Variant report

Variant	esv3323442
Chromosome Location	chr14:55346027-55348775
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:55347965-55348455	GM12878	blood:	n/a	n/a
2	ATF2	chr14:55348036-55348807	GM12878	blood:	n/a	n/a
3	BATF	chr14:55347981-55348418	GM12878	blood:	n/a	n/a
4	BATF	chr14:55347926-55348447	GM12878	blood:	n/a	n/a
5	BCLAF1	chr14:55347924-55348724	GM12878	blood:	n/a	chr14:55348195-55348204
6	BCLAF1	chr14:55347970-55348963	GM12878	blood:	n/a	chr14:55348195-55348204 chr14:55348801-55348810
7	CEBPB	chr14:55348693-55348891	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:55348698-55348933	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:55348709-55348835	A549	lung:	n/a	n/a
10	CTCF	chr14:55348320-55348470	AG09319	gingival:	n/a	n/a
11	CTCF	chr14:55348260-55348410	BJ	skin:	n/a	n/a
12	CTCF	chr14:55348329-55348424	ProgFib	skin:	n/a	n/a
13	CTCF	chr14:55348336-55348382	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr14:55348300-55348330	Kidney_OC	kidney:	n/a	n/a
15	CTCF	chr14:55348240-55348390	NHDF-neo	bronchial:	n/a	n/a
16	CTCF	chr14:55348380-55348530	HCM	heart:	n/a	n/a
17	CTCF	chr14:55348021-55348032	GM19239	blood:	n/a	n/a
18	CTCF	chr14:55348220-55348370	SAEC	small airway:	n/a	n/a
19	CTCF	chr14:55348240-55348390	HCFaa	heart:	n/a	n/a
20	CTCF	chr14:55348078-55348384	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr14:55348760-55348910	AG09319	gingival:	n/a	n/a
22	CTCF	chr14:55348320-55348470	GM12873	blood:	n/a	n/a
23	CTCF	chr14:55348220-55348370	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr14:55348320-55348470	BE2_C	brain:	n/a	n/a
25	CTCF	chr14:55348300-55348450	AG09309	skin:	n/a	n/a
26	CTCF	chr14:55348324-55348425	Fibrobl	skin:	n/a	n/a
27	CTCF	chr14:55348320-55348470	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr14:55348729-55348976	GM12878	blood:	n/a	n/a
29	CTCF	chr14:55348382-55348389	GM12878	blood:	n/a	n/a
30	CTCF	chr14:55347911-55348456	GM12878	blood:	n/a	n/a
31	CTCF	chr14:55348240-55348390	GM06990	blood:	n/a	n/a
32	CTCF	chr14:55348260-55348410	AG10803	skin:	n/a	n/a
33	CTCF	chr14:55348200-55348350	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr14:55348160-55348310	BE2_C	brain:	n/a	n/a
35	CTCF	chr14:55348040-55348190	GM06990	blood:	n/a	n/a
36	CTCF	chr14:55348200-55348350	HCM	heart:	n/a	n/a
37	CTCF	chr14:55348014-55348103	GM12878	blood:	n/a	n/a
38	CTCF	chr14:55348140-55348290	RPTEC	kidney:	n/a	n/a
39	CTCF	chr14:55348260-55348410	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr14:55348300-55348450	AG09319	gingival:	n/a	n/a
41	CTCF	chr14:55347920-55348070	HMEC	breast:	n/a	n/a
42	CTCF	chr14:55347940-55348090	GM12872	blood:	n/a	n/a
43	CTCF	chr14:55348300-55348450	BJ	skin:	n/a	n/a
44	CTCF	chr14:55348280-55348430	HCPEpiC	choroid plexus:	n/a	n/a
45	E2F4	chr14:55348220-55348483	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr14:55347926-55348182	GM12878	blood:	n/a	n/a
47	EBF1	chr14:55348030-55348781	GM12878	blood:	n/a	n/a
48	ELK1	chr14:55348589-55348807	GM12878	blood:	n/a	n/a
49	EP300	chr14:55347820-55350131	SK-N-SH	brain:	n/a	chr14:55348166-55348180 chr14:55348796-55348810 chr14:55348744-55348752
50	EP300	chr14:55347996-55348597	GM12878	blood:	n/a	chr14:55348166-55348180

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55348681-55348731	GM06990	blood:	n/a
2	chr14:55348681-55348731	BE2_C	brain:	n/a
3	chr14:55348681-55348731	HCT-116	colon:	n/a
4	chr14:55348681-55348731	GM12878	blood:	n/a
5	chr14:55348681-55348731	ProgFib	skin:	n/a
6	chr14:55348681-55348731	T-47D	breast:	n/a
7	chr14:55348681-55348731	HRPEpiC	eye:	n/a
8	chr14:55348681-55348731	SK-N-SH_RA	brain:	n/a
9	chr14:55348681-55348731	AG09319	gingival:	n/a
10	chr14:55348681-55348731	AG04449	skin:	fetal
11	chr14:55348681-55348731	IMR90	lung:	fetal
12	chr14:55348681-55348731	HRE	kidney:	n/a
13	chr14:55348681-55348731	HL-60	blood:	n/a
14	chr14:55348681-55348731	HepG2	liver:	n/a
15	chr14:55348681-55348731	ECC-1	luminal epithelium:	n/a
16	chr14:55348681-55348731	HAEpiC	amniotic membrane:	n/a
17	chr14:55348681-55348731	LNCaP	prostate:	n/a
18	chr14:55348681-55348731	HCM	heart:	n/a
19	chr14:55348681-55348731	SAEC	small airway:	n/a
20	chr14:55348681-55348731	U87	brain:	n/a
21	chr14:55348681-55348731	Hela-S3	cervix:	n/a
22	chr14:55348681-55348731	PrEC	prostate:	n/a
23	chr14:55348681-55348731	GM12891	blood:	n/a
24	chr14:55348681-55348731	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:55348681-55348731	NT2-D1	testis:	n/a
26	chr14:55348681-55348731	AG10803	skin:	n/a
27	chr14:55348681-55348731	NHBE	bronchial:	n/a
28	chr14:55348681-55348731	AG04450	lung:	fetal
29	chr14:55348681-55348731	SKMC	muscle:	n/a
30	chr14:55348681-55348731	MCF-7	breast:	n/a
31	chr14:55348681-55348731	Caco-2	colon:	n/a
32	chr14:55348681-55348731	HEEpiC	esophagus:	n/a
33	chr14:55348681-55348731	Jurkat	blood:	n/a
34	chr14:55348681-55348731	PFSK-1	brain:	n/a
35	chr14:55348681-55348731	Hepatocyte	liver:	n/a
36	chr14:55348681-55348731	HIPEpiC	eye:	n/a
37	chr14:55348681-55348731	SK-N-SH	brain:	n/a
38	chr14:55348681-55348731	HUVEC	blood vessel:	n/a
39	chr14:55348681-55348731	MCF10A-Er-Src	breast:	n/a
40	chr14:55348681-55348731	HMEC	breast:	n/a
41	chr14:55348681-55348731	GM19239	blood:	n/a
42	chr14:55348681-55348731	H1-hESC	embryonic stem cell:	embryo
43	chr14:55348681-55348731	CMK	blood:	n/a
44	chr14:55348681-55348731	ovcar-3	ovarian:	n/a
45	chr14:55348681-55348731	SK-N-MC	brain:	n/a
46	chr14:55348681-55348731	GM12892	blood:	n/a
47	chr14:55348681-55348731	PANC-1	pancreas:	n/a
48	chr14:55348681-55348731	HEK293	kidney:	embryo
49	chr14:55348681-55348731	HNPCEpiC	eye:	n/a
50	chr14:55348681-55348731	NH-A	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:55343813..55346930-chr14:55349782..55354238,4	MCF-7	breast:
2	chr14:55343213..55346860-chr14:55368496..55370471,3	MCF-7	breast:
3	chr14:55344081..55346333-chr14:55348656..55350611,2	K562	blood:
4	chr14:55348331..55350043-chr14:55361093..55363707,2	K562	blood:

No data

Variant related genes	Relation type
MIR4308	TF binding region
MIR4308	CpG island
ENSG00000258872	chromatin interactions
ENSG00000265432	chromatin interactions
ENSG00000131979	chromatin interactions

Extended variants
information (count: 132 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10133449	chr14:55346070-55346071	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188253312	chr14:55346078-55346079	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371793677	chr14:55346093-55346094	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs534074191	chr14:55346110-55346111	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs55881030	chr14:55346129-55346130	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs371815857	chr14:55346139-55346140	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs60400770	chr14:55346161-55346162	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs75259980	chr14:55346167-55346168	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs191230953	chr14:55346263-55346264	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs10133650	chr14:55346273-55346274	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs112466784	chr14:55346294-55346295	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs61702394	chr14:55346373-55346374	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs141691618	chr14:55346388-55346389	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150505676	chr14:55346439-55346440	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs140328333	chr14:55346443-55346444	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572581733	chr14:55346472-55346473	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539979544	chr14:55346477-55346478	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144515289	chr14:55346478-55346479	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs527718994	chr14:55346484-55346485	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs184767889	chr14:55346503-55346504	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562423044	chr14:55346520-55346521	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs3945570	chr14:55346602-55346603	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs71412658	chr14:55346626-55346627	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs28757745	chr14:55346671-55346672	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs544332820	chr14:55346723-55346724	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs35476604	chr14:55346727-55346728	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs28542181	chr14:55346773-55346774	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs566584079	chr14:55346784-55346785	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs373449495	chr14:55346785-55346786	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs139779681	chr14:55346790-55346791	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548877874	chr14:55346839-55346840	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs58085261	chr14:55346858-55346859	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs567429248	chr14:55346860-55346861	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs397956284	chr14:55346869-55346870	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs149918054	chr14:55346893-55346894	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189224386	chr14:55346898-55346899	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556185135	chr14:55346904-55346905	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs577605720	chr14:55346909-55346910	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369124329	chr14:55346917-55346918	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145012097	chr14:55346967-55346968	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs554421776	chr14:55347133-55347134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368592440	chr14:55347141-55347142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371417703	chr14:55347146-55347147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34635384	chr14:55347150-55347151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71131237	chr14:55347161-55347162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148945540	chr14:55347172-55347173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181938889	chr14:55347178-55347179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72187597	chr14:55347184-55347185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374740127	chr14:55347186-55347187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371292067	chr14:55347194-55347195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	16397240	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55329400-55347800	Weak transcription	Primary B cells from cord blood	blood
2	chr14:55330800-55347800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr14:55331800-55347600	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr14:55334000-55346200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr14:55337400-55346200	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr14:55337400-55347800	Weak transcription	HSMMtube	muscle
7	chr14:55337600-55346400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr14:55337600-55348600	Weak transcription	Hela-S3	cervix
9	chr14:55343800-55347800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr14:55343800-55348200	Weak transcription	Fetal Intestine Large	intestine
11	chr14:55344000-55346800	Weak transcription	Primary T cells from cord blood	blood
12	chr14:55344000-55347800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr14:55344200-55346200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:55344200-55346200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr14:55344200-55346200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr14:55344200-55346200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr14:55344200-55347600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr14:55344400-55347800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr14:55344800-55346400	Weak transcription	Primary hematopoietic stem cells	blood
20	chr14:55345000-55346200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr14:55345000-55347600	Weak transcription	HUVEC	blood vessel
22	chr14:55345000-55348000	Weak transcription	HepG2	liver
23	chr14:55345400-55347800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr14:55345400-55347800	Weak transcription	GM12878-XiMat	blood
25	chr14:55345400-55348200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr14:55345400-55354800	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr14:55345400-55368200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr14:55345600-55346600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr14:55345600-55346600	Strong transcription	Fetal Intestine Small	intestine
30	chr14:55345600-55347800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr14:55345600-55348000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr14:55345600-55348000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr14:55345800-55346200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr14:55345800-55346200	Enhancers	Liver	Liver
35	chr14:55345800-55347800	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr14:55346000-55347000	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr14:55346000-55347800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr14:55346200-55346400	Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr14:55346200-55346600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr14:55346200-55346600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr14:55346200-55346600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr14:55346200-55346600	Flanking Active TSS	Liver	Liver
43	chr14:55346200-55347000	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr14:55346200-55347000	Active TSS	Duodenum Mucosa	Duodenum
45	chr14:55346200-55347200	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr14:55346200-55347600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr14:55346200-55347800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr14:55346200-55348000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr14:55346400-55346600	Enhancers	Placenta	Placenta
50	chr14:55346400-55346600	Enhancers	Psoas Muscle	Psoas

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