Variant report

Variant	nsv1050491
Chromosome Location	chr14:24426594-24495038
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1181)
CpG islands
(count:1468)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	ARID3A	chr14:24483172-24483507	K562	blood:	n/a	n/a
3	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
4	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
5	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:24439122-24439137	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
9	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
10	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
11	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
12	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
13	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
15	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
16	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
17	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
18	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
19	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
20	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
21	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
22	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
23	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
24	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
25	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
27	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
28	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
29	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
30	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
31	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
32	CEBPD	chr14:24439025-24439361	HepG2	liver:	n/a	n/a
33	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
34	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
35	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
36	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
37	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
38	CHD2	chr14:24439126-24439200	GM12878	blood:	n/a	chr14:24439140-24439150
39	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
40	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
41	CTCF	chr14:24454280-24454430	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr14:24446500-24446650	HMEC	breast:	n/a	n/a
43	CTCF	chr14:24489360-24489510	HepG2	liver:	n/a	n/a
44	CTCF	chr14:24468738-24468758	LNCaP	prostate:	n/a	n/a
45	CTCF	chr14:24483260-24483410	Caco-2	colon:	n/a	n/a
46	CTCF	chr14:24483147-24483522	ECC-1	luminal epithelium:	n/a	n/a
47	CTCF	chr14:24446380-24446530	MCF-7	breast:	n/a	n/a
48	CTCF	chr14:24446548-24446628	GM19239	blood:	n/a	n/a
49	CTCF	chr14:24489280-24489430	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr14:24489276-24489487	MCF-7	breast:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24435159-24435209	ProgFib	skin:	n/a
2	chr14:24458099-24458149	SK-N-MC	brain:	n/a
3	chr14:24457915-24457965	HIPEpiC	eye:	n/a
4	chr14:24476559-24476609	HEK293	kidney:	embryo
5	chr14:24435159-24435209	ProgFib	skin:	n/a
6	chr14:24458099-24458149	SK-N-MC	brain:	n/a
7	chr14:24457915-24457965	HIPEpiC	eye:	n/a
8	chr14:24476559-24476609	HEK293	kidney:	embryo
9	chr14:24458299-24458349	BE2_C	brain:	n/a
10	chr14:24475906-24475956	HCM	heart:	n/a
11	chr14:24438909-24438959	HEK293	kidney:	embryo
12	chr14:24439157-24439207	HMEC	breast:	n/a
13	chr14:24457509-24457559	SKMC	muscle:	n/a
14	chr14:24454443-24454493	SK-N-MC	brain:	n/a
15	chr14:24458014-24458064	A549	lung:	n/a
16	chr14:24458208-24458258	NH-A	brain:	n/a
17	chr14:24457509-24457559	HIPEpiC	eye:	n/a
18	chr14:24458345-24458395	Hepatocyte	liver:	n/a
19	chr14:24438909-24438959	AoSMC	blood vessel:	n/a
20	chr14:24475053-24475103	BJ	skin:	n/a
21	chr14:24435159-24435209	AoSMC	blood vessel:	n/a
22	chr14:24476559-24476609	AoSMC	blood vessel:	n/a
23	chr14:24478620-24478670	IMR90	lung:	fetal
24	chr14:24476082-24476132	HRE	kidney:	n/a
25	chr14:24473832-24473882	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:24475906-24475956	HRPEpiC	eye:	n/a
27	chr14:24457893-24457943	HEEpiC	esophagus:	n/a
28	chr14:24475906-24475956	HNPCEpiC	eye:	n/a
29	chr14:24458208-24458258	HEK293	kidney:	embryo
30	chr14:24478620-24478670	AG09309	skin:	n/a
31	chr14:24435159-24435209	Jurkat	blood:	n/a
32	chr14:24458014-24458064	K562	blood:	n/a
33	chr14:24458345-24458395	BJ	skin:	n/a
34	chr14:24478620-24478670	GM06990	blood:	n/a
35	chr14:24476478-24476528	HepG2	liver:	n/a
36	chr14:24458208-24458258	HRPEpiC	eye:	n/a
37	chr14:24458014-24458064	AG10803	skin:	n/a
38	chr14:24476559-24476609	HCPEpiC	choroid plexus:	n/a
39	chr14:24478620-24478670	NHDF-neo	bronchial:	n/a
40	chr14:24458004-24458054	RPTEC	kidney:	n/a
41	chr14:24457915-24457965	MCF-7	breast:	n/a
42	chr14:24457993-24458043	NT2-D1	testis:	n/a
43	chr14:24476478-24476528	HCM	heart:	n/a
44	chr14:24438909-24438959	AG10803	skin:	n/a
45	chr14:24457893-24457943	HCF	heart:	n/a
46	chr14:24439157-24439207	NHBE	bronchial:	n/a
47	chr14:24457915-24457965	HUVEC	blood vessel:	n/a
48	chr14:24476559-24476609	SK-N-SH_RA	brain:	n/a
49	chr14:24457509-24457559	MCF10A-Er-Src	breast:	n/a
50	chr14:24457915-24457965	AG04449	skin:	fetal

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
2	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
3	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
4	chr14:24421589..24424746-chr14:24425153..24428957,4	MCF-7	breast:
5	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:
6	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
7	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
8	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
9	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:
10	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:
11	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:

(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	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	TF binding region
DHRS4	CpG island
DHRS4L2	CpG island
DHRS4-AS1	CpG island
ENSG00000187630	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000215256	chromatin interactions

Extended variants
information (count: 3237 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3237 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145219936	chr14:24426596-24426597	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs538740547	chr14:24426603-24426604	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs559035336	chr14:24426617-24426618	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs575718978	chr14:24426647-24426648	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142209008	chr14:24426653-24426654	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561204883	chr14:24426692-24426693	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs35429464	chr14:24426698-24426699	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs574795038	chr14:24426709-24426710	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370733434	chr14:24426717-24426718	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs559709978	chr14:24426721-24426722	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs115690102	chr14:24426738-24426739	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs551964888	chr14:24426746-24426747	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562626962	chr14:24426764-24426765	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs66683150	chr14:24426765-24426766	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs75577211	chr14:24426781-24426782	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs76524456	chr14:24426784-24426785	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs13379296	chr14:24426797-24426798	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs550885985	chr14:24426831-24426832	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562808720	chr14:24426875-24426876	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs548415942	chr14:24426926-24426927	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs568316855	chr14:24426938-24426939	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs35550020	chr14:24426950-24426951	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs533442755	chr14:24427006-24427007	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs61999767	chr14:24427021-24427022	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs534069335	chr14:24427038-24427039	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs551780878	chr14:24427094-24427095	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs547746177	chr14:24427101-24427102	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566728519	chr14:24427110-24427111	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539042698	chr14:24427117-24427118	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs558747704	chr14:24427154-24427155	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs146135298	chr14:24427239-24427240	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs184841356	chr14:24427283-24427284	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs554738118	chr14:24427330-24427331	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs574733312	chr14:24427338-24427339	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs540511503	chr14:24427339-24427340	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs377469993	chr14:24427342-24427343	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73600730	chr14:24427358-24427359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs149805904	chr14:24427377-24427378	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs367603379	chr14:24427379-24427380	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370338389	chr14:24427417-24427418	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs375067949	chr14:24427422-24427423	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545802043	chr14:24427439-24427440	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562406066	chr14:24427506-24427507	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs531440918	chr14:24427519-24427520	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372763602	chr14:24427533-24427534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs541995143	chr14:24427547-24427548	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs549451558	chr14:24427572-24427573	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs145694444	chr14:24427573-24427574	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs527508021	chr14:24427580-24427581	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535608697	chr14:24427581-24427582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1251 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	chr14:24423600-24426600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr14:24423600-24430800	Weak transcription	Psoas Muscle	Psoas
5	chr14:24423600-24438800	Weak transcription	Lung	lung
6	chr14:24423600-24438800	Weak transcription	Ovary	ovary
7	chr14:24423800-24427400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr14:24423800-24427400	Weak transcription	HSMMtube	muscle
9	chr14:24423800-24429200	Weak transcription	Fetal Intestine Small	intestine
10	chr14:24423800-24430800	Weak transcription	Fetal Thymus	thymus
11	chr14:24423800-24432400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr14:24423800-24435600	Weak transcription	Primary B cells from cord blood	blood
13	chr14:24423800-24438200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr14:24423800-24438600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr14:24423800-24438600	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr14:24423800-24438800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr14:24423800-24438800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr14:24423800-24438800	Weak transcription	Left Ventricle	heart
19	chr14:24423800-24438800	Weak transcription	Right Ventricle	heart
20	chr14:24423800-24438800	Weak transcription	Osteobl	bone
21	chr14:24424000-24427200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:24424000-24427600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr14:24424000-24428200	Weak transcription	Brain Anterior Caudate	brain
24	chr14:24424000-24429000	Weak transcription	A549	lung
25	chr14:24424000-24435400	Weak transcription	Primary B cells from peripheral blood	blood
26	chr14:24424000-24437400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr14:24424000-24438200	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr14:24424000-24438200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr14:24424000-24438800	Weak transcription	Primary hematopoietic stem cells	blood
30	chr14:24424000-24438800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr14:24424000-24438800	Weak transcription	HSMM	muscle
32	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
33	chr14:24424200-24427200	Weak transcription	Colon Smooth Muscle	Colon
34	chr14:24424200-24435400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr14:24424200-24438200	Weak transcription	Rectal Smooth Muscle	rectum
36	chr14:24424200-24438800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr14:24424200-24438800	Weak transcription	NHEK	skin
38	chr14:24424400-24426800	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr14:24424400-24427400	Weak transcription	Fetal Brain Female	brain
40	chr14:24424400-24427600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr14:24424400-24429200	Weak transcription	Placenta	Placenta
42	chr14:24424400-24429200	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr14:24424400-24429800	Weak transcription	Esophagus	oesophagus
44	chr14:24424400-24430000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr14:24424400-24432200	Weak transcription	Dnd41	blood
46	chr14:24424400-24436600	Weak transcription	Gastric	stomach
47	chr14:24424400-24438000	Weak transcription	Stomach Smooth Muscle	stomach
48	chr14:24424400-24438600	Weak transcription	Brain Hippocampus Middle	brain
49	chr14:24424400-24438800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr14:24424400-24438800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links