Variant report

Variant	esv1844727
Chromosome Location	chr2:54999712-55084583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:714)
CpG islands
(count:122)
Chromatin interactive
region (count:52)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55028658-55028832	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:55049592-55049691	HepG2	liver:	n/a	n/a
3	ATF1	chr2:55054749-55054907	K562	blood:	n/a	n/a
4	ATF1	chr2:55037059-55037360	K562	blood:	n/a	n/a
5	ATF1	chr2:55040792-55041048	K562	blood:	n/a	n/a
6	ATF1	chr2:55031638-55031805	K562	blood:	n/a	n/a
7	ATF2	chr2:55072521-55073040	GM12878	blood:	n/a	n/a
8	BACH1	chr2:55034309-55034313	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr2:55036999-55037253	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:55072300-55072540	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:55065788-55065975	K562	blood:	n/a	n/a
12	BRCA1	chr2:55065770-55066009	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr2:55001025-55001351	K562	blood:	n/a	n/a
14	CBX3	chr2:54999120-55000233	HCT-116	colon:	n/a	n/a
15	CBX3	chr2:55000936-55001398	HCT-116	colon:	n/a	n/a
16	CBX3	chr2:55001056-55001321	K562	blood:	n/a	n/a
17	CEBPB	chr2:55010151-55010347	HepG2	liver:	n/a	chr2:55010156-55010167 chr2:55010156-55010167
18	CEBPB	chr2:55065777-55066064	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:55079001-55079042	K562	blood:	n/a	chr2:55079017-55079028
20	CEBPB	chr2:55078867-55079174	HepG2	liver:	n/a	chr2:55079017-55079028
21	CEBPB	chr2:55003776-55003808	Hela-S3	cervix:	n/a	chr2:55003780-55003791
22	CEBPB	chr2:55049589-55049746	K562	blood:	n/a	n/a
23	CEBPB	chr2:55075956-55076085	A549	lung:	n/a	n/a
24	CEBPB	chr2:55028608-55028799	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:55037037-55037378	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:55037091-55037325	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:55049563-55049783	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:55013386-55013663	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:55072268-55073116	GM12878	blood:	n/a	chr2:55072783-55072796
30	CEBPB	chr2:55075880-55076100	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:55075984-55076052	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:55003661-55003923	HepG2	liver:	n/a	chr2:55003780-55003791
33	CHD2	chr2:55065761-55066026	GM12878	blood:	n/a	n/a
34	CREB1	chr2:55037061-55037360	GM12878	blood:	n/a	n/a
35	CREB1	chr2:55072615-55073013	GM12878	blood:	n/a	n/a
36	CREB1	chr2:55072505-55073124	GM12878	blood:	n/a	n/a
37	CTCF	chr2:55065683-55066154	IMR90	lung:	n/a	chr2:55065864-55065885 chr2:55065869-55065887 chr2:55065870-55065886 chr2:55065871-55065884
38	CTCF	chr2:55012421-55012437	Fibrobl	skin:	n/a	n/a
39	CTCF	chr2:55066660-55066810	GM12873	blood:	n/a	n/a
40	CTCF	chr2:55065760-55065910	NHDF-neo	bronchial:	n/a	chr2:55065864-55065885 chr2:55065869-55065887 chr2:55065870-55065886 chr2:55065871-55065884
41	CTCF	chr2:55000520-55000670	BE2_C	brain:	n/a	n/a
42	CTCF	chr2:55065800-55065950	GM12864	blood:	n/a	chr2:55065864-55065885 chr2:55065869-55065887 chr2:55065870-55065886 chr2:55065871-55065884
43	CTCF	chr2:55065820-55065970	GM06990	blood:	n/a	chr2:55065864-55065885 chr2:55065869-55065887 chr2:55065870-55065886 chr2:55065871-55065884
44	CTCF	chr2:55066180-55066330	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr2:55065840-55065990	WI-38	lung:	n/a	chr2:55065864-55065885 chr2:55065869-55065887 chr2:55065870-55065886 chr2:55065871-55065884
46	CTCF	chr2:55001020-55001170	GM12873	blood:	n/a	n/a
47	CTCF	chr2:55001121-55001124	Medullo	brain:	n/a	n/a
48	CTCF	chr2:55066120-55066270	AG04449	skin:	n/a	n/a
49	CTCF	chr2:55001020-55001170	A549	lung:	n/a	n/a
50	CTCF	chr2:55065760-55065910	BE2_C	brain:	n/a	chr2:55065864-55065885 chr2:55065869-55065887 chr2:55065870-55065886 chr2:55065871-55065884

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55015049-55015099	HCT-116	colon:	n/a
2	chr2:55047815-55047865	AoSMC	blood vessel:	n/a
3	chr2:55015049-55015099	IMR90	lung:	fetal
4	chr2:55047815-55047865	SK-N-MC	brain:	n/a
5	chr2:55047815-55047865	HCT-116	colon:	n/a
6	chr2:55015049-55015099	AG04450	lung:	fetal
7	chr2:55015049-55015099	HRPEpiC	eye:	n/a
8	chr2:55015049-55015099	SK-N-SH	brain:	n/a
9	chr2:55047815-55047865	RPTEC	kidney:	n/a
10	chr2:55015049-55015099	GM12892	blood:	n/a
11	chr2:55015049-55015099	ECC-1	luminal epithelium:	n/a
12	chr2:55015049-55015099	HL-60	blood:	n/a
13	chr2:55015049-55015099	RPTEC	kidney:	n/a
14	chr2:55047815-55047865	HRE	kidney:	n/a
15	chr2:55015049-55015099	PrEC	prostate:	n/a
16	chr2:55015049-55015099	HCF	heart:	n/a
17	chr2:55047815-55047865	HCF	heart:	n/a
18	chr2:55047815-55047865	HL-60	blood:	n/a
19	chr2:55015049-55015099	AG09319	gingival:	n/a
20	chr2:55047815-55047865	AG04450	lung:	fetal
21	chr2:55047815-55047865	ovcar-3	ovarian:	n/a
22	chr2:55047815-55047865	BE2_C	brain:	n/a
23	chr2:55015049-55015099	HCPEpiC	choroid plexus:	n/a
24	chr2:55015049-55015099	HNPCEpiC	eye:	n/a
25	chr2:55047815-55047865	PrEC	prostate:	n/a
26	chr2:55015049-55015099	HepG2	liver:	n/a
27	chr2:55047815-55047865	HEK293	kidney:	embryo
28	chr2:55047815-55047865	PFSK-1	brain:	n/a
29	chr2:55047815-55047865	NH-A	brain:	n/a
30	chr2:55047815-55047865	Hepatocyte	liver:	n/a
31	chr2:55015049-55015099	NH-A	brain:	n/a
32	chr2:55047815-55047865	GM12892	blood:	n/a
33	chr2:55015049-55015099	PANC-1	pancreas:	n/a
34	chr2:55015049-55015099	Hela-S3	cervix:	n/a
35	chr2:55015049-55015099	Hepatocyte	liver:	n/a
36	chr2:55015049-55015099	HAEpiC	amniotic membrane:	n/a
37	chr2:55047815-55047865	CMK	blood:	n/a
38	chr2:55047815-55047865	GM12878	blood:	n/a
39	chr2:55047815-55047865	HCM	heart:	n/a
40	chr2:55047815-55047865	U87	brain:	n/a
41	chr2:55015049-55015099	HIPEpiC	eye:	n/a
42	chr2:55047815-55047865	HUVEC	blood vessel:	n/a
43	chr2:55015049-55015099	HMEC	breast:	n/a
44	chr2:55047815-55047865	PANC-1	pancreas:	n/a
45	chr2:55047815-55047865	GM19239	blood:	n/a
46	chr2:55015049-55015099	SAEC	small airway:	n/a
47	chr2:55015049-55015099	BE2_C	brain:	n/a
48	chr2:55015049-55015099	GM19239	blood:	n/a
49	chr2:55015049-55015099	ovcar-3	ovarian:	n/a
50	chr2:55015049-55015099	MCF-7	breast:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:54994263..54996160-chr2:55006143..55008634,2	K562	blood:
2	chr19:3989800..3990365-chr2:55028993..55029496,2	MCF-7	breast:
3	chr2:55051760..55053947-chr2:55063196..55065513,2	K562	blood:
4	chr2:55066064..55068239-chr2:55070022..55072910,2	K562	blood:
5	chr2:55070043..55071557-chr2:55073869..55075747,2	K562	blood:
6	chr2:55060398..55062114-chr2:55063978..55066536,2	MCF-7	breast:
7	chr2:55042975..55046110-chr2:55047288..55049985,3	K562	blood:
8	chr2:55054994..55056963-chr2:55058842..55061555,2	K562	blood:
9	chr2:55008139..55011075-chr2:55013927..55016853,2	K562	blood:
10	chr2:55050860..55053481-chr2:55056910..55059728,4	K562	blood:
11	chr2:55043190..55047083-chr2:55047288..55051839,4	K562	blood:
12	chr2:55058953..55061884-chr2:55063493..55065215,2	K562	blood:
13	chr2:55060398..55062114-chr2:55063978..55066536,2	MCF-7	breast:
14	chr2:55030699..55032489-chr2:55035995..55037701,2	K562	blood:
15	chr2:55030989..55033813-chr2:55035805..55037701,2	K562	blood:
16	chr2:55077644..55080366-chr2:55082902..55084991,2	K562	blood:
17	chr2:55043075..55045749-chr2:55057343..55058927,2	K562	blood:
18	chr2:55051760..55053947-chr2:55063196..55065513,2	K562	blood:
19	chr2:55008139..55011075-chr2:55013927..55016853,2	K562	blood:
20	chr2:55043075..55045749-chr2:55057343..55058927,2	K562	blood:
21	chr2:55043190..55047083-chr2:55047288..55051839,4	K562	blood:
22	chr2:54999349..55001528-chr2:55002903..55005507,2	MCF-7	breast:
23	chr2:55042975..55046110-chr2:55047288..55049985,3	K562	blood:
24	chr2:55001781..55004496-chr2:55092891..55095421,2	K562	blood:
25	chr17:59492061..59493575-chr2:55052880..55054380,2	MCF-7	breast:
26	chr2:54990315..54991347-chr2:55065566..55066286,4	MCF-7	breast:
27	chr2:55013900..55016291-chr2:55017771..55020544,3	MCF-7	breast:
28	chr2:54990527..54991452-chr2:55065478..55066629,7	MCF-7	breast:
29	chr2:55054994..55056963-chr2:55058842..55061555,2	K562	blood:
30	chr2:54982346..54983733-chr2:55065232..55066304,6	MCF-7	breast:
31	chr2:55065842..55066397-chr2:55402066..55403010,2	MCF-7	breast:
32	chr2:55050860..55053564-chr2:55056333..55059728,3	K562	blood:
33	chr2:55066064..55068907-chr2:55070022..55073567,3	K562	blood:
34	chr2:55078067..55080199-chr2:55091204..55092735,2	MCF-7	breast:
35	chr2:54892587..54893215-chr2:55065584..55066311,2	MCF-7	breast:
36	chr2:54990391..54992574-chr2:55063841..55065808,2	MCF-7	breast:
37	chr2:54950232..54951150-chr2:55065622..55066622,2	MCF-7	breast:
38	chr2:54999349..55001528-chr2:55002903..55005507,2	MCF-7	breast:
39	chr2:55013900..55016291-chr2:55017771..55020544,3	MCF-7	breast:
40	chr2:55070043..55071557-chr2:55073869..55075747,2	K562	blood:
41	chr2:55066064..55068239-chr2:55070022..55072910,2	K562	blood:
42	chr2:55050860..55053481-chr2:55056910..55059728,4	K562	blood:
43	chr2:55058953..55061884-chr2:55063493..55065215,2	K562	blood:
44	chr2:55030989..55033813-chr2:55035805..55037701,2	K562	blood:
45	chr2:54075898..54077445-chr2:55058501..55060039,2	K562	blood:
46	chr2:55010731..55013685-chr2:55129900..55132615,2	K562	blood:
47	chr2:54956388..54959275-chr2:55046945..55049769,2	MCF-7	breast:
48	chr2:55030699..55032489-chr2:55035995..55037701,2	K562	blood:
49	chr2:55066064..55068907-chr2:55070022..55073567,3	K562	blood:
50	chr2:55050860..55053564-chr2:55056333..55059728,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RTN4-4	chr2:55057725-55058202	expReg_chr2_4079_-

No data

Variant related genes	Relation type
RNU7-81P	TF binding region
EML6	TF binding region
RNU7-81P	CpG island
EML6	CpG island
ENSG00000265452	chromatin interactions
ENSG00000214595	chromatin interactions

Extended variants
information (count: 4089 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4089 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4671231	chr2:54999712-54999713	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576784075	chr2:54999714-54999715	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs113211936	chr2:54999748-54999749	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs559804163	chr2:54999793-54999794	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs528772823	chr2:54999887-54999888	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs542485410	chr2:54999904-54999905	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs562242913	chr2:54999933-54999934	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs531058864	chr2:54999934-54999935	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs188216112	chr2:54999938-54999939	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs570879124	chr2:54999945-54999946	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs182089601	chr2:54999952-54999953	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11901245	chr2:54999980-54999981	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs565882481	chr2:55000008-55000009	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs534583604	chr2:55000089-55000090	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs554378467	chr2:55000096-55000097	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs144701715	chr2:55000151-55000152	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs72915587	chr2:55000170-55000171	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs556782067	chr2:55000194-55000195	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs576832081	chr2:55000198-55000199	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs567912440	chr2:55000214-55000215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576667442	chr2:55000251-55000252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545520729	chr2:55000274-55000275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552928410	chr2:55000275-55000276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573605001	chr2:55000282-55000283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34744323	chr2:55000284-55000285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542523985	chr2:55000367-55000368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562331654	chr2:55000408-55000409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147913419	chr2:55000418-55000419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544778389	chr2:55000441-55000442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11125544	chr2:55000451-55000452	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184742301	chr2:55000463-55000464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558513116	chr2:55000484-55000485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546706227	chr2:55000547-55000548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556838488	chr2:55000563-55000564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560523817	chr2:55000568-55000569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140443768	chr2:55000572-55000573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548101712	chr2:55000596-55000597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567966280	chr2:55000602-55000603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536856470	chr2:55000609-55000610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150389739	chr2:55000650-55000651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138152478	chr2:55000660-55000661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572134498	chr2:55000673-55000674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539496182	chr2:55000676-55000677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552727060	chr2:55000686-55000687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572889384	chr2:55000775-55000776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372450908	chr2:55000796-55000797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149208744	chr2:55000844-55000845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72915588	chr2:55000884-55000885	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190032126	chr2:55000940-55000941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181667397	chr2:55000941-55000942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
XY gonadal dysgenesis	20685758	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:54997400-55000600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr2:54997400-55000800	Enhancers	HSMMtube	muscle
3	chr2:54997600-55000600	Enhancers	HSMM	muscle
4	chr2:54997600-55000800	Enhancers	HMEC	breast
5	chr2:54997600-55001400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:54997800-55000600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:54997800-55000600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr2:54997800-55000600	Enhancers	NHDF-Ad	bronchial
9	chr2:54998000-55000200	Enhancers	HUVEC	blood vessel
10	chr2:54998000-55000600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:54998200-54999800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:54998200-55000400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:54998200-55000400	Enhancers	Osteobl	bone
14	chr2:54998400-55000400	Enhancers	Hela-S3	cervix
15	chr2:54998400-55000600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:54998800-54999800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:54999200-54999800	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr2:54999200-55000200	Enhancers	NHLF	lung
19	chr2:54999200-55000600	Enhancers	Stomach Mucosa	stomach
20	chr2:54999400-54999800	Enhancers	NHEK	skin
21	chr2:54999600-54999800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:54999600-54999800	Flanking Active TSS	NH-A	brain
23	chr2:54999800-55000000	Enhancers	Esophagus	oesophagus
24	chr2:54999800-55000000	Enhancers	NH-A	brain
25	chr2:54999800-55000200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:54999800-55000200	Flanking Active TSS	NHEK	skin
27	chr2:54999800-55000600	Enhancers	Gastric	stomach
28	chr2:55000000-55000200	Flanking Active TSS	NH-A	brain
29	chr2:55000200-55000600	Enhancers	Fetal Muscle Trunk	muscle
30	chr2:55000200-55000600	Enhancers	NHEK	skin
31	chr2:55000600-55002200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:55000600-55002600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:55001400-55002400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr2:55002400-55002600	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
35	chr2:55002400-55002800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr2:55002600-55003400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:55003400-55006200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr2:55003600-55004400	Enhancers	Dnd41	blood
39	chr2:55009800-55010200	Enhancers	Primary B cells from peripheral blood	blood
40	chr2:55010200-55012000	Weak transcription	Primary B cells from peripheral blood	blood
41	chr2:55012000-55015200	Enhancers	Primary B cells from peripheral blood	blood
42	chr2:55013200-55014000	Enhancers	HepG2	liver
43	chr2:55013600-55013800	Bivalent Enhancer	Stomach Mucosa	stomach
44	chr2:55013600-55014200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:55013600-55015400	Enhancers	Pancreas	Pancrea
46	chr2:55014000-55014600	Enhancers	Gastric	stomach
47	chr2:55014600-55015000	Weak transcription	Gastric	stomach
48	chr2:55015000-55015400	Enhancers	Gastric	stomach
49	chr2:55015200-55015800	Flanking Active TSS	Primary B cells from peripheral blood	blood
50	chr2:55015800-55016200	Enhancers	Primary B cells from peripheral blood	blood

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