367813-chr3:20369993..20373801,3	K562	blood:
9	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
10	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
11	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
12	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
13	chr3:20255206..20257186-chr3:20272224..20273896,2	K562	blood:
14	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
15	chr3:20225982..20227551-chr3:20349845..20352725,2	K562	blood:
16	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
17	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
18	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:
19	chr3:20381671..20382483-chr3:21592493..21593315,3	MCF-7	breast:
20	chr3:20381763..20382471-chr3:21525223..21526354,4	MCF-7	breast:
21	chr3:20381636..20382451-chr3:20971371..20972187,4	MCF-7	breast:
22	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
23	chr3:20378280..20380658-chr3:21571258..21574044,2	K562	blood:
24	chr3:20358544..20361265-chr3:20365566..20368705,3	K562	blood:
25	chr3:20358544..20361265-chr3:20365566..20368705,3	K562	blood:
26	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
27	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
28	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
29	chr3:20363426..20365605-chr3:20367558..20369154,2	K562	blood:
30	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
31	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
32	chr3:20267223..20267887-chr3:21592292..21593221,2	MCF-7	breast:
33	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
34	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
35	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
36	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
37	chr3:20369262..20370826-chr3:20371574..20373222,2	K562	blood:
38	chr3:20358467..20362257-chr3:20366935..20370675,4	K562	blood:
39	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
40	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
41	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
42	chr3:20269133..20272394-chr3:20272728..20275710,3	K562	blood:
43	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
44	chr20:55749599..55750399-chr3:20381742..20382481,2	MCF-7	breast:
45	chr3:20352341..20352841-chr6:144261197..144261734,2	MCF-7	breast:
46	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
47	chr3:20363426..20365605-chr3:20367558..20369154,2	K562	blood:
48	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:
49	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
50	chr3:20365682..20367813-chr3:20369993..20373801,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595
2	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
3	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
4	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595
5	lnc-KAT2B-6	chr3:20286533-20287951	NONHSAT088619
6	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595
7	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
8	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
9	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
10	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622

No data

Variant related genes	Relation type
RNU6-822P	TF binding region
ENSG00000231304	TF binding region
RNU6-822P	CpG island
ENSG00000231304	CpG island

Extended variants
information (count: 5657 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:5657 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542033063	chr3:20265615-20265616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576004216	chr3:20265637-20265638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537485857	chr3:20265665-20265666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75507184	chr3:20265670-20265671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577514863	chr3:20265702-20265703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77653538	chr3:20265703-20265704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114927338	chr3:20265748-20265749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575104409	chr3:20265770-20265771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs61207556	chr3:20265812-20265813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs371551237	chr3:20265906-20265907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560993833	chr3:20265913-20265914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531194439	chr3:20265979-20265980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147381974	chr3:20266032-20266033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561892442	chr3:20266052-20266053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74500624	chr3:20266149-20266150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532394186	chr3:20266156-20266157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547390775	chr3:20266380-20266381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115216156	chr3:20266465-20266466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2365799	chr3:20266516-20266517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548259454	chr3:20266539-20266540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190130708	chr3:20266602-20266603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534833415	chr3:20266645-20266646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs74320031	chr3:20266692-20266693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79701174	chr3:20266735-20266736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368071808	chr3:20266785-20266786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182725620	chr3:20266839-20266840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535291660	chr3:20266859-20266860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533607951	chr3:20266866-20266867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188495360	chr3:20266948-20266949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147560568	chr3:20266963-20266964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200198921	chr3:20267012-20267013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542478981	chr3:20267045-20267046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560957073	chr3:20267120-20267121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371789840	chr3:20267125-20267126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139436136	chr3:20267177-20267178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564860566	chr3:20267275-20267276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192905147	chr3:20267281-20267282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565785189	chr3:20267332-20267333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77091460	chr3:20267464-20267465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150062983	chr3:20267477-20267478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs184029835	chr3:20267530-20267531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548185880	chr3:20267533-20267534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4858778	chr3:20267543-20267544	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs188926205	chr3:20267551-20267552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs78078666	chr3:20267561-20267562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552406413	chr3:20267570-20267571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372146294	chr3:20267632-20267633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570797541	chr3:20267647-20267648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534739840	chr3:20267673-20267674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556868471	chr3:20267674-20267675	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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

Chromatin state (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20264200-20267600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr3:20264800-20267000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:20265000-20265800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr3:20265000-20265800	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr3:20265200-20267600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:20265800-20267200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:20267000-20268000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr3:20267200-20267800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:20267200-20269800	Enhancers	Liver	Liver
10	chr3:20267400-20267800	Enhancers	Brain Hippocampus Middle	brain
11	chr3:20267600-20267800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:20267600-20267800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:20267600-20267800	Enhancers	Fetal Brain Male	brain
14	chr3:20268000-20271400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr3:20269800-20270400	Flanking Active TSS	Liver	Liver
16	chr3:20270000-20270200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr3:20270400-20271800	Enhancers	Liver	Liver
18	chr3:20271400-20271600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr3:20271800-20272600	Flanking Active TSS	Liver	Liver
20	chr3:20272600-20276000	Enhancers	Liver	Liver
21	chr3:20273400-20273800	Enhancers	Fetal Intestine Large	intestine
22	chr3:20273600-20274600	Enhancers	Fetal Intestine Small	intestine
23	chr3:20273800-20275200	Weak transcription	Fetal Intestine Large	intestine
24	chr3:20274400-20277200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr3:20274600-20275000	Weak transcription	Fetal Intestine Small	intestine
26	chr3:20274600-20275400	Enhancers	Fetal Kidney	kidney
27	chr3:20274600-20275400	Enhancers	Fetal Lung	lung
28	chr3:20275000-20275600	Enhancers	Fetal Intestine Small	intestine
29	chr3:20275200-20275600	Enhancers	Fetal Intestine Large	intestine
30	chr3:20275600-20278000	Weak transcription	Fetal Intestine Large	intestine
31	chr3:20275600-20278000	Weak transcription	Fetal Intestine Small	intestine
32	chr3:20276000-20276600	Weak transcription	Liver	Liver
33	chr3:20276600-20278600	Enhancers	Liver	Liver
34	chr3:20276800-20277400	Enhancers	GM12878-XiMat	blood
35	chr3:20277200-20277400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr3:20278000-20278400	Enhancers	Fetal Intestine Small	intestine
37	chr3:20278000-20278600	Enhancers	Fetal Intestine Large	intestine
38	chr3:20278000-20278600	Enhancers	Stomach Mucosa	stomach
39	chr3:20278400-20282200	Weak transcription	Fetal Intestine Small	intestine
40	chr3:20278600-20282000	Weak transcription	Liver	Liver
41	chr3:20281200-20282400	Enhancers	Ovary	ovary
42	chr3:20281400-20282800	Enhancers	Aorta	Aorta
43	chr3:20281600-20282000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr3:20281600-20282000	Enhancers	Spleen	Spleen
45	chr3:20281600-20282600	Enhancers	Esophagus	oesophagus
46	chr3:20282800-20284000	Weak transcription	Aorta	Aorta
47	chr3:20284000-20284200	Enhancers	Aorta	Aorta
48	chr3:20287200-20289000	Enhancers	GM12878-XiMat	blood
49	chr3:20291800-20292200	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr3:20291800-20292400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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