Variant report

Variant	nsv598430
Chromosome Location	chr5:68832529-68856885
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:567)
CpG islands
(count:428)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:68855731-68856077	GM12878	blood:	n/a	n/a
2	BATF	chr5:68855769-68856236	GM12878	blood:	n/a	n/a
3	BATF	chr5:68856265-68856477	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:68855749-68856242	GM12878	blood:	n/a	chr5:68855979-68855988
5	BCL11A	chr5:68855639-68856223	GM12878	blood:	n/a	chr5:68855979-68855988
6	BCLAF1	chr5:68855724-68856111	K562	blood:	n/a	chr5:68855979-68855988
7	BCLAF1	chr5:68855732-68856164	GM12878	blood:	n/a	chr5:68855979-68855988
8	BCLAF1	chr5:68855724-68856135	GM12878	blood:	n/a	chr5:68855979-68855988
9	BCLAF1	chr5:68855724-68856116	K562	blood:	n/a	chr5:68855979-68855988
10	BHLHE40	chr5:68855820-68856132	HepG2	liver:	n/a	chr5:68855927-68855943 chr5:68855911-68855927
11	BRCA1	chr5:68855848-68856045	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr5:68855601-68856119	K562	blood:	n/a	n/a
13	CBX3	chr5:68855493-68856354	K562	blood:	n/a	n/a
14	CEBPB	chr5:68855845-68856045	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:68834723-68834923	HepG2	liver:	n/a	n/a
16	CEBPB	chr5:68834691-68834785	HepG2	liver:	n/a	n/a
17	CEBPD	chr5:68855760-68856284	K562	blood:	n/a	n/a
18	CHD2	chr5:68855853-68856047	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr5:68855844-68855949	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr5:68855923-68856048	GM12878	blood:	n/a	n/a
21	CREB1	chr5:68855831-68856118	A549	lung:	n/a	n/a
22	CTCF	chr5:68855814-68856146	Lung_OC	lung:	n/a	n/a
23	CTCF	chr5:68855853-68855972	GM19240	blood:	n/a	n/a
24	CTCF	chr5:68855557-68856148	SK-N-SH	brain:	n/a	n/a
25	CTCF	chr5:68855794-68856128	GM10248	blood:	n/a	n/a
26	CTCF	chr5:68855818-68856068	A549	lung:	n/a	n/a
27	CTCF	chr5:68833712-68833856	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr5:68855720-68855870	BJ	skin:	n/a	n/a
29	CTCF	chr5:68855720-68855870	HepG2	liver:	n/a	n/a
30	CTCF	chr5:68855720-68855870	GM12872	blood:	n/a	n/a
31	CTCF	chr5:68855747-68855896	HepG2	liver:	n/a	n/a
32	CTCF	chr5:68855783-68856107	GM10266	blood:	n/a	n/a
33	CTCF	chr5:68855800-68856092	A549	lung:	n/a	n/a
34	CTCF	chr5:68855960-68856110	NHEK	skin:	n/a	n/a
35	CTCF	chr5:68838421-68838427	GM20000	blood:	n/a	n/a
36	CTCF	chr5:68855720-68855870	GM12878	blood:	n/a	n/a
37	CTCF	chr5:68856000-68856150	HVMF	connective:	n/a	n/a
38	CTCF	chr5:68856000-68856150	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr5:68855682-68856139	K562	blood:	n/a	n/a
40	CTCF	chr5:68855980-68856130	GM12865	blood:	n/a	n/a
41	CTCF	chr5:68855720-68855870	GM12866	blood:	n/a	n/a
42	CTCF	chr5:68855980-68856130	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr5:68855846-68856040	GM19238	blood:	n/a	n/a
44	CTCF	chr5:68855720-68855870	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:68855720-68855870	AG04450	lung:	n/a	n/a
46	CTCF	chr5:68855980-68856130	AG09309	skin:	n/a	n/a
47	CTCF	chr5:68855980-68856130	GM12873	blood:	n/a	n/a
48	CTCF	chr5:68855700-68855850	A549	lung:	n/a	n/a
49	CTCF	chr5:68856000-68856150	RPTEC	kidney:	n/a	n/a
50	CTCF	chr5:68855860-68856010	AoAF	blood vessel:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68856065-68856115	NB4	blood:	n/a
2	chr5:68856065-68856115	NB4	blood:	n/a
3	chr5:68855560-68855610	AG10803	skin:	n/a
4	chr5:68855873-68855923	A549	lung:	n/a
5	chr5:68855810-68855860	NH-A	brain:	n/a
6	chr5:68856065-68856115	PrEC	prostate:	n/a
7	chr5:68855560-68855610	HCM	heart:	n/a
8	chr5:68855810-68855860	SAEC	small airway:	n/a
9	chr5:68855810-68855860	HCPEpiC	choroid plexus:	n/a
10	chr5:68852996-68853046	SAEC	small airway:	n/a
11	chr5:68855560-68855610	HCT-116	colon:	n/a
12	chr5:68856062-68856112	GM06990	blood:	n/a
13	chr5:68856077-68856127	LNCaP	prostate:	n/a
14	chr5:68852996-68853046	NT2-D1	testis:	n/a
15	chr5:68856065-68856115	MCF10A-Er-Src	breast:	n/a
16	chr5:68855560-68855610	NH-A	brain:	n/a
17	chr5:68855873-68855923	HNPCEpiC	eye:	n/a
18	chr5:68856065-68856115	AG09309	skin:	n/a
19	chr5:68856062-68856112	HCM	heart:	n/a
20	chr5:68852996-68853046	NH-A	brain:	n/a
21	chr5:68855560-68855610	ECC-1	luminal epithelium:	n/a
22	chr5:68855560-68855610	GM19239	blood:	n/a
23	chr5:68856062-68856112	A549	lung:	n/a
24	chr5:68855873-68855923	HMEC	breast:	n/a
25	chr5:68855810-68855860	CMK	blood:	n/a
26	chr5:68855560-68855610	NT2-D1	testis:	n/a
27	chr5:68856077-68856127	AG04449	skin:	fetal
28	chr5:68852996-68853046	HRE	kidney:	n/a
29	chr5:68856077-68856127	HAEpiC	amniotic membrane:	n/a
30	chr5:68856077-68856127	SK-N-SH_RA	brain:	n/a
31	chr5:68855560-68855610	AG09319	gingival:	n/a
32	chr5:68855873-68855923	MCF-7	breast:	n/a
33	chr5:68856077-68856127	AG09319	gingival:	n/a
34	chr5:68856065-68856115	A549	lung:	n/a
35	chr5:68856065-68856115	SK-N-SH_RA	brain:	n/a
36	chr5:68856062-68856112	AG09309	skin:	n/a
37	chr5:68856077-68856127	ProgFib	skin:	n/a
38	chr5:68856062-68856112	HepG2	liver:	n/a
39	chr5:68856065-68856115	AoSMC	blood vessel:	n/a
40	chr5:68855810-68855860	AG09319	gingival:	n/a
41	chr5:68855560-68855610	SKMC	muscle:	n/a
42	chr5:68856065-68856115	GM12891	blood:	n/a
43	chr5:68855560-68855610	HAEpiC	amniotic membrane:	n/a
44	chr5:68852996-68853046	K562	blood:	n/a
45	chr5:68855873-68855923	ECC-1	luminal epithelium:	n/a
46	chr5:68855873-68855923	AG04450	lung:	fetal
47	chr5:68855560-68855610	MCF10A-Er-Src	breast:	n/a
48	chr5:68856065-68856115	HRPEpiC	eye:	n/a
49	chr5:68852996-68853046	HUVEC	blood vessel:	n/a
50	chr5:68852996-68853046	GM12892	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCLN-1	chr5:68856086-68856428	NONHSAT101929

No data

Variant related genes	Relation type
ENSG00000238740	TF binding region
OCLN	TF binding region
GTF2H2C	TF binding region
ENSG00000238740	CpG island
OCLN	CpG island
GTF2H2C	CpG island

Extended variants
information (count: 253 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557706451	chr5:68832617-68832618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577113039	chr5:68832625-68832626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544167204	chr5:68832640-68832641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7381161	chr5:68832646-68832647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181335305	chr5:68832650-68832651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574551664	chr5:68832663-68832664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542019600	chr5:68832749-68832750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373134497	chr5:68833279-68833280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560307108	chr5:68833605-68833606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568971079	chr5:68833606-68833607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531363581	chr5:68833607-68833608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200271483	chr5:68833837-68833838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185979339	chr5:68833909-68833910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377593765	chr5:68833951-68833952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370624234	chr5:68834017-68834018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545843806	chr5:68834155-68834156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563923583	chr5:68834208-68834209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532072791	chr5:68834219-68834220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550216840	chr5:68834310-68834311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551063957	chr5:68834670-68834671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568038210	chr5:68834714-68834715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75758747	chr5:68835256-68835257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111906095	chr5:68835478-68835479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111963051	chr5:68836458-68836459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2666583	chr5:68838938-68838939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62371755	chr5:68839366-68839367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568708094	chr5:68840639-68840640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374647565	chr5:68840793-68840794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377718385	chr5:68840825-68840826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529478147	chr5:68840860-68840861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547569464	chr5:68840877-68840878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370970569	chr5:68840886-68840887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144743806	chr5:68840898-68840899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539541122	chr5:68840909-68840910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557769604	chr5:68840949-68840950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374290737	chr5:68840951-68840952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569957677	chr5:68840963-68840964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537407554	chr5:68840977-68840978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs556208975	chr5:68840996-68840997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574644845	chr5:68841050-68841051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542082960	chr5:68841091-68841092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553989126	chr5:68841159-68841160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200539187	chr5:68841258-68841259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2666581	chr5:68841325-68841326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2561167	chr5:68841353-68841354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112435330	chr5:68841374-68841375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572218624	chr5:68842313-68842314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545907196	chr5:68842314-68842315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571000746	chr5:68842315-68842316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564168490	chr5:68842354-68842355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pseudo-TORCH syndrome	20727516	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68824000-68855400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr5:68828200-68840800	Weak transcription	Pancreas	Pancrea
3	chr5:68829600-68855400	Weak transcription	Fetal Intestine Small	intestine
4	chr5:68840800-68841000	Enhancers	Pancreas	Pancrea
5	chr5:68840800-68841000	Enhancers	HepG2	liver
6	chr5:68841000-68841200	Weak transcription	Pancreas	Pancrea
7	chr5:68841000-68855200	Weak transcription	HepG2	liver
8	chr5:68844400-68855400	Weak transcription	Fetal Intestine Large	intestine
9	chr5:68845800-68855600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr5:68855000-68855200	Enhancers	Dnd41	blood
11	chr5:68855000-68855600	Enhancers	Primary T cells fromperipheralblood	blood
12	chr5:68855200-68855400	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr5:68855200-68855400	Enhancers	Adipose Nuclei	Adipose
14	chr5:68855200-68855400	Enhancers	Liver	Liver
15	chr5:68855200-68855400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
16	chr5:68855200-68855400	Enhancers	HepG2	liver
17	chr5:68855200-68855400	Enhancers	HUVEC	blood vessel
18	chr5:68855200-68855600	Enhancers	Right Atrium	heart
19	chr5:68855200-68855600	Flanking Active TSS	Dnd41	blood
20	chr5:68855200-68855800	Enhancers	Fetal Brain Male	brain
21	chr5:68855200-68856800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:68855200-68857000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:68855400-68855600	Enhancers	Primary B cells from peripheral blood	blood
24	chr5:68855400-68855600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr5:68855400-68855600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr5:68855400-68855600	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr5:68855400-68855600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr5:68855400-68855600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr5:68855400-68855600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr5:68855400-68855600	Enhancers	Fetal Intestine Large	intestine
31	chr5:68855400-68855600	Enhancers	Fetal Muscle Trunk	muscle
32	chr5:68855400-68855600	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr5:68855400-68855600	Flanking Active TSS	HepG2	liver
34	chr5:68855400-68855600	Enhancers	HMEC	breast
35	chr5:68855400-68855600	Enhancers	NHEK	skin
36	chr5:68855400-68855800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr5:68855400-68855800	Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr5:68855400-68855800	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr5:68855400-68855800	Flanking Active TSS	Liver	Liver
40	chr5:68855400-68855800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr5:68855400-68855800	Flanking Active TSS	HUVEC	blood vessel
42	chr5:68855400-68856200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:68855400-68856200	Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr5:68855400-68856600	Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr5:68855400-68856600	Active TSS	Primary B cells from cord blood	blood
46	chr5:68855400-68856600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
47	chr5:68855400-68856800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr5:68855400-68856800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:68855400-68856800	Active TSS	Primary T cells from cord blood	blood
50	chr5:68855400-68856800	Active TSS	Primary hematopoietic stem cells short term culture	blood

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