Variant report

Variant	esv1794822
Chromosome Location	chr14:35755087-35761366
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:598)
CpG islands
(count:244)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35761081-35761818	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35759977-35760372	HepG2	liver:	n/a	n/a
3	ATF2	chr14:35761056-35761846	GM12878	blood:	n/a	n/a
4	ATF2	chr14:35761033-35761707	GM12878	blood:	n/a	n/a
5	ATF2	chr14:35754385-35755598	GM12878	blood:	n/a	n/a
6	ATF2	chr14:35754239-35755796	GM12878	blood:	n/a	n/a
7	ATF2	chr14:35756617-35757269	GM12878	blood:	n/a	n/a
8	ATF3	chr14:35761088-35761778	A549	lung:	n/a	chr14:35761499-35761508
9	BACH1	chr14:35761241-35761956	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr14:35761159-35761679	GM12878	blood:	n/a	chr14:35761412-35761420
11	BATF	chr14:35754332-35755553	GM12878	blood:	n/a	n/a
12	BATF	chr14:35754462-35755192	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:35754449-35755253	GM12878	blood:	n/a	chr14:35755115-35755124
14	BCL11A	chr14:35754512-35755241	GM12878	blood:	n/a	chr14:35755115-35755124
15	BCL3	chr14:35761106-35762076	A549	lung:	n/a	n/a
16	BCL3	chr14:35761121-35762015	GM12878	blood:	n/a	n/a
17	BCL3	chr14:35761055-35762324	A549	lung:	n/a	n/a
18	BCLAF1	chr14:35754245-35755679	GM12878	blood:	n/a	chr14:35755115-35755124
19	BCLAF1	chr14:35754318-35755358	GM12878	blood:	n/a	chr14:35755115-35755124
20	BCLAF1	chr14:35760949-35761900	GM12878	blood:	n/a	n/a
21	BCLAF1	chr14:35761125-35761849	GM12878	blood:	n/a	n/a
22	BHLHE40	chr14:35754435-35755560	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:35761085-35761833	GM12878	blood:	n/a	n/a
24	BHLHE40	chr14:35756719-35757058	GM12878	blood:	n/a	n/a
25	BHLHE40	chr14:35761227-35761981	HepG2	liver:	n/a	n/a
26	BHLHE40	chr14:35761252-35761995	K562	blood:	n/a	n/a
27	BRCA1	chr14:35761203-35761723	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr14:35761264-35761915	HepG2	liver:	n/a	n/a
29	CBX3	chr14:35761126-35761734	K562	blood:	n/a	n/a
30	CCNT2	chr14:35761345-35762173	K562	blood:	n/a	chr14:35761499-35761508
31	CEBPB	chr14:35761287-35761704	K562	blood:	n/a	n/a
32	CEBPB	chr14:35760930-35761866	GM12878	blood:	n/a	n/a
33	CEBPB	chr14:35761242-35761761	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:35754364-35755796	GM12878	blood:	n/a	n/a
35	CEBPB	chr14:35754602-35755240	GM12878	blood:	n/a	n/a
36	CEBPB	chr14:35761095-35761854	HepG2	liver:	n/a	n/a
37	CEBPB	chr14:35761261-35761749	HepG2	liver:	n/a	n/a
38	CEBPD	chr14:35761042-35762108	HepG2	liver:	n/a	n/a
39	CEBPD	chr14:35761324-35761805	K562	blood:	n/a	n/a
40	CEBPD	chr14:35761184-35762021	HepG2	liver:	n/a	n/a
41	CEBPD	chr14:35760079-35760550	HepG2	liver:	n/a	n/a
42	CHD1	chr14:35761060-35761260	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr14:35761068-35761307	GM12878	blood:	n/a	n/a
44	CHD1	chr14:35754526-35755291	GM12878	blood:	n/a	n/a
45	CHD2	chr14:35756022-35756024	GM12878	blood:	n/a	n/a
46	CHD2	chr14:35754521-35755588	GM12878	blood:	n/a	n/a
47	CHD2	chr14:35761131-35762049	K562	blood:	n/a	n/a
48	CHD2	chr14:35761152-35761854	GM12878	blood:	n/a	n/a
49	CHD2	chr14:35761219-35761887	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr14:35761149-35762068	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35761197-35761247	HNPCEpiC	eye:	n/a
2	chr14:35761197-35761247	AG04449	skin:	fetal
3	chr14:35761165-35761215	ovcar-3	ovarian:	n/a
4	chr14:35761165-35761215	BJ	skin:	n/a
5	chr14:35757441-35757491	GM19239	blood:	n/a
6	chr14:35761165-35761215	AG10803	skin:	n/a
7	chr14:35761197-35761247	HCPEpiC	choroid plexus:	n/a
8	chr14:35761197-35761247	ProgFib	skin:	n/a
9	chr14:35761327-35761377	NHDF-neo	bronchial:	n/a
10	chr14:35761197-35761247	H1-hESC	embryonic stem cell:	embryo
11	chr14:35761165-35761215	GM12878	blood:	n/a
12	chr14:35761165-35761215	HMEC	breast:	n/a
13	chr14:35761197-35761247	SKMC	muscle:	n/a
14	chr14:35761327-35761377	NH-A	brain:	n/a
15	chr14:35761165-35761215	HEK293	kidney:	embryo
16	chr14:35761327-35761377	BJ	skin:	n/a
17	chr14:35757441-35757491	HUVEC	blood vessel:	n/a
18	chr14:35761165-35761215	PrEC	prostate:	n/a
19	chr14:35757441-35757491	NT2-D1	testis:	n/a
20	chr14:35757441-35757491	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:35761197-35761247	GM12892	blood:	n/a
22	chr14:35761197-35761247	Hela-S3	cervix:	n/a
23	chr14:35761197-35761247	NH-A	brain:	n/a
24	chr14:35757441-35757491	AG10803	skin:	n/a
25	chr14:35761165-35761215	NT2-D1	testis:	n/a
26	chr14:35757441-35757491	K562	blood:	n/a
27	chr14:35757441-35757491	NHBE	bronchial:	n/a
28	chr14:35757441-35757491	HMEC	breast:	n/a
29	chr14:35761327-35761377	HepG2	liver:	n/a
30	chr14:35761197-35761247	HCT-116	colon:	n/a
31	chr14:35761165-35761215	HIPEpiC	eye:	n/a
32	chr14:35761165-35761215	K562	blood:	n/a
33	chr14:35757441-35757491	AG09319	gingival:	n/a
34	chr14:35761327-35761377	AG04449	skin:	fetal
35	chr14:35757441-35757491	NHDF-neo	bronchial:	n/a
36	chr14:35761327-35761377	AG09309	skin:	n/a
37	chr14:35761327-35761377	SAEC	small airway:	n/a
38	chr14:35761165-35761215	AG04450	lung:	fetal
39	chr14:35761327-35761377	GM19239	blood:	n/a
40	chr14:35757441-35757491	HRCEpiC	kidney:	n/a
41	chr14:35761327-35761377	AG10803	skin:	n/a
42	chr14:35761327-35761377	RPTEC	kidney:	n/a
43	chr14:35761197-35761247	HEEpiC	esophagus:	n/a
44	chr14:35761165-35761215	IMR90	lung:	fetal
45	chr14:35761327-35761377	GM12878	blood:	n/a
46	chr14:35761165-35761215	GM19239	blood:	n/a
47	chr14:35761327-35761377	Hela-S3	cervix:	n/a
48	chr14:35761327-35761377	ProgFib	skin:	n/a
49	chr14:35757441-35757491	HEEpiC	esophagus:	n/a
50	chr14:35761165-35761215	U87	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35753115..35758805-chr14:35759547..35762790,7	MCF-7	breast:
2	chr14:35761190..35763920-chr14:35872521..35874914,4	K562	blood:
3	chr14:35760689..35762512-chr8:131454589..131456596,2	MCF-7	breast:
4	chr14:35755322..35757615-chr14:35761312..35763223,3	MCF-7	breast:
5	chr14:35753303..35755635-chr14:35756425..35758168,2	MCF-7	breast:
6	chr14:35757192..35766588-chr14:35865950..35877395,53	MCF-7	breast:
7	chr14:35701633..35705447-chr14:35760005..35763215,4	MCF-7	breast:
8	chr14:35757780..35767592-chr14:35866063..35878024,53	MCF-7	breast:
9	chr14:35750207..35752268-chr14:35757042..35759453,2	MCF-7	breast:
10	chr14:35756501..35758878-chr14:35872345..35875637,3	K562	blood:
11	chr14:35753303..35755635-chr14:35756425..35758168,2	MCF-7	breast:
12	chr14:35755039..35756974-chr14:35862913..35865202,2	MCF-7	breast:
13	chr14:35749143..35751383-chr14:35753309..35755474,3	MCF-7	breast:
14	chr14:35760513..35762912-chr14:35858124..35860393,3	K562	blood:
15	chr14:35755418..35758074-chr14:35799307..35801251,2	MCF-7	breast:
16	chr14:35755052..35758727-chr14:35759764..35761284,4	MCF-7	breast:
17	chr14:35750852..35757164-chr14:35871890..35876148,8	MCF-7	breast:
18	chr14:35749937..35752594-chr14:35754898..35756875,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-173D9.3.1-3	chr14:35760251-35760436	l_963_chr14:35700899-35775195_brain

No data

Variant related genes	Relation type
ENSG00000265530	TF binding region
PSMA6	TF binding region
ENSG00000265530	CpG island
PSMA6	CpG island
ENSG00000100902	chromatin interactions
ENSG00000256243	chromatin interactions
ENSG00000240023	chromatin interactions
ENSG00000265530	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000153317	chromatin interactions

Extended variants
information (count: 208 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:208 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10142846	chr14:35755087-35755088	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375738946	chr14:35755129-35755130	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs547560818	chr14:35755196-35755197	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs115531185	chr14:35755200-35755201	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs536703865	chr14:35755204-35755205	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs556618474	chr14:35755216-35755217	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs188540229	chr14:35755235-35755236	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs876996	chr14:35755296-35755297	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs17458137	chr14:35755360-35755361	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555760895	chr14:35755382-35755383	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs572698581	chr14:35755393-35755394	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs534949127	chr14:35755408-35755409	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs555095365	chr14:35755435-35755436	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs573673105	chr14:35755451-35755452	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs542279269	chr14:35755458-35755459	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs574123788	chr14:35755472-35755473	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs562225909	chr14:35755488-35755489	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs575658563	chr14:35755581-35755582	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs193078560	chr14:35755586-35755587	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs143933460	chr14:35755616-35755617	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs565073904	chr14:35755639-35755640	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs527540012	chr14:35755690-35755691	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs184899461	chr14:35755706-35755707	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs561109093	chr14:35755713-35755714	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs4982254	chr14:35755737-35755738	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs202032290	chr14:35755775-35755776	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs373937299	chr14:35755779-35755780	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs397852104	chr14:35755794-35755795	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs577753464	chr14:35755858-35755859	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs75548236	chr14:35755868-35755869	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs189943212	chr14:35755900-35755901	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs551408160	chr14:35755932-35755933	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs191548851	chr14:35756007-35756008	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs117494255	chr14:35756053-35756054	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs566244544	chr14:35756137-35756138	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs527534947	chr14:35756166-35756167	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs535293986	chr14:35756196-35756197	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs554878142	chr14:35756199-35756200	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs148220524	chr14:35756209-35756210	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs577906576	chr14:35756213-35756214	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs141128900	chr14:35756278-35756279	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs17103166	chr14:35756317-35756318	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs560535239	chr14:35756386-35756387	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs17458214	chr14:35756447-35756448	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564852145	chr14:35756455-35756456	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs150729099	chr14:35756500-35756501	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs75464714	chr14:35756575-35756576	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs115097920	chr14:35756590-35756591	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs549824259	chr14:35756627-35756628	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs371888978	chr14:35756636-35756637	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Acute lymphoblastic leukemia	20067559	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD
Cancer	20164920	CNVD

Chromatin state (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35684600-35760800	Weak transcription	HSMM	muscle
2	chr14:35706800-35760800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:35716800-35760600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr14:35716800-35761000	Weak transcription	Spleen	Spleen
5	chr14:35717000-35760800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr14:35722000-35760800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr14:35724200-35756400	Weak transcription	Left Ventricle	heart
8	chr14:35727200-35756400	Weak transcription	Stomach Mucosa	stomach
9	chr14:35727200-35761000	Weak transcription	NHLF	lung
10	chr14:35730200-35760600	Weak transcription	Fetal Brain Female	brain
11	chr14:35731800-35756000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:35734400-35760600	Weak transcription	Right Ventricle	heart
13	chr14:35734400-35760800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr14:35736000-35760800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr14:35737400-35761000	Weak transcription	Gastric	stomach
16	chr14:35738800-35759400	Weak transcription	Placenta	Placenta
17	chr14:35740000-35756600	Weak transcription	NHEK	skin
18	chr14:35741200-35760800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr14:35742800-35755800	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr14:35743200-35756400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr14:35743400-35760800	Weak transcription	HMEC	breast
22	chr14:35743600-35760800	Weak transcription	Brain Anterior Caudate	brain
23	chr14:35743800-35760800	Weak transcription	Osteobl	bone
24	chr14:35744000-35756200	Weak transcription	Liver	Liver
25	chr14:35744000-35757600	Weak transcription	Lung	lung
26	chr14:35744000-35760800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr14:35744000-35760800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr14:35744000-35760800	Weak transcription	Brain Substantia Nigra	brain
29	chr14:35744000-35760800	Weak transcription	Fetal Lung	lung
30	chr14:35744000-35760800	Weak transcription	Rectal Smooth Muscle	rectum
31	chr14:35744000-35761000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:35744400-35756200	Weak transcription	Fetal Intestine Large	intestine
33	chr14:35744400-35760800	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr14:35744800-35760800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr14:35745000-35756600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr14:35745200-35760600	Weak transcription	Fetal Muscle Trunk	muscle
37	chr14:35745200-35760800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr14:35745400-35760800	Weak transcription	Brain Cingulate Gyrus	brain
39	chr14:35745600-35760800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr14:35745800-35760400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr14:35745800-35760800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr14:35746000-35755400	Weak transcription	Fetal Muscle Leg	muscle
43	chr14:35746000-35760800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr14:35746000-35760800	Weak transcription	Brain Hippocampus Middle	brain
45	chr14:35746000-35760800	Weak transcription	Stomach Smooth Muscle	stomach
46	chr14:35746000-35760800	Weak transcription	A549	lung
47	chr14:35746000-35761000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr14:35746200-35755200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr14:35746200-35760800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr14:35746600-35756000	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links