Variant report

Variant	nsv516239
Chromosome Location	chr14:69010690-69025870
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:523)
CpG islands
(count:183)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:69015834-69016038	K562	blood:	n/a	n/a
2	BHLHE40	chr14:69015838-69016044	K562	blood:	n/a	n/a
3	BRCA1	chr14:69015830-69016095	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr14:69013574-69013834	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr14:69014165-69015458	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr14:69010894-69011277	IMR90	lung:	n/a	n/a
7	CEBPB	chr14:69015797-69016155	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr14:69019246-69019678	ECC-1	luminal epithelium:	n/a	chr14:69019276-69019293 chr14:69019279-69019291
9	CEBPB	chr14:69014981-69015387	IMR90	lung:	n/a	n/a
10	CEBPB	chr14:69014297-69014657	IMR90	lung:	n/a	n/a
11	CEBPB	chr14:69014201-69015363	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr14:69014811-69015431	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr14:69013578-69013944	IMR90	lung:	n/a	n/a
14	CEBPB	chr14:69013519-69013980	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr14:69013458-69013910	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr14:69014130-69015423	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr14:69015730-69016117	Hela-S3	cervix:	n/a	n/a
18	CREB1	chr14:69015779-69016094	A549	lung:	n/a	n/a
19	CREB1	chr14:69014273-69014741	A549	lung:	n/a	n/a
20	CREB1	chr14:69014894-69015255	A549	lung:	n/a	n/a
21	CREB1	chr14:69015689-69016179	A549	lung:	n/a	n/a
22	CREB1	chr14:69014239-69014689	A549	lung:	n/a	n/a
23	CREB1	chr14:69014897-69015381	A549	lung:	n/a	n/a
24	CREB1	chr14:69014773-69015380	ECC-1	luminal epithelium:	n/a	n/a
25	CREB1	chr14:69016978-69017465	A549	lung:	n/a	n/a
26	CREB1	chr14:69014875-69015357	ECC-1	luminal epithelium:	n/a	n/a
27	CTCF	chr14:69014260-69014410	SAEC	small airway:	n/a	n/a
28	CTCF	chr14:69014280-69014430	HPF	lung:	n/a	n/a
29	CTCF	chr14:69014260-69014410	BJ	skin:	n/a	n/a
30	CTCF	chr14:69014340-69014490	HRE	kidney:	n/a	n/a
31	CTCF	chr14:69014300-69014450	SAEC	small airway:	n/a	n/a
32	CTCF	chr14:69023120-69023270	WERI-Rb-1	eye:	n/a	chr14:69023208-69023217
33	CTCF	chr14:69023160-69023310	WERI-Rb-1	eye:	n/a	chr14:69023208-69023217
34	CTCF	chr14:69014300-69014450	AG04449	skin:	n/a	n/a
35	CTCF	chr14:69014340-69014490	RPTEC	kidney:	n/a	n/a
36	CTCF	chr14:69013460-69013710	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr14:69014280-69014430	RPTEC	kidney:	n/a	n/a
38	CTCF	chr14:69014320-69014470	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr14:69023164-69023255	H1-hESC	embryonic stem cell:	n/a	chr14:69023208-69023217
40	CTCF	chr14:69014260-69014410	HMF	breast:	n/a	n/a
41	CTCF	chr14:69014260-69014410	HCFaa	heart:	n/a	n/a
42	CTCF	chr14:69014180-69014330	AG09309	skin:	n/a	n/a
43	CTCF	chr14:69014280-69014430	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr14:69013580-69013730	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr14:69022020-69022170	HMF	breast:	n/a	n/a
46	CTCF	chr14:69014360-69014510	AG10803	skin:	n/a	n/a
47	CTCF	chr14:69014265-69014535	A549	lung:	n/a	n/a
48	CTCF	chr14:69014260-69014410	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr14:69014260-69014410	AG09309	skin:	n/a	n/a
50	CTCF	chr14:69013620-69013770	SAEC	small airway:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69015199-69015249	ProgFib	skin:	n/a
2	chr14:69012387-69012437	IMR90	lung:	fetal
3	chr14:69012387-69012437	HPAEpiC	pulmonary alveolar:	n/a
4	chr14:69020214-69020264	AG09319	gingival:	n/a
5	chr14:69015199-69015249	NT2-D1	testis:	n/a
6	chr14:69012387-69012437	AoSMC	blood vessel:	n/a
7	chr14:69012387-69012437	AG04449	skin:	fetal
8	chr14:69012387-69012437	HCF	heart:	n/a
9	chr14:69020214-69020264	HRPEpiC	eye:	n/a
10	chr14:69015199-69015249	AG04450	lung:	fetal
11	chr14:69020214-69020264	NB4	blood:	n/a
12	chr14:69012387-69012437	Caco-2	colon:	n/a
13	chr14:69012387-69012437	SKMC	muscle:	n/a
14	chr14:69015199-69015249	HCT-116	colon:	n/a
15	chr14:69012387-69012437	PANC-1	pancreas:	n/a
16	chr14:69015199-69015249	HRCEpiC	kidney:	n/a
17	chr14:69020214-69020264	K562	blood:	n/a
18	chr14:69015199-69015249	Jurkat	blood:	n/a
19	chr14:69020214-69020264	GM19239	blood:	n/a
20	chr14:69012387-69012437	NB4	blood:	n/a
21	chr14:69012387-69012437	BE2_C	brain:	n/a
22	chr14:69015199-69015249	HEEpiC	esophagus:	n/a
23	chr14:69020214-69020264	AG04450	lung:	fetal
24	chr14:69015199-69015249	NB4	blood:	n/a
25	chr14:69015199-69015249	HCPEpiC	choroid plexus:	n/a
26	chr14:69012387-69012437	GM19239	blood:	n/a
27	chr14:69020214-69020264	T-47D	breast:	n/a
28	chr14:69012387-69012437	U87	brain:	n/a
29	chr14:69015199-69015249	NHDF-neo	bronchial:	n/a
30	chr14:69020214-69020264	HEK293	kidney:	embryo
31	chr14:69015199-69015249	Caco-2	colon:	n/a
32	chr14:69020214-69020264	HMEC	breast:	n/a
33	chr14:69015199-69015249	AG09309	skin:	n/a
34	chr14:69012387-69012437	SAEC	small airway:	n/a
35	chr14:69015199-69015249	PANC-1	pancreas:	n/a
36	chr14:69020214-69020264	NHDF-neo	bronchial:	n/a
37	chr14:69020214-69020264	GM12892	blood:	n/a
38	chr14:69020214-69020264	ovcar-3	ovarian:	n/a
39	chr14:69020214-69020264	RPTEC	kidney:	n/a
40	chr14:69012387-69012437	HNPCEpiC	eye:	n/a
41	chr14:69012387-69012437	NHDF-neo	bronchial:	n/a
42	chr14:69012387-69012437	NT2-D1	testis:	n/a
43	chr14:69020214-69020264	SK-N-SH_RA	brain:	n/a
44	chr14:69012387-69012437	SK-N-SH	brain:	n/a
45	chr14:69015199-69015249	HCM	heart:	n/a
46	chr14:69012387-69012437	GM12892	blood:	n/a
47	chr14:69020214-69020264	HUVEC	blood vessel:	n/a
48	chr14:69012387-69012437	HEK293	kidney:	embryo
49	chr14:69015199-69015249	HepG2	liver:	n/a
50	chr14:69015199-69015249	BJ	skin:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:69015136..69018224-chr14:69257957..69260697,4	MCF-7	breast:
2	chr14:69019342..69021876-chr14:69025131..69028551,3	MCF-7	breast:
3	chr14:69021201..69023551-chr14:69053894..69056000,2	MCF-7	breast:
4	chr14:69013842..69015927-chr14:69025144..69027586,2	MCF-7	breast:
5	chr14:69014425..69017204-chr14:69022282..69023965,2	K562	blood:
6	chr14:69006886..69009005-chr14:69017187..69019247,2	MCF-7	breast:
7	chr14:69010762..69012583-chr14:69020438..69023361,2	MCF-7	breast:
8	chr14:68926068..68927730-chr14:69025760..69028340,2	MCF-7	breast:
9	chr14:69020493..69021482-chr14:69036415..69037377,20	MCF-7	breast:
10	chr14:69018839..69025167-chr14:69255576..69261923,8	MCF-7	breast:
11	chr14:68989438..68991863-chr14:69015676..69017457,2	MCF-7	breast:
12	chr14:69011818..69014393-chr14:69018316..69020253,2	MCF-7	breast:
13	chr14:69020493..69021399-chr14:69036539..69037377,10	MCF-7	breast:
14	chr14:68931650..68935082-chr14:69022199..69024459,3	MCF-7	breast:
15	chr14:68773930..68776459-chr14:69021069..69023168,2	MCF-7	breast:
16	chr14:68943428..68945388-chr14:69016683..69019444,2	MCF-7	breast:
17	chr14:69013020..69016426-chr14:69030419..69035616,4	MCF-7	breast:
18	chr14:69013842..69015927-chr14:69025144..69027586,2	MCF-7	breast:
19	chr14:69019342..69021876-chr14:69025131..69028551,3	MCF-7	breast:
20	chr14:69020386..69021361-chr14:69036539..69037509,4	MCF-7	breast:
21	chr14:68910903..68913112-chr14:69019388..69021979,2	MCF-7	breast:
22	chr14:69022061..69023580-chr14:69250425..69252837,2	MCF-7	breast:
23	chr14:68994426..68996258-chr14:69013993..69016421,2	MCF-7	breast:
24	chr14:69014425..69017204-chr14:69022282..69023965,2	K562	blood:
25	chr14:68925384..68926445-chr14:69020510..69021409,9	MCF-7	breast:
26	chr14:69013506..69014266-chr16:4321574..4322534,2	HCT-116	colon:
27	chr14:69014687..69017316-chr14:69017983..69019961,2	MCF-7	breast:
28	chr14:68925384..68926445-chr14:69020543..69021388,4	MCF-7	breast:
29	chr14:68923760..68926395-chr14:69020012..69022778,2	MCF-7	breast:
30	chr14:69013185..69015813-chr14:69258202..69261056,2	K562	blood:
31	chr14:68932051..68934015-chr14:69017184..69019251,2	MCF-7	breast:
32	chr14:69012905..69014587-chr14:69260400..69263200,2	MCF-7	breast:
33	chr14:69023246..69027101-chr14:69028219..69030991,3	MCF-7	breast:
34	chr14:69009163..69010827-chr14:69260601..69262528,2	MCF-7	breast:
35	chr14:69014687..69017316-chr14:69017983..69019961,2	MCF-7	breast:
36	chr14:68752714..68755212-chr14:69016133..69017803,2	MCF-7	breast:
37	chr14:69012961..69014809-chr14:69260230..69262550,2	MCF-7	breast:
38	chr14:69007812..69009771-chr14:69024457..69026624,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXD2-6	chr14:69012279-69012341	NONHSAT037485
2	lnc-EXD2-5	chr14:69023216-69023577	NONHSAT037486

No data

Variant related genes	Relation type
RAD51B	TF binding region
RAD51B	CpG island
ENSG00000185650	chromatin interactions
ENSG00000182185	chromatin interactions

Extended variants
information (count: 497 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2842331	chr14:69010690-69010691	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs17105821	chr14:69010731-69010732	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs566797667	chr14:69010787-69010788	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534073667	chr14:69010799-69010800	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs11848742	chr14:69010868-69010869	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs573587306	chr14:69010878-69010879	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs2842330	chr14:69010925-69010926	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs544038519	chr14:69010943-69010944	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs11845733	chr14:69010959-69010960	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs574811032	chr14:69010973-69010974	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs17105822	chr14:69011043-69011044	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563101547	chr14:69011059-69011060	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs528017909	chr14:69011071-69011072	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs373198558	chr14:69011094-69011095	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs182208721	chr14:69011147-69011148	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs376301385	chr14:69011171-69011172	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs148013587	chr14:69011195-69011196	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs17828907	chr14:69011205-69011206	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs17828913	chr14:69011294-69011295	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs529790766	chr14:69011331-69011332	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs548239429	chr14:69011482-69011483	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs566474754	chr14:69011547-69011548	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540363869	chr14:69011554-69011555	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs561418376	chr14:69011574-69011575	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs140804980	chr14:69011664-69011665	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572200261	chr14:69011703-69011704	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs375960324	chr14:69011790-69011791	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs560094576	chr14:69011820-69011821	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs2525528	chr14:69011832-69011833	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs528605611	chr14:69011880-69011881	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs546991670	chr14:69011893-69011894	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs79114897	chr14:69011915-69011916	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs80089772	chr14:69011916-69011917	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs76826567	chr14:69011917-69011918	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs74546732	chr14:69011918-69011919	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs12435759	chr14:69011938-69011939	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs17755925	chr14:69011946-69011947	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs150143333	chr14:69011952-69011953	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs2158358	chr14:69011972-69011973	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs188192900	chr14:69012017-69012018	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs138870849	chr14:69012025-69012026	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs142892966	chr14:69012128-69012129	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs531881069	chr14:69012129-69012130	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs376518105	chr14:69012199-69012200	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs551300200	chr14:69012204-69012205	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs8017678	chr14:69012218-69012219	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs577182288	chr14:69012293-69012294	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs2525529	chr14:69012355-69012356	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566534373	chr14:69012395-69012396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527301775	chr14:69012405-69012406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD

Chromatin state (count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:69002400-69016600	Weak transcription	Gastric	stomach
2	chr14:69005000-69013400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:69005000-69015000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:69006000-69014600	Enhancers	NHDF-Ad	bronchial
5	chr14:69006200-69012000	Weak transcription	Lung	lung
6	chr14:69006400-69013200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr14:69006400-69013800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:69006800-69011200	Weak transcription	Placenta	Placenta
9	chr14:69006800-69011600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr14:69006800-69012800	Weak transcription	Esophagus	oesophagus
11	chr14:69006800-69013800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr14:69006800-69014200	Weak transcription	Brain Substantia Nigra	brain
13	chr14:69006800-69014400	Weak transcription	Brain Hippocampus Middle	brain
14	chr14:69006800-69014600	Weak transcription	Brain Angular Gyrus	brain
15	chr14:69007000-69011000	Weak transcription	Left Ventricle	heart
16	chr14:69007000-69011400	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr14:69007200-69013400	Weak transcription	Right Ventricle	heart
18	chr14:69007400-69013600	Weak transcription	Fetal Heart	heart
19	chr14:69007800-69013800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr14:69007800-69014000	Weak transcription	Brain Anterior Caudate	brain
21	chr14:69008000-69013800	Enhancers	HMEC	breast
22	chr14:69008000-69013800	Enhancers	HSMM	muscle
23	chr14:69008200-69013400	Weak transcription	Ovary	ovary
24	chr14:69008400-69010800	Weak transcription	Fetal Thymus	thymus
25	chr14:69008400-69010800	Weak transcription	Stomach Mucosa	stomach
26	chr14:69008400-69011000	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr14:69008400-69011600	Weak transcription	Fetal Intestine Small	intestine
28	chr14:69008400-69011800	Weak transcription	Spleen	Spleen
29	chr14:69008400-69013600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr14:69008400-69013600	Weak transcription	Fetal Kidney	kidney
31	chr14:69008400-69013800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr14:69008400-69014200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:69009000-69012200	Enhancers	Osteobl	bone
34	chr14:69009000-69013400	Enhancers	NHEK	skin
35	chr14:69009000-69013800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:69009000-69023600	Enhancers	Fetal Muscle Leg	muscle
37	chr14:69009200-69010800	Enhancers	Fetal Brain Male	brain
38	chr14:69009200-69012200	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr14:69009200-69013400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:69009200-69016600	Enhancers	Colon Smooth Muscle	Colon
41	chr14:69009400-69013400	Enhancers	Rectal Smooth Muscle	rectum
42	chr14:69009400-69017600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:69009600-69014600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:69009600-69016000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr14:69009800-69010800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:69009800-69012400	Enhancers	Psoas Muscle	Psoas
47	chr14:69009800-69012400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr14:69009800-69013800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr14:69010000-69011000	Weak transcription	Hela-S3	cervix
50	chr14:69010000-69011800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links