Variant report

Variant	nsv1053462
Chromosome Location	chr15:41270067-41396094
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1001)
CpG islands
(count:550)
Chromatin interactive
region (count:128)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1001 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:41353962-41354090	HepG2	liver:	n/a	n/a
2	ATF1	chr15:41293933-41293943	K562	blood:	n/a	n/a
3	BATF	chr15:41296965-41297231	GM12878	blood:	n/a	n/a
4	BATF	chr15:41307256-41307497	GM12878	blood:	n/a	n/a
5	BATF	chr15:41307205-41307541	GM12878	blood:	n/a	n/a
6	BCL11A	chr15:41296740-41296984	GM12878	blood:	n/a	n/a
7	BCL3	chr15:41291350-41291863	A549	lung:	n/a	n/a
8	BCLAF1	chr15:41305903-41306410	GM12878	blood:	n/a	chr15:41306077-41306086
9	BHLHE40	chr15:41314736-41315003	GM12878	blood:	n/a	n/a
10	BHLHE40	chr15:41287996-41288058	K562	blood:	n/a	n/a
11	BHLHE40	chr15:41296907-41296950	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:41314778-41314906	K562	blood:	n/a	n/a
13	BHLHE40	chr15:41357922-41358198	GM12878	blood:	n/a	n/a
14	BRCA1	chr15:41386558-41386567	HepG2	liver:	n/a	n/a
15	CBX3	chr15:41353861-41354196	K562	blood:	n/a	n/a
16	CBX3	chr15:41353873-41354244	K562	blood:	n/a	n/a
17	CCNT2	chr15:41271774-41271957	K562	blood:	n/a	n/a
18	CEBPB	chr15:41291460-41291946	IMR90	lung:	n/a	chr15:41291814-41291823 chr15:41291814-41291823
19	CEBPB	chr15:41335394-41335841	IMR90	lung:	n/a	chr15:41335490-41335501
20	CEBPB	chr15:41335454-41335742	HepG2	liver:	n/a	chr15:41335490-41335501
21	CEBPB	chr15:41305887-41306173	A549	lung:	n/a	chr15:41306036-41306047 chr15:41306129-41306140
22	CEBPB	chr15:41392827-41393023	A549	lung:	n/a	chr15:41392993-41393004
23	CEBPB	chr15:41305841-41306164	Hela-S3	cervix:	n/a	chr15:41306036-41306047 chr15:41306129-41306140
24	CEBPB	chr15:41303999-41304074	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr15:41355865-41355960	HepG2	liver:	n/a	chr15:41355919-41355930
26	CEBPB	chr15:41346838-41346850	K562	blood:	n/a	n/a
27	CEBPB	chr15:41392920-41393093	H1-hESC	embryonic stem cell:	n/a	chr15:41392993-41393004
28	CEBPB	chr15:41305902-41306139	HepG2	liver:	n/a	chr15:41306036-41306047
29	CEBPB	chr15:41337280-41337289	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr15:41392898-41393019	HepG2	liver:	n/a	chr15:41392993-41393004
31	CEBPB	chr15:41335437-41335746	Hela-S3	cervix:	n/a	chr15:41335490-41335501
32	CEBPB	chr15:41335353-41335785	ECC-1	luminal epithelium:	n/a	chr15:41335490-41335501
33	CEBPB	chr15:41305830-41306240	IMR90	lung:	n/a	chr15:41306036-41306047 chr15:41306129-41306140
34	CEBPB	chr15:41338085-41338411	IMR90	lung:	n/a	n/a
35	CEBPB	chr15:41291374-41291984	A549	lung:	n/a	chr15:41291814-41291823 chr15:41291814-41291823
36	CEBPB	chr15:41392829-41393084	IMR90	lung:	n/a	chr15:41392993-41393004
37	CEBPB	chr15:41363904-41364003	IMR90	lung:	n/a	chr15:41363972-41363983
38	CEBPB	chr15:41277169-41277490	IMR90	lung:	n/a	n/a
39	CEBPB	chr15:41392956-41393069	K562	blood:	n/a	chr15:41392993-41393004
40	CEBPB	chr15:41303896-41304210	IMR90	lung:	n/a	n/a
41	CEBPB	chr15:41277871-41278194	IMR90	lung:	n/a	n/a
42	CHD1	chr15:41290510-41292276	IMR90	lung:	n/a	n/a
43	CHD2	chr15:41314935-41314939	GM12878	blood:	n/a	n/a
44	CREB1	chr15:41293691-41293939	A549	lung:	n/a	n/a
45	CTCF	chr15:41314800-41314950	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr15:41310860-41311010	AG10803	skin:	n/a	n/a
47	CTCF	chr15:41302650-41302793	HepG2	liver:	n/a	n/a
48	CTCF	chr15:41310900-41311050	SAEC	small airway:	n/a	n/a
49	CTCF	chr15:41314774-41315016	Lung_OC	lung:	n/a	n/a
50	CTCF	chr15:41315185-41315213	GM12892	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41293531-41293581	Hepatocyte	liver:	n/a
2	chr15:41293531-41293581	Hepatocyte	liver:	n/a
3	chr15:41276343-41276393	BJ	skin:	n/a
4	chr15:41276147-41276197	SK-N-MC	brain:	n/a
5	chr15:41285147-41285197	HAEpiC	amniotic membrane:	n/a
6	chr15:41309253-41309303	HCM	heart:	n/a
7	chr15:41285147-41285197	ECC-1	luminal epithelium:	n/a
8	chr15:41276147-41276197	HMEC	breast:	n/a
9	chr15:41309253-41309303	NH-A	brain:	n/a
10	chr15:41275117-41275167	MCF-7	breast:	n/a
11	chr15:41285147-41285197	RPTEC	kidney:	n/a
12	chr15:41304870-41304920	GM12892	blood:	n/a
13	chr15:41316752-41316802	BE2_C	brain:	n/a
14	chr15:41309253-41309303	AG09309	skin:	n/a
15	chr15:41276343-41276393	HCPEpiC	choroid plexus:	n/a
16	chr15:41285147-41285197	HCF	heart:	n/a
17	chr15:41285147-41285197	NB4	blood:	n/a
18	chr15:41309253-41309303	HCT-116	colon:	n/a
19	chr15:41276147-41276197	HCM	heart:	n/a
20	chr15:41276147-41276197	SK-N-SH_RA	brain:	n/a
21	chr15:41275117-41275167	ovcar-3	ovarian:	n/a
22	chr15:41304870-41304920	NT2-D1	testis:	n/a
23	chr15:41304870-41304920	HUVEC	blood vessel:	n/a
24	chr15:41293531-41293581	LNCaP	prostate:	n/a
25	chr15:41275117-41275167	GM12892	blood:	n/a
26	chr15:41293531-41293581	AG09309	skin:	n/a
27	chr15:41316752-41316802	HEEpiC	esophagus:	n/a
28	chr15:41293531-41293581	GM19239	blood:	n/a
29	chr15:41275117-41275167	ECC-1	luminal epithelium:	n/a
30	chr15:41304870-41304920	AG09309	skin:	n/a
31	chr15:41304870-41304920	HepG2	liver:	n/a
32	chr15:41304870-41304920	IMR90	lung:	fetal
33	chr15:41271499-41271549	HAEpiC	amniotic membrane:	n/a
34	chr15:41285147-41285197	ovcar-3	ovarian:	n/a
35	chr15:41316752-41316802	K562	blood:	n/a
36	chr15:41285147-41285197	K562	blood:	n/a
37	chr15:41276343-41276393	HepG2	liver:	n/a
38	chr15:41276147-41276197	HNPCEpiC	eye:	n/a
39	chr15:41276343-41276393	NHDF-neo	bronchial:	n/a
40	chr15:41276343-41276393	Caco-2	colon:	n/a
41	chr15:41309253-41309303	Caco-2	colon:	n/a
42	chr15:41304870-41304920	U87	brain:	n/a
43	chr15:41316752-41316802	SK-N-MC	brain:	n/a
44	chr15:41275117-41275167	SAEC	small airway:	n/a
45	chr15:41304870-41304920	MCF10A-Er-Src	breast:	n/a
46	chr15:41285147-41285197	Hela-S3	cervix:	n/a
47	chr15:41304870-41304920	HEK293	kidney:	embryo
48	chr15:41285147-41285197	A549	lung:	n/a
49	chr15:41304870-41304920	GM12891	blood:	n/a
50	chr15:41285147-41285197	SK-N-SH	brain:	n/a

(count:128 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:41197511..41199195-chr15:41312839..41314955,3	K562	blood:
2	chr15:41221498..41223245-chr15:41301419..41303112,2	MCF-7	breast:
3	chr15:41234066..41235999-chr15:41310279..41312553,2	MCF-7	breast:
4	chr15:41271609..41273813-chr15:41287467..41290099,2	K562	blood:
5	chr15:41372419..41375425-chr15:41375855..41379166,3	K562	blood:
6	chr15:41384971..41389195-chr15:41407627..41410447,4	MCF-7	breast:
7	chr15:41197772..41199593-chr15:41314407..41315334,7	K562	blood:
8	chr15:41278440..41281104-chr15:41283285..41284820,2	K562	blood:
9	chr15:41304257..41306324-chr15:41623449..41625045,2	K562	blood:
10	chr15:41278440..41281104-chr15:41283285..41284820,2	K562	blood:
11	chr15:41230478..41233329-chr15:41297882..41299703,2	MCF-7	breast:
12	chr15:41264586..41267497-chr15:41281523..41283917,2	MCF-7	breast:
13	chr15:41195917..41196490-chr15:41310542..41311271,2	MCF-7	breast:
14	chr15:41374877..41377715-chr15:41379772..41382441,2	K562	blood:
15	chr15:41243576..41247065-chr15:41269319..41273291,3	MCF-7	breast:
16	chr15:41274207..41275810-chr15:41276649..41279377,2	K562	blood:
17	chr15:41389225..41391040-chr15:41407409..41409110,2	K562	blood:
18	chr15:41276343..41279940-chr15:41283285..41287659,3	K562	blood:
19	chr15:41391555..41394241-chr15:41403159..41405692,2	K562	blood:
20	chr15:41198304..41199036-chr15:41314353..41315333,2	MCF-7	breast:
21	chr15:41269511..41271032-chr15:41281628..41283628,2	K562	blood:
22	chr15:41271634..41273702-chr15:41273927..41275645,2	K562	blood:
23	chr15:41342780..41344966-chr15:41407191..41408966,2	K562	blood:
24	chr15:41276343..41279940-chr15:41283285..41287659,3	K562	blood:
25	chr15:41279189..41280997-chr15:41281365..41284292,2	MCF-7	breast:
26	chr15:41352417..41354404-chr15:41357276..41359773,2	MCF-7	breast:
27	chr15:41237043..41239988-chr15:41288206..41289792,2	K562	blood:
28	chr15:41330998..41333072-chr15:41336486..41338381,2	K562	blood:
29	chr15:41199560..41201206-chr15:41311847..41314635,2	MCF-7	breast:
30	chr15:41344528..41346229-chr15:41370109..41372324,2	MCF-7	breast:
31	chr15:41369235..41371146-chr15:41373294..41375147,2	K562	blood:
32	chr15:41221454..41223191-chr15:41293221..41295361,2	MCF-7	breast:
33	chr15:41391634..41395412-chr15:41405784..41409599,4	K562	blood:
34	chr15:41315566..41320310-chr15:41320724..41323896,4	K562	blood:
35	chr15:41198546..41199236-chr15:41314430..41314991,2	MCF-7	breast:
36	chr15:41229926..41230909-chr15:41310448..41311427,5	MCF-7	breast:
37	chr15:41296905..41299361-chr15:41300610..41302194,2	K562	blood:
38	chr15:41343718..41346047-chr15:41347738..41349539,2	MCF-7	breast:
39	chr15:41326386..41328188-chr15:41329412..41331864,2	K562	blood:
40	chr15:41388020..41390130-chr15:41405775..41409320,4	K562	blood:
41	chr15:41222426..41223378-chr15:41310613..41311459,3	MCF-7	breast:
42	chr15:41389694..41391207-chr15:41395733..41397571,2	MCF-7	breast:
43	chr15:41367609..41370089-chr15:41407814..41410461,2	K562	blood:
44	chr15:41221331..41223458-chr15:41308283..41310657,2	MCF-7	breast:
45	chr15:41234112..41234673-chr15:41314434..41315104,2	MCF-7	breast:
46	chr15:41393874..41395893-chr15:41406370..41408669,2	K562	blood:
47	chr15:41305413..41309160-chr15:41310948..41312697,3	K562	blood:
48	chr15:41229929..41230873-chr15:41310737..41311759,3	MCF-7	breast:
49	chr15:41221470..41223661-chr15:41278817..41281382,2	MCF-7	breast:
50	chr15:41272019..41273702-chr15:41273927..41276843,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC1-4	chr15:41310700-41310826	ENSG00000259521.1
2	lnc-CHAC1-2	chr15:41296731-41297063	ENSG00000259617.1
3	lnc-CHAC1-3	chr15:41303795-41303934	ENSG00000259463.1
4	lnc-RHOV-1	chr15:41320640-41322414	ENSG00000251290
5	lnc-CHAC1-4	chr15:41311661-41311760	ENSG00000259521.1
6	lnc-CHAC1-4	chr15:41316697-41316835	ENSG00000259521.1
7	lnc-CHAC1-4	chr15:41316685-41316740	ENSG00000259521.1
8	lnc-CHAC1-3	chr15:41305225-41305498	ENSG00000259463.1
9	lnc-CHAC1-4	chr15:41309005-41309033	ENSG00000259521.1
10	lnc-CHAC1-4	chr15:41319787-41320091	ENSG00000259521.1
11	lnc-CHAC1-2	chr15:41291472-41291638	ENSG00000259617.1
12	lnc-RHOV-1	chr15:41316067-41317661	ENSG00000251290

No data

Variant related genes	Relation type
ENSG00000259463	TF binding region
ENSG00000259521	TF binding region
CYCSP2	TF binding region
ENSG00000259617	TF binding region
INO80	TF binding region
ENSG00000259463	CpG island
ENSG00000259521	CpG island
CYCSP2	CpG island
ENSG00000259617	CpG island
INO80	CpG island
ENSG00000137804	chromatin interactions
ENSG00000251161	chromatin interactions
ENSG00000187446	chromatin interactions
ENSG00000128908	chromatin interactions
ENSG00000117139	chromatin interactions
ENSG00000104147	chromatin interactions
ENSG00000259617	chromatin interactions
ENSG00000259463	chromatin interactions
ENSG00000128917	chromatin interactions
ENSG00000259521	chromatin interactions
ENSG00000128965	chromatin interactions
ENSG00000178997	chromatin interactions
PTK2	miRNA target sites
EIF4A1	miRNA target sites

Extended variants
information (count: 5126 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5126 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558482602	chr15:41270083-41270084	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141976446	chr15:41270093-41270094	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150693300	chr15:41270103-41270104	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78207750	chr15:41270112-41270113	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs542371641	chr15:41270161-41270162	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs560136520	chr15:41270166-41270167	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139849520	chr15:41270181-41270182	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs193010387	chr15:41270203-41270204	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574672810	chr15:41270240-41270241	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs111746218	chr15:41270270-41270271	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542347216	chr15:41270278-41270279	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs7175362	chr15:41270302-41270303	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs116372089	chr15:41270308-41270309	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575644698	chr15:41270313-41270314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182892626	chr15:41270326-41270327	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs59935357	chr15:41270409-41270410	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs28646225	chr15:41270413-41270414	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs28581708	chr15:41270422-41270423	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564438597	chr15:41270447-41270448	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375519259	chr15:41270459-41270460	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548337297	chr15:41270473-41270474	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146373866	chr15:41270482-41270483	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527517020	chr15:41270506-41270507	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532023766	chr15:41270566-41270567	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs547278820	chr15:41270591-41270592	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532482350	chr15:41270627-41270628	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs570458020	chr15:41270641-41270642	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573405013	chr15:41270686-41270687	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187494021	chr15:41270761-41270762	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555894155	chr15:41270821-41270822	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541310037	chr15:41270895-41270896	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs569702444	chr15:41270899-41270900	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191860547	chr15:41270934-41270935	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555468795	chr15:41270959-41270960	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184284562	chr15:41270970-41270971	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs541686733	chr15:41270971-41270972	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559633750	chr15:41271000-41271001	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558488207	chr15:41271027-41271028	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370678595	chr15:41271057-41271058	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs188627851	chr15:41271100-41271101	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542275070	chr15:41271102-41271103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542467022	chr15:41271153-41271154	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529906325	chr15:41271201-41271202	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555394048	chr15:41271210-41271211	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs144066616	chr15:41271238-41271239	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs529314300	chr15:41271268-41271269	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573828893	chr15:41271306-41271307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542738626	chr15:41271324-41271325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192327784	chr15:41271336-41271337	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs74601039	chr15:41271354-41271355	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3755 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41252800-41270800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:41258800-41270400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:41258800-41270800	Weak transcription	Psoas Muscle	Psoas
4	chr15:41258800-41348400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:41262000-41271400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:41264000-41275400	Weak transcription	Fetal Brain Male	brain
7	chr15:41264600-41271800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr15:41265400-41271600	Weak transcription	Stomach Mucosa	stomach
9	chr15:41266000-41274200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr15:41266200-41275000	Strong transcription	Fetal Muscle Trunk	muscle
11	chr15:41266600-41274000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr15:41266600-41275000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:41266800-41273800	Strong transcription	Muscle Satellite Cultured Cells	--
14	chr15:41266800-41274000	Strong transcription	Osteobl	bone
15	chr15:41266800-41275200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr15:41266800-41277400	Strong transcription	Fetal Muscle Leg	muscle
17	chr15:41266800-41278400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:41266800-41280200	Strong transcription	Fetal Brain Female	brain
19	chr15:41266800-41280400	Strong transcription	Brain Substantia Nigra	brain
20	chr15:41266800-41281400	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr15:41266800-41283800	Strong transcription	A549	lung
22	chr15:41266800-41290000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr15:41266800-41298400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:41267000-41280600	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr15:41267000-41280800	Strong transcription	Brain Germinal Matrix	brain
26	chr15:41267200-41270200	Weak transcription	NHDF-Ad	bronchial
27	chr15:41267200-41272600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr15:41267200-41294800	Strong transcription	Primary T cells from cord blood	blood
29	chr15:41267600-41280600	Strong transcription	Fetal Stomach	stomach
30	chr15:41267600-41294200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr15:41267600-41301200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:41267800-41273400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr15:41267800-41273400	Strong transcription	Lung	lung
34	chr15:41267800-41274400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr15:41267800-41280600	Strong transcription	Fetal Intestine Large	intestine
36	chr15:41267800-41280800	Strong transcription	Ovary	ovary
37	chr15:41267800-41281000	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr15:41267800-41281000	Strong transcription	HUES64 Cell Line	embryonic stem cell
39	chr15:41267800-41282000	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr15:41267800-41284400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr15:41267800-41284600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr15:41267800-41290200	Strong transcription	NHEK	skin
43	chr15:41267800-41290800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr15:41267800-41294200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr15:41267800-41301400	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr15:41268000-41271000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:41268000-41274800	Strong transcription	HSMMtube	muscle
48	chr15:41268000-41274800	Strong transcription	NH-A	brain
49	chr15:41268000-41275000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr15:41268000-41276000	Strong transcription	Thymus	Thymus

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