Variant report

Variant	nsv9124
Chromosome Location	chr14:24424711-24474776
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:626)
CpG islands
(count:1221)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24443416-24443612	HepG2	liver:	n/a	n/a
2	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
3	BACH1	chr14:24439122-24439137	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
6	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
8	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
9	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
11	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
12	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
13	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
14	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
15	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
16	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
18	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
19	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
20	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
21	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
22	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
23	CEBPD	chr14:24439025-24439361	HepG2	liver:	n/a	n/a
24	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
25	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
26	CHD2	chr14:24439126-24439200	GM12878	blood:	n/a	chr14:24439140-24439150
27	CTCF	chr14:24468738-24468758	LNCaP	prostate:	n/a	n/a
28	CTCF	chr14:24446380-24446530	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr14:24446620-24446770	GM12868	blood:	n/a	n/a
30	CTCF	chr14:24446492-24446709	Gliobla	brain:	n/a	n/a
31	CTCF	chr14:24446600-24446750	GM12871	blood:	n/a	n/a
32	CTCF	chr14:24446376-24446701	A549	lung:	n/a	n/a
33	CTCF	chr14:24446580-24446730	GM12865	blood:	n/a	n/a
34	CTCF	chr14:24446380-24446530	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr14:24446580-24446730	Caco-2	colon:	n/a	n/a
36	CTCF	chr14:24435876-24436058	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr14:24446500-24446650	GM12875	blood:	n/a	n/a
38	CTCF	chr14:24446600-24446750	GM06990	blood:	n/a	n/a
39	CTCF	chr14:24454280-24454430	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr14:24446620-24446770	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:24446515-24446685	NHEK	skin:	n/a	n/a
42	CTCF	chr14:24446510-24446675	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:24454260-24454410	HepG2	liver:	n/a	n/a
44	CTCF	chr14:24458460-24458610	HRE	kidney:	n/a	n/a
45	CTCF	chr14:24446540-24446690	AG04449	skin:	n/a	n/a
46	CTCF	chr14:24446560-24446710	HMF	breast:	n/a	n/a
47	CTCF	chr14:24446580-24446730	RPTEC	kidney:	n/a	n/a
48	CTCF	chr14:24458380-24458530	HRE	kidney:	n/a	n/a
49	CTCF	chr14:24446380-24446530	NB4	blood:	n/a	n/a
50	CTCF	chr14:24458380-24458530	AG04450	lung:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24425142-24425192	HRPEpiC	eye:	n/a
2	chr14:24425142-24425192	HRPEpiC	eye:	n/a
3	chr14:24439157-24439207	BE2_C	brain:	n/a
4	chr14:24458004-24458054	AG09309	skin:	n/a
5	chr14:24458000-24458050	ProgFib	skin:	n/a
6	chr14:24439157-24439207	HPAEpiC	pulmonary alveolar:	n/a
7	chr14:24458299-24458349	MCF-7	breast:	n/a
8	chr14:24435159-24435209	K562	blood:	n/a
9	chr14:24425142-24425192	HCPEpiC	choroid plexus:	n/a
10	chr14:24457993-24458043	RPTEC	kidney:	n/a
11	chr14:24438136-24438186	H1-hESC	embryonic stem cell:	embryo
12	chr14:24425142-24425192	Jurkat	blood:	n/a
13	chr14:24457893-24457943	HMEC	breast:	n/a
14	chr14:24438909-24438959	Hepatocyte	liver:	n/a
15	chr14:24458208-24458258	CMK	blood:	n/a
16	chr14:24457509-24457559	AG10803	skin:	n/a
17	chr14:24457993-24458043	Hepatocyte	liver:	n/a
18	chr14:24458345-24458395	HPAEpiC	pulmonary alveolar:	n/a
19	chr14:24458345-24458395	BJ	skin:	n/a
20	chr14:24425142-24425192	MCF-7	breast:	n/a
21	chr14:24458099-24458149	GM19239	blood:	n/a
22	chr14:24473832-24473882	K562	blood:	n/a
23	chr14:24425142-24425192	ProgFib	skin:	n/a
24	chr14:24473832-24473882	AG09319	gingival:	n/a
25	chr14:24425142-24425192	SK-N-SH_RA	brain:	n/a
26	chr14:24438909-24438959	AG10803	skin:	n/a
27	chr14:24439157-24439207	HRCEpiC	kidney:	n/a
28	chr14:24435159-24435209	SK-N-SH	brain:	n/a
29	chr14:24458299-24458349	AG04450	lung:	fetal
30	chr14:24458099-24458149	SKMC	muscle:	n/a
31	chr14:24425142-24425192	HUVEC	blood vessel:	n/a
32	chr14:24439430-24439480	AG04450	lung:	fetal
33	chr14:24457915-24457965	A549	lung:	n/a
34	chr14:24439430-24439480	AG09319	gingival:	n/a
35	chr14:24473832-24473882	AG04449	skin:	fetal
36	chr14:24458014-24458064	H1-hESC	embryonic stem cell:	embryo
37	chr14:24457993-24458043	SK-N-SH_RA	brain:	n/a
38	chr14:24458004-24458054	AG10803	skin:	n/a
39	chr14:24438909-24438959	MCF-7	breast:	n/a
40	chr14:24458099-24458149	NH-A	brain:	n/a
41	chr14:24425012-24425062	Hela-S3	cervix:	n/a
42	chr14:24458014-24458064	RPTEC	kidney:	n/a
43	chr14:24425012-24425062	HepG2	liver:	n/a
44	chr14:24435159-24435209	PrEC	prostate:	n/a
45	chr14:24425012-24425062	GM19239	blood:	n/a
46	chr14:24435159-24435209	Hela-S3	cervix:	n/a
47	chr14:24473832-24473882	NHBE	bronchial:	n/a
48	chr14:24458345-24458395	HMEC	breast:	n/a
49	chr14:24457915-24457965	GM19239	blood:	n/a
50	chr14:24458345-24458395	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:
2	chr14:24421589..24424746-chr14:24425153..24428957,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3

No data

Variant related genes	Relation type
DHRS4-AS1	TF binding region
DHRS4	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	CpG island
DHRS4	CpG island
DHRS4L2	CpG island
ENSG00000215256	chromatin interactions
ENSG00000187630	chromatin interactions
ENSG00000157326	chromatin interactions

Extended variants
information (count: 2447 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2447 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563652746	chr14:24424755-24424756	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs529454179	chr14:24424758-24424759	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182287796	chr14:24424797-24424798	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564176547	chr14:24424810-24424811	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376464477	chr14:24424812-24424813	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566330238	chr14:24424926-24424927	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535333580	chr14:24424969-24424970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116635822	chr14:24424993-24424994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571209554	chr14:24425008-24425009	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536678623	chr14:24425012-24425013	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs187366832	chr14:24425013-24425014	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs556992149	chr14:24425033-24425034	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs573671208	chr14:24425051-24425052	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs10137990	chr14:24425058-24425059	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs568916959	chr14:24425060-24425061	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs539793808	chr14:24425117-24425118	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552744429	chr14:24425121-24425122	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111631601	chr14:24425151-24425152	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	mRNA abundance
19	rs544884466	chr14:24425161-24425162	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs565061470	chr14:24425173-24425174	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs577940489	chr14:24425184-24425185	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs543466543	chr14:24425237-24425238	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs190620270	chr14:24425279-24425280	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563763286	chr14:24425285-24425286	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532211198	chr14:24425287-24425288	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs117354048	chr14:24425325-24425326	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529410466	chr14:24425352-24425353	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543191767	chr14:24425374-24425375	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs2984817	chr14:24425427-24425428	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs144247892	chr14:24425438-24425439	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs200998110	chr14:24425444-24425445	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552084642	chr14:24425466-24425467	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182842712	chr14:24425467-24425468	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530493523	chr14:24425498-24425499	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs187077183	chr14:24425527-24425528	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs190001893	chr14:24425531-24425532	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182869540	chr14:24425532-24425533	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs187463921	chr14:24425533-24425534	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs566308924	chr14:24425534-24425535	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs192690455	chr14:24425536-24425537	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs185663861	chr14:24425551-24425552	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs558781851	chr14:24425553-24425554	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs146577513	chr14:24425600-24425601	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs543754185	chr14:24425642-24425643	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187829975	chr14:24425660-24425661	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs114156090	chr14:24425662-24425663	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142267460	chr14:24425693-24425694	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529597690	chr14:24425708-24425709	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs368190057	chr14:24425709-24425710	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs528671404	chr14:24425720-24425721	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24423400-24429000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr14:24423400-24431000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:24423600-24425200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:24423600-24426600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr14:24423600-24430800	Weak transcription	Psoas Muscle	Psoas
6	chr14:24423600-24438800	Weak transcription	Lung	lung
7	chr14:24423600-24438800	Weak transcription	Ovary	ovary
8	chr14:24423800-24425000	Weak transcription	Fetal Kidney	kidney
9	chr14:24423800-24425600	Weak transcription	HUVEC	blood vessel
10	chr14:24423800-24426400	Weak transcription	Fetal Lung	lung
11	chr14:24423800-24427400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr14:24423800-24427400	Weak transcription	HSMMtube	muscle
13	chr14:24423800-24429200	Weak transcription	Fetal Intestine Small	intestine
14	chr14:24423800-24430800	Weak transcription	Fetal Thymus	thymus
15	chr14:24423800-24432400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:24423800-24435600	Weak transcription	Primary B cells from cord blood	blood
17	chr14:24423800-24438200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr14:24423800-24438600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr14:24423800-24438600	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr14:24423800-24438800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr14:24423800-24438800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr14:24423800-24438800	Weak transcription	Left Ventricle	heart
23	chr14:24423800-24438800	Weak transcription	Right Ventricle	heart
24	chr14:24423800-24438800	Weak transcription	Osteobl	bone
25	chr14:24424000-24424800	Weak transcription	Fetal Stomach	stomach
26	chr14:24424000-24425000	Weak transcription	Stomach Mucosa	stomach
27	chr14:24424000-24425400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr14:24424000-24425800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr14:24424000-24426000	Weak transcription	NHLF	lung
30	chr14:24424000-24426400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:24424000-24427200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:24424000-24427600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr14:24424000-24428200	Weak transcription	Brain Anterior Caudate	brain
34	chr14:24424000-24429000	Weak transcription	A549	lung
35	chr14:24424000-24435400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr14:24424000-24437400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr14:24424000-24438200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr14:24424000-24438200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr14:24424000-24438800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr14:24424000-24438800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr14:24424000-24438800	Weak transcription	HSMM	muscle
42	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
43	chr14:24424200-24424800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr14:24424200-24425000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr14:24424200-24425000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr14:24424200-24427200	Weak transcription	Colon Smooth Muscle	Colon
47	chr14:24424200-24435400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr14:24424200-24438200	Weak transcription	Rectal Smooth Muscle	rectum
49	chr14:24424200-24438800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:24424200-24438800	Weak transcription	NHEK	skin

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