Variant report

Variant	nsv1027667
Chromosome Location	chr5:117891559-118036578
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	BATF	chr5:117966281-117966527	GM12878	blood:	n/a	chr5:117966409-117966419 chr5:117966408-117966419
2	BATF	chr5:118034787-118034986	GM12878	blood:	n/a	chr5:118034906-118034917
3	BCL3	chr5:118025299-118025601	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:118036382-118036558	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:117934828-117934953	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:117968451-117968509	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:118016144-118016302	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:117966977-117967267	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:117898306-117898626	HepG2	liver:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
10	CEBPB	chr5:118029480-118029746	HepG2	liver:	n/a	chr5:118029594-118029605 chr5:118029594-118029607 chr5:118029595-118029606 chr5:118029594-118029605
11	CEBPB	chr5:117898345-117898611	Hela-S3	cervix:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
12	CEBPB	chr5:117980631-117980944	IMR90	lung:	n/a	n/a
13	CEBPB	chr5:117893153-117893464	HepG2	liver:	n/a	chr5:117893294-117893305
14	CEBPB	chr5:117932289-117932583	A549	lung:	n/a	n/a
15	CEBPB	chr5:118001014-118001180	K562	blood:	n/a	n/a
16	CEBPB	chr5:117980695-117980854	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:117980697-117980954	MCF-7	breast:	n/a	n/a
18	CEBPB	chr5:117932234-117932584	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:117898360-117898614	MCF-7	breast:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
20	CEBPB	chr5:117980648-117980924	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:117898380-117898661	K562	blood:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
22	CEBPB	chr5:117898314-117898635	A549	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
23	CEBPB	chr5:117898330-117898641	IMR90	lung:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
24	CEBPB	chr5:117980712-117980912	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:118016169-118016299	IMR90	lung:	n/a	n/a
26	CEBPB	chr5:117898339-117898607	H1-hESC	embryonic stem cell:	n/a	chr5:117898390-117898403 chr5:117898387-117898404 chr5:117898482-117898495 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493 chr5:117898484-117898493
27	CHD2	chr5:118034533-118034719	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr5:117947140-117947290	HAc	cerebellar:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
29	CTCF	chr5:117947180-117947330	BE2_C	brain:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
30	CTCF	chr5:118034480-118034630	GM12873	blood:	n/a	n/a
31	CTCF	chr5:117946879-117947449	SK-N-SH	brain:	n/a	chr5:117947026-117947047 chr5:117947230-117947248 chr5:117947031-117947049 chr5:117947225-117947246
32	CTCF	chr5:118028853-118029069	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:118034540-118034690	GM12878	blood:	n/a	chr5:118034643-118034664 chr5:118034641-118034659
34	CTCF	chr5:118034640-118034790	WERI-Rb-1	eye:	n/a	chr5:118034643-118034664 chr5:118034641-118034659
35	CTCF	chr5:117947200-117947350	GM12870	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
36	CTCF	chr5:118034540-118034690	GM06990	blood:	n/a	chr5:118034643-118034664 chr5:118034641-118034659
37	CTCF	chr5:117947145-117947313	A549	lung:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
38	CTCF	chr5:117928720-117928870	Caco-2	colon:	n/a	chr5:117928819-117928828
39	CTCF	chr5:117928500-117928650	RPTEC	kidney:	n/a	n/a
40	CTCF	chr5:118034550-118034722	LNCaP	prostate:	n/a	chr5:118034643-118034664 chr5:118034641-118034659
41	CTCF	chr5:117947180-117947330	HepG2	liver:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
42	CTCF	chr5:117947108-117947365	ProgFib	skin:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
43	CTCF	chr5:117947117-117947363	K562	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
44	CTCF	chr5:117947160-117947310	HFF-Myc	foreskin:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
45	CTCF	chr5:117947200-117947350	AG04450	lung:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
46	CTCF	chr5:117928800-117928950	HMF	breast:	n/a	chr5:117928819-117928828
47	CTCF	chr5:117947143-117947349	GM13977	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
48	CTCF	chr5:117947135-117947345	Hela-S3	cervix:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
49	CTCF	chr5:117947160-117947310	WERI-Rb-1	eye:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
50	CTCF	chr5:117974657-117974669	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117964718-117964768	AG04450	lung:	fetal
2	chr5:117964718-117964768	RPTEC	kidney:	n/a
3	chr5:117964718-117964768	HMEC	breast:	n/a
4	chr5:117964718-117964768	CMK	blood:	n/a
5	chr5:117964718-117964768	Caco-2	colon:	n/a
6	chr5:117964718-117964768	HepG2	liver:	n/a
7	chr5:117964718-117964768	BJ	skin:	n/a
8	chr5:117964718-117964768	NT2-D1	testis:	n/a
9	chr5:117964718-117964768	PANC-1	pancreas:	n/a
10	chr5:117964718-117964768	NB4	blood:	n/a
11	chr5:117964718-117964768	Hepatocyte	liver:	n/a
12	chr5:117964718-117964768	U87	brain:	n/a
13	chr5:117964718-117964768	PFSK-1	brain:	n/a
14	chr5:117964718-117964768	H1-hESC	embryonic stem cell:	embryo
15	chr5:117964718-117964768	T-47D	breast:	n/a
16	chr5:117964718-117964768	NH-A	brain:	n/a
17	chr5:117964718-117964768	NHDF-neo	bronchial:	n/a
18	chr5:117964718-117964768	AG09309	skin:	n/a
19	chr5:117964718-117964768	GM12878	blood:	n/a
20	chr5:117964718-117964768	ECC-1	luminal epithelium:	n/a
21	chr5:117964718-117964768	GM12892	blood:	n/a
22	chr5:117964718-117964768	HNPCEpiC	eye:	n/a
23	chr5:117964718-117964768	AG10803	skin:	n/a
24	chr5:117964718-117964768	HIPEpiC	eye:	n/a
25	chr5:117964718-117964768	LNCaP	prostate:	n/a
26	chr5:117964718-117964768	SK-N-MC	brain:	n/a
27	chr5:117964718-117964768	SAEC	small airway:	n/a
28	chr5:117964718-117964768	SK-N-SH	brain:	n/a
29	chr5:117964718-117964768	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:117964718-117964768	AoSMC	blood vessel:	n/a
31	chr5:117964718-117964768	HRE	kidney:	n/a
32	chr5:117964718-117964768	HCM	heart:	n/a
33	chr5:117964718-117964768	HCT-116	colon:	n/a
34	chr5:117964718-117964768	HL-60	blood:	n/a
35	chr5:117964718-117964768	AG04449	skin:	fetal
36	chr5:117964718-117964768	IMR90	lung:	fetal
37	chr5:117964718-117964768	A549	lung:	n/a
38	chr5:117964718-117964768	AG09319	gingival:	n/a
39	chr5:117964718-117964768	HAEpiC	amniotic membrane:	n/a
40	chr5:117964718-117964768	HEEpiC	esophagus:	n/a
41	chr5:117964718-117964768	HCPEpiC	choroid plexus:	n/a
42	chr5:117964718-117964768	PrEC	prostate:	n/a
43	chr5:117964718-117964768	MCF-7	breast:	n/a
44	chr5:117964718-117964768	ProgFib	skin:	n/a
45	chr5:117964718-117964768	Hela-S3	cervix:	n/a
46	chr5:117964718-117964768	SK-N-SH_RA	brain:	n/a
47	chr5:117964718-117964768	HEK293	kidney:	embryo
48	chr5:117964718-117964768	BE2_C	brain:	n/a
49	chr5:117964718-117964768	GM06990	blood:	n/a
50	chr5:117964718-117964768	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:118034213..118035082-chr5:118292213..118292973,2	MCF-7	breast:
2	chr5:117997413..117999188-chr5:118002983..118004523,2	MCF-7	breast:
3	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
4	chr5:117946766..117947670-chr5:118127610..118128249,2	MCF-7	breast:
5	chr5:117930634..117932935-chr5:117933519..117935108,2	MCF-7	breast:
6	chr5:118034173..118035130-chr5:118126969..118128409,6	MCF-7	breast:
7	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
8	chr5:117953386..117954146-chr5:118127518..118128022,2	MCF-7	breast:
9	chr5:118030545..118033202-chr5:118033219..118034778,2	MCF-7	breast:
10	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
11	chr5:117893334..117895634-chr5:117899247..117902608,3	K562	blood:
12	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:
13	chr5:117947053..117948753-chr5:118127871..118130563,2	MCF-7	breast:
14	chr5:117911515..117913042-chr5:117914826..117917481,2	MCF-7	breast:
15	chr5:118030545..118033202-chr5:118033219..118034778,2	MCF-7	breast:
16	chr5:117989069..117990852-chr5:117992183..117994675,2	K562	blood:
17	chr5:117997413..117999188-chr5:118002983..118004523,2	MCF-7	breast:
18	chr5:117892457..117896152-chr5:117898946..117902524,3	MCF-7	breast:
19	chr5:117887915..117890272-chr5:117891445..117894908,3	MCF-7	breast:
20	chr3:161088409..161090897-chr5:117945115..117947573,2	MCF-7	breast:
21	chr5:117989069..117990852-chr5:117992183..117994675,2	K562	blood:
22	chr5:117923008..117924830-chr5:117927973..117929496,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-1	chr5:117945434-117945572	XLOC_004527
2	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
3	lnc-DMXL1-1	chr5:117931883-117931916	XLOC_004527
4	lnc-DTWD2-10	chr5:117918641-117918733	l_3002_chr5:117837955-117925717_heart
5	lnc-DTWD2-3	chr5:117897616-117897751	XLOC_004965
6	lnc-DMXL1-1	chr5:117949988-117950046	XLOC_004527
7	lnc-DTWD2-3	chr5:117897616-117897812	XLOC_004965
8	lnc-DMXL1-2	chr5:117916227-117916343	XLOC_004526
9	lnc-DTWD2-3	chr5:117897616-117897812	NR_104610
10	lnc-DTWD2-10	chr5:117925515-117925717	l_3002_chr5:117837955-117925717_heart
11	lnc-DMXL1-1	chr5:117947055-117947122	XLOC_004527
12	lnc-DMXL1-2	chr5:117915349-117915489	XLOC_004526
13	lnc-DMXL1-2	chr5:117912735-117912889	XLOC_004526
14	lnc-DMXL1-1	chr5:117963545-117963787	XLOC_004527
15	lnc-DTWD2-3	chr5:117897616-117897812	NONHSAT103396
16	lnc-DTWD2-3	chr5:117897616-117897826	NONHSAT103403
17	lnc-DTWD2-3	chr5:117897616-117897818	XLOC_004965
18	lnc-DMXL1-2	chr5:117911270-117911381	XLOC_004526
19	lnc-DTWD2-10	chr5:117909342-117909743	l_3002_chr5:117837955-117925717_heart
20	lnc-DMXL1-2	chr5:117916964-117917019	XLOC_004526

Variant related genes	Relation type
ENSG00000249551	TF binding region
ENSG00000249128	TF binding region
ENSG00000250891	TF binding region
ENSG00000249551	CpG island
ENSG00000249128	CpG island
ENSG00000250891	CpG island
ENSG00000196542	chromatin interactions
ENSG00000249128	chromatin interactions
DIABLO	miRNA target sites
SFRS2	miRNA target sites
KRAS	miRNA target sites
DICER1	miRNA target sites
MATR3	miRNA target sites
MARS2	miRNA target sites
DHX57	miRNA target sites
MAT2A	miRNA target sites
MARK2	miRNA target sites

Extended variants
information (count: 4099 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4099 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188363504	chr5:117891586-117891587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181816917	chr5:117891598-117891599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200639305	chr5:117891611-117891612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187196085	chr5:117891617-117891618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191834590	chr5:117891668-117891669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545957208	chr5:117891722-117891723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576805599	chr5:117891861-117891862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs10038758	chr5:117891870-117891871	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs10035809	chr5:117891873-117891874	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs183603539	chr5:117891899-117891900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547495255	chr5:117891939-117891940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560900822	chr5:117891961-117891962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1012695	chr5:117891968-117891969	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs199561837	chr5:117891998-117891999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs386691619	chr5:117891999-117892000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1012696	chr5:117892001-117892002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs75344304	chr5:117892054-117892055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs375795182	chr5:117892060-117892061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10068932	chr5:117892072-117892073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560999501	chr5:117892086-117892087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534661543	chr5:117892146-117892147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554729402	chr5:117892152-117892153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543375924	chr5:117892153-117892154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17144199	chr5:117892157-117892158	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1012697	chr5:117892165-117892166	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs186445911	chr5:117892166-117892167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149039602	chr5:117892176-117892177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545821017	chr5:117892188-117892189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143017220	chr5:117892227-117892228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs114194289	chr5:117892241-117892242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17144204	chr5:117892404-117892405	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs528020450	chr5:117892487-117892488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561062093	chr5:117892492-117892493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530166924	chr5:117892501-117892502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550125802	chr5:117892518-117892519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190226907	chr5:117892524-117892525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs151232091	chr5:117892534-117892535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1366983	chr5:117892552-117892553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374181998	chr5:117892553-117892554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182616010	chr5:117892557-117892558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs76668783	chr5:117892564-117892565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561594911	chr5:117892584-117892585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535251291	chr5:117892601-117892602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146997449	chr5:117892645-117892646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs116357330	chr5:117892711-117892712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138123184	chr5:117892712-117892713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538676266	chr5:117892742-117892743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12652828	chr5:117892743-117892744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150435043	chr5:117892766-117892767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539672903	chr5:117892775-117892776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
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
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117885000-117892600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr5:117885200-117894200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:117885800-117892600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr5:117888600-117892000	Weak transcription	Fetal Heart	heart
5	chr5:117889600-117892000	Weak transcription	Fetal Lung	lung
6	chr5:117889600-117892800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:117889600-117892800	Weak transcription	Left Ventricle	heart
8	chr5:117889600-117894600	Weak transcription	Right Atrium	heart
9	chr5:117889800-117892800	Weak transcription	NHLF	lung
10	chr5:117890200-117894400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:117890600-117892600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr5:117890600-117893200	Weak transcription	Osteobl	bone
13	chr5:117890600-117893400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr5:117890800-117892400	Weak transcription	NHDF-Ad	bronchial
15	chr5:117890800-117892600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr5:117890800-117892800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:117890800-117894200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr5:117891000-117892600	Weak transcription	HMEC	breast
19	chr5:117891000-117892800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:117891200-117891800	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr5:117891400-117891800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:117891800-117894200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr5:117891800-117895000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr5:117892000-117892600	Enhancers	Fetal Heart	heart
25	chr5:117892000-117894400	Enhancers	Fetal Lung	lung
26	chr5:117892400-117892600	Enhancers	NHDF-Ad	bronchial
27	chr5:117892600-117893000	Weak transcription	NHDF-Ad	bronchial
28	chr5:117892600-117893600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr5:117892600-117894000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr5:117892600-117894600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:117892600-117894800	Weak transcription	Fetal Heart	heart
32	chr5:117892600-117895200	Enhancers	HMEC	breast
33	chr5:117892600-117896000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr5:117892800-117893000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr5:117892800-117893200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr5:117892800-117893200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:117892800-117893200	Enhancers	Left Ventricle	heart
38	chr5:117892800-117893800	Enhancers	Fetal Muscle Leg	muscle
39	chr5:117892800-117894600	Enhancers	NHLF	lung
40	chr5:117892800-117895200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr5:117893000-117893400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:117893000-117893800	Enhancers	Placenta	Placenta
43	chr5:117893000-117895200	Enhancers	NHDF-Ad	bronchial
44	chr5:117893200-117893400	Enhancers	Osteobl	bone
45	chr5:117893200-117894600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr5:117893200-117895600	Weak transcription	Left Ventricle	heart
47	chr5:117893400-117893600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr5:117893400-117893800	Weak transcription	Osteobl	bone
49	chr5:117893400-117894000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:117893600-117894000	Weak transcription	Muscle Satellite Cultured Cells	--

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