Variant report

Variant	nsv512352
Chromosome Location	chr14:24442856-24486059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:887)
CpG islands
(count:1162)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
8	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
10	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
12	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
13	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
14	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
15	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
16	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
17	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
18	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
19	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
20	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
21	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
22	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
23	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
26	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
27	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
28	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
29	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
30	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
31	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
32	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
33	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
34	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
35	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
36	CTCF	chr14:24483280-24483430	GM12873	blood:	n/a	n/a
37	CTCF	chr14:24483213-24483468	LNCaP	prostate:	n/a	n/a
38	CTCF	chr14:24483309-24483422	GM12891	blood:	n/a	n/a
39	CTCF	chr14:24483145-24483502	T-47D	breast:	n/a	n/a
40	CTCF	chr14:24457937-24458015	Lung_OC	lung:	n/a	n/a
41	CTCF	chr14:24483206-24483477	K562	blood:	n/a	n/a
42	CTCF	chr14:24483240-24483390	GM06990	blood:	n/a	n/a
43	CTCF	chr14:24483260-24483410	HCFaa	heart:	n/a	n/a
44	CTCF	chr14:24446360-24446510	NHLF	lung:	n/a	n/a
45	CTCF	chr14:24454220-24454370	AG10803	skin:	n/a	n/a
46	CTCF	chr14:24483300-24483450	NB4	blood:	n/a	n/a
47	CTCF	chr14:24483280-24483430	K562	blood:	n/a	n/a
48	CTCF	chr14:24446380-24446530	NB4	blood:	n/a	n/a
49	CTCF	chr14:24483240-24483390	NHLF	lung:	n/a	n/a
50	CTCF	chr14:24483240-24483390	SAEC	small airway:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24458004-24458054	GM12892	blood:	n/a
2	chr14:24454443-24454493	ovcar-3	ovarian:	n/a
3	chr14:24476082-24476132	GM12891	blood:	n/a
4	chr14:24458004-24458054	GM12892	blood:	n/a
5	chr14:24454443-24454493	ovcar-3	ovarian:	n/a
6	chr14:24476082-24476132	GM12891	blood:	n/a
7	chr14:24473832-24473882	AG09309	skin:	n/a
8	chr14:24457893-24457943	RPTEC	kidney:	n/a
9	chr14:24458099-24458149	HUVEC	blood vessel:	n/a
10	chr14:24457993-24458043	NH-A	brain:	n/a
11	chr14:24458000-24458050	Hepatocyte	liver:	n/a
12	chr14:24476478-24476528	GM19239	blood:	n/a
13	chr14:24478620-24478670	BE2_C	brain:	n/a
14	chr14:24458004-24458054	GM12891	blood:	n/a
15	chr14:24458000-24458050	SK-N-MC	brain:	n/a
16	chr14:24473832-24473882	H1-hESC	embryonic stem cell:	embryo
17	chr14:24458000-24458050	HEEpiC	esophagus:	n/a
18	chr14:24476082-24476132	GM12878	blood:	n/a
19	chr14:24454443-24454493	HEEpiC	esophagus:	n/a
20	chr14:24457915-24457965	HNPCEpiC	eye:	n/a
21	chr14:24475053-24475103	HUVEC	blood vessel:	n/a
22	chr14:24473832-24473882	ECC-1	luminal epithelium:	n/a
23	chr14:24476559-24476609	HepG2	liver:	n/a
24	chr14:24454443-24454493	GM12878	blood:	n/a
25	chr14:24476559-24476609	GM12892	blood:	n/a
26	chr14:24457893-24457943	NT2-D1	testis:	n/a
27	chr14:24454443-24454493	HRCEpiC	kidney:	n/a
28	chr14:24476082-24476132	IMR90	lung:	fetal
29	chr14:24458099-24458149	HRCEpiC	kidney:	n/a
30	chr14:24457915-24457965	NHBE	bronchial:	n/a
31	chr14:24457509-24457559	HEEpiC	esophagus:	n/a
32	chr14:24476559-24476609	GM12891	blood:	n/a
33	chr14:24458099-24458149	MCF10A-Er-Src	breast:	n/a
34	chr14:24454443-24454493	AG09309	skin:	n/a
35	chr14:24478620-24478670	GM12892	blood:	n/a
36	chr14:24458345-24458395	HNPCEpiC	eye:	n/a
37	chr14:24457915-24457965	HEK293	kidney:	embryo
38	chr14:24476082-24476132	Hepatocyte	liver:	n/a
39	chr14:24458014-24458064	SK-N-MC	brain:	n/a
40	chr14:24475906-24475956	Caco-2	colon:	n/a
41	chr14:24476082-24476132	T-47D	breast:	n/a
42	chr14:24475053-24475103	NB4	blood:	n/a
43	chr14:24475053-24475103	H1-hESC	embryonic stem cell:	embryo
44	chr14:24476478-24476528	NHDF-neo	bronchial:	n/a
45	chr14:24457915-24457965	MCF-7	breast:	n/a
46	chr14:24478620-24478670	AG04450	lung:	fetal
47	chr14:24458014-24458064	BJ	skin:	n/a
48	chr14:24457915-24457965	SK-N-SH	brain:	n/a
49	chr14:24458299-24458349	ovcar-3	ovarian:	n/a
50	chr14:24475906-24475956	NHDF-neo	bronchial:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
2	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
3	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
4	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:
5	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:
6	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
7	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
8	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
9	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:
10	chr14:24482858..24483785-chr14:24559502..24560237,2	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-AS1	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	CpG island
DHRS4L2	CpG island
ENSG00000225766	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000187630	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000100889	chromatin interactions

Extended variants
information (count: 2187 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2187 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566698776	chr14:24442862-24442863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532573301	chr14:24442867-24442868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2759424	chr14:24442883-24442884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2262496	chr14:24442886-24442887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552798295	chr14:24442897-24442898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2759423	chr14:24442899-24442900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569441775	chr14:24442953-24442954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538576735	chr14:24443038-24443039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546902816	chr14:24443040-24443041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377283404	chr14:24443049-24443050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562080164	chr14:24443051-24443052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200767900	chr14:24443102-24443103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7160979	chr14:24443103-24443104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199510129	chr14:24443139-24443140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568084080	chr14:24443175-24443176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370739546	chr14:24443239-24443240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533837424	chr14:24443261-24443262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553926054	chr14:24443293-24443294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200837279	chr14:24443298-24443299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577065262	chr14:24443328-24443329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2760087	chr14:24443374-24443375	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs199947613	chr14:24443398-24443399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556361804	chr14:24443405-24443406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576252578	chr14:24443406-24443407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542133695	chr14:24443430-24443431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531162777	chr14:24443455-24443456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78155004	chr14:24443465-24443466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76532221	chr14:24443467-24443468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112824005	chr14:24443468-24443469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530061110	chr14:24443484-24443485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540285811	chr14:24443488-24443489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560225218	chr14:24443489-24443490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200716911	chr14:24443503-24443504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532510091	chr14:24443513-24443514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552492865	chr14:24443556-24443557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569463473	chr14:24443560-24443561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191424308	chr14:24443592-24443593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552896204	chr14:24443594-24443595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs112129390	chr14:24443600-24443601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570682351	chr14:24443611-24443612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376390545	chr14:24443624-24443625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371013153	chr14:24443627-24443628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375572865	chr14:24443660-24443661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs80170777	chr14:24443682-24443683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs180958211	chr14:24443684-24443685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376036071	chr14:24443691-24443692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533772356	chr14:24443695-24443696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534847852	chr14:24443721-24443722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150518817	chr14:24443731-24443732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185903642	chr14:24443739-24443740	Weak transcription Enhancers	n/a	n/a	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:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
2	chr14:24439400-24446400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:24439400-24450000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr14:24439400-24451000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr14:24439400-24451200	Weak transcription	Pancreas	Pancrea
6	chr14:24439400-24457600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr14:24440000-24453600	Weak transcription	Dnd41	blood
8	chr14:24442600-24443000	Weak transcription	HepG2	liver
9	chr14:24442800-24456000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr14:24443000-24444200	Enhancers	HepG2	liver
11	chr14:24445000-24446400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr14:24445200-24454600	Weak transcription	Thymus	Thymus
13	chr14:24445200-24456200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr14:24445400-24446000	Weak transcription	Gastric	stomach
15	chr14:24446000-24446200	Enhancers	Gastric	stomach
16	chr14:24446200-24458000	Weak transcription	Gastric	stomach
17	chr14:24446400-24446600	Enhancers	Primary B cells from peripheral blood	blood
18	chr14:24446400-24446800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr14:24446400-24446800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr14:24446400-24447200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr14:24446600-24457400	Weak transcription	Primary B cells from peripheral blood	blood
22	chr14:24448000-24457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr14:24448400-24457400	Weak transcription	Primary T cells fromperipheralblood	blood
24	chr14:24450000-24450400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr14:24450000-24452000	Enhancers	Fetal Intestine Large	intestine
26	chr14:24450000-24452000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr14:24450400-24454200	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr14:24450400-24457400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr14:24450400-24457600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr14:24450800-24452200	Enhancers	HepG2	liver
31	chr14:24451000-24451400	Enhancers	Fetal Intestine Small	intestine
32	chr14:24451000-24451400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
33	chr14:24451200-24451400	Enhancers	Duodenum Mucosa	Duodenum
34	chr14:24451200-24451600	Enhancers	Pancreas	Pancrea
35	chr14:24451200-24451800	Enhancers	Liver	Liver
36	chr14:24451400-24453800	Weak transcription	Fetal Intestine Small	intestine
37	chr14:24451400-24453800	Weak transcription	Fetal Thymus	thymus
38	chr14:24451400-24454400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr14:24451600-24454600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr14:24451800-24457400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr14:24452000-24455400	Weak transcription	Fetal Intestine Large	intestine
42	chr14:24452000-24455800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr14:24452200-24454000	Weak transcription	HepG2	liver
44	chr14:24452600-24457600	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr14:24453600-24453800	Enhancers	Esophagus	oesophagus
46	chr14:24453600-24453800	Enhancers	Small Intestine	intestine
47	chr14:24453600-24457600	Enhancers	Dnd41	blood
48	chr14:24453800-24455200	Weak transcription	Esophagus	oesophagus
49	chr14:24453800-24456400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr14:24453800-24456400	Enhancers	Fetal Intestine Small	intestine

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