Variant report

Variant	nsv1036854
Chromosome Location	chr14:37609535-38013533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3606)
CpG islands
(count:1648)
Chromatin interactive
region (count:247)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3606 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37618944-37619276	K562	blood:	n/a	n/a
2	ARID3A	chr14:37699852-37700129	K562	blood:	n/a	n/a
3	ARID3A	chr14:37664464-37664897	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:37668114-37668178	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:37702064-37702476	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:37715436-37716157	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:37640896-37641730	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:37720992-37722152	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:37666578-37667618	K562	blood:	n/a	n/a
10	ARID3A	chr14:37638798-37638998	K562	blood:	n/a	chr14:37638878-37638894 chr14:37638877-37638893
11	ARID3A	chr14:37636253-37636339	K562	blood:	n/a	n/a
12	ARID3A	chr14:37937245-37937930	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:37702174-37702457	K562	blood:	n/a	n/a
14	ARID3A	chr14:37699763-37700208	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:37665962-37666204	K562	blood:	n/a	n/a
16	ARID3A	chr14:37854210-37854747	HepG2	liver:	n/a	chr14:37854604-37854612
17	ARID3A	chr14:37641543-37641674	K562	blood:	n/a	n/a
18	ARID3A	chr14:37637980-37638323	K562	blood:	n/a	n/a
19	ARID3A	chr14:37612843-37612931	K562	blood:	n/a	n/a
20	ARID3A	chr14:37640439-37641338	K562	blood:	n/a	n/a
21	ARID3A	chr14:37935172-37936858	HepG2	liver:	n/a	n/a
22	ARID3A	chr14:37966619-37967091	HepG2	liver:	n/a	n/a
23	ARID3A	chr14:37618939-37620096	HepG2	liver:	n/a	n/a
24	ARID3A	chr14:37798163-37799893	HepG2	liver:	n/a	n/a
25	ARID3A	chr14:37619710-37620155	K562	blood:	n/a	n/a
26	ARID3A	chr14:37643767-37644084	K562	blood:	n/a	n/a
27	ARID3A	chr14:37996655-37996907	HepG2	liver:	n/a	n/a
28	ARID3A	chr14:37707129-37707415	HepG2	liver:	n/a	n/a
29	ARID3A	chr14:37882908-37883266	HepG2	liver:	n/a	n/a
30	ARID3A	chr14:37667012-37667537	HepG2	liver:	n/a	n/a
31	ARID3A	chr14:37916975-37917561	HepG2	liver:	n/a	n/a
32	ARID3A	chr14:37642484-37642976	K562	blood:	n/a	n/a
33	ARID3A	chr14:37636859-37637271	K562	blood:	n/a	n/a
34	ARID3A	chr14:37747860-37748994	HepG2	liver:	n/a	n/a
35	ARID3A	chr14:37739891-37740124	HepG2	liver:	n/a	n/a
36	ARID3A	chr14:37962806-37963218	HepG2	liver:	n/a	n/a
37	ATF1	chr14:37886466-37886666	K562	blood:	n/a	n/a
38	ATF1	chr14:37868829-37869057	K562	blood:	n/a	n/a
39	ATF1	chr14:37636855-37637252	K562	blood:	n/a	n/a
40	ATF1	chr14:37637957-37638275	K562	blood:	n/a	n/a
41	ATF2	chr14:37641089-37641818	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr14:37636749-37637333	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr14:37636807-37637410	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr14:37641468-37642010	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF3	chr14:37868759-37869025	K562	blood:	n/a	n/a
46	ATF3	chr14:37666986-37667277	K562	blood:	n/a	n/a
47	ATF3	chr14:37641048-37641567	A549	lung:	n/a	n/a
48	ATF3	chr14:37650651-37650943	H1-hESC	embryonic stem cell:	n/a	n/a
49	ATF3	chr14:37639465-37639767	K562	blood:	n/a	n/a
50	BACH1	chr14:37666966-37667533	K562	blood:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37666893-37666943	HIPEpiC	eye:	n/a
2	chr14:37666893-37666943	HIPEpiC	eye:	n/a
3	chr14:37641462-37641512	PANC-1	pancreas:	n/a
4	chr14:37641600-37641650	HPAEpiC	pulmonary alveolar:	n/a
5	chr14:37666931-37666981	GM12891	blood:	n/a
6	chr14:37667261-37667311	SK-N-SH_RA	brain:	n/a
7	chr14:37641261-37641311	HRCEpiC	kidney:	n/a
8	chr14:37667689-37667739	H1-hESC	embryonic stem cell:	embryo
9	chr14:37641134-37641184	MCF10A-Er-Src	breast:	n/a
10	chr14:37641436-37641486	H1-hESC	embryonic stem cell:	embryo
11	chr14:37667230-37667280	SKMC	muscle:	n/a
12	chr14:37641660-37641710	RPTEC	kidney:	n/a
13	chr14:37641964-37642014	SK-N-SH_RA	brain:	n/a
14	chr14:37641726-37641776	PrEC	prostate:	n/a
15	chr14:37641134-37641184	GM12892	blood:	n/a
16	chr14:37667689-37667739	SK-N-SH	brain:	n/a
17	chr14:37666920-37666970	MCF-7	breast:	n/a
18	chr14:37641261-37641311	HIPEpiC	eye:	n/a
19	chr14:37667833-37667883	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:37638478-37638528	HMEC	breast:	n/a
21	chr14:37666893-37666943	H1-hESC	embryonic stem cell:	embryo
22	chr14:37641726-37641776	SK-N-MC	brain:	n/a
23	chr14:37640247-37640297	NH-A	brain:	n/a
24	chr14:37666994-37667044	IMR90	lung:	fetal
25	chr14:37667689-37667739	A549	lung:	n/a
26	chr14:37641436-37641486	K562	blood:	n/a
27	chr14:37640455-37640505	ovcar-3	ovarian:	n/a
28	chr14:37825967-37826017	HRPEpiC	eye:	n/a
29	chr14:37641600-37641650	K562	blood:	n/a
30	chr14:37641191-37641241	AG04450	lung:	fetal
31	chr14:37773865-37773915	NT2-D1	testis:	n/a
32	chr14:37641726-37641776	SK-N-SH	brain:	n/a
33	chr14:37641436-37641486	PANC-1	pancreas:	n/a
34	chr14:37666920-37666970	HRCEpiC	kidney:	n/a
35	chr14:37641134-37641184	Hepatocyte	liver:	n/a
36	chr14:37644675-37644725	SKMC	muscle:	n/a
37	chr14:37667833-37667883	K562	blood:	n/a
38	chr14:37825967-37826017	HRE	kidney:	n/a
39	chr14:37641964-37642014	NB4	blood:	n/a
40	chr14:37773865-37773915	HCPEpiC	choroid plexus:	n/a
41	chr14:37640247-37640297	T-47D	breast:	n/a
42	chr14:37639757-37639807	ovcar-3	ovarian:	n/a
43	chr14:37644675-37644725	MCF-7	breast:	n/a
44	chr14:37667689-37667739	PFSK-1	brain:	n/a
45	chr14:37667689-37667739	AG09319	gingival:	n/a
46	chr14:37667689-37667739	HRE	kidney:	n/a
47	chr14:37667261-37667311	RPTEC	kidney:	n/a
48	chr14:37641436-37641486	GM12878	blood:	n/a
49	chr14:37641436-37641486	HCF	heart:	n/a
50	chr14:37667230-37667280	HCM	heart:	n/a

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr14:37811526..37813219-chr14:38057927..38059734,2	MCF-7	breast:
2	chr14:37680569..37683226-chr14:37683414..37685864,2	MCF-7	breast:
3	chr14:37924566..37927073-chr14:38060566..38062784,2	MCF-7	breast:
4	chr14:38011441..38015766-chr14:38062652..38065926,9	MCF-7	breast:
5	chr14:37639617..37644848-chr14:37662875..37669924,15	K562	blood:
6	chr14:37117193..37117982-chr14:37618414..37619153,3	K562	blood:
7	chr14:37635891..37637422-chr14:37666864..37668416,2	MCF-7	breast:
8	chr14:37720431..37722161-chr14:37725187..37727828,2	MCF-7	breast:
9	chr14:37996620..37999759-chr14:38060620..38062986,3	MCF-7	breast:
10	chr14:37619842..37620362-chr14:37699681..37700515,2	K562	blood:
11	chr14:37638513..37640081-chr14:37646893..37648669,2	MCF-7	breast:
12	chr14:37704717..37707352-chr14:38053028..38056563,4	MCF-7	breast:
13	chr14:37608441..37610002-chr14:37610883..37613279,2	K562	blood:
14	chr14:37697269..37708885-chr14:38056043..38068163,30	MCF-7	breast:
15	chr14:37640829..37643687-chr14:37650994..37653256,2	K562	blood:
16	chr14:37717816..37720206-chr14:38145329..38146961,2	K562	blood:
17	chr14:37730985..37733871-chr14:37737549..37739404,2	MCF-7	breast:
18	chr14:37715306..37715938-chr14:38034662..38035728,3	MCF-7	breast:
19	chr14:37699926..37700451-chr14:38063417..38063967,2	MCF-7	breast:
20	chr14:37996356..38000397-chr14:38056446..38059493,3	MCF-7	breast:
21	chr14:37922237..37924533-chr14:37931027..37932952,2	MCF-7	breast:
22	chr14:37858877..37861783-chr14:37988865..37991123,2	MCF-7	breast:
23	chr14:37984075..37986407-chr14:37992639..37994265,2	MCF-7	breast:
24	chr14:37720748..37721511-chr14:38034504..38035461,3	MCF-7	breast:
25	chr14:37640543..37642943-chr20:48598351..48600093,2	MCF-7	breast:
26	chr14:37723784..37725511-chr14:37726243..37728327,2	MCF-7	breast:
27	chr14:37981930..37983702-chr14:37987537..37990336,2	MCF-7	breast:
28	chr14:37638778..37643112-chr14:37646063..37650865,4	K562	blood:
29	chr14:37639061..37645694-chr14:37661777..37669317,18	MCF-7	breast:
30	chr14:37638513..37640081-chr14:37646893..37648669,2	MCF-7	breast:
31	chr14:37710312..37712829-chr14:37714356..37716232,3	MCF-7	breast:
32	chr14:37709403..37711519-chr14:37714565..37716617,2	K562	blood:
33	chr14:37914831..37917471-chr14:37919271..37922132,2	MCF-7	breast:
34	chr14:37493069..37493723-chr14:37618601..37619945,3	MCF-7	breast:
35	chr14:37730985..37733871-chr14:37737549..37739404,2	MCF-7	breast:
36	chr14:37992113..37994949-chr14:37995785..37998678,3	MCF-7	breast:
37	chr14:37610927..37613306-chr14:37640197..37642903,2	MCF-7	breast:
38	chr14:37884990..37886932-chr14:37888404..37890275,2	K562	blood:
39	chr14:37840146..37842839-chr14:37843811..37846339,2	K562	blood:
40	chr14:37669239..37670769-chr14:37675458..37677421,2	K562	blood:
41	chr14:37640266..37643741-chr14:37700089..37702308,3	MCF-7	breast:
42	chr14:37619842..37620362-chr14:37699681..37700515,2	K562	blood:
43	chr14:37723534..37725938-chr14:37730959..37732560,2	K562	blood:
44	chr14:37652408..37654436-chr14:37665348..37666994,2	MCF-7	breast:
45	chr14:37699123..37701373-chr14:37712703..37714358,2	K562	blood:
46	chr14:37638286..37642814-chr14:37645632..37648854,6	K562	blood:
47	chr14:37992987..37994554-chr14:37998762..38001417,2	K562	blood:
48	chr14:37619150..37623313-chr14:37636849..37639143,3	K562	blood:
49	chr14:37051690..37053277-chr14:37640298..37642030,2	K562	blood:
50	chr14:37679446..37681161-chr14:37683959..37685641,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-537P22.1.1-1	chr14:37717034-37717112	NONHSAT036456
2	lnc-RP11-537P22.1.1-1	chr14:37709629-37709774	NONHSAT036456
3	lnc-RP11-537P22.1.1-1	chr14:37732158-37732474	l_969_chr14:37729807-37741737_76bGuttman_hES
4	lnc-MIPOL1-5	chr14:37641231-37642998	NR_033240
5	lnc-RP11-537P22.1.1-1	chr14:37736143-37736374	NONHSAT036456
6	lnc-RP11-537P22.1.1-1	chr14:37729808-37730221	l_969_chr14:37729807-37741737_76bGuttman_hES
7	lnc-FOXA1-4	chr14:37853626-37855696	NONHSAT036459
8	lnc-TTC6-2	chr14:37869005-37871105	NONHSAT036460
9	lnc-RP11-537P22.1.1-1	chr14:37727929-37730334	NONHSAT036457
10	lnc-RP11-537P22.1.1-1	chr14:37716308-37716445	NONHSAT036456
11	lnc-RP11-537P22.1.1-1	chr14:37734270-37737659	l_969_chr14:37729807-37741737_76bGuttman_hES
12	lnc-RP11-537P22.1.1-1	chr14:37737668-37742505	l_969_chr14:37729807-37741737_76bGuttman_hES

No data

Variant related genes	Relation type
RNU6-886P	TF binding region
MIPOL1	TF binding region
SLC25A21-AS1	TF binding region
SLC25A21	TF binding region
RNU6-273P	TF binding region
RNU6-886P	CpG island
MIPOL1	CpG island
SLC25A21-AS1	CpG island
SLC25A21	CpG island
RNU6-273P	CpG island
ENSG00000198807	chromatin interactions
ENSG00000207046	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000183032	chromatin interactions
ENSG00000107338	chromatin interactions
ENSG00000137261	chromatin interactions
ENSG00000259087	chromatin interactions
ENSG00000258414	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000255872	chromatin interactions
ENSG00000136327	chromatin interactions
ENSG00000258708	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000124216	chromatin interactions

Extended variants
information (count: 14259 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:14259 , 50 per page) page: 1 2 3 4 5 6 7 ... 286

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139817949	chr14:37609564-37609565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542601048	chr14:37609595-37609596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35208965	chr14:37609637-37609638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545581091	chr14:37609727-37609728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565385573	chr14:37609750-37609751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190615590	chr14:37609771-37609772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560868319	chr14:37609860-37609861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541483748	chr14:37609870-37609871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182167905	chr14:37609872-37609873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186810860	chr14:37609942-37609943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34719227	chr14:37610039-37610040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397719802	chr14:37610049-37610050	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562775038	chr14:37610067-37610068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531418649	chr14:37610077-37610078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191580463	chr14:37610079-37610080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550930448	chr14:37610123-37610124	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563094825	chr14:37610126-37610127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571014969	chr14:37610135-37610136	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372320859	chr14:37610161-37610162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533640366	chr14:37610172-37610173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182641938	chr14:37610179-37610180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567128086	chr14:37610212-37610213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536214817	chr14:37610214-37610215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114795901	chr14:37610270-37610271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570320793	chr14:37610282-37610283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57011324	chr14:37610312-37610313	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs559192286	chr14:37610328-37610329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147902935	chr14:37610357-37610358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs572611358	chr14:37610402-37610403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377404287	chr14:37610403-37610404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373789959	chr14:37610418-37610419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541520702	chr14:37610439-37610440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369785969	chr14:37610489-37610490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148232667	chr14:37610497-37610498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147878066	chr14:37610523-37610524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543766132	chr14:37610708-37610709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533050099	chr14:37610713-37610714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567161316	chr14:37610714-37610715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76060696	chr14:37610719-37610720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531458643	chr14:37610801-37610802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544853602	chr14:37610802-37610803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535221791	chr14:37610803-37610804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547194729	chr14:37610851-37610852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554734091	chr14:37610937-37610938	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs139829359	chr14:37610942-37610943	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533984128	chr14:37610970-37610971	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs529664496	chr14:37610972-37610973	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549701422	chr14:37611015-37611016	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570408378	chr14:37611029-37611030	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535133981	chr14:37611033-37611034	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Colorectal cancer	16774939	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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1812 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37598400-37610000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:37608200-37609800	Enhancers	Muscle Satellite Cultured Cells	--
3	chr14:37609200-37609800	Enhancers	HSMM	muscle
4	chr14:37609200-37609800	Enhancers	K562	blood
5	chr14:37609200-37609800	Enhancers	NH-A	brain
6	chr14:37609600-37609800	Enhancers	Fetal Muscle Leg	muscle
7	chr14:37609800-37611800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr14:37609800-37611800	Weak transcription	HSMM	muscle
9	chr14:37609800-37611800	Weak transcription	NH-A	brain
10	chr14:37609800-37614600	Weak transcription	K562	blood
11	chr14:37610000-37610400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr14:37610400-37610800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr14:37610400-37610800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr14:37610400-37618200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr14:37610800-37611600	Weak transcription	Fetal Muscle Leg	muscle
16	chr14:37610800-37612000	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr14:37610800-37612000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr14:37611400-37612800	Enhancers	Placenta Amnion	Placenta Amnion
19	chr14:37611400-37613000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr14:37611600-37613000	Enhancers	Fetal Muscle Leg	muscle
21	chr14:37611800-37612400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr14:37611800-37612400	Enhancers	HSMM	muscle
23	chr14:37611800-37612600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:37611800-37612800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr14:37611800-37612800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr14:37611800-37613000	Enhancers	Muscle Satellite Cultured Cells	--
27	chr14:37611800-37613000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr14:37611800-37613000	Enhancers	HMEC	breast
29	chr14:37611800-37613000	Enhancers	HSMMtube	muscle
30	chr14:37611800-37613000	Enhancers	NH-A	brain
31	chr14:37612000-37612200	Enhancers	Fetal Kidney	kidney
32	chr14:37612000-37612600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr14:37612000-37612600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr14:37612000-37612600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:37612000-37612800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:37612000-37612800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr14:37612000-37613000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr14:37612200-37612400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr14:37612200-37612600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr14:37612200-37612800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr14:37612200-37613400	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr14:37612400-37612600	Enhancers	Hela-S3	cervix
43	chr14:37612400-37612800	Flanking Active TSS	HSMM	muscle
44	chr14:37612400-37613000	Enhancers	NHDF-Ad	bronchial
45	chr14:37612600-37613400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr14:37612600-37614400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:37612600-37614600	Weak transcription	Hela-S3	cervix
48	chr14:37612800-37613000	Enhancers	Fetal Kidney	kidney
49	chr14:37612800-37613000	Enhancers	HSMM	muscle
50	chr14:37613000-37614200	Weak transcription	Muscle Satellite Cultured Cells	--

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