Variant report

Variant	nsv1050663
Chromosome Location	chr10:5737979-5785918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:333)
CpG islands
(count:61)
Chromatin interactive
region (count:73)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5738365-5738366	K562	blood:	n/a	n/a
2	ARID3A	chr10:5739648-5740302	K562	blood:	n/a	n/a
3	BACH1	chr10:5746580-5746627	K562	blood:	n/a	n/a
4	BACH1	chr10:5782020-5782104	K562	blood:	n/a	n/a
5	CEBPB	chr10:5739796-5740140	K562	blood:	n/a	chr10:5739960-5739971
6	CEBPB	chr10:5757502-5757812	H1-hESC	embryonic stem cell:	n/a	chr10:5757661-5757672
7	CEBPB	chr10:5757416-5757816	ECC-1	luminal epithelium:	n/a	chr10:5757661-5757672
8	CEBPB	chr10:5739840-5740127	HepG2	liver:	n/a	chr10:5739960-5739971
9	CEBPB	chr10:5757585-5757752	K562	blood:	n/a	chr10:5757661-5757672
10	CEBPB	chr10:5783380-5783475	HepG2	liver:	n/a	chr10:5783438-5783449 chr10:5783435-5783452 chr10:5783440-5783451 chr10:5783440-5783451
11	CEBPB	chr10:5739870-5740070	IMR90	lung:	n/a	chr10:5739960-5739971
12	CEBPB	chr10:5741198-5741547	K562	blood:	n/a	chr10:5741366-5741377
13	CEBPB	chr10:5783305-5783578	K562	blood:	n/a	chr10:5783438-5783449 chr10:5783435-5783452 chr10:5783440-5783451 chr10:5783440-5783451
14	CEBPB	chr10:5757569-5757769	HepG2	liver:	n/a	chr10:5757661-5757672
15	CEBPB	chr10:5741255-5741460	HepG2	liver:	n/a	chr10:5741366-5741377
16	CEBPB	chr10:5741245-5741471	H1-hESC	embryonic stem cell:	n/a	chr10:5741366-5741377
17	CEBPB	chr10:5741239-5741541	IMR90	lung:	n/a	chr10:5741366-5741377
18	CEBPB	chr10:5757615-5757712	A549	lung:	n/a	chr10:5757661-5757672
19	CEBPB	chr10:5741192-5741515	K562	blood:	n/a	chr10:5741366-5741377
20	CEBPB	chr10:5757362-5757825	ECC-1	luminal epithelium:	n/a	chr10:5757661-5757672
21	CEBPB	chr10:5741244-5741494	A549	lung:	n/a	chr10:5741366-5741377
22	CHD1	chr10:5765807-5765932	GM12878	blood:	n/a	n/a
23	CHD1	chr10:5753181-5753222	GM12878	blood:	n/a	n/a
24	CTCF	chr10:5757682-5758216	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:5757873-5758053	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr10:5779497-5779568	GM10266	blood:	n/a	n/a
27	CTCF	chr10:5779480-5779630	HepG2	liver:	n/a	n/a
28	CTCF	chr10:5785831-5785958	MCF-7	breast:	n/a	n/a
29	CTCF	chr10:5757828-5758053	GM19239	blood:	n/a	n/a
30	CTCF	chr10:5757900-5758050	GM12872	blood:	n/a	n/a
31	CTCF	chr10:5757900-5758035	GM12878	blood:	n/a	n/a
32	CTCF	chr10:5779394-5779608	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr10:5779440-5779590	GM12872	blood:	n/a	n/a
34	CTCF	chr10:5779380-5779530	HCT-116	colon:	n/a	n/a
35	CTCF	chr10:5779312-5779727	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr10:5757930-5758014	GM10248	blood:	n/a	n/a
37	CTCF	chr10:5779480-5779630	AG09319	gingival:	n/a	n/a
38	CTCF	chr10:5779469-5779681	K562	blood:	n/a	n/a
39	CTCF	chr10:5757880-5758030	GM12872	blood:	n/a	n/a
40	CTCF	chr10:5779400-5779550	MCF-7	breast:	n/a	n/a
41	CTCF	chr10:5779380-5779530	RPTEC	kidney:	n/a	n/a
42	CTCF	chr10:5747000-5747150	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr10:5757900-5758050	GM12875	blood:	n/a	n/a
44	CTCF	chr10:5779434-5779548	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:5757840-5757990	GM12878	blood:	n/a	n/a
46	CTCF	chr10:5757880-5758030	GM12875	blood:	n/a	n/a
47	CTCF	chr10:5779420-5779570	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr10:5757840-5758009	MCF-7	breast:	n/a	n/a
49	CTCF	chr10:5779480-5779628	GM20000	blood:	n/a	n/a
50	CTCF	chr10:5785869-5785897	GM19239	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5781747-5781797	U87	brain:	n/a
2	chr10:5781747-5781797	HCPEpiC	choroid plexus:	n/a
3	chr10:5781747-5781797	HPAEpiC	pulmonary alveolar:	n/a
4	chr10:5781747-5781797	HL-60	blood:	n/a
5	chr10:5781747-5781797	HRPEpiC	eye:	n/a
6	chr10:5781747-5781797	Hepatocyte	liver:	n/a
7	chr10:5781747-5781797	PANC-1	pancreas:	n/a
8	chr10:5781747-5781797	H1-hESC	embryonic stem cell:	embryo
9	chr10:5781747-5781797	Caco-2	colon:	n/a
10	chr10:5781747-5781797	HCF	heart:	n/a
11	chr10:5781747-5781797	LNCaP	prostate:	n/a
12	chr10:5781747-5781797	Jurkat	blood:	n/a
13	chr10:5781747-5781797	HNPCEpiC	eye:	n/a
14	chr10:5781747-5781797	PrEC	prostate:	n/a
15	chr10:5781747-5781797	AG09319	gingival:	n/a
16	chr10:5781747-5781797	HCM	heart:	n/a
17	chr10:5781747-5781797	CMK	blood:	n/a
18	chr10:5781747-5781797	A549	lung:	n/a
19	chr10:5781747-5781797	SAEC	small airway:	n/a
20	chr10:5781747-5781797	HUVEC	blood vessel:	n/a
21	chr10:5781747-5781797	NHDF-neo	bronchial:	n/a
22	chr10:5781747-5781797	AG10803	skin:	n/a
23	chr10:5781747-5781797	SK-N-SH	brain:	n/a
24	chr10:5781747-5781797	SK-N-MC	brain:	n/a
25	chr10:5781747-5781797	K562	blood:	n/a
26	chr10:5781747-5781797	T-47D	breast:	n/a
27	chr10:5781747-5781797	NT2-D1	testis:	n/a
28	chr10:5781747-5781797	HEEpiC	esophagus:	n/a
29	chr10:5781747-5781797	AG04450	lung:	fetal
30	chr10:5781747-5781797	HMEC	breast:	n/a
31	chr10:5781747-5781797	IMR90	lung:	fetal
32	chr10:5781747-5781797	HCT-116	colon:	n/a
33	chr10:5781747-5781797	GM19239	blood:	n/a
34	chr10:5781747-5781797	GM12892	blood:	n/a
35	chr10:5781747-5781797	GM12891	blood:	n/a
36	chr10:5781747-5781797	PFSK-1	brain:	n/a
37	chr10:5781747-5781797	HAEpiC	amniotic membrane:	n/a
38	chr10:5781747-5781797	MCF10A-Er-Src	breast:	n/a
39	chr10:5781747-5781797	AG09309	skin:	n/a
40	chr10:5781747-5781797	HRCEpiC	kidney:	n/a
41	chr10:5781747-5781797	GM06990	blood:	n/a
42	chr10:5781747-5781797	Hela-S3	cervix:	n/a
43	chr10:5781747-5781797	ProgFib	skin:	n/a
44	chr10:5781747-5781797	HepG2	liver:	n/a
45	chr10:5781747-5781797	MCF-7	breast:	n/a
46	chr10:5781747-5781797	NB4	blood:	n/a
47	chr10:5781747-5781797	SK-N-SH_RA	brain:	n/a
48	chr10:5781747-5781797	HIPEpiC	eye:	n/a
49	chr10:5781747-5781797	NH-A	brain:	n/a
50	chr10:5781747-5781797	NHBE	bronchial:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:5767552..5769962-chr10:5775840..5778685,2	MCF-7	breast:
2	chr10:5766311..5769267-chr10:5770852..5774721,4	K562	blood:
3	chr10:5772075..5775852-chr10:5776811..5780345,4	K562	blood:
4	chr10:5780274..5783194-chr10:5784148..5786108,3	K562	blood:
5	chr10:5487728..5489402-chr10:5743832..5746682,2	MCF-7	breast:
6	chr10:5748194..5752835-chr10:5754048..5756817,4	MCF-7	breast:
7	chr10:5739796..5741781-chr10:5749171..5751664,2	K562	blood:
8	chr10:5732189..5734942-chr10:5774754..5777305,2	K562	blood:
9	chr10:5781025..5783578-chr10:5784148..5786676,3	K562	blood:
10	chr10:5758553..5760843-chr10:5766010..5768055,2	MCF-7	breast:
11	chr10:5758294..5759916-chr10:5768801..5770809,2	K562	blood:
12	chr10:5757345..5759947-chr10:5761882..5764434,2	K562	blood:
13	chr10:5733545..5736331-chr10:5766284..5768389,2	K562	blood:
14	chr10:5781966..5784201-chr10:5791463..5794331,2	K562	blood:
15	chr10:5762001..5764340-chr10:5764704..5766280,2	K562	blood:
16	chr10:5751112..5753798-chr10:5754382..5757716,3	K562	blood:
17	chr10:5760893..5762838-chr10:5855669..5858245,2	K562	blood:
18	chr10:5775152..5778135-chr10:5781961..5783823,3	K562	blood:
19	chr10:5726626..5728206-chr10:5753168..5755087,2	K562	blood:
20	chr10:5707719..5709670-chr10:5755550..5758097,2	MCF-7	breast:
21	chr10:5725933..5727611-chr10:5766306..5768774,2	MCF-7	breast:
22	chr10:5749331..5751583-chr10:5752146..5753784,2	MCF-7	breast:
23	chr10:5748219..5750363-chr10:5854486..5857836,3	K562	blood:
24	chr10:5733731..5736743-chr10:5750015..5755601,4	MCF-7	breast:
25	chr10:5729840..5732495-chr10:5739235..5741106,2	MCF-7	breast:
26	chr10:5727747..5730181-chr10:5782433..5784785,2	K562	blood:
27	chr10:5734698..5736593-chr10:5746537..5749432,2	MCF-7	breast:
28	chr10:5748091..5753661-chr10:5757526..5761076,4	K562	blood:
29	chr10:5706900..5709374-chr10:5740250..5741979,2	MCF-7	breast:
30	chr10:5758553..5760843-chr10:5766010..5768055,2	MCF-7	breast:
31	chr10:5762001..5764340-chr10:5764704..5766280,2	K562	blood:
32	chr10:5735790..5738712-chr10:5931841..5933412,2	MCF-7	breast:
33	chr10:5775152..5778135-chr10:5781961..5783823,3	K562	blood:
34	chr10:5724274..5728540-chr10:5734829..5741563,8	MCF-7	breast:
35	chr10:5749811..5754744-chr10:5757295..5761114,5	MCF-7	breast:
36	chr10:5749331..5751583-chr10:5752146..5753784,2	MCF-7	breast:
37	chr10:5754503..5756653-chr10:5756794..5759759,2	K562	blood:
38	chr10:5771904..5773618-chr10:5783797..5785914,2	K562	blood:
39	chr10:5725557..5727727-chr10:5778800..5780889,3	MCF-7	breast:
40	chr10:5775178..5776755-chr10:5781337..5783023,2	K562	blood:
41	chr10:5727335..5729854-chr10:5777449..5779108,2	K562	blood:
42	chr10:5725582..5728827-chr10:5752793..5758658,6	MCF-7	breast:
43	chr10:5733787..5736575-chr10:5751182..5753712,2	MCF-7	breast:
44	chr10:5730140..5732838-chr10:5762555..5765263,2	MCF-7	breast:
45	chr10:5781284..5783375-chr10:5788559..5791168,2	MCF-7	breast:
46	chr10:5779411..5780958-chr10:5853296..5855552,2	K562	blood:
47	chr10:5766311..5769267-chr10:5770852..5774721,4	K562	blood:
48	chr10:5733360..5736300-chr10:5737628..5741126,5	MCF-7	breast:
49	chr10:5725406..5728715-chr10:5747568..5751515,5	MCF-7	breast:
50	chr10:5782641..5784620-chr10:5787406..5789176,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALML3-1	chr10:5762507-5762574	NONHSAT011175
2	lnc-CALML3-1	chr10:5756098-5756170	NONHSAT011175
3	lnc-GDI2-1	chr10:5754383-5754651	ENSG00000226647.2
4	lnc-FBXO18-4	chr10:5769024-5769086	NONHSAT011181
5	lnc-FBXO18-4	chr10:5772450-5772739	NONHSAT011181
6	lnc-GDI2-1	chr10:5755711-5756386	ENSG00000226647.2
7	lnc-CALML3-1	chr10:5751493-5751626	NONHSAT011176
8	lnc-GDI2-1	chr10:5785810-5786030	ENSG00000226647.1
9	lnc-GDI2-1	chr10:5754177-5754651	ENSG00000226647.1
10	lnc-CALML3-1	chr10:5754357-5754502	NONHSAT011176
11	lnc-CALML3-1	chr10:5741411-5741700	NONHSAT011177
12	lnc-GDI2-1	chr10:5754137-5754651	ENSG00000226647.2
13	lnc-FBXO18-4	chr10:5768789-5768920	NONHSAT011181
14	lnc-CALML3-1	chr10:5751493-5751626	NONHSAT011177
15	lnc-CALML3-1	chr10:5754786-5754835	NONHSAT011176
16	lnc-CALML3-1	chr10:5759622-5759713	NONHSAT011175
17	lnc-GDI2-1	chr10:5785810-5786030	ENSG00000226647.2
18	lnc-CALML3-1	chr10:5754786-5754881	NONHSAT011175

No data

Variant related genes	Relation type
FAM208B	TF binding region
ENSG00000226647	TF binding region
FAM208B	CpG island
ENSG00000226647	CpG island
ENSG00000134452	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000134461	chromatin interactions
ENSG00000226647	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000272764	chromatin interactions

Extended variants
information (count: 1862 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1862 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9423726	chr10:5737979-5737980	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568287838	chr10:5737990-5737991	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs535720702	chr10:5738005-5738006	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs57103262	chr10:5738017-5738018	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs575169443	chr10:5738033-5738034	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs59827083	chr10:5738044-5738045	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs553870117	chr10:5738060-5738061	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs574523184	chr10:5738071-5738072	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs374834521	chr10:5738101-5738102	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs181875676	chr10:5738105-5738106	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs540439871	chr10:5738140-5738141	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs114792216	chr10:5738146-5738147	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs574279269	chr10:5738159-5738160	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs544874410	chr10:5738162-5738163	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs562782306	chr10:5738163-5738164	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs565532316	chr10:5738200-5738201	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs533368919	chr10:5738235-5738236	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs551759406	chr10:5738246-5738247	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs560586183	chr10:5738270-5738271	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs528686323	chr10:5738291-5738292	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs527759590	chr10:5738344-5738345	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs140634705	chr10:5738355-5738356	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs184185852	chr10:5738400-5738401	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs554269267	chr10:5738402-5738403	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs575889542	chr10:5738429-5738430	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs150389717	chr10:5738431-5738432	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs550852122	chr10:5738435-5738436	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs115208850	chr10:5738452-5738453	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs539052441	chr10:5738453-5738454	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs189364038	chr10:5738472-5738473	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs111991596	chr10:5738564-5738565	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs75924593	chr10:5738650-5738651	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs9423946	chr10:5738670-5738671	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376460679	chr10:5738704-5738705	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs72774058	chr10:5738714-5738715	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs576654801	chr10:5738743-5738744	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs181777966	chr10:5738753-5738754	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs369434944	chr10:5738780-5738781	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs185164139	chr10:5738834-5738835	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs202062438	chr10:5738835-5738836	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs12414547	chr10:5738848-5738849	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs559836421	chr10:5738850-5738851	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs560485499	chr10:5738877-5738878	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs372610702	chr10:5738912-5738913	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs530037256	chr10:5738961-5738962	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs570413394	chr10:5739032-5739033	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs7908235	chr10:5739054-5739055	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs543101812	chr10:5739063-5739064	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs143404951	chr10:5739073-5739074	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs190949060	chr10:5739074-5739075	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5728800-5746800	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr10:5734800-5763400	Weak transcription	HSMM	muscle
3	chr10:5735200-5738800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr10:5735200-5739000	Weak transcription	Fetal Intestine Large	intestine
5	chr10:5735200-5739400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr10:5735200-5739400	Weak transcription	Lung	lung
7	chr10:5735200-5739400	Weak transcription	Pancreas	Pancrea
8	chr10:5735200-5739800	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr10:5735200-5743000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:5735200-5749000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr10:5735200-5750600	Weak transcription	Gastric	stomach
12	chr10:5735200-5767000	Weak transcription	Fetal Muscle Leg	muscle
13	chr10:5735400-5738000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:5735400-5738000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr10:5735400-5738200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr10:5735400-5738200	Weak transcription	Right Atrium	heart
17	chr10:5735400-5738400	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr10:5735400-5738600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr10:5735400-5739200	Weak transcription	Fetal Heart	heart
20	chr10:5735400-5739200	Weak transcription	Fetal Intestine Small	intestine
21	chr10:5735400-5739400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr10:5735400-5739400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr10:5735400-5739400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr10:5735400-5739600	Weak transcription	Colonic Mucosa	Colon
25	chr10:5735400-5744800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:5735400-5750800	Weak transcription	Spleen	Spleen
27	chr10:5735400-5761600	Weak transcription	NHEK	skin
28	chr10:5735400-5762000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr10:5735600-5739000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr10:5735800-5739000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr10:5735800-5741800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr10:5735800-5752800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr10:5736000-5739600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr10:5736200-5739200	Weak transcription	Thymus	Thymus
35	chr10:5736200-5739400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr10:5736200-5739600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr10:5736200-5740000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr10:5736200-5740200	Weak transcription	A549	lung
39	chr10:5736200-5742600	Weak transcription	Brain Angular Gyrus	brain
40	chr10:5736200-5751600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr10:5736400-5738200	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr10:5736400-5738200	Weak transcription	Fetal Thymus	thymus
43	chr10:5736400-5738200	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr10:5736400-5739000	Weak transcription	Duodenum Mucosa	Duodenum
45	chr10:5736400-5739200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr10:5736400-5741000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr10:5736400-5753000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:5736600-5738600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr10:5736600-5739000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr10:5736600-5741600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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