Variant report

Variant	nsv882766
Chromosome Location	chr5:117893138-118032245
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	BCL3	chr5:118025299-118025601	GM12878	blood:	n/a	n/a
3	BHLHE40	chr5:117934828-117934953	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:117968451-117968509	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr5:117932289-117932583	A549	lung:	n/a	n/a
6	CEBPB	chr5:117980712-117980912	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:117980648-117980924	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:117980697-117980954	MCF-7	breast:	n/a	n/a
9	CEBPB	chr5:117980631-117980944	IMR90	lung:	n/a	n/a
10	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
11	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
12	CEBPB	chr5:118016169-118016299	IMR90	lung:	n/a	n/a
13	CEBPB	chr5:118016144-118016302	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:117966977-117967267	Hela-S3	cervix:	n/a	n/a
15	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
16	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
17	CEBPB	chr5:118001014-118001180	K562	blood:	n/a	n/a
18	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
19	CEBPB	chr5:117980695-117980854	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr5:118029480-118029746	HepG2	liver:	n/a	chr5:118029594-118029605 chr5:118029594-118029607 chr5:118029595-118029606 chr5:118029594-118029605
21	CEBPB	chr5:117932234-117932584	HepG2	liver:	n/a	n/a
22	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
23	CEBPB	chr5:117893153-117893464	HepG2	liver:	n/a	chr5:117893294-117893305
24	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
25	CTCF	chr5:117947160-117947310	GM12875	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
26	CTCF	chr5:117947145-117947313	A549	lung:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
27	CTCF	chr5:117947160-117947310	GM12867	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
28	CTCF	chr5:117947120-117947270	HRE	kidney:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
29	CTCF	chr5:117928660-117928810	NHLF	lung:	n/a	n/a
30	CTCF	chr5:117947180-117947330	GM12801	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
31	CTCF	chr5:117928800-117928950	NHDF-neo	bronchial:	n/a	chr5:117928819-117928828
32	CTCF	chr5:118028820-118028970	HEK293	kidney:	n/a	n/a
33	CTCF	chr5:117947180-117947330	AG04450	lung:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
34	CTCF	chr5:117947135-117947345	Hela-S3	cervix:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
35	CTCF	chr5:117947180-117947330	RPTEC	kidney:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
36	CTCF	chr5:117947119-117947325	GM12892	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
37	CTCF	chr5:117947180-117947330	WERI-Rb-1	eye:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
38	CTCF	chr5:117947160-117947310	HPF	lung:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
39	CTCF	chr5:117928700-117928850	AG10803	skin:	n/a	chr5:117928819-117928828
40	CTCF	chr5:117947120-117947270	GM12872	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
41	CTCF	chr5:117974617-117974710	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:117928840-117928990	BJ	skin:	n/a	n/a
43	CTCF	chr5:117964780-117964930	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr5:117947140-117947290	HPAF	blood vessel:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
45	CTCF	chr5:117942761-117942871	NHEK	skin:	n/a	n/a
46	CTCF	chr5:117947117-117947363	K562	blood:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
47	CTCF	chr5:117964760-117964910	AG09319	gingival:	n/a	n/a
48	CTCF	chr5:117947077-117947310	A549	lung:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
49	CTCF	chr5:117947220-117947370	AoAF	blood vessel:	n/a	chr5:117947230-117947248 chr5:117947225-117947246
50	CTCF	chr5:117953762-117953825	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117964718-117964768	HRPEpiC	eye:	n/a
2	chr5:117964718-117964768	SK-N-SH_RA	brain:	n/a
3	chr5:117964718-117964768	HCT-116	colon:	n/a
4	chr5:117964718-117964768	SK-N-MC	brain:	n/a
5	chr5:117964718-117964768	AG09319	gingival:	n/a
6	chr5:117964718-117964768	HIPEpiC	eye:	n/a
7	chr5:117964718-117964768	SAEC	small airway:	n/a
8	chr5:117964718-117964768	A549	lung:	n/a
9	chr5:117964718-117964768	RPTEC	kidney:	n/a
10	chr5:117964718-117964768	AG04449	skin:	fetal
11	chr5:117964718-117964768	BJ	skin:	n/a
12	chr5:117964718-117964768	GM12891	blood:	n/a
13	chr5:117964718-117964768	T-47D	breast:	n/a
14	chr5:117964718-117964768	AG10803	skin:	n/a
15	chr5:117964718-117964768	Hela-S3	cervix:	n/a
16	chr5:117964718-117964768	U87	brain:	n/a
17	chr5:117964718-117964768	HRE	kidney:	n/a
18	chr5:117964718-117964768	SKMC	muscle:	n/a
19	chr5:117964718-117964768	SK-N-SH	brain:	n/a
20	chr5:117964718-117964768	Hepatocyte	liver:	n/a
21	chr5:117964718-117964768	ECC-1	luminal epithelium:	n/a
22	chr5:117964718-117964768	H1-hESC	embryonic stem cell:	embryo
23	chr5:117964718-117964768	NHDF-neo	bronchial:	n/a
24	chr5:117964718-117964768	GM12892	blood:	n/a
25	chr5:117964718-117964768	HUVEC	blood vessel:	n/a
26	chr5:117964718-117964768	AG04450	lung:	fetal
27	chr5:117964718-117964768	GM19239	blood:	n/a
28	chr5:117964718-117964768	PANC-1	pancreas:	n/a
29	chr5:117964718-117964768	HNPCEpiC	eye:	n/a
30	chr5:117964718-117964768	HCF	heart:	n/a
31	chr5:117964718-117964768	HEK293	kidney:	embryo
32	chr5:117964718-117964768	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:117964718-117964768	Jurkat	blood:	n/a
34	chr5:117964718-117964768	HEEpiC	esophagus:	n/a
35	chr5:117964718-117964768	LNCaP	prostate:	n/a
36	chr5:117964718-117964768	AoSMC	blood vessel:	n/a
37	chr5:117964718-117964768	PFSK-1	brain:	n/a
38	chr5:117964718-117964768	AG09309	skin:	n/a
39	chr5:117964718-117964768	HRCEpiC	kidney:	n/a
40	chr5:117964718-117964768	MCF10A-Er-Src	breast:	n/a
41	chr5:117964718-117964768	NT2-D1	testis:	n/a
42	chr5:117964718-117964768	HMEC	breast:	n/a
43	chr5:117964718-117964768	HAEpiC	amniotic membrane:	n/a
44	chr5:117964718-117964768	HL-60	blood:	n/a
45	chr5:117964718-117964768	GM12878	blood:	n/a
46	chr5:117964718-117964768	CMK	blood:	n/a
47	chr5:117964718-117964768	IMR90	lung:	fetal
48	chr5:117964718-117964768	Caco-2	colon:	n/a
49	chr5:117964718-117964768	NHBE	bronchial:	n/a
50	chr5:117964718-117964768	PrEC	prostate:	n/a

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

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

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
ENSG00000249128	chromatin interactions
ENSG00000196542	chromatin interactions
DICER1	miRNA target sites
DIABLO	miRNA target sites
MATR3	miRNA target sites
MARS2	miRNA target sites
DHX57	miRNA target sites
MARK2	miRNA target sites
KRAS	miRNA target sites
MAT2A	miRNA target sites
SFRS2	miRNA target sites

Extended variants
information (count: 4023 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4023 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7737007	chr5:117893138-117893139	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568711867	chr5:117893148-117893149	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs183064959	chr5:117893162-117893163	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs547216723	chr5:117893163-117893164	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs550408096	chr5:117893177-117893178	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs570399831	chr5:117893208-117893209	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs554886116	chr5:117893212-117893213	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs539076064	chr5:117893216-117893217	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs552965492	chr5:117893230-117893231	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs374748297	chr5:117893239-117893240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs535405430	chr5:117893265-117893266	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs555130855	chr5:117893268-117893269	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs7737327	chr5:117893338-117893339	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs543850373	chr5:117893351-117893352	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs188952930	chr5:117893360-117893361	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs193084907	chr5:117893382-117893383	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs138199754	chr5:117893400-117893401	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs114330010	chr5:117893408-117893409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149571657	chr5:117893409-117893410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554588172	chr5:117893412-117893413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144229712	chr5:117893490-117893491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371786536	chr5:117893501-117893502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550615206	chr5:117893548-117893549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141260841	chr5:117893556-117893557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140206584	chr5:117893601-117893602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142250921	chr5:117893633-117893634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185305520	chr5:117893646-117893647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61663324	chr5:117893682-117893683	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs555243481	chr5:117893727-117893728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7737856	chr5:117893795-117893796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs537630312	chr5:117893825-117893826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375138415	chr5:117893832-117893833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146382805	chr5:117893905-117893906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7737893	chr5:117893919-117893920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs13168827	chr5:117893945-117893946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188174090	chr5:117893983-117893984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553362886	chr5:117893992-117893993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7704356	chr5:117894016-117894017	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs144375115	chr5:117894068-117894069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562383704	chr5:117894120-117894121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191679030	chr5:117894159-117894160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372787597	chr5:117894233-117894234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564748783	chr5:117894248-117894249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554440745	chr5:117894294-117894295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184228839	chr5:117894336-117894337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546296256	chr5:117894345-117894346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76311044	chr5:117894352-117894353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572694035	chr5:117894358-117894359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116081234	chr5:117894364-117894365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188107442	chr5:117894394-117894395	Enhancers Weak transcription	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:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117885200-117894200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr5:117889600-117894600	Weak transcription	Right Atrium	heart
3	chr5:117890200-117894400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:117890600-117893200	Weak transcription	Osteobl	bone
5	chr5:117890600-117893400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr5:117890800-117894200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr5:117891800-117894200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr5:117891800-117895000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:117892000-117894400	Enhancers	Fetal Lung	lung
10	chr5:117892600-117893600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr5:117892600-117894000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr5:117892600-117894600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:117892600-117894800	Weak transcription	Fetal Heart	heart
14	chr5:117892600-117895200	Enhancers	HMEC	breast
15	chr5:117892600-117896000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:117892800-117893200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:117892800-117893200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:117892800-117893200	Enhancers	Left Ventricle	heart
19	chr5:117892800-117893800	Enhancers	Fetal Muscle Leg	muscle
20	chr5:117892800-117894600	Enhancers	NHLF	lung
21	chr5:117892800-117895200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:117893000-117893400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:117893000-117893800	Enhancers	Placenta	Placenta
24	chr5:117893000-117895200	Enhancers	NHDF-Ad	bronchial
25	chr5:117893200-117893400	Enhancers	Osteobl	bone
26	chr5:117893200-117894600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:117893200-117895600	Weak transcription	Left Ventricle	heart
28	chr5:117893400-117893600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr5:117893400-117893800	Weak transcription	Osteobl	bone
30	chr5:117893400-117894000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:117893600-117894000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr5:117893600-117895000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr5:117893800-117894600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:117893800-117894600	Enhancers	Osteobl	bone
35	chr5:117894000-117894200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr5:117894000-117895000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr5:117894200-117894400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr5:117894200-117894600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr5:117894200-117894600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:117894400-117895000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr5:117894400-117895800	Weak transcription	Fetal Lung	lung
42	chr5:117894600-117895600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:117894600-117897800	Active TSS	Right Atrium	heart
44	chr5:117894800-117896800	Enhancers	Fetal Heart	heart
45	chr5:117895000-117896400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr5:117895200-117901200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:117895400-117895800	Enhancers	Brain Germinal Matrix	brain
48	chr5:117895600-117895800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr5:117895600-117896200	Active TSS	Left Ventricle	heart
50	chr5:117895600-117896400	Enhancers	Ovary	ovary

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