Variant report

Variant	nsv1036717
Chromosome Location	chr14:24446705-24489426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:908)
CpG islands
(count:1163)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24483172-24483507	K562	blood:	n/a	n/a
3	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
4	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
7	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
9	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
12	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
13	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
14	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
15	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
16	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
17	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
18	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
19	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
20	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
21	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
22	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
23	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
24	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
25	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
26	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
28	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
29	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
30	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
31	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
32	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
33	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
34	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
35	CTCF	chr14:24489340-24489490	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr14:24446600-24446750	NHEK	skin:	n/a	n/a
37	CTCF	chr14:24446620-24446770	GM12872	blood:	n/a	n/a
38	CTCF	chr14:24446580-24446730	Caco-2	colon:	n/a	n/a
39	CTCF	chr14:24458502-24458607	GM19238	blood:	n/a	n/a
40	CTCF	chr14:24483240-24483390	GM12878	blood:	n/a	n/a
41	CTCF	chr14:24483180-24483330	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr14:24483280-24483430	GM12867	blood:	n/a	n/a
43	CTCF	chr14:24483280-24483430	RPTEC	kidney:	n/a	n/a
44	CTCF	chr14:24483194-24483516	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr14:24483220-24483370	HAc	cerebellar:	n/a	n/a
46	CTCF	chr14:24489360-24489510	GM12865	blood:	n/a	n/a
47	CTCF	chr14:24483205-24483492	A549	lung:	n/a	n/a
48	CTCF	chr14:24483240-24483390	HFF	foreskin:	n/a	n/a
49	CTCF	chr14:24489340-24489490	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr14:24446580-24446730	AG09309	skin:	n/a	n/a

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24458299-24458349	SKMC	muscle:	n/a
2	chr14:24458000-24458050	Hela-S3	cervix:	n/a
3	chr14:24478620-24478670	GM12891	blood:	n/a
4	chr14:24475053-24475103	ProgFib	skin:	n/a
5	chr14:24458299-24458349	SKMC	muscle:	n/a
6	chr14:24458000-24458050	Hela-S3	cervix:	n/a
7	chr14:24478620-24478670	GM12891	blood:	n/a
8	chr14:24475053-24475103	ProgFib	skin:	n/a
9	chr14:24457509-24457559	GM12891	blood:	n/a
10	chr14:24458099-24458149	HEK293	kidney:	embryo
11	chr14:24457509-24457559	HL-60	blood:	n/a
12	chr14:24458299-24458349	HRE	kidney:	n/a
13	chr14:24458000-24458050	HCF	heart:	n/a
14	chr14:24475053-24475103	A549	lung:	n/a
15	chr14:24476082-24476132	Jurkat	blood:	n/a
16	chr14:24475906-24475956	HCPEpiC	choroid plexus:	n/a
17	chr14:24478620-24478670	CMK	blood:	n/a
18	chr14:24458014-24458064	HCF	heart:	n/a
19	chr14:24457915-24457965	GM12878	blood:	n/a
20	chr14:24457915-24457965	K562	blood:	n/a
21	chr14:24458208-24458258	HIPEpiC	eye:	n/a
22	chr14:24458208-24458258	SAEC	small airway:	n/a
23	chr14:24457893-24457943	NHBE	bronchial:	n/a
24	chr14:24458345-24458395	MCF10A-Er-Src	breast:	n/a
25	chr14:24457993-24458043	HepG2	liver:	n/a
26	chr14:24458299-24458349	HL-60	blood:	n/a
27	chr14:24458345-24458395	NT2-D1	testis:	n/a
28	chr14:24458000-24458050	AG09319	gingival:	n/a
29	chr14:24457993-24458043	GM12891	blood:	n/a
30	chr14:24478620-24478670	ProgFib	skin:	n/a
31	chr14:24458014-24458064	ECC-1	luminal epithelium:	n/a
32	chr14:24476478-24476528	HCM	heart:	n/a
33	chr14:24458099-24458149	AG09309	skin:	n/a
34	chr14:24458099-24458149	IMR90	lung:	fetal
35	chr14:24457915-24457965	NT2-D1	testis:	n/a
36	chr14:24476559-24476609	PFSK-1	brain:	n/a
37	chr14:24473832-24473882	HCM	heart:	n/a
38	chr14:24457509-24457559	RPTEC	kidney:	n/a
39	chr14:24476559-24476609	K562	blood:	n/a
40	chr14:24457993-24458043	ovcar-3	ovarian:	n/a
41	chr14:24457509-24457559	HCM	heart:	n/a
42	chr14:24457509-24457559	MCF-7	breast:	n/a
43	chr14:24454443-24454493	K562	blood:	n/a
44	chr14:24458208-24458258	HMEC	breast:	n/a
45	chr14:24473832-24473882	AG04449	skin:	fetal
46	chr14:24458099-24458149	HAEpiC	amniotic membrane:	n/a
47	chr14:24457509-24457559	HMEC	breast:	n/a
48	chr14:24475906-24475956	A549	lung:	n/a
49	chr14:24457893-24457943	H1-hESC	embryonic stem cell:	embryo
50	chr14:24458208-24458258	HepG2	liver:	n/a

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

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

Extended variants
information (count: 2106 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2106 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553272556	chr14:24446708-24446709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141977159	chr14:24446731-24446732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529461554	chr14:24446732-24446733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188700761	chr14:24446739-24446740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs58192612	chr14:24446746-24446747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397958824	chr14:24446750-24446751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544328516	chr14:24446798-24446799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373147847	chr14:24446808-24446809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545118660	chr14:24446813-24446814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540488795	chr14:24446824-24446825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560468374	chr14:24446831-24446832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376134329	chr14:24446833-24446834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146153493	chr14:24446878-24446879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377358225	chr14:24446896-24446897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527795128	chr14:24446922-24446923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191649098	chr14:24446992-24446993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140204699	chr14:24446993-24446994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs550673475	chr14:24446994-24446995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567491410	chr14:24447034-24447035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376918856	chr14:24447043-24447044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561883682	chr14:24447044-24447045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546847867	chr14:24447066-24447067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184726004	chr14:24447080-24447081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539349069	chr14:24447084-24447085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142132089	chr14:24447093-24447094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189648443	chr14:24447094-24447095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146374013	chr14:24447099-24447100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139601318	chr14:24447101-24447102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180786425	chr14:24447112-24447113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs59082073	chr14:24447114-24447115	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs370340256	chr14:24447129-24447130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539718643	chr14:24447130-24447131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373495440	chr14:24447137-24447138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187615643	chr14:24447141-24447142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546110242	chr14:24447150-24447151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189214915	chr14:24447166-24447167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs60909389	chr14:24447167-24447168	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs544251898	chr14:24447173-24447174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28578611	chr14:24447203-24447204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs58653994	chr14:24447231-24447232	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs181562061	chr14:24447235-24447236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560773397	chr14:24447297-24447298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555017345	chr14:24447300-24447301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185700528	chr14:24447340-24447341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552857257	chr14:24447352-24447353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145163470	chr14:24447363-24447364	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
47	rs190457506	chr14:24447378-24447379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148720201	chr14:24447384-24447385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568160103	chr14:24447423-24447424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12878559	chr14:24447431-24447432	Weak transcription	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:913 , 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	chr14:24439400-24450000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr14:24439400-24451000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr14:24439400-24451200	Weak transcription	Pancreas	Pancrea
5	chr14:24439400-24457600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr14:24440000-24453600	Weak transcription	Dnd41	blood
7	chr14:24442800-24456000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr14:24445200-24454600	Weak transcription	Thymus	Thymus
9	chr14:24445200-24456200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr14:24446200-24458000	Weak transcription	Gastric	stomach
11	chr14:24446400-24446800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:24446400-24446800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr14:24446400-24447200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr14:24446600-24457400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr14:24448000-24457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr14:24448400-24457400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr14:24450000-24450400	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr14:24450000-24452000	Enhancers	Fetal Intestine Large	intestine
19	chr14:24450000-24452000	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr14:24450400-24454200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr14:24450400-24457400	Weak transcription	Primary hematopoietic stem cells	blood
22	chr14:24450400-24457600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr14:24450800-24452200	Enhancers	HepG2	liver
24	chr14:24451000-24451400	Enhancers	Fetal Intestine Small	intestine
25	chr14:24451000-24451400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr14:24451200-24451400	Enhancers	Duodenum Mucosa	Duodenum
27	chr14:24451200-24451600	Enhancers	Pancreas	Pancrea
28	chr14:24451200-24451800	Enhancers	Liver	Liver
29	chr14:24451400-24453800	Weak transcription	Fetal Intestine Small	intestine
30	chr14:24451400-24453800	Weak transcription	Fetal Thymus	thymus
31	chr14:24451400-24454400	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr14:24451600-24454600	Weak transcription	Duodenum Mucosa	Duodenum
33	chr14:24451800-24457400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr14:24452000-24455400	Weak transcription	Fetal Intestine Large	intestine
35	chr14:24452000-24455800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr14:24452200-24454000	Weak transcription	HepG2	liver
37	chr14:24452600-24457600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr14:24453600-24453800	Enhancers	Esophagus	oesophagus
39	chr14:24453600-24453800	Enhancers	Small Intestine	intestine
40	chr14:24453600-24457600	Enhancers	Dnd41	blood
41	chr14:24453800-24455200	Weak transcription	Esophagus	oesophagus
42	chr14:24453800-24456400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr14:24453800-24456400	Enhancers	Fetal Intestine Small	intestine
44	chr14:24453800-24457000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr14:24453800-24457000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:24453800-24457000	Enhancers	NHEK	skin
47	chr14:24453800-24457600	Enhancers	Fetal Thymus	thymus
48	chr14:24454000-24454200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr14:24454000-24455200	Enhancers	A549	lung
50	chr14:24454000-24455400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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