Variant report

Variant	esv3358123
Chromosome Location	chr14:55359251-55378030
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	chr14:55359897-55360240	K562	blood:	n/a	n/a
2	ARID3A	chr14:55369457-55370106	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:55359876-55360266	HepG2	liver:	n/a	n/a
4	ATF2	chr14:55369631-55370101	GM12878	blood:	n/a	n/a
5	ATF2	chr14:55367373-55367979	GM12878	blood:	n/a	n/a
6	BACH1	chr14:55368473-55368676	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr14:55359992-55360241	GM12878	blood:	n/a	chr14:55360141-55360152 chr14:55360142-55360152
8	BCLAF1	chr14:55368645-55369241	GM12878	blood:	n/a	chr14:55368916-55368924 chr14:55368996-55369005 chr14:55368993-55369006
9	BCLAF1	chr14:55368760-55369343	GM12878	blood:	n/a	chr14:55368916-55368924 chr14:55368996-55369005 chr14:55368993-55369006
10	BHLHE40	chr14:55369915-55370002	K562	blood:	n/a	n/a
11	BHLHE40	chr14:55368944-55370096	HepG2	liver:	n/a	chr14:55368993-55369009
12	BHLHE40	chr14:55359974-55360181	K562	blood:	n/a	n/a
13	BHLHE40	chr14:55368574-55369625	K562	blood:	n/a	chr14:55368993-55369009
14	BHLHE40	chr14:55368855-55369669	GM12878	blood:	n/a	chr14:55368993-55369009
15	BRCA1	chr14:55369363-55369546	HepG2	liver:	n/a	n/a
16	BRCA1	chr14:55369321-55369517	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr14:55368666-55368974	Hela-S3	cervix:	n/a	n/a
18	CCNT2	chr14:55368738-55369879	K562	blood:	n/a	n/a
19	CEBPB	chr14:55369741-55369908	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:55367355-55367734	Hela-S3	cervix:	n/a	chr14:55367675-55367688 chr14:55367549-55367560 chr14:55367703-55367714 chr14:55367548-55367561
21	CEBPB	chr14:55376501-55376857	K562	blood:	n/a	chr14:55376665-55376678 chr14:55376667-55376676 chr14:55376667-55376676 chr14:55376667-55376676
22	CEBPB	chr14:55376511-55376843	Hela-S3	cervix:	n/a	chr14:55376665-55376678 chr14:55376667-55376676 chr14:55376667-55376676 chr14:55376667-55376676
23	CEBPB	chr14:55367500-55367682	H1-hESC	embryonic stem cell:	n/a	chr14:55367549-55367560 chr14:55367548-55367561
24	CEBPB	chr14:55368176-55368189	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:55376503-55376846	IMR90	lung:	n/a	chr14:55376665-55376678 chr14:55376667-55376676 chr14:55376667-55376676 chr14:55376667-55376676
26	CEBPB	chr14:55376513-55376846	H1-hESC	embryonic stem cell:	n/a	chr14:55376665-55376678 chr14:55376667-55376676 chr14:55376667-55376676 chr14:55376667-55376676
27	CEBPB	chr14:55368747-55369205	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:55365993-55366577	HepG2	liver:	n/a	chr14:55366425-55366436
29	CEBPB	chr14:55368170-55368343	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:55368753-55369050	K562	blood:	n/a	n/a
31	CEBPB	chr14:55368754-55369926	HepG2	liver:	n/a	n/a
32	CEBPB	chr14:55367252-55367739	IMR90	lung:	n/a	chr14:55367675-55367688 chr14:55367549-55367560 chr14:55367703-55367714 chr14:55367548-55367561
33	CEBPB	chr14:55369658-55369798	K562	blood:	n/a	n/a
34	CEBPB	chr14:55367458-55367726	HepG2	liver:	n/a	chr14:55367675-55367688 chr14:55367549-55367560 chr14:55367703-55367714 chr14:55367548-55367561
35	CEBPB	chr14:55368493-55369496	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:55368619-55369233	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr14:55376477-55376830	K562	blood:	n/a	chr14:55376665-55376678 chr14:55376667-55376676 chr14:55376667-55376676 chr14:55376667-55376676
38	CEBPB	chr14:55376445-55376871	MCF-7	breast:	n/a	chr14:55376665-55376678 chr14:55376667-55376676 chr14:55376667-55376676 chr14:55376667-55376676
39	CEBPB	chr14:55376595-55376902	A549	lung:	n/a	chr14:55376665-55376678 chr14:55376667-55376676 chr14:55376667-55376676 chr14:55376667-55376676
40	CEBPB	chr14:55368764-55369136	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:55368785-55369124	IMR90	lung:	n/a	n/a
42	CEBPB	chr14:55367441-55367682	A549	lung:	n/a	chr14:55367549-55367560 chr14:55367548-55367561
43	CEBPB	chr14:55368846-55369035	HepG2	liver:	n/a	n/a
44	CEBPB	chr14:55370378-55370480	HepG2	liver:	n/a	chr14:55370428-55370439 chr14:55370427-55370440 chr14:55370427-55370438
45	CEBPB	chr14:55366315-55366568	IMR90	lung:	n/a	chr14:55366425-55366436
46	CEBPB	chr14:55366050-55366568	K562	blood:	n/a	chr14:55366425-55366436
47	CEBPB	chr14:55368762-55369135	K562	blood:	n/a	n/a
48	CEBPB	chr14:55368578-55369119	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr14:55367344-55367822	MCF-7	breast:	n/a	chr14:55367675-55367688 chr14:55367549-55367560 chr14:55367703-55367714 chr14:55367548-55367561
50	CEBPB	chr14:55370348-55370548	K562	blood:	n/a	chr14:55370428-55370439 chr14:55370427-55370440 chr14:55370427-55370438

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55373834-55373884	U87	brain:	n/a
2	chr14:55369781-55369831	HEK293	kidney:	embryo
3	chr14:55373834-55373884	U87	brain:	n/a
4	chr14:55369781-55369831	HEK293	kidney:	embryo
5	chr14:55368706-55368756	AG04449	skin:	fetal
6	chr14:55369959-55370009	SK-N-SH_RA	brain:	n/a
7	chr14:55369030-55369080	HEEpiC	esophagus:	n/a
8	chr14:55368442-55368492	PANC-1	pancreas:	n/a
9	chr14:55368706-55368756	Jurkat	blood:	n/a
10	chr14:55368706-55368756	HRE	kidney:	n/a
11	chr14:55369460-55369510	H1-hESC	embryonic stem cell:	embryo
12	chr14:55369460-55369510	HMEC	breast:	n/a
13	chr14:55369212-55369262	SK-N-SH_RA	brain:	n/a
14	chr14:55369030-55369080	AG10803	skin:	n/a
15	chr14:55368924-55368974	GM12878	blood:	n/a
16	chr14:55368706-55368756	SK-N-SH	brain:	n/a
17	chr14:55369959-55370009	GM12892	blood:	n/a
18	chr14:55368706-55368756	RPTEC	kidney:	n/a
19	chr14:55369460-55369510	AG04450	lung:	fetal
20	chr14:55368706-55368756	HCM	heart:	n/a
21	chr14:55368924-55368974	CMK	blood:	n/a
22	chr14:55369861-55369911	Hela-S3	cervix:	n/a
23	chr14:55368706-55368756	SK-N-SH_RA	brain:	n/a
24	chr14:55368343-55368393	HCPEpiC	choroid plexus:	n/a
25	chr14:55369781-55369831	ECC-1	luminal epithelium:	n/a
26	chr14:55368343-55368393	HNPCEpiC	eye:	n/a
27	chr14:55368706-55368756	CMK	blood:	n/a
28	chr14:55366874-55366924	GM12878	blood:	n/a
29	chr14:55368343-55368393	HAEpiC	amniotic membrane:	n/a
30	chr14:55368924-55368974	HRPEpiC	eye:	n/a
31	chr14:55369212-55369262	T-47D	breast:	n/a
32	chr14:55369861-55369911	RPTEC	kidney:	n/a
33	chr14:55369959-55370009	SAEC	small airway:	n/a
34	chr14:55368442-55368492	HNPCEpiC	eye:	n/a
35	chr14:55369959-55370009	SK-N-MC	brain:	n/a
36	chr14:55368343-55368393	H1-hESC	embryonic stem cell:	embryo
37	chr14:55369030-55369080	AG04450	lung:	fetal
38	chr14:55368706-55368756	T-47D	breast:	n/a
39	chr14:55369460-55369510	SK-N-MC	brain:	n/a
40	chr14:55369212-55369262	Caco-2	colon:	n/a
41	chr14:55369861-55369911	HIPEpiC	eye:	n/a
42	chr14:55368442-55368492	ovcar-3	ovarian:	n/a
43	chr14:55368343-55368393	ProgFib	skin:	n/a
44	chr14:55368706-55368756	ProgFib	skin:	n/a
45	chr14:55366874-55366924	IMR90	lung:	fetal
46	chr14:55373834-55373884	HL-60	blood:	n/a
47	chr14:55369460-55369510	HCM	heart:	n/a
48	chr14:55368343-55368393	AG09309	skin:	n/a
49	chr14:55369861-55369911	Hepatocyte	liver:	n/a
50	chr14:55369460-55369510	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:114250712..114251342-chr14:55359858..55360579,2	MCF-7	breast:
2	chr14:55359557..55360396-chr14:55599807..55600483,2	MCF-7	breast:
3	chr14:55368751..55370631-chr14:55518308..55520538,2	K562	blood:
4	chr14:55289701..55291395-chr14:55367160..55368912,2	MCF-7	breast:
5	chr14:55032510..55035314-chr14:55358663..55360584,2	MCF-7	breast:
6	chr14:55368974..55369574-chr6:27100348..27100871,2	Hela-S3	cervix:
7	chr14:55368060..55369582-chr14:55493883..55496744,2	MCF-7	breast:
8	chr14:55368284..55370170-chr14:55376140..55380944,4	MCF-7	breast:
9	chr14:55368556..55370568-chr14:55372065..55374377,3	MCF-7	breast:
10	chr14:55372048..55373585-chr14:55492566..55495202,2	K562	blood:
11	chr14:55030801..55036234-chr14:55366700..55372024,9	MCF-7	breast:
12	chr14:55368311..55371330-chr14:55594542..55598408,4	MCF-7	breast:
13	chr14:55348331..55350043-chr14:55361093..55363707,2	K562	blood:
14	chr14:55368105..55371463-chr14:55516987..55520396,7	MCF-7	breast:
15	chr14:55369487..55370112-chrX:70585640..70586564,2	Hela-S3	cervix:
16	chr14:55369172..55369944-chr19:35264069..35264965,2	HCT-116	colon:
17	chr14:55361522..55363244-chr14:55517974..55519538,2	MCF-7	breast:
18	chr14:55032369..55034172-chr14:55367637..55369968,2	K562	blood:
19	chr14:55343213..55346860-chr14:55368496..55370471,3	MCF-7	breast:
20	chr14:55247890..55252413-chr14:55368163..55370491,5	MCF-7	breast:
21	chr14:55360231..55364033-chr14:55366282..55369580,4	K562	blood:
22	chr14:55365292..55366794-chr14:55367173..55368937,2	K562	blood:
23	chr14:55367425..55371142-chr14:55516489..55521777,7	MCF-7	breast:
24	chr14:55369324..55371934-chr14:55373929..55376733,3	K562	blood:
25	chr14:55365292..55366794-chr14:55367173..55368937,2	K562	blood:
26	chr14:55279326..55281967-chr14:55362988..55365196,2	MCF-7	breast:
27	chr14:55354060..55356270-chr14:55359922..55362227,2	K562	blood:
28	chr14:55351951..55354870-chr14:55368126..55370512,5	MCF-7	breast:
29	chr14:54954247..54955899-chr14:55367178..55369078,2	MCF-7	breast:
30	chr14:55359687..55364414-chr14:55366282..55370012,8	K562	blood:
31	chr14:55359081..55363562-chr14:55365386..55370539,12	MCF-7	breast:
32	chr14:55367938..55370447-chr14:55374823..55378227,3	K562	blood:
33	chr1:145381572..145383182-chr14:55371948..55373600,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SAMD4A-3	chr14:55369024-55370518	NONHSAT036977

Variant related genes	Relation type
GCH1	TF binding region
GCH1	CpG island
ENSG00000197045	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000147133	chromatin interactions
ENSG00000256195	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000198554	chromatin interactions
ENSG00000020577	chromatin interactions
ENSG00000131981	chromatin interactions
ENSG00000180008	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000131979	chromatin interactions
ENSG00000153896	chromatin interactions
ENSG00000265432	chromatin interactions
ENSG00000168175	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000258872	chromatin interactions

Extended variants
information (count: 789 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:789 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182032583	chr14:55359267-55359268	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs531621840	chr14:55359320-55359321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs550107138	chr14:55359385-55359386	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571848552	chr14:55359404-55359405	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs116829666	chr14:55359448-55359449	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs548050499	chr14:55359508-55359509	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs566260746	chr14:55359519-55359520	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs542636881	chr14:55359560-55359561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs533903425	chr14:55359570-55359571	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs149060032	chr14:55359594-55359595	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs143009532	chr14:55359602-55359603	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs148202994	chr14:55359613-55359614	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs35265487	chr14:55359635-55359636	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575149365	chr14:55359642-55359643	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs113585929	chr14:55359653-55359654	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
16	rs577564841	chr14:55359654-55359655	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs145610220	chr14:55359655-55359656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs553587378	chr14:55359656-55359657	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112165923	chr14:55359664-55359665	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
20	rs142520205	chr14:55359690-55359691	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571388746	chr14:55359725-55359726	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs376263783	chr14:55359726-55359727	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs527604849	chr14:55359759-55359760	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150563865	chr14:55359764-55359765	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs138196765	chr14:55359789-55359790	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs149591874	chr14:55359793-55359794	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565271447	chr14:55359803-55359804	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs17832263	chr14:55359822-55359823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs75116139	chr14:55359831-55359832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115665619	chr14:55359862-55359863	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs186171240	chr14:55359872-55359873	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs77285555	chr14:55359878-55359879	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs568438218	chr14:55359887-55359888	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs78886498	chr14:55359933-55359934	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs189076786	chr14:55359945-55359946	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs537945852	chr14:55359965-55359966	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs114876991	chr14:55359974-55359975	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs117641016	chr14:55359993-55359994	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs116626090	chr14:55360045-55360046	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs10133661	chr14:55360056-55360057	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs147221759	chr14:55360126-55360127	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs3783641	chr14:55360139-55360140	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs542458297	chr14:55360143-55360144	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs554744699	chr14:55360169-55360170	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs3783642	chr14:55360203-55360204	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs543883165	chr14:55360224-55360225	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs116213604	chr14:55360252-55360253	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs114694951	chr14:55360265-55360266	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs541403801	chr14:55360311-55360312	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs115254999	chr14:55360320-55360321	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	16397240	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55345400-55368200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:55348400-55368200	Weak transcription	Gastric	stomach
3	chr14:55349000-55366400	Weak transcription	Hela-S3	cervix
4	chr14:55349200-55367400	Weak transcription	Fetal Intestine Large	intestine
5	chr14:55349200-55367400	Weak transcription	Thymus	Thymus
6	chr14:55349400-55367800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr14:55349600-55367200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr14:55349600-55368000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr14:55350000-55366400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr14:55353600-55365800	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr14:55354000-55367200	Weak transcription	Primary T cells from cord blood	blood
12	chr14:55355200-55360400	Weak transcription	HMEC	breast
13	chr14:55355200-55362000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr14:55355600-55359400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:55355600-55360000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:55355800-55359800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr14:55356000-55362000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr14:55356000-55362000	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr14:55356000-55362000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:55356000-55362600	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr14:55356000-55368000	Weak transcription	Spleen	Spleen
22	chr14:55356400-55362200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr14:55356400-55362400	Weak transcription	Lung	lung
24	chr14:55356400-55365600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr14:55356400-55368000	Weak transcription	Small Intestine	intestine
26	chr14:55356600-55367800	Weak transcription	K562	blood
27	chr14:55356800-55360000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr14:55356800-55360000	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr14:55356800-55360200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr14:55356800-55364200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr14:55356800-55365400	Weak transcription	Fetal Intestine Small	intestine
32	chr14:55357000-55361800	Weak transcription	NHEK	skin
33	chr14:55357400-55361000	Weak transcription	HepG2	liver
34	chr14:55357600-55362200	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr14:55358000-55360000	Weak transcription	Primary B cells from peripheral blood	blood
36	chr14:55358200-55367400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:55358400-55361800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr14:55358600-55367200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr14:55359000-55359600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:55359000-55359600	Weak transcription	GM12878-XiMat	blood
41	chr14:55359000-55360400	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr14:55359000-55361200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr14:55359000-55362000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr14:55359000-55364200	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr14:55359000-55366600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr14:55359000-55367400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr14:55359200-55360200	Weak transcription	Liver	Liver
48	chr14:55359400-55367400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr14:55359600-55360000	Enhancers	GM12878-XiMat	blood
50	chr14:55359600-55367000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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