Variant report

Variant	nsv975776
Chromosome Location	chr10:61569234-61574091
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	BATF	chr10:61569202-61569382	GM12878	blood:	n/a	n/a
2	BCLAF1	chr10:61569046-61569389	GM12878	blood:	n/a	n/a
3	BHLHE40	chr10:61569136-61569475	HepG2	liver:	n/a	n/a
4	BHLHE40	chr10:61569139-61569496	K562	blood:	n/a	n/a
5	BHLHE40	chr10:61569146-61569366	GM12878	blood:	n/a	n/a
6	BRCA1	chr10:61569327-61569373	HepG2	liver:	n/a	n/a
7	CHD2	chr10:61569163-61569403	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr10:61569282-61569402	GM12878	blood:	n/a	n/a
9	CTCF	chr10:61569540-61569690	GM12871	blood:	n/a	n/a
10	CTCF	chr10:61569156-61569458	GM12892	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
11	CTCF	chr10:61569260-61569410	AG04450	lung:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
12	CTCF	chr10:61569184-61569446	HepG2	liver:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
13	CTCF	chr10:61569200-61569350	AG09309	skin:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
14	CTCF	chr10:61569260-61569410	HA-sp	spinal cord:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
15	CTCF	chr10:61569240-61569390	WERI-Rb-1	eye:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
16	CTCF	chr10:61569260-61569410	GM12865	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
17	CTCF	chr10:61569240-61569390	AG04449	skin:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
18	CTCF	chr10:61569240-61569390	HEK293	kidney:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
19	CTCF	chr10:61569260-61569410	GM06990	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
20	CTCF	chr10:61569220-61569370	WERI-Rb-1	eye:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
21	CTCF	chr10:61569240-61569390	HBMEC	blood vessel:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
22	CTCF	chr10:61569232-61569416	GM20000	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
23	CTCF	chr10:61569260-61569410	HBMEC	blood vessel:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
24	CTCF	chr10:61569158-61569447	MCF-7	breast:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
25	CTCF	chr10:61569240-61569390	GM12865	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
26	CTCF	chr10:61569197-61569450	LNCaP	prostate:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
27	CTCF	chr10:61569131-61569468	ECC-1	luminal epithelium:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
28	CTCF	chr10:61569220-61569370	HMEC	breast:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
29	CTCF	chr10:61569200-61569445	LNCaP	prostate:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
30	CTCF	chr10:61569240-61569390	GM12873	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
31	CTCF	chr10:61569220-61569370	HAc	cerebellar:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
32	CTCF	chr10:61569260-61569410	WI-38	lung:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
33	CTCF	chr10:61569175-61569450	Hela-S3	cervix:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
34	CTCF	chr10:61569200-61569350	GM12871	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
35	CTCF	chr10:61569162-61569459	NHEK	skin:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
36	CTCF	chr10:61569099-61569538	T-47D	breast:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
37	CTCF	chr10:61569240-61569390	HPF	lung:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
38	CTCF	chr10:61569240-61569390	HepG2	liver:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
39	CTCF	chr10:61569165-61569489	Spleen_OC	spleen:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
40	CTCF	chr10:61569480-61569630	NHLF	lung:	n/a	n/a
41	CTCF	chr10:61569240-61569390	HUVEC	blood vessel:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
42	CTCF	chr10:61569200-61569350	GM12801	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
43	CTCF	chr10:61569171-61569455	K562	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
44	CTCF	chr10:61569108-61569513	K562	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
45	CTCF	chr10:61569240-61569390	AG10803	skin:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
46	CTCF	chr10:61569240-61569390	GM12870	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
47	CTCF	chr10:61569240-61569390	GM12871	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
48	CTCF	chr10:61569220-61569370	HMF	breast:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
49	CTCF	chr10:61569210-61569446	GM13976	blood:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322
50	CTCF	chr10:61569260-61569410	MCF-7	breast:	n/a	chr10:61569299-61569320 chr10:61569306-61569319 chr10:61569310-61569319 chr10:61569304-61569322

No.	Distal block	Cell Line	Cell type
1	chr10:61568113..61570689-chr10:61665672..61667670,4	K562	blood:
2	chr10:61385405..61386688-chr10:61568618..61569756,12	MCF-7	breast:
3	chr10:61385518..61386497-chr10:61568741..61570237,8	MCF-7	breast:
4	chr10:61568903..61569775-chr10:61807632..61808158,2	MCF-7	breast:
5	chr10:61385493..61386429-chr10:61568847..61570051,6	K562	blood:
6	chr10:61385856..61386422-chr10:61568698..61569339,2	MCF-7	breast:

Variant related genes	Relation type
CCDC6	TF binding region
ENSG00000108091	chromatin interactions

Extended variants
information (count: 175 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:175 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377083462	chr10:61569247-61569248	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs540150473	chr10:61569256-61569257	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs537192133	chr10:61569322-61569323	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs115392816	chr10:61569358-61569359	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7895724	chr10:61569410-61569411	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs375733440	chr10:61569423-61569424	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs2137904	chr10:61569446-61569447	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs200750286	chr10:61569485-61569486	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112862717	chr10:61569586-61569587	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146832318	chr10:61569590-61569591	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs34217404	chr10:61569624-61569625	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs186265710	chr10:61569671-61569672	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs574603460	chr10:61569673-61569674	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs12262735	chr10:61569816-61569817	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs113257555	chr10:61569837-61569838	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs139612536	chr10:61569841-61569842	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375923320	chr10:61569852-61569853	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs561843131	chr10:61569944-61569945	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544880402	chr10:61569973-61569974	Enhancers Genic enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs112510529	chr10:61570037-61570038	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113310706	chr10:61570092-61570093	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs540277540	chr10:61570137-61570138	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562163647	chr10:61570149-61570150	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182794745	chr10:61570162-61570163	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529387979	chr10:61570168-61570169	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187038543	chr10:61570176-61570177	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189931439	chr10:61570196-61570197	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533595980	chr10:61570237-61570238	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142638609	chr10:61570246-61570247	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs377099155	chr10:61570253-61570254	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552103122	chr10:61570314-61570315	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567214550	chr10:61570320-61570321	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533742018	chr10:61570367-61570368	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548704650	chr10:61570373-61570374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7075215	chr10:61570411-61570412	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs530035041	chr10:61570439-61570440	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537561140	chr10:61570448-61570449	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs4948243	chr10:61570450-61570451	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs577411535	chr10:61570460-61570461	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531431129	chr10:61570465-61570466	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538485658	chr10:61570529-61570530	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543528937	chr10:61570550-61570551	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4948244	chr10:61570574-61570575	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs537359390	chr10:61570681-61570682	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540590434	chr10:61570721-61570722	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs182615565	chr10:61570743-61570744	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs529504239	chr10:61570744-61570745	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs34296169	chr10:61570769-61570770	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs574011372	chr10:61570803-61570804	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs4948366	chr10:61570840-61570841	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Obesity	21956041	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Urothelial carcinoma	21177765	CNVD
abnormal development	18461090	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	20643615	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61537600-61582800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:61548600-61573000	Strong transcription	Dnd41	blood
3	chr10:61549600-61572000	Strong transcription	Liver	Liver
4	chr10:61549600-61579600	Strong transcription	Primary B cells from cord blood	blood
5	chr10:61550400-61569400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr10:61553000-61571000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:61554800-61571000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr10:61556000-61583800	Strong transcription	Primary B cells from peripheral blood	blood
9	chr10:61556200-61573800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:61556200-61573800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr10:61556200-61574800	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr10:61556200-61574800	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr10:61556600-61573000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr10:61556800-61570400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr10:61556800-61574600	Strong transcription	Primary T cells from cord blood	blood
16	chr10:61557400-61573400	Strong transcription	Adipose Nuclei	Adipose
17	chr10:61557400-61574600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr10:61561000-61572800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr10:61561000-61574000	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr10:61561000-61574600	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr10:61561200-61571800	Strong transcription	HSMM	muscle
22	chr10:61561200-61574000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:61561200-61574600	Strong transcription	HepG2	liver
24	chr10:61561600-61572600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr10:61561600-61572800	Strong transcription	Osteobl	bone
26	chr10:61561600-61573600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr10:61561800-61571600	Strong transcription	Duodenum Smooth Muscle	Duodenum
28	chr10:61562000-61573400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr10:61562200-61574600	Strong transcription	Fetal Thymus	thymus
30	chr10:61562400-61572600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr10:61562600-61571600	Strong transcription	GM12878-XiMat	blood
32	chr10:61562600-61573000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr10:61562600-61573400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr10:61562800-61571600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr10:61562800-61571600	Strong transcription	H9 Cell Line	embryonic stem cell
36	chr10:61562800-61571600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr10:61562800-61571600	Strong transcription	Sigmoid Colon	Sigmoid Colon
38	chr10:61562800-61571600	Strong transcription	Thymus	Thymus
39	chr10:61562800-61572400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr10:61562800-61572600	Strong transcription	Fetal Intestine Large	intestine
41	chr10:61562800-61572600	Strong transcription	HMEC	breast
42	chr10:61562800-61572800	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr10:61562800-61574200	Strong transcription	Placenta	Placenta
44	chr10:61562800-61574400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr10:61563000-61571000	Strong transcription	Fetal Intestine Small	intestine
46	chr10:61563000-61572800	Strong transcription	Fetal Muscle Trunk	muscle
47	chr10:61563200-61571600	Strong transcription	Fetal Muscle Leg	muscle
48	chr10:61563400-61571000	Strong transcription	NHEK	skin
49	chr10:61563600-61577600	Weak transcription	Right Atrium	heart
50	chr10:61564200-61576800	Strong transcription	Monocytes-CD14+_RO01746	blood

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