Variant report

Variant	nsv459943
Chromosome Location	chr2:169756930-169799010
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:612)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:169777121-169777531	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:169775223-169775312	K562	blood:	n/a	n/a
3	ARID3A	chr2:169797892-169798475	K562	blood:	n/a	n/a
4	ARID3A	chr2:169792336-169793247	K562	blood:	n/a	n/a
5	ARID3A	chr2:169777082-169777494	K562	blood:	n/a	n/a
6	ATF1	chr2:169792194-169793101	K562	blood:	n/a	n/a
7	ATF1	chr2:169764852-169765181	K562	blood:	n/a	n/a
8	ATF1	chr2:169797936-169798078	K562	blood:	n/a	n/a
9	ATF2	chr2:169796331-169796855	GM12878	blood:	n/a	n/a
10	ATF3	chr2:169792385-169793031	K562	blood:	n/a	n/a
11	BACH1	chr2:169777116-169777307	K562	blood:	n/a	n/a
12	BACH1	chr2:169792614-169792814	K562	blood:	n/a	n/a
13	BACH1	chr2:169770937-169771086	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:169798189-169798368	K562	blood:	n/a	n/a
15	BATF	chr2:169796430-169796832	GM12878	blood:	n/a	n/a
16	BATF	chr2:169796401-169796869	GM12878	blood:	n/a	n/a
17	BCL3	chr2:169792532-169792882	K562	blood:	n/a	n/a
18	BCLAF1	chr2:169792451-169793033	K562	blood:	n/a	n/a
19	BHLHE40	chr2:169792005-169793016	K562	blood:	n/a	n/a
20	CBX3	chr2:169792347-169793039	K562	blood:	n/a	n/a
21	CBX3	chr2:169792124-169793154	K562	blood:	n/a	n/a
22	CBX3	chr2:169772027-169772582	K562	blood:	n/a	n/a
23	CBX3	chr2:169764781-169765361	K562	blood:	n/a	n/a
24	CBX3	chr2:169771947-169772599	K562	blood:	n/a	n/a
25	CCNT2	chr2:169792316-169793036	K562	blood:	n/a	n/a
26	CCNT2	chr2:169764887-169765118	K562	blood:	n/a	n/a
27	CCNT2	chr2:169797891-169798146	K562	blood:	n/a	n/a
28	CCNT2	chr2:169777172-169777407	K562	blood:	n/a	n/a
29	CEBPB	chr2:169766925-169767021	K562	blood:	n/a	n/a
30	CEBPB	chr2:169770012-169770324	H1-hESC	embryonic stem cell:	n/a	chr2:169770258-169770271
31	CEBPB	chr2:169792375-169792926	K562	blood:	n/a	n/a
32	CEBPB	chr2:169769997-169770357	HepG2	liver:	n/a	chr2:169770258-169770271
33	CEBPB	chr2:169792253-169793378	K562	blood:	n/a	n/a
34	CEBPB	chr2:169797889-169798201	K562	blood:	n/a	n/a
35	CEBPB	chr2:169795615-169795918	IMR90	lung:	n/a	chr2:169795775-169795792 chr2:169795780-169795791 chr2:169795780-169795789
36	CEBPB	chr2:169795603-169795959	K562	blood:	n/a	chr2:169795775-169795792 chr2:169795780-169795791 chr2:169795780-169795789
37	CEBPB	chr2:169792328-169793242	K562	blood:	n/a	n/a
38	CEBPB	chr2:169795646-169795860	A549	lung:	n/a	chr2:169795775-169795792 chr2:169795780-169795791 chr2:169795780-169795789
39	CEBPB	chr2:169777188-169777424	K562	blood:	n/a	n/a
40	CEBPB	chr2:169795599-169795938	HepG2	liver:	n/a	chr2:169795775-169795792 chr2:169795780-169795791 chr2:169795780-169795789
41	CEBPB	chr2:169769971-169770381	MCF-7	breast:	n/a	chr2:169770258-169770271
42	CEBPD	chr2:169797844-169798291	K562	blood:	n/a	n/a
43	CEBPD	chr2:169797705-169798306	K562	blood:	n/a	n/a
44	CEBPD	chr2:169792229-169793310	K562	blood:	n/a	n/a
45	CEBPD	chr2:169792237-169793172	K562	blood:	n/a	n/a
46	CHD2	chr2:169792571-169793041	K562	blood:	n/a	n/a
47	CREB1	chr2:169792176-169793290	K562	blood:	n/a	n/a
48	CTCF	chr2:169777180-169777330	K562	blood:	n/a	chr2:169777279-169777289 chr2:169777276-169777294 chr2:169777271-169777292 chr2:169777277-169777293
49	CTCF	chr2:169777577-169777660	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr2:169776888-169777996	A549	lung:	n/a	chr2:169777279-169777289 chr2:169777276-169777294 chr2:169777271-169777292 chr2:169777277-169777293

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:169756942-169756992	CMK	blood:	n/a
2	chr2:169780101-169780151	BE2_C	brain:	n/a
3	chr2:169756942-169756992	CMK	blood:	n/a
4	chr2:169780101-169780151	BE2_C	brain:	n/a
5	chr2:169757561-169757611	HUVEC	blood vessel:	n/a
6	chr2:169763832-169763882	AG09309	skin:	n/a
7	chr2:169769616-169769666	HIPEpiC	eye:	n/a
8	chr2:169763832-169763882	HL-60	blood:	n/a
9	chr2:169757561-169757611	SAEC	small airway:	n/a
10	chr2:169756942-169756992	LNCaP	prostate:	n/a
11	chr2:169769616-169769666	RPTEC	kidney:	n/a
12	chr2:169756942-169756992	A549	lung:	n/a
13	chr2:169763832-169763882	HCPEpiC	choroid plexus:	n/a
14	chr2:169769501-169769551	AG09309	skin:	n/a
15	chr2:169769616-169769666	Caco-2	colon:	n/a
16	chr2:169756942-169756992	PANC-1	pancreas:	n/a
17	chr2:169780101-169780151	Caco-2	colon:	n/a
18	chr2:169757561-169757611	T-47D	breast:	n/a
19	chr2:169757561-169757611	GM06990	blood:	n/a
20	chr2:169756942-169756992	HMEC	breast:	n/a
21	chr2:169769501-169769551	CMK	blood:	n/a
22	chr2:169769616-169769666	H1-hESC	embryonic stem cell:	embryo
23	chr2:169787256-169787306	GM19239	blood:	n/a
24	chr2:169787256-169787306	SK-N-SH_RA	brain:	n/a
25	chr2:169757618-169757668	MCF-7	breast:	n/a
26	chr2:169769616-169769666	SK-N-SH_RA	brain:	n/a
27	chr2:169769501-169769551	Hela-S3	cervix:	n/a
28	chr2:169757618-169757668	HEK293	kidney:	embryo
29	chr2:169763832-169763882	RPTEC	kidney:	n/a
30	chr2:169756942-169756992	HCT-116	colon:	n/a
31	chr2:169780101-169780151	PANC-1	pancreas:	n/a
32	chr2:169764700-169764750	HMEC	breast:	n/a
33	chr2:169769616-169769666	NHBE	bronchial:	n/a
34	chr2:169763832-169763882	HMEC	breast:	n/a
35	chr2:169764700-169764750	NHDF-neo	bronchial:	n/a
36	chr2:169769616-169769666	K562	blood:	n/a
37	chr2:169763832-169763882	HRCEpiC	kidney:	n/a
38	chr2:169757561-169757611	SK-N-SH_RA	brain:	n/a
39	chr2:169780101-169780151	MCF-7	breast:	n/a
40	chr2:169757618-169757668	GM12892	blood:	n/a
41	chr2:169769616-169769666	HMEC	breast:	n/a
42	chr2:169757780-169757830	HCPEpiC	choroid plexus:	n/a
43	chr2:169756942-169756992	GM06990	blood:	n/a
44	chr2:169757780-169757830	MCF10A-Er-Src	breast:	n/a
45	chr2:169764700-169764750	HepG2	liver:	n/a
46	chr2:169763832-169763882	SK-N-SH	brain:	n/a
47	chr2:169787256-169787306	Jurkat	blood:	n/a
48	chr2:169769616-169769666	HCT-116	colon:	n/a
49	chr2:169769501-169769551	SKMC	muscle:	n/a
50	chr2:169780101-169780151	HL-60	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:169758144..169760837-chr22:21355170..21356774,2	K562	blood:
2	chr2:169755958..169758089-chr2:169767448..169770171,2	K562	blood:
3	chr2:169757947..169761015-chr2:169767482..169770079,3	MCF-7	breast:
4	chr2:169760230..169762214-chr2:169762274..169764034,2	MCF-7	breast:
5	chr2:169798515..169802093-chr2:169802233..169805225,4	K562	blood:
6	chr2:169757947..169761015-chr2:169767482..169770079,3	MCF-7	breast:
7	chr2:169628746..169631542-chr2:169795260..169797198,2	K562	blood:
8	chr2:169627058..169629094-chr2:169775848..169778213,2	K562	blood:
9	chr2:169629920..169631115-chr2:169776779..169777787,11	K562	blood:
10	chr2:169755958..169758089-chr2:169767448..169770171,2	K562	blood:
11	chr2:169202892..169203802-chr2:169776914..169777707,3	K562	blood:
12	chr2:169786175..169787842-chr2:169790022..169792069,2	MCF-7	breast:
13	chr2:169791653..169794074-chr2:169983204..169985929,2	K562	blood:
14	chr2:169782114..169785281-chr2:169786393..169790786,5	K562	blood:
15	chr2:169756337..169758641-chr2:169759610..169762037,2	K562	blood:
16	chr2:169782114..169785281-chr2:169786393..169790786,5	K562	blood:
17	chr2:169628645..169630407-chr2:169772441..169774167,2	K562	blood:
18	chr2:169786046..169790721-chr2:169791105..169793269,7	K562	blood:
19	chr2:169792449..169795110-chr2:169797440..169799933,3	K562	blood:
20	chr2:169797130..169797902-chr4:70311918..70312713,2	MCF-7	breast:
21	chr2:169202611..169203586-chr2:169776930..169777698,2	MCF-7	breast:
22	chr2:169786175..169787842-chr2:169790022..169792069,2	MCF-7	breast:
23	chr2:169757381..169760101-chr2:169762347..169764988,3	K562	blood:
24	chr2:169746271..169749176-chr2:169755167..169756945,2	K562	blood:
25	chr2:169782114..169784208-chr2:169788090..169790755,2	K562	blood:
26	chr2:169792537..169795729-chr2:169800668..169803473,3	K562	blood:
27	chr2:169629906..169631239-chr2:169776809..169777837,8	MCF-7	breast:
28	chr2:168992688..168993571-chr2:169776875..169777426,2	K562	blood:
29	chr2:169763531..169766205-chr2:169769452..169771867,3	K562	blood:
30	chr2:161488018..161488821-chr2:169795050..169795992,2	MCF-7	breast:
31	chr2:169792449..169795110-chr2:169797440..169799933,3	K562	blood:
32	chr2:169775702..169778963-chr2:169780525..169783462,3	K562	blood:
33	chr2:169769700..169774524-chr2:169775649..169779398,6	K562	blood:
34	chr2:169786046..169790721-chr2:169791105..169793269,7	K562	blood:
35	chr2:169790519..169792634-chr2:169793983..169795668,2	K562	blood:
36	chr2:169775702..169778963-chr2:169780525..169783462,3	K562	blood:
37	chr2:169629191..169630841-chr2:169776722..169777731,4	MCF-7	breast:
38	chr2:169760230..169762214-chr2:169762274..169764034,2	MCF-7	breast:
39	chr2:169204183..169204820-chr2:169776794..169777318,2	K562	blood:
40	chr2:169775702..169778664-chr2:169780525..169782299,2	K562	blood:
41	chr2:169775702..169778664-chr2:169780525..169782299,2	K562	blood:
42	chr2:169782114..169784208-chr2:169788090..169790755,2	K562	blood:
43	chr2:169733481..169736243-chr2:169763377..169765605,2	K562	blood:
44	chr2:169790519..169792634-chr2:169793983..169795668,2	K562	blood:
45	chr2:169757280..169761059-chr2:169762984..169765763,4	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ABCB11	hsa-miR-33a-5p	chr2:169780122-169780131

Variant related genes	Relation type
G6PC2	TF binding region
SPC25	TF binding region
G6PC2	CpG island
SPC25	CpG island
ENSG00000152254	chromatin interactions
ENSG00000152253	chromatin interactions
ENSG00000230513	chromatin interactions
ENSG00000184436	chromatin interactions

Extended variants
information (count: 1707 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:1707 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540524	chr2:169756930-169756931	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185834197	chr2:169756937-169756938	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs574277631	chr2:169756942-169756943	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543259035	chr2:169756944-169756945	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs80124478	chr2:169756968-169756969	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs78707420	chr2:169756971-169756972	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563195006	chr2:169757007-169757008	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2232314	chr2:169757129-169757130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545445542	chr2:169757158-169757159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs559320978	chr2:169757187-169757188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs180947575	chr2:169757200-169757201	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370637177	chr2:169757213-169757214	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs143041179	chr2:169757341-169757342	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs1402837	chr2:169757354-169757355	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
15	rs542908897	chr2:169757389-169757390	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs77580782	chr2:169757396-169757397	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2232315	chr2:169757432-169757433	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs570325987	chr2:169757436-169757437	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34238785	chr2:169757492-169757493	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573225	chr2:169757541-169757542	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs34746523	chr2:169757548-169757549	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566043787	chr2:169757561-169757562	Weak transcription Enhancers Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2232316	chr2:169757562-169757563	Weak transcription Enhancers Active TSS	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs148215323	chr2:169757618-169757619	Weak transcription Enhancers Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs568218940	chr2:169757679-169757680	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375476582	chr2:169757697-169757698	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536809298	chr2:169757781-169757782	Weak transcription Enhancers Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368619514	chr2:169757793-169757794	Weak transcription Enhancers Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs368382511	chr2:169757864-169757865	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372008743	chr2:169757889-169757890	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143670077	chr2:169757900-169757901	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577033273	chr2:169757902-169757903	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs510399	chr2:169757917-169757918	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546055009	chr2:169757921-169757922	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34725343	chr2:169757923-169757924	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs142189264	chr2:169757930-169757931	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375350062	chr2:169757933-169757934	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149874491	chr2:169757953-169757954	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371294159	chr2:169757996-169757997	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs375874967	chr2:169757998-169757999	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369755574	chr2:169758016-169758017	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs368329614	chr2:169758024-169758025	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201561079	chr2:169758029-169758030	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs376403545	chr2:169758033-169758034	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs199682245	chr2:169758044-169758045	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540732196	chr2:169758118-169758119	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs6715133	chr2:169758147-169758148	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs561721548	chr2:169758148-169758149	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs530633250	chr2:169758205-169758206	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs544000668	chr2:169758206-169758207	Weak transcription Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Breast cancer	22522925	CNVD
Sudden cardiac death	19188705	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169747000-169757600	Weak transcription	Pancreas	Pancrea
2	chr2:169756600-169757200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr2:169756600-169758000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr2:169756800-169757000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:169756800-169757800	Enhancers	Brain Cingulate Gyrus	brain
6	chr2:169757000-169760400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:169757200-169757400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr2:169757400-169762000	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr2:169757600-169757800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr2:169757600-169757800	Enhancers	Ovary	ovary
11	chr2:169757600-169757800	Enhancers	Pancreas	Pancrea
12	chr2:169760000-169760200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:169760200-169760600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:169760400-169760600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr2:169760600-169762200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr2:169760600-169762400	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr2:169760600-169763400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr2:169761400-169764400	Weak transcription	K562	blood
19	chr2:169762000-169762200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr2:169762200-169762400	Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr2:169762200-169765800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr2:169762400-169763000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr2:169762400-169764800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:169762800-169765200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr2:169763000-169763600	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr2:169763000-169763800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr2:169763200-169763400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr2:169763200-169763400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:169763200-169764000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr2:169763200-169765200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:169763200-169765400	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:169763400-169763800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr2:169763400-169764400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr2:169763400-169764400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr2:169763400-169764600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr2:169763400-169764600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:169763400-169764600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr2:169763400-169765400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:169763600-169766400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr2:169763800-169764200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr2:169763800-169764400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:169763800-169766800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr2:169764000-169764400	Enhancers	HMEC	breast
44	chr2:169764000-169764600	Enhancers	Spleen	Spleen
45	chr2:169764000-169764800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr2:169764000-169765000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr2:169764200-169764600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr2:169764200-169765000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr2:169764400-169764800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr2:169764400-169765400	Enhancers	K562	blood

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