Variant report

Variant	esv3352463
Chromosome Location	chr10:44789446-44792444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr10:44790521-44790815	GM12878	blood:	n/a	n/a
2	BCL3	chr10:44790369-44790780	GM12878	blood:	n/a	n/a
3	BHLHE40	chr10:44791083-44791469	GM12878	blood:	n/a	n/a
4	CEBPB	chr10:44790789-44790979	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:44789236-44789628	IMR90	lung:	n/a	n/a
6	CHD2	chr10:44791241-44791467	GM12878	blood:	n/a	n/a
7	CHD2	chr10:44790424-44790440	GM12878	blood:	n/a	n/a
8	CTCF	chr10:44790647-44790685	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr10:44790326-44790428	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr10:44790260-44790410	GM12873	blood:	n/a	n/a
11	CTCF	chr10:44791205-44791216	GM19239	blood:	n/a	n/a
12	CTCF	chr10:44790606-44790727	GM19239	blood:	n/a	n/a
13	EP300	chr10:44791130-44791519	GM12878	blood:	n/a	n/a
14	EP300	chr10:44791201-44791526	GM12878	blood:	n/a	n/a
15	EP300	chr10:44791113-44791554	GM12878	blood:	n/a	n/a
16	MAFK	chr10:44792154-44792250	HepG2	liver:	n/a	n/a
17	MAFK	chr10:44792194-44792256	HepG2	liver:	n/a	n/a
18	MAX	chr10:44790417-44790711	K562	blood:	n/a	n/a
19	MYC	chr10:44790591-44790620	MCF-7	breast:	n/a	n/a
20	MYC	chr10:44790911-44790971	MCF-7	breast:	n/a	n/a
21	MYC	chr10:44790761-44790771	MCF-7	breast:	n/a	n/a
22	MYC	chr10:44790614-44790746	MCF-7	breast:	n/a	n/a
23	MYC	chr10:44790622-44790675	MCF-7	breast:	n/a	n/a
24	PAX5	chr10:44790918-44791451	GM12878	blood:	n/a	chr10:44791411-44791420
25	POLR2A	chr10:44789249-44789681	U87	brain:	n/a	n/a
26	POLR2A	chr10:44788687-44789713	U87	brain:	n/a	n/a
27	POLR2A	chr10:44790566-44790620	Gliobla	brain:	n/a	n/a
28	POLR2A	chr10:44790894-44791036	Gliobla	brain:	n/a	n/a
29	POLR2A	chr10:44790658-44790784	A549	lung:	n/a	n/a
30	POLR2A	chr10:44791040-44791054	Gliobla	brain:	n/a	n/a
31	POLR2A	chr10:44790797-44790808	A549	lung:	n/a	n/a
32	POLR2A	chr10:44789239-44789708	U87	brain:	n/a	n/a
33	RUNX3	chr10:44790953-44791457	GM12878	blood:	n/a	chr10:44791218-44791233 chr10:44791199-44791214
34	RUNX3	chr10:44791011-44791435	GM12878	blood:	n/a	chr10:44791218-44791233 chr10:44791199-44791214
35	STAT3	chr10:44789407-44789567	MCF10A-Er-Src	breast:	n/a	chr10:44789525-44789533
36	STAT3	chr10:44789397-44789572	MCF10A-Er-Src	breast:	n/a	chr10:44789525-44789533
37	WRNIP1	chr10:44790933-44791385	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:44789589-44789639	HNPCEpiC	eye:	n/a
2	chr10:44789589-44789639	AG09309	skin:	n/a
3	chr10:44789589-44789639	AoSMC	blood vessel:	n/a
4	chr10:44789589-44789639	PFSK-1	brain:	n/a
5	chr10:44789589-44789639	AG04449	skin:	fetal
6	chr10:44789589-44789639	NH-A	brain:	n/a
7	chr10:44789589-44789639	HAEpiC	amniotic membrane:	n/a
8	chr10:44789589-44789639	PANC-1	pancreas:	n/a
9	chr10:44789589-44789639	HRPEpiC	eye:	n/a
10	chr10:44789589-44789639	SAEC	small airway:	n/a
11	chr10:44789589-44789639	AG09319	gingival:	n/a
12	chr10:44789589-44789639	SK-N-SH	brain:	n/a
13	chr10:44789589-44789639	SK-N-SH_RA	brain:	n/a
14	chr10:44789589-44789639	NT2-D1	testis:	n/a
15	chr10:44789589-44789639	MCF-7	breast:	n/a
16	chr10:44789589-44789639	RPTEC	kidney:	n/a
17	chr10:44789589-44789639	HEEpiC	esophagus:	n/a
18	chr10:44789589-44789639	H1-hESC	embryonic stem cell:	embryo
19	chr10:44789589-44789639	HCT-116	colon:	n/a
20	chr10:44789589-44789639	NHDF-neo	bronchial:	n/a
21	chr10:44789589-44789639	HUVEC	blood vessel:	n/a
22	chr10:44789589-44789639	IMR90	lung:	fetal
23	chr10:44789589-44789639	HepG2	liver:	n/a
24	chr10:44789589-44789639	Hela-S3	cervix:	n/a
25	chr10:44789589-44789639	LNCaP	prostate:	n/a
26	chr10:44789589-44789639	Hepatocyte	liver:	n/a
27	chr10:44789589-44789639	AG10803	skin:	n/a
28	chr10:44789589-44789639	BJ	skin:	n/a
29	chr10:44789589-44789639	HRE	kidney:	n/a
30	chr10:44789589-44789639	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:44789589-44789639	GM06990	blood:	n/a
32	chr10:44789589-44789639	ECC-1	luminal epithelium:	n/a
33	chr10:44789589-44789639	SKMC	muscle:	n/a
34	chr10:44789589-44789639	HCF	heart:	n/a
35	chr10:44789589-44789639	HMEC	breast:	n/a
36	chr10:44789589-44789639	NHBE	bronchial:	n/a
37	chr10:44789589-44789639	NB4	blood:	n/a
38	chr10:44789589-44789639	GM12892	blood:	n/a
39	chr10:44789589-44789639	HIPEpiC	eye:	n/a
40	chr10:44789589-44789639	U87	brain:	n/a
41	chr10:44789589-44789639	AG04450	lung:	fetal
42	chr10:44789589-44789639	HCM	heart:	n/a
43	chr10:44789589-44789639	HRCEpiC	kidney:	n/a
44	chr10:44789589-44789639	HL-60	blood:	n/a
45	chr10:44789589-44789639	HEK293	kidney:	embryo
46	chr10:44789589-44789639	MCF10A-Er-Src	breast:	n/a
47	chr10:44789589-44789639	A549	lung:	n/a
48	chr10:44789589-44789639	BE2_C	brain:	n/a
49	chr10:44789589-44789639	ProgFib	skin:	n/a
50	chr10:44789589-44789639	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:44790586..44792742-chr10:44798450..44801246,2	K562	blood:
2	chr10:44755013..44756692-chr10:44790155..44792136,2	MCF-7	breast:
3	chr10:44790196..44793217-chr10:44793221..44795884,3	MCF-7	breast:
4	chr10:44790481..44792534-chr10:44792786..44795587,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CXCL12-1	chr10:44789285-44789628	XLOC_008795

No data

Variant related genes	Relation type
ENSG00000229116	TF binding region
ENSG00000229116	CpG island

Extended variants
information (count: 111 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577740498	chr10:44789451-44789452	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs190814093	chr10:44789471-44789472	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs374314246	chr10:44789474-44789475	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs141749672	chr10:44789500-44789501	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs72788791	chr10:44789554-44789555	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533219597	chr10:44789555-44789556	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs560691153	chr10:44789583-44789584	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs809601	chr10:44789602-44789603	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs182611882	chr10:44789619-44789620	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs150847373	chr10:44789654-44789655	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs74357308	chr10:44789700-44789701	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs189526062	chr10:44789713-44789714	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192217140	chr10:44789716-44789717	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs188047286	chr10:44789735-44789736	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs569485804	chr10:44789755-44789756	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs138228150	chr10:44789801-44789802	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs550105613	chr10:44789821-44789822	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs74688633	chr10:44789871-44789872	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs573122543	chr10:44789883-44789884	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs192982382	chr10:44789886-44789887	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs558778403	chr10:44789896-44789897	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs577307319	chr10:44789917-44789918	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs147246972	chr10:44789947-44789948	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs808972	chr10:44789989-44789990	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs140983076	chr10:44789994-44789995	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs144919017	chr10:44790025-44790026	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs138862184	chr10:44790037-44790038	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs542477333	chr10:44790052-44790053	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs374021619	chr10:44790088-44790089	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs561268045	chr10:44790100-44790101	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs549049603	chr10:44790142-44790143	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs182596997	chr10:44790168-44790169	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs78708646	chr10:44790193-44790194	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs540272871	chr10:44790256-44790257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs57055606	chr10:44790341-44790342	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs187673103	chr10:44790352-44790353	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs550699422	chr10:44790363-44790364	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs534206105	chr10:44790368-44790369	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs530335479	chr10:44790369-44790370	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs548587333	chr10:44790378-44790379	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs192131007	chr10:44790386-44790387	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs533930997	chr10:44790422-44790423	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs558870137	chr10:44790431-44790432	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs374767724	chr10:44790508-44790509	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs372934518	chr10:44790526-44790527	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs367737192	chr10:44790532-44790533	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs79405863	chr10:44790554-44790555	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs12763236	chr10:44790562-44790563	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs554931057	chr10:44790578-44790579	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs537917900	chr10:44790591-44790592	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Lung cancer	18438408	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
Mental retardation	21062444	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	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
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44787800-44790800	Enhancers	Fetal Heart	heart
2	chr10:44787800-44791600	Enhancers	Ovary	ovary
3	chr10:44788200-44790400	Weak transcription	Pancreas	Pancrea
4	chr10:44788200-44790600	Weak transcription	Spleen	Spleen
5	chr10:44788200-44791000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr10:44788400-44789800	Enhancers	Fetal Kidney	kidney
7	chr10:44788600-44789800	Enhancers	NHLF	lung
8	chr10:44788600-44791200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:44788600-44791600	Enhancers	NHDF-Ad	bronchial
10	chr10:44789000-44789800	Bivalent Enhancer	Fetal Stomach	stomach
11	chr10:44789000-44790000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr10:44789000-44790000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:44789000-44790000	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr10:44789000-44790200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr10:44789000-44791400	Enhancers	GM12878-XiMat	blood
16	chr10:44789000-44791600	Enhancers	Right Ventricle	heart
17	chr10:44789200-44789800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:44789200-44789800	Enhancers	Fetal Lung	lung
19	chr10:44789200-44789800	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr10:44789200-44789800	Enhancers	HepG2	liver
21	chr10:44789200-44789800	Enhancers	NH-A	brain
22	chr10:44789200-44790000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
23	chr10:44789200-44790000	Enhancers	Brain Anterior Caudate	brain
24	chr10:44789200-44790200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr10:44789200-44790200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
26	chr10:44789200-44790200	Enhancers	Colon Smooth Muscle	Colon
27	chr10:44789200-44790200	Enhancers	Right Atrium	heart
28	chr10:44789200-44790400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr10:44789200-44790400	Weak transcription	Brain Substantia Nigra	brain
30	chr10:44789200-44790400	Weak transcription	Gastric	stomach
31	chr10:44789200-44791000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr10:44789200-44791000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr10:44789200-44791200	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr10:44789200-44791400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr10:44789200-44791400	Enhancers	Rectal Smooth Muscle	rectum
36	chr10:44789200-44796600	Weak transcription	Fetal Brain Female	brain
37	chr10:44789400-44789600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr10:44789400-44789600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr10:44789400-44789600	Bivalent Enhancer	Fetal Thymus	thymus
40	chr10:44789400-44789600	Active TSS	Stomach Smooth Muscle	stomach
41	chr10:44789400-44789600	Enhancers	Osteobl	bone
42	chr10:44789400-44789800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr10:44789400-44789800	Weak transcription	Left Ventricle	heart
44	chr10:44789400-44789800	Weak transcription	Lung	lung
45	chr10:44789400-44790000	Enhancers	Adipose Nuclei	Adipose
46	chr10:44789400-44790000	Bivalent Enhancer	Fetal Intestine Small	intestine
47	chr10:44789400-44791000	Weak transcription	Brain Hippocampus Middle	brain
48	chr10:44789400-44791200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr10:44789400-44791600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr10:44789600-44789800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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