Variant report

Variant	nsv871791
Chromosome Location	chr1:104043185-104342898
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	ARID3A	chr1:104068425-104069462	K562	blood:	n/a	n/a
2	ARID3A	chr1:104332136-104332202	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:104103048-104103509	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:104076441-104076543	K562	blood:	n/a	n/a
5	ARID3A	chr1:104068398-104069159	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:104104781-104104969	HepG2	liver:	n/a	n/a
7	ATF2	chr1:104068246-104068748	GM12878	blood:	n/a	n/a
8	ATF2	chr1:104060167-104060706	GM12878	blood:	n/a	n/a
9	ATF2	chr1:104060069-104060653	GM12878	blood:	n/a	n/a
10	ATF2	chr1:104104531-104104991	GM12878	blood:	n/a	n/a
11	ATF2	chr1:104068276-104068823	GM12878	blood:	n/a	n/a
12	BATF	chr1:104163708-104163856	GM12878	blood:	n/a	n/a
13	BATF	chr1:104069996-104070255	GM12878	blood:	n/a	chr1:104070131-104070142
14	BATF	chr1:104069989-104070340	GM12878	blood:	n/a	chr1:104070131-104070142
15	BATF	chr1:104059876-104060357	GM12878	blood:	n/a	chr1:104060014-104060024 chr1:104060094-104060103
16	BATF	chr1:104163710-104163876	GM12878	blood:	n/a	n/a
17	BATF	chr1:104068947-104069203	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:104163692-104163866	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:104163716-104163847	GM12878	blood:	n/a	n/a
20	BCL3	chr1:104081714-104081999	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:104104511-104104987	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:104057548-104057847	GM12878	blood:	n/a	n/a
23	BCLAF1	chr1:104068286-104068884	GM12878	blood:	n/a	n/a
24	BHLHE40	chr1:104068347-104069164	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:104163686-104163884	HepG2	liver:	n/a	n/a
26	BHLHE40	chr1:104104614-104104992	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:104069904-104070362	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:104067893-104069179	K562	blood:	n/a	n/a
29	BRCA1	chr1:104068338-104068741	HepG2	liver:	n/a	chr1:104068541-104068550
30	BRCA1	chr1:104068257-104069233	Hela-S3	cervix:	n/a	chr1:104068541-104068550
31	BRCA1	chr1:104068332-104068755	H1-hESC	embryonic stem cell:	n/a	chr1:104068541-104068550
32	BRCA1	chr1:104068347-104068826	GM12878	blood:	n/a	chr1:104068541-104068550
33	BRCA1	chr1:104326501-104326782	GM12878	blood:	n/a	n/a
34	CBX3	chr1:104068335-104068703	K562	blood:	n/a	n/a
35	CBX3	chr1:104068298-104068668	K562	blood:	n/a	n/a
36	CCNT2	chr1:104068442-104069153	K562	blood:	n/a	n/a
37	CEBPB	chr1:104117717-104117917	HepG2	liver:	n/a	chr1:104117799-104117810
38	CEBPB	chr1:104120629-104120899	HepG2	liver:	n/a	chr1:104120781-104120792 chr1:104120780-104120791 chr1:104120780-104120793
39	CEBPB	chr1:104071533-104071833	HepG2	liver:	n/a	chr1:104071695-104071706
40	CEBPB	chr1:104103108-104103415	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:104067855-104068146	K562	blood:	n/a	n/a
42	CEBPB	chr1:104071591-104071848	IMR90	lung:	n/a	chr1:104071695-104071706
43	CEBPB	chr1:104109284-104109624	IMR90	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
44	CEBPB	chr1:104109287-104109643	HepG2	liver:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
45	CEBPB	chr1:104128801-104129380	HepG2	liver:	n/a	chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128959-104128968 chr1:104128957-104128970
46	CEBPB	chr1:104104662-104104945	Hela-S3	cervix:	n/a	chr1:104104711-104104723
47	CEBPB	chr1:104069315-104069645	K562	blood:	n/a	chr1:104069437-104069448
48	CEBPB	chr1:104109313-104109613	A549	lung:	n/a	chr1:104109438-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109515-104109526 chr1:104109440-104109449 chr1:104109438-104109449 chr1:104109440-104109451 chr1:104109440-104109451 chr1:104109440-104109449 chr1:104109438-104109451 chr1:104109440-104109449
49	CEBPB	chr1:104117700-104117982	IMR90	lung:	n/a	chr1:104117799-104117810
50	CEBPB	chr1:104074143-104074222	HepG2	liver:	n/a	chr1:104074178-104074189

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:104160257-104160307	ovcar-3	ovarian:	n/a
2	chr1:104068490-104068540	Jurkat	blood:	n/a
3	chr1:104160257-104160307	ovcar-3	ovarian:	n/a
4	chr1:104068490-104068540	Jurkat	blood:	n/a
5	chr1:104097670-104097720	AG04449	skin:	fetal
6	chr1:104068567-104068617	HL-60	blood:	n/a
7	chr1:104068567-104068617	NT2-D1	testis:	n/a
8	chr1:104160257-104160307	MCF10A-Er-Src	breast:	n/a
9	chr1:104068312-104068362	SAEC	small airway:	n/a
10	chr1:104239696-104239746	HCPEpiC	choroid plexus:	n/a
11	chr1:104068567-104068617	HRE	kidney:	n/a
12	chr1:104096517-104096567	Hepatocyte	liver:	n/a
13	chr1:104068419-104068469	ECC-1	luminal epithelium:	n/a
14	chr1:104068935-104068985	U87	brain:	n/a
15	chr1:104068312-104068362	AG09309	skin:	n/a
16	chr1:104068419-104068469	ovcar-3	ovarian:	n/a
17	chr1:104068301-104068351	HRE	kidney:	n/a
18	chr1:104068704-104068754	GM19239	blood:	n/a
19	chr1:104068704-104068754	AoSMC	blood vessel:	n/a
20	chr1:104068121-104068171	SK-N-SH_RA	brain:	n/a
21	chr1:104111877-104111927	NT2-D1	testis:	n/a
22	chr1:104239696-104239746	ovcar-3	ovarian:	n/a
23	chr1:104160257-104160307	A549	lung:	n/a
24	chr1:104068664-104068714	HL-60	blood:	n/a
25	chr1:104239696-104239746	HEEpiC	esophagus:	n/a
26	chr1:104097670-104097720	GM06990	blood:	n/a
27	chr1:104065263-104065313	HepG2	liver:	n/a
28	chr1:104068704-104068754	HUVEC	blood vessel:	n/a
29	chr1:104096517-104096567	HMEC	breast:	n/a
30	chr1:104112143-104112193	HCM	heart:	n/a
31	chr1:104068419-104068469	HRE	kidney:	n/a
32	chr1:104068121-104068171	PrEC	prostate:	n/a
33	chr1:104112143-104112193	K562	blood:	n/a
34	chr1:104097670-104097720	HL-60	blood:	n/a
35	chr1:104068301-104068351	NT2-D1	testis:	n/a
36	chr1:104068312-104068362	HCPEpiC	choroid plexus:	n/a
37	chr1:104068419-104068469	HCT-116	colon:	n/a
38	chr1:104068704-104068754	ECC-1	luminal epithelium:	n/a
39	chr1:104113039-104113089	CMK	blood:	n/a
40	chr1:104068301-104068351	IMR90	lung:	fetal
41	chr1:104068490-104068540	HCM	heart:	n/a
42	chr1:104068935-104068985	GM12891	blood:	n/a
43	chr1:104068567-104068617	HCF	heart:	n/a
44	chr1:104096621-104096671	HCT-116	colon:	n/a
45	chr1:104068118-104068168	HPAEpiC	pulmonary alveolar:	n/a
46	chr1:104096517-104096567	HCPEpiC	choroid plexus:	n/a
47	chr1:104068121-104068171	GM12878	blood:	n/a
48	chr1:104065263-104065313	HIPEpiC	eye:	n/a
49	chr1:104111877-104111927	MCF-7	breast:	n/a
50	chr1:104068118-104068168	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:104330211..104331667-chr1:104674701..104675769,4	MCF-7	breast:
2	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
3	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
4	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
5	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:
6	chr1:104067350..104071361-chr1:104071688..104074634,4	K562	blood:
7	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
8	chr1:104068373..104071907-chr1:104081557..104086760,7	K562	blood:
9	chr1:104067956..104068800-chr18:9474823..9475445,2	Hela-S3	cervix:
10	chr1:104067350..104070075-chr1:104070516..104073483,5	K562	blood:
11	chr1:104067221..104069850-chr1:104074751..104077723,3	MCF-7	breast:
12	chr1:104087556..104090106-chr1:104096002..104097509,2	K562	blood:
13	chr1:104330809..104331725-chr1:104675161..104675727,2	MCF-7	breast:
14	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
15	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:
16	chr1:104120354..104123298-chr1:104128850..104131166,2	K562	blood:
17	chr1:104075755..104077597-chr1:104090154..104091919,2	K562	blood:
18	chr1:104067752..104069863-chr1:104085885..104087467,2	MCF-7	breast:
19	chr1:104320249..104323301-chr1:104334806..104337281,3	K562	blood:
20	chr1:104068563..104070409-chr1:104091369..104094625,4	MCF-7	breast:
21	chr1:104084688..104087612-chr1:104092885..104095420,2	K562	blood:
22	chr1:104307678..104310486-chr1:104333154..104335185,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
2	lnc-AMY1B-1	chr1:104068018-104068115	XLOC_000945
3	lnc-AMY1B-1	chr1:104068018-104068105	XLOC_000945
4	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
5	lnc-AMY1B-1	chr1:104068018-104068139	XLOC_000945
6	lnc-AMY1B-1	chr1:104068018-104068083	ENSG00000224613.2
7	lnc-RNPC3-4	chr1:104066184-104066501	NONHSAT004893

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNPC3	hsa-miR-192-5p	chr1:104096163-104096184

Variant related genes	Relation type
AMY1C	TF binding region
ACTG1P4	TF binding region
AMY1A	TF binding region
ENSG00000224613	TF binding region
RNPC3	TF binding region
AMY1B	TF binding region
ENSG00000234441	TF binding region
AMY2A	TF binding region
AMYP1	TF binding region
RN7SKP285	TF binding region
AMY2B	TF binding region
AMY1C	CpG island
ACTG1P4	CpG island
AMY1A	CpG island
ENSG00000224613	CpG island
RNPC3	CpG island
AMY1B	CpG island
ENSG00000234441	CpG island
AMY2A	CpG island
AMYP1	CpG island
RN7SKP285	CpG island
AMY2B	CpG island
ENSG00000224613	chromatin interactions
ENSG00000185946	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000240038	chromatin interactions
TOMM34	miRNA target sites

Extended variants
information (count: 3639 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:3639 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12125927	chr1:104043185-104043186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147331925	chr1:104043219-104043220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369758840	chr1:104043232-104043233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72694406	chr1:104043239-104043240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563810571	chr1:104043260-104043261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148788086	chr1:104043342-104043343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376158795	chr1:104043369-104043370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569499413	chr1:104043421-104043422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536835479	chr1:104043456-104043457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529128161	chr1:104043463-104043464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375726215	chr1:104043465-104043466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184244381	chr1:104043512-104043513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537609929	chr1:104043535-104043536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533160155	chr1:104043575-104043576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551143003	chr1:104043603-104043604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375509486	chr1:104043651-104043652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188958459	chr1:104043659-104043660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555381663	chr1:104043662-104043663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142278268	chr1:104043663-104043664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181058784	chr1:104043675-104043676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150812386	chr1:104043764-104043765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78848391	chr1:104043801-104043802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
23	rs186321804	chr1:104043803-104043804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114644480	chr1:104043860-104043861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139332338	chr1:104043869-104043870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547945127	chr1:104043872-104043873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74109116	chr1:104043878-104043879	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs369543789	chr1:104043912-104043913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528480178	chr1:104043923-104043924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540885515	chr1:104043948-104043949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533640571	chr1:104044017-104044018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533121179	chr1:104044051-104044052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551544067	chr1:104044063-104044064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553394951	chr1:104044089-104044090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190033813	chr1:104044137-104044138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530595096	chr1:104044151-104044152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549115381	chr1:104044159-104044160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567338945	chr1:104044167-104044168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180788047	chr1:104044201-104044202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186219826	chr1:104044249-104044250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372862040	chr1:104044253-104044254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190895945	chr1:104044254-104044255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571901115	chr1:104044277-104044278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534708809	chr1:104044354-104044355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539000258	chr1:104044364-104044365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144284741	chr1:104044424-104044425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557505767	chr1:104044442-104044443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181984037	chr1:104044500-104044501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575453346	chr1:104044504-104044505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536309762	chr1:104044506-104044507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Cancer	22429812	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Lung cancer	17086460	CNVD
Gastric cancer	16891809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Multiple myeloma	17550852	CNVD
Schizophrenia	20967226	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:1570 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104040600-104043600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:104040600-104044000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr1:104043000-104043200	Enhancers	Aorta	Aorta
4	chr1:104043200-104046400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr1:104043200-104067400	Weak transcription	Aorta	Aorta
6	chr1:104043600-104044600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr1:104044000-104044600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:104046000-104047200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr1:104046200-104046800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr1:104046200-104047000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:104046200-104047200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:104046400-104046800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:104046400-104046800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr1:104046400-104047000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr1:104050000-104067400	Weak transcription	Left Ventricle	heart
16	chr1:104051800-104052400	Enhancers	HUVEC	blood vessel
17	chr1:104052000-104052600	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr1:104052200-104052600	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr1:104054400-104066200	Weak transcription	Psoas Muscle	Psoas
20	chr1:104054800-104062600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr1:104056200-104060600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:104056400-104056600	Enhancers	HMEC	breast
23	chr1:104056400-104056800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr1:104056400-104057600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:104056400-104059800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:104056600-104056800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr1:104056600-104056800	Enhancers	Osteobl	bone
28	chr1:104056800-104058400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:104056800-104058400	Weak transcription	Osteobl	bone
30	chr1:104057200-104058200	Weak transcription	HMEC	breast
31	chr1:104057600-104059000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:104057800-104058600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr1:104058200-104060400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:104058200-104060400	Enhancers	NH-A	brain
35	chr1:104058200-104060600	Enhancers	HMEC	breast
36	chr1:104058400-104059800	Enhancers	Osteobl	bone
37	chr1:104058400-104060400	Enhancers	NHEK	skin
38	chr1:104058400-104060600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:104058400-104060600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:104058600-104059600	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr1:104058800-104060000	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:104058800-104060600	Enhancers	HUVEC	blood vessel
43	chr1:104059000-104059200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr1:104059200-104060400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:104059400-104060200	Enhancers	GM12878-XiMat	blood
46	chr1:104059600-104060000	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr1:104059800-104067400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:104059800-104067400	Weak transcription	Osteobl	bone
49	chr1:104060200-104060400	Enhancers	Fetal Heart	heart
50	chr1:104060200-104060400	Enhancers	Sigmoid Colon	Sigmoid Colon

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