Variant report

Variant	esv1792421
Chromosome Location	chr7:98737119-98752081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:598)
CpG islands
(count:1040)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:98740390-98740536	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:98740935-98740942	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:98739849-98740049	HepG2	liver:	n/a	n/a
4	ATF2	chr7:98741810-98742219	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:98741758-98742097	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr7:98741715-98742204	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:98741335-98742191	K562	blood:	n/a	n/a
8	BHLHE40	chr7:98740393-98741090	K562	blood:	n/a	n/a
9	BHLHE40	chr7:98741623-98742244	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:98741050-98741216	GM12878	blood:	n/a	n/a
11	BRCA1	chr7:98740938-98741164	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr7:98740958-98741229	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr7:98740373-98741114	K562	blood:	n/a	n/a
14	CCNT2	chr7:98741124-98742122	K562	blood:	n/a	n/a
15	CEBPB	chr7:98740649-98740661	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr7:98741958-98742210	K562	blood:	n/a	n/a
17	CEBPB	chr7:98741017-98741030	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:98737337-98737617	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:98742024-98742247	HepG2	liver:	n/a	n/a
20	CEBPD	chr7:98741618-98742103	HepG2	liver:	n/a	n/a
21	CEBPD	chr7:98741716-98741958	HepG2	liver:	n/a	n/a
22	CHD1	chr7:98741322-98741426	GM12878	blood:	n/a	n/a
23	CHD2	chr7:98740941-98741182	GM12878	blood:	n/a	n/a
24	CHD2	chr7:98740244-98741321	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr7:98741514-98742227	GM12878	blood:	n/a	chr7:98741825-98741835 chr7:98741820-98741830
26	CHD2	chr7:98739893-98742174	Hela-S3	cervix:	n/a	chr7:98741825-98741835 chr7:98741820-98741830
27	CHD2	chr7:98740911-98741450	HepG2	liver:	n/a	n/a
28	CHD2	chr7:98740656-98741680	K562	blood:	n/a	n/a
29	CREB1	chr7:98740370-98742338	HepG2	liver:	n/a	n/a
30	CREB1	chr7:98740469-98741329	A549	lung:	n/a	n/a
31	CREB1	chr7:98741565-98742007	A549	lung:	n/a	n/a
32	CREB1	chr7:98740848-98741444	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:98739700-98739850	HMEC	breast:	n/a	n/a
34	CTCF	chr7:98740700-98740850	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr7:98739760-98739910	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr7:98739757-98739831	MCF-7	breast:	n/a	n/a
37	CTCF	chr7:98741920-98742070	AG09319	gingival:	n/a	n/a
38	CTCF	chr7:98739640-98739790	SAEC	small airway:	n/a	n/a
39	CTCF	chr7:98739600-98739750	HMEC	breast:	n/a	n/a
40	CTCF	chr7:98739900-98740050	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr7:98741880-98742030	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr7:98741930-98742063	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr7:98742080-98742230	RPTEC	kidney:	n/a	n/a
44	CTCF	chr7:98741880-98742030	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr7:98739640-98739790	NHEK	skin:	n/a	n/a
46	CTCF	chr7:98739960-98740110	K562	blood:	n/a	n/a
47	CTCF	chr7:98741900-98742050	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr7:98739749-98739829	Fibrobl	skin:	n/a	n/a
49	CTCF	chr7:98741880-98742030	Caco-2	colon:	n/a	n/a
50	CTCF	chr7:98741920-98742070	AG04449	skin:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:98744600-98744650	T-47D	breast:	n/a
2	chr7:98741983-98742033	IMR90	lung:	fetal
3	chr7:98741587-98741637	SK-N-SH_RA	brain:	n/a
4	chr7:98744600-98744650	T-47D	breast:	n/a
5	chr7:98741983-98742033	IMR90	lung:	fetal
6	chr7:98741587-98741637	SK-N-SH_RA	brain:	n/a
7	chr7:98741946-98741996	Jurkat	blood:	n/a
8	chr7:98739496-98739546	Hepatocyte	liver:	n/a
9	chr7:98741665-98741715	Hela-S3	cervix:	n/a
10	chr7:98740022-98740072	NB4	blood:	n/a
11	chr7:98741983-98742033	U87	brain:	n/a
12	chr7:98739698-98739748	ProgFib	skin:	n/a
13	chr7:98741983-98742033	NB4	blood:	n/a
14	chr7:98741989-98742039	AoSMC	blood vessel:	n/a
15	chr7:98741946-98741996	ProgFib	skin:	n/a
16	chr7:98739627-98739677	HEK293	kidney:	embryo
17	chr7:98739782-98739832	SAEC	small airway:	n/a
18	chr7:98739698-98739748	HEK293	kidney:	embryo
19	chr7:98741989-98742039	ovcar-3	ovarian:	n/a
20	chr7:98740022-98740072	HMEC	breast:	n/a
21	chr7:98741665-98741715	NB4	blood:	n/a
22	chr7:98741946-98741996	HAEpiC	amniotic membrane:	n/a
23	chr7:98741357-98741407	SK-N-SH	brain:	n/a
24	chr7:98742398-98742448	NT2-D1	testis:	n/a
25	chr7:98741989-98742039	PFSK-1	brain:	n/a
26	chr7:98740022-98740072	NHBE	bronchial:	n/a
27	chr7:98741665-98741715	Jurkat	blood:	n/a
28	chr7:98739698-98739748	HRCEpiC	kidney:	n/a
29	chr7:98739782-98739832	T-47D	breast:	n/a
30	chr7:98741636-98741686	HNPCEpiC	eye:	n/a
31	chr7:98741587-98741637	ProgFib	skin:	n/a
32	chr7:98741946-98741996	Hela-S3	cervix:	n/a
33	chr7:98744600-98744650	HRE	kidney:	n/a
34	chr7:98739496-98739546	HCT-116	colon:	n/a
35	chr7:98741989-98742039	NT2-D1	testis:	n/a
36	chr7:98741946-98741996	BJ	skin:	n/a
37	chr7:98741636-98741686	AG04450	lung:	fetal
38	chr7:98739496-98739546	GM19239	blood:	n/a
39	chr7:98740022-98740072	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:98741636-98741686	HMEC	breast:	n/a
41	chr7:98741599-98741649	IMR90	lung:	fetal
42	chr7:98741636-98741686	HEEpiC	esophagus:	n/a
43	chr7:98741989-98742039	ProgFib	skin:	n/a
44	chr7:98741587-98741637	HRCEpiC	kidney:	n/a
45	chr7:98741636-98741686	LNCaP	prostate:	n/a
46	chr7:98739496-98739546	RPTEC	kidney:	n/a
47	chr7:98742099-98742149	GM06990	blood:	n/a
48	chr7:98741665-98741715	BE2_C	brain:	n/a
49	chr7:98741587-98741637	Jurkat	blood:	n/a
50	chr7:98741636-98741686	GM19239	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:98740498..98742801-chr7:98868578..98871943,3	MCF-7	breast:
2	chr7:98725270..98727490-chr7:98735625..98737953,2	K562	blood:
3	chr7:98738148..98740026-chr7:98743359..98745839,2	MCF-7	breast:
4	chr7:98744404..98747208-chr7:98758596..98760579,2	MCF-7	breast:
5	chr1:212032006..212034997-chr7:98739173..98741161,3	MCF-7	breast:
6	chr7:98739038..98741115-chr7:98797135..98798989,2	K562	blood:
7	chr7:98739982..98741583-chr7:99034501..99036509,2	K562	blood:
8	chr7:98741722..98743418-chr7:98744692..98747371,2	MCF-7	breast:
9	chr7:98742101..98744840-chr7:98747144..98750541,3	K562	blood:
10	chr7:98703474..98705646-chr7:98736902..98738750,2	K562	blood:
11	chr7:98744627..98747517-chr7:98820164..98821746,2	MCF-7	breast:
12	chr7:98739979..98741519-chr7:99062135..99063958,2	K562	blood:
13	chr7:98739425..98742547-chr7:98743617..98746560,5	K562	blood:
14	chr7:98685362..98687722-chr7:98738938..98740939,2	K562	blood:
15	chr7:98737351..98739969-chr7:98796808..98799355,2	MCF-7	breast:
16	chr7:98666324..98669111-chr7:98738998..98741505,2	MCF-7	breast:
17	chr7:98739484..98741856-chr7:99035435..99038061,2	K562	blood:
18	chr7:98729782..98731427-chr7:98738611..98740186,2	MCF-7	breast:
19	chr7:98740342..98743513-chr7:98744665..98747630,5	MCF-7	breast:
20	chr7:98738526..98746153-chr7:98804876..98809686,18	MCF-7	breast:
21	chr7:98722011..98724574-chr7:98735793..98737369,2	K562	blood:
22	chr10:126480012..126480539-chr7:98741134..98741832,2	Hela-S3	cervix:
23	chr16:70557729..70558362-chr7:98741012..98741830,2	Hela-S3	cervix:
24	chr7:98740238..98742349-chr7:98859373..98862218,2	MCF-7	breast:
25	chr7:98746993..98748569-chr7:98768043..98771030,2	MCF-7	breast:
26	chr7:98749796..98751324-chr7:98758015..98760030,2	MCF-7	breast:
27	chr7:98738717..98741614-chr7:98773276..98775542,2	K562	blood:
28	chr7:98741100..98743568-chr7:98748333..98750378,3	MCF-7	breast:
29	chr7:98725464..98728251-chr7:98738859..98741076,3	K562	blood:
30	chr7:98738519..98741248-chr7:98774626..98776239,2	MCF-7	breast:
31	chr7:98740149..98740762-chr8:104426797..104427597,2	Hela-S3	cervix:
32	chr7:98742101..98744840-chr7:98747144..98750541,3	K562	blood:
33	chr7:98737541..98740084-chr7:98792661..98794883,2	MCF-7	breast:
34	chr7:98678288..98682057-chr7:98738982..98742511,4	MCF-7	breast:
35	chr7:98725984..98728681-chr7:98745631..98748345,2	MCF-7	breast:
36	chr7:98741779..98743305-chr7:98813050..98816035,2	MCF-7	breast:
37	chr7:98702976..98705646-chr7:98736902..98739331,2	K562	blood:
38	chr7:98739614..98743126-chr7:98922770..98926033,5	MCF-7	breast:
39	chr7:98739456..98741292-chr7:98918688..98921036,2	MCF-7	breast:
40	chr7:26240253..26241081-chr7:98741273..98742046,2	Hela-S3	cervix:
41	chr7:98738148..98740026-chr7:98743359..98745839,2	MCF-7	breast:
42	chr7:98745845..98748521-chr7:98754573..98756801,2	K562	blood:
43	chr7:98738431..98740200-chr7:98866049..98867571,2	MCF-7	breast:
44	chr7:98645170..98647801-chr7:98738848..98740476,2	MCF-7	breast:

No data

Variant related genes	Relation type
SMURF1	TF binding region
SMURF1	CpG island
ENSG00000122566	chromatin interactions
ENSG00000203791	chromatin interactions
ENSG00000164934	chromatin interactions
ENSG00000106246	chromatin interactions
ENSG00000164933	chromatin interactions
ENSG00000241468	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000241685	chromatin interactions
ENSG00000160917	chromatin interactions
ENSG00000198742	chromatin interactions
ENSG00000002079	chromatin interactions
ENSG00000248919	chromatin interactions
ENSG00000258539	chromatin interactions
ENSG00000185467	chromatin interactions

Extended variants
information (count: 526 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572013419	chr7:98737139-98737140	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs376965579	chr7:98737246-98737247	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs542619478	chr7:98737285-98737286	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs560595423	chr7:98737320-98737321	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs531195818	chr7:98737335-98737336	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140781739	chr7:98737399-98737400	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs531858002	chr7:98737432-98737433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532358545	chr7:98737483-98737484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547240170	chr7:98737498-98737499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566172776	chr7:98737642-98737643	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs76866976	chr7:98737659-98737660	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs10241277	chr7:98737685-98737686	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs568674786	chr7:98737709-98737710	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs570275722	chr7:98737723-98737724	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs539640694	chr7:98737781-98737782	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs547719923	chr7:98737789-98737790	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs537427319	chr7:98737829-98737830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200126952	chr7:98737903-98737904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200891452	chr7:98737904-98737905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11421940	chr7:98737905-98737906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186776246	chr7:98738035-98738036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571134072	chr7:98738037-98738038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370184866	chr7:98738055-98738056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377679938	chr7:98738067-98738068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145819795	chr7:98738086-98738087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536104674	chr7:98738097-98738098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11975084	chr7:98738139-98738140	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs56709249	chr7:98738180-98738181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs57919161	chr7:98738252-98738253	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554226809	chr7:98738274-98738275	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs12705027	chr7:98738317-98738318	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs375116669	chr7:98738328-98738329	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs564851607	chr7:98738347-98738348	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs532265341	chr7:98738348-98738349	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs541222748	chr7:98738377-98738378	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567695420	chr7:98738417-98738418	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs57050114	chr7:98738428-98738429	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559329898	chr7:98738474-98738475	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs370859084	chr7:98738484-98738485	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs60083526	chr7:98738497-98738498	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs548735363	chr7:98738532-98738533	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563751824	chr7:98738566-98738567	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138872019	chr7:98738619-98738620	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs552573470	chr7:98738711-98738712	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs28609623	chr7:98738731-98738732	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs142799580	chr7:98738793-98738794	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147439616	chr7:98738933-98738934	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs183109092	chr7:98738998-98738999	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs117439848	chr7:98739016-98739017	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs574105733	chr7:98739142-98739143	Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98707200-98739400	Weak transcription	Thymus	Thymus
2	chr7:98710000-98739200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr7:98714800-98739400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr7:98722000-98739600	Weak transcription	Primary B cells from cord blood	blood
5	chr7:98722200-98738600	Weak transcription	Fetal Intestine Small	intestine
6	chr7:98722400-98739400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:98723600-98738600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:98723800-98738600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:98725000-98739600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:98730800-98738000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr7:98730800-98739400	Weak transcription	Right Ventricle	heart
12	chr7:98730800-98739600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr7:98731000-98739600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:98731400-98738600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr7:98731800-98738400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:98731800-98739400	Weak transcription	Fetal Intestine Large	intestine
17	chr7:98732200-98738200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:98732200-98738400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr7:98732200-98739400	Weak transcription	K562	blood
20	chr7:98732200-98739600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr7:98732800-98738400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr7:98733800-98738600	Weak transcription	Duodenum Mucosa	Duodenum
23	chr7:98733800-98738600	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr7:98733800-98739400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:98734200-98737400	Enhancers	Adipose Nuclei	Adipose
26	chr7:98734200-98738400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:98734400-98737200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:98734400-98738800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:98734600-98738200	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr7:98734600-98739200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr7:98734800-98737200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:98734800-98737200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr7:98735000-98737200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr7:98735000-98737600	Enhancers	HMEC	breast
35	chr7:98735200-98737200	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr7:98735200-98738400	Weak transcription	Small Intestine	intestine
37	chr7:98735200-98738600	Enhancers	Liver	Liver
38	chr7:98735200-98738600	Weak transcription	GM12878-XiMat	blood
39	chr7:98735200-98738600	Enhancers	HepG2	liver
40	chr7:98735200-98739400	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr7:98735200-98739600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:98735200-98739600	Weak transcription	Lung	lung
43	chr7:98735400-98737200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:98735400-98737200	Enhancers	Brain Angular Gyrus	brain
45	chr7:98735400-98737400	Enhancers	NH-A	brain
46	chr7:98735400-98737400	Enhancers	Osteobl	bone
47	chr7:98735400-98738000	Enhancers	Colon Smooth Muscle	Colon
48	chr7:98735400-98738200	Weak transcription	Esophagus	oesophagus
49	chr7:98735400-98738200	Weak transcription	Right Atrium	heart
50	chr7:98735400-98738400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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