Variant report

Variant	nsv582090
Chromosome Location	chr2:57595408-57665702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:57600561-57601162	HCT-116	colon:	n/a	n/a
2	BACH1	chr2:57623493-57623938	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr2:57656947-57657199	GM12878	blood:	n/a	n/a
4	BRCA1	chr2:57625938-57625986	GM12878	blood:	n/a	n/a
5	CBX3	chr2:57600551-57601256	HCT-116	colon:	n/a	n/a
6	CEBPB	chr2:57644218-57644262	A549	lung:	n/a	n/a
7	CEBPB	chr2:57635068-57635356	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr2:57630938-57631021	A549	lung:	n/a	chr2:57630962-57630975
9	CEBPB	chr2:57653300-57653715	HepG2	liver:	n/a	n/a
10	CEBPB	chr2:57595173-57595845	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:57595285-57595780	HCT-116	colon:	n/a	n/a
12	CTCF	chr2:57604200-57604350	HEEpiC	esophagus:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
13	CTCF	chr2:57616310-57616331	GM20000	blood:	n/a	n/a
14	CTCF	chr2:57604222-57604362	SK-N-SH_RA	brain:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
15	CTCF	chr2:57604180-57604330	SK-N-SH_RA	brain:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
16	CTCF	chr2:57604240-57604390	RPTEC	kidney:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
17	CTCF	chr2:57604272-57604354	ProgFib	skin:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
18	CTCF	chr2:57604014-57604604	HCT-116	colon:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
19	CTCF	chr2:57604220-57604370	HCT-116	colon:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
20	CTCF	chr2:57604280-57604430	SK-N-SH_RA	brain:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
21	CTCF	chr2:57604260-57604410	WERI-Rb-1	eye:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
22	CTCF	chr2:57604153-57604426	IMR90	lung:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
23	CTCF	chr2:57604257-57604378	HepG2	liver:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
24	CTCF	chr2:57604200-57604350	HMF	breast:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
25	CTCF	chr2:57604226-57604357	GM10266	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
26	CTCF	chr2:57604220-57604370	HepG2	liver:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
27	CTCF	chr2:57604201-57604419	Hela-S3	cervix:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
28	CTCF	chr2:57604209-57604431	HepG2	liver:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
29	CTCF	chr2:57604227-57604379	GM12878	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
30	CTCF	chr2:57604121-57604498	GM12878	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
31	CTCF	chr2:57604192-57604447	H1-hESC	embryonic stem cell:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
32	CTCF	chr2:57604200-57604350	HCPEpiC	choroid plexus:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
33	CTCF	chr2:57604240-57604390	GM12872	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
34	CTCF	chr2:57604303-57604311	GM20000	blood:	n/a	n/a
35	CTCF	chr2:57604220-57604370	HMEC	breast:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
36	CTCF	chr2:57625775-57625970	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:57604220-57604370	HCPEpiC	choroid plexus:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
38	CTCF	chr2:57604200-57604350	HA-sp	spinal cord:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
39	CTCF	chr2:57604139-57604410	SK-N-SH_RA	brain:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
40	CTCF	chr2:57604260-57604410	GM12871	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
41	CTCF	chr2:57604202-57604410	GM13977	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
42	CTCF	chr2:57604340-57604490	A549	lung:	n/a	n/a
43	CTCF	chr2:57604229-57604389	LNCaP	prostate:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
44	CTCF	chr2:57604220-57604370	MCF-7	breast:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
45	CTCF	chr2:57604200-57604350	HRPEpiC	eye:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
46	CTCF	chr2:57604240-57604390	NHEK	skin:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
47	CTCF	chr2:57604200-57604350	HRE	kidney:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
48	CTCF	chr2:57604240-57604390	HMEC	breast:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
49	CTCF	chr2:57604180-57604330	GM12874	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319
50	CTCF	chr2:57604260-57604410	GM12878	blood:	n/a	chr2:57604302-57604318 chr2:57604303-57604324 chr2:57604301-57604319

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:57634837-57634887	MCF-7	breast:	n/a
2	chr2:57634837-57634887	A549	lung:	n/a
3	chr2:57634837-57634887	HRPEpiC	eye:	n/a
4	chr2:57634837-57634887	T-47D	breast:	n/a
5	chr2:57634837-57634887	NT2-D1	testis:	n/a
6	chr2:57634837-57634887	NHBE	bronchial:	n/a
7	chr2:57634837-57634887	GM06990	blood:	n/a
8	chr2:57634837-57634887	AG09309	skin:	n/a
9	chr2:57634837-57634887	ProgFib	skin:	n/a
10	chr2:57634837-57634887	HEEpiC	esophagus:	n/a
11	chr2:57634837-57634887	AG04450	lung:	fetal
12	chr2:57634837-57634887	HCPEpiC	choroid plexus:	n/a
13	chr2:57634837-57634887	HCF	heart:	n/a
14	chr2:57634837-57634887	PFSK-1	brain:	n/a
15	chr2:57634837-57634887	AG09319	gingival:	n/a
16	chr2:57634837-57634887	LNCaP	prostate:	n/a
17	chr2:57634837-57634887	BE2_C	brain:	n/a
18	chr2:57634837-57634887	Hela-S3	cervix:	n/a
19	chr2:57634837-57634887	HAEpiC	amniotic membrane:	n/a
20	chr2:57634837-57634887	Caco-2	colon:	n/a
21	chr2:57634837-57634887	GM12891	blood:	n/a
22	chr2:57634837-57634887	U87	brain:	n/a
23	chr2:57634837-57634887	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:57634837-57634887	IMR90	lung:	fetal
25	chr2:57634837-57634887	NB4	blood:	n/a
26	chr2:57634837-57634887	BJ	skin:	n/a
27	chr2:57634837-57634887	ECC-1	luminal epithelium:	n/a
28	chr2:57634837-57634887	PrEC	prostate:	n/a
29	chr2:57634837-57634887	SK-N-MC	brain:	n/a
30	chr2:57634837-57634887	HCM	heart:	n/a
31	chr2:57634837-57634887	NHDF-neo	bronchial:	n/a
32	chr2:57634837-57634887	K562	blood:	n/a
33	chr2:57634837-57634887	SK-N-SH	brain:	n/a
34	chr2:57634837-57634887	AG04449	skin:	fetal
35	chr2:57634837-57634887	HRCEpiC	kidney:	n/a
36	chr2:57634837-57634887	HIPEpiC	eye:	n/a
37	chr2:57634837-57634887	AG10803	skin:	n/a
38	chr2:57634837-57634887	NH-A	brain:	n/a
39	chr2:57634837-57634887	HRE	kidney:	n/a
40	chr2:57634837-57634887	GM19239	blood:	n/a
41	chr2:57634837-57634887	ovcar-3	ovarian:	n/a
42	chr2:57634837-57634887	SK-N-SH_RA	brain:	n/a
43	chr2:57634837-57634887	GM12878	blood:	n/a
44	chr2:57634837-57634887	HMEC	breast:	n/a
45	chr2:57634837-57634887	HUVEC	blood vessel:	n/a
46	chr2:57634837-57634887	RPTEC	kidney:	n/a
47	chr2:57634837-57634887	H1-hESC	embryonic stem cell:	embryo
48	chr2:57634837-57634887	HEK293	kidney:	embryo
49	chr2:57634837-57634887	HL-60	blood:	n/a
50	chr2:57634837-57634887	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:57602104..57602641-chr2:57724502..57725135,2	MCF-7	breast:
2	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
3	chr2:57603852..57604740-chr2:57724321..57725273,3	MCF-7	breast:
4	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:
5	chr2:57631506..57633055-chr2:57645760..57647304,2	MCF-7	breast:
6	chr2:57633446..57635721-chr2:57643662..57645382,2	MCF-7	breast:
7	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:
8	chr2:57603431..57604465-chr2:57724481..57725285,5	MCF-7	breast:
9	chr2:57011309..57011934-chr2:57604188..57604743,2	MCF-7	breast:
10	chr2:57627476..57629537-chr2:57644280..57646195,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VRK2-16	chr2:57659475-57659520	NONHSAT070834
2	lnc-FANCL-8	chr2:57657275-57657340	NONHSAT070833
3	lnc-FANCL-8	chr2:57656683-57656947	NONHSAT070833
4	lnc-FANCL-8	chr2:57657781-57657828	NONHSAT070833

Variant related genes	Relation type
ENSG00000270569	TF binding region
ENSG00000270569	CpG island

Extended variants
information (count: 1339 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6743780	chr2:57595408-57595409	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189621124	chr2:57595441-57595442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551213166	chr2:57595516-57595517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571071183	chr2:57595555-57595556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141163345	chr2:57595566-57595567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182099161	chr2:57595593-57595594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs144599859	chr2:57595607-57595608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535593250	chr2:57595609-57595610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6715855	chr2:57595620-57595621	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs575548636	chr2:57595654-57595655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537863049	chr2:57595670-57595671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557997822	chr2:57595726-57595727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146675859	chr2:57595763-57595764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17048786	chr2:57595852-57595853	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs140276386	chr2:57595860-57595861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186737874	chr2:57595866-57595867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34404668	chr2:57595893-57595894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35366591	chr2:57595917-57595918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189932338	chr2:57595936-57595937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183053008	chr2:57595941-57595942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150329102	chr2:57595966-57595967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551108499	chr2:57595980-57595981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577809403	chr2:57596059-57596060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558025384	chr2:57596060-57596061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533489663	chr2:57596124-57596125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546780151	chr2:57596127-57596128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138252355	chr2:57596226-57596227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149616543	chr2:57596324-57596325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553015869	chr2:57596338-57596339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188623108	chr2:57596359-57596360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72935541	chr2:57596367-57596368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143368669	chr2:57596375-57596376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139343174	chr2:57596376-57596377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192997125	chr2:57596405-57596406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534124139	chr2:57596432-57596433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185603096	chr2:57596441-57596442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374948569	chr2:57596454-57596455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188035693	chr2:57596474-57596475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs55658488	chr2:57596585-57596586	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs10199165	chr2:57596612-57596613	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562572223	chr2:57596650-57596651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540429261	chr2:57596670-57596671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576082037	chr2:57596689-57596690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7570448	chr2:57596690-57596691	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs369531459	chr2:57596727-57596728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192562933	chr2:57596736-57596737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533441112	chr2:57596790-57596791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546841688	chr2:57596794-57596795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143354039	chr2:57596814-57596815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13406256	chr2:57596841-57596842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

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
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
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
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57593600-57601000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:57595200-57595800	Enhancers	HMEC	breast
3	chr2:57595400-57595800	Enhancers	NHEK	skin
4	chr2:57595800-57599600	Weak transcription	NHEK	skin
5	chr2:57595800-57600000	Weak transcription	HMEC	breast
6	chr2:57596200-57596800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:57598000-57598400	Enhancers	HSMMtube	muscle
8	chr2:57598200-57598400	Enhancers	HSMM	muscle
9	chr2:57598400-57599800	Weak transcription	HSMMtube	muscle
10	chr2:57598400-57602000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:57598600-57599600	Weak transcription	HSMM	muscle
12	chr2:57599000-57601400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:57599400-57601400	Enhancers	HUVEC	blood vessel
14	chr2:57599600-57600200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:57599600-57601400	Enhancers	NHEK	skin
16	chr2:57599600-57601800	Enhancers	HSMM	muscle
17	chr2:57599600-57601800	Enhancers	NHDF-Ad	bronchial
18	chr2:57599800-57600000	Active TSS	A549	lung
19	chr2:57599800-57601400	Enhancers	HSMMtube	muscle
20	chr2:57600000-57600200	Flanking Active TSS	A549	lung
21	chr2:57600000-57601000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:57600000-57601200	Enhancers	NH-A	brain
23	chr2:57600000-57601400	Enhancers	HMEC	breast
24	chr2:57600200-57601800	Enhancers	A549	lung
25	chr2:57601000-57601200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:57605600-57606400	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr2:57613400-57614000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:57623200-57624000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr2:57623400-57623800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:57623400-57624000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:57623400-57624200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:57623400-57624200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:57623400-57624200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:57623400-57624200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:57623400-57624200	Enhancers	A549	lung
36	chr2:57623400-57624200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr2:57623400-57624400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr2:57623600-57624000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr2:57623800-57624000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:57623800-57625000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:57623800-57625200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr2:57624000-57624200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr2:57624000-57634800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr2:57624200-57624800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:57624800-57625400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:57625000-57625200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr2:57629000-57629400	Enhancers	Fetal Brain Female	brain
48	chr2:57629000-57630400	Enhancers	Fetal Lung	lung
49	chr2:57633400-57633600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:57633400-57636000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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