Variant report

Variant	esv2761313
Chromosome Location	chr7:26340970-26389772
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:647)
CpG islands
(count:122)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:26387719-26388817	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:26382847-26383769	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:26345271-26345506	HepG2	liver:	n/a	n/a
4	ATF1	chr7:26348750-26349005	K562	blood:	n/a	n/a
5	ATF2	chr7:26354011-26354443	GM12878	blood:	n/a	n/a
6	ATF2	chr7:26354033-26354389	GM12878	blood:	n/a	n/a
7	BACH1	chr7:26342689-26342892	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:26387710-26388012	GM12878	blood:	n/a	n/a
9	BATF	chr7:26368517-26368790	GM12878	blood:	n/a	chr7:26368626-26368637
10	BCL11A	chr7:26387790-26388028	GM12878	blood:	n/a	n/a
11	BCLAF1	chr7:26353927-26354422	GM12878	blood:	n/a	chr7:26354255-26354264
12	BCLAF1	chr7:26375530-26375981	GM12878	blood:	n/a	chr7:26375730-26375739
13	BHLHE40	chr7:26375681-26375915	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:26361025-26361369	K562	blood:	n/a	n/a
15	BHLHE40	chr7:26387774-26388167	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:26348831-26348899	K562	blood:	n/a	n/a
17	BHLHE40	chr7:26369545-26369855	K562	blood:	n/a	n/a
18	BHLHE40	chr7:26386308-26386359	K562	blood:	n/a	n/a
19	BHLHE40	chr7:26346876-26347017	K562	blood:	n/a	n/a
20	BHLHE40	chr7:26386574-26386876	GM12878	blood:	n/a	n/a
21	CEBPB	chr7:26383594-26383776	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:26372420-26372627	HepG2	liver:	n/a	chr7:26372523-26372534
23	CEBPB	chr7:26345103-26345761	HepG2	liver:	n/a	chr7:26345392-26345403
24	CEBPB	chr7:26383475-26383795	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:26345107-26345448	HepG2	liver:	n/a	chr7:26345392-26345403
26	CEBPB	chr7:26351533-26351783	IMR90	lung:	n/a	chr7:26351672-26351681 chr7:26351670-26351683 chr7:26351672-26351683
27	CEBPB	chr7:26351532-26351720	HepG2	liver:	n/a	chr7:26351672-26351681 chr7:26351670-26351683 chr7:26351672-26351683
28	CEBPB	chr7:26382882-26383876	HepG2	liver:	n/a	chr7:26383148-26383159
29	CEBPB	chr7:26345458-26345670	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:26383038-26383242	HepG2	liver:	n/a	chr7:26383148-26383159
31	CEBPB	chr7:26348771-26349058	K562	blood:	n/a	n/a
32	CEBPB	chr7:26351611-26351693	K562	blood:	n/a	chr7:26351672-26351681 chr7:26351670-26351683 chr7:26351672-26351683
33	CEBPB	chr7:26351658-26351688	A549	lung:	n/a	chr7:26351672-26351681 chr7:26351670-26351683 chr7:26351672-26351683
34	CEBPB	chr7:26345112-26345758	HepG2	liver:	n/a	chr7:26345392-26345403
35	CEBPB	chr7:26383134-26383214	K562	blood:	n/a	chr7:26383148-26383159
36	CEBPB	chr7:26382947-26383881	HepG2	liver:	n/a	chr7:26383148-26383159
37	CEBPB	chr7:26348699-26349071	K562	blood:	n/a	n/a
38	CEBPB	chr7:26387861-26388151	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:26345171-26345709	K562	blood:	n/a	chr7:26345392-26345403
40	CEBPB	chr7:26345070-26345698	HepG2	liver:	n/a	chr7:26345392-26345403
41	CEBPB	chr7:26382963-26383374	HepG2	liver:	n/a	chr7:26383148-26383159
42	CEBPD	chr7:26345006-26345443	HepG2	liver:	n/a	chr7:26345270-26345281
43	CEBPD	chr7:26348662-26349100	K562	blood:	n/a	n/a
44	CEBPD	chr7:26345136-26345625	HepG2	liver:	n/a	chr7:26345270-26345281
45	CHD1	chr7:26375753-26376092	GM12878	blood:	n/a	n/a
46	CHD2	chr7:26348743-26348897	K562	blood:	n/a	n/a
47	CHD2	chr7:26375759-26375874	GM12878	blood:	n/a	n/a
48	CHD2	chr7:26387745-26388446	GM12878	blood:	n/a	n/a
49	CTCF	chr7:26387640-26387790	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:26376180-26376330	GM12872	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:26341566-26341616	AG09319	gingival:	n/a
2	chr7:26341566-26341616	HCF	heart:	n/a
3	chr7:26370519-26370569	K562	blood:	n/a
4	chr7:26370519-26370569	HUVEC	blood vessel:	n/a
5	chr7:26370519-26370569	SK-N-SH_RA	brain:	n/a
6	chr7:26341566-26341616	HCM	heart:	n/a
7	chr7:26341566-26341616	HL-60	blood:	n/a
8	chr7:26370519-26370569	NB4	blood:	n/a
9	chr7:26341566-26341616	ovcar-3	ovarian:	n/a
10	chr7:26370519-26370569	ovcar-3	ovarian:	n/a
11	chr7:26370519-26370569	HepG2	liver:	n/a
12	chr7:26341566-26341616	SAEC	small airway:	n/a
13	chr7:26341566-26341616	SK-N-SH_RA	brain:	n/a
14	chr7:26370519-26370569	HCM	heart:	n/a
15	chr7:26341566-26341616	HUVEC	blood vessel:	n/a
16	chr7:26370519-26370569	BJ	skin:	n/a
17	chr7:26370519-26370569	GM06990	blood:	n/a
18	chr7:26370519-26370569	SK-N-SH	brain:	n/a
19	chr7:26341566-26341616	GM12878	blood:	n/a
20	chr7:26370519-26370569	SK-N-MC	brain:	n/a
21	chr7:26341566-26341616	HepG2	liver:	n/a
22	chr7:26341566-26341616	HMEC	breast:	n/a
23	chr7:26370519-26370569	CMK	blood:	n/a
24	chr7:26370519-26370569	HCT-116	colon:	n/a
25	chr7:26370519-26370569	GM12878	blood:	n/a
26	chr7:26370519-26370569	Jurkat	blood:	n/a
27	chr7:26370519-26370569	BE2_C	brain:	n/a
28	chr7:26341566-26341616	HRPEpiC	eye:	n/a
29	chr7:26341566-26341616	RPTEC	kidney:	n/a
30	chr7:26370519-26370569	AG10803	skin:	n/a
31	chr7:26341566-26341616	ProgFib	skin:	n/a
32	chr7:26341566-26341616	ECC-1	luminal epithelium:	n/a
33	chr7:26370519-26370569	NT2-D1	testis:	n/a
34	chr7:26341566-26341616	U87	brain:	n/a
35	chr7:26370519-26370569	HL-60	blood:	n/a
36	chr7:26341566-26341616	HRCEpiC	kidney:	n/a
37	chr7:26341566-26341616	NT2-D1	testis:	n/a
38	chr7:26341566-26341616	NH-A	brain:	n/a
39	chr7:26341566-26341616	BE2_C	brain:	n/a
40	chr7:26370519-26370569	NHDF-neo	bronchial:	n/a
41	chr7:26341566-26341616	AG04450	lung:	fetal
42	chr7:26370519-26370569	H1-hESC	embryonic stem cell:	embryo
43	chr7:26370519-26370569	GM12891	blood:	n/a
44	chr7:26370519-26370569	HNPCEpiC	eye:	n/a
45	chr7:26341566-26341616	H1-hESC	embryonic stem cell:	embryo
46	chr7:26341566-26341616	T-47D	breast:	n/a
47	chr7:26370519-26370569	GM19239	blood:	n/a
48	chr7:26370519-26370569	HIPEpiC	eye:	n/a
49	chr7:26370519-26370569	Hela-S3	cervix:	n/a
50	chr7:26370519-26370569	HCF	heart:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:26340483..26343827-chr7:26348426..26350723,3	K562	blood:
2	chr7:26343995..26346313-chr7:26352554..26355349,2	K562	blood:
3	chr7:26253560..26255433-chr7:26347806..26350350,2	K562	blood:
4	chr7:26237797..26240269-chr7:26356166..26359044,2	MCF-7	breast:
5	chr7:26330311..26333159-chr7:26344268..26346177,2	K562	blood:
6	chr7:26372399..26374092-chr7:26382837..26384720,2	MCF-7	breast:
7	chr7:26240262..26243244-chr7:26384656..26387797,3	MCF-7	breast:
8	chr7:26239461..26241633-chr7:26350906..26352685,2	MCF-7	breast:
9	chr7:26353571..26356318-chr7:26357830..26359410,2	K562	blood:
10	chr7:26332240..26334107-chr7:26341731..26343972,2	MCF-7	breast:
11	chr7:26238829..26241871-chr7:26366847..26369878,3	MCF-7	breast:
12	chr7:26344840..26346808-chr7:26358431..26360772,2	K562	blood:
13	chr7:26239258..26242569-chr7:26344673..26347382,3	K562	blood:
14	chr7:26388712..26391203-chr7:26393919..26396186,2	MCF-7	breast:
15	chr7:26238955..26241719-chr7:26366641..26368444,2	K562	blood:
16	chr7:26375094..26376675-chr7:26376861..26378996,2	K562	blood:
17	chr7:26330233..26332997-chr7:26343202..26346610,3	MCF-7	breast:
18	chr7:26369795..26371338-chr7:26373306..26375843,2	MCF-7	breast:
19	chr7:26343922..26347367-chr7:26351241..26354054,3	K562	blood:
20	chr7:26375094..26376675-chr7:26376861..26378996,2	K562	blood:
21	chr7:26330677..26332957-chr7:26384822..26387116,2	MCF-7	breast:
22	chr7:26337541..26339633-chr7:26341931..26343497,2	MCF-7	breast:
23	chr7:26347459..26349895-chr7:26355478..26358331,2	MCF-7	breast:
24	chr7:26364731..26367327-chr7:26371858..26374794,2	K562	blood:
25	chr7:26339720..26342269-chr7:26343705..26346837,3	MCF-7	breast:
26	chr7:26337033..26341522-chr7:26343910..26346140,5	K562	blood:
27	chr7:26340483..26343827-chr7:26348426..26350723,3	K562	blood:
28	chr7:26339720..26342269-chr7:26343705..26346837,3	MCF-7	breast:
29	chr7:26238981..26240863-chr7:26385040..26387955,2	MCF-7	breast:
30	chr7:26343995..26346313-chr7:26352554..26355349,2	K562	blood:
31	chr7:26239072..26241329-chr7:26379066..26381218,2	MCF-7	breast:
32	chr7:26340732..26342659-chr7:26342750..26344382,2	MCF-7	breast:
33	chr7:26366431..26368895-chr7:26373379..26376096,2	K562	blood:
34	chr7:26386222..26388194-chr7:26390840..26392963,3	MCF-7	breast:
35	chr7:26343922..26347367-chr7:26351241..26354054,3	K562	blood:
36	chr7:26340732..26342659-chr7:26342750..26344382,2	MCF-7	breast:
37	chr7:25933522..25935904-chr7:26366723..26369511,2	K562	blood:
38	chr7:26337033..26341522-chr7:26343910..26346140,5	K562	blood:
39	chr7:26389446..26391389-chr7:26400125..26402977,3	K562	blood:
40	chr7:26330256..26333180-chr7:26342684..26345768,4	K562	blood:
41	chr7:26344840..26346808-chr7:26358431..26360772,2	K562	blood:
42	chr7:26382800..26384799-chr7:26387254..26389366,2	K562	blood:
43	chr7:26384575..26386800-chr7:26402613..26404629,2	MCF-7	breast:
44	chr7:26341541..26343807-chr7:26346274..26348081,2	K562	blood:
45	chr7:26225325..26227141-chr7:26354018..26356821,2	K562	blood:
46	chr7:26335516..26340174-chr7:26340453..26343647,5	K562	blood:
47	chr7:26348261..26349909-chr7:26403707..26405412,2	MCF-7	breast:
48	chr7:26366431..26368895-chr7:26373379..26376096,2	K562	blood:
49	chr7:26364731..26367327-chr7:26371858..26374794,2	K562	blood:
50	chr7:26335544..26340174-chr7:26340481..26343647,5	K562	blood:

No data

Variant related genes	Relation type
SNX10	TF binding region
SNX10	CpG island
ENSG00000122566	chromatin interactions
ENSG00000086300	chromatin interactions
ENSG00000122565	chromatin interactions

Extended variants
information (count: 1874 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1874 , 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	rs17153429	chr7:26340970-26340971	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182827459	chr7:26340985-26340986	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11525780	chr7:26341007-26341008	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs35934277	chr7:26341039-26341040	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs79391342	chr7:26341091-26341092	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527977529	chr7:26341240-26341241	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561808536	chr7:26341271-26341272	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547856339	chr7:26341290-26341291	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561268874	chr7:26341291-26341292	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530315791	chr7:26341356-26341357	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189214479	chr7:26341366-26341367	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75898209	chr7:26341370-26341371	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144536908	chr7:26341390-26341391	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538863432	chr7:26341396-26341397	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547220364	chr7:26341441-26341442	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75119606	chr7:26341546-26341547	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146634703	chr7:26341553-26341554	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534607366	chr7:26341567-26341568	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76776135	chr7:26341607-26341608	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538981934	chr7:26341611-26341612	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs80100657	chr7:26341643-26341644	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144784233	chr7:26341656-26341657	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536621779	chr7:26341658-26341659	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372187522	chr7:26341699-26341700	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557047175	chr7:26341738-26341739	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557828356	chr7:26341742-26341743	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576848562	chr7:26341766-26341767	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs115551448	chr7:26341776-26341777	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552859556	chr7:26341825-26341826	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567815876	chr7:26341841-26341842	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs142274851	chr7:26341884-26341885	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541764077	chr7:26342005-26342006	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561539704	chr7:26342090-26342091	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35323038	chr7:26342092-26342093	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs202216699	chr7:26342095-26342096	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs10271777	chr7:26342125-26342126	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs193092649	chr7:26342126-26342127	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184488275	chr7:26342157-26342158	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs10271591	chr7:26342161-26342162	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs187450693	chr7:26342162-26342163	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150729859	chr7:26342192-26342193	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs118105146	chr7:26342209-26342210	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528235583	chr7:26342226-26342227	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569996379	chr7:26342245-26342246	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548099705	chr7:26342265-26342266	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567992583	chr7:26342278-26342279	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191829105	chr7:26342300-26342301	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs6970564	chr7:26342359-26342360	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs372170540	chr7:26342378-26342379	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs570570030	chr7:26342459-26342460	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Breast cancer	18852474	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26332400-26347000	Weak transcription	HMEC	breast
2	chr7:26332600-26347400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:26332600-26347400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr7:26332800-26342000	Weak transcription	Fetal Intestine Small	intestine
5	chr7:26332800-26343000	Weak transcription	Spleen	Spleen
6	chr7:26332800-26346200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:26332800-26346400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr7:26332800-26346600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr7:26333400-26344600	Weak transcription	Placenta	Placenta
10	chr7:26333600-26346600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:26333600-26351400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr7:26333800-26346800	Weak transcription	Pancreas	Pancrea
13	chr7:26334000-26341000	Weak transcription	HepG2	liver
14	chr7:26334200-26346200	Weak transcription	K562	blood
15	chr7:26334400-26341000	Weak transcription	Brain Angular Gyrus	brain
16	chr7:26334600-26344800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr7:26334600-26344800	Weak transcription	Thymus	Thymus
18	chr7:26335000-26344600	Weak transcription	Fetal Thymus	thymus
19	chr7:26335000-26344800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr7:26335000-26353000	Weak transcription	GM12878-XiMat	blood
21	chr7:26335200-26342200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr7:26335200-26344800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr7:26335200-26344800	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr7:26335200-26344800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr7:26335200-26386400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr7:26335400-26343200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr7:26338400-26341000	Weak transcription	Liver	Liver
28	chr7:26338600-26343200	Strong transcription	Primary B cells from peripheral blood	blood
29	chr7:26339000-26342400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr7:26339800-26342600	Genic enhancers	Primary monocytes fromperipheralblood	blood
31	chr7:26339800-26343200	Genic enhancers	Primary neutrophils fromperipheralblood	blood
32	chr7:26340000-26342600	Strong transcription	Primary hematopoietic stem cells	blood
33	chr7:26340200-26341400	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr7:26340200-26342600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr7:26340200-26343000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr7:26340600-26342200	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr7:26340600-26342600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:26340600-26343000	Strong transcription	Primary B cells from cord blood	blood
39	chr7:26340800-26341000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:26340800-26342000	Strong transcription	Primary T cells from cord blood	blood
41	chr7:26341000-26341200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr7:26341000-26341200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:26341000-26341400	Enhancers	Brain Angular Gyrus	brain
44	chr7:26341000-26342200	Strong transcription	Liver	Liver
45	chr7:26341000-26342400	Strong transcription	HepG2	liver
46	chr7:26341200-26342000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr7:26341200-26342600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:26341400-26342600	Genic enhancers	Monocytes-CD14+_RO01746	blood
49	chr7:26341800-26343000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:26342000-26342200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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