Variant report

Variant	nsv983840
Chromosome Location	chr14:70696676-70714926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:151)
CpG islands
(count:490)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:151 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:70704443-70705035	K562	blood:	n/a	n/a
2	ATF1	chr14:70704474-70704876	K562	blood:	n/a	n/a
3	ATF3	chr14:70704454-70704749	K562	blood:	n/a	n/a
4	BACH1	chr14:70704503-70704674	K562	blood:	n/a	n/a
5	BCL11A	chr14:70706539-70706794	GM12878	blood:	n/a	n/a
6	BCL11A	chr14:70706560-70706847	GM12878	blood:	n/a	n/a
7	BHLHE40	chr14:70704459-70705108	K562	blood:	n/a	n/a
8	BHLHE40	chr14:70698871-70699221	GM12878	blood:	n/a	n/a
9	CBX3	chr14:70704442-70704798	K562	blood:	n/a	n/a
10	CBX3	chr14:70704481-70704763	K562	blood:	n/a	n/a
11	CCNT2	chr14:70704435-70704849	K562	blood:	n/a	n/a
12	CEBPB	chr14:70704563-70704695	K562	blood:	n/a	n/a
13	CEBPB	chr14:70698623-70698820	HepG2	liver:	n/a	chr14:70698699-70698708 chr14:70698699-70698708
14	CEBPB	chr14:70704426-70704827	K562	blood:	n/a	n/a
15	CEBPB	chr14:70705506-70705790	K562	blood:	n/a	n/a
16	CEBPB	chr14:70704396-70704787	K562	blood:	n/a	n/a
17	CEBPB	chr14:70698678-70698720	A549	lung:	n/a	chr14:70698699-70698708 chr14:70698699-70698708
18	CEBPD	chr14:70704284-70704895	K562	blood:	n/a	n/a
19	CEBPD	chr14:70704341-70704966	K562	blood:	n/a	n/a
20	CHD2	chr14:70704598-70704755	K562	blood:	n/a	n/a
21	CHD2	chr14:70706600-70706984	GM12878	blood:	n/a	n/a
22	CUX1	chr14:70698994-70699406	GM12878	blood:	n/a	chr14:70699224-70699238
23	CUX1	chr14:70704285-70705529	K562	blood:	n/a	n/a
24	EBF1	chr14:70706441-70707010	GM12878	blood:	n/a	chr14:70706699-70706710
25	EBF1	chr14:70706426-70706967	GM12878	blood:	n/a	chr14:70706699-70706710
26	EBF1	chr14:70706368-70706984	GM12878	blood:	n/a	chr14:70706699-70706710
27	EGR1	chr14:70704472-70704759	K562	blood:	n/a	n/a
28	EP300	chr14:70706395-70706972	GM12878	blood:	n/a	n/a
29	EP300	chr14:70704415-70705120	K562	blood:	n/a	n/a
30	EP300	chr14:70704460-70704827	K562	blood:	n/a	n/a
31	EP300	chr14:70706551-70706923	GM12878	blood:	n/a	n/a
32	ETS1	chr14:70704499-70704760	K562	blood:	n/a	n/a
33	ETS1	chr14:70704407-70704800	K562	blood:	n/a	n/a
34	FOSL1	chr14:70704506-70704764	K562	blood:	n/a	n/a
35	GABPA	chr14:70704393-70704797	K562	blood:	n/a	n/a
36	GABPA	chr14:70704438-70704795	K562	blood:	n/a	n/a
37	GATA1	chr14:70704244-70705177	K562	blood:	n/a	n/a
38	GATA1	chr14:70704450-70704816	K562	blood:	n/a	n/a
39	GATA1	chr14:70704170-70705677	PBDE	blood:	n/a	n/a
40	GATA1	chr14:70711424-70711964	PBDE	blood:	n/a	n/a
41	GATA1	chr14:70704433-70704962	PBDEFetal	blood:	n/a	n/a
42	GATA2	chr14:70704290-70704878	K562	blood:	n/a	n/a
43	GATA2	chr14:70704344-70704895	K562	blood:	n/a	n/a
44	GATA2	chr14:70704423-70704895	K562	blood:	n/a	n/a
45	HDAC2	chr14:70704470-70704746	K562	blood:	n/a	n/a
46	HDAC2	chr14:70704199-70704430	K562	blood:	n/a	n/a
47	HDAC2	chr14:70704440-70704780	K562	blood:	n/a	n/a
48	HMGN3	chr14:70704517-70704819	K562	blood:	n/a	n/a
49	IRF1	chr14:70704471-70705011	K562	blood:	n/a	n/a
50	IRF1	chr14:70704432-70704994	K562	blood:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70701049-70701099	LNCaP	prostate:	n/a
2	chr14:70701049-70701099	HAEpiC	amniotic membrane:	n/a
3	chr14:70701049-70701099	LNCaP	prostate:	n/a
4	chr14:70701049-70701099	HAEpiC	amniotic membrane:	n/a
5	chr14:70701025-70701075	GM19239	blood:	n/a
6	chr14:70699208-70699258	NT2-D1	testis:	n/a
7	chr14:70714389-70714439	Hepatocyte	liver:	n/a
8	chr14:70701435-70701485	HepG2	liver:	n/a
9	chr14:70701025-70701075	PrEC	prostate:	n/a
10	chr14:70699208-70699258	SAEC	small airway:	n/a
11	chr14:70698703-70698753	Jurkat	blood:	n/a
12	chr14:70699208-70699258	HAEpiC	amniotic membrane:	n/a
13	chr14:70701049-70701099	HRE	kidney:	n/a
14	chr14:70701025-70701075	GM12891	blood:	n/a
15	chr14:70701049-70701099	ProgFib	skin:	n/a
16	chr14:70701025-70701075	SK-N-SH_RA	brain:	n/a
17	chr14:70701435-70701485	SAEC	small airway:	n/a
18	chr14:70700886-70700936	NHDF-neo	bronchial:	n/a
19	chr14:70698703-70698753	HCT-116	colon:	n/a
20	chr14:70701025-70701075	Jurkat	blood:	n/a
21	chr14:70701435-70701485	AG09309	skin:	n/a
22	chr14:70701025-70701075	SAEC	small airway:	n/a
23	chr14:70698703-70698753	HAEpiC	amniotic membrane:	n/a
24	chr14:70699208-70699258	SKMC	muscle:	n/a
25	chr14:70701025-70701075	HCPEpiC	choroid plexus:	n/a
26	chr14:70698703-70698753	NHBE	bronchial:	n/a
27	chr14:70701435-70701485	HRPEpiC	eye:	n/a
28	chr14:70701025-70701075	A549	lung:	n/a
29	chr14:70701049-70701099	MCF10A-Er-Src	breast:	n/a
30	chr14:70701049-70701099	SK-N-MC	brain:	n/a
31	chr14:70701435-70701485	NB4	blood:	n/a
32	chr14:70701263-70701313	AG09319	gingival:	n/a
33	chr14:70701049-70701099	HEK293	kidney:	embryo
34	chr14:70701049-70701099	AG04450	lung:	fetal
35	chr14:70701025-70701075	K562	blood:	n/a
36	chr14:70698703-70698753	HIPEpiC	eye:	n/a
37	chr14:70698703-70698753	AG04450	lung:	fetal
38	chr14:70701263-70701313	AG04450	lung:	fetal
39	chr14:70699208-70699258	GM19239	blood:	n/a
40	chr14:70701435-70701485	BE2_C	brain:	n/a
41	chr14:70699208-70699258	HCM	heart:	n/a
42	chr14:70714389-70714439	HRPEpiC	eye:	n/a
43	chr14:70701263-70701313	AoSMC	blood vessel:	n/a
44	chr14:70700886-70700936	AG09309	skin:	n/a
45	chr14:70698703-70698753	AG09319	gingival:	n/a
46	chr14:70701263-70701313	PANC-1	pancreas:	n/a
47	chr14:70701025-70701075	LNCaP	prostate:	n/a
48	chr14:70714389-70714439	NH-A	brain:	n/a
49	chr14:70700886-70700936	HEEpiC	esophagus:	n/a
50	chr14:70699208-70699258	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:70691907..70694267-chr14:70697780..70699341,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SMOC1-2	chr14:70696735-70696904	ENSG00000258422
2	lnc-SMOC1-2	chr14:70696735-70696898	ENSG00000258422
3	lnc-SLC8A3-3	chr14:70712470-70714518	NR_003951
4	lnc-SMOC1-2	chr14:70696735-70696825	ENSG00000258422

No data

Variant related genes	Relation type
ADAM21P1	TF binding region
ENSG00000270610	TF binding region
ADAM21P1	CpG island
ENSG00000270610	CpG island

Extended variants
information (count: 714 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115283652	chr14:70696709-70696710	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551116508	chr14:70696783-70696784	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs569616771	chr14:70696797-70696798	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs147133960	chr14:70696802-70696803	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs369479815	chr14:70696806-70696807	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs556092232	chr14:70696935-70696936	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs574334013	chr14:70696976-70696977	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs71423392	chr14:70696993-70696994	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs367612703	chr14:70696997-70696998	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs578048648	chr14:70697071-70697072	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545469706	chr14:70697091-70697092	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563576062	chr14:70697097-70697098	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs530044074	chr14:70697113-70697114	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs139079708	chr14:70697138-70697139	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542569483	chr14:70697147-70697148	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs41350744	chr14:70697154-70697155	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs527452154	chr14:70697192-70697193	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs529118671	chr14:70697211-70697212	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs149913144	chr14:70697241-70697242	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs559479435	chr14:70697272-70697273	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs532918697	chr14:70697278-70697279	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs114037620	chr14:70697288-70697289	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs117123938	chr14:70697342-70697343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376864838	chr14:70697424-70697425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371330365	chr14:70697426-70697427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116523993	chr14:70697529-70697530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117519845	chr14:70697574-70697575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139943948	chr14:70697635-70697636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578118132	chr14:70697666-70697667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190198532	chr14:70697682-70697683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182769949	chr14:70697686-70697687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575608824	chr14:70697698-70697699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143377720	chr14:70697729-70697730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560921019	chr14:70697756-70697757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573628136	chr14:70697781-70697782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540909788	chr14:70697782-70697783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72731897	chr14:70697813-70697814	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533145185	chr14:70697824-70697825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528182283	chr14:70697846-70697847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187490349	chr14:70697862-70697863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556183027	chr14:70697881-70697882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530586869	chr14:70697906-70697907	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs549019617	chr14:70697946-70697947	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs567247378	chr14:70697959-70697960	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528836806	chr14:70697994-70697995	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs74062855	chr14:70698020-70698021	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs146743800	chr14:70698023-70698024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs57482885	chr14:70698033-70698034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71395630	chr14:70698041-70698042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs36078348	chr14:70698043-70698044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70691000-70703400	Weak transcription	K562	blood
2	chr14:70696400-70697200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:70696400-70697400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr14:70696400-70697400	Enhancers	H1 Cell Line	embryonic stem cell
5	chr14:70696400-70697400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr14:70696400-70697400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr14:70696400-70697600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr14:70696400-70697600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr14:70696400-70697600	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr14:70696600-70697200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr14:70697000-70697400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr14:70697200-70697400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr14:70697200-70697400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr14:70697400-70699200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr14:70697400-70719400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:70697600-70699200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr14:70699200-70699400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr14:70699200-70699400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr14:70700800-70701800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr14:70701800-70721200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr14:70703400-70704800	Enhancers	K562	blood
22	chr14:70704200-70705000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr14:70704200-70705200	Enhancers	Placenta	Placenta
24	chr14:70704400-70706400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr14:70704600-70705000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:70704600-70705000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr14:70704600-70705000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr14:70704800-70705600	Flanking Active TSS	K562	blood
29	chr14:70705000-70706000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:70705600-70706400	Enhancers	K562	blood
31	chr14:70706000-70706200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
32	chr14:70706000-70706400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
33	chr14:70706000-70706400	Enhancers	GM12878-XiMat	blood
34	chr14:70706000-70706800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:70706200-70706400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
36	chr14:70706200-70706400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
37	chr14:70706200-70706600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr14:70706200-70706600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
39	chr14:70706200-70706600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr14:70706200-70706800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr14:70706200-70707000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr14:70706200-70707000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr14:70706200-70707200	Enhancers	Primary B cells from peripheral blood	blood
44	chr14:70706400-70706800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr14:70706400-70707000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr14:70706800-70707200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:70707000-70711800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr14:70711800-70712400	Enhancers	HMEC	breast
49	chr14:70711800-70712600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr14:70712000-70713600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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