Variant report

Variant	nsv948724
Chromosome Location	chr14:79484233-79614043
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:79557750-79558236	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr14:79557693-79558133	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:79560132-79560350	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr14:79557773-79558093	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr14:79557757-79558076	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr14:79557714-79558287	H1-hESC	embryonic stem cell:	n/a	chr14:79558092-79558105 chr14:79558092-79558103
7	CEBPB	chr14:79601619-79601724	IMR90	lung:	n/a	chr14:79601695-79601708
8	CEBPB	chr14:79559878-79560134	HepG2	liver:	n/a	chr14:79560020-79560031 chr14:79560018-79560031
9	CEBPB	chr14:79605965-79606029	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:79510018-79510268	A549	lung:	n/a	chr14:79510123-79510136
11	CEBPB	chr14:79523178-79523744	IMR90	lung:	n/a	n/a
12	CEBPB	chr14:79497978-79498031	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr14:79511642-79511933	A549	lung:	n/a	n/a
14	CREB1	chr14:79511763-79511975	A549	lung:	n/a	n/a
15	CTCF	chr14:79557806-79557852	Medullo	brain:	n/a	n/a
16	CTCF	chr14:79511620-79511770	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr14:79557960-79558110	Caco-2	colon:	n/a	n/a
18	CTCF	chr14:79598444-79598545	GM13976	blood:	n/a	n/a
19	CTCF	chr14:79558058-79558175	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:79511800-79511950	GM12869	blood:	n/a	chr14:79511824-79511832
21	CTCF	chr14:79558031-79558198	GM12878	blood:	n/a	n/a
22	CTCF	chr14:79558070-79558173	Lung_OC	lung:	n/a	n/a
23	CTCF	chr14:79488945-79488997	GM20000	blood:	n/a	n/a
24	CTCF	chr14:79546420-79546570	WERI-Rb-1	eye:	n/a	chr14:79546476-79546489
25	CTCF	chr14:79558046-79558193	LNCaP	prostate:	n/a	n/a
26	CTCF	chr14:79546412-79546471	GM20000	blood:	n/a	n/a
27	CTCF	chr14:79511480-79511630	HBMEC	blood vessel:	n/a	chr14:79511521-79511539
28	CTCF	chr14:79557921-79558251	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr14:79557780-79557930	HA-sp	spinal cord:	n/a	n/a
30	CTCF	chr14:79520000-79520150	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr14:79533567-79533689	GM13977	blood:	n/a	n/a
32	CTCF	chr14:79557980-79558130	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:79558040-79558187	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr14:79558064-79558189	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr14:79558020-79558170	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr14:79558100-79558250	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:79558051-79558196	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:79511400-79511550	HCFaa	heart:	n/a	chr14:79511521-79511539
39	CTCF	chr14:79543629-79543639	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr14:79558096-79558176	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr14:79558045-79558195	Medullo	brain:	n/a	n/a
42	CTCF	chr14:79511520-79511670	HMEC	breast:	n/a	chr14:79511521-79511539
43	CTCF	chr14:79557960-79558110	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr14:79511540-79511690	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr14:79511580-79511730	HMF	breast:	n/a	n/a
46	CTCF	chr14:79558020-79558170	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr14:79558020-79558170	Caco-2	colon:	n/a	n/a
48	E2F4	chr14:79551061-79551135	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr14:79537861-79537864	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr14:79488402-79488550	MCF10A-Er-Src	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:79558823-79558873	HCM	heart:	n/a
2	chr14:79529179-79529229	NT2-D1	testis:	n/a
3	chr14:79529179-79529229	AG04449	skin:	fetal
4	chr14:79558823-79558873	BJ	skin:	n/a
5	chr14:79558823-79558873	PrEC	prostate:	n/a
6	chr14:79529179-79529229	Hela-S3	cervix:	n/a
7	chr14:79511907-79511957	GM12878	blood:	n/a
8	chr14:79558823-79558873	HIPEpiC	eye:	n/a
9	chr14:79558823-79558873	GM06990	blood:	n/a
10	chr14:79529179-79529229	SK-N-SH_RA	brain:	n/a
11	chr14:79511907-79511957	SK-N-SH	brain:	n/a
12	chr14:79558823-79558873	HL-60	blood:	n/a
13	chr14:79529179-79529229	GM12892	blood:	n/a
14	chr14:79511907-79511957	Caco-2	colon:	n/a
15	chr14:79529179-79529229	HCPEpiC	choroid plexus:	n/a
16	chr14:79529179-79529229	HepG2	liver:	n/a
17	chr14:79529179-79529229	Jurkat	blood:	n/a
18	chr14:79529179-79529229	SK-N-SH	brain:	n/a
19	chr14:79529179-79529229	GM19239	blood:	n/a
20	chr14:79558823-79558873	HRCEpiC	kidney:	n/a
21	chr14:79558823-79558873	SK-N-MC	brain:	n/a
22	chr14:79558823-79558873	HCPEpiC	choroid plexus:	n/a
23	chr14:79511907-79511957	HepG2	liver:	n/a
24	chr14:79511907-79511957	Hela-S3	cervix:	n/a
25	chr14:79511907-79511957	HCPEpiC	choroid plexus:	n/a
26	chr14:79511907-79511957	AoSMC	blood vessel:	n/a
27	chr14:79558823-79558873	K562	blood:	n/a
28	chr14:79558823-79558873	SAEC	small airway:	n/a
29	chr14:79558823-79558873	HEEpiC	esophagus:	n/a
30	chr14:79529179-79529229	Hepatocyte	liver:	n/a
31	chr14:79511907-79511957	CMK	blood:	n/a
32	chr14:79529179-79529229	HEK293	kidney:	embryo
33	chr14:79529179-79529229	K562	blood:	n/a
34	chr14:79558823-79558873	SK-N-SH_RA	brain:	n/a
35	chr14:79511907-79511957	GM06990	blood:	n/a
36	chr14:79529179-79529229	HRPEpiC	eye:	n/a
37	chr14:79511907-79511957	HCM	heart:	n/a
38	chr14:79529179-79529229	MCF-7	breast:	n/a
39	chr14:79558823-79558873	U87	brain:	n/a
40	chr14:79511907-79511957	HNPCEpiC	eye:	n/a
41	chr14:79558823-79558873	Jurkat	blood:	n/a
42	chr14:79558823-79558873	NHBE	bronchial:	n/a
43	chr14:79558823-79558873	HNPCEpiC	eye:	n/a
44	chr14:79558823-79558873	LNCaP	prostate:	n/a
45	chr14:79529179-79529229	MCF10A-Er-Src	breast:	n/a
46	chr14:79558823-79558873	SK-N-SH	brain:	n/a
47	chr14:79529179-79529229	PFSK-1	brain:	n/a
48	chr14:79511907-79511957	PFSK-1	brain:	n/a
49	chr14:79529179-79529229	T-47D	breast:	n/a
50	chr14:79511907-79511957	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:79557622..79558152-chr15:97180235..97181024,2	MCF-7	breast:
2	chr14:79554622..79556371-chr14:79563139..79566085,2	K562	blood:
3	chr14:79573779..79574636-chr15:68722745..68723313,2	MCF-7	breast:
4	chr14:79554622..79556371-chr14:79563139..79566085,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIO2-5	chr14:79538510-79538846	ENSG00000258829.1
2	lnc-DIO2-5	chr14:79540891-79541105	ENSG00000258829.1
3	lnc-DIO2-5	chr14:79538475-79538818	ENSG00000258829.1
4	lnc-DIO2-5	chr14:79540891-79541110	ENSG00000258829.1

No data

Variant related genes	Relation type
ENSG00000258829	TF binding region
ENSG00000258829	CpG island

Extended variants
information (count: 3745 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3745 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8016232	chr14:79484233-79484234	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561712834	chr14:79484245-79484246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141432805	chr14:79484281-79484282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576176052	chr14:79484373-79484374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs150844553	chr14:79484383-79484384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs8017027	chr14:79484394-79484395	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs111472527	chr14:79484432-79484433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs555540223	chr14:79484493-79484494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563344561	chr14:79484496-79484497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547213329	chr14:79484511-79484512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371866924	chr14:79484617-79484618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs67838149	chr14:79484635-79484636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10148545	chr14:79484638-79484639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11628160	chr14:79484640-79484641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573569442	chr14:79484654-79484655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs33953818	chr14:79484681-79484682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2964900	chr14:79484708-79484709	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs77639066	chr14:79484714-79484715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540944448	chr14:79484720-79484721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369271050	chr14:79484782-79484783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144524979	chr14:79484785-79484786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139712877	chr14:79484811-79484812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571366466	chr14:79484844-79484845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78978758	chr14:79484869-79484870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74622233	chr14:79484946-79484947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556676813	chr14:79484948-79484949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373927958	chr14:79484951-79484952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576576495	chr14:79484964-79484965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75026814	chr14:79485003-79485004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555668092	chr14:79485099-79485100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375227884	chr14:79485101-79485102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572094020	chr14:79485126-79485127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541069068	chr14:79485153-79485154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567463297	chr14:79485155-79485156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115109660	chr14:79485243-79485244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs578012405	chr14:79485284-79485285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553800399	chr14:79485327-79485328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543564141	chr14:79485342-79485343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190182874	chr14:79485392-79485393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529125876	chr14:79485432-79485433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35144231	chr14:79485464-79485465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373300378	chr14:79485530-79485531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145292926	chr14:79485533-79485534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2938031	chr14:79485596-79485597	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs528087014	chr14:79485612-79485613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551348837	chr14:79485660-79485661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571162746	chr14:79485718-79485719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147228628	chr14:79485818-79485819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550426566	chr14:79485843-79485844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140278600	chr14:79485850-79485851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79478200-79485400	Weak transcription	Colon Smooth Muscle	Colon
2	chr14:79478400-79485200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr14:79482400-79485800	Enhancers	Osteobl	bone
4	chr14:79482600-79486200	Enhancers	HSMM	muscle
5	chr14:79482600-79486200	Enhancers	NHLF	lung
6	chr14:79482800-79486000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr14:79482800-79486200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:79483800-79484800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr14:79483800-79484800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr14:79483800-79485000	Weak transcription	NHEK	skin
11	chr14:79483800-79485200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr14:79483800-79485400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:79483800-79487800	Weak transcription	Fetal Muscle Leg	muscle
14	chr14:79484000-79484400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:79484000-79484800	Weak transcription	NHDF-Ad	bronchial
16	chr14:79484000-79485200	Weak transcription	HMEC	breast
17	chr14:79484200-79485400	Weak transcription	NH-A	brain
18	chr14:79484200-79487400	Weak transcription	HSMMtube	muscle
19	chr14:79484400-79485800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr14:79484800-79485200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr14:79484800-79485600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr14:79484800-79485600	Enhancers	NHDF-Ad	bronchial
23	chr14:79485000-79485600	Enhancers	NHEK	skin
24	chr14:79485200-79485400	Enhancers	Rectal Smooth Muscle	rectum
25	chr14:79485200-79485600	Enhancers	HMEC	breast
26	chr14:79485200-79485600	Enhancers	HUVEC	blood vessel
27	chr14:79485400-79485600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr14:79485400-79485600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr14:79485400-79485600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr14:79485400-79485600	Enhancers	Colon Smooth Muscle	Colon
31	chr14:79485400-79485800	Enhancers	NH-A	brain
32	chr14:79485600-79494600	Weak transcription	HUVEC	blood vessel
33	chr14:79486000-79487600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr14:79486200-79487200	Weak transcription	HSMM	muscle
35	chr14:79486200-79487800	Weak transcription	NHLF	lung
36	chr14:79487200-79489400	Enhancers	HSMM	muscle
37	chr14:79487400-79489000	Enhancers	HSMMtube	muscle
38	chr14:79487600-79488800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr14:79487800-79488200	Enhancers	Brain Substantia Nigra	brain
40	chr14:79487800-79488400	Enhancers	Brain Cingulate Gyrus	brain
41	chr14:79487800-79488400	Enhancers	Brain Germinal Matrix	brain
42	chr14:79487800-79488400	Enhancers	Fetal Muscle Leg	muscle
43	chr14:79488000-79488200	Enhancers	NHLF	lung
44	chr14:79488000-79488400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:79488000-79488400	Enhancers	Brain Hippocampus Middle	brain
46	chr14:79488000-79488400	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr14:79489400-79490400	Weak transcription	HSMM	muscle
48	chr14:79490400-79491800	Enhancers	HSMM	muscle
49	chr14:79493600-79495800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:79493800-79495400	Enhancers	Primary monocytes fromperipheralblood	blood

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