Variant report

Variant	nsv875026
Chromosome Location	chr2:128378563-128445585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1348)
CpG islands
(count:4152)
Chromatin interactive
region (count:105)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1348 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:128402852-128402944	HepG2	liver:	n/a	n/a
2	ATF1	chr2:128395319-128395639	K562	blood:	n/a	n/a
3	ATF2	chr2:128395213-128395669	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:128407243-128407554	GM12878	blood:	n/a	n/a
5	ATF2	chr2:128395260-128395633	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:128390643-128391096	GM12878	blood:	n/a	n/a
7	ATF3	chr2:128401745-128401880	K562	blood:	n/a	n/a
8	BACH1	chr2:128433263-128433279	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr2:128395358-128395563	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:128390676-128391052	GM12878	blood:	n/a	n/a
11	BCL3	chr2:128419470-128419729	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:128407395-128407643	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:128396128-128396261	K562	blood:	n/a	n/a
14	BHLHE40	chr2:128395747-128395861	K562	blood:	n/a	n/a
15	BHLHE40	chr2:128407298-128407596	K562	blood:	n/a	n/a
16	BHLHE40	chr2:128438887-128438934	K562	blood:	n/a	n/a
17	BHLHE40	chr2:128420479-128420809	HepG2	liver:	n/a	n/a
18	BHLHE40	chr2:128409996-128410017	K562	blood:	n/a	n/a
19	BHLHE40	chr2:128385528-128385592	K562	blood:	n/a	n/a
20	BHLHE40	chr2:128428369-128428376	K562	blood:	n/a	n/a
21	BRCA1	chr2:128407346-128407624	Hela-S3	cervix:	n/a	n/a
22	CCNT2	chr2:128404581-128404775	K562	blood:	n/a	chr2:128404664-128404684
23	CCNT2	chr2:128395299-128395499	K562	blood:	n/a	n/a
24	CEBPB	chr2:128416210-128416533	A549	lung:	n/a	chr2:128416367-128416380
25	CEBPB	chr2:128416241-128416520	H1-hESC	embryonic stem cell:	n/a	chr2:128416367-128416380
26	CEBPB	chr2:128402725-128402856	HepG2	liver:	n/a	chr2:128402781-128402792
27	CEBPB	chr2:128395844-128396166	K562	blood:	n/a	chr2:128396018-128396029
28	CEBPB	chr2:128395872-128396195	IMR90	lung:	n/a	chr2:128396018-128396029
29	CEBPB	chr2:128422983-128423217	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:128416184-128416557	HepG2	liver:	n/a	chr2:128416367-128416380
31	CEBPB	chr2:128395864-128396191	HepG2	liver:	n/a	chr2:128396018-128396029
32	CEBPB	chr2:128395924-128396104	HepG2	liver:	n/a	chr2:128396018-128396029
33	CEBPB	chr2:128395817-128396208	K562	blood:	n/a	chr2:128396018-128396029
34	CEBPB	chr2:128387780-128387794	A549	lung:	n/a	n/a
35	CEBPB	chr2:128440790-128440899	HepG2	liver:	n/a	chr2:128440848-128440859
36	CEBPB	chr2:128387706-128387873	HepG2	liver:	n/a	chr2:128387774-128387785
37	CEBPB	chr2:128426685-128426998	IMR90	lung:	n/a	chr2:128426846-128426857
38	CEBPB	chr2:128441707-128441911	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:128416210-128416537	IMR90	lung:	n/a	chr2:128416367-128416380
40	CEBPB	chr2:128387560-128388007	MCF-7	breast:	n/a	chr2:128387774-128387785
41	CEBPB	chr2:128395791-128396221	MCF-7	breast:	n/a	chr2:128396018-128396029
42	CEBPB	chr2:128395866-128396205	HepG2	liver:	n/a	chr2:128396018-128396029
43	CEBPB	chr2:128423094-128423101	K562	blood:	n/a	n/a
44	CEBPB	chr2:128416286-128416432	K562	blood:	n/a	chr2:128416367-128416380
45	CEBPB	chr2:128416289-128416419	HepG2	liver:	n/a	chr2:128416367-128416380
46	CEBPB	chr2:128416202-128416545	HepG2	liver:	n/a	chr2:128416367-128416380
47	CEBPB	chr2:128395924-128396209	H1-hESC	embryonic stem cell:	n/a	chr2:128396018-128396029
48	CEBPB	chr2:128426745-128426882	HepG2	liver:	n/a	chr2:128426846-128426857
49	CEBPB	chr2:128416198-128416513	K562	blood:	n/a	chr2:128416367-128416380
50	CEBPB	chr2:128395370-128395570	Hela-S3	cervix:	n/a	n/a

(count:4152 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:128381653-128381703	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:128389103-128389153	GM06990	blood:	n/a
3	chr2:128422224-128422274	MCF10A-Er-Src	breast:	n/a
4	chr2:128419650-128419700	MCF10A-Er-Src	breast:	n/a
5	chr2:128381653-128381703	HPAEpiC	pulmonary alveolar:	n/a
6	chr2:128389103-128389153	GM06990	blood:	n/a
7	chr2:128422224-128422274	MCF10A-Er-Src	breast:	n/a
8	chr2:128419650-128419700	MCF10A-Er-Src	breast:	n/a
9	chr2:128440247-128440297	GM12878	blood:	n/a
10	chr2:128410602-128410652	NB4	blood:	n/a
11	chr2:128382383-128382433	MCF10A-Er-Src	breast:	n/a
12	chr2:128407154-128407204	ECC-1	luminal epithelium:	n/a
13	chr2:128433157-128433207	T-47D	breast:	n/a
14	chr2:128381689-128381739	MCF-7	breast:	n/a
15	chr2:128433309-128433359	H1-hESC	embryonic stem cell:	embryo
16	chr2:128381835-128381885	LNCaP	prostate:	n/a
17	chr2:128381745-128381795	HIPEpiC	eye:	n/a
18	chr2:128410029-128410079	NHDF-neo	bronchial:	n/a
19	chr2:128412420-128412470	NT2-D1	testis:	n/a
20	chr2:128412420-128412470	AG04450	lung:	fetal
21	chr2:128433373-128433423	HRE	kidney:	n/a
22	chr2:128433489-128433539	BJ	skin:	n/a
23	chr2:128403133-128403183	HCF	heart:	n/a
24	chr2:128385752-128385802	Hela-S3	cervix:	n/a
25	chr2:128433373-128433423	MCF-7	breast:	n/a
26	chr2:128422307-128422357	HNPCEpiC	eye:	n/a
27	chr2:128422179-128422229	SK-N-SH_RA	brain:	n/a
28	chr2:128410029-128410079	HNPCEpiC	eye:	n/a
29	chr2:128381877-128381927	HRPEpiC	eye:	n/a
30	chr2:128382383-128382433	HNPCEpiC	eye:	n/a
31	chr2:128402415-128402465	HCF	heart:	n/a
32	chr2:128410029-128410079	SK-N-SH_RA	brain:	n/a
33	chr2:128403286-128403336	H1-hESC	embryonic stem cell:	embryo
34	chr2:128410803-128410853	NT2-D1	testis:	n/a
35	chr2:128433058-128433108	NHBE	bronchial:	n/a
36	chr2:128420784-128420834	Caco-2	colon:	n/a
37	chr2:128381877-128381927	U87	brain:	n/a
38	chr2:128440247-128440297	SK-N-SH	brain:	n/a
39	chr2:128388876-128388926	U87	brain:	n/a
40	chr2:128385752-128385802	RPTEC	kidney:	n/a
41	chr2:128410689-128410739	A549	lung:	n/a
42	chr2:128410602-128410652	CMK	blood:	n/a
43	chr2:128422433-128422483	Hela-S3	cervix:	n/a
44	chr2:128433309-128433359	HepG2	liver:	n/a
45	chr2:128421828-128421878	HRCEpiC	kidney:	n/a
46	chr2:128439171-128439221	NHDF-neo	bronchial:	n/a
47	chr2:128402415-128402465	BE2_C	brain:	n/a
48	chr2:128402294-128402344	HEK293	kidney:	embryo
49	chr2:128433309-128433359	HEEpiC	esophagus:	n/a
50	chr2:128422224-128422274	NB4	blood:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:128380533..128382202-chr2:128389367..128391180,2	K562	blood:
2	chr2:128431316..128432995-chr2:128434172..128435952,2	K562	blood:
3	chr2:128349017..128351644-chr2:128387621..128389792,2	MCF-7	breast:
4	chr2:128389859..128392516-chr2:128399643..128401704,2	K562	blood:
5	chr2:128372104..128373861-chr2:128379908..128381447,2	K562	blood:
6	chr2:128422795..128425949-chr2:128427793..128430552,3	MCF-7	breast:
7	chr2:128385318..128388983-chr2:128393086..128394739,3	MCF-7	breast:
8	chr2:128433955..128435747-chr2:128462860..128464885,2	K562	blood:
9	chr2:128281712..128283571-chr2:128434827..128436741,2	K562	blood:
10	chr2:128282410..128284022-chr2:128394708..128396398,2	MCF-7	breast:
11	chr2:128402343..128404793-chr2:128407484..128409770,2	MCF-7	breast:
12	chr2:128386978..128389867-chr2:128392766..128396164,5	MCF-7	breast:
13	chr2:128388233..128390478-chr2:128396235..128397787,2	K562	blood:
14	chr2:128420447..128422567-chr2:128457609..128460284,2	K562	blood:
15	chr2:128367073..128368593-chr2:128390549..128393243,2	K562	blood:
16	chr2:128411945..128414716-chr2:128419531..128422215,2	MCF-7	breast:
17	chr17:41464681..41467245-chr2:128400919..128402419,3	K562	blood:
18	chr2:128389859..128392516-chr2:128399643..128401704,2	K562	blood:
19	chr2:128422795..128425949-chr2:128427793..128430552,3	MCF-7	breast:
20	chr2:128389876..128393259-chr2:128457359..128460267,4	K562	blood:
21	chr2:128396062..128398700-chr2:128403094..128404905,3	K562	blood:
22	chr2:128420579..128422835-chr2:128429985..128431797,2	MCF-7	breast:
23	chr2:128388233..128390478-chr2:128396235..128397787,2	K562	blood:
24	chr2:128375722..128378691-chr2:128379848..128382679,2	MCF-7	breast:
25	chr2:128379959..128382926-chr2:128418686..128421294,2	K562	blood:
26	chr2:128408594..128410279-chr2:128415629..128417148,2	K562	blood:
27	chr17:41464756..41466583-chr2:128402419..128403919,2	K562	blood:
28	chr2:128434245..128436993-chr2:128458435..128460018,2	K562	blood:
29	chr2:128410612..128413068-chr2:128414602..128416410,3	K562	blood:
30	chr2:128395122..128397868-chr2:128458445..128462393,4	MCF-7	breast:
31	chr2:128388582..128390159-chr2:128390369..128392220,2	K562	blood:
32	chr2:128282097..128285637-chr2:128404430..128407235,3	MCF-7	breast:
33	chr2:128407793..128410279-chr2:128415629..128417878,2	K562	blood:
34	chr2:128379152..128382886-chr2:128385919..128388760,4	K562	blood:
35	chr2:128408594..128410279-chr2:128415629..128417148,2	K562	blood:
36	chr2:128435093..128437638-chr2:128440757..128442672,3	K562	blood:
37	chr2:128435093..128437638-chr2:128440757..128442672,3	K562	blood:
38	chr2:128375941..128378223-chr2:128378920..128381001,2	K562	blood:
39	chr2:128396263..128398888-chr2:128399161..128401002,2	MCF-7	breast:
40	chr2:128410612..128413068-chr2:128414602..128416399,2	K562	blood:
41	chr2:128441597..128444680-chr2:128458427..128461316,5	MCF-7	breast:
42	chr2:128388188..128389976-chr2:128397282..128399225,3	MCF-7	breast:
43	chr2:128399168..128401965-chr2:128403212..128405574,3	MCF-7	breast:
44	chr2:128406114..128408879-chr2:128412310..128414037,2	MCF-7	breast:
45	chr2:128431990..128439027-chr2:128456236..128461918,10	K562	blood:
46	chr2:128281499..128284149-chr2:128402816..128405194,3	K562	blood:
47	chr2:128385318..128388983-chr2:128393086..128394739,3	MCF-7	breast:
48	chr2:128282521..128284586-chr2:128401987..128404000,3	MCF-7	breast:
49	chr2:128395249..128397685-chr2:128567372..128568887,2	K562	blood:
50	chr2:128275312..128279572-chr2:128410107..128412898,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LIMS2-2	chr2:128383572-128384423	ENSG00000272789.1
2	lnc-LIMS2-1	chr2:128394380-128394796	NONHSAT074176
3	lnc-LIMS2-1	chr2:128391285-128394251	NONHSAT074176

No data

Variant related genes	Relation type
GPR17	TF binding region
LIMS2	TF binding region
ENSG00000272789	TF binding region
MYO7B	TF binding region
GPR17	CpG island
LIMS2	CpG island
ENSG00000272789	CpG island
MYO7B	CpG island
ENSG00000136709	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000173349	chromatin interactions
ENSG00000163166	chromatin interactions
ENSG00000272789	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000144230	chromatin interactions
ENSG00000072163	chromatin interactions
ENSG00000169994	chromatin interactions

Extended variants
information (count: 3432 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3432 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2245711	chr2:128378563-128378564	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117771518	chr2:128378573-128378574	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535327730	chr2:128378587-128378588	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372658893	chr2:128378593-128378594	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181158036	chr2:128378622-128378623	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575452616	chr2:128378673-128378674	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs146016713	chr2:128378786-128378787	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs543615076	chr2:128378795-128378796	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557038994	chr2:128378824-128378825	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11291906	chr2:128378829-128378830	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573632691	chr2:128378834-128378835	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs397985840	chr2:128378839-128378840	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs72843376	chr2:128378840-128378841	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs542248841	chr2:128378847-128378848	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558913624	chr2:128378849-128378850	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76931720	chr2:128378855-128378856	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs77648153	chr2:128378856-128378857	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554312244	chr2:128378862-128378863	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571348358	chr2:128378874-128378875	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368262353	chr2:128378878-128378879	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544906476	chr2:128378885-128378886	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574373130	chr2:128378902-128378903	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139823420	chr2:128379035-128379036	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs185652595	chr2:128379047-128379048	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs550475615	chr2:128379082-128379083	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs563835503	chr2:128379161-128379162	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs529357012	chr2:128379208-128379209	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs549441541	chr2:128379268-128379269	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs575877013	chr2:128379292-128379293	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs12105828	chr2:128379328-128379329	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs60935161	chr2:128379340-128379341	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs190685797	chr2:128379342-128379343	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs370307386	chr2:128379369-128379370	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs571816329	chr2:128379382-128379383	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs181024288	chr2:128379414-128379415	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs186005153	chr2:128379427-128379428	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs573721015	chr2:128379428-128379429	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs73953661	chr2:128379438-128379439	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs77782292	chr2:128379482-128379483	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs375559203	chr2:128379544-128379545	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs61744148	chr2:128379563-128379564	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs374621759	chr2:128379586-128379587	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs372919338	chr2:128379596-128379597	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs61745260	chr2:128379609-128379610	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs370843350	chr2:128379610-128379611	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs142561271	chr2:128379611-128379612	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs201359831	chr2:128379615-128379616	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs202160591	chr2:128379655-128379656	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs549504666	chr2:128379683-128379684	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs56189444	chr2:128379697-128379698	Strong transcription Enhancers Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2736 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:128359200-128395200	Strong transcription	Duodenum Mucosa	Duodenum
2	chr2:128371000-128391600	Strong transcription	Fetal Intestine Large	intestine
3	chr2:128371400-128390800	Strong transcription	Fetal Intestine Small	intestine
4	chr2:128372600-128378600	Weak transcription	Colonic Mucosa	Colon
5	chr2:128373000-128380800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr2:128373200-128379400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr2:128376000-128379200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr2:128376400-128379000	Enhancers	Thymus	Thymus
9	chr2:128376600-128381000	Weak transcription	HSMM	muscle
10	chr2:128376600-128391200	Weak transcription	HSMMtube	muscle
11	chr2:128376800-128380200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr2:128377200-128378600	Flanking Active TSS	Primary B cells from cord blood	blood
13	chr2:128377200-128379400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr2:128377400-128379400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr2:128377600-128379400	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr2:128377800-128379200	Weak transcription	Spleen	Spleen
17	chr2:128377800-128380000	Enhancers	Primary hematopoietic stem cells	blood
18	chr2:128377800-128382800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr2:128378000-128380600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr2:128378400-128379200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr2:128378400-128380000	Weak transcription	Fetal Thymus	thymus
22	chr2:128378400-128392000	Enhancers	Primary B cells from peripheral blood	blood
23	chr2:128378400-128393600	Genic enhancers	Dnd41	blood
24	chr2:128378600-128383400	Strong transcription	Colonic Mucosa	Colon
25	chr2:128378600-128385000	Enhancers	Primary B cells from cord blood	blood
26	chr2:128379000-128381000	Weak transcription	Thymus	Thymus
27	chr2:128379000-128387600	Weak transcription	Right Atrium	heart
28	chr2:128379200-128379800	Enhancers	Spleen	Spleen
29	chr2:128379200-128382800	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr2:128379200-128386600	Strong transcription	Rectal Mucosa Donor 31	rectum
31	chr2:128379400-128382600	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr2:128379400-128382600	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr2:128379400-128383800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr2:128379400-128388000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:128379800-128380000	Weak transcription	Spleen	Spleen
36	chr2:128380000-128380200	Enhancers	Right Ventricle	heart
37	chr2:128380000-128382200	Enhancers	Fetal Thymus	thymus
38	chr2:128380000-128382400	Genic enhancers	Spleen	Spleen
39	chr2:128380000-128383000	Weak transcription	Primary hematopoietic stem cells	blood
40	chr2:128380200-128382600	Weak transcription	Right Ventricle	heart
41	chr2:128380200-128383600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr2:128380400-128382200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:128380600-128381600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:128380600-128381800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:128380600-128381800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr2:128380600-128382600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:128380800-128381800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr2:128380800-128382200	Enhancers	NH-A	brain
49	chr2:128380800-128382800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:128381000-128381400	Enhancers	HSMM	muscle

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