Variant report

Variant	nsv1044267
Chromosome Location	chr10:581928-645916
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:2995)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr10:603843-604054	K562	blood:	n/a	chr10:603936-603945
2	ATF3	chr10:603849-604150	H1-hESC	embryonic stem cell:	n/a	chr10:603936-603945
3	BATF	chr10:590435-590657	GM12878	blood:	n/a	n/a
4	BHLHE40	chr10:587767-588048	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:639950-640123	K562	blood:	n/a	chr10:640070-640079 chr10:640064-640085 chr10:640068-640081 chr10:640069-640078
6	BHLHE40	chr10:629787-629980	K562	blood:	n/a	chr10:629835-629844 chr10:629836-629845 chr10:629835-629844
7	CEBPB	chr10:640267-640478	A549	lung:	n/a	n/a
8	CEBPB	chr10:643580-643734	HepG2	liver:	n/a	n/a
9	CEBPB	chr10:626623-627083	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:585836-586136	IMR90	lung:	n/a	chr10:585977-585988
11	CEBPB	chr10:639844-640483	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:584917-585255	IMR90	lung:	n/a	n/a
13	CEBPB	chr10:643535-643697	A549	lung:	n/a	n/a
14	CEBPB	chr10:617766-618133	IMR90	lung:	n/a	n/a
15	CEBPB	chr10:644198-645135	IMR90	lung:	n/a	n/a
16	CHD2	chr10:601726-601734	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr10:634200-634350	AG09309	skin:	n/a	n/a
18	CTCF	chr10:634160-634310	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr10:631516-631759	MCF-7	breast:	n/a	n/a
20	CTCF	chr10:634156-634320	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr10:634199-634267	GM12892	blood:	n/a	n/a
22	CTCF	chr10:634160-634310	HAc	cerebellar:	n/a	n/a
23	CTCF	chr10:583600-583750	GM12865	blood:	n/a	chr10:583643-583659
24	CTCF	chr10:634121-634337	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:619380-619530	HAc	cerebellar:	n/a	n/a
26	CTCF	chr10:634180-634330	HCFaa	heart:	n/a	n/a
27	CTCF	chr10:631961-631995	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr10:631503-631725	MCF-7	breast:	n/a	n/a
29	CTCF	chr10:634202-634270	GM19239	blood:	n/a	n/a
30	CTCF	chr10:634140-634290	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr10:634164-634497	MCF-7	breast:	n/a	chr10:634453-634466
32	CTCF	chr10:631540-631690	Caco-2	colon:	n/a	n/a
33	CTCF	chr10:634180-634330	SAEC	small airway:	n/a	n/a
34	CTCF	chr10:634200-634350	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr10:619320-619470	MCF-7	breast:	n/a	n/a
36	CTCF	chr10:634162-634412	T-47D	breast:	n/a	n/a
37	CTCF	chr10:588255-588262	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr10:634180-634330	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr10:631560-631710	MCF-7	breast:	n/a	n/a
40	CTCF	chr10:631415-631834	T-47D	breast:	n/a	n/a
41	CTCF	chr10:634160-634310	HEK293	kidney:	n/a	n/a
42	CTCF	chr10:634169-634313	ProgFib	skin:	n/a	n/a
43	CTCF	chr10:634200-634350	HFF	foreskin:	n/a	n/a
44	CTCF	chr10:625440-625590	Caco-2	colon:	n/a	n/a
45	CTCF	chr10:634117-634348	MCF-7	breast:	n/a	n/a
46	CTCF	chr10:634160-634310	HPF	lung:	n/a	n/a
47	CTCF	chr10:634160-634310	AG04449	skin:	n/a	n/a
48	CTCF	chr10:634180-634330	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr10:631560-631710	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr10:631560-631710	HBMEC	blood vessel:	n/a	n/a

(count:2995 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:616995-617045	LNCaP	prostate:	n/a
2	chr10:641641-641691	GM12892	blood:	n/a
3	chr10:589375-589425	NHBE	bronchial:	n/a
4	chr10:612266-612316	LNCaP	prostate:	n/a
5	chr10:629565-629615	PrEC	prostate:	n/a
6	chr10:601816-601866	RPTEC	kidney:	n/a
7	chr10:616995-617045	LNCaP	prostate:	n/a
8	chr10:641641-641691	GM12892	blood:	n/a
9	chr10:589375-589425	NHBE	bronchial:	n/a
10	chr10:612266-612316	LNCaP	prostate:	n/a
11	chr10:629565-629615	PrEC	prostate:	n/a
12	chr10:601816-601866	RPTEC	kidney:	n/a
13	chr10:589143-589193	HCM	heart:	n/a
14	chr10:617105-617155	Hepatocyte	liver:	n/a
15	chr10:641641-641691	CMK	blood:	n/a
16	chr10:633154-633204	NHBE	bronchial:	n/a
17	chr10:640996-641046	AG09319	gingival:	n/a
18	chr10:633154-633204	IMR90	lung:	fetal
19	chr10:629582-629632	GM19239	blood:	n/a
20	chr10:601759-601809	Hepatocyte	liver:	n/a
21	chr10:617105-617155	BE2_C	brain:	n/a
22	chr10:612391-612441	HCM	heart:	n/a
23	chr10:629565-629615	AG04450	lung:	fetal
24	chr10:630671-630721	CMK	blood:	n/a
25	chr10:590014-590064	GM12891	blood:	n/a
26	chr10:640770-640820	Hela-S3	cervix:	n/a
27	chr10:631304-631354	HAEpiC	amniotic membrane:	n/a
28	chr10:604461-604511	GM12878	blood:	n/a
29	chr10:640770-640820	AG04450	lung:	fetal
30	chr10:632914-632964	A549	lung:	n/a
31	chr10:641641-641691	ECC-1	luminal epithelium:	n/a
32	chr10:582370-582420	U87	brain:	n/a
33	chr10:641615-641665	AG04449	skin:	fetal
34	chr10:593275-593325	GM12878	blood:	n/a
35	chr10:590541-590591	SK-N-SH_RA	brain:	n/a
36	chr10:627679-627729	PrEC	prostate:	n/a
37	chr10:629565-629615	HEK293	kidney:	embryo
38	chr10:587122-587172	HRPEpiC	eye:	n/a
39	chr10:603950-604000	AG09319	gingival:	n/a
40	chr10:590541-590591	Hepatocyte	liver:	n/a
41	chr10:589375-589425	PFSK-1	brain:	n/a
42	chr10:601759-601809	AG09319	gingival:	n/a
43	chr10:616959-617009	GM12891	blood:	n/a
44	chr10:604032-604082	RPTEC	kidney:	n/a
45	chr10:612391-612441	HUVEC	blood vessel:	n/a
46	chr10:636140-636190	AG09319	gingival:	n/a
47	chr10:604461-604511	BE2_C	brain:	n/a
48	chr10:603950-604000	GM06990	blood:	n/a
49	chr10:601816-601866	GM12892	blood:	n/a
50	chr10:627679-627729	SK-N-SH	brain:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:
2	chr10:642832..645382-chr10:657753..659444,2	MCF-7	breast:
3	chr10:580078..582771-chr10:585483..587204,2	MCF-7	breast:
4	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
5	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
6	chr10:588433..590625-chr10:591503..594544,3	MCF-7	breast:
7	chr10:589190..591988-chr10:602233..604449,2	K562	blood:
8	chr10:585455..588115-chr10:589415..592524,3	MCF-7	breast:
9	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
10	chr10:633910..634891-chr10:834953..835643,3	MCF-7	breast:
11	chr10:593219..595264-chr10:597541..599754,3	MCF-7	breast:
12	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
13	chr10:588433..590625-chr10:591503..594544,3	MCF-7	breast:
14	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
15	chr10:584008..586633-chr10:587341..589161,2	MCF-7	breast:
16	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
17	chr10:585109..589667-chr10:591108..594165,5	MCF-7	breast:
18	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
19	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
20	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
21	chr10:586974..589540-chr10:590949..592732,2	K562	blood:
22	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
23	chr10:565187..567915-chr10:586471..588342,2	MCF-7	breast:
24	chr10:634748..636656-chr10:637964..639591,2	K562	blood:
25	chr10:586974..589540-chr10:590949..592732,2	K562	blood:
26	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
27	chr10:638624..640408-chr10:644679..647011,2	MCF-7	breast:
28	chr10:591027..592678-chr10:670118..672515,2	MCF-7	breast:
29	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
30	chr10:632878..635792-chr10:829676..832349,2	MCF-7	breast:
31	chr10:585455..588115-chr10:589415..592524,3	MCF-7	breast:
32	chr10:582102..583966-chr10:587212..590042,3	K562	blood:
33	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
34	chr10:641312..643673-chr10:645720..648516,2	MCF-7	breast:
35	chr10:584008..586633-chr10:587341..589161,2	MCF-7	breast:
36	chr10:641312..643673-chr10:645720..648516,2	MCF-7	breast:
37	chr10:625995..627810-chr10:664687..667494,2	K562	blood:
38	chr10:583403..585208-chr10:714450..715956,2	K562	blood:
39	chr10:589190..591988-chr10:602233..604449,2	K562	blood:
40	chr10:585109..589667-chr10:591108..594165,5	MCF-7	breast:
41	chr10:577006..578982-chr10:591616..594323,2	MCF-7	breast:
42	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:
43	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
44	chr10:572682..575293-chr10:584649..586274,2	MCF-7	breast:
45	chr10:630264..632276-chr10:643488..645388,2	MCF-7	breast:
46	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
47	chr10:582102..583966-chr10:587212..590042,3	K562	blood:
48	chr10:627398..630591-chr10:632947..634840,3	K562	blood:
49	chr10:632427..634199-chr10:639895..642783,2	K562	blood:
50	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:

No data

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

Extended variants
information (count: 4107 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4107 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563821567	chr10:581936-581937	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532893628	chr10:581957-581958	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549363534	chr10:581965-581966	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182032838	chr10:582002-582003	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558127596	chr10:582008-582009	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529522017	chr10:582010-582011	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549656837	chr10:582021-582022	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566116759	chr10:582051-582052	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs377578125	chr10:582052-582053	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184533357	chr10:582070-582071	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140852433	chr10:582072-582073	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555952826	chr10:582116-582117	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78142899	chr10:582119-582120	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573978325	chr10:582125-582126	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541730109	chr10:582126-582127	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555648653	chr10:582129-582130	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572283186	chr10:582130-582131	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138509564	chr10:582147-582148	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563987879	chr10:582185-582186	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532854912	chr10:582199-582200	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370884678	chr10:582248-582249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563094211	chr10:582252-582253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372969126	chr10:582272-582273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140624579	chr10:582273-582274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549379971	chr10:582286-582287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12761663	chr10:582311-582312	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs71494914	chr10:582313-582314	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs551992816	chr10:582317-582318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138290274	chr10:582319-582320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537493227	chr10:582321-582322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181437592	chr10:582335-582336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567517672	chr10:582362-582363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536633681	chr10:582364-582365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs113509750	chr10:582370-582371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534642725	chr10:582382-582383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186876636	chr10:582391-582392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577419788	chr10:582395-582396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191319811	chr10:582427-582428	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs12761875	chr10:582431-582432	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs546965310	chr10:582435-582436	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs12761882	chr10:582442-582443	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs577981283	chr10:582443-582444	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs573691279	chr10:582444-582445	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs149611938	chr10:582454-582455	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs559123429	chr10:582464-582465	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs528753146	chr10:582538-582539	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs552103209	chr10:582557-582558	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs565447647	chr10:582575-582576	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs146669763	chr10:582586-582587	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs550928268	chr10:582592-582593	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1888 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:557800-582200	Weak transcription	Osteobl	bone
2	chr10:568600-582000	Weak transcription	Right Atrium	heart
3	chr10:568600-582400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:572000-582000	Weak transcription	NH-A	brain
5	chr10:573200-587200	Weak transcription	Gastric	stomach
6	chr10:573200-587800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:573800-582600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:575000-582000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr10:577000-582000	Weak transcription	Brain Substantia Nigra	brain
10	chr10:577000-582000	Weak transcription	Psoas Muscle	Psoas
11	chr10:577000-582800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr10:578400-582200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr10:578400-587800	Weak transcription	Fetal Muscle Leg	muscle
14	chr10:578800-582200	Weak transcription	Right Ventricle	heart
15	chr10:579200-582000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr10:579600-582000	Weak transcription	Brain Anterior Caudate	brain
17	chr10:579800-582600	Weak transcription	Brain Angular Gyrus	brain
18	chr10:579800-587200	Weak transcription	Pancreas	Pancrea
19	chr10:580200-582800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr10:580400-582000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr10:580400-582400	Weak transcription	Brain Hippocampus Middle	brain
22	chr10:580400-582800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr10:580400-583000	Weak transcription	Fetal Stomach	stomach
24	chr10:580400-585400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr10:580600-587600	Weak transcription	Fetal Intestine Small	intestine
26	chr10:581000-582200	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr10:581000-583800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:581200-583000	Weak transcription	Fetal Brain Male	brain
29	chr10:581200-583400	Enhancers	Left Ventricle	heart
30	chr10:581200-587200	Weak transcription	Esophagus	oesophagus
31	chr10:581200-587600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr10:581400-582600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr10:581400-583200	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr10:581400-583600	Enhancers	Colon Smooth Muscle	Colon
35	chr10:581600-582800	Weak transcription	Adipose Nuclei	Adipose
36	chr10:581800-583200	Enhancers	Ovary	ovary
37	chr10:581800-583200	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr10:581800-583400	Enhancers	Stomach Smooth Muscle	stomach
39	chr10:582000-582200	Enhancers	Right Atrium	heart
40	chr10:582000-582200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr10:582000-582400	Enhancers	Psoas Muscle	Psoas
42	chr10:582000-582800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr10:582000-583200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr10:582000-583200	Enhancers	NH-A	brain
45	chr10:582000-583600	Enhancers	Brain Substantia Nigra	brain
46	chr10:582000-583800	Enhancers	Brain Anterior Caudate	brain
47	chr10:582000-585800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr10:582200-582600	Weak transcription	Right Atrium	heart
49	chr10:582200-582600	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr10:582200-583000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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