Variant report

Variant	esv3382652
Chromosome Location	chr14:71373549-71376347
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	chr14:71373929-71374421	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:71375376-71375583	HepG2	liver:	n/a	n/a
3	ATF3	chr14:71373936-71374105	K562	blood:	n/a	n/a
4	BACH1	chr14:71374691-71375583	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr14:71373588-71374162	A549	lung:	n/a	chr14:71374105-71374114
6	BCLAF1	chr14:71374946-71375591	GM12878	blood:	n/a	chr14:71375147-71375160 chr14:71375151-71375164 chr14:71375190-71375203 chr14:71375153-71375162 chr14:71375150-71375159 chr14:71375150-71375163
7	BCLAF1	chr14:71373665-71374534	GM12878	blood:	n/a	chr14:71374105-71374114
8	BCLAF1	chr14:71373808-71374512	GM12878	blood:	n/a	chr14:71374105-71374114
9	BHLHE40	chr14:71374690-71374766	K562	blood:	n/a	n/a
10	BHLHE40	chr14:71373820-71375496	GM12878	blood:	n/a	chr14:71374478-71374494 chr14:71373994-71374010 chr14:71374414-71374430 chr14:71375147-71375163
11	BHLHE40	chr14:71374018-71374164	K562	blood:	n/a	n/a
12	BRCA1	chr14:71373881-71374156	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr14:71373817-71374017	HepG2	liver:	n/a	n/a
14	CCNT2	chr14:71373788-71374788	K562	blood:	n/a	chr14:71374729-71374738
15	CEBPB	chr14:71373564-71374336	Hela-S3	cervix:	n/a	chr14:71373719-71373732
16	CEBPB	chr14:71373580-71373884	HepG2	liver:	n/a	chr14:71373719-71373732
17	CEBPB	chr14:71373557-71374209	MCF-7	breast:	n/a	chr14:71373719-71373732
18	CEBPB	chr14:71375383-71375499	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr14:71375263-71375870	Hela-S3	cervix:	n/a	n/a
20	CEBPD	chr14:71373950-71374417	HepG2	liver:	n/a	n/a
21	CHD1	chr14:71373870-71376082	GM12878	blood:	n/a	chr14:71374730-71374740 chr14:71375143-71375153 chr14:71375196-71375206 chr14:71374847-71374857
22	CHD1	chr14:71375261-71375778	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr14:71373422-71376760	IMR90	lung:	n/a	chr14:71374730-71374740 chr14:71375143-71375153 chr14:71375196-71375206 chr14:71374847-71374857
24	CHD1	chr14:71374587-71374670	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr14:71373862-71375543	Hela-S3	cervix:	n/a	chr14:71374730-71374740 chr14:71375143-71375153 chr14:71375196-71375206 chr14:71374847-71374857
26	CHD2	chr14:71373843-71375362	GM12878	blood:	n/a	chr14:71374730-71374740 chr14:71375143-71375153 chr14:71375196-71375206 chr14:71374847-71374857
27	CHD2	chr14:71375336-71375578	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr14:71375664-71375807	GM12878	blood:	n/a	n/a
29	CHD2	chr14:71375394-71375548	HepG2	liver:	n/a	n/a
30	CHD2	chr14:71374633-71375054	HepG2	liver:	n/a	chr14:71374730-71374740 chr14:71374847-71374857
31	CHD2	chr14:71373901-71374207	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr14:71373973-71374173	HepG2	liver:	n/a	n/a
33	CREB1	chr14:71373910-71374128	A549	lung:	n/a	n/a
34	CREB1	chr14:71373796-71374263	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr14:71373785-71374346	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr14:71373794-71374995	GM12878	blood:	n/a	n/a
37	CREB1	chr14:71373840-71374453	A549	lung:	n/a	n/a
38	CTBP2	chr14:71374665-71375575	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr14:71374978-71375139	ProgFib	skin:	n/a	n/a
40	CTCF	chr14:71373904-71374374	GM19239	blood:	n/a	chr14:71374100-71374110 chr14:71374130-71374143
41	CTCF	chr14:71373940-71374090	HCFaa	heart:	n/a	n/a
42	CTCF	chr14:71374000-71374150	GM12873	blood:	n/a	chr14:71374100-71374110 chr14:71374130-71374143
43	CTCF	chr14:71373980-71374130	BE2_C	brain:	n/a	chr14:71374100-71374110
44	CTCF	chr14:71373759-71374447	K562	blood:	n/a	chr14:71374100-71374110 chr14:71374130-71374143
45	CTCF	chr14:71374020-71374170	HAc	cerebellar:	n/a	chr14:71374100-71374110 chr14:71374130-71374143
46	CTCF	chr14:71374020-71374170	WI-38	lung:	n/a	chr14:71374100-71374110 chr14:71374130-71374143
47	CTCF	chr14:71373740-71373890	K562	blood:	n/a	n/a
48	CTCF	chr14:71374960-71375110	GM12866	blood:	n/a	n/a
49	CTCF	chr14:71373860-71374330	HepG2	liver:	n/a	chr14:71374100-71374110 chr14:71374130-71374143
50	CTCF	chr14:71374020-71374170	NHLF	lung:	n/a	chr14:71374100-71374110 chr14:71374130-71374143

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:71374299-71374349	PrEC	prostate:	n/a
2	chr14:71375349-71375399	HCM	heart:	n/a
3	chr14:71373858-71373908	PANC-1	pancreas:	n/a
4	chr14:71375319-71375369	NHDF-neo	bronchial:	n/a
5	chr14:71374299-71374349	PrEC	prostate:	n/a
6	chr14:71375349-71375399	HCM	heart:	n/a
7	chr14:71373858-71373908	PANC-1	pancreas:	n/a
8	chr14:71375319-71375369	NHDF-neo	bronchial:	n/a
9	chr14:71373978-71374028	Hela-S3	cervix:	n/a
10	chr14:71374302-71374352	HAEpiC	amniotic membrane:	n/a
11	chr14:71373980-71374030	HEK293	kidney:	embryo
12	chr14:71373980-71374030	LNCaP	prostate:	n/a
13	chr14:71375319-71375369	AG09319	gingival:	n/a
14	chr14:71373858-71373908	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:71374612-71374662	HRCEpiC	kidney:	n/a
16	chr14:71375319-71375369	HRPEpiC	eye:	n/a
17	chr14:71375319-71375369	Caco-2	colon:	n/a
18	chr14:71375319-71375369	HRCEpiC	kidney:	n/a
19	chr14:71373980-71374030	K562	blood:	n/a
20	chr14:71373978-71374028	AG10803	skin:	n/a
21	chr14:71375319-71375369	HEK293	kidney:	embryo
22	chr14:71374612-71374662	IMR90	lung:	fetal
23	chr14:71373858-71373908	GM12878	blood:	n/a
24	chr14:71374302-71374352	H1-hESC	embryonic stem cell:	embryo
25	chr14:71375319-71375369	GM12892	blood:	n/a
26	chr14:71375349-71375399	T-47D	breast:	n/a
27	chr14:71373978-71374028	AoSMC	blood vessel:	n/a
28	chr14:71375349-71375399	PrEC	prostate:	n/a
29	chr14:71375319-71375369	LNCaP	prostate:	n/a
30	chr14:71375349-71375399	HUVEC	blood vessel:	n/a
31	chr14:71374299-71374349	HepG2	liver:	n/a
32	chr14:71375349-71375399	AG04450	lung:	fetal
33	chr14:71374784-71374834	HCM	heart:	n/a
34	chr14:71374784-71374834	NHBE	bronchial:	n/a
35	chr14:71374612-71374662	T-47D	breast:	n/a
36	chr14:71374612-71374662	GM19239	blood:	n/a
37	chr14:71373888-71373938	NHDF-neo	bronchial:	n/a
38	chr14:71374302-71374352	AoSMC	blood vessel:	n/a
39	chr14:71373888-71373938	Jurkat	blood:	n/a
40	chr14:71373978-71374028	BE2_C	brain:	n/a
41	chr14:71374299-71374349	K562	blood:	n/a
42	chr14:71375319-71375369	GM19239	blood:	n/a
43	chr14:71374299-71374349	ProgFib	skin:	n/a
44	chr14:71373888-71373938	HEEpiC	esophagus:	n/a
45	chr14:71375349-71375399	AoSMC	blood vessel:	n/a
46	chr14:71375319-71375369	NH-A	brain:	n/a
47	chr14:71373858-71373908	NHBE	bronchial:	n/a
48	chr14:71373888-71373938	GM12892	blood:	n/a
49	chr14:71374784-71374834	AoSMC	blood vessel:	n/a
50	chr14:71373888-71373938	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:71373548..71375387-chr14:71412068..71413840,2	MCF-7	breast:
2	chr14:71368982..71370871-chr14:71374486..71376080,2	K562	blood:
3	chr14:71374157..71374728-chr2:38603975..38604567,2	Hela-S3	cervix:
4	chr14:71373774..71374385-chr17:61045448..61046114,2	Hela-S3	cervix:
5	chr14:71373840..71374362-chr8:136469426..136469930,2	MCF-7	breast:
6	chr14:71372585..71374647-chr14:71376260..71377778,2	K562	blood:
7	chr14:71373975..71375521-chr14:71375860..71378276,2	MCF-7	breast:

Variant related genes	Relation type
PCNX	TF binding region
PCNX	CpG island
ENSG00000119787	chromatin interactions
ENSG00000100731	chromatin interactions
ENSG00000266411	chromatin interactions
ENSG00000131773	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538189689	chr14:71373565-71373566	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs556561818	chr14:71373574-71373575	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs2240341	chr14:71373580-71373581	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs535123824	chr14:71373624-71373625	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563600049	chr14:71373626-71373627	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs10144691	chr14:71373627-71373628	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs200100805	chr14:71373629-71373630	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs149548923	chr14:71373653-71373654	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs146025912	chr14:71373664-71373665	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558029449	chr14:71373680-71373681	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs377633508	chr14:71373686-71373687	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576290820	chr14:71373747-71373748	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs140031717	chr14:71373767-71373768	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561856370	chr14:71373773-71373774	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529152372	chr14:71373787-71373788	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541870991	chr14:71373862-71373863	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs547318861	chr14:71373906-71373907	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs527830136	chr14:71373936-71373937	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs371011049	chr14:71373963-71373964	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs552245395	chr14:71374005-71374006	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs564372347	chr14:71374081-71374082	Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs3122098	chr14:71374087-71374088	Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs3094891	chr14:71374088-71374089	Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs143556921	chr14:71374092-71374093	Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs550318831	chr14:71374111-71374112	Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs568672483	chr14:71374160-71374161	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs536105466	chr14:71374163-71374164	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs547080204	chr14:71374229-71374230	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs565675471	chr14:71374232-71374233	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs539581558	chr14:71374278-71374279	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs146815725	chr14:71374282-71374283	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs28397070	chr14:71374311-71374312	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs148523058	chr14:71374330-71374331	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs576179022	chr14:71374334-71374335	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs536868346	chr14:71374363-71374364	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs34907416	chr14:71374383-71374384	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs76961858	chr14:71374386-71374387	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs541318359	chr14:71374463-71374464	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs3122097	chr14:71374524-71374525	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs3094890	chr14:71374525-71374526	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs556580107	chr14:71374543-71374544	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs560327711	chr14:71374546-71374547	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs113468911	chr14:71374562-71374563	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs199898507	chr14:71374592-71374593	Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs371986953	chr14:71374618-71374619	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs141085703	chr14:71374653-71374654	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs545920002	chr14:71374657-71374658	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566932318	chr14:71374672-71374673	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs2526882	chr14:71374702-71374703	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs201812061	chr14:71374711-71374712	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71364000-71373800	Weak transcription	Small Intestine	intestine
2	chr14:71364200-71373600	Weak transcription	Lung	lung
3	chr14:71368600-71373600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:71368800-71373600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr14:71370800-71373600	Enhancers	Fetal Lung	lung
6	chr14:71371000-71373600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr14:71371200-71373600	Weak transcription	Colonic Mucosa	Colon
8	chr14:71371200-71373600	Enhancers	HSMM	muscle
9	chr14:71371200-71374200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:71371600-71373800	Flanking Active TSS	HSMMtube	muscle
11	chr14:71371800-71373600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr14:71372000-71373600	Enhancers	Fetal Heart	heart
13	chr14:71372200-71373600	Weak transcription	Placenta	Placenta
14	chr14:71372400-71373600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr14:71372400-71373600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr14:71372400-71373600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr14:71372400-71373600	Weak transcription	Fetal Muscle Trunk	muscle
18	chr14:71372400-71373600	Weak transcription	Gastric	stomach
19	chr14:71372400-71373600	Weak transcription	Left Ventricle	heart
20	chr14:71372600-71373600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr14:71372800-71373600	Enhancers	Fetal Intestine Large	intestine
22	chr14:71372800-71374000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
23	chr14:71373000-71373600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr14:71373000-71373600	Enhancers	Primary B cells from peripheral blood	blood
25	chr14:71373000-71373600	Enhancers	Primary T cells from cord blood	blood
26	chr14:71373000-71373600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
27	chr14:71373000-71373600	Enhancers	Liver	Liver
28	chr14:71373000-71373600	Flanking Active TSS	Brain Angular Gyrus	brain
29	chr14:71373000-71373600	Flanking Active TSS	Rectal Smooth Muscle	rectum
30	chr14:71373000-71373800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr14:71373000-71374000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:71373000-71374000	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr14:71373000-71374000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr14:71373000-71374000	Enhancers	Stomach Mucosa	stomach
35	chr14:71373000-71374800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr14:71373200-71373600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr14:71373200-71373600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr14:71373200-71373600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
39	chr14:71373200-71373600	Enhancers	Fetal Brain Male	brain
40	chr14:71373200-71373800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr14:71373200-71373800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr14:71373200-71373800	Flanking Active TSS	Fetal Kidney	kidney
43	chr14:71373200-71373800	Weak transcription	Spleen	Spleen
44	chr14:71373200-71373800	Flanking Active TSS	Osteobl	bone
45	chr14:71373200-71374000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr14:71373200-71374000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr14:71373200-71374000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr14:71373200-71374000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr14:71373200-71374200	Active TSS	Right Atrium	heart
50	chr14:71373200-71374400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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