Variant report

Variant	nsv519458
Chromosome Location	chr14:35702857-35715411
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr14:35705679-35705717	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr14:35703265-35703611	IMR90	lung:	n/a	chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703429-35703440 chr14:35703428-35703439
3	CEBPB	chr14:35703505-35703517	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr14:35703290-35703519	A549	lung:	n/a	chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703429-35703440 chr14:35703428-35703439
5	CEBPB	chr14:35703263-35703569	MCF-7	breast:	n/a	chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703429-35703440 chr14:35703428-35703439
6	CEBPB	chr14:35704458-35704589	HepG2	liver:	n/a	chr14:35704481-35704492
7	CEBPB	chr14:35703262-35703609	HepG2	liver:	n/a	chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703429-35703440 chr14:35703428-35703439
8	CEBPB	chr14:35703309-35703540	Hela-S3	cervix:	n/a	chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703430-35703439 chr14:35703429-35703440 chr14:35703428-35703439
9	CHD2	chr14:35703507-35703531	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr14:35706317-35706414	MCF-7	breast:	n/a	n/a
11	CTCF	chr14:35706374-35706384	GM12891	blood:	n/a	n/a
12	CTCF	chr14:35706315-35706434	MCF-7	breast:	n/a	n/a
13	CTCF	chr14:35706377-35706380	MCF-7	breast:	n/a	n/a
14	CTCF	chr14:35706334-35706439	MCF-7	breast:	n/a	n/a
15	CTCF	chr14:35706326-35706371	Lung_OC	lung:	n/a	n/a
16	CTCF	chr14:35704578-35704643	GM13976	blood:	n/a	n/a
17	FOS	chr14:35703214-35703611	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr14:35703218-35703547	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr14:35703183-35703693	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr14:35703185-35703696	MCF10A-Er-Src	breast:	n/a	n/a
21	GATA3	chr14:35703248-35703539	T-47D	breast:	n/a	n/a
22	GATA3	chr14:35703236-35703502	T-47D	breast:	n/a	n/a
23	JUN	chr14:35713206-35713341	HepG2	liver:	n/a	n/a
24	MAFK	chr14:35703462-35703473	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAFK	chr14:35715014-35715038	H1-hESC	embryonic stem cell:	n/a	n/a
26	MYC	chr14:35703157-35703686	MCF10A-Er-Src	breast:	n/a	n/a
27	MYC	chr14:35703197-35703624	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr14:35712027-35712040	MCF-7	breast:	n/a	n/a
29	POLR2A	chr14:35711129-35711270	ProgFib	skin:	n/a	n/a
30	POLR2A	chr14:35703025-35703730	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr14:35712616-35712644	MCF-7	breast:	n/a	n/a
32	POLR2A	chr14:35712639-35712644	MCF-7	breast:	n/a	n/a
33	RUNX3	chr14:35712649-35713088	GM12878	blood:	n/a	n/a
34	STAT3	chr14:35703170-35703646	MCF10A-Er-Src	breast:	n/a	chr14:35703431-35703439
35	STAT3	chr14:35703242-35703876	MCF10A-Er-Src	breast:	n/a	chr14:35703431-35703439
36	STAT3	chr14:35703243-35703691	MCF10A-Er-Src	breast:	n/a	chr14:35703431-35703439
37	STAT3	chr14:35703252-35703617	MCF10A-Er-Src	breast:	n/a	chr14:35703431-35703439
38	STAT3	chr14:35705892-35706020	MCF10A-Er-Src	breast:	n/a	n/a
39	TCF7L2	chr14:35711536-35711736	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:35694745..35697043-chr14:35701937..35704486,2	MCF-7	breast:
2	chr14:35714388..35715903-chr14:35719645..35721798,2	MCF-7	breast:
3	chr14:35713971..35716399-chr14:35872514..35875136,2	MCF-7	breast:
4	chr14:35698917..35700420-chr14:35714304..35715826,2	MCF-7	breast:
5	chr14:35701570..35704183-chr14:35804617..35807506,4	MCF-7	breast:
6	chr14:35688349..35704994-chr14:35861790..35878218,62	MCF-7	breast:
7	chr14:35698822..35700476-chr14:35705196..35707061,2	MCF-7	breast:
8	chr14:35711794..35714036-chr14:35837683..35839377,2	MCF-7	breast:
9	chr14:35703500..35705028-chr14:35708204..35710934,2	MCF-7	breast:
10	chr14:35681924..35684171-chr14:35710768..35712492,2	MCF-7	breast:
11	chr14:35706016..35708901-chr14:35873653..35875984,5	MCF-7	breast:
12	chr14:35708125..35710807-chr14:35761300..35763864,2	MCF-7	breast:
13	chr14:35702282..35704520-chr14:35800753..35803790,5	MCF-7	breast:
14	chr14:35705860..35707392-chr14:35712096..35713861,2	MCF-7	breast:
15	chr14:35705470..35707557-chr14:35709197..35711039,2	K562	blood:
16	chr14:35701633..35705447-chr14:35760005..35763215,4	MCF-7	breast:
17	chr14:35707379..35710076-chr14:35710482..35713240,2	MCF-7	breast:
18	chr14:35683362..35686230-chr14:35702094..35703639,2	MCF-7	breast:
19	chr14:35705860..35707392-chr14:35712096..35713861,2	MCF-7	breast:
20	chr14:35700495..35703278-chr14:35704050..35706629,2	K562	blood:
21	chr14:35709151..35713105-chr14:35760006..35762827,3	MCF-7	breast:
22	chr14:35699579..35702448-chr14:35709536..35711264,2	MCF-7	breast:
23	chr14:35701265..35703150-chr14:35798175..35799719,2	MCF-7	breast:
24	chr14:35711337..35713419-chr14:35730009..35732772,2	MCF-7	breast:
25	chr14:35711268..35715087-chr14:35870152..35873955,3	MCF-7	breast:
26	chr14:35701125..35703592-chr14:35762146..35764422,2	MCF-7	breast:
27	chr14:35695193..35706000-chr14:35866255..35879159,42	MCF-7	breast:
28	chr14:35705470..35707557-chr14:35709197..35711039,2	K562	blood:
29	chr14:35707379..35710076-chr14:35710482..35713240,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-173D9.3.1-3	chr14:35704702-35704801	l_963_chr14:35700899-35775195_brain
2	lnc-RP11-173D9.3.1-3	chr14:35703077-35703223	l_963_chr14:35700899-35775195_brain
3	lnc-RP11-173D9.3.1-3	chr14:35704074-35704252	l_963_chr14:35700899-35775195_brain
4	lnc-PPP2R3C-4	chr14:35715251-35715712	l_962_chr14:35668508-35676460_thyroid
5	lnc-PPP2R3C-4	chr14:35704820-35705215	l_962_chr14:35668508-35676460_thyroid
6	lnc-PPP2R3C-4	chr14:35704130-35704256	l_962_chr14:35668508-35676460_thyroid
7	lnc-PPP2R3C-4	chr14:35714373-35714399	l_962_chr14:35668508-35676460_thyroid
8	lnc-PPP2R3C-4	chr14:35704706-35704801	l_962_chr14:35668508-35676460_thyroid

Variant related genes	Relation type
RPL7AP3	TF binding region
ENSG00000265530	chromatin interactions
ENSG00000240392	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000256243	chromatin interactions
ENSG00000100902	chromatin interactions

Extended variants
information (count: 483 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:483 , 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	rs8181982	chr14:35702857-35702858	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542987008	chr14:35702879-35702880	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs563245113	chr14:35702901-35702902	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs373652497	chr14:35702910-35702911	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs138214803	chr14:35702911-35702912	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs79533887	chr14:35702923-35702924	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs561675357	chr14:35703041-35703042	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs531578122	chr14:35703135-35703136	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs559548899	chr14:35703158-35703159	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs369574013	chr14:35703175-35703176	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs528254511	chr14:35703180-35703181	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs542771560	chr14:35703209-35703210	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs185677288	chr14:35703266-35703267	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs562010157	chr14:35703307-35703308	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs116351206	chr14:35703335-35703336	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs143602025	chr14:35703340-35703341	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs570849048	chr14:35703354-35703355	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs372817531	chr14:35703398-35703399	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs191171851	chr14:35703431-35703432	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs546955260	chr14:35703437-35703438	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs377131086	chr14:35703485-35703486	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs74660260	chr14:35703501-35703502	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs2899831	chr14:35703521-35703522	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs35634238	chr14:35703545-35703546	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs568016946	chr14:35703550-35703551	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs147194164	chr14:35703607-35703608	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs112446279	chr14:35703634-35703635	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs115017046	chr14:35703639-35703640	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs182495054	chr14:35703660-35703661	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs552980399	chr14:35703670-35703671	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs28397717	chr14:35703711-35703712	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs541610133	chr14:35703765-35703766	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs562218799	chr14:35703768-35703769	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs115714305	chr14:35703772-35703773	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs370220185	chr14:35703827-35703828	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs149388511	chr14:35703830-35703831	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs17103120	chr14:35703839-35703840	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs574735731	chr14:35703855-35703856	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs377202613	chr14:35703860-35703861	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs533347945	chr14:35703863-35703864	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs532064563	chr14:35703883-35703884	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs376143290	chr14:35703894-35703895	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs561893479	chr14:35703896-35703897	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs398056986	chr14:35703900-35703901	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs572127728	chr14:35703935-35703936	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs113472481	chr14:35703944-35703945	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs117981306	chr14:35703995-35703996	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs529494027	chr14:35704025-35704026	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs565745004	chr14:35704061-35704062	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs112265616	chr14:35704125-35704126	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	3 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:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35643400-35724000	Weak transcription	Left Ventricle	heart
2	chr14:35650800-35707800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr14:35661000-35736400	Weak transcription	Fetal Intestine Small	intestine
4	chr14:35672000-35742200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr14:35674400-35711200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr14:35674800-35737000	Weak transcription	Lung	lung
7	chr14:35678000-35719600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr14:35680800-35729800	Weak transcription	Primary B cells from cord blood	blood
9	chr14:35681000-35729800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr14:35684000-35706800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr14:35684600-35737000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr14:35684600-35760800	Weak transcription	HSMM	muscle
13	chr14:35684800-35703000	Weak transcription	HMEC	breast
14	chr14:35686800-35735800	Weak transcription	Fetal Intestine Large	intestine
15	chr14:35687400-35716400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr14:35690200-35730000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr14:35690600-35735800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr14:35691200-35735800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:35693800-35717000	Weak transcription	HSMMtube	muscle
20	chr14:35694600-35726800	Weak transcription	K562	blood
21	chr14:35698600-35704200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr14:35699000-35703800	Enhancers	Primary hematopoietic stem cells	blood
23	chr14:35699000-35704000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr14:35699000-35704200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr14:35699200-35717200	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr14:35699800-35735800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr14:35700200-35703000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr14:35700200-35729600	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr14:35700200-35738000	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr14:35700400-35703400	Weak transcription	HepG2	liver
31	chr14:35700400-35712400	Weak transcription	GM12878-XiMat	blood
32	chr14:35700400-35716600	Weak transcription	Fetal Thymus	thymus
33	chr14:35700400-35717400	Weak transcription	Thymus	Thymus
34	chr14:35700400-35729600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr14:35700400-35735800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr14:35700600-35704200	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr14:35700600-35729200	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr14:35700800-35703800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr14:35700800-35709600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr14:35700800-35717400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr14:35701200-35704600	Weak transcription	Primary T cells from cord blood	blood
42	chr14:35702600-35703800	Enhancers	Dnd41	blood
43	chr14:35702800-35703200	Weak transcription	Liver	Liver
44	chr14:35702800-35703200	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr14:35702800-35703200	Weak transcription	NHDF-Ad	bronchial
46	chr14:35702800-35703800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr14:35702800-35708000	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr14:35703000-35703800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:35703000-35703800	Enhancers	HMEC	breast
50	chr14:35703200-35703400	Enhancers	Liver	Liver

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