Variant report

Variant	nsv1035855
Chromosome Location	chr14:67935684-67964355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:488)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:67954819-67955693	GM12878	blood:	n/a	n/a
2	ATF2	chr14:67959748-67960269	GM12878	blood:	n/a	n/a
3	ATF2	chr14:67954759-67955830	GM12878	blood:	n/a	n/a
4	BATF	chr14:67954916-67955636	GM12878	blood:	n/a	n/a
5	BATF	chr14:67954843-67955690	GM12878	blood:	n/a	n/a
6	BCL11A	chr14:67955249-67955651	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:67954761-67955701	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
8	BCL11A	chr14:67954907-67955245	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
9	BCL3	chr14:67954848-67955694	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
10	BCL3	chr14:67954795-67955606	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
11	BCLAF1	chr14:67954817-67955786	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
12	BCLAF1	chr14:67954691-67955722	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
13	BHLHE40	chr14:67963909-67964086	K562	blood:	n/a	n/a
14	BHLHE40	chr14:67954835-67955721	GM12878	blood:	n/a	n/a
15	CBX3	chr14:67960035-67960357	K562	blood:	n/a	n/a
16	CBX3	chr14:67959916-67960503	HCT-116	colon:	n/a	n/a
17	CBX3	chr14:67960033-67960467	K562	blood:	n/a	n/a
18	CEBPB	chr14:67955284-67955597	GM12878	blood:	n/a	n/a
19	CEBPB	chr14:67939661-67939765	HepG2	liver:	n/a	chr14:67939708-67939719
20	CEBPB	chr14:67954924-67955210	GM12878	blood:	n/a	n/a
21	CEBPB	chr14:67956934-67957172	HepG2	liver:	n/a	chr14:67957015-67957026 chr14:67957062-67957073
22	CEBPB	chr14:67954719-67955853	GM12878	blood:	n/a	n/a
23	CHD2	chr14:67954787-67955724	GM12878	blood:	n/a	n/a
24	CREB1	chr14:67954884-67955760	GM12878	blood:	n/a	n/a
25	CTCF	chr14:67940576-67940719	H1-hESC	embryonic stem cell:	n/a	chr14:67940658-67940671
26	CTCF	chr14:67952540-67952690	AG04449	skin:	n/a	chr14:67952602-67952611
27	CTCF	chr14:67952460-67952610	RPTEC	kidney:	n/a	n/a
28	CTCF	chr14:67952480-67952630	K562	blood:	n/a	chr14:67952602-67952611
29	CTCF	chr14:67952600-67952750	GM12864	blood:	n/a	chr14:67952602-67952611
30	CTCF	chr14:67955531-67955622	GM12878	blood:	n/a	n/a
31	CTCF	chr14:67952580-67952730	GM12875	blood:	n/a	chr14:67952602-67952611
32	CTCF	chr14:67954800-67954950	GM12865	blood:	n/a	n/a
33	CTCF	chr14:67952480-67952630	HMF	breast:	n/a	chr14:67952602-67952611
34	CTCF	chr14:67952520-67952670	HRPEpiC	eye:	n/a	chr14:67952602-67952611
35	CTCF	chr14:67952420-67952570	SAEC	small airway:	n/a	n/a
36	CTCF	chr14:67954900-67955050	GM12874	blood:	n/a	n/a
37	CTCF	chr14:67952520-67952670	HepG2	liver:	n/a	chr14:67952602-67952611
38	CTCF	chr14:67955393-67955700	GM12878	blood:	n/a	n/a
39	CTCF	chr14:67940565-67940748	K562	blood:	n/a	chr14:67940658-67940671
40	CTCF	chr14:67952480-67952630	GM12872	blood:	n/a	chr14:67952602-67952611
41	CTCF	chr14:67952569-67952636	HepG2	liver:	n/a	chr14:67952602-67952611
42	CTCF	chr14:67952560-67952710	GM12865	blood:	n/a	chr14:67952602-67952611
43	CTCF	chr14:67952340-67952490	HCT-116	colon:	n/a	n/a
44	CTCF	chr14:67954860-67955150	GM12869	blood:	n/a	n/a
45	CTCF	chr14:67952560-67952710	GM12874	blood:	n/a	chr14:67952602-67952611
46	CTCF	chr14:67954800-67954950	GM12864	blood:	n/a	n/a
47	CTCF	chr14:67952480-67952630	GM12873	blood:	n/a	chr14:67952602-67952611
48	CTCF	chr14:67952540-67952690	HBMEC	blood vessel:	n/a	chr14:67952602-67952611
49	CTCF	chr14:67955080-67955230	GM12873	blood:	n/a	n/a
50	CTCF	chr14:67954860-67955010	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67940178-67940228	GM12878	blood:	n/a
2	chr14:67940178-67940228	ProgFib	skin:	n/a
3	chr14:67943755-67943805	GM12891	blood:	n/a
4	chr14:67940425-67940475	K562	blood:	n/a
5	chr14:67940425-67940475	SK-N-MC	brain:	n/a
6	chr14:67937737-67937787	NT2-D1	testis:	n/a
7	chr14:67940035-67940085	BE2_C	brain:	n/a
8	chr14:67940035-67940085	A549	lung:	n/a
9	chr14:67940035-67940085	SAEC	small airway:	n/a
10	chr14:67940425-67940475	HRE	kidney:	n/a
11	chr14:67943755-67943805	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:67940669-67940719	NHBE	bronchial:	n/a
13	chr14:67943755-67943805	HEEpiC	esophagus:	n/a
14	chr14:67937737-67937787	NHBE	bronchial:	n/a
15	chr14:67940035-67940085	AoSMC	blood vessel:	n/a
16	chr14:67957839-67957889	HEEpiC	esophagus:	n/a
17	chr14:67940425-67940475	PANC-1	pancreas:	n/a
18	chr14:67937737-67937787	HEEpiC	esophagus:	n/a
19	chr14:67940669-67940719	HUVEC	blood vessel:	n/a
20	chr14:67940425-67940475	HMEC	breast:	n/a
21	chr14:67943755-67943805	ECC-1	luminal epithelium:	n/a
22	chr14:67940178-67940228	HRPEpiC	eye:	n/a
23	chr14:67941820-67941870	HIPEpiC	eye:	n/a
24	chr14:67943755-67943805	LNCaP	prostate:	n/a
25	chr14:67940425-67940475	U87	brain:	n/a
26	chr14:67957839-67957889	HRPEpiC	eye:	n/a
27	chr14:67940178-67940228	HEK293	kidney:	embryo
28	chr14:67943755-67943805	ovcar-3	ovarian:	n/a
29	chr14:67940425-67940475	ProgFib	skin:	n/a
30	chr14:67941820-67941870	SK-N-SH_RA	brain:	n/a
31	chr14:67937737-67937787	BJ	skin:	n/a
32	chr14:67940035-67940085	PrEC	prostate:	n/a
33	chr14:67941820-67941870	GM06990	blood:	n/a
34	chr14:67957839-67957889	IMR90	lung:	fetal
35	chr14:67940425-67940475	GM12878	blood:	n/a
36	chr14:67940035-67940085	NB4	blood:	n/a
37	chr14:67937737-67937787	HAEpiC	amniotic membrane:	n/a
38	chr14:67941820-67941870	ECC-1	luminal epithelium:	n/a
39	chr14:67940669-67940719	Jurkat	blood:	n/a
40	chr14:67943755-67943805	BE2_C	brain:	n/a
41	chr14:67940425-67940475	GM06990	blood:	n/a
42	chr14:67940669-67940719	RPTEC	kidney:	n/a
43	chr14:67957839-67957889	HIPEpiC	eye:	n/a
44	chr14:67940178-67940228	HMEC	breast:	n/a
45	chr14:67940035-67940085	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:67940425-67940475	LNCaP	prostate:	n/a
47	chr14:67940035-67940085	K562	blood:	n/a
48	chr14:67940669-67940719	SK-N-SH_RA	brain:	n/a
49	chr14:67957839-67957889	T-47D	breast:	n/a
50	chr14:67943755-67943805	AG09319	gingival:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:67908880..67909947-chr14:67946478..67947292,3	MCF-7	breast:
2	chr14:67907067..67911151-chr14:67944659..67948573,6	MCF-7	breast:
3	chr14:67960402..67962099-chr14:67962938..67964502,2	MCF-7	breast:
4	chr14:67919473..67920342-chr14:67946537..67947177,3	MCF-7	breast:
5	chr14:67954443..67956751-chr14:67999962..68001506,2	MCF-7	breast:
6	chr14:67944442..67947234-chr14:67997536..68000572,3	MCF-7	breast:
7	chr14:67944168..67950756-chr14:67978926..67983400,9	MCF-7	breast:
8	chr14:67945813..67949224-chr14:67990739..67993658,4	MCF-7	breast:
9	chr14:67946462..67947472-chr14:68000220..68001028,4	MCF-7	breast:
10	chr14:67946842..67948505-chr14:67958854..67960376,2	MCF-7	breast:
11	chr14:67952500..67954302-chr14:67954353..67956306,2	K562	blood:
12	chr14:67955748..67958630-chr14:67960758..67962478,3	MCF-7	breast:
13	chr14:67937786..67940325-chr14:67940798..67942852,2	MCF-7	breast:
14	chr14:67946457..67947472-chr14:68000217..68001213,11	MCF-7	breast:
15	chr14:67908929..67909688-chr14:67946732..67947393,3	MCF-7	breast:
16	chr14:67935396..67937435-chr14:67945472..67948247,2	MCF-7	breast:
17	chr14:67928154..67928999-chr14:67946524..67947358,3	MCF-7	breast:
18	chr14:67937786..67940325-chr14:67940798..67942852,2	MCF-7	breast:
19	chr14:67928466..67932816-chr14:67938653..67942762,5	MCF-7	breast:
20	chr14:67932706..67934759-chr14:67935532..67938182,2	K562	blood:
21	chr14:67945819..67948998-chr14:67952251..67955708,4	MCF-7	breast:
22	chr14:67935565..67937568-chr14:67945579..67947744,3	MCF-7	breast:
23	chr14:67953372..67955912-chr14:67957756..67960248,2	K562	blood:
24	chr14:67919473..67920365-chr14:67946537..67947323,6	MCF-7	breast:
25	chr14:67945430..67947453-chr14:67950590..67952638,3	MCF-7	breast:
26	chr14:67946481..67947300-chr14:67979982..67980806,3	MCF-7	breast:
27	chr14:67958532..67960462-chr14:67983895..67986078,2	MCF-7	breast:
28	chr14:67945641..67948338-chr14:67966357..67969353,2	MCF-7	breast:
29	chr14:67946150..67948174-chr14:67950017..67952096,2	MCF-7	breast:
30	chr14:67912599..67913704-chr14:67946532..67947321,6	MCF-7	breast:
31	chr14:67950772..67953650-chr14:67961025..67964119,3	MCF-7	breast:
32	chr14:67939344..67942070-chr14:67946929..67950674,3	MCF-7	breast:
33	chr14:67913108..67915439-chr14:67935952..67938092,2	MCF-7	breast:
34	chr14:67939344..67942070-chr14:67946929..67950674,3	MCF-7	breast:
35	chr14:67908947..67909688-chr14:67946562..67947331,3	MCF-7	breast:
36	chr14:67928246..67929078-chr14:67946550..67947331,3	MCF-7	breast:
37	chr14:67938787..67940976-chr14:67998285..68000377,3	MCF-7	breast:
38	chr14:67950772..67953650-chr14:67961025..67964119,3	MCF-7	breast:
39	chr14:67903388..67905312-chr14:67950420..67951946,2	MCF-7	breast:
40	chr14:67935396..67937435-chr14:67945472..67948247,2	MCF-7	breast:
41	chr14:67945315..67948095-chr14:67972222..67974425,2	MCF-7	breast:
42	chr14:67932881..67935193-chr14:67939104..67941762,2	MCF-7	breast:
43	chr14:67925170..67927732-chr14:67942012..67943534,2	K562	blood:
44	chr14:67945430..67947453-chr14:67950590..67952638,3	MCF-7	breast:
45	chr14:67946150..67948174-chr14:67950017..67952096,2	MCF-7	breast:
46	chr14:67946842..67948505-chr14:67958854..67960376,2	MCF-7	breast:
47	chr14:67950274..67952126-chr14:67954353..67957172,2	MCF-7	breast:
48	chr14:67945105..67947990-chr14:67956817..67958766,2	MCF-7	breast:
49	chr14:67912569..67913643-chr14:67946452..67947328,6	MCF-7	breast:
50	chr14:67935565..67937568-chr14:67945579..67947744,3	MCF-7	breast:

No data

Variant related genes	Relation type
TMEM229B	TF binding region
TMEM229B	CpG island
ENSG00000054690	chromatin interactions
ENSG00000198133	chromatin interactions
ENSG00000265993	chromatin interactions

Extended variants
information (count: 1116 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1116 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545348550	chr14:67935706-67935707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs571839406	chr14:67935736-67935737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564127974	chr14:67935753-67935754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369385458	chr14:67935757-67935758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182686072	chr14:67935772-67935773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs374239409	chr14:67935779-67935780	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549471035	chr14:67935780-67935781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532584898	chr14:67935827-67935828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187011072	chr14:67935842-67935843	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs148699882	chr14:67935902-67935903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547552702	chr14:67935933-67935934	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs376312967	chr14:67935936-67935937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141327105	chr14:67935992-67935993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs1315737	chr14:67936045-67936046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs551351653	chr14:67936053-67936054	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11312015	chr14:67936065-67936066	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs191497974	chr14:67936087-67936088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571793095	chr14:67936114-67936115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs537395503	chr14:67936152-67936153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537269311	chr14:67936182-67936183	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555938919	chr14:67936190-67936191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150784254	chr14:67936214-67936215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs117948490	chr14:67936255-67936256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs117616274	chr14:67936264-67936265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552768250	chr14:67936284-67936285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60226469	chr14:67936310-67936311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115559568	chr14:67936337-67936338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs142291421	chr14:67936363-67936364	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372182380	chr14:67936364-67936365	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184514499	chr14:67936366-67936367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557325919	chr14:67936375-67936376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs575681179	chr14:67936396-67936397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543003296	chr14:67936408-67936409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs1315736	chr14:67936423-67936424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs528931832	chr14:67936462-67936463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540737778	chr14:67936471-67936472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs1315735	chr14:67936482-67936483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs532942803	chr14:67936483-67936484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs11623116	chr14:67936493-67936494	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551654858	chr14:67936509-67936510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569962066	chr14:67936530-67936531	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542629197	chr14:67936566-67936567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530964617	chr14:67936569-67936570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs549377684	chr14:67936576-67936577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs11623164	chr14:67936612-67936613	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567637122	chr14:67936615-67936616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560919278	chr14:67936621-67936622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187487629	chr14:67936631-67936632	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs193274623	chr14:67936713-67936714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538857065	chr14:67936721-67936722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:842 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67928800-67946600	Weak transcription	Pancreas	Pancrea
2	chr14:67929600-67942600	Weak transcription	Lung	lung
3	chr14:67929800-67938600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr14:67931200-67939600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr14:67931400-67939000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:67931800-67938600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:67932000-67939600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr14:67932800-67937600	Weak transcription	Primary T cells from cord blood	blood
9	chr14:67932800-67939200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:67932800-67940000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:67933000-67954400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr14:67933200-67939400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr14:67934000-67936400	Weak transcription	Small Intestine	intestine
14	chr14:67934400-67939400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr14:67934600-67938800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr14:67934600-67939000	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr14:67934600-67950600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:67934800-67939200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr14:67934800-67946800	Weak transcription	Placenta	Placenta
20	chr14:67935000-67977200	Weak transcription	Brain Angular Gyrus	brain
21	chr14:67935200-67936600	Weak transcription	Colonic Mucosa	Colon
22	chr14:67935200-67937800	Weak transcription	Thymus	Thymus
23	chr14:67935200-67938400	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr14:67935200-67946800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr14:67935200-67952200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr14:67935400-67935800	Weak transcription	Duodenum Mucosa	Duodenum
27	chr14:67935400-67935800	Weak transcription	Fetal Thymus	thymus
28	chr14:67935400-67936400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr14:67935400-67936600	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr14:67935400-67936600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr14:67935400-67938600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr14:67935400-67940200	Weak transcription	Fetal Intestine Large	intestine
33	chr14:67935400-67945200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr14:67935600-67937400	Weak transcription	Fetal Intestine Small	intestine
35	chr14:67935800-67936000	Enhancers	Fetal Thymus	thymus
36	chr14:67935800-67937400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:67935800-67937400	Enhancers	Duodenum Mucosa	Duodenum
38	chr14:67936000-67939600	Weak transcription	Fetal Thymus	thymus
39	chr14:67936000-67952000	Weak transcription	Brain Substantia Nigra	brain
40	chr14:67936400-67936600	Enhancers	Small Intestine	intestine
41	chr14:67936400-67937000	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr14:67936600-67936800	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr14:67936600-67937200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr14:67936600-67937400	Enhancers	Colonic Mucosa	Colon
45	chr14:67936800-67937200	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr14:67936800-67938600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr14:67937000-67937200	Active TSS	Spleen	Spleen
48	chr14:67937000-67939800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr14:67937200-67937400	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr14:67937200-67937600	Weak transcription	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links