Variant report

Variant	nsv982875
Chromosome Location	chr10:50324703-50328326
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:50325483-50325774	K562	blood:	n/a	chr10:50325613-50325626 chr10:50325613-50325624 chr10:50325634-50325645 chr10:50325613-50325626
2	CEBPB	chr10:50325467-50325766	HepG2	liver:	n/a	chr10:50325613-50325626 chr10:50325613-50325624 chr10:50325634-50325645 chr10:50325613-50325626
3	CTCF	chr10:50326709-50326713	LNCaP	prostate:	n/a	n/a
4	E2F4	chr10:50327947-50328167	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F6	chr10:50327936-50328104	K562	blood:	n/a	n/a
6	FOS	chr10:50327898-50328205	MCF10A-Er-Src	breast:	n/a	chr10:50328037-50328045
7	FOS	chr10:50327886-50328183	MCF10A-Er-Src	breast:	n/a	chr10:50328037-50328045
8	FOS	chr10:50327908-50328189	MCF10A-Er-Src	breast:	n/a	chr10:50328037-50328045
9	FOS	chr10:50327894-50328176	MCF10A-Er-Src	breast:	n/a	chr10:50328037-50328045
10	GATA2	chr10:50326474-50326884	SH-SY5Y	brain:	n/a	chr10:50326543-50326550
11	GATA3	chr10:50327161-50327607	SH-SY5Y	brain:	n/a	n/a
12	GATA3	chr10:50326086-50326582	SH-SY5Y	brain:	n/a	chr10:50326543-50326550
13	HCFC1	chr10:50325466-50325469	K562	blood:	n/a	n/a
14	MAFK	chr10:50325587-50325872	HepG2	liver:	n/a	n/a
15	MAFK	chr10:50325617-50325826	K562	blood:	n/a	n/a
16	MAFK	chr10:50325658-50325760	HepG2	liver:	n/a	n/a
17	MAX	chr10:50327813-50328125	H1-hESC	embryonic stem cell:	n/a	chr10:50327966-50327975
18	MAX	chr10:50327844-50328118	H1-hESC	embryonic stem cell:	n/a	chr10:50327966-50327975
19	MAX	chr10:50327800-50328217	K562	blood:	n/a	chr10:50327966-50327975
20	MXI1	chr10:50327705-50328241	IMR90	lung:	n/a	n/a
21	MYC	chr10:50327789-50328102	K562	blood:	n/a	chr10:50327966-50327975
22	MYC	chr10:50327805-50328195	MCF10A-Er-Src	breast:	n/a	chr10:50327966-50327975
23	MYC	chr10:50327838-50328214	MCF10A-Er-Src	breast:	n/a	chr10:50327966-50327975
24	NFYA	chr10:50326520-50326834	K562	blood:	n/a	chr10:50326668-50326681 chr10:50326668-50326683 chr10:50326668-50326682 chr10:50326668-50326686 chr10:50326670-50326680
25	NFYB	chr10:50326511-50326863	GM12878	blood:	n/a	chr10:50326851-50326861 chr10:50326668-50326681 chr10:50326668-50326683 chr10:50326668-50326682 chr10:50326670-50326680
26	NFYB	chr10:50326521-50326876	K562	blood:	n/a	chr10:50326851-50326861 chr10:50326668-50326681 chr10:50326668-50326683 chr10:50326668-50326682 chr10:50326670-50326680
27	RCOR1	chr10:50326472-50327140	K562	blood:	n/a	n/a
28	RCOR1	chr10:50327787-50328443	IMR90	lung:	n/a	n/a
29	STAT3	chr10:50325456-50325640	MCF10A-Er-Src	breast:	n/a	n/a
30	STAT3	chr10:50328172-50328372	MCF10A-Er-Src	breast:	n/a	chr10:50328278-50328285
31	STAT3	chr10:50327952-50328212	MCF10A-Er-Src	breast:	n/a	n/a
32	STAT3	chr10:50327872-50328112	MCF10A-Er-Src	breast:	n/a	n/a
33	TAL1	chr10:50326540-50326618	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:50326783-50326833	SK-N-SH	brain:	n/a
2	chr10:50326783-50326833	SKMC	muscle:	n/a
3	chr10:50326783-50326833	GM12892	blood:	n/a
4	chr10:50326783-50326833	NHBE	bronchial:	n/a
5	chr10:50326783-50326833	NHDF-neo	bronchial:	n/a
6	chr10:50326783-50326833	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:50326783-50326833	AoSMC	blood vessel:	n/a
8	chr10:50326783-50326833	HCF	heart:	n/a
9	chr10:50326783-50326833	ProgFib	skin:	n/a
10	chr10:50326783-50326833	HRE	kidney:	n/a
11	chr10:50326783-50326833	HRCEpiC	kidney:	n/a
12	chr10:50326783-50326833	AG04450	lung:	fetal
13	chr10:50326783-50326833	T-47D	breast:	n/a
14	chr10:50326783-50326833	SK-N-SH_RA	brain:	n/a
15	chr10:50326783-50326833	H1-hESC	embryonic stem cell:	embryo
16	chr10:50326783-50326833	HL-60	blood:	n/a
17	chr10:50326783-50326833	Jurkat	blood:	n/a
18	chr10:50326783-50326833	PANC-1	pancreas:	n/a
19	chr10:50326783-50326833	MCF-7	breast:	n/a
20	chr10:50326783-50326833	HepG2	liver:	n/a
21	chr10:50326783-50326833	IMR90	lung:	fetal
22	chr10:50326783-50326833	BJ	skin:	n/a
23	chr10:50326783-50326833	A549	lung:	n/a
24	chr10:50326783-50326833	HUVEC	blood vessel:	n/a
25	chr10:50326783-50326833	GM19239	blood:	n/a
26	chr10:50326783-50326833	HIPEpiC	eye:	n/a
27	chr10:50326783-50326833	HEEpiC	esophagus:	n/a
28	chr10:50326783-50326833	GM12878	blood:	n/a
29	chr10:50326783-50326833	BE2_C	brain:	n/a
30	chr10:50326783-50326833	HRPEpiC	eye:	n/a
31	chr10:50326783-50326833	Hepatocyte	liver:	n/a
32	chr10:50326783-50326833	HNPCEpiC	eye:	n/a
33	chr10:50326783-50326833	HEK293	kidney:	embryo
34	chr10:50326783-50326833	NH-A	brain:	n/a
35	chr10:50326783-50326833	NB4	blood:	n/a
36	chr10:50326783-50326833	GM06990	blood:	n/a
37	chr10:50326783-50326833	RPTEC	kidney:	n/a
38	chr10:50326783-50326833	Hela-S3	cervix:	n/a
39	chr10:50326783-50326833	HCPEpiC	choroid plexus:	n/a
40	chr10:50326783-50326833	Caco-2	colon:	n/a
41	chr10:50326783-50326833	NT2-D1	testis:	n/a
42	chr10:50326783-50326833	SK-N-MC	brain:	n/a
43	chr10:50326783-50326833	HCM	heart:	n/a
44	chr10:50326783-50326833	K562	blood:	n/a
45	chr10:50326783-50326833	MCF10A-Er-Src	breast:	n/a
46	chr10:50326783-50326833	AG09319	gingival:	n/a
47	chr10:50326783-50326833	CMK	blood:	n/a
48	chr10:50326783-50326833	AG09309	skin:	n/a
49	chr10:50326783-50326833	ECC-1	luminal epithelium:	n/a
50	chr10:50326783-50326833	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:50327680..50329332-chr10:50338988..50341061,2	K562	blood:
2	chr10:50314500..50318570-chr10:50326499..50328270,3	K562	blood:
3	chr10:50321527..50324998-chr10:50325157..50328658,6	K562	blood:
4	chr10:50281055..50283973-chr10:50326395..50329291,2	K562	blood:
5	chr10:50322283..50325786-chr10:50341748..50344745,3	K562	blood:
6	chr10:50322609..50324135-chr10:50326068..50328008,2	K562	blood:

Variant related genes	Relation type
FAM170B-AS1	TF binding region
VSTM4	TF binding region
FAM170B-AS1	CpG island
VSTM4	CpG island
ENSG00000165633	chromatin interactions
ENSG00000172538	chromatin interactions

Extended variants
information (count: 126 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:126 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540317025	chr10:50324818-50324819	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs575223051	chr10:50324871-50324872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555599037	chr10:50324904-50324905	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs11100989	chr10:50324915-50324916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs369439612	chr10:50324994-50324995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs114358695	chr10:50325034-50325035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11100990	chr10:50325055-50325056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs540435870	chr10:50325078-50325079	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577904707	chr10:50325079-50325080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs148236020	chr10:50325089-50325090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs532480100	chr10:50325108-50325109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550892758	chr10:50325109-50325110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568914043	chr10:50325117-50325118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs80143911	chr10:50325146-50325147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141895041	chr10:50325183-50325184	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150219192	chr10:50325281-50325282	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs138747949	chr10:50325293-50325294	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs142986402	chr10:50325314-50325315	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs117206547	chr10:50325319-50325320	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147449392	chr10:50325339-50325340	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs187613469	chr10:50325342-50325343	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575484383	chr10:50325405-50325406	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536266739	chr10:50325434-50325435	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369438774	chr10:50325474-50325475	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs117586087	chr10:50325493-50325494	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs573324135	chr10:50325504-50325505	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs540352244	chr10:50325524-50325525	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs140206093	chr10:50325529-50325530	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs113530745	chr10:50325530-50325531	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs376293429	chr10:50325563-50325564	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs4532948	chr10:50325572-50325573	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs375143146	chr10:50325573-50325574	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs61167870	chr10:50325587-50325588	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs559872270	chr10:50325605-50325606	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs34080129	chr10:50325607-50325608	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs527427166	chr10:50325608-50325609	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs551975193	chr10:50325627-50325628	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs570485143	chr10:50325635-50325636	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs4412679	chr10:50325660-50325661	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs4497320	chr10:50325739-50325740	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs569221791	chr10:50325826-50325827	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs536529575	chr10:50325839-50325840	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs556851179	chr10:50325840-50325841	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs573155271	chr10:50325871-50325872	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs144338514	chr10:50325908-50325909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192099240	chr10:50325919-50325920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184084167	chr10:50325934-50325935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs117703348	chr10:50325940-50325941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562638719	chr10:50326051-50326052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs118050559	chr10:50326060-50326061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Hypotonia	21948486	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50323800-50326200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:50323800-50327800	Weak transcription	NH-A	brain
3	chr10:50324000-50324800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:50324000-50325000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr10:50324000-50325000	Enhancers	Ovary	ovary
6	chr10:50324000-50325200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr10:50324000-50325200	Weak transcription	Adipose Nuclei	Adipose
8	chr10:50324000-50325400	Enhancers	Liver	Liver
9	chr10:50324000-50325600	Weak transcription	Brain Angular Gyrus	brain
10	chr10:50324000-50325800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr10:50324000-50327200	Enhancers	Fetal Thymus	thymus
12	chr10:50324000-50328200	Weak transcription	HSMMtube	muscle
13	chr10:50324000-50343600	Weak transcription	Right Atrium	heart
14	chr10:50324200-50325000	Enhancers	Fetal Muscle Trunk	muscle
15	chr10:50324200-50325400	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr10:50324200-50325400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr10:50324200-50325600	Weak transcription	K562	blood
18	chr10:50324200-50326600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr10:50324200-50328400	Weak transcription	Fetal Stomach	stomach
20	chr10:50324400-50327200	Enhancers	Fetal Muscle Leg	muscle
21	chr10:50324600-50324800	Enhancers	Spleen	Spleen
22	chr10:50324800-50325000	Enhancers	Brain Hippocampus Middle	brain
23	chr10:50324800-50328200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr10:50325000-50325800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr10:50325000-50338600	Weak transcription	Fetal Muscle Trunk	muscle
26	chr10:50325000-50339400	Weak transcription	Ovary	ovary
27	chr10:50325200-50325400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:50325200-50326000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr10:50325200-50326000	Enhancers	Adipose Nuclei	Adipose
30	chr10:50325400-50325600	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr10:50325400-50327200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr10:50325400-50328000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr10:50325600-50325800	Enhancers	Brain Cingulate Gyrus	brain
34	chr10:50325600-50325800	Enhancers	Stomach Smooth Muscle	stomach
35	chr10:50325600-50326400	Enhancers	Brain Angular Gyrus	brain
36	chr10:50325600-50327000	Enhancers	K562	blood
37	chr10:50325800-50326000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr10:50325800-50327000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr10:50325800-50327800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr10:50326000-50326400	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr10:50326200-50326400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr10:50326200-50326600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr10:50326200-50327000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr10:50326200-50327000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr10:50326400-50326800	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr10:50326400-50327800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr10:50326600-50326800	Enhancers	Thymus	Thymus
48	chr10:50326600-50327000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr10:50326600-50327200	Enhancers	Fetal Lung	lung
50	chr10:50326800-50327000	Enhancers	Primary hematopoietic stem cells	blood

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