Variant report

Variant	nsv949662
Chromosome Location	chr5:60047974-60488379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4645)
CpG islands
(count:3359)
Chromatin interactive
region (count:279)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:4645 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
2	ARID3A	chr5:60459138-60459436	K562	blood:	n/a	n/a
3	ARID3A	chr5:60106314-60106972	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:60140010-60140140	K562	blood:	n/a	n/a
5	ARID3A	chr5:60314308-60314387	K562	blood:	n/a	chr5:60314370-60314386
6	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
8	ARID3A	chr5:60457952-60459426	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:60463345-60463470	K562	blood:	n/a	n/a
10	ARID3A	chr5:60451899-60451986	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:60116461-60117150	K562	blood:	n/a	n/a
12	ARID3A	chr5:60458031-60458279	K562	blood:	n/a	n/a
13	ARID3A	chr5:60274848-60275124	K562	blood:	n/a	n/a
14	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
15	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
16	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
17	ATF1	chr5:60274513-60275143	K562	blood:	n/a	n/a
18	ATF1	chr5:60458155-60458714	K562	blood:	n/a	n/a
19	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
20	ATF1	chr5:60105880-60106051	K562	blood:	n/a	n/a
21	ATF1	chr5:60137790-60137795	K562	blood:	n/a	n/a
22	ATF1	chr5:60380627-60380816	K562	blood:	n/a	n/a
23	ATF1	chr5:60383271-60383277	K562	blood:	n/a	n/a
24	ATF1	chr5:60140322-60140612	K562	blood:	n/a	n/a
25	ATF1	chr5:60116465-60117242	K562	blood:	n/a	n/a
26	ATF1	chr5:60148865-60149065	K562	blood:	n/a	n/a
27	ATF1	chr5:60396369-60396602	K562	blood:	n/a	n/a
28	ATF1	chr5:60098191-60098391	K562	blood:	n/a	n/a
29	ATF2	chr5:60122280-60122899	GM12878	blood:	n/a	n/a
30	ATF2	chr5:60122399-60122938	GM12878	blood:	n/a	n/a
31	ATF2	chr5:60457991-60458459	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
33	ATF2	chr5:60457869-60459425	GM12878	blood:	n/a	n/a
34	ATF3	chr5:60139979-60140240	K562	blood:	n/a	chr5:60140013-60140022
35	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
36	ATF3	chr5:60106451-60106930	A549	lung:	n/a	chr5:60106679-60106693
37	BACH1	chr5:60139641-60140505	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr5:60457791-60459109	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr5:60140730-60140830	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr5:60274899-60275146	K562	blood:	n/a	n/a
42	BACH1	chr5:60458014-60458112	K562	blood:	n/a	n/a
43	BATF	chr5:60473553-60473796	GM12878	blood:	n/a	n/a
44	BATF	chr5:60347149-60347471	GM12878	blood:	n/a	chr5:60347322-60347333 chr5:60347323-60347333
45	BATF	chr5:60458142-60458470	GM12878	blood:	n/a	n/a
46	BATF	chr5:60122447-60122875	GM12878	blood:	n/a	chr5:60122677-60122688
47	BATF	chr5:60122489-60122819	GM12878	blood:	n/a	chr5:60122677-60122688
48	BATF	chr5:60117975-60118244	GM12878	blood:	n/a	n/a
49	BATF	chr5:60057199-60057512	GM12878	blood:	n/a	n/a
50	BATF	chr5:60057258-60057503	GM12878	blood:	n/a	n/a

(count:3359 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60472989-60473039	GM12891	blood:	n/a
2	chr5:60241003-60241053	GM12892	blood:	n/a
3	chr5:60240817-60240867	RPTEC	kidney:	n/a
4	chr5:60139420-60139470	U87	brain:	n/a
5	chr5:60472989-60473039	GM12891	blood:	n/a
6	chr5:60241003-60241053	GM12892	blood:	n/a
7	chr5:60240817-60240867	RPTEC	kidney:	n/a
8	chr5:60139420-60139470	U87	brain:	n/a
9	chr5:60240838-60240888	ovcar-3	ovarian:	n/a
10	chr5:60141082-60141132	HepG2	liver:	n/a
11	chr5:60428301-60428351	ProgFib	skin:	n/a
12	chr5:60240891-60240941	HEK293	kidney:	embryo
13	chr5:60457901-60457951	PFSK-1	brain:	n/a
14	chr5:60059120-60059170	MCF10A-Er-Src	breast:	n/a
15	chr5:60455790-60455840	HAEpiC	amniotic membrane:	n/a
16	chr5:60187211-60187261	HL-60	blood:	n/a
17	chr5:60428301-60428351	AG09319	gingival:	n/a
18	chr5:60458176-60458226	HL-60	blood:	n/a
19	chr5:60459327-60459377	ProgFib	skin:	n/a
20	chr5:60139516-60139566	AG04450	lung:	fetal
21	chr5:60138761-60138811	A549	lung:	n/a
22	chr5:60464888-60464938	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:60459327-60459377	MCF-7	breast:	n/a
24	chr5:60240670-60240720	ECC-1	luminal epithelium:	n/a
25	chr5:60240926-60240976	LNCaP	prostate:	n/a
26	chr5:60241428-60241478	BJ	skin:	n/a
27	chr5:60050299-60050349	AG04449	skin:	fetal
28	chr5:60139938-60139988	BE2_C	brain:	n/a
29	chr5:60458483-60458533	Caco-2	colon:	n/a
30	chr5:60428301-60428351	GM12891	blood:	n/a
31	chr5:60240891-60240941	HPAEpiC	pulmonary alveolar:	n/a
32	chr5:60457841-60457891	ovcar-3	ovarian:	n/a
33	chr5:60240670-60240720	AoSMC	blood vessel:	n/a
34	chr5:60458778-60458828	IMR90	lung:	fetal
35	chr5:60241424-60241474	HIPEpiC	eye:	n/a
36	chr5:60059120-60059170	RPTEC	kidney:	n/a
37	chr5:60458483-60458533	HUVEC	blood vessel:	n/a
38	chr5:60458778-60458828	K562	blood:	n/a
39	chr5:60050299-60050349	GM12891	blood:	n/a
40	chr5:60241003-60241053	HL-60	blood:	n/a
41	chr5:60140824-60140874	K562	blood:	n/a
42	chr5:60132712-60132762	HRCEpiC	kidney:	n/a
43	chr5:60137757-60137807	HEEpiC	esophagus:	n/a
44	chr5:60142446-60142496	T-47D	breast:	n/a
45	chr5:60456037-60456087	HCF	heart:	n/a
46	chr5:60139708-60139758	ECC-1	luminal epithelium:	n/a
47	chr5:60241636-60241686	AoSMC	blood vessel:	n/a
48	chr5:60138838-60138888	ProgFib	skin:	n/a
49	chr5:60138761-60138811	T-47D	breast:	n/a
50	chr5:60073995-60074045	MCF-7	breast:	n/a

(count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
2	chr5:60087441..60089276-chr5:60089305..60090863,2	MCF-7	breast:
3	chr5:60351342..60352964-chr5:60353710..60356675,2	K562	blood:
4	chr5:60450120..60453584-chr5:60455423..60459976,7	MCF-7	breast:
5	chr2:25194755..25195595-chr5:60240745..60241487,2	Hela-S3	cervix:
6	chr5:60432909..60434440-chr5:60438125..60440670,2	K562	blood:
7	chr5:60412981..60415103-chr5:60419112..60420959,2	K562	blood:
8	chr5:60464487..60466680-chr5:60468300..60471010,2	K562	blood:
9	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
10	chr3:51422419..51423111-chr5:60457900..60458841,2	HCT-116	colon:
11	chr5:60320010..60322208-chr5:60331308..60333222,2	MCF-7	breast:
12	chr5:60411996..60414710-chr5:60433336..60435161,2	K562	blood:
13	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
14	chr5:60472733..60477448-chr5:60625158..60628299,7	MCF-7	breast:
15	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
16	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
17	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
18	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
19	chr12:46384250..46385111-chr5:60458221..60458844,2	Hela-S3	cervix:
20	chr5:60117200..60119232-chr5:60122303..60124424,2	K562	blood:
21	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
22	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
23	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
24	chr5:60351204..60351892-chr5:60434644..60435198,2	MCF-7	breast:
25	chr1:16840577..16841087-chr5:60458118..60458962,2	Hela-S3	cervix:
26	chr5:60239789..60242454-chr5:60245834..60249187,6	MCF-7	breast:
27	chr17:57967665..57970523-chr5:60456925..60459540,2	MCF-7	breast:
28	chr5:60143868..60145505-chr5:60146013..60148610,2	K562	blood:
29	chr5:60440723..60443859-chr5:60448886..60452084,3	K562	blood:
30	chr5:60254798..60255532-chr5:60954065..60954863,2	K562	blood:
31	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
32	chr5:60433928..60435922-chr5:60454326..60456231,2	K562	blood:
33	chr5:60474350..60475293-chr5:60600116..60600975,7	MCF-7	breast:
34	chr5:60320010..60322208-chr5:60331308..60333222,2	MCF-7	breast:
35	chr5:60464941..60466921-chr5:60605078..60607461,2	MCF-7	breast:
36	chr5:60150200..60152775-chr5:60153410..60154990,2	MCF-7	breast:
37	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
38	chr5:60111228..60113761-chr5:60138428..60140266,2	MCF-7	breast:
39	chr5:60473247..60475039-chr5:60548494..60550640,2	MCF-7	breast:
40	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
41	chr5:60369695..60372434-chr5:60457768..60459538,2	K562	blood:
42	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
43	chr5:60463125..60463841-chr5:60626532..60627147,2	MCF-7	breast:
44	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
45	chr5:60431315..60433087-chr5:60453432..60456427,3	K562	blood:
46	chr5:60355470..60357785-chr5:60423437..60426318,2	K562	blood:
47	chr5:60454421..60471345-chr5:60622342..60633215,36	MCF-7	breast:
48	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
49	chr5:60470829..60473385-chr5:60478345..60480116,2	K562	blood:
50	chr5:60046195..60048141-chr5:60138648..60140514,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFAF2-3	chr5:60464189-60465734	NONHSAT101659
2	lnc-ERCC8-1	chr5:60162284-60162762	ENSG00000272308.1
3	lnc-NDUFAF2-4	chr5:60487377-60487523	NONHSAT101662
4	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655
5	lnc-NDUFAF2-2	chr5:60476179-60476265	NR_109908
6	lnc-NDUFAF2-2	chr5:60457897-60458353	ENSG00000251279.1
7	lnc-C5orf43-6	chr5:60466567-60467690	NONHSAT101660
8	lnc-NDUFAF2-2	chr5:60475531-60475654	NR_109908
9	lnc-NDUFAF2-1	chr5:60215204-60215400	ENSG00000233847.1
10	lnc-NDUFAF2-2	chr5:60474133-60476024	NONHSAT101661
11	lnc-NDUFAF2-2	chr5:60475531-60475654	ENSG00000251279.1
12	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1
13	lnc-NDUFAF2-2	chr5:60458334-60460554	NONHSAT101658
14	lnc-ZSWIM6-4	chr5:60368953-60369018	NONHSAT101655
15	lnc-NDUFAF2-2	chr5:60476179-60476265	ENSG00000251279.1
16	lnc-NDUFAF2-2	chr5:60476179-60476280	NONHSAT101661
17	lnc-NDUFAF2-2	chr5:60458143-60458353	NR_109908
18	lnc-NDUFAF2-2	chr5:60476586-60479163	NONHSAT101661
19	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ELOVL7	hsa-miR-21-5p	chr5:60048157-60048175
2	ELOVL7	hsa-miR-21-5p	chr5:60049832-60049858

Variant related genes	Relation type
ENSG00000251279	TF binding region
NDUFAF2	TF binding region
ENSG00000269267	TF binding region
ELOVL7	TF binding region
ENSG00000272308	TF binding region
SMIM15	TF binding region
ERCC8	TF binding region
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
ENSG00000251279	CpG island
NDUFAF2	CpG island
ENSG00000269267	CpG island
ELOVL7	CpG island
ENSG00000272308	CpG island
SMIM15	CpG island
ERCC8	CpG island
GNL3LP1	CpG island
ENSG00000233847	CpG island
ENSG00000100982	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000101898	chromatin interactions
ENSG00000196352	chromatin interactions
ENSG00000256940	chromatin interactions
ENSG00000143761	chromatin interactions
ENSG00000249279	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000054267	chromatin interactions
ENSG00000073756	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000101294	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000251682	chromatin interactions
ENSG00000110925	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000111679	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000112977	chromatin interactions
ENSG00000021355	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000125686	chromatin interactions
ENSG00000267308	chromatin interactions
ENSG00000145050	chromatin interactions
ENSG00000173457	chromatin interactions
ENSG00000139218	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000130449	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000152904	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000214174	chromatin interactions
ENSG00000206652	chromatin interactions

Extended variants
information (count: 14769 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:14769 , 50 per page) page: 1 2 3 4 5 6 7 ... 296

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs702564	chr5:60047974-60047975	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs180924470	chr5:60047980-60047981	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558691224	chr5:60047992-60047993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs16878354	chr5:60048028-60048029	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559509009	chr5:60048097-60048098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534997805	chr5:60048139-60048140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184922158	chr5:60048161-60048162	Weak transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
8	rs189679004	chr5:60048255-60048256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562358304	chr5:60048278-60048279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145164561	chr5:60048366-60048367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551185355	chr5:60048426-60048427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182035598	chr5:60048428-60048429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112591812	chr5:60048545-60048546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373029299	chr5:60048546-60048547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578241770	chr5:60048551-60048552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565558664	chr5:60048577-60048578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534571677	chr5:60048591-60048592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554570089	chr5:60048634-60048635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574674172	chr5:60048673-60048674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536887293	chr5:60048692-60048693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200554830	chr5:60048772-60048773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186175219	chr5:60048779-60048780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72417102	chr5:60048780-60048781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576598701	chr5:60048792-60048793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376624477	chr5:60048802-60048803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545908072	chr5:60048815-60048816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs147562358	chr5:60048874-60048875	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573155671	chr5:60048966-60048967	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542201081	chr5:60048971-60048972	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576029297	chr5:60048972-60048973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs149021475	chr5:60048982-60048983	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs551819564	chr5:60049026-60049027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570605053	chr5:60049042-60049043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35840031	chr5:60049052-60049053	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2219333	chr5:60049119-60049120	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575747711	chr5:60049123-60049124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373855389	chr5:60049141-60049142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs192016127	chr5:60049161-60049162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs73759411	chr5:60049240-60049241	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs565722148	chr5:60049271-60049272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs183295547	chr5:60049300-60049301	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs548161158	chr5:60049335-60049336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568299789	chr5:60049358-60049359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs13358053	chr5:60049577-60049578	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs188349011	chr5:60049723-60049724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567566830	chr5:60049752-60049753	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs116305438	chr5:60049753-60049754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539199950	chr5:60049764-60049765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567831775	chr5:60049805-60049806	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190989135	chr5:60049924-60049925	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Contiguous gene syndrome	19525295	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4656 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60040800-60066600	Weak transcription	Fetal Intestine Small	intestine
2	chr5:60042200-60050000	Weak transcription	Fetal Intestine Large	intestine
3	chr5:60042200-60052000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr5:60042600-60055800	Weak transcription	Brain Hippocampus Middle	brain
5	chr5:60044800-60081600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr5:60044800-60098000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:60045000-60056600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr5:60045200-60048800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr5:60045200-60065000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr5:60045200-60084400	Weak transcription	Brain Angular Gyrus	brain
11	chr5:60046000-60061000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:60046200-60065000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:60050000-60051000	Strong transcription	Fetal Intestine Large	intestine
14	chr5:60051000-60057000	Weak transcription	Fetal Intestine Large	intestine
15	chr5:60056600-60058000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:60057000-60057600	Strong transcription	Fetal Intestine Large	intestine
17	chr5:60057600-60061200	Weak transcription	Fetal Intestine Large	intestine
18	chr5:60057600-60092200	Weak transcription	Brain Anterior Caudate	brain
19	chr5:60057600-60093200	Weak transcription	Pancreas	Pancrea
20	chr5:60057800-60074800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr5:60058000-60066200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr5:60060600-60069600	Weak transcription	Esophagus	oesophagus
23	chr5:60061000-60061800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:60061000-60062000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr5:60061200-60061600	Enhancers	Fetal Intestine Large	intestine
26	chr5:60061200-60061800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr5:60061600-60066000	Weak transcription	Fetal Intestine Large	intestine
28	chr5:60061800-60067800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr5:60061800-60075200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr5:60062000-60064200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:60062600-60062800	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr5:60062800-60067600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr5:60063800-60065000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:60064000-60065400	Enhancers	Brain Substantia Nigra	brain
35	chr5:60064200-60064400	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr5:60064200-60065400	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr5:60064200-60065600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr5:60064400-60065000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr5:60065000-60065200	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr5:60065000-60065600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:60065000-60065600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:60065200-60091800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr5:60065200-60101200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr5:60065600-60070200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:60065600-60070600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:60065600-60078000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:60066000-60068600	Strong transcription	Fetal Intestine Large	intestine
48	chr5:60066200-60068200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr5:60066600-60068600	Strong transcription	Fetal Intestine Small	intestine
50	chr5:60067600-60068200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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