Variant report

Variant	esv2763020
Chromosome Location	chr13:50105055-50192259
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	ARID3A	chr13:50161077-50161152	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:50181294-50181522	K562	blood:	n/a	n/a
3	ARID3A	chr13:50161361-50161950	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:50134434-50134784	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:50181305-50181495	HepG2	liver:	n/a	n/a
6	ATF2	chr13:50159392-50159732	GM12878	blood:	n/a	n/a
7	ATF2	chr13:50145690-50146288	GM12878	blood:	n/a	n/a
8	ATF2	chr13:50145626-50146173	GM12878	blood:	n/a	n/a
9	ATF3	chr13:50159404-50159991	GM12878	blood:	n/a	chr13:50159561-50159570 chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159875-50159884 chr13:50159754-50159763
10	ATF3	chr13:50159391-50159975	HepG2	liver:	n/a	chr13:50159561-50159570 chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159875-50159884 chr13:50159754-50159763
11	ATF3	chr13:50159508-50159900	K562	blood:	n/a	chr13:50159561-50159570 chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159875-50159884 chr13:50159754-50159763
12	ATF3	chr13:50159608-50159828	GM12878	blood:	n/a	chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159754-50159763
13	ATF3	chr13:50159435-50159946	H1-hESC	embryonic stem cell:	n/a	chr13:50159561-50159570 chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159875-50159884 chr13:50159754-50159763
14	ATF3	chr13:50159506-50159894	H1-hESC	embryonic stem cell:	n/a	chr13:50159561-50159570 chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159875-50159884 chr13:50159754-50159763
15	ATF3	chr13:50159511-50159888	HepG2	liver:	n/a	chr13:50159561-50159570 chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159875-50159884 chr13:50159754-50159763
16	ATF3	chr13:50159573-50159874	K562	blood:	n/a	chr13:50159736-50159745 chr13:50159706-50159726 chr13:50159725-50159745 chr13:50159736-50159756 chr13:50159754-50159763
17	BACH1	chr13:50181291-50181324	K562	blood:	n/a	n/a
18	BACH1	chr13:50181187-50181550	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr13:50114793-50115029	H1-hESC	embryonic stem cell:	n/a	chr13:50114913-50114927
20	BATF	chr13:50145645-50146016	GM12878	blood:	n/a	n/a
21	BATF	chr13:50146050-50146368	GM12878	blood:	n/a	n/a
22	BATF	chr13:50146077-50146332	GM12878	blood:	n/a	n/a
23	BATF	chr13:50144463-50144729	GM12878	blood:	n/a	chr13:50144518-50144527
24	BATF	chr13:50145747-50146053	GM12878	blood:	n/a	n/a
25	BCL11A	chr13:50145639-50146047	GM12878	blood:	n/a	n/a
26	BCL11A	chr13:50146042-50146312	GM12878	blood:	n/a	n/a
27	BCL11A	chr13:50145718-50145994	GM12878	blood:	n/a	n/a
28	BCL11A	chr13:50146070-50146365	GM12878	blood:	n/a	n/a
29	BCLAF1	chr13:50181082-50181563	GM12878	blood:	n/a	n/a
30	BHLHE40	chr13:50161385-50162070	HepG2	liver:	n/a	n/a
31	BHLHE40	chr13:50158980-50160236	K562	blood:	n/a	chr13:50159589-50159605 chr13:50159736-50159745 chr13:50159734-50159747 chr13:50159974-50159990 chr13:50159737-50159746 chr13:50159736-50159745 chr13:50159730-50159751
32	BHLHE40	chr13:50181263-50181518	HepG2	liver:	n/a	n/a
33	BHLHE40	chr13:50159293-50160367	HepG2	liver:	n/a	chr13:50159589-50159605 chr13:50159736-50159745 chr13:50159734-50159747 chr13:50159974-50159990 chr13:50159737-50159746 chr13:50159736-50159745 chr13:50159730-50159751
34	BHLHE40	chr13:50159588-50159851	A549	lung:	n/a	chr13:50159589-50159605 chr13:50159736-50159745 chr13:50159734-50159747 chr13:50159737-50159746 chr13:50159736-50159745 chr13:50159730-50159751
35	BHLHE40	chr13:50145695-50146199	GM12878	blood:	n/a	n/a
36	BHLHE40	chr13:50181180-50181459	K562	blood:	n/a	n/a
37	BHLHE40	chr13:50181195-50181543	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:50134491-50134757	HepG2	liver:	n/a	n/a
39	BHLHE40	chr13:50141587-50141920	K562	blood:	n/a	n/a
40	BHLHE40	chr13:50159515-50160027	GM12878	blood:	n/a	chr13:50159589-50159605 chr13:50159736-50159745 chr13:50159734-50159747 chr13:50159974-50159990 chr13:50159737-50159746 chr13:50159736-50159745 chr13:50159730-50159751
41	BHLHE40	chr13:50171223-50171526	K562	blood:	n/a	chr13:50171344-50171353 chr13:50171344-50171353
42	BRCA1	chr13:50159631-50159642	GM12878	blood:	n/a	n/a
43	BRCA1	chr13:50181238-50181495	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr13:50181392-50181398	HepG2	liver:	n/a	n/a
45	BRCA1	chr13:50181196-50181459	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr13:50141604-50141930	K562	blood:	n/a	n/a
47	CCNT2	chr13:50159349-50160020	K562	blood:	n/a	n/a
48	CCNT2	chr13:50171489-50171719	K562	blood:	n/a	n/a
49	CCNT2	chr13:50114899-50115099	K562	blood:	n/a	n/a
50	CEBPB	chr13:50134464-50134743	MCF-7	breast:	n/a	chr13:50134589-50134601

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50159779-50159829	MCF-7	breast:	n/a
2	chr13:50160670-50160720	MCF10A-Er-Src	breast:	n/a
3	chr13:50160670-50160720	GM12892	blood:	n/a
4	chr13:50159867-50159917	Hepatocyte	liver:	n/a
5	chr13:50160670-50160720	AG04450	lung:	fetal
6	chr13:50160670-50160720	SK-N-SH	brain:	n/a
7	chr13:50159768-50159818	HRCEpiC	kidney:	n/a
8	chr13:50155502-50155552	RPTEC	kidney:	n/a
9	chr13:50159387-50159437	HCT-116	colon:	n/a
10	chr13:50159867-50159917	IMR90	lung:	fetal
11	chr13:50159138-50159188	SK-N-MC	brain:	n/a
12	chr13:50160670-50160720	AG04449	skin:	fetal
13	chr13:50159768-50159818	BE2_C	brain:	n/a
14	chr13:50123613-50123663	SK-N-SH_RA	brain:	n/a
15	chr13:50155502-50155552	HCPEpiC	choroid plexus:	n/a
16	chr13:50160350-50160400	A549	lung:	n/a
17	chr13:50123613-50123663	MCF10A-Er-Src	breast:	n/a
18	chr13:50159387-50159437	HepG2	liver:	n/a
19	chr13:50107026-50107076	ProgFib	skin:	n/a
20	chr13:50162325-50162375	HRCEpiC	kidney:	n/a
21	chr13:50160095-50160145	MCF10A-Er-Src	breast:	n/a
22	chr13:50159779-50159829	Caco-2	colon:	n/a
23	chr13:50160670-50160720	HMEC	breast:	n/a
24	chr13:50107026-50107076	GM19239	blood:	n/a
25	chr13:50160350-50160400	AG04449	skin:	fetal
26	chr13:50162325-50162375	SKMC	muscle:	n/a
27	chr13:50159798-50159848	Caco-2	colon:	n/a
28	chr13:50159138-50159188	AG04450	lung:	fetal
29	chr13:50159138-50159188	IMR90	lung:	fetal
30	chr13:50159779-50159829	GM12892	blood:	n/a
31	chr13:50160062-50160112	HepG2	liver:	n/a
32	chr13:50134640-50134690	HUVEC	blood vessel:	n/a
33	chr13:50159138-50159188	SK-N-SH_RA	brain:	n/a
34	chr13:50159138-50159188	NH-A	brain:	n/a
35	chr13:50134640-50134690	HNPCEpiC	eye:	n/a
36	chr13:50190584-50190634	SAEC	small airway:	n/a
37	chr13:50159779-50159829	K562	blood:	n/a
38	chr13:50162325-50162375	GM06990	blood:	n/a
39	chr13:50159798-50159848	MCF-7	breast:	n/a
40	chr13:50190584-50190634	HRE	kidney:	n/a
41	chr13:50159387-50159437	LNCaP	prostate:	n/a
42	chr13:50160670-50160720	HCF	heart:	n/a
43	chr13:50190584-50190634	AG04449	skin:	fetal
44	chr13:50107026-50107076	LNCaP	prostate:	n/a
45	chr13:50160350-50160400	HCM	heart:	n/a
46	chr13:50155502-50155552	Hela-S3	cervix:	n/a
47	chr13:50160350-50160400	HCT-116	colon:	n/a
48	chr13:50159138-50159188	MCF10A-Er-Src	breast:	n/a
49	chr13:50134640-50134690	HIPEpiC	eye:	n/a
50	chr13:50159387-50159437	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:50134779..50137828-chr13:50140921..50142745,3	MCF-7	breast:
2	chr13:50071647..50073472-chr13:50180377..50183221,3	MCF-7	breast:
3	chr13:50127837..50130111-chr13:50134111..50136962,3	MCF-7	breast:
4	chr13:50022863..50025187-chr13:50116857..50119478,2	K562	blood:
5	chr13:50143614..50146624-chr13:50158019..50161696,4	MCF-7	breast:
6	chr1:144533809..144534431-chr13:50159258..50160240,2	Hela-S3	cervix:
7	chr13:50123244..50123850-chr13:50179491..50180112,2	MCF-7	breast:
8	chr13:50153114..50155193-chr13:50155306..50157479,2	MCF-7	breast:
9	chr13:50191955..50193680-chr13:50196033..50197758,2	MCF-7	breast:
10	chr13:50068857..50071479-chr13:50143285..50145487,2	MCF-7	breast:
11	chr13:50126796..50128354-chr13:50131796..50134070,2	MCF-7	breast:
12	chr13:50045650..50047733-chr13:50190939..50192914,2	MCF-7	breast:
13	chr13:50132912..50136766-chr13:50158156..50162933,6	MCF-7	breast:
14	chr13:50134986..50135758-chr13:50143919..50144828,2	MCF-7	breast:
15	chr13:50068598..50070239-chr13:50135700..50137416,2	MCF-7	breast:
16	chr13:50016992..50019784-chr13:50159235..50161344,2	K562	blood:
17	chr13:50157525..50159034-chr13:50176178..50177840,2	MCF-7	breast:
18	chr13:50134458..50136628-chr13:50139261..50141252,2	MCF-7	breast:
19	chr13:50134505..50135459-chr13:50143778..50144515,3	MCF-7	breast:
20	chr13:50142756..50146527-chr13:50158016..50161593,4	MCF-7	breast:
21	chr13:50143262..50147042-chr13:50150087..50153613,4	MCF-7	breast:
22	chr13:50133873..50136164-chr13:50144707..50146572,2	MCF-7	breast:
23	chr13:50126796..50128354-chr13:50131796..50134070,2	MCF-7	breast:
24	chr13:50182731..50184724-chr13:50185681..50187681,2	K562	blood:
25	chr13:50133873..50136164-chr13:50144707..50146572,2	MCF-7	breast:
26	chr13:50087217..50089138-chr13:50160277..50162233,2	MCF-7	breast:
27	chr13:50157525..50159034-chr13:50176178..50177840,2	MCF-7	breast:
28	chr13:50038641..50040451-chr13:50143314..50145864,2	MCF-7	breast:
29	chr13:50140695..50143077-chr13:50154599..50156492,2	K562	blood:
30	chr13:50124973..50127457-chr13:50130944..50133269,2	MCF-7	breast:
31	chr13:50127837..50130111-chr13:50134111..50136962,3	MCF-7	breast:
32	chr13:50091935..50095583-chr13:50159811..50161648,3	MCF-7	breast:
33	chr13:50158880..50161532-chr13:50167908..50169542,2	MCF-7	breast:
34	chr13:50129638..50131635-chr13:50134638..50136314,2	MCF-7	breast:
35	chr13:50147102..50149993-chr13:50155282..50157133,2	MCF-7	breast:
36	chr13:50134458..50136628-chr13:50139261..50141252,2	MCF-7	breast:
37	chr13:50140129..50142488-chr13:50158778..50160378,3	MCF-7	breast:
38	chr13:49854962..49855868-chr13:50180880..50181856,2	K562	blood:
39	chr13:50158665..50162522-chr13:50168019..50171007,4	MCF-7	breast:
40	chr13:50123244..50123850-chr13:50179491..50180112,2	MCF-7	breast:
41	chr13:50137662..50139363-chr13:50159195..50160839,2	MCF-7	breast:
42	chr13:50018091..50020783-chr13:50160403..50162609,2	MCF-7	breast:
43	chr13:50017307..50019773-chr13:50138937..50140601,2	MCF-7	breast:
44	chr13:50149299..50151085-chr13:50153245..50155110,2	MCF-7	breast:
45	chr13:50147102..50149993-chr13:50155282..50157133,2	MCF-7	breast:
46	chr13:50148788..50150757-chr13:50155991..50157502,2	K562	blood:
47	chr13:50134986..50135758-chr13:50143919..50144828,2	MCF-7	breast:
48	chr13:50149299..50151085-chr13:50153245..50155110,2	MCF-7	breast:
49	chr13:49820000..49822078-chr13:50177732..50179319,2	K562	blood:
50	chr13:50017613..50020080-chr13:50178535..50181318,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARL11-3	chr13:50191636-50192101	NONHSAT033754

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RCBTB1	hsa-miR-26b-5p	chr13:50106528-50106521
2	RCBTB1	hsa-miR-26b-5p	chr13:50106522-50106541

Variant related genes	Relation type
ENSG00000176882	TF binding region
RCBTB1	TF binding region
ENSG00000176882	CpG island
RCBTB1	CpG island
ENSG00000201699	chromatin interactions
ENSG00000136169	chromatin interactions
ENSG00000102547	chromatin interactions
ENSG00000234127	chromatin interactions
ENSG00000215462	chromatin interactions
ENSG00000102543	chromatin interactions
ENSG00000136147	chromatin interactions
ENSG00000236577	chromatin interactions
ENSG00000136144	chromatin interactions

Extended variants
information (count: 3577 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:3577 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9568239	chr13:50105055-50105056	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535133402	chr13:50105103-50105104	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7331262	chr13:50105142-50105143	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs568461512	chr13:50105148-50105149	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535683718	chr13:50105154-50105155	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10559021	chr13:50105216-50105217	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71078858	chr13:50105223-50105224	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556853625	chr13:50105230-50105231	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117486538	chr13:50105243-50105244	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575513298	chr13:50105244-50105245	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7331330	chr13:50105299-50105300	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs563324237	chr13:50105377-50105378	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557338492	chr13:50105385-50105386	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572458382	chr13:50105390-50105391	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542831395	chr13:50105440-50105441	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555248578	chr13:50105445-50105446	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374171203	chr13:50105458-50105459	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561861856	chr13:50105492-50105493	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574908921	chr13:50105497-50105498	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542439006	chr13:50105502-50105503	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9535257	chr13:50105518-50105519	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs531249635	chr13:50105519-50105520	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182580200	chr13:50105540-50105541	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148013171	chr13:50105599-50105600	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187190589	chr13:50105663-50105664	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549212288	chr13:50105698-50105699	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192825022	chr13:50105704-50105705	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs4941644	chr13:50105705-50105706	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs375046839	chr13:50105717-50105718	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577440005	chr13:50105734-50105735	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117308143	chr13:50105753-50105754	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568916747	chr13:50105754-50105755	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539350041	chr13:50105781-50105782	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7989504	chr13:50105782-50105783	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs183632921	chr13:50105787-50105788	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533576182	chr13:50105802-50105803	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555041023	chr13:50105810-50105811	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9562892	chr13:50105858-50105859	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs571632706	chr13:50105900-50105901	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4942838	chr13:50105907-50105908	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs4942839	chr13:50105954-50105955	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs575862609	chr13:50105994-50105995	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs113988609	chr13:50106009-50106010	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4942840	chr13:50106078-50106079	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs150571538	chr13:50106115-50106116	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372400658	chr13:50106116-50106117	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528781793	chr13:50106156-50106157	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559536186	chr13:50106163-50106164	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561896667	chr13:50106169-50106170	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529396862	chr13:50106197-50106198	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Osteosarcoma	21215367	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50075000-50143800	Weak transcription	Small Intestine	intestine
2	chr13:50077600-50114000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr13:50080000-50107000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr13:50086400-50113600	Weak transcription	Brain Angular Gyrus	brain
5	chr13:50086600-50106200	Strong transcription	Fetal Thymus	thymus
6	chr13:50086600-50108800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr13:50086600-50114200	Weak transcription	Fetal Brain Female	brain
8	chr13:50088200-50113600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:50088400-50151000	Weak transcription	Psoas Muscle	Psoas
10	chr13:50088600-50134200	Weak transcription	Stomach Mucosa	stomach
11	chr13:50089200-50107400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr13:50089400-50114200	Weak transcription	Colon Smooth Muscle	Colon
13	chr13:50090000-50113600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr13:50090000-50122800	Weak transcription	Ovary	ovary
15	chr13:50090000-50123600	Weak transcription	Esophagus	oesophagus
16	chr13:50090200-50114200	Weak transcription	Aorta	Aorta
17	chr13:50090200-50117800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr13:50090400-50106600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr13:50090400-50113400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr13:50090400-50114200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr13:50091000-50114200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr13:50091400-50138800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr13:50091800-50107600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr13:50092000-50108000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr13:50092000-50112200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr13:50092000-50114200	Weak transcription	Fetal Brain Male	brain
27	chr13:50092200-50105400	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr13:50092200-50105800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr13:50092200-50113400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr13:50093000-50108000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:50093800-50113400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr13:50094000-50112000	Weak transcription	HSMMtube	muscle
33	chr13:50094000-50114200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr13:50094200-50107800	Weak transcription	HepG2	liver
35	chr13:50094600-50113600	Weak transcription	Gastric	stomach
36	chr13:50094600-50113800	Weak transcription	Pancreas	Pancrea
37	chr13:50094600-50120000	Weak transcription	Spleen	Spleen
38	chr13:50094600-50141600	Weak transcription	Right Ventricle	heart
39	chr13:50095000-50120400	Weak transcription	A549	lung
40	chr13:50096000-50108000	Weak transcription	Lung	lung
41	chr13:50096600-50106800	Weak transcription	Fetal Kidney	kidney
42	chr13:50097600-50113600	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr13:50097600-50114000	Weak transcription	Fetal Lung	lung
44	chr13:50097800-50107800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr13:50097800-50113400	Weak transcription	NHLF	lung
46	chr13:50097800-50113600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr13:50097800-50135000	Weak transcription	Colonic Mucosa	Colon
48	chr13:50098000-50114200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr13:50098200-50114000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr13:50100200-50112200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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