Variant report

Variant	nsv606043
Chromosome Location	chr7:7473563-7571420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:744)
CpG islands
(count:367)
Chromatin interactive
region (count:51)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7557252-7557767	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:7539535-7539872	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:7532230-7532480	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:7478472-7478836	HepG2	liver:	n/a	n/a
5	ATF1	chr7:7491171-7491232	K562	blood:	n/a	n/a
6	ATF3	chr7:7478333-7478974	A549	lung:	n/a	n/a
7	ATF3	chr7:7532156-7532521	A549	lung:	n/a	n/a
8	BATF	chr7:7526033-7526318	GM12878	blood:	n/a	n/a
9	BCL3	chr7:7532070-7532569	A549	lung:	n/a	chr7:7532369-7532378 chr7:7532368-7532377
10	BHLHE40	chr7:7560979-7561131	K562	blood:	n/a	n/a
11	BRCA1	chr7:7532171-7532474	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr7:7478442-7478892	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr7:7478353-7479081	HCT-116	colon:	n/a	n/a
14	CBX3	chr7:7523735-7524001	K562	blood:	n/a	n/a
15	CBX3	chr7:7532102-7532612	HCT-116	colon:	n/a	chr7:7532457-7532468
16	CBX3	chr7:7532097-7532528	HCT-116	colon:	n/a	chr7:7532457-7532468
17	CBX3	chr7:7478342-7479021	HCT-116	colon:	n/a	n/a
18	CBX3	chr7:7523666-7524128	HCT-116	colon:	n/a	n/a
19	CBX3	chr7:7488708-7488988	K562	blood:	n/a	n/a
20	CBX3	chr7:7487828-7488056	K562	blood:	n/a	n/a
21	CBX3	chr7:7523736-7524068	K562	blood:	n/a	n/a
22	CEBPB	chr7:7478329-7479033	A549	lung:	n/a	n/a
23	CEBPB	chr7:7531866-7532502	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:7532075-7532460	A549	lung:	n/a	n/a
25	CEBPB	chr7:7520250-7520589	HepG2	liver:	n/a	chr7:7520412-7520423
26	CEBPB	chr7:7478405-7479121	HCT-116	colon:	n/a	n/a
27	CEBPB	chr7:7536097-7536200	K562	blood:	n/a	chr7:7536140-7536149 chr7:7536140-7536151
28	CEBPB	chr7:7557324-7557777	Hela-S3	cervix:	n/a	chr7:7557601-7557614 chr7:7557517-7557528 chr7:7557519-7557530
29	CEBPB	chr7:7478047-7478248	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:7532197-7532397	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:7531901-7532655	HCT-116	colon:	n/a	n/a
32	CEBPB	chr7:7520268-7520560	A549	lung:	n/a	chr7:7520412-7520423
33	CEBPB	chr7:7539620-7539869	A549	lung:	n/a	n/a
34	CEBPB	chr7:7532020-7532562	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:7557355-7557804	HepG2	liver:	n/a	chr7:7557601-7557614 chr7:7557517-7557528 chr7:7557519-7557530
36	CEBPB	chr7:7515331-7515524	Hela-S3	cervix:	n/a	chr7:7515407-7515424
37	CEBPB	chr7:7539607-7539831	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:7520258-7520579	K562	blood:	n/a	chr7:7520412-7520423
39	CEBPB	chr7:7557443-7557663	A549	lung:	n/a	chr7:7557601-7557614 chr7:7557517-7557528 chr7:7557519-7557530
40	CEBPB	chr7:7520258-7520594	IMR90	lung:	n/a	chr7:7520412-7520423
41	CEBPB	chr7:7478398-7479050	A549	lung:	n/a	n/a
42	CEBPB	chr7:7532058-7532468	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:7532209-7532390	K562	blood:	n/a	n/a
44	CEBPB	chr7:7532103-7532546	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr7:7532128-7532397	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:7532110-7532576	MCF-7	breast:	n/a	n/a
47	CEBPB	chr7:7532109-7532434	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:7532050-7532659	HCT-116	colon:	n/a	n/a
49	CEBPB	chr7:7529182-7529519	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:7478474-7478949	A549	lung:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7557590-7557640	HMEC	breast:	n/a
2	chr7:7557590-7557640	HMEC	breast:	n/a
3	chr7:7530676-7530726	HCM	heart:	n/a
4	chr7:7504884-7504934	HNPCEpiC	eye:	n/a
5	chr7:7504884-7504934	AG09319	gingival:	n/a
6	chr7:7557741-7557791	HRPEpiC	eye:	n/a
7	chr7:7474236-7474286	NB4	blood:	n/a
8	chr7:7478820-7478870	HCF	heart:	n/a
9	chr7:7474236-7474286	K562	blood:	n/a
10	chr7:7474236-7474286	IMR90	lung:	fetal
11	chr7:7504884-7504934	RPTEC	kidney:	n/a
12	chr7:7504884-7504934	ProgFib	skin:	n/a
13	chr7:7557741-7557791	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:7530676-7530726	ovcar-3	ovarian:	n/a
15	chr7:7474236-7474286	T-47D	breast:	n/a
16	chr7:7504884-7504934	HCT-116	colon:	n/a
17	chr7:7557590-7557640	SKMC	muscle:	n/a
18	chr7:7504884-7504934	BJ	skin:	n/a
19	chr7:7557741-7557791	Jurkat	blood:	n/a
20	chr7:7557741-7557791	ProgFib	skin:	n/a
21	chr7:7504884-7504934	PANC-1	pancreas:	n/a
22	chr7:7557741-7557791	Hela-S3	cervix:	n/a
23	chr7:7557741-7557791	NT2-D1	testis:	n/a
24	chr7:7504884-7504934	Caco-2	colon:	n/a
25	chr7:7557741-7557791	AG04449	skin:	fetal
26	chr7:7557590-7557640	AG04450	lung:	fetal
27	chr7:7557590-7557640	NB4	blood:	n/a
28	chr7:7557590-7557640	LNCaP	prostate:	n/a
29	chr7:7557590-7557640	GM12892	blood:	n/a
30	chr7:7478820-7478870	BJ	skin:	n/a
31	chr7:7474236-7474286	AoSMC	blood vessel:	n/a
32	chr7:7557741-7557791	A549	lung:	n/a
33	chr7:7504884-7504934	HRPEpiC	eye:	n/a
34	chr7:7504884-7504934	HCM	heart:	n/a
35	chr7:7557590-7557640	HUVEC	blood vessel:	n/a
36	chr7:7504884-7504934	NH-A	brain:	n/a
37	chr7:7557741-7557791	BJ	skin:	n/a
38	chr7:7504884-7504934	SK-N-SH	brain:	n/a
39	chr7:7557590-7557640	NT2-D1	testis:	n/a
40	chr7:7478820-7478870	HRCEpiC	kidney:	n/a
41	chr7:7530676-7530726	K562	blood:	n/a
42	chr7:7504884-7504934	Jurkat	blood:	n/a
43	chr7:7557590-7557640	HCM	heart:	n/a
44	chr7:7557590-7557640	HCF	heart:	n/a
45	chr7:7530676-7530726	A549	lung:	n/a
46	chr7:7478820-7478870	MCF-7	breast:	n/a
47	chr7:7557590-7557640	SK-N-SH	brain:	n/a
48	chr7:7557741-7557791	CMK	blood:	n/a
49	chr7:7474236-7474286	GM06990	blood:	n/a
50	chr7:7504884-7504934	A549	lung:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:7517874..7521544-chr7:7521578..7525558,4	MCF-7	breast:
2	chr7:7547719..7549678-chr7:7550952..7552917,2	MCF-7	breast:
3	chr7:7565660..7568561-chr7:7568925..7570438,2	MCF-7	breast:
4	chr7:7560179..7562918-chr7:7563350..7565628,2	K562	blood:
5	chr7:7528603..7532505-chr7:7533349..7536188,3	K562	blood:
6	chr7:7486591..7488164-chr7:7496470..7498337,2	K562	blood:
7	chr7:7494613..7496722-chr7:7496760..7498364,2	K562	blood:
8	chr7:7492127..7496167-chr7:7498814..7501004,3	K562	blood:
9	chr7:7530006..7532448-chr7:7539748..7541894,2	MCF-7	breast:
10	chr7:7565685..7567431-chr7:7571979..7573747,2	MCF-7	breast:
11	chr7:7494613..7496722-chr7:7496760..7498364,2	K562	blood:
12	chr7:7536315..7539063-chr7:7547524..7550241,2	MCF-7	breast:
13	chr7:7484454..7487980-chr7:7492862..7495926,3	MCF-7	breast:
14	chr7:7532093..7533691-chr7:7544218..7547045,2	MCF-7	breast:
15	chr7:7531005..7532947-chr7:7534688..7536787,2	K562	blood:
16	chr7:7531005..7532947-chr7:7534688..7536787,2	K562	blood:
17	chr7:7536586..7539525-chr7:7557347..7559308,2	MCF-7	breast:
18	chr7:7528603..7532505-chr7:7533349..7536188,3	K562	blood:
19	chr7:7521873..7525191-chr7:7530979..7533379,3	MCF-7	breast:
20	chr7:7562049..7564854-chr7:7565202..7567272,2	MCF-7	breast:
21	chr7:7521538..7523619-chr7:7523634..7525398,2	MCF-7	breast:
22	chr11:103022096..103022829-chr7:7557065..7557847,2	MCF-7	breast:
23	chr7:7470914..7472671-chr7:7492916..7494632,2	MCF-7	breast:
24	chr7:7492127..7496167-chr7:7498814..7501004,3	K562	blood:
25	chr7:7556776..7558526-chr7:7562736..7564916,2	MCF-7	breast:
26	chr7:7565660..7568561-chr7:7568925..7570438,2	MCF-7	breast:
27	chr1:234735823..234738754-chr7:7542030..7544124,2	MCF-7	breast:
28	chr7:7457858..7459653-chr7:7472855..7475146,2	K562	blood:
29	chr1:17230904..17232961-chr7:7534309..7535829,3	MCF-7	breast:
30	chr1:17231251..17232970-chr7:7534309..7535809,2	MCF-7	breast:
31	chr7:7562049..7564854-chr7:7565202..7567272,2	MCF-7	breast:
32	chr7:7547719..7549678-chr7:7550952..7552917,2	MCF-7	breast:
33	chr7:7484454..7487980-chr7:7492862..7495926,3	MCF-7	breast:
34	chr7:7486546..7488260-chr7:7605611..7607554,2	MCF-7	breast:
35	chr20:52681572..52682154-chr7:7496312..7497133,2	MCF-7	breast:
36	chr7:7521538..7523619-chr7:7523634..7525398,2	MCF-7	breast:
37	chr7:7556776..7558526-chr7:7562736..7564916,2	MCF-7	breast:
38	chr7:7571296..7573446-chr7:7605747..7607706,2	MCF-7	breast:
39	chr7:7530006..7532448-chr7:7539748..7541894,2	MCF-7	breast:
40	chr7:7523488..7525479-chr7:7527617..7529829,2	K562	blood:
41	chr7:7536315..7539063-chr7:7547524..7550241,2	MCF-7	breast:
42	chr7:7486591..7488164-chr7:7496470..7498337,2	K562	blood:
43	chr7:7473373..7475762-chr7:7594753..7597282,2	MCF-7	breast:
44	chr7:7560179..7562918-chr7:7563350..7565628,2	K562	blood:
45	chr7:7551131..7553753-chr7:7566696..7569417,2	MCF-7	breast:
46	chr7:7523488..7525479-chr7:7527617..7529829,2	K562	blood:
47	chr7:7521873..7525191-chr7:7530979..7533379,3	MCF-7	breast:
48	chr7:7517874..7521544-chr7:7521578..7525558,4	MCF-7	breast:
49	chr7:7536586..7539525-chr7:7557347..7559308,2	MCF-7	breast:
50	chr7:7551131..7553753-chr7:7566696..7569417,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPA3-4	chr7:7556936-7557632	l_3359_chr7:7556673-7558351_thyroid
2	lnc-RPA3-4	chr7:7556674-7556934	l_3359_chr7:7556673-7558351_thyroid
3	lnc-RPA3-3	chr7:7561312-7561345	l_3360_chr7:7558465-7570482_kidney
4	lnc-RPA3-4	chr7:7558315-7558351	l_3359_chr7:7556673-7558351_thyroid
5	lnc-RPA3-3	chr7:7570393-7570482	l_3360_chr7:7558465-7570482_kidney
6	lnc-RPA3-3	chr7:7560844-7560899	l_3360_chr7:7558465-7570482_kidney
7	lnc-RPA3-3	chr7:7569370-7569400	l_3360_chr7:7558465-7570482_kidney
8	lnc-RPA3-3	chr7:7558466-7559078	l_3360_chr7:7558465-7570482_kidney

No data

Variant related genes	Relation type
COL28A1	TF binding region
COL28A1	CpG island
ENSG00000272426	chromatin interactions
ENSG00000272894	chromatin interactions
ENSG00000164654	chromatin interactions

Extended variants
information (count: 4317 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4317 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6463692	chr7:7473563-7473564	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564130800	chr7:7473571-7473572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531607238	chr7:7473581-7473582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187415324	chr7:7473590-7473591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77430010	chr7:7473605-7473606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148191524	chr7:7473614-7473615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548689347	chr7:7473621-7473622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190629178	chr7:7473642-7473643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183020429	chr7:7473656-7473657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552707984	chr7:7473662-7473663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555820970	chr7:7473817-7473818	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs573782803	chr7:7473830-7473831	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs185701151	chr7:7473845-7473846	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs541203355	chr7:7473989-7473990	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs538514691	chr7:7474003-7474004	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs141222030	chr7:7474028-7474029	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs113755272	chr7:7474051-7474052	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs533285275	chr7:7474110-7474111	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs375870281	chr7:7474117-7474118	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs535121082	chr7:7474131-7474132	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs553362332	chr7:7474141-7474142	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs147372657	chr7:7474147-7474148	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs578040858	chr7:7474178-7474179	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs190356848	chr7:7474221-7474222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557903388	chr7:7474236-7474237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576194030	chr7:7474237-7474238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182980624	chr7:7474241-7474242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543683459	chr7:7474242-7474243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs187403762	chr7:7474257-7474258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529210628	chr7:7474305-7474306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375311957	chr7:7474306-7474307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs193177574	chr7:7474344-7474345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183646844	chr7:7474378-7474379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570388320	chr7:7474384-7474385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs17167690	chr7:7474432-7474433	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs571001820	chr7:7474439-7474440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531857510	chr7:7474451-7474452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550051845	chr7:7474464-7474465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568375000	chr7:7474561-7474562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535750747	chr7:7474569-7474570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546962199	chr7:7474604-7474605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565556957	chr7:7474607-7474608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539506207	chr7:7474608-7474609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189090223	chr7:7474623-7474624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527444169	chr7:7474668-7474669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549330172	chr7:7474681-7474682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576173836	chr7:7474699-7474700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537200032	chr7:7474701-7474702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555602069	chr7:7474770-7474771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573952856	chr7:7474787-7474788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7455200-7478600	Weak transcription	Pancreas	Pancrea
2	chr7:7464600-7480200	Weak transcription	Aorta	Aorta
3	chr7:7465000-7477800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:7465000-7478600	Weak transcription	Gastric	stomach
5	chr7:7467200-7478800	Weak transcription	Ovary	ovary
6	chr7:7468000-7473800	Weak transcription	Fetal Kidney	kidney
7	chr7:7468400-7484400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr7:7469400-7477600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:7469600-7478800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:7469800-7478400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:7472200-7476200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr7:7472800-7473800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:7472800-7474600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:7472800-7474600	Enhancers	HSMM	muscle
15	chr7:7472800-7475000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:7473200-7474200	Enhancers	HSMMtube	muscle
17	chr7:7473200-7474800	Enhancers	NHDF-Ad	bronchial
18	chr7:7473400-7473600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:7473400-7473600	Enhancers	Fetal Intestine Small	intestine
20	chr7:7473400-7474000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr7:7473400-7474200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:7473400-7474200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr7:7473400-7474400	Enhancers	A549	lung
24	chr7:7473400-7474400	Enhancers	Osteobl	bone
25	chr7:7473400-7474600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr7:7473400-7474600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:7473400-7475000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr7:7473600-7474200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:7473600-7474800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr7:7473600-7475000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:7473800-7474000	Enhancers	Small Intestine	intestine
32	chr7:7473800-7474200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:7473800-7474400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr7:7473800-7474400	Enhancers	Fetal Kidney	kidney
35	chr7:7473800-7474800	Enhancers	Fetal Lung	lung
36	chr7:7474000-7474400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:7474000-7478200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr7:7474200-7474400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:7474200-7474600	Enhancers	Fetal Intestine Large	intestine
40	chr7:7474200-7475200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr7:7474200-7478400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr7:7474200-7478400	Weak transcription	HSMMtube	muscle
43	chr7:7474400-7475400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr7:7474400-7477000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:7474400-7478000	Weak transcription	A549	lung
46	chr7:7474400-7478000	Weak transcription	Osteobl	bone
47	chr7:7474400-7483200	Weak transcription	Fetal Kidney	kidney
48	chr7:7474600-7474800	Enhancers	Fetal Stomach	stomach
49	chr7:7474600-7475000	Weak transcription	HSMM	muscle
50	chr7:7474600-7475400	Weak transcription	Fetal Intestine Large	intestine

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