Variant report

Variant	nsv4960
Chromosome Location	chr5:112200199-112218299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:112214510-112214780	K562	blood:	n/a	n/a
2	ATF3	chr5:112214444-112214852	K562	blood:	n/a	n/a
3	BHLHE40	chr5:112214495-112214855	K562	blood:	n/a	n/a
4	CCNT2	chr5:112214489-112214886	K562	blood:	n/a	n/a
5	CEBPB	chr5:112211644-112211870	K562	blood:	n/a	n/a
6	CEBPB	chr5:112211566-112211873	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:112200935-112201156	H1-hESC	embryonic stem cell:	n/a	chr5:112201038-112201049
8	CEBPB	chr5:112206747-112207024	A549	lung:	n/a	n/a
9	CEBPB	chr5:112211579-112211792	A549	lung:	n/a	n/a
10	CEBPB	chr5:112212238-112212339	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr5:112200972-112201113	A549	lung:	n/a	chr5:112201038-112201049
12	CEBPB	chr5:112206707-112207052	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:112206740-112206978	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:112200927-112201186	HepG2	liver:	n/a	chr5:112201038-112201049
15	CEBPB	chr5:112200905-112201196	K562	blood:	n/a	chr5:112201038-112201049
16	CEBPB	chr5:112211562-112211859	IMR90	lung:	n/a	n/a
17	CEBPB	chr5:112211600-112211855	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr5:112200882-112201173	IMR90	lung:	n/a	chr5:112201038-112201049
19	CHD2	chr5:112212153-112212417	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr5:112207480-112207630	GM12866	blood:	n/a	n/a
21	CTCF	chr5:112211132-112211156	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:112211840-112211990	NHEK	skin:	n/a	chr5:112211935-112211944
23	CUX1	chr5:112214643-112215014	K562	blood:	n/a	n/a
24	E2F4	chr5:112211575-112211783	MCF10A-Er-Src	breast:	n/a	n/a
25	ELF1	chr5:112214438-112214790	K562	blood:	n/a	n/a
26	EP300	chr5:112214634-112214736	GM12878	blood:	n/a	chr5:112214637-112214646 chr5:112214638-112214647
27	EP300	chr5:112214433-112214956	K562	blood:	n/a	chr5:112214637-112214646 chr5:112214638-112214647
28	FOS	chr5:112214484-112214831	MCF10A-Er-Src	breast:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
29	FOS	chr5:112214471-112214871	MCF10A-Er-Src	breast:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
30	FOS	chr5:112215503-112215672	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr5:112214425-112214838	MCF10A-Er-Src	breast:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
32	FOS	chr5:112215489-112215642	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:112214493-112214831	MCF10A-Er-Src	breast:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
34	FOS	chr5:112211584-112211811	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:112211680-112211776	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr5:112211591-112211793	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:112214471-112214832	K562	blood:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
38	FOS	chr5:112211596-112211856	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL1	chr5:112214421-112214838	K562	blood:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214636-112214647 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
40	FOSL1	chr5:112214345-112214945	HCT-116	colon:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214636-112214647 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
41	FOSL1	chr5:112214516-112214819	K562	blood:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214636-112214647 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
42	GABPA	chr5:112214445-112214822	K562	blood:	n/a	n/a
43	GATA2	chr5:112214396-112214862	K562	blood:	n/a	n/a
44	HDAC2	chr5:112214404-112214841	K562	blood:	n/a	chr5:112214549-112214563
45	HDAC2	chr5:112214504-112214853	K562	blood:	n/a	chr5:112214549-112214563
46	IRF1	chr5:112214482-112214818	K562	blood:	n/a	chr5:112214792-112214802 chr5:112214637-112214646
47	JUN	chr5:112214453-112215024	K562	blood:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
48	JUN	chr5:112202327-112202543	HepG2	liver:	n/a	chr5:112202405-112202418 chr5:112202406-112202415
49	JUN	chr5:112214471-112214869	K562	blood:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650
50	JUN	chr5:112214415-112214957	K562	blood:	n/a	chr5:112214637-112214647 chr5:112214636-112214648 chr5:112214638-112214646 chr5:112214638-112214645 chr5:112214637-112214646 chr5:112214639-112214650

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112203375-112203425	H1-hESC	embryonic stem cell:	embryo
2	chr5:112203375-112203425	GM19239	blood:	n/a
3	chr5:112203375-112203425	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:112203375-112203425	HEK293	kidney:	embryo
5	chr5:112203375-112203425	HCT-116	colon:	n/a
6	chr5:112203375-112203425	MCF10A-Er-Src	breast:	n/a
7	chr5:112203375-112203425	K562	blood:	n/a
8	chr5:112203375-112203425	AG09319	gingival:	n/a
9	chr5:112203375-112203425	GM12891	blood:	n/a
10	chr5:112203375-112203425	HRCEpiC	kidney:	n/a
11	chr5:112203375-112203425	CMK	blood:	n/a
12	chr5:112203375-112203425	ProgFib	skin:	n/a
13	chr5:112203375-112203425	HAEpiC	amniotic membrane:	n/a
14	chr5:112203375-112203425	MCF-7	breast:	n/a
15	chr5:112203375-112203425	Caco-2	colon:	n/a
16	chr5:112203375-112203425	Hela-S3	cervix:	n/a
17	chr5:112203375-112203425	GM12892	blood:	n/a
18	chr5:112203375-112203425	ovcar-3	ovarian:	n/a
19	chr5:112203375-112203425	PrEC	prostate:	n/a
20	chr5:112203375-112203425	HEEpiC	esophagus:	n/a
21	chr5:112203375-112203425	NB4	blood:	n/a
22	chr5:112203375-112203425	HRPEpiC	eye:	n/a
23	chr5:112203375-112203425	HL-60	blood:	n/a
24	chr5:112203375-112203425	GM06990	blood:	n/a
25	chr5:112203375-112203425	SAEC	small airway:	n/a
26	chr5:112203375-112203425	RPTEC	kidney:	n/a
27	chr5:112203375-112203425	SKMC	muscle:	n/a
28	chr5:112203375-112203425	U87	brain:	n/a
29	chr5:112203375-112203425	SK-N-SH	brain:	n/a
30	chr5:112203375-112203425	HIPEpiC	eye:	n/a
31	chr5:112203375-112203425	IMR90	lung:	fetal
32	chr5:112203375-112203425	HMEC	breast:	n/a
33	chr5:112203375-112203425	BJ	skin:	n/a
34	chr5:112203375-112203425	AG04449	skin:	fetal
35	chr5:112203375-112203425	AG09309	skin:	n/a
36	chr5:112203375-112203425	LNCaP	prostate:	n/a
37	chr5:112203375-112203425	BE2_C	brain:	n/a
38	chr5:112203375-112203425	GM12878	blood:	n/a
39	chr5:112203375-112203425	PANC-1	pancreas:	n/a
40	chr5:112203375-112203425	A549	lung:	n/a
41	chr5:112203375-112203425	PFSK-1	brain:	n/a
42	chr5:112203375-112203425	NH-A	brain:	n/a
43	chr5:112203375-112203425	HCF	heart:	n/a
44	chr5:112203375-112203425	AG10803	skin:	n/a
45	chr5:112203375-112203425	HRE	kidney:	n/a
46	chr5:112203375-112203425	NT2-D1	testis:	n/a
47	chr5:112203375-112203425	SK-N-MC	brain:	n/a
48	chr5:112203375-112203425	AG04450	lung:	fetal
49	chr5:112203375-112203425	HNPCEpiC	eye:	n/a
50	chr5:112203375-112203425	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:112213405..112216248-chr5:112216805..112218995,2	K562	blood:
2	chr5:112213405..112216248-chr5:112216805..112218995,2	K562	blood:
3	chr5:112199637..112202533-chr5:112210303..112212318,2	MCF-7	breast:
4	chr5:112195269..112200241-chr5:112214225..112218967,7	MCF-7	breast:
5	chr5:112214124..112215918-chr5:112256466..112258811,2	MCF-7	breast:
6	chr5:112201095..112203323-chr5:112277431..112279323,2	K562	blood:
7	chr5:112206451..112208757-chr5:112210968..112212741,2	MCF-7	breast:
8	chr5:112194408..112196977-chr5:112198175..112200544,3	MCF-7	breast:
9	chr5:112202124..112203911-chr5:112204966..112207266,2	K562	blood:
10	chr5:112213045..112215334-chr5:112215360..112217961,2	K562	blood:
11	chr5:112195239..112200315-chr5:112255126..112261929,8	MCF-7	breast:
12	chr5:112200659..112202447-chr5:112205231..112207652,2	K562	blood:
13	chr5:112204419..112206839-chr5:112213966..112216300,2	K562	blood:
14	chr5:112197996..112200677-chr5:112212037..112214219,2	K562	blood:
15	chr5:112195408..112199487-chr5:112199566..112202603,4	K562	blood:
16	chr5:112200659..112202447-chr5:112205231..112207652,2	K562	blood:
17	chr5:112210185..112212366-chr5:112214528..112217503,2	K562	blood:
18	chr5:112195906..112198557-chr5:112198644..112200582,4	MCF-7	breast:
19	chr5:112211665..112213695-chr5:112223485..112225532,2	K562	blood:
20	chr5:112214521..112217440-chr5:112219552..112222525,2	MCF-7	breast:
21	chr5:112202124..112203911-chr5:112204966..112207266,2	K562	blood:
22	chr5:112202949..112204762-chr5:112314290..112317071,2	MCF-7	breast:
23	chr5:112210185..112212366-chr5:112214528..112217503,2	K562	blood:
24	chr5:112213045..112215334-chr5:112215360..112217961,2	K562	blood:
25	chr5:112200124..112202418-chr5:112211371..112213575,2	MCF-7	breast:
26	chr5:112204419..112206839-chr5:112213966..112216300,2	K562	blood:
27	chr5:112196333..112202800-chr5:112202907..112207825,7	MCF-7	breast:
28	chr5:112206451..112208757-chr5:112210968..112212741,2	MCF-7	breast:
29	chr5:112203523..112205062-chr5:112311681..112313579,2	K562	blood:
30	chr5:112200900..112202532-chr5:112232608..112235513,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	REEP5	hsa-miR-17-5p	chr5:112214296-112214318

Variant related genes	Relation type
XBP1P1	TF binding region
SRP19	TF binding region
XBP1P1	CpG island
SRP19	CpG island
ENSG00000129625	chromatin interactions
ENSG00000153037	chromatin interactions
ENSG00000272389	chromatin interactions
ENSG00000272869	chromatin interactions
ENSG00000172795	chromatin interactions
ENSG00000249947	chromatin interactions

Extended variants
information (count: 843 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540093237	chr5:112200235-112200236	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs565379044	chr5:112200236-112200237	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs369947658	chr5:112200246-112200247	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs374031980	chr5:112200259-112200260	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs377663477	chr5:112200277-112200278	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs368060006	chr5:112200307-112200308	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs201542559	chr5:112200308-112200309	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs541623905	chr5:112200310-112200311	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs372961557	chr5:112200349-112200350	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs148840201	chr5:112200359-112200360	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559658089	chr5:112200376-112200377	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs144099306	chr5:112200415-112200416	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs147944769	chr5:112200422-112200423	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141132771	chr5:112200425-112200426	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs200209563	chr5:112200428-112200429	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs3193238	chr5:112200429-112200430	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376976330	chr5:112200448-112200449	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370060492	chr5:112200462-112200463	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200681026	chr5:112200467-112200468	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs201810812	chr5:112200477-112200478	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs56159470	chr5:112200478-112200479	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs189981308	chr5:112200482-112200483	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs150798120	chr5:112200486-112200487	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs540913538	chr5:112200512-112200513	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs559475531	chr5:112200537-112200538	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530511250	chr5:112200564-112200565	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141137994	chr5:112200636-112200637	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570537359	chr5:112200641-112200642	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs79363512	chr5:112200660-112200661	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546793344	chr5:112200664-112200665	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs182994585	chr5:112200674-112200675	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs535391593	chr5:112200712-112200713	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs556825456	chr5:112200718-112200719	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs576077421	chr5:112200772-112200773	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs3822652	chr5:112200786-112200787	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs3822653	chr5:112200787-112200788	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546108677	chr5:112200884-112200885	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs541138415	chr5:112200929-112200930	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs147595200	chr5:112200943-112200944	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs17290456	chr5:112200971-112200972	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs149066799	chr5:112200981-112200982	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs143071115	chr5:112200985-112200986	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs187533926	chr5:112200998-112200999	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs148257961	chr5:112201017-112201018	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs141258219	chr5:112201040-112201041	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs2545156	chr5:112201054-112201055	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs528215670	chr5:112201060-112201061	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs495794	chr5:112201094-112201095	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs567951909	chr5:112201142-112201143	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs74593183	chr5:112201153-112201154	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Lung cancer	20668451	CNVD
adenomatous polyposis	20649969	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	22014273	CNVD
Colorectal cancer	23471846	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Sezary syndrome	18413736	CNVD
Cancer	17440070	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:822 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112197800-112211800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:112198000-112205000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:112198200-112200200	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
4	chr5:112198200-112202200	Weak transcription	Fetal Kidney	kidney
5	chr5:112198400-112200200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr5:112198400-112200200	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr5:112198400-112200400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr5:112198400-112200800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr5:112198400-112211200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:112198400-112220600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr5:112198600-112200600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
12	chr5:112198600-112201000	Genic enhancers	Osteobl	bone
13	chr5:112198600-112201200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr5:112198600-112205600	Weak transcription	Fetal Brain Male	brain
15	chr5:112198600-112206600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
16	chr5:112198600-112206800	Strong transcription	H9 Cell Line	embryonic stem cell
17	chr5:112198600-112206800	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr5:112198600-112206800	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr5:112198600-112207000	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr5:112198600-112207000	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr5:112198600-112207400	Strong transcription	Rectal Mucosa Donor 31	rectum
22	chr5:112198600-112208800	Strong transcription	Fetal Thymus	thymus
23	chr5:112198800-112206800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:112198800-112206800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:112198800-112207200	Strong transcription	Fetal Muscle Trunk	muscle
26	chr5:112198800-112208800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr5:112199000-112200200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr5:112199000-112200600	Strong transcription	Thymus	Thymus
29	chr5:112199000-112200800	Strong transcription	Ovary	ovary
30	chr5:112199000-112201200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
31	chr5:112199000-112201200	Strong transcription	Rectal Smooth Muscle	rectum
32	chr5:112199000-112206800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr5:112199000-112207000	Strong transcription	Placenta	Placenta
34	chr5:112199000-112207200	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr5:112199000-112208000	Strong transcription	Primary B cells from peripheral blood	blood
36	chr5:112199000-112226000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:112199200-112201000	Strong transcription	NHDF-Ad	bronchial
38	chr5:112199200-112203400	Weak transcription	Stomach Mucosa	stomach
39	chr5:112199200-112206200	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr5:112199200-112206400	Strong transcription	Monocytes-CD14+_RO01746	blood
41	chr5:112199200-112207200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:112199200-112210200	Weak transcription	Psoas Muscle	Psoas
43	chr5:112199200-112213200	Weak transcription	Fetal Heart	heart
44	chr5:112199200-112213400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:112199400-112200200	Enhancers	Brain Angular Gyrus	brain
46	chr5:112199400-112200200	Weak transcription	Colon Smooth Muscle	Colon
47	chr5:112199400-112200400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr5:112199400-112200600	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr5:112199400-112200600	Strong transcription	HMEC	breast
50	chr5:112199400-112200600	Strong transcription	K562	blood

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