Variant report

Variant	esv3392795
Chromosome Location	chr10:46147995-46170942
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:731)
CpG islands
(count:795)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:731 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:46150304-46150339	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:46167853-46168612	HepG2	liver:	n/a	n/a
3	ATF1	chr10:46156450-46156572	K562	blood:	n/a	n/a
4	ATF1	chr10:46152214-46152277	K562	blood:	n/a	n/a
5	ATF2	chr10:46148813-46149349	GM12878	blood:	n/a	n/a
6	ATF2	chr10:46167889-46168477	GM12878	blood:	n/a	n/a
7	BACH1	chr10:46167812-46168617	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr10:46157638-46157843	GM12878	blood:	n/a	chr10:46157746-46157757
9	BATF	chr10:46157597-46157840	GM12878	blood:	n/a	chr10:46157746-46157757
10	BCLAF1	chr10:46167595-46168410	GM12878	blood:	n/a	chr10:46168230-46168239 chr10:46168224-46168237
11	BCLAF1	chr10:46167390-46168501	GM12878	blood:	n/a	chr10:46168230-46168239 chr10:46168224-46168237
12	BHLHE40	chr10:46168352-46168615	A549	lung:	n/a	n/a
13	BHLHE40	chr10:46167662-46168605	HepG2	liver:	n/a	chr10:46168224-46168240
14	BHLHE40	chr10:46167585-46168551	GM12878	blood:	n/a	chr10:46168224-46168240
15	BRCA1	chr10:46168004-46168080	HepG2	liver:	n/a	n/a
16	BRCA1	chr10:46168085-46168369	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr10:46168082-46168214	H1-hESC	embryonic stem cell:	n/a	n/a
18	CCNT2	chr10:46167817-46168282	K562	blood:	n/a	chr10:46168238-46168247
19	CEBPB	chr10:46157329-46157384	A549	lung:	n/a	n/a
20	CEBPB	chr10:46152503-46152839	A549	lung:	n/a	n/a
21	CEBPB	chr10:46160234-46160477	K562	blood:	n/a	chr10:46160329-46160340
22	CEBPB	chr10:46152521-46152851	A549	lung:	n/a	n/a
23	CEBPB	chr10:46167682-46168448	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr10:46167616-46168260	MCF-7	breast:	n/a	n/a
25	CEBPB	chr10:46152532-46152732	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:46157190-46157394	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:46152590-46152879	A549	lung:	n/a	n/a
28	CEBPB	chr10:46167842-46168114	HepG2	liver:	n/a	n/a
29	CEBPB	chr10:46152480-46152825	MCF-7	breast:	n/a	n/a
30	CEBPB	chr10:46168671-46168988	HepG2	liver:	n/a	n/a
31	CEBPB	chr10:46167847-46168212	A549	lung:	n/a	n/a
32	CEBPB	chr10:46167682-46168406	IMR90	lung:	n/a	n/a
33	CEBPB	chr10:46152497-46152834	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr10:46167897-46168139	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:46160373-46160393	A549	lung:	n/a	n/a
36	CEBPB	chr10:46167675-46169013	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:46148631-46148831	HepG2	liver:	n/a	chr10:46148721-46148732
38	CEBPB	chr10:46160295-46160513	IMR90	lung:	n/a	chr10:46160329-46160340
39	CEBPB	chr10:46160272-46160420	HepG2	liver:	n/a	chr10:46160329-46160340
40	CEBPB	chr10:46167613-46168447	A549	lung:	n/a	n/a
41	CEBPB	chr10:46149925-46150122	HepG2	liver:	n/a	n/a
42	CEBPB	chr10:46152455-46152828	K562	blood:	n/a	n/a
43	CEBPB	chr10:46152566-46152838	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:46152582-46152790	K562	blood:	n/a	n/a
45	CEBPB	chr10:46167847-46168384	HepG2	liver:	n/a	n/a
46	CEBPB	chr10:46152487-46152846	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:46157241-46157495	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr10:46167906-46168202	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr10:46167889-46168067	K562	blood:	n/a	n/a
50	CEBPB	chr10:46152562-46152769	Hela-S3	cervix:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:46168597-46168647	HNPCEpiC	eye:	n/a
2	chr10:46168231-46168281	RPTEC	kidney:	n/a
3	chr10:46168597-46168647	HNPCEpiC	eye:	n/a
4	chr10:46168231-46168281	RPTEC	kidney:	n/a
5	chr10:46168597-46168647	GM12891	blood:	n/a
6	chr10:46168377-46168427	PANC-1	pancreas:	n/a
7	chr10:46169183-46169233	NHDF-neo	bronchial:	n/a
8	chr10:46158095-46158145	A549	lung:	n/a
9	chr10:46167626-46167676	HIPEpiC	eye:	n/a
10	chr10:46168377-46168427	ECC-1	luminal epithelium:	n/a
11	chr10:46158095-46158145	Hepatocyte	liver:	n/a
12	chr10:46168403-46168453	NH-A	brain:	n/a
13	chr10:46168446-46168496	NHBE	bronchial:	n/a
14	chr10:46164062-46164112	SKMC	muscle:	n/a
15	chr10:46168377-46168427	HL-60	blood:	n/a
16	chr10:46167626-46167676	Jurkat	blood:	n/a
17	chr10:46168377-46168427	HIPEpiC	eye:	n/a
18	chr10:46168597-46168647	BJ	skin:	n/a
19	chr10:46168403-46168453	HAEpiC	amniotic membrane:	n/a
20	chr10:46167678-46167728	GM12891	blood:	n/a
21	chr10:46158095-46158145	MCF-7	breast:	n/a
22	chr10:46167626-46167676	AoSMC	blood vessel:	n/a
23	chr10:46168446-46168496	AG04449	skin:	fetal
24	chr10:46168403-46168453	HRE	kidney:	n/a
25	chr10:46168403-46168453	MCF-7	breast:	n/a
26	chr10:46168597-46168647	HCPEpiC	choroid plexus:	n/a
27	chr10:46169183-46169233	AG10803	skin:	n/a
28	chr10:46167626-46167676	NHBE	bronchial:	n/a
29	chr10:46169183-46169233	Hepatocyte	liver:	n/a
30	chr10:46164062-46164112	RPTEC	kidney:	n/a
31	chr10:46169183-46169233	Jurkat	blood:	n/a
32	chr10:46168403-46168453	ProgFib	skin:	n/a
33	chr10:46168597-46168647	GM06990	blood:	n/a
34	chr10:46168551-46168601	NB4	blood:	n/a
35	chr10:46168396-46168446	SK-N-SH	brain:	n/a
36	chr10:46168231-46168281	GM12892	blood:	n/a
37	chr10:46168551-46168601	A549	lung:	n/a
38	chr10:46168597-46168647	AG09309	skin:	n/a
39	chr10:46168220-46168270	HIPEpiC	eye:	n/a
40	chr10:46168551-46168601	SK-N-MC	brain:	n/a
41	chr10:46168403-46168453	HCF	heart:	n/a
42	chr10:46167678-46167728	AoSMC	blood vessel:	n/a
43	chr10:46168403-46168453	AG04449	skin:	fetal
44	chr10:46167678-46167728	LNCaP	prostate:	n/a
45	chr10:46168396-46168446	LNCaP	prostate:	n/a
46	chr10:46158095-46158145	NH-A	brain:	n/a
47	chr10:46167626-46167676	GM06990	blood:	n/a
48	chr10:46168403-46168453	NT2-D1	testis:	n/a
49	chr10:46169183-46169233	BJ	skin:	n/a
50	chr10:46169183-46169233	AG04449	skin:	fetal

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:46154690..46156464-chr10:46158011..46159852,2	K562	blood:
2	chr10:46168142..46168698-chr21:43430172..43430948,2	HCT-116	colon:
3	chr10:46163208..46166100-chr10:46169984..46171505,2	K562	blood:
4	chr10:46167759..46168599-chr16:3450730..3451510,2	HCT-116	colon:
5	chr10:46154690..46156464-chr10:46158011..46159852,2	K562	blood:
6	chr10:46163208..46166100-chr10:46169984..46171505,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCH8-3	chr10:46158990-46159290	NR_104256
2	lnc-MARCH8-3	chr10:46148432-46148507	NR_104256
3	lnc-MARCH8-3	chr10:46168127-46168261	NR_104256

No data

Variant related genes	Relation type
ZFAND4	TF binding region
CTGLF10P	TF binding region
ZFAND4	CpG island
CTGLF10P	CpG island
ENSG00000173276	chromatin interactions
ENSG00000103343	chromatin interactions
ENSG00000140987	chromatin interactions

Extended variants
information (count: 867 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538263077	chr10:46148018-46148019	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556347917	chr10:46148046-46148047	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138332491	chr10:46148079-46148080	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562826511	chr10:46148096-46148097	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181740368	chr10:46148103-46148104	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186802306	chr10:46148104-46148105	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546045435	chr10:46148218-46148219	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17157944	chr10:46148266-46148267	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs531182023	chr10:46148278-46148279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543031982	chr10:46148279-46148280	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17157945	chr10:46148301-46148302	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs35337666	chr10:46148309-46148310	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112814546	chr10:46148321-46148322	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7091141	chr10:46148326-46148327	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs191712132	chr10:46148397-46148398	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376839873	chr10:46148407-46148408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565858055	chr10:46148438-46148439	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs539813146	chr10:46148485-46148486	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs200492499	chr10:46148488-46148489	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs201496199	chr10:46148493-46148494	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs376115051	chr10:46148514-46148515	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369488761	chr10:46148522-46148523	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553043896	chr10:46148524-46148525	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200878133	chr10:46148525-46148526	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376340912	chr10:46148535-46148536	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200155845	chr10:46148548-46148549	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569981135	chr10:46148569-46148570	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143852505	chr10:46148603-46148604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556498941	chr10:46148604-46148605	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150264254	chr10:46148644-46148645	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs535931833	chr10:46148648-46148649	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs553980765	chr10:46148652-46148653	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs572257528	chr10:46148689-46148690	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs546006711	chr10:46148714-46148715	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs17696005	chr10:46148750-46148751	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs576315189	chr10:46148816-46148817	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs543737138	chr10:46148819-46148820	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs74754124	chr10:46148839-46148840	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs531762900	chr10:46148895-46148896	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs183933434	chr10:46148908-46148909	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs149400808	chr10:46148910-46148911	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs559187656	chr10:46148926-46148927	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs555572005	chr10:46148938-46148939	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs533124765	chr10:46149016-46149017	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs551585115	chr10:46149094-46149095	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs569893374	chr10:46149095-46149096	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs530823451	chr10:46149118-46149119	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs549045613	chr10:46149150-46149151	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs551461732	chr10:46149153-46149154	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs535483343	chr10:46149197-46149198	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21138945	CNVD
Autism	19287141	CNVD
Intellectual disability	21948486	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	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
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:46090600-46167600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:46098200-46153400	Weak transcription	HSMM	muscle
3	chr10:46104400-46151400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:46108000-46155800	Weak transcription	Brain Angular Gyrus	brain
5	chr10:46108400-46149400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr10:46108400-46167000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr10:46108600-46149200	Weak transcription	Brain Hippocampus Middle	brain
8	chr10:46108600-46155400	Weak transcription	Fetal Intestine Small	intestine
9	chr10:46110200-46153800	Weak transcription	NH-A	brain
10	chr10:46110800-46156800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:46112200-46152400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr10:46119800-46148200	Weak transcription	Colonic Mucosa	Colon
13	chr10:46120000-46157800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr10:46120200-46148400	Weak transcription	Small Intestine	intestine
15	chr10:46122200-46154600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr10:46122200-46157200	Weak transcription	Gastric	stomach
17	chr10:46122400-46149000	Weak transcription	Brain Substantia Nigra	brain
18	chr10:46122400-46156400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr10:46133800-46157800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr10:46137200-46167000	Weak transcription	Right Ventricle	heart
21	chr10:46137600-46149000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr10:46137600-46156600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr10:46137600-46167200	Weak transcription	Ovary	ovary
24	chr10:46138000-46148200	Weak transcription	Fetal Brain Female	brain
25	chr10:46138400-46156600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr10:46138600-46148000	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr10:46139400-46148000	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr10:46140600-46150200	Weak transcription	HepG2	liver
29	chr10:46141600-46148200	Weak transcription	HUVEC	blood vessel
30	chr10:46141800-46148800	Strong transcription	Primary B cells from cord blood	blood
31	chr10:46142400-46158000	Weak transcription	A549	lung
32	chr10:46142800-46148200	Weak transcription	Spleen	Spleen
33	chr10:46142800-46152200	Weak transcription	Thymus	Thymus
34	chr10:46142800-46155200	Weak transcription	Pancreas	Pancrea
35	chr10:46142800-46155600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr10:46142800-46156400	Weak transcription	Fetal Stomach	stomach
37	chr10:46142800-46156800	Weak transcription	Lung	lung
38	chr10:46142800-46167000	Weak transcription	Esophagus	oesophagus
39	chr10:46142800-46167000	Weak transcription	Psoas Muscle	Psoas
40	chr10:46142800-46167000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr10:46142800-46167200	Weak transcription	Aorta	Aorta
42	chr10:46143000-46154400	Weak transcription	Fetal Muscle Leg	muscle
43	chr10:46143000-46156200	Weak transcription	Fetal Muscle Trunk	muscle
44	chr10:46143200-46148200	Weak transcription	GM12878-XiMat	blood
45	chr10:46143200-46153600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr10:46143200-46154400	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr10:46143200-46155800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr10:46143200-46167000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr10:46143200-46167200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr10:46143200-46167400	Weak transcription	Left Ventricle	heart

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