Variant report

Variant	nsv934153
Chromosome Location	chr5:60004982-60309751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2826)
CpG islands
(count:2624)
Chromatin interactive
region (count:134)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2826 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60106314-60106972	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:60116461-60117150	K562	blood:	n/a	n/a
3	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
5	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
6	ARID3A	chr5:60274848-60275124	K562	blood:	n/a	n/a
7	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
8	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:60140010-60140140	K562	blood:	n/a	n/a
10	ATF1	chr5:60137790-60137795	K562	blood:	n/a	n/a
11	ATF1	chr5:60105880-60106051	K562	blood:	n/a	n/a
12	ATF1	chr5:60148865-60149065	K562	blood:	n/a	n/a
13	ATF1	chr5:60018170-60018424	K562	blood:	n/a	n/a
14	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
15	ATF1	chr5:60098191-60098391	K562	blood:	n/a	n/a
16	ATF1	chr5:60274513-60275143	K562	blood:	n/a	n/a
17	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
18	ATF1	chr5:60116465-60117242	K562	blood:	n/a	n/a
19	ATF1	chr5:60140322-60140612	K562	blood:	n/a	n/a
20	ATF2	chr5:60122399-60122938	GM12878	blood:	n/a	n/a
21	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
22	ATF2	chr5:60122280-60122899	GM12878	blood:	n/a	n/a
23	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
24	ATF3	chr5:60139979-60140240	K562	blood:	n/a	chr5:60140013-60140022
25	ATF3	chr5:60106451-60106930	A549	lung:	n/a	chr5:60106679-60106693
26	BACH1	chr5:60274899-60275146	K562	blood:	n/a	n/a
27	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr5:60139641-60140505	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr5:60140730-60140830	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr5:60117975-60118244	GM12878	blood:	n/a	n/a
31	BATF	chr5:60034409-60034644	GM12878	blood:	n/a	n/a
32	BATF	chr5:60057258-60057503	GM12878	blood:	n/a	n/a
33	BATF	chr5:60122489-60122819	GM12878	blood:	n/a	chr5:60122677-60122688
34	BATF	chr5:60122447-60122875	GM12878	blood:	n/a	chr5:60122677-60122688
35	BATF	chr5:60057199-60057512	GM12878	blood:	n/a	n/a
36	BATF	chr5:60034434-60034644	GM12878	blood:	n/a	n/a
37	BCL11A	chr5:60057304-60057451	GM12878	blood:	n/a	n/a
38	BCL11A	chr5:60122417-60122906	GM12878	blood:	n/a	n/a
39	BCL11A	chr5:60122515-60122796	GM12878	blood:	n/a	n/a
40	BCL11A	chr5:60057285-60057534	GM12878	blood:	n/a	n/a
41	BCL3	chr5:60106438-60107052	A549	lung:	n/a	n/a
42	BCL3	chr5:60125467-60125724	GM12878	blood:	n/a	n/a
43	BCLAF1	chr5:60122249-60122828	GM12878	blood:	n/a	n/a
44	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
45	BHLHE40	chr5:60148834-60149083	K562	blood:	n/a	n/a
46	BHLHE40	chr5:60093321-60093343	K562	blood:	n/a	n/a
47	BHLHE40	chr5:60240684-60241301	GM12878	blood:	n/a	chr5:60241008-60241024
48	BHLHE40	chr5:60057704-60057885	HepG2	liver:	n/a	n/a
49	BHLHE40	chr5:60139908-60140548	K562	blood:	n/a	n/a
50	BHLHE40	chr5:60241820-60242140	K562	blood:	n/a	n/a

(count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60139941-60139991	HNPCEpiC	eye:	n/a
2	chr5:60139941-60139991	HNPCEpiC	eye:	n/a
3	chr5:60059120-60059170	IMR90	lung:	fetal
4	chr5:60240891-60240941	MCF10A-Er-Src	breast:	n/a
5	chr5:60240926-60240976	HRPEpiC	eye:	n/a
6	chr5:60240817-60240867	SK-N-SH	brain:	n/a
7	chr5:60137757-60137807	ECC-1	luminal epithelium:	n/a
8	chr5:60240952-60241002	HRPEpiC	eye:	n/a
9	chr5:60240817-60240867	ProgFib	skin:	n/a
10	chr5:60187211-60187261	NHBE	bronchial:	n/a
11	chr5:60240568-60240618	AG09309	skin:	n/a
12	chr5:60039648-60039698	NB4	blood:	n/a
13	chr5:60039414-60039464	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:60059120-60059170	HCPEpiC	choroid plexus:	n/a
15	chr5:60139516-60139566	AoSMC	blood vessel:	n/a
16	chr5:60187211-60187261	NHDF-neo	bronchial:	n/a
17	chr5:60139293-60139343	LNCaP	prostate:	n/a
18	chr5:60240568-60240618	SK-N-SH	brain:	n/a
19	chr5:60240817-60240867	HRPEpiC	eye:	n/a
20	chr5:60050299-60050349	ovcar-3	ovarian:	n/a
21	chr5:60139293-60139343	ovcar-3	ovarian:	n/a
22	chr5:60039414-60039464	BJ	skin:	n/a
23	chr5:60240817-60240867	HCT-116	colon:	n/a
24	chr5:60139941-60139991	SKMC	muscle:	n/a
25	chr5:60148273-60148323	AG09309	skin:	n/a
26	chr5:60050299-60050349	MCF10A-Er-Src	breast:	n/a
27	chr5:60142446-60142496	NHDF-neo	bronchial:	n/a
28	chr5:60240838-60240888	Hepatocyte	liver:	n/a
29	chr5:60138761-60138811	HCM	heart:	n/a
30	chr5:60148273-60148323	LNCaP	prostate:	n/a
31	chr5:60139941-60139991	GM12878	blood:	n/a
32	chr5:60139420-60139470	HRE	kidney:	n/a
33	chr5:60139516-60139566	NB4	blood:	n/a
34	chr5:60139516-60139566	NT2-D1	testis:	n/a
35	chr5:60040736-60040786	GM12892	blood:	n/a
36	chr5:60240891-60240941	Hela-S3	cervix:	n/a
37	chr5:60138883-60138933	HNPCEpiC	eye:	n/a
38	chr5:60240838-60240888	MCF-7	breast:	n/a
39	chr5:60240838-60240888	ovcar-3	ovarian:	n/a
40	chr5:60239580-60239630	AG10803	skin:	n/a
41	chr5:60139941-60139991	RPTEC	kidney:	n/a
42	chr5:60239580-60239630	ovcar-3	ovarian:	n/a
43	chr5:60240870-60240920	MCF-7	breast:	n/a
44	chr5:60139516-60139566	HCM	heart:	n/a
45	chr5:60148273-60148323	SKMC	muscle:	n/a
46	chr5:60239580-60239630	RPTEC	kidney:	n/a
47	chr5:60187211-60187261	AG04449	skin:	fetal
48	chr5:60240926-60240976	HEEpiC	esophagus:	n/a
49	chr5:60241324-60241374	GM19239	blood:	n/a
50	chr5:60139938-60139988	SK-N-SH_RA	brain:	n/a

(count:134 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:60089577..60091620-chr5:60092032..60093773,2	K562	blood:
2	chr5:59993402..59996272-chr5:60048809..60051606,2	MCF-7	breast:
3	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
4	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
5	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
6	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
7	chr5:59998145..60001535-chr5:60003151..60006329,3	K562	blood:
8	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
9	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
10	chr5:60231929..60237280-chr5:60239098..60242865,6	MCF-7	breast:
11	chr5:60050521..60052217-chr5:60052630..60054560,2	MCF-7	breast:
12	chr5:60268329..60270384-chr5:60275561..60277405,2	K562	blood:
13	chr5:60274623..60276264-chr5:60290570..60293305,2	K562	blood:
14	chr5:60017651..60020271-chr5:60037416..60040413,2	MCF-7	breast:
15	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
16	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
17	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
18	chr5:60090547..60092252-chr5:60093927..60095567,2	K562	blood:
19	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
20	chr5:60239789..60242454-chr5:60245834..60249187,6	MCF-7	breast:
21	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
22	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:
23	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
24	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
25	chr5:59973507..59975333-chr5:60177921..60180223,2	MCF-7	breast:
26	chr5:60238110..60240722-chr5:60956482..60958434,2	MCF-7	breast:
27	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:
28	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:
29	chr5:60134031..60135823-chr5:60138767..60140768,2	MCF-7	breast:
30	chr5:60050521..60052217-chr5:60052630..60054560,2	MCF-7	breast:
31	chr5:60091814..60093851-chr5:60098024..60100657,2	K562	blood:
32	chr5:59995891..59998683-chr5:60261062..60263658,2	K562	blood:
33	chr1:156698013..156698560-chr5:60240745..60241454,2	Hela-S3	cervix:
34	chr5:59995721..59997582-chr5:60231998..60233519,2	K562	blood:
35	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
36	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
37	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
38	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
39	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
40	chr5:60141307..60144527-chr5:60240837..60243388,3	K562	blood:
41	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
42	chr5:59973247..59973801-chr5:60224508..60225118,3	K562	blood:
43	chr5:60117200..60119232-chr5:60122303..60124424,2	K562	blood:
44	chr5:60062138..60063887-chr5:60122646..60125586,2	K562	blood:
45	chr5:60082437..60084997-chr5:60089364..60092082,2	MCF-7	breast:
46	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
47	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
48	chr5:60104371..60107157-chr5:60107584..60109673,3	MCF-7	breast:
49	chr5:60138882..60141126-chr5:60148557..60150953,2	MCF-7	breast:
50	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1
2	lnc-ERCC8-1	chr5:60162284-60162762	ENSG00000272308.1
3	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655
4	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1
5	lnc-NDUFAF2-1	chr5:60215204-60215400	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
NDUFAF2	TF binding region
KRT8P31	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
KRT8P31	CpG island
ELOVL7	CpG island
ENSG00000272308	CpG island
ERCC8	CpG island
GNL3LP1	CpG island
ENSG00000233847	CpG island
ENSG00000250148	chromatin interactions
ENSG00000112977	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000251279	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000035499	chromatin interactions

Extended variants
information (count: 10332 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:10332 , 50 per page) page: 1 2 3 4 5 6 7 ... 207

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149552591	chr5:60005015-60005016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532235597	chr5:60005199-60005200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189393355	chr5:60005314-60005315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565685014	chr5:60005318-60005319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528063613	chr5:60005331-60005332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376620421	chr5:60005459-60005460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548187244	chr5:60005516-60005517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568397262	chr5:60005547-60005548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537334270	chr5:60005564-60005565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538167134	chr5:60005601-60005602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570508307	chr5:60005606-60005607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370229052	chr5:60005610-60005611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370607553	chr5:60005645-60005646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539931877	chr5:60005668-60005669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76023700	chr5:60005706-60005707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572924660	chr5:60005720-60005721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9686489	chr5:60005736-60005737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs555329472	chr5:60005743-60005744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368050725	chr5:60005753-60005754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs386403911	chr5:60005754-60005755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs386403912	chr5:60005766-60005767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575576583	chr5:60005860-60005861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77659605	chr5:60005865-60005866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7736518	chr5:60005866-60005867	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs564710609	chr5:60005886-60005887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566766133	chr5:60005956-60005957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181679360	chr5:60005997-60005998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77595860	chr5:60005998-60005999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559517703	chr5:60006035-60006036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528178803	chr5:60006039-60006040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548247986	chr5:60006043-60006044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561664576	chr5:60006065-60006066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148471974	chr5:60006074-60006075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143765224	chr5:60006117-60006118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147186498	chr5:60006151-60006152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539231035	chr5:60006163-60006164	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185918042	chr5:60006277-60006278	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566661205	chr5:60006289-60006290	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535548743	chr5:60006302-60006303	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs140554399	chr5:60006325-60006326	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189628436	chr5:60006327-60006328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs6449487	chr5:60006341-60006342	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs10939863	chr5:60006379-60006380	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs558138663	chr5:60006408-60006409	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs144295790	chr5:60006427-60006428	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs372353542	chr5:60006439-60006440	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560658091	chr5:60006458-60006459	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs72755178	chr5:60006482-60006483	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs116191252	chr5:60006531-60006532	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79259071	chr5:60006558-60006559	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Contiguous gene syndrome	19525295	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2937 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60003400-60005800	Weak transcription	Placenta	Placenta
2	chr5:60005800-60006200	Enhancers	Placenta	Placenta
3	chr5:60012000-60012200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:60013000-60013400	Enhancers	NHEK	skin
5	chr5:60013000-60013800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:60013000-60013800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:60013400-60014200	Flanking Active TSS	NHEK	skin
8	chr5:60013400-60014800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:60013400-60014800	Enhancers	HMEC	breast
10	chr5:60013800-60014200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr5:60013800-60014200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:60014200-60014800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:60014200-60015200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:60014200-60015600	Enhancers	NHEK	skin
15	chr5:60014800-60016400	Weak transcription	HMEC	breast
16	chr5:60015600-60016400	Weak transcription	NHEK	skin
17	chr5:60016400-60016600	Enhancers	NHEK	skin
18	chr5:60016400-60016800	Enhancers	HMEC	breast
19	chr5:60018400-60018600	Active TSS	Sigmoid Colon	Sigmoid Colon
20	chr5:60018800-60019000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:60019800-60020000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:60020200-60032800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:60020600-60023000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr5:60023200-60023400	Bivalent Enhancer	Aorta	Aorta
25	chr5:60024800-60025600	ZNF genes & repeats	Fetal Intestine Small	intestine
26	chr5:60025000-60025600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:60025000-60027800	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr5:60025600-60033000	Weak transcription	Fetal Intestine Small	intestine
29	chr5:60025600-60035400	Weak transcription	Fetal Intestine Large	intestine
30	chr5:60031200-60031800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr5:60031400-60031600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr5:60031600-60032400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr5:60031600-60033200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr5:60031600-60033200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr5:60031800-60032800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:60032200-60033000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr5:60032400-60033200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:60032600-60033000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:60032600-60033200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:60032800-60033200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:60032800-60033200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:60032800-60035600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:60033000-60033200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr5:60033000-60033200	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr5:60033200-60034000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr5:60033200-60039200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:60034800-60035800	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr5:60035400-60035600	Strong transcription	Fetal Intestine Large	intestine
49	chr5:60035400-60035600	ZNF genes & repeats	Lung	lung
50	chr5:60035400-60036400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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