Variant report

Variant	nsv1046588
Chromosome Location	chr10:49790254-49806169
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:94)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:94 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr10:49793186-49793487	K562	blood:	n/a	n/a
2	CBX3	chr10:49793180-49793569	K562	blood:	n/a	n/a
3	CEBPB	chr10:49795893-49796226	A549	lung:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
4	CEBPB	chr10:49795893-49796258	IMR90	lung:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
5	CEBPB	chr10:49795942-49796213	K562	blood:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
6	CEBPB	chr10:49799768-49799917	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:49799815-49799900	K562	blood:	n/a	n/a
8	CEBPB	chr10:49797344-49797659	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:49799776-49800050	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr10:49799725-49799968	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:49795889-49796260	HepG2	liver:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
12	CEBPB	chr10:49796007-49796120	Hela-S3	cervix:	n/a	chr10:49796069-49796080 chr10:49796071-49796082 chr10:49796069-49796082
13	CTBP2	chr10:49802801-49803278	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr10:49802100-49802250	WI-38	lung:	n/a	n/a
15	CTCF	chr10:49803100-49803250	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr10:49803651-49803704	GM13976	blood:	n/a	n/a
17	EBF1	chr10:49802778-49803311	GM12878	blood:	n/a	chr10:49803129-49803138 chr10:49802948-49802959
18	EBF1	chr10:49802797-49803204	GM12878	blood:	n/a	chr10:49803129-49803138 chr10:49802948-49802959
19	EP300	chr10:49802941-49803028	GM12878	blood:	n/a	n/a
20	FOS	chr10:49797460-49797884	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr10:49797376-49797785	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr10:49797469-49797681	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr10:49797369-49797802	MCF10A-Er-Src	breast:	n/a	n/a
24	HDAC2	chr10:49802885-49803304	H1-hESC	embryonic stem cell:	n/a	n/a
25	JUND	chr10:49803168-49803185	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAFK	chr10:49797437-49797735	IMR90	lung:	n/a	n/a
27	MAX	chr10:49791362-49791382	NB4	blood:	n/a	n/a
28	MAX	chr10:49797288-49797814	SK-N-SH	brain:	n/a	n/a
29	MAX	chr10:49797311-49797807	SK-N-SH	brain:	n/a	n/a
30	MAZ	chr10:49797055-49798894	IMR90	lung:	n/a	n/a
31	MXI1	chr10:49804257-49804271	HepG2	liver:	n/a	n/a
32	MXI1	chr10:49803133-49803199	H1-hESC	embryonic stem cell:	n/a	n/a
33	MXI1	chr10:49796786-49798079	IMR90	lung:	n/a	n/a
34	MYC	chr10:49797367-49797848	MCF10A-Er-Src	breast:	n/a	n/a
35	MYC	chr10:49797353-49797770	MCF10A-Er-Src	breast:	n/a	n/a
36	NANOG	chr10:49802803-49803212	H1-hESC	embryonic stem cell:	n/a	n/a
37	NANOG	chr10:49802853-49803199	H1-hESC	embryonic stem cell:	n/a	n/a
38	NFIC	chr10:49797265-49797883	SK-N-SH	brain:	n/a	n/a
39	NFYB	chr10:49805494-49805717	K562	blood:	n/a	n/a
40	NFYB	chr10:49794503-49794687	GM12878	blood:	n/a	n/a
41	POLR2A	chr10:49795056-49798551	U87	brain:	n/a	n/a
42	POLR2A	chr10:49797187-49797324	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr10:49805797-49806915	U87	brain:	n/a	n/a
44	POLR2A	chr10:49793286-49794417	U87	brain:	n/a	n/a
45	POLR2A	chr10:49797040-49798551	U87	brain:	n/a	n/a
46	POLR2A	chr10:49798933-49799820	U87	brain:	n/a	n/a
47	POLR2A	chr10:49790311-49792405	U87	brain:	n/a	n/a
48	POLR2A	chr10:49796980-49797112	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr10:49804769-49805245	U87	brain:	n/a	n/a
50	POLR2A	chr10:49799851-49800334	U87	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:49797259-49797309	HMEC	breast:	n/a
2	chr10:49799349-49799399	HL-60	blood:	n/a
3	chr10:49797259-49797309	AG04450	lung:	fetal
4	chr10:49799349-49799399	Hepatocyte	liver:	n/a
5	chr10:49797259-49797309	AG04449	skin:	fetal
6	chr10:49799349-49799399	PANC-1	pancreas:	n/a
7	chr10:49802919-49802969	SK-N-MC	brain:	n/a
8	chr10:49802919-49802969	HUVEC	blood vessel:	n/a
9	chr10:49797259-49797309	HCM	heart:	n/a
10	chr10:49799349-49799399	HRE	kidney:	n/a
11	chr10:49799349-49799399	HCF	heart:	n/a
12	chr10:49799349-49799399	A549	lung:	n/a
13	chr10:49799349-49799399	SAEC	small airway:	n/a
14	chr10:49802919-49802969	A549	lung:	n/a
15	chr10:49797259-49797309	HIPEpiC	eye:	n/a
16	chr10:49802919-49802969	IMR90	lung:	fetal
17	chr10:49797259-49797309	AG09309	skin:	n/a
18	chr10:49797259-49797309	IMR90	lung:	fetal
19	chr10:49799349-49799399	T-47D	breast:	n/a
20	chr10:49797259-49797309	SK-N-SH	brain:	n/a
21	chr10:49797259-49797309	HRPEpiC	eye:	n/a
22	chr10:49802919-49802969	GM12878	blood:	n/a
23	chr10:49799349-49799399	SK-N-SH_RA	brain:	n/a
24	chr10:49802919-49802969	HIPEpiC	eye:	n/a
25	chr10:49802919-49802969	Caco-2	colon:	n/a
26	chr10:49799349-49799399	HMEC	breast:	n/a
27	chr10:49799349-49799399	HepG2	liver:	n/a
28	chr10:49802919-49802969	ovcar-3	ovarian:	n/a
29	chr10:49802919-49802969	MCF-7	breast:	n/a
30	chr10:49802919-49802969	HEK293	kidney:	embryo
31	chr10:49797259-49797309	GM06990	blood:	n/a
32	chr10:49797259-49797309	GM12892	blood:	n/a
33	chr10:49797259-49797309	HCF	heart:	n/a
34	chr10:49799349-49799399	GM12892	blood:	n/a
35	chr10:49799349-49799399	HPAEpiC	pulmonary alveolar:	n/a
36	chr10:49799349-49799399	AG10803	skin:	n/a
37	chr10:49799349-49799399	NHDF-neo	bronchial:	n/a
38	chr10:49802919-49802969	SKMC	muscle:	n/a
39	chr10:49797259-49797309	GM12878	blood:	n/a
40	chr10:49797259-49797309	K562	blood:	n/a
41	chr10:49797259-49797309	HAEpiC	amniotic membrane:	n/a
42	chr10:49802919-49802969	GM19239	blood:	n/a
43	chr10:49802919-49802969	HCF	heart:	n/a
44	chr10:49802919-49802969	HCM	heart:	n/a
45	chr10:49799349-49799399	ProgFib	skin:	n/a
46	chr10:49802919-49802969	PFSK-1	brain:	n/a
47	chr10:49799349-49799399	HCM	heart:	n/a
48	chr10:49802919-49802969	ECC-1	luminal epithelium:	n/a
49	chr10:49797259-49797309	HL-60	blood:	n/a
50	chr10:49797259-49797309	T-47D	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:49803449..49806328-chr10:49810436..49812286,2	K562	blood:
2	chr10:49804878..49807273-chr10:49811904..49814201,2	MCF-7	breast:
3	chr10:49794436..49796437-chr10:49820833..49823076,2	K562	blood:
4	chr10:49790222..49791861-chr10:49794010..49795750,2	K562	blood:
5	chr10:49798672..49801517-chr10:49802040..49804201,3	MCF-7	breast:
6	chr10:49804967..49805487-chr18:43382414..43383035,2	MCF-7	breast:
7	chr10:49784932..49786991-chr10:49803496..49805915,2	K562	blood:
8	chr10:49798672..49801517-chr10:49802040..49804201,3	MCF-7	breast:
9	chr10:49776352..49778788-chr10:49787790..49790511,2	K562	blood:
10	chr10:49730671..49732812-chr10:49799416..49802228,2	K562	blood:

No data

Variant related genes	Relation type
ARHGAP22	TF binding region
ARHGAP22	CpG island
ENSG00000128805	chromatin interactions

Extended variants
information (count: 722 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185724757	chr10:49790280-49790281	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141009442	chr10:49790311-49790312	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538409204	chr10:49790326-49790327	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143656770	chr10:49790352-49790353	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551590834	chr10:49790402-49790403	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34137758	chr10:49790427-49790428	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528161647	chr10:49790432-49790433	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190090832	chr10:49790461-49790462	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557771055	chr10:49790463-49790464	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181742646	chr10:49790515-49790516	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17010841	chr10:49790550-49790551	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs113288978	chr10:49790565-49790566	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10745278	chr10:49790579-49790580	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs10745279	chr10:49790587-49790588	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs537015400	chr10:49790588-49790589	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555716492	chr10:49790659-49790660	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554055243	chr10:49790702-49790703	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs61838376	chr10:49790728-49790729	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535118357	chr10:49790732-49790733	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536298683	chr10:49790788-49790789	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74130549	chr10:49790839-49790840	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556601290	chr10:49790878-49790879	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186355047	chr10:49790920-49790921	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541938585	chr10:49790963-49790964	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2289808	chr10:49790972-49790973	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs188604855	chr10:49790981-49790982	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142982949	chr10:49790998-49790999	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376059568	chr10:49791013-49791014	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370486035	chr10:49791048-49791049	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151085571	chr10:49791064-49791065	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77031687	chr10:49791070-49791071	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200749941	chr10:49791084-49791085	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528114148	chr10:49791086-49791087	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575901270	chr10:49791107-49791108	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185292982	chr10:49791109-49791110	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs138838300	chr10:49791110-49791111	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs551965474	chr10:49791120-49791121	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs144669976	chr10:49791121-49791122	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs190004521	chr10:49791142-49791143	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs146683289	chr10:49791143-49791144	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs373930027	chr10:49791145-49791146	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs140291555	chr10:49791149-49791150	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs79069617	chr10:49791150-49791151	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs137922552	chr10:49791161-49791162	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200771176	chr10:49791162-49791163	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200954930	chr10:49791172-49791173	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs578160763	chr10:49791180-49791181	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs370077074	chr10:49791191-49791192	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs375658712	chr10:49791195-49791196	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs149533104	chr10:49791196-49791197	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49786200-49792800	Enhancers	Brain Substantia Nigra	brain
2	chr10:49787000-49791800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr10:49787600-49790600	Enhancers	Brain Hippocampus Middle	brain
4	chr10:49787800-49791200	Weak transcription	Spleen	Spleen
5	chr10:49787800-49791400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:49787800-49792400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:49787800-49793200	Weak transcription	Gastric	stomach
8	chr10:49787800-49796800	Weak transcription	Right Atrium	heart
9	chr10:49788000-49792600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:49788000-49792800	Strong transcription	HUVEC	blood vessel
11	chr10:49788000-49796000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:49788200-49792200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:49788200-49792800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:49788200-49795600	Strong transcription	Osteobl	bone
15	chr10:49788200-49795800	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr10:49788600-49790600	Weak transcription	Ovary	ovary
17	chr10:49788600-49790800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr10:49788600-49792600	Strong transcription	NHDF-Ad	bronchial
19	chr10:49788800-49791000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr10:49788800-49791200	Weak transcription	Brain Anterior Caudate	brain
21	chr10:49788800-49791400	Weak transcription	Brain Angular Gyrus	brain
22	chr10:49788800-49791400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:49788800-49793400	Strong transcription	HSMM	muscle
24	chr10:49788800-49795000	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr10:49788800-49797200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr10:49789000-49790600	Enhancers	Primary B cells from peripheral blood	blood
27	chr10:49789000-49791000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr10:49789000-49791200	Strong transcription	HMEC	breast
29	chr10:49789000-49791400	Weak transcription	Colon Smooth Muscle	Colon
30	chr10:49789000-49793000	Strong transcription	NH-A	brain
31	chr10:49789200-49790400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr10:49789400-49793400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr10:49789800-49790400	Enhancers	Primary B cells from cord blood	blood
34	chr10:49789800-49792600	Strong transcription	HSMMtube	muscle
35	chr10:49790000-49791200	Weak transcription	Pancreas	Pancrea
36	chr10:49790000-49791600	Enhancers	Adipose Nuclei	Adipose
37	chr10:49790200-49791400	Strong transcription	Aorta	Aorta
38	chr10:49790200-49791400	Strong transcription	NHLF	lung
39	chr10:49790200-49792000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr10:49790400-49791400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr10:49790400-49793000	Weak transcription	Primary B cells from cord blood	blood
42	chr10:49790600-49791400	Enhancers	Ovary	ovary
43	chr10:49790600-49793400	Weak transcription	Primary B cells from peripheral blood	blood
44	chr10:49790600-49794800	Weak transcription	Brain Hippocampus Middle	brain
45	chr10:49790800-49792400	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr10:49791000-49792400	Enhancers	Brain Cingulate Gyrus	brain
47	chr10:49791000-49796200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr10:49791200-49791400	Enhancers	Pancreas	Pancrea
49	chr10:49791200-49791400	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr10:49791200-49791400	Enhancers	Spleen	Spleen

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