Variant report

Variant	nsv902323
Chromosome Location	chr14:104381687-104464809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1258)
CpG islands
(count:1772)
Chromatin interactive
region (count:75)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1258 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:104387594-104388187	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:104392287-104392636	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:104390391-104390599	K562	blood:	n/a	n/a
4	ARID3A	chr14:104387839-104388285	K562	blood:	n/a	n/a
5	ATF1	chr14:104409999-104410408	K562	blood:	n/a	n/a
6	ATF1	chr14:104387695-104388200	K562	blood:	n/a	n/a
7	ATF2	chr14:104387490-104388186	GM12878	blood:	n/a	n/a
8	ATF2	chr14:104387798-104388049	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr14:104387779-104388059	HepG2	liver:	n/a	n/a
10	ATF3	chr14:104387715-104388049	K562	blood:	n/a	n/a
11	ATF3	chr14:104410083-104410329	K562	blood:	n/a	n/a
12	ATF3	chr14:104387684-104388249	A549	lung:	n/a	n/a
13	BACH1	chr14:104387882-104388222	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr14:104387944-104388221	K562	blood:	n/a	n/a
15	BACH1	chr14:104410119-104410343	K562	blood:	n/a	n/a
16	BATF	chr14:104387756-104388048	GM12878	blood:	n/a	n/a
17	BCL3	chr14:104387524-104388188	A549	lung:	n/a	chr14:104387969-104387982 chr14:104387962-104387970
18	BCL3	chr14:104399236-104399430	GM12878	blood:	n/a	n/a
19	BCLAF1	chr14:104387667-104388090	GM12878	blood:	n/a	chr14:104387969-104387982 chr14:104387962-104387970
20	BCLAF1	chr14:104387721-104388211	K562	blood:	n/a	chr14:104387969-104387982 chr14:104387962-104387970
21	BCLAF1	chr14:104387592-104388197	GM12878	blood:	n/a	chr14:104387969-104387982 chr14:104387962-104387970
22	BHLHE40	chr14:104387483-104388194	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:104400049-104400535	HepG2	liver:	n/a	n/a
24	BHLHE40	chr14:104410093-104410571	K562	blood:	n/a	n/a
25	BHLHE40	chr14:104390302-104390356	K562	blood:	n/a	n/a
26	BHLHE40	chr14:104387560-104388184	K562	blood:	n/a	n/a
27	BHLHE40	chr14:104408483-104408814	K562	blood:	n/a	n/a
28	BHLHE40	chr14:104392167-104392476	HepG2	liver:	n/a	n/a
29	BHLHE40	chr14:104430418-104430483	K562	blood:	n/a	n/a
30	BHLHE40	chr14:104439749-104439766	K562	blood:	n/a	n/a
31	BRCA1	chr14:104387889-104388105	GM12878	blood:	n/a	n/a
32	BRCA1	chr14:104387767-104388072	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr14:104387662-104388202	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr14:104387525-104388088	HepG2	liver:	n/a	n/a
35	CBX3	chr14:104455396-104455737	K562	blood:	n/a	n/a
36	CBX3	chr14:104387653-104388214	K562	blood:	n/a	n/a
37	CBX3	chr14:104455399-104455697	K562	blood:	n/a	n/a
38	CBX3	chr14:104455372-104455863	HCT-116	colon:	n/a	n/a
39	CBX3	chr14:104455307-104455762	HCT-116	colon:	n/a	n/a
40	CBX3	chr14:104413306-104413742	HCT-116	colon:	n/a	n/a
41	CBX3	chr14:104387791-104388083	K562	blood:	n/a	n/a
42	CCNT2	chr14:104387640-104388232	K562	blood:	n/a	chr14:104388000-104388009
43	CCNT2	chr14:104410065-104410335	K562	blood:	n/a	n/a
44	CEBPB	chr14:104387203-104387556	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:104438295-104438485	HepG2	liver:	n/a	chr14:104438309-104438320
46	CEBPB	chr14:104387234-104388151	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:104396376-104397128	MCF-7	breast:	n/a	chr14:104396944-104396956
48	CEBPB	chr14:104415826-104416016	A549	lung:	n/a	n/a
49	CEBPB	chr14:104463259-104463336	HepG2	liver:	n/a	chr14:104463301-104463312
50	CEBPB	chr14:104423536-104423707	HepG2	liver:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104395165-104395215	MCF10A-Er-Src	breast:	n/a
2	chr14:104394831-104394881	MCF-7	breast:	n/a
3	chr14:104394831-104394881	MCF10A-Er-Src	breast:	n/a
4	chr14:104395165-104395215	MCF10A-Er-Src	breast:	n/a
5	chr14:104394831-104394881	MCF-7	breast:	n/a
6	chr14:104394831-104394881	MCF10A-Er-Src	breast:	n/a
7	chr14:104395485-104395535	NH-A	brain:	n/a
8	chr14:104391679-104391729	ovcar-3	ovarian:	n/a
9	chr14:104387210-104387260	GM12891	blood:	n/a
10	chr14:104387812-104387862	HEK293	kidney:	embryo
11	chr14:104436418-104436468	A549	lung:	n/a
12	chr14:104395165-104395215	NH-A	brain:	n/a
13	chr14:104399023-104399073	HEEpiC	esophagus:	n/a
14	chr14:104394530-104394580	HCF	heart:	n/a
15	chr14:104385416-104385466	RPTEC	kidney:	n/a
16	chr14:104387583-104387633	GM19239	blood:	n/a
17	chr14:104395165-104395215	ECC-1	luminal epithelium:	n/a
18	chr14:104391679-104391729	HCM	heart:	n/a
19	chr14:104440623-104440673	ProgFib	skin:	n/a
20	chr14:104388553-104388603	HepG2	liver:	n/a
21	chr14:104388018-104388068	Jurkat	blood:	n/a
22	chr14:104395165-104395215	GM12878	blood:	n/a
23	chr14:104436057-104436107	GM12891	blood:	n/a
24	chr14:104440623-104440673	AG10803	skin:	n/a
25	chr14:104385850-104385900	MCF10A-Er-Src	breast:	n/a
26	chr14:104388185-104388235	AG10803	skin:	n/a
27	chr14:104387923-104387973	T-47D	breast:	n/a
28	chr14:104436057-104436107	HL-60	blood:	n/a
29	chr14:104387812-104387862	AG04449	skin:	fetal
30	chr14:104440623-104440673	Caco-2	colon:	n/a
31	chr14:104388097-104388147	HIPEpiC	eye:	n/a
32	chr14:104391679-104391729	CMK	blood:	n/a
33	chr14:104436161-104436211	SK-N-SH_RA	brain:	n/a
34	chr14:104384599-104384649	LNCaP	prostate:	n/a
35	chr14:104395165-104395215	HCPEpiC	choroid plexus:	n/a
36	chr14:104394530-104394580	HRCEpiC	kidney:	n/a
37	chr14:104387812-104387862	GM12878	blood:	n/a
38	chr14:104388185-104388235	HL-60	blood:	n/a
39	chr14:104387923-104387973	MCF10A-Er-Src	breast:	n/a
40	chr14:104395165-104395215	HRCEpiC	kidney:	n/a
41	chr14:104384599-104384649	NT2-D1	testis:	n/a
42	chr14:104395429-104395479	AG04449	skin:	fetal
43	chr14:104394530-104394580	HepG2	liver:	n/a
44	chr14:104388185-104388235	RPTEC	kidney:	n/a
45	chr14:104436418-104436468	LNCaP	prostate:	n/a
46	chr14:104388018-104388068	AG04449	skin:	fetal
47	chr14:104394530-104394580	NH-A	brain:	n/a
48	chr14:104391679-104391729	HRE	kidney:	n/a
49	chr14:104387812-104387862	HMEC	breast:	n/a
50	chr14:104388553-104388603	GM12878	blood:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:104387945..104390196-chr14:104396396..104397958,2	MCF-7	breast:
2	chr14:104447828..104450385-chr14:104462611..104464716,2	MCF-7	breast:
3	chr14:104403831..104408776-chr14:104408810..104412826,6	K562	blood:
4	chr14:104389161..104391143-chr14:104411439..104413629,2	K562	blood:
5	chr14:104447828..104450385-chr14:104462611..104464716,2	MCF-7	breast:
6	chr14:104382782..104384998-chr14:104387935..104389559,2	K562	blood:
7	chr14:104313555..104317821-chr14:104384318..104388009,4	MCF-7	breast:
8	chr14:104399690..104401761-chr14:104403081..104405618,2	K562	blood:
9	chr14:104391843..104393363-chr14:104396413..104398370,2	K562	blood:
10	chr14:104391843..104393363-chr14:104396413..104398370,2	K562	blood:
11	chr14:104383824..104385771-chr14:104411318..104413343,2	K562	blood:
12	chr14:104383824..104385771-chr14:104411318..104413343,2	K562	blood:
13	chr14:104385987..104387958-chr14:104398361..104401155,2	MCF-7	breast:
14	chr14:104383999..104386148-chr14:104386377..104388170,2	MCF-7	breast:
15	chr14:104387638..104390416-chr14:104390451..104394175,4	K562	blood:
16	chr14:104459245..104461701-chr4:2817391..2818995,2	MCF-7	breast:
17	chr14:104403769..104405537-chr14:104408994..104411713,3	MCF-7	breast:
18	chr14:104393603..104397064-chr14:104407702..104410726,3	K562	blood:
19	chr14:104388901..104390862-chr14:104393087..104395291,2	MCF-7	breast:
20	chr14:104399690..104401761-chr14:104403081..104405618,2	K562	blood:
21	chr14:104394897..104396539-chr14:104399297..104402064,2	MCF-7	breast:
22	chr14:104408709..104411499-chr14:104426104..104427639,2	MCF-7	breast:
23	chr14:104393603..104396242-chr14:104407114..104410000,4	K562	blood:
24	chr14:104383824..104386788-chr14:104411318..104413343,3	K562	blood:
25	chr14:104387417..104388130-chr5:177631502..177632011,2	Hela-S3	cervix:
26	chr14:104389161..104391143-chr14:104411439..104413629,2	K562	blood:
27	chr14:104418207..104420448-chr14:104423783..104426563,2	MCF-7	breast:
28	chr14:104387945..104390196-chr14:104396396..104397958,2	MCF-7	breast:
29	chr14:104377058..104380322-chr14:104382660..104385611,3	MCF-7	breast:
30	chr14:104094616..104096793-chr14:104389564..104391467,2	K562	blood:
31	chr14:104385710..104388983-chr14:104393675..104397966,4	MCF-7	breast:
32	chr14:104380212..104384984-chr14:104386073..104389493,7	MCF-7	breast:
33	chr14:104384353..104387196-chr14:104404625..104406851,3	MCF-7	breast:
34	chr14:104395726..104398249-chr14:104421446..104423004,2	K562	blood:
35	chr14:104403769..104405537-chr14:104408994..104411713,3	MCF-7	breast:
36	chr1:45477949..45478595-chr14:104387345..104388090,2	Hela-S3	cervix:
37	chr14:104380356..104382278-chr14:104382804..104385092,2	MCF-7	breast:
38	chr14:104312474..104314028-chr14:104433639..104437208,3	MCF-7	breast:
39	chr14:104194524..104196710-chr14:104385033..104387734,2	MCF-7	breast:
40	chr14:104395726..104398249-chr14:104421446..104423004,2	K562	blood:
41	chr14:104422761..104424603-chr14:104427460..104430127,2	MCF-7	breast:
42	chr14:104367293..104369155-chr14:104426158..104428921,2	K562	blood:
43	chr14:104400120..104402233-chr14:104410455..104413050,2	MCF-7	breast:
44	chr14:104391863..104393842-chr14:104396870..104399828,2	K562	blood:
45	chr14:104419063..104421166-chr14:104423566..104426306,2	MCF-7	breast:
46	chr14:104419063..104421166-chr14:104423566..104426306,2	MCF-7	breast:
47	chr14:104380212..104384984-chr14:104386073..104389493,7	MCF-7	breast:
48	chr14:104393603..104397064-chr14:104407702..104410726,3	K562	blood:
49	chr14:104385710..104388983-chr14:104393675..104397966,4	MCF-7	breast:
50	chr14:104387889..104389624-chr14:104583359..104585962,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf2-1	chr14:104398228-104398810	l_1076_chr14:104398227-104400802_kidney
2	lnc-TDRD9-AS1-2	chr14:104387807-104387875	NONHSAT040231
3	lnc-C14orf2-1	chr14:104398863-104400802	l_1076_chr14:104398227-104400802_kidney

No data

Variant related genes	Relation type
ENSG00000264439	TF binding region
TDRD9	TF binding region
C14orf2	TF binding region
RD3L	TF binding region
ENSG00000264439	CpG island
TDRD9	CpG island
C14orf2	CpG island
RD3L	CpG island
ENSG00000258735	chromatin interactions
ENSG00000156411	chromatin interactions
ENSG00000269963	chromatin interactions
ENSG00000227729	chromatin interactions
ENSG00000207568	chromatin interactions
ENSG00000126214	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000166183	chromatin interactions
ENSG00000088808	chromatin interactions
ENSG00000156414	chromatin interactions
ENSG00000100711	chromatin interactions
ENSG00000126088	chromatin interactions

Extended variants
information (count: 3444 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3444 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11850704	chr14:104381687-104381688	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573385134	chr14:104381719-104381720	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs545177878	chr14:104381770-104381771	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577542174	chr14:104381794-104381795	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558810076	chr14:104381796-104381797	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs575575612	chr14:104381802-104381803	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138073886	chr14:104381808-104381809	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561263848	chr14:104381830-104381831	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs149079400	chr14:104381831-104381832	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540262785	chr14:104381854-104381855	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559774346	chr14:104381866-104381867	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532079222	chr14:104381903-104381904	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143096495	chr14:104381910-104381911	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs571520158	chr14:104381914-104381915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs115514663	chr14:104381921-104381922	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs566231012	chr14:104381986-104381987	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550991725	chr14:104382004-104382005	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs3783310	chr14:104382013-104382014	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs536213345	chr14:104382014-104382015	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12895592	chr14:104382032-104382033	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs566944154	chr14:104382101-104382102	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539151899	chr14:104382106-104382107	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs376509294	chr14:104382120-104382121	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369189451	chr14:104382121-104382122	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs3783311	chr14:104382124-104382125	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs368243427	chr14:104382169-104382170	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554557488	chr14:104382228-104382229	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs76224845	chr14:104382265-104382266	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs559339333	chr14:104382294-104382295	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs559735766	chr14:104382333-104382334	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs17101928	chr14:104382339-104382340	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs192264045	chr14:104382340-104382341	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184279837	chr14:104382361-104382362	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs199787171	chr14:104382419-104382420	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs544706374	chr14:104382440-104382441	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs531005914	chr14:104382463-104382464	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs17101930	chr14:104382464-104382465	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs76690622	chr14:104382501-104382502	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550389100	chr14:104382552-104382553	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs545283259	chr14:104382584-104382585	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs2887387	chr14:104382588-104382589	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs187256036	chr14:104382652-104382653	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141161756	chr14:104382657-104382658	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs566856776	chr14:104382710-104382711	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs533713726	chr14:104382750-104382751	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs567333619	chr14:104382769-104382770	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530046756	chr14:104382818-104382819	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs370124539	chr14:104382835-104382836	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs35274830	chr14:104382914-104382915	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs398044073	chr14:104382919-104382920	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104363200-104387000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:104375000-104385800	Weak transcription	Small Intestine	intestine
3	chr14:104375800-104384200	Strong transcription	Dnd41	blood
4	chr14:104376000-104384800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr14:104376600-104384200	Weak transcription	Right Atrium	heart
6	chr14:104376800-104382200	Weak transcription	Pancreas	Pancrea
7	chr14:104376800-104386200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:104376800-104387000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr14:104376800-104387000	Weak transcription	Stomach Mucosa	stomach
10	chr14:104377200-104384800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr14:104377200-104385600	Strong transcription	Fetal Intestine Small	intestine
12	chr14:104377200-104386400	Weak transcription	Fetal Heart	heart
13	chr14:104377200-104386800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr14:104377400-104381800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr14:104377400-104383000	Strong transcription	Adipose Nuclei	Adipose
16	chr14:104377400-104383200	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr14:104377400-104383200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr14:104377400-104383800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr14:104377400-104384400	Strong transcription	Placenta	Placenta
20	chr14:104377400-104384600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr14:104377400-104384600	Strong transcription	Primary B cells from peripheral blood	blood
22	chr14:104377400-104384600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr14:104377400-104384600	Strong transcription	Liver	Liver
24	chr14:104377400-104384600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr14:104377400-104384600	Strong transcription	Fetal Intestine Large	intestine
26	chr14:104377400-104384600	Strong transcription	Fetal Muscle Trunk	muscle
27	chr14:104377400-104384600	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr14:104377400-104384800	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr14:104377400-104384800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr14:104377400-104384800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr14:104377400-104384800	Strong transcription	Duodenum Mucosa	Duodenum
32	chr14:104377400-104384800	Strong transcription	Thymus	Thymus
33	chr14:104377400-104385200	Strong transcription	Fetal Brain Female	brain
34	chr14:104377400-104385200	Strong transcription	Fetal Muscle Leg	muscle
35	chr14:104377400-104386000	Strong transcription	Fetal Stomach	stomach
36	chr14:104377600-104381800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr14:104377600-104381800	Strong transcription	Fetal Lung	lung
38	chr14:104377600-104382600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr14:104377600-104382800	Strong transcription	Osteobl	bone
40	chr14:104377600-104383600	Strong transcription	Skeletal Muscle Female	skeletal muscle
41	chr14:104377600-104383800	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr14:104377600-104384200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr14:104377600-104384400	Strong transcription	Spleen	Spleen
44	chr14:104377600-104384600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:104377600-104384600	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr14:104377600-104384600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr14:104377600-104384600	Strong transcription	Rectal Mucosa Donor 29	rectum
48	chr14:104377600-104384600	Strong transcription	Stomach Smooth Muscle	stomach
49	chr14:104377600-104384600	Strong transcription	A549	lung
50	chr14:104377600-104384800	Strong transcription	Primary T helper cells PMA-I stimulated	--

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