Variant report

Variant	nsv549761
Chromosome Location	chr10:595504-642943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:2381)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr10:603849-604150	H1-hESC	embryonic stem cell:	n/a	chr10:603936-603945
2	ATF3	chr10:603843-604054	K562	blood:	n/a	chr10:603936-603945
3	BHLHE40	chr10:629787-629980	K562	blood:	n/a	chr10:629835-629844 chr10:629836-629845 chr10:629835-629844
4	BHLHE40	chr10:639950-640123	K562	blood:	n/a	chr10:640070-640079 chr10:640064-640085 chr10:640068-640081 chr10:640069-640078
5	CEBPB	chr10:626623-627083	IMR90	lung:	n/a	n/a
6	CEBPB	chr10:640267-640478	A549	lung:	n/a	n/a
7	CEBPB	chr10:639844-640483	IMR90	lung:	n/a	n/a
8	CEBPB	chr10:617766-618133	IMR90	lung:	n/a	n/a
9	CHD2	chr10:601726-601734	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr10:631391-631847	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr10:631501-631768	K562	blood:	n/a	n/a
12	CTCF	chr10:634180-634330	HMF	breast:	n/a	n/a
13	CTCF	chr10:634180-634330	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr10:619320-619470	K562	blood:	n/a	n/a
15	CTCF	chr10:631900-632050	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr10:634200-634350	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr10:634160-634310	HPF	lung:	n/a	n/a
18	CTCF	chr10:634180-634330	AG09319	gingival:	n/a	n/a
19	CTCF	chr10:631880-632030	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr10:634180-634330	K562	blood:	n/a	n/a
21	CTCF	chr10:634160-634310	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr10:634109-634324	Fibrobl	skin:	n/a	n/a
23	CTCF	chr10:634160-634310	HEK293	kidney:	n/a	n/a
24	CTCF	chr10:619240-619390	HRE	kidney:	n/a	n/a
25	CTCF	chr10:634160-634310	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr10:631560-631710	K562	blood:	n/a	n/a
27	CTCF	chr10:634199-634267	GM12892	blood:	n/a	n/a
28	CTCF	chr10:634160-634310	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr10:631920-632070	HepG2	liver:	n/a	n/a
30	CTCF	chr10:634180-634330	HCFaa	heart:	n/a	n/a
31	CTCF	chr10:634200-634350	AG09319	gingival:	n/a	n/a
32	CTCF	chr10:634220-634370	WI-38	lung:	n/a	n/a
33	CTCF	chr10:631560-631710	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr10:634180-634330	BJ	skin:	n/a	n/a
35	CTCF	chr10:634191-634308	HepG2	liver:	n/a	n/a
36	CTCF	chr10:634180-634330	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr10:631540-631690	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr10:619316-619506	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr10:631580-631730	Caco-2	colon:	n/a	n/a
40	CTCF	chr10:634175-634287	K562	blood:	n/a	n/a
41	CTCF	chr10:634200-634350	AG04449	skin:	n/a	n/a
42	CTCF	chr10:631503-631725	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:631411-631838	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr10:619282-619694	K562	blood:	n/a	n/a
45	CTCF	chr10:603380-603530	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr10:634200-634350	AG09309	skin:	n/a	n/a
47	CTCF	chr10:637620-637770	GM12872	blood:	n/a	n/a
48	CTCF	chr10:619320-619470	MCF-7	breast:	n/a	n/a
49	CTCF	chr10:631580-631730	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr10:612312-612381	H1-hESC	embryonic stem cell:	n/a	chr10:612342-612351

(count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:636140-636190	SAEC	small airway:	n/a
2	chr10:612314-612364	Caco-2	colon:	n/a
3	chr10:636140-636190	SAEC	small airway:	n/a
4	chr10:612314-612364	Caco-2	colon:	n/a
5	chr10:636331-636381	PrEC	prostate:	n/a
6	chr10:612314-612364	NHDF-neo	bronchial:	n/a
7	chr10:640738-640788	GM12892	blood:	n/a
8	chr10:636241-636291	BJ	skin:	n/a
9	chr10:629625-629675	A549	lung:	n/a
10	chr10:601759-601809	HNPCEpiC	eye:	n/a
11	chr10:636331-636381	BJ	skin:	n/a
12	chr10:630384-630434	RPTEC	kidney:	n/a
13	chr10:641626-641676	GM19239	blood:	n/a
14	chr10:629565-629615	H1-hESC	embryonic stem cell:	embryo
15	chr10:640085-640135	Hela-S3	cervix:	n/a
16	chr10:629565-629615	HCT-116	colon:	n/a
17	chr10:641615-641665	AG04450	lung:	fetal
18	chr10:601816-601866	ovcar-3	ovarian:	n/a
19	chr10:612266-612316	GM12892	blood:	n/a
20	chr10:640061-640111	HRCEpiC	kidney:	n/a
21	chr10:640770-640820	IMR90	lung:	fetal
22	chr10:629625-629675	NH-A	brain:	n/a
23	chr10:640085-640135	IMR90	lung:	fetal
24	chr10:616995-617045	SK-N-SH	brain:	n/a
25	chr10:617105-617155	HCPEpiC	choroid plexus:	n/a
26	chr10:641626-641676	IMR90	lung:	fetal
27	chr10:623056-623106	U87	brain:	n/a
28	chr10:641641-641691	Caco-2	colon:	n/a
29	chr10:629625-629675	AG04449	skin:	fetal
30	chr10:631304-631354	NHBE	bronchial:	n/a
31	chr10:636331-636381	HepG2	liver:	n/a
32	chr10:616959-617009	HEK293	kidney:	embryo
33	chr10:640770-640820	AG09309	skin:	n/a
34	chr10:601816-601866	HEEpiC	esophagus:	n/a
35	chr10:639935-639985	NHDF-neo	bronchial:	n/a
36	chr10:623056-623106	HAEpiC	amniotic membrane:	n/a
37	chr10:630942-630992	PFSK-1	brain:	n/a
38	chr10:604032-604082	NH-A	brain:	n/a
39	chr10:641626-641676	HRPEpiC	eye:	n/a
40	chr10:641615-641665	HEEpiC	esophagus:	n/a
41	chr10:604461-604511	GM12878	blood:	n/a
42	chr10:636076-636126	ovcar-3	ovarian:	n/a
43	chr10:641615-641665	GM19239	blood:	n/a
44	chr10:640085-640135	CMK	blood:	n/a
45	chr10:636390-636440	Jurkat	blood:	n/a
46	chr10:612266-612316	PrEC	prostate:	n/a
47	chr10:636390-636440	PANC-1	pancreas:	n/a
48	chr10:632914-632964	SK-N-SH_RA	brain:	n/a
49	chr10:636076-636126	GM06990	blood:	n/a
50	chr10:623056-623106	AG04450	lung:	fetal

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
2	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
3	chr10:629648..631897-chr10:633164..636396,3	MCF-7	breast:
4	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
5	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
6	chr10:632878..635792-chr10:829676..832349,2	MCF-7	breast:
7	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:
8	chr10:642832..645382-chr10:657753..659444,2	MCF-7	breast:
9	chr10:634748..636656-chr10:637964..639591,2	K562	blood:
10	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
11	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
12	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
13	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
14	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
15	chr10:593219..595264-chr10:597541..599754,3	MCF-7	breast:
16	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
17	chr10:636273..639205-chr10:641067..642739,2	MCF-7	breast:
18	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
19	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
20	chr10:634195..634721-chr10:829974..830911,3	MCF-7	breast:
21	chr10:632427..634199-chr10:639895..642783,2	K562	blood:
22	chr10:634748..636656-chr10:637964..639591,2	K562	blood:
23	chr10:589190..591988-chr10:602233..604449,2	K562	blood:
24	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
25	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
26	chr10:627398..630591-chr10:632947..634840,3	K562	blood:
27	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
28	chr10:641312..643673-chr10:645720..648516,2	MCF-7	breast:
29	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
30	chr10:636273..639205-chr10:641067..642739,2	MCF-7	breast:
31	chr10:638624..640408-chr10:644679..647011,2	MCF-7	breast:
32	chr10:631818..632398-chr3:122337364..122338295,2	MCF-7	breast:
33	chr10:630264..632276-chr10:643488..645388,2	MCF-7	breast:
34	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
35	chr10:633910..634891-chr10:834953..835643,3	MCF-7	breast:
36	chr10:634649..636667-chr10:654000..655714,2	MCF-7	breast:
37	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
38	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
39	chr10:625995..627810-chr10:664687..667494,2	K562	blood:
40	chr10:632427..634199-chr10:639895..642783,2	K562	blood:
41	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:

No data

Variant related genes	Relation type
DIP2C	TF binding region
DIP2C	CpG island
ENSG00000151240	chromatin interactions

Extended variants
information (count: 3134 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3134 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs865289	chr10:595504-595505	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187902063	chr10:595560-595561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535295426	chr10:595562-595563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555154039	chr10:595563-595564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572147698	chr10:595564-595565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534321510	chr10:595569-595570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557737445	chr10:595580-595581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1251342	chr10:595594-595595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs544143419	chr10:595600-595601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139429573	chr10:595608-595609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574260818	chr10:595650-595651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543237760	chr10:595665-595666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11253136	chr10:595674-595675	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs59999413	chr10:595681-595682	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374936093	chr10:595718-595719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78030666	chr10:595719-595720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367790664	chr10:595738-595739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117408151	chr10:595749-595750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533032590	chr10:595762-595763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549645046	chr10:595768-595769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191142894	chr10:595831-595832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79946723	chr10:595870-595871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144384598	chr10:595873-595874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs60820926	chr10:595876-595877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7914425	chr10:595877-595878	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7905658	chr10:595943-595944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145244782	chr10:595946-595947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11461177	chr10:595947-595948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184773326	chr10:595958-595959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557433672	chr10:595961-595962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376758398	chr10:595993-595994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369273748	chr10:596036-596037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537067199	chr10:596057-596058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7917823	chr10:596093-596094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142405596	chr10:596136-596137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189429844	chr10:596156-596157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181832753	chr10:596164-596165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7917949	chr10:596170-596171	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573225226	chr10:596175-596176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139636856	chr10:596181-596182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565069358	chr10:596186-596187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530799085	chr10:596196-596197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185453772	chr10:596197-596198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550602086	chr10:596245-596246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144270232	chr10:596256-596257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529192218	chr10:596318-596319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374089198	chr10:596426-596427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149731580	chr10:596490-596491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548863395	chr10:596498-596499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559331745	chr10:596569-596570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	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
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
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD

Chromatin state (count:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:583200-604800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr10:590600-596000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:591200-595600	Enhancers	Placenta	Placenta
4	chr10:591400-595600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:592400-596000	Enhancers	Brain Anterior Caudate	brain
6	chr10:592600-595600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr10:592600-595600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr10:592800-595600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:592800-596200	Enhancers	Brain Cingulate Gyrus	brain
10	chr10:592800-596200	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr10:593000-595600	Enhancers	Left Ventricle	heart
12	chr10:593000-596000	Enhancers	Fetal Brain Male	brain
13	chr10:593400-596400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr10:593600-596000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr10:593600-602800	Weak transcription	Fetal Intestine Small	intestine
16	chr10:593600-605000	Weak transcription	NH-A	brain
17	chr10:593800-597800	Weak transcription	Fetal Kidney	kidney
18	chr10:593800-600600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:594000-596600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr10:594000-596800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr10:594000-596800	Weak transcription	Esophagus	oesophagus
22	chr10:594000-596800	Weak transcription	Fetal Stomach	stomach
23	chr10:594000-596800	Weak transcription	Right Atrium	heart
24	chr10:594000-597200	Weak transcription	Fetal Muscle Leg	muscle
25	chr10:594000-597400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:594000-597400	Weak transcription	Brain Substantia Nigra	brain
27	chr10:594000-601400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr10:594000-601800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr10:594000-604000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr10:594200-597800	Weak transcription	Fetal Brain Female	brain
31	chr10:594200-602800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr10:594200-604000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr10:594600-596200	Weak transcription	Pancreas	Pancrea
34	chr10:594600-599000	Weak transcription	Lung	lung
35	chr10:594600-600400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr10:594600-601600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr10:594600-604000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr10:594600-604000	Weak transcription	Brain Germinal Matrix	brain
39	chr10:594800-596600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr10:594800-597600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr10:595000-596000	Enhancers	Ovary	ovary
42	chr10:595200-595600	Enhancers	Psoas Muscle	Psoas
43	chr10:595200-595800	Enhancers	Spleen	Spleen
44	chr10:595200-597600	Enhancers	Colon Smooth Muscle	Colon
45	chr10:595200-602800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr10:595400-595600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr10:595400-595600	Enhancers	Fetal Muscle Trunk	muscle
48	chr10:595400-596000	Enhancers	Right Ventricle	heart
49	chr10:595400-596800	Weak transcription	Brain Angular Gyrus	brain
50	chr10:595400-597000	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links