Variant report

Variant	nsv581776
Chromosome Location	chr2:48763382-48913019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1447)
CpG islands
(count:1772)
Chromatin interactive
region (count:48)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1447 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:48832723-48833286	K562	blood:	n/a	n/a
2	ARID3A	chr2:48850023-48850151	K562	blood:	n/a	n/a
3	ARID3A	chr2:48834779-48835112	K562	blood:	n/a	n/a
4	ARID3A	chr2:48827388-48827716	K562	blood:	n/a	chr2:48827687-48827703
5	ARID3A	chr2:48816377-48816687	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:48793805-48793997	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:48772426-48772615	K562	blood:	n/a	n/a
8	ARID3A	chr2:48800039-48800306	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:48772588-48772694	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:48816337-48816665	K562	blood:	n/a	n/a
11	ATF1	chr2:48904722-48905003	K562	blood:	n/a	n/a
12	ATF1	chr2:48832810-48833265	K562	blood:	n/a	n/a
13	ATF1	chr2:48878247-48878500	K562	blood:	n/a	n/a
14	ATF2	chr2:48812780-48813200	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr2:48834690-48835094	K562	blood:	n/a	n/a
16	ATF3	chr2:48772405-48772657	K562	blood:	n/a	n/a
17	ATF3	chr2:48832914-48833249	K562	blood:	n/a	n/a
18	BHLHE40	chr2:48772416-48772721	K562	blood:	n/a	n/a
19	BHLHE40	chr2:48874042-48874175	K562	blood:	n/a	n/a
20	BHLHE40	chr2:48834871-48834971	K562	blood:	n/a	n/a
21	BHLHE40	chr2:48827501-48827675	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:48832874-48833229	K562	blood:	n/a	n/a
23	CBX3	chr2:48832078-48833351	K562	blood:	n/a	n/a
24	CBX3	chr2:48834627-48835227	K562	blood:	n/a	n/a
25	CBX3	chr2:48834288-48835170	HCT-116	colon:	n/a	n/a
26	CBX3	chr2:48832720-48833279	K562	blood:	n/a	n/a
27	CBX3	chr2:48772283-48772746	K562	blood:	n/a	n/a
28	CBX3	chr2:48834298-48835187	HCT-116	colon:	n/a	n/a
29	CBX3	chr2:48840504-48840934	K562	blood:	n/a	n/a
30	CBX3	chr2:48772430-48772704	K562	blood:	n/a	n/a
31	CCNT2	chr2:48832431-48833255	K562	blood:	n/a	n/a
32	CCNT2	chr2:48860293-48860625	K562	blood:	n/a	n/a
33	CCNT2	chr2:48834963-48835190	K562	blood:	n/a	n/a
34	CEBPB	chr2:48834900-48835181	K562	blood:	n/a	n/a
35	CEBPB	chr2:48800037-48800329	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:48862820-48862911	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:48832603-48833395	K562	blood:	n/a	chr2:48832738-48832749
38	CEBPB	chr2:48884167-48884430	IMR90	lung:	n/a	chr2:48884297-48884308
39	CEBPB	chr2:48765362-48765619	IMR90	lung:	n/a	chr2:48765466-48765477
40	CEBPB	chr2:48850005-48850195	K562	blood:	n/a	n/a
41	CEBPB	chr2:48834855-48835202	K562	blood:	n/a	n/a
42	CEBPB	chr2:48884176-48884466	A549	lung:	n/a	chr2:48884297-48884308
43	CEBPB	chr2:48834235-48835238	HCT-116	colon:	n/a	n/a
44	CEBPB	chr2:48872685-48872904	K562	blood:	n/a	n/a
45	CEBPB	chr2:48832893-48833217	K562	blood:	n/a	n/a
46	CEBPB	chr2:48832679-48832801	HepG2	liver:	n/a	chr2:48832738-48832749
47	CEBPB	chr2:48765341-48765586	A549	lung:	n/a	chr2:48765466-48765477
48	CEBPB	chr2:48765340-48765594	HepG2	liver:	n/a	chr2:48765466-48765477
49	CEBPB	chr2:48832568-48833313	K562	blood:	n/a	chr2:48832738-48832749
50	CEBPB	chr2:48884207-48884456	HepG2	liver:	n/a	chr2:48884297-48884308

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:48796213-48796263	GM12892	blood:	n/a
2	chr2:48828358-48828408	NB4	blood:	n/a
3	chr2:48844728-48844778	NHBE	bronchial:	n/a
4	chr2:48796213-48796263	GM12892	blood:	n/a
5	chr2:48828358-48828408	NB4	blood:	n/a
6	chr2:48844728-48844778	NHBE	bronchial:	n/a
7	chr2:48842061-48842111	ECC-1	luminal epithelium:	n/a
8	chr2:48844892-48844942	SK-N-SH_RA	brain:	n/a
9	chr2:48814721-48814771	HCPEpiC	choroid plexus:	n/a
10	chr2:48845068-48845118	GM12892	blood:	n/a
11	chr2:48795067-48795117	Hepatocyte	liver:	n/a
12	chr2:48825037-48825087	Caco-2	colon:	n/a
13	chr2:48813184-48813234	ProgFib	skin:	n/a
14	chr2:48787750-48787800	AG09309	skin:	n/a
15	chr2:48800297-48800347	HRPEpiC	eye:	n/a
16	chr2:48808114-48808164	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:48845068-48845118	AG04449	skin:	fetal
18	chr2:48807373-48807423	HUVEC	blood vessel:	n/a
19	chr2:48787750-48787800	IMR90	lung:	fetal
20	chr2:48796151-48796201	K562	blood:	n/a
21	chr2:48796213-48796263	HCM	heart:	n/a
22	chr2:48795994-48796044	AG04450	lung:	fetal
23	chr2:48844971-48845021	ECC-1	luminal epithelium:	n/a
24	chr2:48795067-48795117	NHDF-neo	bronchial:	n/a
25	chr2:48848421-48848471	BE2_C	brain:	n/a
26	chr2:48787750-48787800	ECC-1	luminal epithelium:	n/a
27	chr2:48844195-48844245	BJ	skin:	n/a
28	chr2:48843645-48843695	NHDF-neo	bronchial:	n/a
29	chr2:48845068-48845118	BE2_C	brain:	n/a
30	chr2:48787750-48787800	T-47D	breast:	n/a
31	chr2:48806508-48806558	H1-hESC	embryonic stem cell:	embryo
32	chr2:48845068-48845118	HIPEpiC	eye:	n/a
33	chr2:48842430-48842480	SK-N-SH_RA	brain:	n/a
34	chr2:48844763-48844813	Hela-S3	cervix:	n/a
35	chr2:48844984-48845034	AoSMC	blood vessel:	n/a
36	chr2:48787750-48787800	U87	brain:	n/a
37	chr2:48825037-48825087	HepG2	liver:	n/a
38	chr2:48825037-48825087	HRE	kidney:	n/a
39	chr2:48843645-48843695	SKMC	muscle:	n/a
40	chr2:48828358-48828408	NHDF-neo	bronchial:	n/a
41	chr2:48806508-48806558	AG09319	gingival:	n/a
42	chr2:48807373-48807423	NHDF-neo	bronchial:	n/a
43	chr2:48825037-48825087	ECC-1	luminal epithelium:	n/a
44	chr2:48844892-48844942	NHDF-neo	bronchial:	n/a
45	chr2:48814721-48814771	SK-N-SH_RA	brain:	n/a
46	chr2:48845068-48845118	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:48806508-48806558	HEK293	kidney:	embryo
48	chr2:48806508-48806558	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:48844908-48844958	HMEC	breast:	n/a
50	chr2:48800297-48800347	A549	lung:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:48793447..48794436-chr2:48816095..48816687,2	K562	blood:
2	chr2:48773207..48775322-chr2:48777456..48778973,2	K562	blood:
3	chr2:48831692..48834380-chr2:48844421..48846212,2	K562	blood:
4	chr2:48827218..48827809-chr2:49717926..49718495,2	MCF-7	breast:
5	chr2:48838000..48839540-chr2:48843056..48846037,2	K562	blood:
6	chr2:48793739..48794249-chr2:48815968..48816646,2	MCF-7	breast:
7	chr2:48837425..48839347-chr2:48846973..48850503,3	K562	blood:
8	chr2:48788958..48790786-chr2:48792304..48795204,2	K562	blood:
9	chr2:48904136..48905986-chr2:48910089..48911674,2	K562	blood:
10	chr2:48761161..48764089-chr2:48767205..48768713,2	K562	blood:
11	chr2:48899103..48900749-chr2:48945263..48947505,2	MCF-7	breast:
12	chr2:48806857..48808745-chr2:48811544..48813174,2	MCF-7	breast:
13	chr2:48793384..48794350-chr2:48816086..48816820,5	MCF-7	breast:
14	chr2:48837425..48839347-chr2:48846973..48850503,3	K562	blood:
15	chr2:48901897..48904285-chr2:48937962..48940671,2	K562	blood:
16	chr2:48338188..48338961-chr2:48816027..48816580,2	MCF-7	breast:
17	chr2:48793384..48794350-chr2:48816086..48816820,5	MCF-7	breast:
18	chr2:48772382..48773067-chr2:48815926..48816979,3	K562	blood:
19	chr2:48904136..48905986-chr2:48910089..48911674,2	K562	blood:
20	chr2:48764687..48766642-chr2:48801802..48803658,2	MCF-7	breast:
21	chr2:48793447..48794436-chr2:48816095..48816687,2	K562	blood:
22	chr2:48828639..48830451-chr2:48830570..48832149,2	K562	blood:
23	chr2:48767423..48771041-chr2:48771579..48775293,4	K562	blood:
24	chr2:48773822..48775873-chr2:48777456..48780403,2	K562	blood:
25	chr2:48828639..48830451-chr2:48830570..48832149,2	K562	blood:
26	chr2:48793739..48794249-chr2:48815968..48816646,2	MCF-7	breast:
27	chr2:48788958..48790786-chr2:48792304..48795204,2	K562	blood:
28	chr2:48845784..48847693-chr2:48848992..48850627,2	K562	blood:
29	chr2:48761161..48764089-chr2:48767205..48768713,2	K562	blood:
30	chr2:48901300..48903356-chr2:48907687..48909663,2	K562	blood:
31	chr2:48676760..48679121-chr2:48771521..48774088,2	K562	blood:
32	chr2:48764687..48766642-chr2:48801802..48803658,2	MCF-7	breast:
33	chr2:48827557..48828940-chr2:49173265..49174447,4	MCF-7	breast:
34	chr2:48697799..48698704-chr2:48819681..48820191,2	MCF-7	breast:
35	chr2:48698168..48698704-chr2:48816044..48816581,2	MCF-7	breast:
36	chr2:48901300..48903356-chr2:48907687..48909663,2	K562	blood:
37	chr2:48803645..48806256-chr2:48816244..48817751,2	K562	blood:
38	chr2:48845784..48847693-chr2:48848992..48850627,2	K562	blood:
39	chr2:48767423..48771041-chr2:48771579..48775293,4	K562	blood:
40	chr2:48736001..48737694-chr2:48761849..48763956,2	K562	blood:
41	chr2:48773822..48775873-chr2:48777456..48780403,2	K562	blood:
42	chr2:48822120..48826399-chr2:48830586..48834373,3	K562	blood:
43	chr2:48803645..48806256-chr2:48816244..48817751,2	K562	blood:
44	chr2:48822120..48826399-chr2:48830586..48834373,3	K562	blood:
45	chr2:48826097..48828718-chr2:49093582..49095780,2	K562	blood:
46	chr2:48772065..48772805-chr2:50719351..50720113,2	K562	blood:
47	chr2:48772382..48773067-chr2:48815926..48816979,3	K562	blood:
48	chr2:48773207..48775322-chr2:48777456..48778973,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LHCGR-1	chr2:48859428-48860260	NONHSAT070627
2	lnc-LHCGR-1	chr2:48873569-48873753	NONHSAT070627
3	lnc-LHCGR-1	chr2:48859995-48860492	NONHSAT070628
4	lnc-LHCGR-1	chr2:48895709-48895804	NONHSAT070627
5	lnc-STON1-1	chr2:48771035-48771088	NONHSAT070624
6	lnc-LHCGR-1	chr2:48874168-48874258	NONHSAT070627
7	lnc-STON1-1	chr2:48774439-48775286	NONHSAT070624
8	lnc-STON1-1	chr2:48786942-48787278	NONHSAT070624

No data

Variant related genes	Relation type
STON1	TF binding region
GTF2A1L	TF binding region
TPT1P11	TF binding region
LHCGR	TF binding region
STON1-GTF2A1L	TF binding region
STON1	CpG island
GTF2A1L	CpG island
TPT1P11	CpG island
LHCGR	CpG island
STON1-GTF2A1L	CpG island
ENSG00000068781	chromatin interactions
ENSG00000242441	chromatin interactions
ENSG00000243244	chromatin interactions
ENSG00000162869	chromatin interactions

Extended variants
information (count: 6823 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:6823 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11695393	chr2:48763382-48763383	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368763567	chr2:48763396-48763397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373375644	chr2:48763405-48763406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192804328	chr2:48763406-48763407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543180080	chr2:48763410-48763411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549789451	chr2:48763422-48763423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549325987	chr2:48763484-48763485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568462168	chr2:48763493-48763494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143917538	chr2:48763505-48763506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532264018	chr2:48763518-48763519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs535882232	chr2:48763519-48763520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547538835	chr2:48763543-48763544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376641177	chr2:48763564-48763565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532226155	chr2:48763573-48763574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369084798	chr2:48763585-48763586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550754983	chr2:48763617-48763618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372901920	chr2:48763621-48763622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548797156	chr2:48763627-48763628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183974982	chr2:48763632-48763633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148896901	chr2:48763684-48763685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540312014	chr2:48763687-48763688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574715628	chr2:48763710-48763711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537326998	chr2:48763723-48763724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117171759	chr2:48763726-48763727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11689512	chr2:48763742-48763743	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs569335347	chr2:48763743-48763744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111352932	chr2:48763781-48763782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553061933	chr2:48763791-48763792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72872778	chr2:48763805-48763806	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs187195880	chr2:48763822-48763823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539615824	chr2:48763823-48763824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560742638	chr2:48763891-48763892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192054991	chr2:48763906-48763907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77738919	chr2:48763909-48763910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543329624	chr2:48763910-48763911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557942126	chr2:48763917-48763918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184459430	chr2:48763936-48763937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532028071	chr2:48764120-48764121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190383138	chr2:48764160-48764161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77125975	chr2:48764161-48764162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548249680	chr2:48764203-48764204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115640619	chr2:48764232-48764233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115347509	chr2:48764263-48764264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115883507	chr2:48764295-48764296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537622434	chr2:48764356-48764357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182071084	chr2:48764371-48764372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185880507	chr2:48764431-48764432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74879345	chr2:48764437-48764438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188991346	chr2:48764464-48764465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180878614	chr2:48764488-48764489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Bladder cancer	21909424	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
small cell lung cancer	20016488	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
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	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
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1022 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48758000-48766000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:48758800-48769000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:48758800-48772400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr2:48759000-48765200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:48759000-48765400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr2:48759000-48772600	Weak transcription	Fetal Muscle Leg	muscle
7	chr2:48759000-48775200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr2:48759000-48787000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr2:48759000-48787400	Weak transcription	Psoas Muscle	Psoas
10	chr2:48759000-48827600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr2:48759200-48766000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr2:48759200-48767000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:48759200-48793200	Weak transcription	Fetal Lung	lung
14	chr2:48759400-48767000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr2:48759400-48775200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:48760000-48766200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:48760000-48770800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:48760000-48771000	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr2:48760000-48772000	Weak transcription	Lung	lung
20	chr2:48760000-48772400	Weak transcription	Right Atrium	heart
21	chr2:48760200-48764800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr2:48760200-48767000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr2:48760200-48767000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:48760400-48767400	Weak transcription	Ovary	ovary
25	chr2:48760400-48772800	Weak transcription	Left Ventricle	heart
26	chr2:48762000-48767000	Weak transcription	Placenta	Placenta
27	chr2:48762200-48767600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr2:48762400-48763400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:48762400-48767400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr2:48762600-48769000	Weak transcription	Colon Smooth Muscle	Colon
31	chr2:48762600-48775000	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr2:48762800-48765800	Weak transcription	Fetal Stomach	stomach
33	chr2:48762800-48767000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr2:48763200-48763400	Enhancers	Stomach Smooth Muscle	stomach
35	chr2:48763400-48766200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr2:48763400-48769000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr2:48764800-48768000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr2:48765200-48767200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:48765400-48765600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr2:48765600-48767200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr2:48765800-48766800	ZNF genes & repeats	Fetal Stomach	stomach
42	chr2:48766000-48766200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:48766000-48768600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr2:48766200-48766600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:48766200-48767200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:48766200-48769000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:48766600-48766800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:48766800-48767800	Strong transcription	Fetal Stomach	stomach
49	chr2:48766800-48779600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr2:48767000-48767200	Enhancers	Aorta	Aorta

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