Variant report

Variant	nsv947726
Chromosome Location	chr10:5008069-5012084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr10:5010586-5011926	A549	lung:	n/a	n/a
2	BCL3	chr10:5008350-5009779	A549	lung:	n/a	chr10:5008426-5008435
3	BCL3	chr10:5006044-5008338	A549	lung:	n/a	n/a
4	FOXA2	chr10:5007998-5008347	A549	lung:	n/a	n/a
5	HEY1	chr10:5008919-5009286	HepG2	liver:	n/a	n/a
6	HEY1	chr10:5010411-5010587	HepG2	liver:	n/a	n/a
7	HEY1	chr10:5009315-5012006	HepG2	liver:	n/a	n/a
8	HEY1	chr10:5007854-5008488	HepG2	liver:	n/a	n/a
9	HEY1	chr10:5005313-5008731	HepG2	liver:	n/a	n/a
10	HEY1	chr10:5011439-5011829	HepG2	liver:	n/a	n/a
11	JUND	chr10:5006865-5008577	A549	lung:	n/a	n/a
12	JUND	chr10:5010942-5011195	HepG2	liver:	n/a	n/a
13	JUND	chr10:5010905-5011868	A549	lung:	n/a	n/a
14	JUND	chr10:5009035-5009849	A549	lung:	n/a	n/a
15	JUND	chr10:5009911-5010773	A549	lung:	n/a	n/a
16	JUND	chr10:5008124-5008357	HepG2	liver:	n/a	n/a
17	POLR2A	chr10:5006471-5008272	HepG2	liver:	n/a	n/a
18	POLR2A	chr10:5010297-5010674	HepG2	liver:	n/a	n/a
19	POLR2A	chr10:5009574-5009633	HepG2	liver:	n/a	n/a
20	POLR2A	chr10:5010947-5011296	A549	lung:	n/a	n/a
21	POLR2A	chr10:5009451-5009713	A549	lung:	n/a	n/a
22	POLR2A	chr10:5011344-5011646	A549	lung:	n/a	n/a
23	POLR2A	chr10:5010790-5011963	A549	lung:	n/a	n/a
24	POLR2A	chr10:5008954-5009249	A549	lung:	n/a	n/a
25	POLR2A	chr10:5008769-5008902	HepG2	liver:	n/a	n/a
26	POLR2A	chr10:5008275-5008528	HepG2	liver:	n/a	n/a
27	POLR2A	chr10:5009437-5009730	HepG2	liver:	n/a	n/a
28	POLR2A	chr10:5009452-5009619	A549	lung:	n/a	n/a
29	POLR2A	chr10:5009060-5009186	A549	lung:	n/a	n/a
30	POLR2A	chr10:5009442-5009728	A549	lung:	n/a	n/a
31	POLR2A	chr10:5011293-5011912	A549	lung:	n/a	n/a
32	POLR2A	chr10:5010858-5011980	HepG2	liver:	n/a	n/a
33	POLR2A	chr10:5009083-5009233	A549	lung:	n/a	n/a
34	POLR2A	chr10:5011322-5012148	HepG2	liver:	n/a	n/a
35	POLR2A	chr10:5010317-5010790	A549	lung:	n/a	n/a
36	POLR2A	chr10:5007829-5008120	A549	lung:	n/a	n/a
37	POLR2A	chr10:5009922-5010256	A549	lung:	n/a	n/a
38	POLR2A	chr10:5011346-5011642	A549	lung:	n/a	n/a
39	POLR2A	chr10:5008654-5008794	HepG2	liver:	n/a	n/a
40	POLR2A	chr10:5006930-5008241	HepG2	liver:	n/a	n/a
41	POLR2A	chr10:5008163-5008342	A549	lung:	n/a	n/a
42	POLR2A	chr10:5008445-5008753	A549	lung:	n/a	n/a
43	POLR2A	chr10:5008370-5008386	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr10:5010947-5011276	A549	lung:	n/a	n/a
45	POLR2A	chr10:5011660-5011951	A549	lung:	n/a	n/a
46	POLR2A	chr10:5010178-5010336	HepG2	liver:	n/a	n/a
47	POLR2A	chr10:5008568-5008746	HepG2	liver:	n/a	n/a
48	POLR2A	chr10:5009942-5010151	A549	lung:	n/a	n/a
49	POLR2A	chr10:5007834-5008345	A549	lung:	n/a	n/a
50	POLR2A	chr10:5008947-5009777	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5009644-5009694	LNCaP	prostate:	n/a
2	chr10:5009644-5009694	HAEpiC	amniotic membrane:	n/a
3	chr10:5009644-5009694	AoSMC	blood vessel:	n/a
4	chr10:5009644-5009694	NB4	blood:	n/a
5	chr10:5009644-5009694	BE2_C	brain:	n/a
6	chr10:5009644-5009694	HL-60	blood:	n/a
7	chr10:5009644-5009694	H1-hESC	embryonic stem cell:	embryo
8	chr10:5009644-5009694	SKMC	muscle:	n/a
9	chr10:5009644-5009694	PrEC	prostate:	n/a
10	chr10:5009644-5009694	GM12892	blood:	n/a
11	chr10:5009644-5009694	AG09309	skin:	n/a
12	chr10:5009644-5009694	HIPEpiC	eye:	n/a
13	chr10:5009644-5009694	A549	lung:	n/a
14	chr10:5009644-5009694	HRE	kidney:	n/a
15	chr10:5009644-5009694	AG10803	skin:	n/a
16	chr10:5009644-5009694	HCT-116	colon:	n/a
17	chr10:5009644-5009694	Hepatocyte	liver:	n/a
18	chr10:5009644-5009694	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:5009644-5009694	HUVEC	blood vessel:	n/a
20	chr10:5009644-5009694	MCF10A-Er-Src	breast:	n/a
21	chr10:5009644-5009694	ProgFib	skin:	n/a
22	chr10:5009644-5009694	NT2-D1	testis:	n/a
23	chr10:5009644-5009694	GM06990	blood:	n/a
24	chr10:5009644-5009694	PFSK-1	brain:	n/a
25	chr10:5009644-5009694	SK-N-SH_RA	brain:	n/a
26	chr10:5009644-5009694	NH-A	brain:	n/a
27	chr10:5009644-5009694	HCF	heart:	n/a
28	chr10:5009644-5009694	CMK	blood:	n/a
29	chr10:5009644-5009694	Caco-2	colon:	n/a
30	chr10:5009644-5009694	BJ	skin:	n/a
31	chr10:5009644-5009694	NHDF-neo	bronchial:	n/a
32	chr10:5009644-5009694	PANC-1	pancreas:	n/a
33	chr10:5009644-5009694	AG09319	gingival:	n/a
34	chr10:5009644-5009694	AG04450	lung:	fetal
35	chr10:5009644-5009694	HRPEpiC	eye:	n/a
36	chr10:5009644-5009694	HMEC	breast:	n/a
37	chr10:5009644-5009694	AG04449	skin:	fetal
38	chr10:5009644-5009694	SAEC	small airway:	n/a
39	chr10:5009644-5009694	K562	blood:	n/a
40	chr10:5009644-5009694	T-47D	breast:	n/a
41	chr10:5009644-5009694	U87	brain:	n/a
42	chr10:5009644-5009694	HCPEpiC	choroid plexus:	n/a
43	chr10:5009644-5009694	GM12891	blood:	n/a
44	chr10:5009644-5009694	HCM	heart:	n/a
45	chr10:5009644-5009694	HEK293	kidney:	embryo
46	chr10:5009644-5009694	ECC-1	luminal epithelium:	n/a
47	chr10:5009644-5009694	RPTEC	kidney:	n/a
48	chr10:5009644-5009694	MCF-7	breast:	n/a
49	chr10:5009644-5009694	GM19239	blood:	n/a
50	chr10:5009644-5009694	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:5005241..5007443-chr10:5009347..5011794,2	MCF-7	breast:
2	chr10:5008134..5010940-chr10:5050778..5053121,2	K562	blood:
3	chr10:5003815..5006768-chr10:5008724..5010986,2	K562	blood:
4	chr10:5007151..5009513-chr10:5009943..5012449,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238840	TF binding region
ENSG00000238840	CpG island
ENSG00000187134	chromatin interactions
ENSG00000238840	chromatin interactions

Extended variants
information (count: 255 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117982876	chr10:5008071-5008072	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs542411116	chr10:5008083-5008084	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs561442757	chr10:5008090-5008091	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs375996832	chr10:5008093-5008094	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371787687	chr10:5008106-5008107	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs1138567	chr10:5008124-5008125	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs140293636	chr10:5008130-5008131	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200575896	chr10:5008132-5008133	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs1138569	chr10:5008133-5008134	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs1138570	chr10:5008134-5008135	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs149693250	chr10:5008137-5008138	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs146428466	chr10:5008140-5008141	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375072627	chr10:5008146-5008147	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs1138571	chr10:5008147-5008148	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200176428	chr10:5008148-5008149	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369850900	chr10:5008152-5008153	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs1138573	chr10:5008153-5008154	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs1138574	chr10:5008156-5008157	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs1138575	chr10:5008161-5008162	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs140835897	chr10:5008167-5008168	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs1138576	chr10:5008177-5008178	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs374368331	chr10:5008180-5008181	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138675307	chr10:5008181-5008182	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs149295644	chr10:5008183-5008184	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs530323152	chr10:5008201-5008202	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs112094476	chr10:5008213-5008214	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201114964	chr10:5008217-5008218	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs377740457	chr10:5008235-5008236	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs567399421	chr10:5008278-5008279	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs369447611	chr10:5008292-5008293	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs199888300	chr10:5008302-5008303	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs540848916	chr10:5008317-5008318	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556156942	chr10:5008328-5008329	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs570924786	chr10:5008357-5008358	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs538218277	chr10:5008358-5008359	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7908994	chr10:5008383-5008384	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs571969675	chr10:5008397-5008398	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs542848301	chr10:5008428-5008429	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs554465478	chr10:5008439-5008440	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs147876533	chr10:5008450-5008451	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs543537415	chr10:5008461-5008462	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs41298224	chr10:5008475-5008476	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs139444003	chr10:5008505-5008506	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs184138086	chr10:5008519-5008520	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs188688701	chr10:5008526-5008527	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs548331889	chr10:5008534-5008535	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs201649634	chr10:5008553-5008554	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs560101331	chr10:5008558-5008559	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs112068046	chr10:5008571-5008572	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548789443	chr10:5008591-5008592	Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4998200-5023800	Weak transcription	Gastric	stomach
2	chr10:5004200-5008400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:5004800-5023800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr10:5005200-5008400	Active TSS	Liver	Liver
5	chr10:5005600-5008200	Active TSS	Duodenum Smooth Muscle	Duodenum
6	chr10:5005600-5009600	Active TSS	Right Atrium	heart
7	chr10:5005800-5009000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr10:5005800-5011000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:5005800-5027400	Weak transcription	Fetal Stomach	stomach
10	chr10:5005800-5045800	Weak transcription	HSMMtube	muscle
11	chr10:5006000-5023800	Weak transcription	Esophagus	oesophagus
12	chr10:5006000-5023800	Weak transcription	Left Ventricle	heart
13	chr10:5006000-5024000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr10:5006200-5011000	Weak transcription	Ovary	ovary
15	chr10:5006200-5011200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:5006800-5010800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr10:5006800-5011200	Weak transcription	Osteobl	bone
18	chr10:5007200-5008600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:5007200-5009400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr10:5007200-5010600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr10:5007200-5011200	Weak transcription	Aorta	Aorta
22	chr10:5007200-5011600	Weak transcription	Fetal Heart	heart
23	chr10:5007200-5021600	Weak transcription	Brain Cingulate Gyrus	brain
24	chr10:5007200-5023200	Weak transcription	Fetal Intestine Large	intestine
25	chr10:5007200-5023600	Weak transcription	Fetal Intestine Small	intestine
26	chr10:5007200-5023800	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr10:5007400-5008200	Enhancers	Fetal Brain Male	brain
28	chr10:5007400-5010800	Weak transcription	Fetal Brain Female	brain
29	chr10:5007400-5011000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr10:5007400-5023800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr10:5007400-5023800	Weak transcription	Right Ventricle	heart
32	chr10:5007400-5024200	Weak transcription	NHEK	skin
33	chr10:5007600-5010800	Weak transcription	Brain Germinal Matrix	brain
34	chr10:5007800-5008200	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr10:5008000-5008200	Flanking Bivalent TSS/Enh	HepG2	liver
36	chr10:5008000-5008200	Flanking Active TSS	NHDF-Ad	bronchial
37	chr10:5008000-5008800	Enhancers	Stomach Mucosa	stomach
38	chr10:5008000-5009600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr10:5008000-5009600	Transcr. at gene 5' and 3'	A549	lung
40	chr10:5008000-5010800	Weak transcription	Psoas Muscle	Psoas
41	chr10:5008000-5011000	Weak transcription	K562	blood
42	chr10:5008200-5008400	Active TSS	NHDF-Ad	bronchial
43	chr10:5008200-5009200	Active TSS	Adipose Nuclei	Adipose
44	chr10:5008200-5009200	Active TSS	HepG2	liver
45	chr10:5008200-5021000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr10:5008200-5044000	Weak transcription	Fetal Brain Male	brain
47	chr10:5008400-5008800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:5008400-5008800	Transcr. at gene 5' and 3'	Liver	Liver
49	chr10:5008400-5010800	Weak transcription	NHDF-Ad	bronchial
50	chr10:5008600-5009600	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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