Variant report

Variant	nsv518041
Chromosome Location	chr12:49618043-49645240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1378)
CpG islands
(count:854)
Chromatin interactive
region (count:101)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:49628799-49629195	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:49645163-49645547	K562	blood:	n/a	n/a
3	ARID3A	chr12:49626430-49628023	K562	blood:	n/a	n/a
4	ARID3A	chr12:49628931-49629146	K562	blood:	n/a	n/a
5	ARID3A	chr12:49628242-49628540	HepG2	liver:	n/a	n/a
6	ATF1	chr12:49627637-49627972	K562	blood:	n/a	n/a
7	ATF1	chr12:49639518-49639616	K562	blood:	n/a	n/a
8	ATF1	chr12:49630325-49630603	K562	blood:	n/a	n/a
9	ATF1	chr12:49626744-49627287	K562	blood:	n/a	n/a
10	ATF2	chr12:49628875-49629157	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:49627375-49628015	GM12878	blood:	n/a	n/a
12	ATF2	chr12:49628903-49629214	GM12878	blood:	n/a	n/a
13	ATF2	chr12:49628083-49628615	GM12878	blood:	n/a	n/a
14	ATF2	chr12:49628092-49628706	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr12:49645159-49645383	K562	blood:	n/a	n/a
16	ATF3	chr12:49628100-49628640	A549	lung:	n/a	n/a
17	ATF3	chr12:49628808-49629248	A549	lung:	n/a	chr12:49629135-49629144
18	BACH1	chr12:49628096-49628572	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:49626930-49627188	K562	blood:	n/a	n/a
20	BACH1	chr12:49628166-49628368	K562	blood:	n/a	n/a
21	BCL3	chr12:49626735-49627306	K562	blood:	n/a	chr12:49626779-49626788
22	BCL3	chr12:49627978-49628584	A549	lung:	n/a	chr12:49628414-49628423 chr12:49628408-49628421
23	BCLAF1	chr12:49628133-49628703	GM12878	blood:	n/a	chr12:49628414-49628423 chr12:49628408-49628421
24	BCLAF1	chr12:49628863-49629306	GM12878	blood:	n/a	chr12:49629140-49629153
25	BCLAF1	chr12:49627372-49628131	GM12878	blood:	n/a	n/a
26	BCLAF1	chr12:49626517-49627303	K562	blood:	n/a	chr12:49626779-49626788
27	BCLAF1	chr12:49628877-49629217	GM12878	blood:	n/a	chr12:49629140-49629153
28	BCLAF1	chr12:49628199-49628711	GM12878	blood:	n/a	chr12:49628414-49628423 chr12:49628408-49628421
29	BHLHE40	chr12:49628198-49628544	HepG2	liver:	n/a	chr12:49628411-49628427 chr12:49628408-49628424
30	BHLHE40	chr12:49629002-49629238	K562	blood:	n/a	n/a
31	BHLHE40	chr12:49627485-49627488	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:49627708-49628540	K562	blood:	n/a	chr12:49628411-49628427 chr12:49628408-49628424
33	BHLHE40	chr12:49628205-49628591	GM12878	blood:	n/a	chr12:49628411-49628427 chr12:49628408-49628424
34	BHLHE40	chr12:49626126-49626239	K562	blood:	n/a	n/a
35	BHLHE40	chr12:49626691-49627484	K562	blood:	n/a	n/a
36	BHLHE40	chr12:49628108-49628327	A549	lung:	n/a	n/a
37	BHLHE40	chr12:49639597-49639675	K562	blood:	n/a	n/a
38	BRCA1	chr12:49628025-49628608	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr12:49628143-49628305	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr12:49628179-49628441	GM12878	blood:	n/a	n/a
41	BRCA1	chr12:49628823-49629216	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr12:49626581-49628575	K562	blood:	n/a	n/a
43	CBX3	chr12:49626715-49627179	K562	blood:	n/a	n/a
44	CCNT2	chr12:49626752-49627440	K562	blood:	n/a	n/a
45	CCNT2	chr12:49629001-49629257	K562	blood:	n/a	n/a
46	CCNT2	chr12:49627650-49628606	K562	blood:	n/a	chr12:49628393-49628413
47	CEBPB	chr12:49628202-49629302	A549	lung:	n/a	chr12:49628925-49628934 chr12:49628923-49628934 chr12:49628925-49628934 chr12:49628923-49628936 chr12:49628925-49628934
48	CEBPB	chr12:49628714-49629315	MCF-7	breast:	n/a	chr12:49628925-49628934 chr12:49628923-49628934 chr12:49628925-49628934 chr12:49628923-49628936 chr12:49628925-49628934
49	CEBPB	chr12:49628201-49628341	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr12:49619453-49619635	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49621078-49621128	GM06990	blood:	n/a
2	chr12:49631720-49631770	HCT-116	colon:	n/a
3	chr12:49627934-49627984	HRPEpiC	eye:	n/a
4	chr12:49629119-49629169	A549	lung:	n/a
5	chr12:49627624-49627674	CMK	blood:	n/a
6	chr12:49628356-49628406	HCF	heart:	n/a
7	chr12:49628458-49628508	HMEC	breast:	n/a
8	chr12:49631720-49631770	PFSK-1	brain:	n/a
9	chr12:49620920-49620970	HCT-116	colon:	n/a
10	chr12:49629133-49629183	GM12891	blood:	n/a
11	chr12:49621078-49621128	SKMC	muscle:	n/a
12	chr12:49629187-49629237	PrEC	prostate:	n/a
13	chr12:49621078-49621128	HRPEpiC	eye:	n/a
14	chr12:49629187-49629237	AG09319	gingival:	n/a
15	chr12:49620920-49620970	HEK293	kidney:	embryo
16	chr12:49620920-49620970	AG10803	skin:	n/a
17	chr12:49629119-49629169	SKMC	muscle:	n/a
18	chr12:49629133-49629183	BE2_C	brain:	n/a
19	chr12:49621078-49621128	HCPEpiC	choroid plexus:	n/a
20	chr12:49629133-49629183	HEK293	kidney:	embryo
21	chr12:49631720-49631770	BJ	skin:	n/a
22	chr12:49631720-49631770	GM12891	blood:	n/a
23	chr12:49624394-49624444	Hela-S3	cervix:	n/a
24	chr12:49627746-49627796	AG04450	lung:	fetal
25	chr12:49628458-49628508	NH-A	brain:	n/a
26	chr12:49629187-49629237	SK-N-SH	brain:	n/a
27	chr12:49628520-49628570	HCPEpiC	choroid plexus:	n/a
28	chr12:49628356-49628406	Hela-S3	cervix:	n/a
29	chr12:49621078-49621128	HIPEpiC	eye:	n/a
30	chr12:49627746-49627796	AG09319	gingival:	n/a
31	chr12:49629133-49629183	AoSMC	blood vessel:	n/a
32	chr12:49627624-49627674	GM19239	blood:	n/a
33	chr12:49624394-49624444	AG09309	skin:	n/a
34	chr12:49628520-49628570	ProgFib	skin:	n/a
35	chr12:49628458-49628508	HIPEpiC	eye:	n/a
36	chr12:49629187-49629237	HepG2	liver:	n/a
37	chr12:49629187-49629237	PANC-1	pancreas:	n/a
38	chr12:49629187-49629237	MCF10A-Er-Src	breast:	n/a
39	chr12:49629133-49629183	ProgFib	skin:	n/a
40	chr12:49627624-49627674	A549	lung:	n/a
41	chr12:49627010-49627060	GM12878	blood:	n/a
42	chr12:49628356-49628406	Caco-2	colon:	n/a
43	chr12:49624394-49624444	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:49629187-49629237	HAEpiC	amniotic membrane:	n/a
45	chr12:49628520-49628570	HMEC	breast:	n/a
46	chr12:49627010-49627060	HRPEpiC	eye:	n/a
47	chr12:49621078-49621128	HCF	heart:	n/a
48	chr12:49629119-49629169	Jurkat	blood:	n/a
49	chr12:49627934-49627984	HEK293	kidney:	embryo
50	chr12:49627934-49627984	HL-60	blood:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:49582252..49584303-chr12:49626991..49629513,3	MCF-7	breast:
2	chr12:49581061..49584023-chr12:49626756..49629853,3	K562	blood:
3	chr12:49504151..49505106-chr12:49628922..49629557,2	K562	blood:
4	chr12:49617947..49619571-chr12:49625520..49628045,3	K562	blood:
5	chr12:49451583..49453949-chr12:49625558..49628294,2	K562	blood:
6	chr12:49627091..49630045-chr12:49647467..49650114,2	MCF-7	breast:
7	chr12:49632513..49636593-chr12:49658328..49660482,3	MCF-7	breast:
8	chr12:49628441..49630011-chr12:49661441..49664264,2	MCF-7	breast:
9	chr12:49608287..49611416-chr12:49615384..49618103,4	K562	blood:
10	chr12:49628644..49630691-chr12:49633942..49636514,2	MCF-7	breast:
11	chr12:49524425..49525138-chr12:49628498..49629103,2	Hela-S3	cervix:
12	chr12:49523221..49526191-chr12:49645076..49648524,3	K562	blood:
13	chr12:49608287..49610880-chr12:49615814..49620950,5	K562	blood:
14	chr12:49628391..49630050-chr12:49633833..49636685,2	MCF-7	breast:
15	chr12:49617947..49619523-chr12:49625520..49627493,2	K562	blood:
16	chr12:49606836..49608508-chr12:49621883..49624285,2	K562	blood:
17	chr12:49482053..49482666-chr12:49626599..49627456,2	K562	blood:
18	chr12:49513866..49528454-chr12:49616957..49635747,92	K562	blood:
19	chr12:49628644..49630691-chr12:49633942..49636514,2	MCF-7	breast:
20	chr12:49612799..49614334-chr12:49623991..49626335,2	K562	blood:
21	chr12:49480667..49484099-chr12:49627128..49630502,6	K562	blood:
22	chr12:49481249..49484156-chr12:49632283..49634121,2	K562	blood:
23	chr12:49581406..49583552-chr12:49621389..49622908,2	MCF-7	breast:
24	chr12:49626870..49630016-chr12:49656039..49660011,4	MCF-7	breast:
25	chr12:49453100..49454681-chr12:49629053..49631692,2	MCF-7	breast:
26	chr12:49627452..49628272-chr17:41465817..41466453,2	NB4	blood:
27	chr12:49410482..49414207-chr12:49626901..49628539,3	K562	blood:
28	chr12:49498025..49500103-chr12:49626582..49628144,2	K562	blood:
29	chr12:49579518..49583719-chr12:49624804..49628256,4	K562	blood:
30	chr12:49627964..49628871-chrX:154842972..154843491,2	Hela-S3	cervix:
31	chr12:49491448..49492070-chr12:49628718..49629572,2	MCF-7	breast:
32	chr12:49644322..49648565-chr12:49657211..49660431,8	MCF-7	breast:
33	chr12:49523038..49525426-chr12:49632544..49634215,5	K562	blood:
34	chr12:49451583..49453085-chr12:49626794..49628619,2	K562	blood:
35	chr12:49628216..49628907-chr5:33441080..33441962,2	Hela-S3	cervix:
36	chr12:49638137..49641048-chr12:49657465..49660850,5	K562	blood:
37	chr12:49524620..49525974-chr12:49627554..49629013,4	NB4	blood:
38	chr12:49638606..49640494-chr12:49646285..49648515,2	MCF-7	breast:
39	chr12:49502508..49504183-chr12:49633326..49635390,2	K562	blood:
40	chr12:49582901..49584858-chr12:49624494..49626461,2	MCF-7	breast:
41	chr12:49625768..49629972-chr12:49657225..49660229,8	MCF-7	breast:
42	chr12:49580612..49583821-chr12:49626954..49630010,6	MCF-7	breast:
43	chr12:49218140..49220739-chr12:49625372..49627807,2	K562	blood:
44	chr12:49523889..49527940-chr12:49626125..49630578,10	MCF-7	breast:
45	chr12:49619700..49621201-chr12:49627678..49629883,2	MCF-7	breast:
46	chr12:49523243..49526269-chr12:49642508..49650672,7	K562	blood:
47	chr12:49504257..49506648-chr12:49625633..49628380,2	MCF-7	breast:
48	chr12:49495156..49497539-chr12:49627737..49630589,2	MCF-7	breast:
49	chr12:49481716..49483159-chr12:49628651..49629622,5	MCF-7	breast:
50	chr12:49624371..49632888-chr12:49655742..49664182,29	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TUBA1C-3	chr12:49621874-49621949	NONHSAT028088
2	lnc-TUBA1A-1	chr12:49627352-49627921	ENSG00000258101.1

No data

Variant related genes	Relation type
TUBA1C	TF binding region
TUBA1C	CpG island
ENSG00000200309	chromatin interactions
ENSG00000167548	chromatin interactions
ENSG00000257346	chromatin interactions
ENSG00000151093	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000167552	chromatin interactions
ENSG00000167535	chromatin interactions
ENSG00000139636	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000151092	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000181929	chromatin interactions
ENSG00000113407	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000139549	chromatin interactions

Extended variants
information (count: 974 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:974 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11834543	chr12:49618043-49618044	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114955317	chr12:49618066-49618067	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs538652581	chr12:49618087-49618088	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs552495805	chr12:49618088-49618089	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs35493053	chr12:49618103-49618104	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs530300334	chr12:49618113-49618114	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs571458480	chr12:49618114-49618115	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs75145560	chr12:49618130-49618131	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs556757707	chr12:49618140-49618141	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs148589250	chr12:49618154-49618155	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs375613185	chr12:49618211-49618212	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs552792548	chr12:49618221-49618222	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs74710198	chr12:49618247-49618248	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs144474743	chr12:49618250-49618251	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs559984835	chr12:49618301-49618302	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs530373286	chr12:49618313-49618314	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs146123068	chr12:49618348-49618349	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs140106868	chr12:49618393-49618394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs182678054	chr12:49618401-49618402	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs79416240	chr12:49618512-49618513	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs11834620	chr12:49618519-49618520	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs530307472	chr12:49618594-49618595	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs28496109	chr12:49618634-49618635	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs547161071	chr12:49618651-49618652	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs140639275	chr12:49618665-49618666	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs188071784	chr12:49618667-49618668	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs530827067	chr12:49618675-49618676	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs532596321	chr12:49618841-49618842	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs192968950	chr12:49618851-49618852	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs569203768	chr12:49618885-49618886	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs144065337	chr12:49618886-49618887	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs550454328	chr12:49618892-49618893	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs150956626	chr12:49618987-49618988	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs184686953	chr12:49619006-49619007	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs140736076	chr12:49619013-49619014	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs572868334	chr12:49619030-49619031	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs552607460	chr12:49619032-49619033	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs149662252	chr12:49619034-49619035	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs575297304	chr12:49619046-49619047	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs544961900	chr12:49619078-49619079	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs555657472	chr12:49619121-49619122	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs77846406	chr12:49619134-49619135	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs56244620	chr12:49619135-49619136	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs570858015	chr12:49619149-49619150	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs189241381	chr12:49619179-49619180	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs145446471	chr12:49619203-49619204	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs540836972	chr12:49619205-49619206	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs560700365	chr12:49619211-49619212	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs532518631	chr12:49619221-49619222	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs546254770	chr12:49619256-49619257	Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49610200-49625800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr12:49612200-49620200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr12:49614200-49618400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
4	chr12:49615200-49618600	Enhancers	Fetal Muscle Leg	muscle
5	chr12:49615200-49625600	Weak transcription	Placenta	Placenta
6	chr12:49616000-49618400	Enhancers	Fetal Muscle Trunk	muscle
7	chr12:49616400-49618400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr12:49616400-49619800	Enhancers	Brain Hippocampus Middle	brain
9	chr12:49616600-49619000	Weak transcription	K562	blood
10	chr12:49616800-49618800	Weak transcription	HMEC	breast
11	chr12:49616800-49619400	Weak transcription	A549	lung
12	chr12:49616800-49621000	Weak transcription	Fetal Brain Female	brain
13	chr12:49616800-49624400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:49616800-49625800	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr12:49616800-49626000	Weak transcription	Adipose Nuclei	Adipose
16	chr12:49617000-49618400	Enhancers	HSMMtube	muscle
17	chr12:49617000-49618600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr12:49617000-49619400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr12:49617000-49619400	Weak transcription	NHEK	skin
20	chr12:49617000-49619600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:49617000-49619600	Weak transcription	Fetal Thymus	thymus
22	chr12:49617000-49624000	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr12:49617200-49619400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:49617200-49619400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr12:49617200-49619400	Weak transcription	Osteobl	bone
26	chr12:49617200-49619600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:49617200-49620000	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr12:49617400-49618200	Weak transcription	Spleen	Spleen
29	chr12:49617400-49619400	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr12:49617400-49619600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:49617600-49619400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr12:49617600-49620800	Weak transcription	Fetal Brain Male	brain
33	chr12:49617600-49625600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:49617600-49625800	Weak transcription	NHDF-Ad	bronchial
35	chr12:49617600-49626000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr12:49617800-49619000	Weak transcription	NHLF	lung
37	chr12:49617800-49619400	Weak transcription	HSMM	muscle
38	chr12:49617800-49620800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:49617800-49621400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:49617800-49621400	Weak transcription	Brain Angular Gyrus	brain
41	chr12:49617800-49621400	Weak transcription	Brain Cingulate Gyrus	brain
42	chr12:49617800-49621400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr12:49618000-49618400	Weak transcription	Primary B cells from cord blood	blood
44	chr12:49618000-49619400	Weak transcription	Brain Substantia Nigra	brain
45	chr12:49618000-49620600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:49618000-49621400	Weak transcription	Brain Anterior Caudate	brain
47	chr12:49618200-49618800	Enhancers	Spleen	Spleen
48	chr12:49618400-49619200	Enhancers	Primary B cells from cord blood	blood
49	chr12:49618400-49619400	Weak transcription	HSMMtube	muscle
50	chr12:49618400-49619400	Enhancers	Monocytes-CD14+_RO01746	blood

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