Variant report

Variant	nsv1002926
Chromosome Location	chr4:70061849-70105434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:143)
CpG islands
(count:245)
Chromatin interactive
region (count:3)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:143 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
2	ATF1	chr4:70087666-70087866	K562	blood:	n/a	n/a
3	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
4	BCL3	chr4:70080358-70080837	A549	lung:	n/a	n/a
5	BHLHE40	chr4:70087582-70087589	K562	blood:	n/a	n/a
6	CEBPB	chr4:70077980-70078075	K562	blood:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
7	CEBPB	chr4:70077864-70078215	IMR90	lung:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
8	CEBPB	chr4:70077881-70078188	HepG2	liver:	n/a	chr4:70078030-70078041 chr4:70078032-70078043
9	CEBPB	chr4:70080509-70080873	A549	lung:	n/a	n/a
10	CEBPD	chr4:70105414-70105831	K562	blood:	n/a	n/a
11	CTCF	chr4:70089049-70089337	K562	blood:	n/a	n/a
12	CTCF	chr4:70089077-70089312	MCF-7	breast:	n/a	n/a
13	CTCF	chr4:70070599-70070664	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr4:70089103-70089279	A549	lung:	n/a	n/a
15	CTCF	chr4:70105330-70105377	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr4:70097000-70097025	GM13977	blood:	n/a	n/a
17	CTCF	chr4:70099241-70099301	GM10248	blood:	n/a	n/a
18	CTCF	chr4:70105420-70105570	Caco-2	colon:	n/a	n/a
19	CTCF	chr4:70089105-70089251	K562	blood:	n/a	n/a
20	CTCF	chr4:70078196-70078250	GM13976	blood:	n/a	n/a
21	CTCF	chr4:70089054-70089358	A549	lung:	n/a	n/a
22	CTCF	chr4:70089045-70089320	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:70077161-70077220	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr4:70098014-70098052	Lung_OC	lung:	n/a	n/a
25	CTCF	chr4:70081934-70082033	GM10248	blood:	n/a	n/a
26	CTCF	chr4:70089120-70089270	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr4:70082912-70082994	GM10248	blood:	n/a	n/a
28	CTCF	chr4:70105384-70105645	K562	blood:	n/a	n/a
29	CTCF	chr4:70089071-70089282	HepG2	liver:	n/a	n/a
30	CTCF	chr4:70089188-70089262	LNCaP	prostate:	n/a	n/a
31	CTCF	chr4:70089095-70089280	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:70100451-70100491	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr4:70089126-70089248	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:70096114-70096171	GM10266	blood:	n/a	n/a
35	CTCF	chr4:70089005-70089293	HepG2	liver:	n/a	n/a
36	CTCF	chr4:70089088-70089310	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:70089131-70089152	Gliobla	brain:	n/a	n/a
38	CTCF	chr4:70097033-70097046	GM13977	blood:	n/a	n/a
39	CTCF	chr4:70071636-70071728	GM13977	blood:	n/a	n/a
40	CTCF	chr4:70089128-70089240	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr4:70089080-70089230	HepG2	liver:	n/a	n/a
42	CTCF	chr4:70089151-70089329	LNCaP	prostate:	n/a	n/a
43	E2F4	chr4:70101266-70101267	MCF10A-Er-Src	breast:	n/a	n/a
44	EGR1	chr4:70087499-70087785	K562	blood:	n/a	n/a
45	EP300	chr4:70080278-70081011	A549	lung:	n/a	n/a
46	EP300	chr4:70080436-70080904	A549	lung:	n/a	n/a
47	FOS	chr4:70062387-70062626	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:70062379-70062485	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr4:70062305-70062621	MCF10A-Er-Src	breast:	n/a	n/a
50	FOSL2	chr4:70080425-70080929	A549	lung:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:70066318-70066368	AG09309	skin:	n/a
2	chr4:70066318-70066368	AG09309	skin:	n/a
3	chr4:70064835-70064885	GM12878	blood:	n/a
4	chr4:70080453-70080503	MCF-7	breast:	n/a
5	chr4:70065325-70065375	NHDF-neo	bronchial:	n/a
6	chr4:70066318-70066368	BJ	skin:	n/a
7	chr4:70065325-70065375	PFSK-1	brain:	n/a
8	chr4:70064835-70064885	H1-hESC	embryonic stem cell:	embryo
9	chr4:70080453-70080503	HRCEpiC	kidney:	n/a
10	chr4:70066318-70066368	NHDF-neo	bronchial:	n/a
11	chr4:70065325-70065375	SKMC	muscle:	n/a
12	chr4:70065325-70065375	HNPCEpiC	eye:	n/a
13	chr4:70080453-70080503	PFSK-1	brain:	n/a
14	chr4:70066318-70066368	ovcar-3	ovarian:	n/a
15	chr4:70064835-70064885	HEEpiC	esophagus:	n/a
16	chr4:70066318-70066368	IMR90	lung:	fetal
17	chr4:70065325-70065375	NH-A	brain:	n/a
18	chr4:70064835-70064885	HCM	heart:	n/a
19	chr4:70065325-70065375	ovcar-3	ovarian:	n/a
20	chr4:70065325-70065375	HEEpiC	esophagus:	n/a
21	chr4:70080453-70080503	Caco-2	colon:	n/a
22	chr4:70066318-70066368	HL-60	blood:	n/a
23	chr4:70080453-70080503	HepG2	liver:	n/a
24	chr4:70064835-70064885	SK-N-SH_RA	brain:	n/a
25	chr4:70065325-70065375	GM19239	blood:	n/a
26	chr4:70064835-70064885	Hela-S3	cervix:	n/a
27	chr4:70065325-70065375	H1-hESC	embryonic stem cell:	embryo
28	chr4:70066318-70066368	GM06990	blood:	n/a
29	chr4:70064835-70064885	Hepatocyte	liver:	n/a
30	chr4:70080453-70080503	HCF	heart:	n/a
31	chr4:70065325-70065375	HRE	kidney:	n/a
32	chr4:70080453-70080503	HRE	kidney:	n/a
33	chr4:70065325-70065375	CMK	blood:	n/a
34	chr4:70066318-70066368	HRCEpiC	kidney:	n/a
35	chr4:70066318-70066368	GM12878	blood:	n/a
36	chr4:70066318-70066368	NB4	blood:	n/a
37	chr4:70066318-70066368	T-47D	breast:	n/a
38	chr4:70066318-70066368	HRE	kidney:	n/a
39	chr4:70080453-70080503	A549	lung:	n/a
40	chr4:70080453-70080503	HMEC	breast:	n/a
41	chr4:70066318-70066368	AG09319	gingival:	n/a
42	chr4:70065325-70065375	ECC-1	luminal epithelium:	n/a
43	chr4:70064835-70064885	K562	blood:	n/a
44	chr4:70066318-70066368	LNCaP	prostate:	n/a
45	chr4:70066318-70066368	HepG2	liver:	n/a
46	chr4:70066318-70066368	MCF-7	breast:	n/a
47	chr4:70064835-70064885	PANC-1	pancreas:	n/a
48	chr4:70066318-70066368	HCM	heart:	n/a
49	chr4:70064835-70064885	HRCEpiC	kidney:	n/a
50	chr4:70080453-70080503	HCPEpiC	choroid plexus:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69673177..69674687-chr4:70085938..70087696,2	MCF-7	breast:
2	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:
3	chr4:70060045..70062674-chr4:70067007..70069842,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-1	chr4:70066190-70066296	ENSG00000250696.1
2	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70066138-70066296	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
5	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
7	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1

No data

Variant related genes	Relation type
ENSG00000250696	TF binding region
ENSG00000268803	TF binding region
UGT2B11	TF binding region
ENSG00000249763	TF binding region
ENSG00000250696	CpG island
ENSG00000268803	CpG island
UGT2B11	CpG island
ENSG00000249763	CpG island

Extended variants
information (count: 1149 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549485076	chr4:70061849-70061850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116530341	chr4:70061874-70061875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72501233	chr4:70061879-70061880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs574820757	chr4:70061890-70061891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551697547	chr4:70061911-70061912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571568705	chr4:70061942-70061943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189053963	chr4:70061969-70061970	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs192624638	chr4:70062012-70062013	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs577417158	chr4:70062021-70062022	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs535941846	chr4:70062028-70062029	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs568831078	chr4:70062052-70062053	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs183582160	chr4:70062054-70062055	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs546312968	chr4:70062059-70062060	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575621389	chr4:70062064-70062065	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs77042210	chr4:70062094-70062095	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs371792861	chr4:70062145-70062146	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs74725542	chr4:70062198-70062199	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs578201590	chr4:70062233-70062234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369742960	chr4:70062241-70062242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116587535	chr4:70062252-70062253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375026406	chr4:70062306-70062307	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs114655822	chr4:70062333-70062334	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs186544993	chr4:70062340-70062341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs150944320	chr4:70062351-70062352	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs563019748	chr4:70062385-70062386	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs531690224	chr4:70062388-70062389	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs551806623	chr4:70062445-70062446	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs577404030	chr4:70062474-70062475	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs139437129	chr4:70062502-70062503	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs533865447	chr4:70062549-70062550	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs547696154	chr4:70062562-70062563	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs567329733	chr4:70062582-70062583	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs6818137	chr4:70062598-70062599	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs191372314	chr4:70062616-70062617	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs575743336	chr4:70062617-70062618	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs62298912	chr4:70062640-70062641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538214339	chr4:70062682-70062683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558154564	chr4:70062718-70062719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572035923	chr4:70062741-70062742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12502502	chr4:70062750-70062751	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs79230142	chr4:70062757-70062758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114147785	chr4:70062775-70062776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184697241	chr4:70062784-70062785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146745294	chr4:70062806-70062807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527957717	chr4:70062858-70062859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371339218	chr4:70062862-70062863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189753237	chr4:70062889-70062890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116357188	chr4:70062914-70062915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545392320	chr4:70062922-70062923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181864160	chr4:70062923-70062924	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70059800-70066800	Weak transcription	Liver	Liver
2	chr4:70062000-70063200	Enhancers	HMEC	breast
3	chr4:70062400-70063000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:70062600-70063400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:70066800-70067800	Strong transcription	Liver	Liver
6	chr4:70067800-70070600	Weak transcription	Liver	Liver
7	chr4:70076400-70076600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:70076800-70077800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr4:70077800-70078200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr4:70080400-70080800	Enhancers	HepG2	liver
11	chr4:70080600-70081200	Enhancers	Rectal Smooth Muscle	rectum
12	chr4:70080800-70081200	Enhancers	A549	lung
13	chr4:70085800-70086000	Enhancers	Fetal Intestine Large	intestine
14	chr4:70086000-70086400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:70086000-70087000	Weak transcription	Fetal Intestine Large	intestine
16	chr4:70086400-70087400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:70087000-70087600	Enhancers	Fetal Intestine Large	intestine
18	chr4:70087200-70088600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr4:70087400-70087600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:70088600-70090200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr4:70090200-70091000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:70090400-70090600	Enhancers	HepG2	liver
23	chr4:70090600-70091000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:70090600-70091000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr4:70090600-70091000	Enhancers	Fetal Stomach	stomach
26	chr4:70104600-70106600	Enhancers	Fetal Intestine Large	intestine
27	chr4:70105000-70106600	Enhancers	Fetal Intestine Small	intestine
28	chr4:70105000-70106600	Enhancers	HepG2	liver
29	chr4:70105200-70106000	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr4:70105200-70106400	Enhancers	Duodenum Mucosa	Duodenum
31	chr4:70105200-70106400	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr4:70105200-70106600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:70105200-70106800	Enhancers	Stomach Mucosa	stomach
34	chr4:70105400-70105800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:70105400-70106200	Enhancers	Primary hematopoietic stem cells short term culture	blood

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