Variant report

Variant	nsv1019307
Chromosome Location	chr5:60295350-60409077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:779)
CpG islands
(count:122)
Chromatin interactive
region (count:52)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:779 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60314308-60314387	K562	blood:	n/a	chr5:60314370-60314386
2	ATF1	chr5:60380627-60380816	K562	blood:	n/a	n/a
3	ATF1	chr5:60396369-60396602	K562	blood:	n/a	n/a
4	ATF1	chr5:60383271-60383277	K562	blood:	n/a	n/a
5	BATF	chr5:60347149-60347471	GM12878	blood:	n/a	chr5:60347322-60347333 chr5:60347323-60347333
6	BHLHE40	chr5:60394223-60394250	K562	blood:	n/a	n/a
7	BRCA1	chr5:60306630-60306773	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr5:60395733-60395752	GM12878	blood:	n/a	n/a
9	CBX3	chr5:60344265-60344917	HCT-116	colon:	n/a	n/a
10	CBX3	chr5:60348517-60349283	HCT-116	colon:	n/a	n/a
11	CBX3	chr5:60348580-60349211	HCT-116	colon:	n/a	n/a
12	CBX3	chr5:60344262-60344845	HCT-116	colon:	n/a	n/a
13	CBX3	chr5:60351230-60351719	HCT-116	colon:	n/a	n/a
14	CCNT2	chr5:60336974-60337076	K562	blood:	n/a	n/a
15	CCNT2	chr5:60381800-60382000	K562	blood:	n/a	n/a
16	CEBPB	chr5:60392408-60392424	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:60392258-60392431	HepG2	liver:	n/a	chr5:60392376-60392387
18	CEBPB	chr5:60348547-60349210	HCT-116	colon:	n/a	n/a
19	CEBPB	chr5:60344184-60345032	HCT-116	colon:	n/a	chr5:60344922-60344933
20	CEBPB	chr5:60368758-60368954	K562	blood:	n/a	chr5:60368867-60368880 chr5:60368867-60368878 chr5:60368867-60368880
21	CEBPB	chr5:60346092-60346408	A549	lung:	n/a	n/a
22	CEBPB	chr5:60362736-60363029	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:60318989-60319403	IMR90	lung:	n/a	n/a
24	CEBPB	chr5:60362776-60362998	K562	blood:	n/a	n/a
25	CEBPB	chr5:60362769-60362975	A549	lung:	n/a	n/a
26	CEBPB	chr5:60325897-60326281	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:60348499-60349238	HCT-116	colon:	n/a	n/a
28	CEBPB	chr5:60316420-60316597	K562	blood:	n/a	n/a
29	CEBPB	chr5:60346097-60346421	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:60348698-60349132	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:60316396-60316638	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:60359586-60359731	K562	blood:	n/a	chr5:60359610-60359621
33	CEBPB	chr5:60359605-60359663	HepG2	liver:	n/a	chr5:60359610-60359621
34	CEBPB	chr5:60316342-60316622	A549	lung:	n/a	n/a
35	CEBPB	chr5:60346083-60346428	K562	blood:	n/a	n/a
36	CEBPB	chr5:60346090-60346426	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:60316358-60316620	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:60364086-60364309	HepG2	liver:	n/a	chr5:60364243-60364256
39	CEBPB	chr5:60362758-60363051	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:60346107-60346376	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr5:60316337-60316539	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:60392231-60392503	K562	blood:	n/a	chr5:60392376-60392387
43	CEBPB	chr5:60316315-60316656	MCF-7	breast:	n/a	n/a
44	CHD2	chr5:60306738-60306820	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr5:60341376-60341462	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr5:60351216-60351699	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:60351333-60351568	T-47D	breast:	n/a	n/a
48	CTCF	chr5:60306480-60307038	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:60351360-60351510	Caco-2	colon:	n/a	n/a
50	CTCF	chr5:60351237-60351560	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60346051-60346101	HCPEpiC	choroid plexus:	n/a
2	chr5:60346051-60346101	BE2_C	brain:	n/a
3	chr5:60346051-60346101	HUVEC	blood vessel:	n/a
4	chr5:60346051-60346101	HCT-116	colon:	n/a
5	chr5:60346051-60346101	HAEpiC	amniotic membrane:	n/a
6	chr5:60346051-60346101	ovcar-3	ovarian:	n/a
7	chr5:60325493-60325543	PrEC	prostate:	n/a
8	chr5:60325493-60325543	MCF10A-Er-Src	breast:	n/a
9	chr5:60325493-60325543	AoSMC	blood vessel:	n/a
10	chr5:60325493-60325543	GM06990	blood:	n/a
11	chr5:60346051-60346101	AoSMC	blood vessel:	n/a
12	chr5:60346051-60346101	HL-60	blood:	n/a
13	chr5:60325493-60325543	GM12892	blood:	n/a
14	chr5:60346051-60346101	NHBE	bronchial:	n/a
15	chr5:60346051-60346101	AG09309	skin:	n/a
16	chr5:60346051-60346101	HepG2	liver:	n/a
17	chr5:60346051-60346101	HMEC	breast:	n/a
18	chr5:60346051-60346101	GM12892	blood:	n/a
19	chr5:60346051-60346101	SK-N-SH	brain:	n/a
20	chr5:60346051-60346101	SK-N-SH_RA	brain:	n/a
21	chr5:60325493-60325543	HAEpiC	amniotic membrane:	n/a
22	chr5:60325493-60325543	GM19239	blood:	n/a
23	chr5:60325493-60325543	AG10803	skin:	n/a
24	chr5:60325493-60325543	GM12878	blood:	n/a
25	chr5:60325493-60325543	Hela-S3	cervix:	n/a
26	chr5:60346051-60346101	SAEC	small airway:	n/a
27	chr5:60325493-60325543	HEEpiC	esophagus:	n/a
28	chr5:60325493-60325543	HCT-116	colon:	n/a
29	chr5:60325493-60325543	K562	blood:	n/a
30	chr5:60346051-60346101	IMR90	lung:	fetal
31	chr5:60325493-60325543	NT2-D1	testis:	n/a
32	chr5:60325493-60325543	PFSK-1	brain:	n/a
33	chr5:60346051-60346101	GM12891	blood:	n/a
34	chr5:60346051-60346101	AG04449	skin:	fetal
35	chr5:60325493-60325543	AG09309	skin:	n/a
36	chr5:60346051-60346101	MCF10A-Er-Src	breast:	n/a
37	chr5:60346051-60346101	GM19239	blood:	n/a
38	chr5:60346051-60346101	Hepatocyte	liver:	n/a
39	chr5:60346051-60346101	U87	brain:	n/a
40	chr5:60325493-60325543	ECC-1	luminal epithelium:	n/a
41	chr5:60346051-60346101	NT2-D1	testis:	n/a
42	chr5:60346051-60346101	Jurkat	blood:	n/a
43	chr5:60325493-60325543	LNCaP	prostate:	n/a
44	chr5:60325493-60325543	HNPCEpiC	eye:	n/a
45	chr5:60325493-60325543	CMK	blood:	n/a
46	chr5:60325493-60325543	HCM	heart:	n/a
47	chr5:60325493-60325543	HIPEpiC	eye:	n/a
48	chr5:60325493-60325543	HRE	kidney:	n/a
49	chr5:60325493-60325543	A549	lung:	n/a
50	chr5:60346051-60346101	SK-N-MC	brain:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
2	chr5:60388764..60392434-chr5:60393819..60396676,3	K562	blood:
3	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
4	chr5:60320010..60322208-chr5:60331308..60333222,2	MCF-7	breast:
5	chr5:60334340..60336285-chr5:60341216..60344077,2	K562	blood:
6	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
7	chr5:60355470..60357785-chr5:60423437..60426318,2	K562	blood:
8	chr5:60350790..60351716-chr5:61229541..61230428,4	MCF-7	breast:
9	chr5:60321206..60323750-chr5:60323786..60326003,2	K562	blood:
10	chr5:60355839..60357550-chr5:60458247..60459791,2	MCF-7	breast:
11	chr5:60388764..60392434-chr5:60393819..60396676,3	K562	blood:
12	chr5:60385727..60388209-chr5:60393407..60396007,2	K562	blood:
13	chr5:60330521..60333236-chr5:60333963..60336641,2	K562	blood:
14	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
15	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
16	chr5:60351160..60351880-chr5:60764388..60765010,2	MCF-7	breast:
17	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
18	chr5:60351342..60352964-chr5:60353710..60356675,2	K562	blood:
19	chr5:60353410..60356120-chr5:60624338..60627119,3	MCF-7	breast:
20	chr5:60324520..60326950-chr5:60332622..60334608,2	K562	blood:
21	chr5:60351749..60354289-chr5:60357222..60359514,2	K562	blood:
22	chr5:60320010..60322208-chr5:60331308..60333222,2	MCF-7	breast:
23	chr5:60334340..60336285-chr5:60341216..60344077,2	K562	blood:
24	chr5:60365711..60368002-chr5:60369594..60371777,2	K562	blood:
25	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
26	chr5:60308495..60310817-chr5:60337811..60340272,2	K562	blood:
27	chr5:60311498..60313138-chr5:60318136..60319841,2	K562	blood:
28	chr5:60318175..60320382-chr5:60629060..60630909,2	K562	blood:
29	chr5:60393939..60396673-chr5:60399417..60401955,2	K562	blood:
30	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
31	chr5:60372533..60374046-chr5:60626026..60628135,2	MCF-7	breast:
32	chr5:60351204..60351892-chr5:60434644..60435198,2	MCF-7	breast:
33	chr5:60308495..60310817-chr5:60337811..60340272,2	K562	blood:
34	chr5:60393939..60396673-chr5:60399417..60401955,2	K562	blood:
35	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
36	chr5:60311498..60313138-chr5:60318136..60319841,2	K562	blood:
37	chr5:60369695..60372434-chr5:60457768..60459538,2	K562	blood:
38	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
39	chr5:60365711..60368002-chr5:60369594..60371777,2	K562	blood:
40	chr5:60393939..60398083-chr5:60399417..60401955,3	K562	blood:
41	chr5:60351749..60354289-chr5:60357222..60359514,2	K562	blood:
42	chr5:60345949..60348661-chr5:60350845..60353374,3	K562	blood:
43	chr5:60393939..60398083-chr5:60399417..60401955,3	K562	blood:
44	chr5:60324520..60326950-chr5:60332622..60334608,2	K562	blood:
45	chr5:60385727..60388209-chr5:60393407..60396007,2	K562	blood:
46	chr5:60351609..60354587-chr5:60627368..60629896,3	MCF-7	breast:
47	chr5:60330521..60333236-chr5:60333963..60336641,2	K562	blood:
48	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
49	chr5:60351342..60352964-chr5:60353710..60356675,2	K562	blood:
50	chr5:60240835..60243505-chr5:60324746..60327313,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM6-4	chr5:60368953-60369018	NONHSAT101655

No data

Variant related genes	Relation type
NDUFAF2	TF binding region
NDUFAF2	CpG island
ENSG00000188725	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000130449	chromatin interactions

Extended variants
information (count: 3663 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3663 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564576338	chr5:60295388-60295389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532295226	chr5:60295389-60295390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539952264	chr5:60295419-60295420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185303288	chr5:60295441-60295442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375414397	chr5:60295450-60295451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557854348	chr5:60295483-60295484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34805931	chr5:60295510-60295511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369148554	chr5:60295530-60295531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191155507	chr5:60295536-60295537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183327053	chr5:60295572-60295573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs386688457	chr5:60295580-60295581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs56043434	chr5:60295581-60295582	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs537323610	chr5:60295586-60295587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187038935	chr5:60295668-60295669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530445983	chr5:60295679-60295680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550213123	chr5:60295698-60295699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs55659107	chr5:60295704-60295705	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs539558325	chr5:60295754-60295755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554938362	chr5:60295809-60295810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191385286	chr5:60295879-60295880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555383614	chr5:60295903-60295904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573616545	chr5:60295913-60295914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183296599	chr5:60295939-60295940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536125238	chr5:60295998-60295999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556120614	chr5:60296092-60296093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575665345	chr5:60296118-60296119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544628382	chr5:60296171-60296172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140200508	chr5:60296210-60296211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142136235	chr5:60296235-60296236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540749437	chr5:60296265-60296266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76535696	chr5:60296342-60296343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553578727	chr5:60296445-60296446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146379261	chr5:60296468-60296469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139701124	chr5:60296469-60296470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371583553	chr5:60296475-60296476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145128694	chr5:60296481-60296482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35786913	chr5:60296482-60296483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201967156	chr5:60296483-60296484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397882009	chr5:60296485-60296486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376051872	chr5:60296502-60296503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs290505	chr5:60296556-60296557	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs188134914	chr5:60296652-60296653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570472590	chr5:60296715-60296716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532862714	chr5:60296769-60296770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191658755	chr5:60296781-60296782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566926426	chr5:60296930-60296931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536061876	chr5:60297012-60297013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182288995	chr5:60297051-60297052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569563140	chr5:60297090-60297091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538585950	chr5:60297177-60297178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Contiguous gene syndrome	19525295	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60266200-60317400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:60289600-60296400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr5:60290000-60296400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr5:60290000-60296400	Weak transcription	NHEK	skin
5	chr5:60290000-60297000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:60290200-60296800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:60290200-60298400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr5:60290200-60298400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr5:60290400-60296400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr5:60291200-60296600	Weak transcription	Fetal Brain Female	brain
11	chr5:60292200-60297800	Weak transcription	Pancreas	Pancrea
12	chr5:60292200-60305800	Weak transcription	Ovary	ovary
13	chr5:60293800-60296400	Weak transcription	Brain Angular Gyrus	brain
14	chr5:60295000-60304200	Weak transcription	HepG2	liver
15	chr5:60295200-60295400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr5:60295200-60295400	Enhancers	Fetal Brain Male	brain
17	chr5:60295200-60296200	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr5:60295200-60296400	Weak transcription	Aorta	Aorta
19	chr5:60295400-60296400	Weak transcription	Fetal Brain Male	brain
20	chr5:60296000-60296400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:60296000-60296600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:60296000-60296800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:60296000-60297000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr5:60296000-60298400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:60296200-60296600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:60296200-60297000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr5:60296400-60296800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr5:60296400-60296800	Enhancers	NHDF-Ad	bronchial
29	chr5:60296400-60297000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr5:60296400-60297000	Enhancers	Fetal Brain Male	brain
31	chr5:60296400-60297000	Enhancers	NHEK	skin
32	chr5:60296400-60297200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:60296400-60297200	Enhancers	Aorta	Aorta
34	chr5:60296400-60297200	Enhancers	Colon Smooth Muscle	Colon
35	chr5:60296400-60298000	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr5:60296600-60300000	Enhancers	Fetal Brain Female	brain
37	chr5:60296800-60297000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr5:60296800-60297200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:60297000-60297200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr5:60297000-60297400	Weak transcription	Fetal Brain Male	brain
41	chr5:60297000-60299800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:60297200-60300800	Weak transcription	Aorta	Aorta
43	chr5:60297400-60298200	Enhancers	Fetal Brain Male	brain
44	chr5:60297800-60298000	Enhancers	Pancreas	Pancrea
45	chr5:60298000-60298200	Weak transcription	Pancreas	Pancrea
46	chr5:60298200-60299400	Weak transcription	Fetal Brain Male	brain
47	chr5:60298400-60298600	Enhancers	Brain Angular Gyrus	brain
48	chr5:60298400-60299200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:60299400-60300000	Enhancers	Fetal Brain Male	brain
50	chr5:60299800-60300600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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