Variant report

Variant	nsv1017095
Chromosome Location	chr5:60050600-60414783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3321)
CpG islands
(count:2320)
Chromatin interactive
region (count:169)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3321 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

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	chr5:60314308-60314387	K562	blood:	n/a	chr5:60314370-60314386
3	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:60106314-60106972	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:60140010-60140140	K562	blood:	n/a	n/a
6	ARID3A	chr5:60116461-60117150	K562	blood:	n/a	n/a
7	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
8	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
9	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:60274848-60275124	K562	blood:	n/a	n/a
11	ATF1	chr5:60148865-60149065	K562	blood:	n/a	n/a
12	ATF1	chr5:60098191-60098391	K562	blood:	n/a	n/a
13	ATF1	chr5:60140322-60140612	K562	blood:	n/a	n/a
14	ATF1	chr5:60137790-60137795	K562	blood:	n/a	n/a
15	ATF1	chr5:60274513-60275143	K562	blood:	n/a	n/a
16	ATF1	chr5:60116465-60117242	K562	blood:	n/a	n/a
17	ATF1	chr5:60396369-60396602	K562	blood:	n/a	n/a
18	ATF1	chr5:60383271-60383277	K562	blood:	n/a	n/a
19	ATF1	chr5:60105880-60106051	K562	blood:	n/a	n/a
20	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
21	ATF1	chr5:60380627-60380816	K562	blood:	n/a	n/a
22	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
23	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
24	ATF2	chr5:60122280-60122899	GM12878	blood:	n/a	n/a
25	ATF2	chr5:60122399-60122938	GM12878	blood:	n/a	n/a
26	ATF3	chr5:60139979-60140240	K562	blood:	n/a	chr5:60140013-60140022
27	ATF3	chr5:60106451-60106930	A549	lung:	n/a	chr5:60106679-60106693
28	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
29	BACH1	chr5:60140730-60140830	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:60274899-60275146	K562	blood:	n/a	n/a
31	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr5:60139641-60140505	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr5:60057199-60057512	GM12878	blood:	n/a	n/a
34	BATF	chr5:60347149-60347471	GM12878	blood:	n/a	chr5:60347322-60347333 chr5:60347323-60347333
35	BATF	chr5:60122489-60122819	GM12878	blood:	n/a	chr5:60122677-60122688
36	BATF	chr5:60057258-60057503	GM12878	blood:	n/a	n/a
37	BATF	chr5:60117975-60118244	GM12878	blood:	n/a	n/a
38	BATF	chr5:60122447-60122875	GM12878	blood:	n/a	chr5:60122677-60122688
39	BCL11A	chr5:60122417-60122906	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:60122515-60122796	GM12878	blood:	n/a	n/a
41	BCL11A	chr5:60057304-60057451	GM12878	blood:	n/a	n/a
42	BCL11A	chr5:60057285-60057534	GM12878	blood:	n/a	n/a
43	BCL3	chr5:60106438-60107052	A549	lung:	n/a	n/a
44	BCL3	chr5:60125467-60125724	GM12878	blood:	n/a	n/a
45	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
46	BCLAF1	chr5:60122249-60122828	GM12878	blood:	n/a	n/a
47	BHLHE40	chr5:60116487-60117300	K562	blood:	n/a	n/a
48	BHLHE40	chr5:60139760-60140304	HepG2	liver:	n/a	chr5:60139813-60139829
49	BHLHE40	chr5:60240872-60241581	K562	blood:	n/a	chr5:60241008-60241024
50	BHLHE40	chr5:60148834-60149083	K562	blood:	n/a	n/a

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60240891-60240941	HEK293	kidney:	embryo
2	chr5:60240817-60240867	SKMC	muscle:	n/a
3	chr5:60240891-60240941	HEK293	kidney:	embryo
4	chr5:60240817-60240867	SKMC	muscle:	n/a
5	chr5:60240952-60241002	SKMC	muscle:	n/a
6	chr5:60187211-60187261	HIPEpiC	eye:	n/a
7	chr5:60240838-60240888	Hepatocyte	liver:	n/a
8	chr5:60187211-60187261	SK-N-MC	brain:	n/a
9	chr5:60139941-60139991	PrEC	prostate:	n/a
10	chr5:60139420-60139470	U87	brain:	n/a
11	chr5:60240952-60241002	HepG2	liver:	n/a
12	chr5:60139420-60139470	LNCaP	prostate:	n/a
13	chr5:60139708-60139758	GM12891	blood:	n/a
14	chr5:60138761-60138811	Jurkat	blood:	n/a
15	chr5:60241324-60241374	MCF10A-Er-Src	breast:	n/a
16	chr5:60142446-60142496	CMK	blood:	n/a
17	chr5:60139293-60139343	LNCaP	prostate:	n/a
18	chr5:60241324-60241374	HCPEpiC	choroid plexus:	n/a
19	chr5:60240838-60240888	GM06990	blood:	n/a
20	chr5:60139941-60139991	SK-N-MC	brain:	n/a
21	chr5:60241003-60241053	HEK293	kidney:	embryo
22	chr5:60139938-60139988	GM12878	blood:	n/a
23	chr5:60073995-60074045	Hela-S3	cervix:	n/a
24	chr5:60240891-60240941	IMR90	lung:	fetal
25	chr5:60240926-60240976	HCPEpiC	choroid plexus:	n/a
26	chr5:60240817-60240867	GM12891	blood:	n/a
27	chr5:60241019-60241069	NB4	blood:	n/a
28	chr5:60139420-60139470	HAEpiC	amniotic membrane:	n/a
29	chr5:60325493-60325543	HMEC	breast:	n/a
30	chr5:60240926-60240976	AG04450	lung:	fetal
31	chr5:60138883-60138933	HCF	heart:	n/a
32	chr5:60241003-60241053	U87	brain:	n/a
33	chr5:60241636-60241686	SKMC	muscle:	n/a
34	chr5:60148273-60148323	H1-hESC	embryonic stem cell:	embryo
35	chr5:60241428-60241478	HRCEpiC	kidney:	n/a
36	chr5:60138761-60138811	PrEC	prostate:	n/a
37	chr5:60240838-60240888	GM12878	blood:	n/a
38	chr5:60148273-60148323	GM06990	blood:	n/a
39	chr5:60139938-60139988	AG09319	gingival:	n/a
40	chr5:60138838-60138888	HRCEpiC	kidney:	n/a
41	chr5:60241424-60241474	PrEC	prostate:	n/a
42	chr5:60059120-60059170	SK-N-SH	brain:	n/a
43	chr5:60241019-60241069	HEEpiC	esophagus:	n/a
44	chr5:60240891-60240941	LNCaP	prostate:	n/a
45	chr5:60240870-60240920	GM12878	blood:	n/a
46	chr5:60073995-60074045	HMEC	breast:	n/a
47	chr5:60240568-60240618	SKMC	muscle:	n/a
48	chr5:60137757-60137807	A549	lung:	n/a
49	chr5:60241003-60241053	HCT-116	colon:	n/a
50	chr5:60239580-60239630	AG04449	skin:	fetal

(count:169 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr5:60351609..60354587-chr5:60627368..60629896,3	MCF-7	breast:
2	chr5:60119778..60121322-chr5:60121327..60122978,2	K562	blood:
3	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
4	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
5	chr5:60412981..60415103-chr5:60419112..60420959,2	K562	blood:
6	chr5:60111228..60113761-chr5:60138428..60140266,2	MCF-7	breast:
7	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
8	chr5:60087441..60089276-chr5:60089305..60090863,2	MCF-7	breast:
9	chr5:60104199..60107112-chr5:60138183..60141170,2	MCF-7	breast:
10	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
11	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
12	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
13	chr5:60351342..60352964-chr5:60353710..60356675,2	K562	blood:
14	chr5:59993402..59996272-chr5:60048809..60051606,2	MCF-7	breast:
15	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
16	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
17	chr5:60042570..60044385-chr5:60079016..60080838,2	K562	blood:
18	chr5:60117200..60119232-chr5:60122303..60124424,2	K562	blood:
19	chr5:60365711..60368002-chr5:60369594..60371777,2	K562	blood:
20	chr2:25194755..25195595-chr5:60240745..60241487,2	Hela-S3	cervix:
21	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
22	chr5:60393939..60398083-chr5:60399417..60401955,3	K562	blood:
23	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
24	chr5:60138677..60141411-chr5:60155273..60157219,2	MCF-7	breast:
25	chr5:60115551..60118264-chr5:60126347..60128654,2	MCF-7	breast:
26	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
27	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
28	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
29	chr5:60369695..60372434-chr5:60457768..60459538,2	K562	blood:
30	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
31	chr5:60330521..60333236-chr5:60333963..60336641,2	K562	blood:
32	chr5:60393939..60398083-chr5:60399417..60401955,3	K562	blood:
33	chr5:60308495..60310817-chr5:60337811..60340272,2	K562	blood:
34	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
35	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
36	chr5:60141307..60144527-chr5:60240837..60243388,3	K562	blood:
37	chr5:60150200..60152775-chr5:60153410..60154990,2	MCF-7	breast:
38	chr5:60318175..60320382-chr5:60629060..60630909,2	K562	blood:
39	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
40	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
41	chr5:60274623..60276264-chr5:60290570..60293305,2	K562	blood:
42	chr5:60134031..60135823-chr5:60138767..60140768,2	MCF-7	breast:
43	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
44	chr5:60240835..60243505-chr5:60324746..60327313,2	MCF-7	breast:
45	chr5:60393939..60396673-chr5:60399417..60401955,2	K562	blood:
46	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
47	chr5:60100541..60102761-chr5:60130219..60132557,2	K562	blood:
48	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
49	chr5:60050521..60052217-chr5:60052630..60054560,2	MCF-7	breast:
50	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFAF2-1	chr5:60215204-60215400	ENSG00000233847.1
2	lnc-ERCC8-1	chr5:60162284-60162762	ENSG00000272308.1
3	lnc-ZSWIM6-4	chr5:60368953-60369018	NONHSAT101655
4	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1
5	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1
6	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655

No data

Variant related genes	Relation type
NDUFAF2	TF binding region
ENSG00000269267	TF binding region
ELOVL7	TF binding region
ENSG00000272308	TF binding region
ERCC8	TF binding region
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
NDUFAF2	CpG island
ENSG00000269267	CpG island
ELOVL7	CpG island
ENSG00000272308	CpG island
ERCC8	CpG island
GNL3LP1	CpG island
ENSG00000233847	CpG island
ENSG00000121068	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000112977	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000130449	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000115137	chromatin interactions

Extended variants
information (count: 12345 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:12345 , 50 per page) page: 1 2 3 4 5 6 7 ... 247

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546154166	chr5:60050608-60050609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs146313717	chr5:60050637-60050638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs367806058	chr5:60050643-60050644	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs367629382	chr5:60050669-60050670	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368479805	chr5:60050675-60050676	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372205505	chr5:60050695-60050696	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs13156137	chr5:60050708-60050709	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575720882	chr5:60050718-60050719	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544573200	chr5:60050719-60050720	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182320358	chr5:60050729-60050730	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs578247798	chr5:60050754-60050755	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540506541	chr5:60050762-60050763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560716503	chr5:60050775-60050776	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375993556	chr5:60050880-60050881	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574116262	chr5:60050885-60050886	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186942369	chr5:60050889-60050890	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532226800	chr5:60050966-60050967	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561398605	chr5:60050973-60050974	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78320971	chr5:60050988-60050989	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530469647	chr5:60051074-60051075	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs371522054	chr5:60051214-60051215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs550149583	chr5:60051232-60051233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191405522	chr5:60051237-60051238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185058175	chr5:60051256-60051257	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569172005	chr5:60051258-60051259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546548576	chr5:60051267-60051268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188645157	chr5:60051303-60051304	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536040161	chr5:60051318-60051319	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs549504896	chr5:60051340-60051341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs151317671	chr5:60051341-60051342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374338830	chr5:60051376-60051377	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538283433	chr5:60051392-60051393	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535150994	chr5:60051416-60051417	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs578257415	chr5:60051422-60051423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548389966	chr5:60051432-60051433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534522692	chr5:60051433-60051434	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554128517	chr5:60051471-60051472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs368310964	chr5:60051483-60051484	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574180018	chr5:60051524-60051525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113096760	chr5:60051600-60051601	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76910489	chr5:60051604-60051605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539081917	chr5:60051639-60051640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574977456	chr5:60051658-60051659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543830409	chr5:60051739-60051740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76075715	chr5:60051837-60051838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs5868252	chr5:60051960-60051961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193179133	chr5:60051986-60051987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150450495	chr5:60051991-60051992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138441962	chr5:60052008-60052009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529137165	chr5:60052012-60052013	Weak transcription	n/a	n/a	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:3510 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60040800-60066600	Weak transcription	Fetal Intestine Small	intestine
2	chr5:60042200-60052000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr5:60042600-60055800	Weak transcription	Brain Hippocampus Middle	brain
4	chr5:60044800-60081600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr5:60044800-60098000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr5:60045000-60056600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:60045200-60065000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:60045200-60084400	Weak transcription	Brain Angular Gyrus	brain
9	chr5:60046000-60061000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:60046200-60065000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:60050000-60051000	Strong transcription	Fetal Intestine Large	intestine
12	chr5:60051000-60057000	Weak transcription	Fetal Intestine Large	intestine
13	chr5:60056600-60058000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr5:60057000-60057600	Strong transcription	Fetal Intestine Large	intestine
15	chr5:60057600-60061200	Weak transcription	Fetal Intestine Large	intestine
16	chr5:60057600-60092200	Weak transcription	Brain Anterior Caudate	brain
17	chr5:60057600-60093200	Weak transcription	Pancreas	Pancrea
18	chr5:60057800-60074800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr5:60058000-60066200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr5:60060600-60069600	Weak transcription	Esophagus	oesophagus
21	chr5:60061000-60061800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:60061000-60062000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:60061200-60061600	Enhancers	Fetal Intestine Large	intestine
24	chr5:60061200-60061800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr5:60061600-60066000	Weak transcription	Fetal Intestine Large	intestine
26	chr5:60061800-60067800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr5:60061800-60075200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr5:60062000-60064200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:60062600-60062800	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr5:60062800-60067600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr5:60063800-60065000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:60064000-60065400	Enhancers	Brain Substantia Nigra	brain
33	chr5:60064200-60064400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr5:60064200-60065400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr5:60064200-60065600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:60064400-60065000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr5:60065000-60065200	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr5:60065000-60065600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr5:60065000-60065600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:60065200-60091800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr5:60065200-60101200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:60065600-60070200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr5:60065600-60070600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr5:60065600-60078000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:60066000-60068600	Strong transcription	Fetal Intestine Large	intestine
46	chr5:60066200-60068200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:60066600-60068600	Strong transcription	Fetal Intestine Small	intestine
48	chr5:60067600-60068200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr5:60067800-60068000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr5:60067800-60068400	Enhancers	HUES48 Cell Line	embryonic stem cell

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