Variant report

Variant	esv3423260
Chromosome Location	chr3:141204887-141207435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:627)
CpG islands
(count:671)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141204602-141205135	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:141206589-141206612	K562	blood:	n/a	n/a
3	ATF2	chr3:141206413-141207085	GM12878	blood:	n/a	n/a
4	ATF2	chr3:141206631-141207016	GM12878	blood:	n/a	n/a
5	BACH1	chr3:141206233-141206877	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:141206694-141206981	GM12878	blood:	n/a	n/a
7	BCLAF1	chr3:141206184-141207039	GM12878	blood:	n/a	chr3:141206443-141206456 chr3:141206447-141206460
8	BCLAF1	chr3:141206371-141207002	GM12878	blood:	n/a	chr3:141206443-141206456 chr3:141206447-141206460
9	BCLAF1	chr3:141205789-141206182	GM12878	blood:	n/a	chr3:141205857-141205870 chr3:141206114-141206123
10	BHLHE40	chr3:141205409-141207051	GM12878	blood:	n/a	chr3:141206446-141206462 chr3:141206249-141206265
11	BHLHE40	chr3:141205842-141206094	A549	lung:	n/a	n/a
12	BHLHE40	chr3:141205262-141206829	HepG2	liver:	n/a	chr3:141206446-141206462 chr3:141206249-141206265
13	BHLHE40	chr3:141204515-141204900	K562	blood:	n/a	n/a
14	BHLHE40	chr3:141205733-141206940	K562	blood:	n/a	chr3:141206446-141206462 chr3:141206249-141206265
15	BRCA1	chr3:141206020-141206049	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:141206486-141206909	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr3:141205427-141205675	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr3:141204967-141205089	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr3:141205983-141206025	HepG2	liver:	n/a	n/a
20	BRCA1	chr3:141205390-141205785	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr3:141204535-141204995	K562	blood:	n/a	n/a
22	CBX3	chr3:141206397-141207020	K562	blood:	n/a	n/a
23	CCNT2	chr3:141205713-141206856	K562	blood:	n/a	chr3:141206548-141206557
24	CEBPB	chr3:141206590-141206894	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:141205431-141206029	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:141206615-141206853	HepG2	liver:	n/a	n/a
27	CEBPD	chr3:141205686-141206179	HepG2	liver:	n/a	n/a
28	CHD1	chr3:141204883-141204890	GM12878	blood:	n/a	n/a
29	CHD1	chr3:141205952-141206066	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr3:141205787-141207595	IMR90	lung:	n/a	chr3:141206600-141206607
31	CHD1	chr3:141206907-141207237	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr3:141206219-141207048	GM12878	blood:	n/a	chr3:141206600-141206607
33	CHD2	chr3:141206453-141206937	GM12878	blood:	n/a	chr3:141206600-141206607
34	CHD2	chr3:141205350-141206901	Hela-S3	cervix:	n/a	chr3:141206600-141206607
35	CHD2	chr3:141205235-141206080	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr3:141205427-141205611	GM12878	blood:	n/a	n/a
37	CHD2	chr3:141205967-141206060	K562	blood:	n/a	n/a
38	CHD2	chr3:141205817-141206131	GM12878	blood:	n/a	n/a
39	CHD2	chr3:141206588-141206938	K562	blood:	n/a	chr3:141206600-141206607
40	CHD2	chr3:141205352-141206186	HepG2	liver:	n/a	n/a
41	CHD2	chr3:141206563-141206913	HepG2	liver:	n/a	chr3:141206600-141206607
42	CHD2	chr3:141205545-141205725	K562	blood:	n/a	n/a
43	CHD2	chr3:141206517-141206747	H1-hESC	embryonic stem cell:	n/a	chr3:141206600-141206607
44	CREB1	chr3:141205790-141206831	A549	lung:	n/a	n/a
45	CREB1	chr3:141205610-141207011	HepG2	liver:	n/a	n/a
46	CTBP2	chr3:141205522-141206871	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr3:141206700-141206850	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr3:141206628-141206801	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:141206620-141206770	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr3:141206573-141206580	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141205758-141205808	H1-hESC	embryonic stem cell:	embryo
2	chr3:141206348-141206398	T-47D	breast:	n/a
3	chr3:141206102-141206152	HEEpiC	esophagus:	n/a
4	chr3:141205767-141205817	GM06990	blood:	n/a
5	chr3:141205540-141205590	HRE	kidney:	n/a
6	chr3:141205758-141205808	HCM	heart:	n/a
7	chr3:141205623-141205673	HUVEC	blood vessel:	n/a
8	chr3:141205767-141205817	A549	lung:	n/a
9	chr3:141206903-141206953	SK-N-SH	brain:	n/a
10	chr3:141206694-141206744	IMR90	lung:	fetal
11	chr3:141206903-141206953	Jurkat	blood:	n/a
12	chr3:141205623-141205673	HEEpiC	esophagus:	n/a
13	chr3:141205649-141205699	IMR90	lung:	fetal
14	chr3:141206759-141206809	SKMC	muscle:	n/a
15	chr3:141206348-141206398	A549	lung:	n/a
16	chr3:141206348-141206398	Hepatocyte	liver:	n/a
17	chr3:141205649-141205699	HMEC	breast:	n/a
18	chr3:141206694-141206744	ProgFib	skin:	n/a
19	chr3:141205758-141205808	Caco-2	colon:	n/a
20	chr3:141206102-141206152	SAEC	small airway:	n/a
21	chr3:141206694-141206744	HRE	kidney:	n/a
22	chr3:141206028-141206078	GM06990	blood:	n/a
23	chr3:141206759-141206809	RPTEC	kidney:	n/a
24	chr3:141206102-141206152	HNPCEpiC	eye:	n/a
25	chr3:141205767-141205817	PANC-1	pancreas:	n/a
26	chr3:141205767-141205817	NHDF-neo	bronchial:	n/a
27	chr3:141206759-141206809	AG10803	skin:	n/a
28	chr3:141206102-141206152	Caco-2	colon:	n/a
29	chr3:141206694-141206744	HCM	heart:	n/a
30	chr3:141205649-141205699	ovcar-3	ovarian:	n/a
31	chr3:141206759-141206809	HL-60	blood:	n/a
32	chr3:141205767-141205817	ProgFib	skin:	n/a
33	chr3:141205623-141205673	SK-N-MC	brain:	n/a
34	chr3:141206694-141206744	AG09309	skin:	n/a
35	chr3:141205540-141205590	CMK	blood:	n/a
36	chr3:141206694-141206744	MCF10A-Er-Src	breast:	n/a
37	chr3:141205758-141205808	NT2-D1	testis:	n/a
38	chr3:141205758-141205808	T-47D	breast:	n/a
39	chr3:141206102-141206152	GM12892	blood:	n/a
40	chr3:141206028-141206078	HEK293	kidney:	embryo
41	chr3:141206903-141206953	GM19239	blood:	n/a
42	chr3:141206903-141206953	IMR90	lung:	fetal
43	chr3:141205767-141205817	GM12878	blood:	n/a
44	chr3:141206028-141206078	ECC-1	luminal epithelium:	n/a
45	chr3:141205623-141205673	HL-60	blood:	n/a
46	chr3:141206903-141206953	HRE	kidney:	n/a
47	chr3:141206694-141206744	PrEC	prostate:	n/a
48	chr3:141206348-141206398	MCF10A-Er-Src	breast:	n/a
49	chr3:141205649-141205699	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:141205649-141205699	GM06990	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:141085187..141087816-chr3:141204878..141206678,4	MCF-7	breast:
2	chr3:141085737..141089975-chr3:141204779..141207356,5	K562	blood:
3	chr12:120729229..120730031-chr3:141205706..141206699,3	Hela-S3	cervix:
4	chr3:141206890..141209130-chr3:141222372..141224478,3	MCF-7	breast:
5	chr12:72057082..72057894-chr3:141205927..141206704,2	HCT-116	colon:
6	chr3:141205894..141211656-chr3:141222007..141226023,7	K562	blood:
7	chr3:141206272..141206931-chr7:5569362..5570306,2	Hela-S3	cervix:
8	chr3:141205080..141206779-chr6:76458156..76460847,2	MCF-7	breast:
9	chr3:141189849..141195094-chr3:141204829..141208801,7	MCF-7	breast:
10	chr3:141203440..141205280-chr3:141224808..141226638,2	K562	blood:
11	chr3:141205921..141208089-chr3:141225217..141227159,2	MCF-7	breast:
12	chr3:141206322..141208347-chr3:141274984..141277409,3	K562	blood:
13	chr3:141206855..141208513-chr3:141245393..141248171,2	MCF-7	breast:
14	chr18:12883912..12884619-chr3:141205723..141206246,2	Hela-S3	cervix:
15	chr3:141204551..141207938-chr3:141241119..141245308,6	MCF-7	breast:
16	chr3:141194536..141196661-chr3:141202566..141205649,3	K562	blood:

No data

Variant related genes	Relation type
RASA2	TF binding region
RASA2	CpG island
ENSG00000250170	chromatin interactions
ENSG00000215606	chromatin interactions
ENSG00000175354	chromatin interactions
ENSG00000177311	chromatin interactions
ENSG00000196586	chromatin interactions
ENSG00000249417	chromatin interactions
ENSG00000133858	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 90 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:90 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374681787	chr3:141204943-141204944	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs532877393	chr3:141204971-141204972	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs370232099	chr3:141205008-141205009	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs555519697	chr3:141205027-141205028	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs138976639	chr3:141205058-141205059	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs368741343	chr3:141205063-141205064	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs142228370	chr3:141205173-141205174	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs3821712	chr3:141205185-141205186	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs79024127	chr3:141205188-141205189	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs369826952	chr3:141205192-141205193	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs188438242	chr3:141205193-141205194	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs534844840	chr3:141205194-141205195	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs117352895	chr3:141205211-141205212	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs115823107	chr3:141205265-141205266	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs150911176	chr3:141205282-141205283	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs558646446	chr3:141205283-141205284	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs575752285	chr3:141205303-141205304	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs542655024	chr3:141205326-141205327	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs9833339	chr3:141205360-141205361	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs12695736	chr3:141205465-141205466	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs375668483	chr3:141205521-141205522	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs534599801	chr3:141205523-141205524	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs575383002	chr3:141205551-141205552	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs3806647	chr3:141205563-141205564	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532520250	chr3:141205571-141205572	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs3806648	chr3:141205572-141205573	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs563034993	chr3:141205627-141205628	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs376171560	chr3:141205673-141205674	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs548678689	chr3:141205697-141205698	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs561268236	chr3:141205703-141205704	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs528399465	chr3:141205710-141205711	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs13064789	chr3:141205720-141205721	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs111296302	chr3:141205723-141205724	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs546828028	chr3:141205773-141205774	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs571477198	chr3:141205774-141205775	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs9713110	chr3:141205825-141205826	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs538827438	chr3:141205930-141205931	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs201352230	chr3:141205942-141205943	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs200191034	chr3:141205951-141205952	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs372336063	chr3:141205957-141205958	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs376313232	chr3:141205963-141205964	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs536687230	chr3:141205996-141205997	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs554683720	chr3:141206025-141206026	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs369569203	chr3:141206046-141206047	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs573160719	chr3:141206095-141206096	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs534225581	chr3:141206111-141206112	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs558782989	chr3:141206137-141206138	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs117367539	chr3:141206207-141206208	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs544398776	chr3:141206218-141206219	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs563071305	chr3:141206220-141206221	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21509527	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141201200-141205400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr3:141201400-141205400	Enhancers	Placenta	Placenta
3	chr3:141203000-141205600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr3:141203400-141205600	Enhancers	Lung	lung
5	chr3:141203800-141205200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr3:141203800-141205200	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:141203800-141205200	Enhancers	Primary T cells fromperipheralblood	blood
8	chr3:141203800-141205200	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr3:141203800-141205400	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr3:141204000-141205000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr3:141204000-141205000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr3:141204000-141205400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:141204000-141205400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:141204200-141205200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr3:141204200-141205200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr3:141204200-141205200	Enhancers	Fetal Intestine Large	intestine
17	chr3:141204200-141205200	Enhancers	Dnd41	blood
18	chr3:141204200-141205600	Flanking Active TSS	HUVEC	blood vessel
19	chr3:141204200-141205800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr3:141204200-141208000	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr3:141204400-141205000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:141204400-141205000	Enhancers	Duodenum Smooth Muscle	Duodenum
23	chr3:141204400-141205000	Enhancers	NH-A	brain
24	chr3:141204400-141205200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr3:141204400-141205200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:141204400-141205200	Enhancers	HSMM	muscle
27	chr3:141204400-141205800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
28	chr3:141204600-141205000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr3:141204600-141205000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:141204600-141205000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr3:141204600-141205000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr3:141204600-141205000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:141204600-141205000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr3:141204600-141205000	Enhancers	Right Atrium	heart
35	chr3:141204600-141205000	Flanking Active TSS	HepG2	liver
36	chr3:141204600-141205200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr3:141204600-141205200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr3:141204600-141205200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:141204600-141205200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr3:141204600-141205200	Enhancers	Brain Hippocampus Middle	brain
41	chr3:141204600-141205400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:141204600-141205400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr3:141204600-141205400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:141204600-141205400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr3:141204600-141205400	Enhancers	Fetal Thymus	thymus
46	chr3:141204600-141205400	Enhancers	Left Ventricle	heart
47	chr3:141204600-141205400	Enhancers	Stomach Mucosa	stomach
48	chr3:141204600-141205400	Flanking Active TSS	A549	lung
49	chr3:141204600-141205400	Enhancers	HSMMtube	muscle
50	chr3:141204600-141205600	Flanking Active TSS	Primary T cells from cord blood	blood

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