Variant report

Variant	nsv1050694
Chromosome Location	chr10:4290802-4306798
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	ATF1	chr10:4304785-4304985	K562	blood:	n/a	n/a
2	ATF1	chr10:4296957-4297180	K562	blood:	n/a	n/a
3	BCL3	chr10:4304633-4304899	GM12878	blood:	n/a	n/a
4	BCL3	chr10:4304705-4304906	GM12878	blood:	n/a	n/a
5	CBX3	chr10:4302647-4303081	HCT-116	colon:	n/a	n/a
6	CEBPB	chr10:4296947-4297179	A549	lung:	n/a	n/a
7	CEBPB	chr10:4305189-4305928	Hela-S3	cervix:	n/a	chr10:4305239-4305250
8	CEBPB	chr10:4305612-4305739	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:4296845-4297267	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr10:4296810-4297453	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:4292740-4292819	HepG2	liver:	n/a	chr10:4292773-4292784
12	CTCF	chr10:4300325-4300371	A549	lung:	n/a	n/a
13	CTCF	chr10:4290829-4290961	GM19240	blood:	n/a	chr10:4290882-4290903
14	CTCF	chr10:4290801-4290982	GM19239	blood:	n/a	chr10:4290882-4290903
15	CTCF	chr10:4290826-4290944	GM19238	blood:	n/a	chr10:4290882-4290903
16	CTCF	chr10:4290809-4290943	Spleen_OC	spleen:	n/a	chr10:4290882-4290903
17	CTCF	chr10:4300340-4300490	HepG2	liver:	n/a	n/a
18	CTCF	chr10:4290848-4290968	NHEK	skin:	n/a	chr10:4290882-4290903
19	E2F4	chr10:4302505-4303001	MCF10A-Er-Src	breast:	n/a	n/a
20	EP300	chr10:4296923-4297217	SK-N-SH_RA	brain:	n/a	chr10:4297021-4297028
21	EP300	chr10:4302522-4303279	SK-N-SH	brain:	n/a	chr10:4302890-4302899 chr10:4302889-4302898 chr10:4303205-4303219
22	EP300	chr10:4296249-4297489	SK-N-SH	brain:	n/a	chr10:4296873-4296887 chr10:4297021-4297028
23	EP300	chr10:4302723-4303153	SK-N-SH_RA	brain:	n/a	chr10:4302890-4302899 chr10:4302889-4302898
24	EP300	chr10:4296854-4297218	Hela-S3	cervix:	n/a	chr10:4296873-4296887 chr10:4297021-4297028
25	FOS	chr10:4302642-4303096	MCF10A-Er-Src	breast:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302888-4302899 chr10:4302890-4302899 chr10:4302889-4302898
26	FOS	chr10:4302657-4303090	MCF10A-Er-Src	breast:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302888-4302899 chr10:4302890-4302899 chr10:4302889-4302898
27	FOS	chr10:4302638-4303268	HUVEC	blood vessel:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302888-4302899 chr10:4302890-4302899 chr10:4302889-4302898
28	FOS	chr10:4298071-4298251	MCF10A-Er-Src	breast:	n/a	chr10:4298181-4298188 chr10:4298181-4298189 chr10:4298180-4298190 chr10:4298181-4298189
29	FOS	chr10:4291998-4292904	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr10:4302686-4303078	MCF10A-Er-Src	breast:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302888-4302899 chr10:4302890-4302899 chr10:4302889-4302898
31	FOS	chr10:4296890-4297238	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr10:4291998-4292950	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr10:4296895-4297167	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr10:4292040-4292659	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr10:4296922-4297168	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr10:4302649-4303087	MCF10A-Er-Src	breast:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302888-4302899 chr10:4302890-4302899 chr10:4302889-4302898
37	FOS	chr10:4292007-4292946	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr10:4298120-4298248	MCF10A-Er-Src	breast:	n/a	chr10:4298181-4298188 chr10:4298181-4298189 chr10:4298180-4298190 chr10:4298181-4298189
39	FOS	chr10:4296905-4297216	MCF10A-Er-Src	breast:	n/a	n/a
40	FOSL1	chr10:4302640-4303182	HCT-116	colon:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302890-4302899 chr10:4302889-4302898
41	FOSL1	chr10:4302602-4303158	HCT-116	colon:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302890-4302899 chr10:4302889-4302898
42	FOSL2	chr10:4302625-4303142	A549	lung:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302890-4302899 chr10:4302889-4302898
43	FOSL2	chr10:4296600-4297405	SK-N-SH	brain:	n/a	n/a
44	FOSL2	chr10:4302606-4303194	SK-N-SH	brain:	n/a	chr10:4302890-4302898 chr10:4302891-4302898 chr10:4302890-4302899 chr10:4302889-4302898
45	GATA3	chr10:4302527-4303262	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr10:4296703-4297378	SK-N-SH	brain:	n/a	n/a
47	GATA3	chr10:4305164-4305757	MCF-7	breast:	n/a	n/a
48	GATA3	chr10:4305222-4305685	T-47D	breast:	n/a	n/a
49	GATA3	chr10:4305331-4305611	MCF-7	breast:	n/a	n/a
50	GATA3	chr10:4305118-4305759	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4296406-4296456	ECC-1	luminal epithelium:	n/a
2	chr10:4296406-4296456	PFSK-1	brain:	n/a
3	chr10:4296406-4296456	HPAEpiC	pulmonary alveolar:	n/a
4	chr10:4296406-4296456	NB4	blood:	n/a
5	chr10:4296406-4296456	BJ	skin:	n/a
6	chr10:4296406-4296456	GM12878	blood:	n/a
7	chr10:4296406-4296456	Hela-S3	cervix:	n/a
8	chr10:4296406-4296456	HCT-116	colon:	n/a
9	chr10:4296406-4296456	HRCEpiC	kidney:	n/a
10	chr10:4296406-4296456	MCF-7	breast:	n/a
11	chr10:4296406-4296456	PANC-1	pancreas:	n/a
12	chr10:4296406-4296456	BE2_C	brain:	n/a
13	chr10:4296406-4296456	GM12892	blood:	n/a
14	chr10:4296406-4296456	HRE	kidney:	n/a
15	chr10:4296406-4296456	PrEC	prostate:	n/a
16	chr10:4296406-4296456	Caco-2	colon:	n/a
17	chr10:4296406-4296456	HEK293	kidney:	embryo
18	chr10:4296406-4296456	H1-hESC	embryonic stem cell:	embryo
19	chr10:4296406-4296456	GM06990	blood:	n/a
20	chr10:4296406-4296456	RPTEC	kidney:	n/a
21	chr10:4296406-4296456	AG09309	skin:	n/a
22	chr10:4296406-4296456	LNCaP	prostate:	n/a
23	chr10:4296406-4296456	HAEpiC	amniotic membrane:	n/a
24	chr10:4296406-4296456	HIPEpiC	eye:	n/a
25	chr10:4296406-4296456	AG04449	skin:	fetal
26	chr10:4296406-4296456	Hepatocyte	liver:	n/a
27	chr10:4296406-4296456	HCPEpiC	choroid plexus:	n/a
28	chr10:4296406-4296456	NH-A	brain:	n/a
29	chr10:4296406-4296456	T-47D	breast:	n/a
30	chr10:4296406-4296456	NT2-D1	testis:	n/a
31	chr10:4296406-4296456	HepG2	liver:	n/a
32	chr10:4296406-4296456	HCM	heart:	n/a
33	chr10:4296406-4296456	ProgFib	skin:	n/a
34	chr10:4296406-4296456	GM19239	blood:	n/a
35	chr10:4296406-4296456	A549	lung:	n/a
36	chr10:4296406-4296456	AG10803	skin:	n/a
37	chr10:4296406-4296456	U87	brain:	n/a
38	chr10:4296406-4296456	HCF	heart:	n/a
39	chr10:4296406-4296456	NHBE	bronchial:	n/a
40	chr10:4296406-4296456	AG09319	gingival:	n/a
41	chr10:4296406-4296456	NHDF-neo	bronchial:	n/a
42	chr10:4296406-4296456	ovcar-3	ovarian:	n/a
43	chr10:4296406-4296456	AG04450	lung:	fetal
44	chr10:4296406-4296456	CMK	blood:	n/a
45	chr10:4296406-4296456	HNPCEpiC	eye:	n/a
46	chr10:4296406-4296456	SAEC	small airway:	n/a
47	chr10:4296406-4296456	SK-N-SH	brain:	n/a
48	chr10:4296406-4296456	HRPEpiC	eye:	n/a
49	chr10:4296406-4296456	SKMC	muscle:	n/a
50	chr10:4296406-4296456	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:4304386..4306768-chr10:4318241..4320361,3	MCF-7	breast:
2	chr10:4243895..4246337-chr10:4299306..4301962,2	MCF-7	breast:
3	chr10:3825342..3830573-chr10:4304925..4310190,7	MCF-7	breast:
4	chr10:3823986..3829739-chr10:4306109..4310504,8	MCF-7	breast:
5	chr10:3826008..3828712-chr10:4299777..4301639,2	MCF-7	breast:
6	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:
7	chr10:3824875..3826995-chr10:4293449..4295482,2	MCF-7	breast:
8	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:

Variant related genes	Relation type
LINC00702	TF binding region
LINC00702	CpG island
ENSG00000067082	chromatin interactions

Extended variants
information (count: 777 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568314168	chr10:4290810-4290811	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs535774763	chr10:4290825-4290826	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77999857	chr10:4290845-4290846	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs191148540	chr10:4290860-4290861	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs77423508	chr10:4290869-4290870	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs141405627	chr10:4290909-4290910	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs558484498	chr10:4290957-4290958	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs115901159	chr10:4290985-4290986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146436712	chr10:4291033-4291034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553249049	chr10:4291139-4291140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533685113	chr10:4291143-4291144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574660995	chr10:4291220-4291221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78555602	chr10:4291266-4291267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149390080	chr10:4291348-4291349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7089752	chr10:4291386-4291387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545880344	chr10:4291449-4291450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564098400	chr10:4291481-4291482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144726983	chr10:4291522-4291523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546668370	chr10:4291544-4291545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182526106	chr10:4291609-4291610	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs113306440	chr10:4291636-4291637	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs368443190	chr10:4291666-4291667	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs377456615	chr10:4291679-4291680	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs370182331	chr10:4291680-4291681	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs376115109	chr10:4291682-4291683	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs551126267	chr10:4291698-4291699	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs370693261	chr10:4291735-4291736	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs541235559	chr10:4291761-4291762	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs540088386	chr10:4291771-4291772	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558628185	chr10:4291784-4291785	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs570456952	chr10:4291804-4291805	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559577146	chr10:4291837-4291838	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs534733503	chr10:4291842-4291843	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs553085545	chr10:4291890-4291891	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs574548216	chr10:4291898-4291899	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs188325346	chr10:4291902-4291903	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs557070381	chr10:4291927-4291928	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs117902411	chr10:4291928-4291929	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs546067518	chr10:4291941-4291942	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs548281686	chr10:4292002-4292003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs367906668	chr10:4292003-4292004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148102175	chr10:4292005-4292006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1923391	chr10:4292023-4292024	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs201127481	chr10:4292045-4292046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367714745	chr10:4292049-4292050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529343968	chr10:4292084-4292085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547159703	chr10:4292089-4292090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191071055	chr10:4292101-4292102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563568059	chr10:4292107-4292108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs202231526	chr10:4292137-4292138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4276000-4292200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:4285200-4291800	Weak transcription	Psoas Muscle	Psoas
3	chr10:4285600-4296200	Weak transcription	Fetal Muscle Leg	muscle
4	chr10:4286000-4292400	Weak transcription	Right Ventricle	heart
5	chr10:4286000-4294800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr10:4286800-4296200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr10:4288400-4291000	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr10:4288600-4291800	Weak transcription	Aorta	Aorta
9	chr10:4289000-4293000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr10:4289400-4301400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr10:4289600-4296400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr10:4289800-4291600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr10:4289800-4291800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:4290000-4291600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr10:4290000-4291600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr10:4290000-4291600	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr10:4290000-4291600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr10:4290000-4291600	Weak transcription	NH-A	brain
19	chr10:4290000-4291600	Weak transcription	NHLF	lung
20	chr10:4290000-4291800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr10:4290000-4291800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr10:4290000-4291800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr10:4290000-4291800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:4290000-4292200	Weak transcription	Hela-S3	cervix
25	chr10:4290000-4297800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr10:4290200-4291600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:4290200-4291600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr10:4290200-4291600	Weak transcription	HMEC	breast
29	chr10:4290200-4291600	Weak transcription	NHDF-Ad	bronchial
30	chr10:4290200-4291600	Weak transcription	NHEK	skin
31	chr10:4290200-4291600	Weak transcription	Osteobl	bone
32	chr10:4291000-4296400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr10:4291600-4291800	Enhancers	Rectal Smooth Muscle	rectum
34	chr10:4291600-4292000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:4291600-4292200	Enhancers	NH-A	brain
36	chr10:4291600-4292200	Enhancers	NHDF-Ad	bronchial
37	chr10:4291600-4292400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr10:4291600-4292600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr10:4291600-4292600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr10:4291600-4292600	Enhancers	NHLF	lung
41	chr10:4291600-4292600	Enhancers	Osteobl	bone
42	chr10:4291600-4293000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr10:4291600-4293600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr10:4291600-4294400	Enhancers	HMEC	breast
45	chr10:4291600-4294600	Enhancers	NHEK	skin
46	chr10:4291800-4292000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr10:4291800-4292000	Enhancers	Psoas Muscle	Psoas
48	chr10:4291800-4292400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr10:4291800-4292600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr10:4291800-4292600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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