Variant report

Variant	nsv1048046
Chromosome Location	chr14:67932876-67958467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:430)
CpG islands
(count:490)
Chromatin interactive
region (count:50)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr14:67954759-67955830	GM12878	blood:	n/a	n/a
3	BATF	chr14:67954843-67955690	GM12878	blood:	n/a	n/a
4	BATF	chr14:67954916-67955636	GM12878	blood:	n/a	n/a
5	BCL11A	chr14:67954761-67955701	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
6	BCL11A	chr14:67954907-67955245	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
7	BCL11A	chr14:67955249-67955651	GM12878	blood:	n/a	n/a
8	BCL3	chr14:67954848-67955694	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
9	BCL3	chr14:67954795-67955606	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
10	BCLAF1	chr14:67954817-67955786	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
11	BCLAF1	chr14:67954691-67955722	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
12	BHLHE40	chr14:67954835-67955721	GM12878	blood:	n/a	n/a
13	CEBPB	chr14:67954719-67955853	GM12878	blood:	n/a	n/a
14	CEBPB	chr14:67954924-67955210	GM12878	blood:	n/a	n/a
15	CEBPB	chr14:67955284-67955597	GM12878	blood:	n/a	n/a
16	CEBPB	chr14:67939661-67939765	HepG2	liver:	n/a	chr14:67939708-67939719
17	CEBPB	chr14:67956934-67957172	HepG2	liver:	n/a	chr14:67957015-67957026 chr14:67957062-67957073
18	CHD2	chr14:67954787-67955724	GM12878	blood:	n/a	n/a
19	CREB1	chr14:67954884-67955760	GM12878	blood:	n/a	n/a
20	CTCF	chr14:67934380-67934530	GM12865	blood:	n/a	n/a
21	CTCF	chr14:67934420-67934570	GM12871	blood:	n/a	n/a
22	CTCF	chr14:67952520-67952670	WERI-Rb-1	eye:	n/a	chr14:67952602-67952611
23	CTCF	chr14:67934400-67934550	HRE	kidney:	n/a	n/a
24	CTCF	chr14:67934420-67934570	GM12869	blood:	n/a	n/a
25	CTCF	chr14:67955435-67955572	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr14:67934294-67934634	GM12878	blood:	n/a	n/a
27	CTCF	chr14:67934380-67934530	GM12878	blood:	n/a	n/a
28	CTCF	chr14:67934440-67934590	GM12870	blood:	n/a	n/a
29	CTCF	chr14:67952520-67952670	HepG2	liver:	n/a	chr14:67952602-67952611
30	CTCF	chr14:67934302-67934517	A549	lung:	n/a	n/a
31	CTCF	chr14:67934340-67934490	HEK293	kidney:	n/a	n/a
32	CTCF	chr14:67940576-67940719	H1-hESC	embryonic stem cell:	n/a	chr14:67940658-67940671
33	CTCF	chr14:67934420-67934570	HFF	foreskin:	n/a	n/a
34	CTCF	chr14:67934420-67934570	AG04449	skin:	n/a	n/a
35	CTCF	chr14:67952503-67952728	K562	blood:	n/a	chr14:67952602-67952611
36	CTCF	chr14:67934380-67934530	GM12864	blood:	n/a	n/a
37	CTCF	chr14:67934435-67934469	A549	lung:	n/a	n/a
38	CTCF	chr14:67952608-67952614	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr14:67934396-67934523	GM10248	blood:	n/a	n/a
40	CTCF	chr14:67934320-67934470	AG09309	skin:	n/a	n/a
41	CTCF	chr14:67952560-67952710	HUVEC	blood vessel:	n/a	chr14:67952602-67952611
42	CTCF	chr14:67934340-67934490	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr14:67952340-67952490	HCT-116	colon:	n/a	n/a
44	CTCF	chr14:67934360-67934510	GM12874	blood:	n/a	n/a
45	CTCF	chr14:67934340-67934490	NHLF	lung:	n/a	n/a
46	CTCF	chr14:67932960-67933110	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr14:67955004-67955056	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr14:67954980-67955130	GM06990	blood:	n/a	n/a
49	CTCF	chr14:67952480-67952630	K562	blood:	n/a	chr14:67952602-67952611
50	CTCF	chr14:67954860-67955010	GM12878	blood:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67943755-67943805	HRPEpiC	eye:	n/a
2	chr14:67943755-67943805	SAEC	small airway:	n/a
3	chr14:67943755-67943805	HRPEpiC	eye:	n/a
4	chr14:67943755-67943805	SAEC	small airway:	n/a
5	chr14:67941820-67941870	BJ	skin:	n/a
6	chr14:67940425-67940475	HCPEpiC	choroid plexus:	n/a
7	chr14:67941820-67941870	GM12878	blood:	n/a
8	chr14:67940035-67940085	K562	blood:	n/a
9	chr14:67943755-67943805	AG09309	skin:	n/a
10	chr14:67941820-67941870	PANC-1	pancreas:	n/a
11	chr14:67957839-67957889	HIPEpiC	eye:	n/a
12	chr14:67937737-67937787	HCT-116	colon:	n/a
13	chr14:67940669-67940719	Jurkat	blood:	n/a
14	chr14:67940425-67940475	NB4	blood:	n/a
15	chr14:67940178-67940228	BJ	skin:	n/a
16	chr14:67940425-67940475	AoSMC	blood vessel:	n/a
17	chr14:67957839-67957889	PFSK-1	brain:	n/a
18	chr14:67940425-67940475	BE2_C	brain:	n/a
19	chr14:67940669-67940719	MCF-7	breast:	n/a
20	chr14:67940035-67940085	Hela-S3	cervix:	n/a
21	chr14:67941820-67941870	Jurkat	blood:	n/a
22	chr14:67940035-67940085	T-47D	breast:	n/a
23	chr14:67943755-67943805	SK-N-MC	brain:	n/a
24	chr14:67941820-67941870	SK-N-SH_RA	brain:	n/a
25	chr14:67957839-67957889	RPTEC	kidney:	n/a
26	chr14:67943755-67943805	Jurkat	blood:	n/a
27	chr14:67937737-67937787	MCF-7	breast:	n/a
28	chr14:67937737-67937787	HEEpiC	esophagus:	n/a
29	chr14:67940035-67940085	SK-N-SH	brain:	n/a
30	chr14:67937737-67937787	AG10803	skin:	n/a
31	chr14:67937737-67937787	H1-hESC	embryonic stem cell:	embryo
32	chr14:67940178-67940228	A549	lung:	n/a
33	chr14:67940035-67940085	NHDF-neo	bronchial:	n/a
34	chr14:67937737-67937787	LNCaP	prostate:	n/a
35	chr14:67957839-67957889	GM12892	blood:	n/a
36	chr14:67940035-67940085	GM12891	blood:	n/a
37	chr14:67940035-67940085	GM19239	blood:	n/a
38	chr14:67941820-67941870	Caco-2	colon:	n/a
39	chr14:67941820-67941870	HMEC	breast:	n/a
40	chr14:67941820-67941870	GM12892	blood:	n/a
41	chr14:67940035-67940085	AoSMC	blood vessel:	n/a
42	chr14:67940178-67940228	PFSK-1	brain:	n/a
43	chr14:67937737-67937787	U87	brain:	n/a
44	chr14:67937737-67937787	GM06990	blood:	n/a
45	chr14:67940669-67940719	NHBE	bronchial:	n/a
46	chr14:67940035-67940085	BJ	skin:	n/a
47	chr14:67957839-67957889	SK-N-SH_RA	brain:	n/a
48	chr14:67937737-67937787	GM12878	blood:	n/a
49	chr14:67940178-67940228	HAEpiC	amniotic membrane:	n/a
50	chr14:67957839-67957889	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:67939344..67942070-chr14:67946929..67950674,3	MCF-7	breast:
2	chr14:67908947..67909688-chr14:67946562..67947331,3	MCF-7	breast:
3	chr14:67944168..67950756-chr14:67978926..67983400,9	MCF-7	breast:
4	chr14:67908880..67909947-chr14:67946478..67947292,3	MCF-7	breast:
5	chr14:67939344..67942070-chr14:67946929..67950674,3	MCF-7	breast:
6	chr14:67945105..67947990-chr14:67956817..67958766,2	MCF-7	breast:
7	chr14:67944442..67947234-chr14:67997536..68000572,3	MCF-7	breast:
8	chr14:67937786..67940325-chr14:67940798..67942852,2	MCF-7	breast:
9	chr14:67955748..67958630-chr14:67960758..67962478,3	MCF-7	breast:
10	chr14:67907067..67911151-chr14:67944659..67948573,6	MCF-7	breast:
11	chr14:67946457..67947472-chr14:68000217..68001213,11	MCF-7	breast:
12	chr14:67953372..67955912-chr14:67957756..67960248,2	K562	blood:
13	chr14:67952500..67954302-chr14:67954353..67956306,2	K562	blood:
14	chr14:67919473..67920365-chr14:67946537..67947323,6	MCF-7	breast:
15	chr14:67935565..67937568-chr14:67945579..67947744,3	MCF-7	breast:
16	chr14:67946150..67948174-chr14:67950017..67952096,2	MCF-7	breast:
17	chr14:67935396..67937435-chr14:67945472..67948247,2	MCF-7	breast:
18	chr14:67913108..67915439-chr14:67935952..67938092,2	MCF-7	breast:
19	chr14:67908929..67909688-chr14:67946732..67947393,3	MCF-7	breast:
20	chr14:67945105..67947990-chr14:67956817..67958766,2	MCF-7	breast:
21	chr14:67946481..67947300-chr14:67979982..67980806,3	MCF-7	breast:
22	chr14:67919473..67920342-chr14:67946537..67947177,3	MCF-7	breast:
23	chr14:67946150..67948174-chr14:67950017..67952096,2	MCF-7	breast:
24	chr14:67950274..67952126-chr14:67954353..67957172,2	MCF-7	breast:
25	chr14:67903388..67905312-chr14:67950420..67951946,2	MCF-7	breast:
26	chr14:67928466..67932816-chr14:67938653..67942762,5	MCF-7	breast:
27	chr14:67954053..67956925-chr14:67980005..67982672,2	MCF-7	breast:
28	chr14:67946762..67947287-chr14:67969455..67970025,2	MCF-7	breast:
29	chr14:67928154..67928999-chr14:67946524..67947358,3	MCF-7	breast:
30	chr14:67946842..67948505-chr14:67958854..67960376,2	MCF-7	breast:
31	chr14:67935396..67937435-chr14:67945472..67948247,2	MCF-7	breast:
32	chr14:67914287..67914992-chr14:67934220..67935041,2	MCF-7	breast:
33	chr14:67912599..67913704-chr14:67946532..67947321,6	MCF-7	breast:
34	chr14:67954443..67956751-chr14:67999962..68001506,2	MCF-7	breast:
35	chr14:67945315..67948095-chr14:67972222..67974425,2	MCF-7	breast:
36	chr14:67946462..67947472-chr14:68000220..68001028,4	MCF-7	breast:
37	chr14:67925170..67927732-chr14:67942012..67943534,2	K562	blood:
38	chr14:67938787..67940976-chr14:67998285..68000377,3	MCF-7	breast:
39	chr14:67932881..67935193-chr14:67939104..67941762,2	MCF-7	breast:
40	chr14:67945813..67949224-chr14:67990739..67993658,4	MCF-7	breast:
41	chr14:67950772..67953650-chr14:67961025..67964119,3	MCF-7	breast:
42	chr14:67945641..67948338-chr14:67966357..67969353,2	MCF-7	breast:
43	chr14:67928246..67929078-chr14:67946550..67947331,3	MCF-7	breast:
44	chr14:67945819..67948998-chr14:67952251..67955708,4	MCF-7	breast:
45	chr14:67935565..67937568-chr14:67945579..67947744,3	MCF-7	breast:
46	chr14:67937786..67940325-chr14:67940798..67942852,2	MCF-7	breast:
47	chr14:67912569..67913643-chr14:67946452..67947328,6	MCF-7	breast:
48	chr14:67945430..67947453-chr14:67950590..67952638,3	MCF-7	breast:
49	chr14:67945430..67947453-chr14:67950590..67952638,3	MCF-7	breast:
50	chr14:67932706..67934759-chr14:67935532..67938182,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEK2-2	chr14:67933821-67934635	NONHSAT037445

No data

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

Extended variants
information (count: 992 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:992 , 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	rs575285683	chr14:67932896-67932897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372706482	chr14:67932962-67932963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143791937	chr14:67932973-67932974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554663742	chr14:67932987-67932988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573078066	chr14:67933007-67933008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139608335	chr14:67933054-67933055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565222046	chr14:67933089-67933090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181949649	chr14:67933090-67933091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544619813	chr14:67933119-67933120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376516601	chr14:67933147-67933148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529998013	chr14:67933175-67933176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548281514	chr14:67933222-67933223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370303851	chr14:67933280-67933281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187032128	chr14:67933282-67933283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576078028	chr14:67933305-67933306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76672232	chr14:67933326-67933327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149723420	chr14:67933339-67933340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571151513	chr14:67933346-67933347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538179035	chr14:67933354-67933355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115759698	chr14:67933414-67933415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568878297	chr14:67933525-67933526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536205766	chr14:67933540-67933541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554751708	chr14:67933553-67933554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188960720	chr14:67933583-67933584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145557814	chr14:67933659-67933660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148436877	chr14:67933660-67933661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576939301	chr14:67933665-67933666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs57229350	chr14:67933670-67933671	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs181365827	chr14:67933690-67933691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112903127	chr14:67933691-67933692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185640301	chr14:67933704-67933705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560251937	chr14:67933707-67933708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs397852017	chr14:67933712-67933713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs398043793	chr14:67933732-67933733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs398025489	chr14:67933733-67933734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561803969	chr14:67933734-67933735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75023382	chr14:67933742-67933743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190004606	chr14:67933744-67933745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180860720	chr14:67933758-67933759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546250964	chr14:67933774-67933775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564542320	chr14:67933799-67933800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11851098	chr14:67933804-67933805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs377415706	chr14:67933829-67933830	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs375625753	chr14:67933855-67933856	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs144567624	chr14:67933895-67933896	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs568766393	chr14:67933899-67933900	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs113621920	chr14:67933911-67933912	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs548189084	chr14:67933928-67933929	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs35645080	chr14:67933937-67933938	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs566597311	chr14:67933938-67933939	Weak transcription Enhancers	lncRNA	n/a	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:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67927800-67935400	Enhancers	Fetal Thymus	thymus
2	chr14:67928200-67935200	Enhancers	Thymus	Thymus
3	chr14:67928600-67934400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr14:67928800-67933800	Weak transcription	Fetal Intestine Large	intestine
5	chr14:67928800-67946600	Weak transcription	Pancreas	Pancrea
6	chr14:67929000-67934000	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr14:67929200-67933800	Weak transcription	Fetal Intestine Small	intestine
8	chr14:67929600-67942600	Weak transcription	Lung	lung
9	chr14:67929800-67938600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr14:67930200-67934000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr14:67930400-67935400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr14:67931200-67939600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr14:67931400-67939000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:67931800-67938600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr14:67932000-67934000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr14:67932000-67934200	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr14:67932000-67939600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr14:67932200-67933800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr14:67932200-67934200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr14:67932400-67933800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr14:67932400-67934000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr14:67932600-67933200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr14:67932600-67933200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr14:67932600-67934000	Enhancers	Duodenum Mucosa	Duodenum
25	chr14:67932600-67934400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr14:67932800-67933000	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr14:67932800-67933800	Weak transcription	Placenta	Placenta
28	chr14:67932800-67934000	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr14:67932800-67937600	Weak transcription	Primary T cells from cord blood	blood
30	chr14:67932800-67939200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:67932800-67940000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr14:67933000-67954400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr14:67933200-67934000	Enhancers	Small Intestine	intestine
34	chr14:67933200-67939400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr14:67933800-67934400	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr14:67933800-67934800	Enhancers	Placenta	Placenta
37	chr14:67933800-67935200	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr14:67933800-67935400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr14:67933800-67935400	Enhancers	Fetal Intestine Large	intestine
40	chr14:67933800-67935600	Enhancers	Fetal Intestine Small	intestine
41	chr14:67934000-67934400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr14:67934000-67934600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr14:67934000-67934600	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr14:67934000-67935200	Enhancers	Primary T cells fromperipheralblood	blood
45	chr14:67934000-67935200	Flanking Active TSS	Duodenum Mucosa	Duodenum
46	chr14:67934000-67935400	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr14:67934000-67936400	Weak transcription	Small Intestine	intestine
48	chr14:67934200-67934400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr14:67934200-67934400	Bivalent Enhancer	HepG2	liver
50	chr14:67934200-67934600	Enhancers	Primary T helper cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links