Variant report

Variant	nsv1053322
Chromosome Location	chr10:4279301-4306798
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:415)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	CBX3	chr10:4285844-4286362	HCT-116	colon:	n/a	n/a
7	CEBPB	chr10:4296810-4297453	IMR90	lung:	n/a	n/a
8	CEBPB	chr10:4285804-4286368	HCT-116	colon:	n/a	n/a
9	CEBPB	chr10:4305612-4305739	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:4284615-4285259	HCT-116	colon:	n/a	n/a
11	CEBPB	chr10:4284358-4285073	Hela-S3	cervix:	n/a	chr10:4284406-4284417
12	CEBPB	chr10:4305189-4305928	Hela-S3	cervix:	n/a	chr10:4305239-4305250
13	CEBPB	chr10:4282853-4283500	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:4292740-4292819	HepG2	liver:	n/a	chr10:4292773-4292784
15	CEBPB	chr10:4282886-4283178	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr10:4296947-4297179	A549	lung:	n/a	n/a
17	CEBPB	chr10:4285878-4286272	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr10:4285751-4286264	IMR90	lung:	n/a	n/a
19	CEBPB	chr10:4284004-4284995	IMR90	lung:	n/a	chr10:4284406-4284417
20	CEBPB	chr10:4296845-4297267	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:4288948-4289680	IMR90	lung:	n/a	n/a
22	CTCF	chr10:4285626-4285734	A549	lung:	n/a	n/a
23	CTCF	chr10:4290809-4290943	Spleen_OC	spleen:	n/a	chr10:4290882-4290903
24	CTCF	chr10:4288900-4289050	HCFaa	heart:	n/a	n/a
25	CTCF	chr10:4288940-4289090	HMF	breast:	n/a	n/a
26	CTCF	chr10:4288940-4289090	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr10:4290829-4290961	GM19240	blood:	n/a	chr10:4290882-4290903
28	CTCF	chr10:4284680-4284830	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr10:4284460-4284610	AG10803	skin:	n/a	n/a
30	CTCF	chr10:4284640-4284790	HAc	cerebellar:	n/a	n/a
31	CTCF	chr10:4290826-4290944	GM19238	blood:	n/a	chr10:4290882-4290903
32	CTCF	chr10:4288940-4289090	AG10803	skin:	n/a	n/a
33	CTCF	chr10:4288960-4289110	AG04449	skin:	n/a	n/a
34	CTCF	chr10:4284080-4284230	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr10:4284820-4284970	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr10:4288900-4289050	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr10:4288960-4289110	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr10:4290848-4290968	NHEK	skin:	n/a	chr10:4290882-4290903
39	CTCF	chr10:4284760-4284910	AG10803	skin:	n/a	n/a
40	CTCF	chr10:4288940-4289090	BJ	skin:	n/a	n/a
41	CTCF	chr10:4290801-4290982	GM19239	blood:	n/a	chr10:4290882-4290903
42	CTCF	chr10:4300325-4300371	A549	lung:	n/a	n/a
43	CTCF	chr10:4288980-4289130	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr10:4300340-4300490	HepG2	liver:	n/a	n/a
45	CTCF	chr10:4288960-4289110	HPAF	blood vessel:	n/a	n/a
46	E2F4	chr10:4289182-4289539	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr10:4285828-4286219	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr10:4302505-4303001	MCF10A-Er-Src	breast:	n/a	n/a
49	EP300	chr10:4284609-4285117	Hela-S3	cervix:	n/a	chr10:4284958-4284974
50	EP300	chr10:4285810-4286257	SK-N-SH_RA	brain:	n/a	chr10:4286082-4286091 chr10:4286163-4286177

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4296406-4296456	Jurkat	blood:	n/a
2	chr10:4296406-4296456	PANC-1	pancreas:	n/a
3	chr10:4296406-4296456	BE2_C	brain:	n/a
4	chr10:4296406-4296456	MCF-7	breast:	n/a
5	chr10:4296406-4296456	HPAEpiC	pulmonary alveolar:	n/a
6	chr10:4296406-4296456	IMR90	lung:	fetal
7	chr10:4296406-4296456	HEK293	kidney:	embryo
8	chr10:4296406-4296456	GM12891	blood:	n/a
9	chr10:4296406-4296456	T-47D	breast:	n/a
10	chr10:4296406-4296456	NH-A	brain:	n/a
11	chr10:4296406-4296456	SK-N-MC	brain:	n/a
12	chr10:4296406-4296456	A549	lung:	n/a
13	chr10:4296406-4296456	AG09319	gingival:	n/a
14	chr10:4296406-4296456	HCPEpiC	choroid plexus:	n/a
15	chr10:4296406-4296456	HNPCEpiC	eye:	n/a
16	chr10:4296406-4296456	HUVEC	blood vessel:	n/a
17	chr10:4296406-4296456	NT2-D1	testis:	n/a
18	chr10:4296406-4296456	SKMC	muscle:	n/a
19	chr10:4296406-4296456	HCM	heart:	n/a
20	chr10:4296406-4296456	AG10803	skin:	n/a
21	chr10:4296406-4296456	ECC-1	luminal epithelium:	n/a
22	chr10:4296406-4296456	PrEC	prostate:	n/a
23	chr10:4296406-4296456	GM12878	blood:	n/a
24	chr10:4296406-4296456	ProgFib	skin:	n/a
25	chr10:4296406-4296456	HL-60	blood:	n/a
26	chr10:4296406-4296456	NB4	blood:	n/a
27	chr10:4296406-4296456	HRCEpiC	kidney:	n/a
28	chr10:4296406-4296456	BJ	skin:	n/a
29	chr10:4296406-4296456	LNCaP	prostate:	n/a
30	chr10:4296406-4296456	HIPEpiC	eye:	n/a
31	chr10:4296406-4296456	HRE	kidney:	n/a
32	chr10:4296406-4296456	NHDF-neo	bronchial:	n/a
33	chr10:4296406-4296456	HCT-116	colon:	n/a
34	chr10:4296406-4296456	Hela-S3	cervix:	n/a
35	chr10:4296406-4296456	CMK	blood:	n/a
36	chr10:4296406-4296456	H1-hESC	embryonic stem cell:	embryo
37	chr10:4296406-4296456	AG04450	lung:	fetal
38	chr10:4296406-4296456	AG09309	skin:	n/a
39	chr10:4296406-4296456	ovcar-3	ovarian:	n/a
40	chr10:4296406-4296456	AG04449	skin:	fetal
41	chr10:4296406-4296456	AoSMC	blood vessel:	n/a
42	chr10:4296406-4296456	GM12892	blood:	n/a
43	chr10:4296406-4296456	SAEC	small airway:	n/a
44	chr10:4296406-4296456	U87	brain:	n/a
45	chr10:4296406-4296456	SK-N-SH	brain:	n/a
46	chr10:4296406-4296456	K562	blood:	n/a
47	chr10:4296406-4296456	PFSK-1	brain:	n/a
48	chr10:4296406-4296456	HepG2	liver:	n/a
49	chr10:4296406-4296456	HEEpiC	esophagus:	n/a
50	chr10:4296406-4296456	GM06990	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:3826852..3829310-chr10:4280995..4283154,3	MCF-7	breast:
2	chr10:4278158..4281099-chr10:4281519..4283245,2	MCF-7	breast:
3	chr10:4243895..4246337-chr10:4299306..4301962,2	MCF-7	breast:
4	chr10:3824875..3826995-chr10:4293449..4295482,2	MCF-7	breast:
5	chr10:4280040..4281988-chr10:4283638..4285219,2	MCF-7	breast:
6	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:
7	chr10:4280040..4281988-chr10:4283638..4285219,2	MCF-7	breast:
8	chr10:4275653..4277576-chr10:4279450..4282362,2	K562	blood:
9	chr10:4304386..4306768-chr10:4318241..4320361,3	MCF-7	breast:
10	chr10:3825342..3830573-chr10:4304925..4310190,7	MCF-7	breast:
11	chr10:3823986..3829739-chr10:4306109..4310504,8	MCF-7	breast:
12	chr10:3826008..3828712-chr10:4299777..4301639,2	MCF-7	breast:
13	chr10:4278158..4281099-chr10:4281519..4283245,2	MCF-7	breast:
14	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF6-14	chr10:4284529-4284775	NONHSAT011085
2	lnc-KLF6-7	chr10:4285696-4285957	XLOC_008700
3	lnc-KLF6-6	chr10:4282814-4283144	XLOC_008701
4	lnc-KLF6-7	chr10:4285696-4285879	ENSG00000233117.2
5	lnc-KLF6-7	chr10:4285696-4285879	NR_108040
6	lnc-KLF6-7	chr10:4286015-4286104	NR_108040
7	lnc-KLF6-7	chr10:4285696-4285981	XLOC_008700
8	lnc-KLF6-7	chr10:4285696-4285728	NONHSAT011084
9	lnc-KLF6-7	chr10:4286015-4286104	ENSG00000233117.2
10	lnc-KLF6-14	chr10:4284539-4284771	NONHSAT011086
11	lnc-KLF6-7	chr10:4285696-4285835	XLOC_008700
12	lnc-KLF6-7	chr10:4285142-4285301	XLOC_008700

No data

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

Extended variants
information (count: 1298 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117955211	chr10:4279301-4279302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574964547	chr10:4279304-4279305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72776593	chr10:4279305-4279306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563615339	chr10:4279334-4279335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145806209	chr10:4279369-4279370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549389487	chr10:4279374-4279375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566193952	chr10:4279391-4279392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375081579	chr10:4279405-4279406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532119069	chr10:4279409-4279410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547460937	chr10:4279450-4279451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184275978	chr10:4279496-4279497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138636745	chr10:4279501-4279502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548222212	chr10:4279504-4279505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188604397	chr10:4279606-4279607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537313337	chr10:4279613-4279614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80318446	chr10:4279721-4279722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558994428	chr10:4279726-4279727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76758277	chr10:4279732-4279733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570816816	chr10:4279797-4279798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368839915	chr10:4279824-4279825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533757438	chr10:4279832-4279833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534845624	chr10:4279843-4279844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553427133	chr10:4279852-4279853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548720219	chr10:4279876-4279877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78764342	chr10:4279915-4279916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574223702	chr10:4279993-4279994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542427173	chr10:4280043-4280044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181639183	chr10:4280048-4280049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372583340	chr10:4280101-4280102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575537864	chr10:4280102-4280103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567368401	chr10:4280140-4280141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564581144	chr10:4280179-4280180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532132193	chr10:4280195-4280196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540797063	chr10:4280210-4280211	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377258362	chr10:4280211-4280212	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12262394	chr10:4280270-4280271	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs548426225	chr10:4280310-4280311	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10795143	chr10:4280313-4280314	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs530834008	chr10:4280328-4280329	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150743410	chr10:4280330-4280331	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570903810	chr10:4280336-4280337	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139071380	chr10:4280344-4280345	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs553223634	chr10:4280357-4280358	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12269255	chr10:4280406-4280407	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs535534613	chr10:4280497-4280498	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs149511122	chr10:4280510-4280511	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs536509980	chr10:4280526-4280527	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs546137601	chr10:4280543-4280544	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs76278199	chr10:4280550-4280551	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs576798915	chr10:4280557-4280558	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4257400-4282400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:4272400-4283200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:4275200-4282800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr10:4276000-4292200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:4276200-4281400	Weak transcription	NHDF-Ad	bronchial
6	chr10:4276400-4281400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr10:4276600-4284000	Weak transcription	Left Ventricle	heart
8	chr10:4278000-4280200	Weak transcription	Aorta	Aorta
9	chr10:4278400-4282800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr10:4279200-4283200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr10:4280200-4280400	Enhancers	Placenta Amnion	Placenta Amnion
12	chr10:4280200-4280600	ZNF genes & repeats	Aorta	Aorta
13	chr10:4280200-4282400	Weak transcription	NH-A	brain
14	chr10:4280400-4280600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr10:4280400-4280600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr10:4280400-4280600	Enhancers	Right Atrium	heart
17	chr10:4280400-4281200	Enhancers	Stomach Smooth Muscle	stomach
18	chr10:4280600-4281200	Genic enhancers	Aorta	Aorta
19	chr10:4280600-4282400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr10:4280600-4282800	Weak transcription	Right Atrium	heart
21	chr10:4280600-4283200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr10:4281200-4282200	Weak transcription	Aorta	Aorta
23	chr10:4281200-4282800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr10:4281400-4281600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr10:4281400-4282800	Enhancers	NHDF-Ad	bronchial
26	chr10:4281600-4282000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:4282000-4282800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:4282000-4283600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr10:4282000-4286200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr10:4282200-4282600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr10:4282200-4282800	Active TSS	Aorta	Aorta
32	chr10:4282200-4286400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr10:4282400-4282800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr10:4282400-4282800	Enhancers	NH-A	brain
35	chr10:4282400-4282800	Enhancers	Osteobl	bone
36	chr10:4282400-4283200	Enhancers	Placenta Amnion	Placenta Amnion
37	chr10:4282400-4283600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr10:4282400-4283600	Enhancers	HUVEC	blood vessel
39	chr10:4282400-4284200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr10:4282400-4285000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr10:4282600-4282800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr10:4282600-4282800	Enhancers	NHLF	lung
43	chr10:4282600-4284000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:4282600-4284000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr10:4282800-4283000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr10:4282800-4283000	Flanking Active TSS	Aorta	Aorta
47	chr10:4282800-4283000	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr10:4282800-4283000	Flanking Active TSS	NH-A	brain
49	chr10:4282800-4283200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr10:4282800-4283200	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links