Variant report

Variant	nsv498021
Chromosome Location	chr14:71874708-72128721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2343)
CpG islands
(count:1100)
Chromatin interactive
region (count:91)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2343 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:72115437-72115988	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:72022399-72022774	K562	blood:	n/a	n/a
3	ARID3A	chr14:71912076-71912104	K562	blood:	n/a	n/a
4	ARID3A	chr14:72015057-72015208	K562	blood:	n/a	n/a
5	ARID3A	chr14:71885636-71886025	K562	blood:	n/a	chr14:71885851-71885867
6	ARID3A	chr14:72125944-72126209	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:72004217-72004524	K562	blood:	n/a	n/a
8	ATF1	chr14:72041880-72042021	K562	blood:	n/a	n/a
9	ATF1	chr14:71988484-71988598	K562	blood:	n/a	n/a
10	ATF2	chr14:71897143-71898130	GM12878	blood:	n/a	n/a
11	ATF2	chr14:72064609-72065142	GM12878	blood:	n/a	n/a
12	ATF2	chr14:72021007-72021468	GM12878	blood:	n/a	n/a
13	ATF2	chr14:71897147-71898087	GM12878	blood:	n/a	n/a
14	ATF2	chr14:72064690-72065350	GM12878	blood:	n/a	n/a
15	ATF2	chr14:71964092-71965239	GM12878	blood:	n/a	n/a
16	ATF2	chr14:72113644-72114374	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr14:71990473-71991708	GM12878	blood:	n/a	n/a
18	ATF2	chr14:71990429-71991710	GM12878	blood:	n/a	n/a
19	ATF2	chr14:71939075-71939754	GM12878	blood:	n/a	n/a
20	ATF2	chr14:72113723-72114157	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr14:71911075-71911433	GM12878	blood:	n/a	n/a
22	ATF2	chr14:71938962-71939577	GM12878	blood:	n/a	n/a
23	ATF2	chr14:72021773-72023123	GM12878	blood:	n/a	n/a
24	ATF2	chr14:72021788-72023092	GM12878	blood:	n/a	n/a
25	ATF2	chr14:71964179-71965702	GM12878	blood:	n/a	n/a
26	BACH1	chr14:71975963-71976059	K562	blood:	n/a	n/a
27	BACH1	chr14:71883163-71883432	K562	blood:	n/a	n/a
28	BACH1	chr14:72127364-72127412	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr14:71883175-71883429	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr14:72059409-72059474	K562	blood:	n/a	n/a
31	BATF	chr14:72073726-72074185	GM12878	blood:	n/a	n/a
32	BATF	chr14:72021889-72022673	GM12878	blood:	n/a	n/a
33	BATF	chr14:71934190-71934526	GM12878	blood:	n/a	chr14:71934371-71934382
34	BATF	chr14:72030378-72030790	GM12878	blood:	n/a	n/a
35	BATF	chr14:71964313-71964891	GM12878	blood:	n/a	chr14:71964591-71964602
36	BATF	chr14:71939051-71939395	GM12878	blood:	n/a	n/a
37	BATF	chr14:71964376-71965040	GM12878	blood:	n/a	chr14:71964591-71964602
38	BATF	chr14:72030420-72030768	GM12878	blood:	n/a	n/a
39	BATF	chr14:72065036-72065364	GM12878	blood:	n/a	n/a
40	BATF	chr14:72033069-72033355	GM12878	blood:	n/a	n/a
41	BATF	chr14:71990493-71991254	GM12878	blood:	n/a	n/a
42	BATF	chr14:71990699-71991189	GM12878	blood:	n/a	n/a
43	BATF	chr14:71911172-71911563	GM12878	blood:	n/a	n/a
44	BATF	chr14:71939098-71939376	GM12878	blood:	n/a	n/a
45	BATF	chr14:72064661-72065370	GM12878	blood:	n/a	n/a
46	BATF	chr14:72021719-72022913	GM12878	blood:	n/a	n/a
47	BATF	chr14:71911210-71911466	GM12878	blood:	n/a	n/a
48	BCL11A	chr14:72085453-72085786	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:71964449-71964825	GM12878	blood:	n/a	n/a
50	BCL11A	chr14:71964344-71964885	GM12878	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:72041267-72041317	GM19239	blood:	n/a
2	chr14:72061746-72061796	BE2_C	brain:	n/a
3	chr14:72041267-72041317	GM19239	blood:	n/a
4	chr14:72061746-72061796	BE2_C	brain:	n/a
5	chr14:72041267-72041317	ProgFib	skin:	n/a
6	chr14:71953890-71953940	BJ	skin:	n/a
7	chr14:71954034-71954084	AG04449	skin:	fetal
8	chr14:72113798-72113848	ovcar-3	ovarian:	n/a
9	chr14:72041267-72041317	SKMC	muscle:	n/a
10	chr14:71953890-71953940	HAEpiC	amniotic membrane:	n/a
11	chr14:72061746-72061796	AG09309	skin:	n/a
12	chr14:72006683-72006733	AoSMC	blood vessel:	n/a
13	chr14:72006683-72006733	HIPEpiC	eye:	n/a
14	chr14:71954034-71954084	NT2-D1	testis:	n/a
15	chr14:72113798-72113848	NH-A	brain:	n/a
16	chr14:71955729-71955779	AG04450	lung:	fetal
17	chr14:72117181-72117231	HNPCEpiC	eye:	n/a
18	chr14:72061746-72061796	MCF-7	breast:	n/a
19	chr14:71994749-71994799	NB4	blood:	n/a
20	chr14:71954034-71954084	ProgFib	skin:	n/a
21	chr14:72113798-72113848	SK-N-MC	brain:	n/a
22	chr14:71954034-71954084	HIPEpiC	eye:	n/a
23	chr14:71955729-71955779	NB4	blood:	n/a
24	chr14:71954034-71954084	SKMC	muscle:	n/a
25	chr14:72113798-72113848	IMR90	lung:	fetal
26	chr14:72117181-72117231	T-47D	breast:	n/a
27	chr14:72006683-72006733	NHDF-neo	bronchial:	n/a
28	chr14:71954034-71954084	MCF10A-Er-Src	breast:	n/a
29	chr14:72088434-72088484	GM06990	blood:	n/a
30	chr14:71949117-71949167	HCM	heart:	n/a
31	chr14:72041267-72041317	AG09309	skin:	n/a
32	chr14:71953890-71953940	SK-N-SH_RA	brain:	n/a
33	chr14:71996050-71996100	HRPEpiC	eye:	n/a
34	chr14:72083707-72083757	GM19239	blood:	n/a
35	chr14:72041267-72041317	Jurkat	blood:	n/a
36	chr14:72117181-72117231	HUVEC	blood vessel:	n/a
37	chr14:71996050-71996100	IMR90	lung:	fetal
38	chr14:72006683-72006733	SK-N-SH_RA	brain:	n/a
39	chr14:72117181-72117231	RPTEC	kidney:	n/a
40	chr14:71875703-71875753	AG09309	skin:	n/a
41	chr14:71905595-71905645	HCF	heart:	n/a
42	chr14:71875703-71875753	SK-N-SH	brain:	n/a
43	chr14:71896386-71896436	A549	lung:	n/a
44	chr14:72053146-72053196	Caco-2	colon:	n/a
45	chr14:71954034-71954084	BE2_C	brain:	n/a
46	chr14:72083707-72083757	HMEC	breast:	n/a
47	chr14:71875703-71875753	SKMC	muscle:	n/a
48	chr14:72061746-72061796	AG09319	gingival:	n/a
49	chr14:72117181-72117231	GM06990	blood:	n/a
50	chr14:72053146-72053196	LNCaP	prostate:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:71786621..71788325-chr14:71990859..71992775,2	MCF-7	breast:
2	chr14:72000187..72002970-chr14:72003263..72006662,3	MCF-7	breast:
3	chr14:72064708..72067406-chr14:72108018..72110332,2	K562	blood:
4	chr14:71956888..71959124-chr14:71962522..71965043,2	K562	blood:
5	chr14:72044399..72046285-chr14:72058005..72060824,2	K562	blood:
6	chr14:72079358..72081183-chr14:72081812..72085209,3	MCF-7	breast:
7	chr14:71998902..72001502-chr14:72003507..72006121,3	K562	blood:
8	chr14:71899659..71902752-chr14:71906518..71909457,3	MCF-7	breast:
9	chr14:72044562..72046264-chr14:72073210..72075565,2	MCF-7	breast:
10	chr14:71784631..71787414-chr14:71876832..71879827,2	K562	blood:
11	chr14:72105812..72107340-chr14:72111060..72113226,2	MCF-7	breast:
12	chr14:71915843..71917991-chr14:71921566..71923548,2	MCF-7	breast:
13	chr14:71998182..71998851-chrX:12964802..12965547,2	MCF-7	breast:
14	chr14:72104934..72106796-chr14:72107368..72110088,2	MCF-7	breast:
15	chr14:71894769..71896723-chr14:71920391..71921906,2	MCF-7	breast:
16	chr14:72036232..72038025-chr14:72039204..72041312,2	MCF-7	breast:
17	chr14:71780361..71782666-chr14:71883933..71885964,2	MCF-7	breast:
18	chr14:72097989..72100709-chr14:72101548..72105731,3	MCF-7	breast:
19	chr14:72107137..72109592-chr14:72112007..72114588,3	K562	blood:
20	chr14:71877114..71877785-chr5:30096829..30097526,2	MCF-7	breast:
21	chr14:71786940..71788976-chr14:72077565..72079206,2	MCF-7	breast:
22	chr14:71949964..71951465-chr14:71958875..71960889,2	K562	blood:
23	chr14:71949964..71951465-chr14:71958875..71960889,2	K562	blood:
24	chr14:71956692..71959417-chr14:71961232..71963280,2	MCF-7	breast:
25	chr14:72037181..72039839-chr14:72063450..72065135,2	MCF-7	breast:
26	chr14:72014462..72017337-chr14:72017571..72020406,2	MCF-7	breast:
27	chr14:71942357..71943227-chr14:71967306..71967809,2	MCF-7	breast:
28	chr14:72096584..72098763-chr14:72104877..72106791,2	MCF-7	breast:
29	chr14:72038823..72040937-chr14:72089563..72092048,2	MCF-7	breast:
30	chr14:72096584..72098763-chr14:72104877..72106791,2	MCF-7	breast:
31	chr14:71910831..71913161-chr14:71915505..71918179,2	MCF-7	breast:
32	chr14:72051242..72053047-chr14:72057398..72060318,2	MCF-7	breast:
33	chr14:72107137..72109592-chr14:72112007..72114588,3	K562	blood:
34	chr14:71956692..71959417-chr14:71961232..71963280,2	MCF-7	breast:
35	chr14:71760323..71761838-chr14:71875710..71878506,2	MCF-7	breast:
36	chr14:72098961..72100634-chr14:72106164..72107861,2	MCF-7	breast:
37	chr14:71877515..71880070-chr14:71885947..71887689,2	MCF-7	breast:
38	chr14:71786410..71788050-chr14:71885965..71888835,2	MCF-7	breast:
39	chr14:71786904..71788917-chr14:71937053..71939016,2	MCF-7	breast:
40	chr14:71786578..71788917-chr14:72067175..72069776,2	MCF-7	breast:
41	chr14:71890976..71893718-chr14:71893758..71896619,2	K562	blood:
42	chr14:72105812..72107340-chr14:72111060..72113226,2	MCF-7	breast:
43	chr14:72030442..72031945-chr14:72036768..72039737,2	K562	blood:
44	chr14:71869375..71872292-chr14:71882867..71885400,2	MCF-7	breast:
45	chr14:71908040..71909554-chr14:71914806..71916309,2	K562	blood:
46	chr14:71785913..71788316-chr14:72114370..72116896,2	MCF-7	breast:
47	chr14:72104934..72106796-chr14:72107368..72110088,2	MCF-7	breast:
48	chr14:71786624..71789494-chr14:72079631..72081639,2	MCF-7	breast:
49	chr14:71931431..71933043-chr14:71940078..71941973,2	MCF-7	breast:
50	chr14:71998902..72001502-chr14:72003507..72006121,3	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIPA1L1-2	chr14:71996029-71996087	NONHSAT037631
2	lnc-SIPA1L1-2	chr14:71995416-71995457	NONHSAT037631
3	lnc-SIPA1L1-2	chr14:71932999-71933639	NONHSAT037636
4	lnc-SIPA1L1-2	chr14:71996029-71996087	NONHSAT037640
5	lnc-SIPA1L1-2	chr14:71955871-71956294	NONHSAT037636
6	lnc-C14orf57-1	chr14:71937646-71939072	ENSG00000251156
7	lnc-SIPA1L1-2	chr14:72040206-72040517	NONHSAT037631
8	lnc-SIPA1L1-2	chr14:71905719-71905991	NONHSAT037636
9	lnc-SIPA1L1-2	chr14:71979460-71979562	NONHSAT037631
10	lnc-SIPA1L1-2	chr14:71935828-71936281	NONHSAT037636
11	lnc-SIPA1L1-2	chr14:71882693-71883000	NONHSAT037638
12	lnc-SIPA1L1-2	chr14:71954578-71956420	NONHSAT037641
13	lnc-C14orf57-1	chr14:71927903-71931274	ENSG00000251156
14	lnc-SIPA1L1-2	chr14:71915406-71915673	NONHSAT037639
15	lnc-SIPA1L1-2	chr14:71882582-71883023	NONHSAT037636
16	lnc-SIPA1L1-2	chr14:71880665-71880731	NONHSAT037631
17	lnc-SIPA1L1-2	chr14:71880665-71880733	NONHSAT037636
18	lnc-SIPA1L1-2	chr14:72040206-72041803	NONHSAT037640
19	lnc-SIPA1L1-2	chr14:71884847-71884914	NONHSAT037636
20	lnc-SIPA1L1-2	chr14:71880671-71880819	NONHSAT037638
21	lnc-SIPA1L1-2	chr14:71915246-71915481	NONHSAT037636
22	lnc-SIPA1L1-2	chr14:71933858-71933964	NONHSAT037636
23	lnc-SIPA1L1-2	chr14:71979460-71979562	NONHSAT037640
24	lnc-SIPA1L1-2	chr14:71933902-71933964	NONHSAT037640

No data

Variant related genes	Relation type
RN7SL683P	TF binding region
SIPA1L1	TF binding region
RN7SL683P	CpG island
SIPA1L1	CpG island
ENSG00000197555	chromatin interactions
ENSG00000242330	chromatin interactions
ENSG00000259146	chromatin interactions
KBTBD6	miRNA target sites
KLF4	miRNA target sites

Extended variants
information (count: 8897 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:8897 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181460587	chr14:71874716-71874717	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs538054633	chr14:71874729-71874730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548520503	chr14:71874764-71874765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566520634	chr14:71874765-71874766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs138653921	chr14:71874791-71874792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140412514	chr14:71874901-71874902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571758495	chr14:71874937-71874938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538634096	chr14:71874970-71874971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556968593	chr14:71874983-71874984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575251071	chr14:71875008-71875009	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs142075806	chr14:71875075-71875076	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150374581	chr14:71875088-71875089	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs186409791	chr14:71875126-71875127	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541896242	chr14:71875181-71875182	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550680241	chr14:71875190-71875191	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573318879	chr14:71875195-71875196	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540863990	chr14:71875265-71875266	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs190758914	chr14:71875278-71875279	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138180391	chr14:71875285-71875286	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375713706	chr14:71875323-71875324	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544212375	chr14:71875334-71875335	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs149550544	chr14:71875337-71875338	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369671434	chr14:71875359-71875360	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546223598	chr14:71875399-71875400	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529736842	chr14:71875440-71875441	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182275888	chr14:71875490-71875491	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548463133	chr14:71875552-71875553	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564806444	chr14:71875649-71875650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574441859	chr14:71875672-71875673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs527489999	chr14:71875674-71875675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543529614	chr14:71875698-71875699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552375328	chr14:71875713-71875714	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571633428	chr14:71875751-71875752	Weak transcription Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs538711016	chr14:71875754-71875755	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184896205	chr14:71875760-71875761	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs144291307	chr14:71875766-71875767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576622182	chr14:71875810-71875811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536258741	chr14:71875821-71875822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs11627196	chr14:71875838-71875839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs372148866	chr14:71875848-71875849	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573528721	chr14:71875869-71875870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534111478	chr14:71875876-71875877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs17178192	chr14:71875909-71875910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs199741609	chr14:71875911-71875912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377700979	chr14:71875913-71875914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577383435	chr14:71875926-71875927	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs116571984	chr14:71875938-71875939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs372657466	chr14:71875961-71875962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs377735064	chr14:71875983-71875984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs116253989	chr14:71876009-71876010	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:5927 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71851400-71878200	Weak transcription	Pancreas	Pancrea
2	chr14:71859000-71878200	Weak transcription	Lung	lung
3	chr14:71861000-71885200	Weak transcription	K562	blood
4	chr14:71861400-71875200	Weak transcription	Brain Anterior Caudate	brain
5	chr14:71862600-71878200	Weak transcription	Spleen	Spleen
6	chr14:71866000-71877400	Weak transcription	Stomach Mucosa	stomach
7	chr14:71866000-71877600	Weak transcription	HepG2	liver
8	chr14:71866000-71889000	Weak transcription	Dnd41	blood
9	chr14:71866200-71875000	Weak transcription	NH-A	brain
10	chr14:71866800-71875400	Weak transcription	Fetal Thymus	thymus
11	chr14:71867000-71875200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr14:71867200-71892200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr14:71867800-71877400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr14:71867800-71881600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr14:71867800-71885000	Weak transcription	Brain Substantia Nigra	brain
16	chr14:71868000-71875000	Weak transcription	HSMMtube	muscle
17	chr14:71868000-71875200	Weak transcription	HSMM	muscle
18	chr14:71868000-71875600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr14:71868000-71876600	Weak transcription	Fetal Lung	lung
20	chr14:71868000-71878000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr14:71868000-71878200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr14:71868200-71875200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr14:71868200-71877400	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr14:71868200-71891400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr14:71868400-71875200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr14:71868400-71878200	Weak transcription	HMEC	breast
27	chr14:71868400-71881200	Weak transcription	NHLF	lung
28	chr14:71869000-71875000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr14:71869000-71875800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr14:71869400-71874800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr14:71869400-71875400	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr14:71869400-71878000	Weak transcription	NHEK	skin
33	chr14:71869400-71878200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr14:71869600-71875000	Weak transcription	NHDF-Ad	bronchial
35	chr14:71869600-71904200	Weak transcription	Hela-S3	cervix
36	chr14:71869800-71875000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr14:71870600-71878200	Weak transcription	Duodenum Mucosa	Duodenum
38	chr14:71870600-71891000	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr14:71871000-71877600	Weak transcription	Primary T cells from cord blood	blood
40	chr14:71871400-71880600	Weak transcription	Primary B cells from peripheral blood	blood
41	chr14:71871600-71874800	Weak transcription	Osteobl	bone
42	chr14:71871600-71899600	Weak transcription	Primary B cells from cord blood	blood
43	chr14:71872400-71877400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:71872600-71877200	Weak transcription	GM12878-XiMat	blood
45	chr14:71872600-71885000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr14:71872800-71874800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr14:71872800-71877400	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr14:71874400-71874800	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr14:71874400-71875000	Weak transcription	Aorta	Aorta
50	chr14:71874400-71877600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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