Variant report

Variant	nsv894710
Chromosome Location	chr10:588126-639750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:422)
CpG islands
(count:2261)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr10:629787-629980	K562	blood:	n/a	chr10:629835-629844 chr10:629836-629845 chr10:629835-629844
5	CEBPB	chr10:617766-618133	IMR90	lung:	n/a	n/a
6	CEBPB	chr10:626623-627083	IMR90	lung:	n/a	n/a
7	CHD2	chr10:601726-601734	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr10:634218-634278	GM12878	blood:	n/a	n/a
9	CTCF	chr10:634160-634310	BE2_C	brain:	n/a	n/a
10	CTCF	chr10:634180-634330	AG09309	skin:	n/a	n/a
11	CTCF	chr10:631525-631730	MCF-7	breast:	n/a	n/a
12	CTCF	chr10:634120-634270	HA-sp	spinal cord:	n/a	n/a
13	CTCF	chr10:634180-634330	Caco-2	colon:	n/a	n/a
14	CTCF	chr10:634131-634334	MCF-7	breast:	n/a	n/a
15	CTCF	chr10:631516-631759	MCF-7	breast:	n/a	n/a
16	CTCF	chr10:634160-634310	HVMF	connective:	n/a	n/a
17	CTCF	chr10:634160-634310	HEK293	kidney:	n/a	n/a
18	CTCF	chr10:631880-632030	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr10:637580-637730	GM12866	blood:	n/a	n/a
20	CTCF	chr10:634180-634330	HCFaa	heart:	n/a	n/a
21	CTCF	chr10:634160-634310	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:619320-619470	HEK293	kidney:	n/a	n/a
23	CTCF	chr10:634160-634310	HepG2	liver:	n/a	n/a
24	CTCF	chr10:634180-634330	SAEC	small airway:	n/a	n/a
25	CTCF	chr10:634160-634310	HAc	cerebellar:	n/a	n/a
26	CTCF	chr10:634180-634330	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr10:619320-619494	K562	blood:	n/a	n/a
28	CTCF	chr10:637620-637770	GM12872	blood:	n/a	n/a
29	CTCF	chr10:631523-631759	T-47D	breast:	n/a	n/a
30	CTCF	chr10:634180-634330	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr10:634162-634412	T-47D	breast:	n/a	n/a
32	CTCF	chr10:631580-631730	MCF-7	breast:	n/a	n/a
33	CTCF	chr10:634200-634350	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr10:634220-634370	RPTEC	kidney:	n/a	n/a
35	CTCF	chr10:631529-631825	K562	blood:	n/a	n/a
36	CTCF	chr10:619322-619487	MCF-7	breast:	n/a	n/a
37	CTCF	chr10:588255-588262	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr10:631515-631722	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr10:634200-634350	AG09309	skin:	n/a	n/a
40	CTCF	chr10:631920-632070	HepG2	liver:	n/a	n/a
41	CTCF	chr10:631391-631847	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr10:633305-633359	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr10:634180-634330	HRE	kidney:	n/a	n/a
44	CTCF	chr10:634180-634330	AG10803	skin:	n/a	n/a
45	CTCF	chr10:634191-634308	HepG2	liver:	n/a	n/a
46	CTCF	chr10:615814-615836	GM13976	blood:	n/a	n/a
47	CTCF	chr10:619320-619470	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr10:634164-634497	MCF-7	breast:	n/a	chr10:634453-634466
49	CTCF	chr10:634180-634330	HVMF	connective:	n/a	n/a
50	CTCF	chr10:631520-631670	HepG2	liver:	n/a	n/a

(count:2261 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:604032-604082	RPTEC	kidney:	n/a
2	chr10:601816-601866	HCM	heart:	n/a
3	chr10:629582-629632	GM19239	blood:	n/a
4	chr10:589375-589425	T-47D	breast:	n/a
5	chr10:604032-604082	RPTEC	kidney:	n/a
6	chr10:601816-601866	HCM	heart:	n/a
7	chr10:629582-629632	GM19239	blood:	n/a
8	chr10:589375-589425	T-47D	breast:	n/a
9	chr10:636241-636291	HCM	heart:	n/a
10	chr10:636331-636381	HRPEpiC	eye:	n/a
11	chr10:604523-604573	GM06990	blood:	n/a
12	chr10:617105-617155	IMR90	lung:	fetal
13	chr10:633154-633204	BJ	skin:	n/a
14	chr10:603950-604000	GM12878	blood:	n/a
15	chr10:604032-604082	BJ	skin:	n/a
16	chr10:593275-593325	ovcar-3	ovarian:	n/a
17	chr10:616959-617009	HUVEC	blood vessel:	n/a
18	chr10:601816-601866	NHDF-neo	bronchial:	n/a
19	chr10:633154-633204	HIPEpiC	eye:	n/a
20	chr10:630384-630434	LNCaP	prostate:	n/a
21	chr10:636331-636381	HUVEC	blood vessel:	n/a
22	chr10:633154-633204	MCF-7	breast:	n/a
23	chr10:593275-593325	SK-N-SH	brain:	n/a
24	chr10:636331-636381	SK-N-SH	brain:	n/a
25	chr10:629582-629632	HMEC	breast:	n/a
26	chr10:630671-630721	AG09319	gingival:	n/a
27	chr10:630310-630360	T-47D	breast:	n/a
28	chr10:612314-612364	ProgFib	skin:	n/a
29	chr10:604523-604573	HEK293	kidney:	embryo
30	chr10:616959-617009	Caco-2	colon:	n/a
31	chr10:604461-604511	PFSK-1	brain:	n/a
32	chr10:630671-630721	NHBE	bronchial:	n/a
33	chr10:631304-631354	AG09319	gingival:	n/a
34	chr10:632914-632964	AG09319	gingival:	n/a
35	chr10:604461-604511	HEK293	kidney:	embryo
36	chr10:612391-612441	MCF-7	breast:	n/a
37	chr10:629625-629675	H1-hESC	embryonic stem cell:	embryo
38	chr10:589217-589267	SK-N-SH_RA	brain:	n/a
39	chr10:629582-629632	HIPEpiC	eye:	n/a
40	chr10:601816-601866	SK-N-SH	brain:	n/a
41	chr10:636076-636126	CMK	blood:	n/a
42	chr10:630942-630992	HAEpiC	amniotic membrane:	n/a
43	chr10:589217-589267	NH-A	brain:	n/a
44	chr10:612314-612364	AG09309	skin:	n/a
45	chr10:629625-629675	PrEC	prostate:	n/a
46	chr10:631304-631354	HRE	kidney:	n/a
47	chr10:593275-593325	AG09309	skin:	n/a
48	chr10:636076-636126	MCF10A-Er-Src	breast:	n/a
49	chr10:630671-630721	BE2_C	brain:	n/a
50	chr10:627679-627729	SK-N-SH_RA	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
2	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
3	chr10:588040..589570-chr10:591232..593419,2	K562	blood:
4	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
5	chr10:577006..578982-chr10:591616..594323,2	MCF-7	breast:
6	chr10:632878..635792-chr10:829676..832349,2	MCF-7	breast:
7	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
8	chr10:586974..589540-chr10:590949..592732,2	K562	blood:
9	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
10	chr10:631818..632398-chr3:122337364..122338295,2	MCF-7	breast:
11	chr10:632427..634199-chr10:639895..642783,2	K562	blood:
12	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
13	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
14	chr10:585455..588115-chr10:589415..592524,3	MCF-7	breast:
15	chr10:589190..591988-chr10:602233..604449,2	K562	blood:
16	chr10:634195..634721-chr10:829974..830911,3	MCF-7	breast:
17	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
18	chr10:588433..590625-chr10:591503..594544,3	MCF-7	breast:
19	chr10:591027..592678-chr10:670118..672515,2	MCF-7	breast:
20	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
21	chr10:589190..591988-chr10:602233..604449,2	K562	blood:
22	chr10:627398..630591-chr10:632947..634840,3	K562	blood:
23	chr10:636273..639205-chr10:641067..642739,2	MCF-7	breast:
24	chr10:588433..590625-chr10:591503..594544,3	MCF-7	breast:
25	chr10:584008..586633-chr10:587341..589161,2	MCF-7	breast:
26	chr10:634748..636656-chr10:637964..639591,2	K562	blood:
27	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
28	chr10:585109..589667-chr10:591108..594165,5	MCF-7	breast:
29	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
30	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:
31	chr10:585109..589667-chr10:591108..594165,5	MCF-7	breast:
32	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
33	chr10:629648..631897-chr10:633164..636396,3	MCF-7	breast:
34	chr10:593219..595264-chr10:597541..599754,3	MCF-7	breast:
35	chr10:565187..567915-chr10:586471..588342,2	MCF-7	breast:
36	chr10:634649..636667-chr10:654000..655714,2	MCF-7	breast:
37	chr10:638624..640408-chr10:644679..647011,2	MCF-7	breast:
38	chr10:591597..594748-chr10:659292..660981,3	MCF-7	breast:
39	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
40	chr10:633910..634891-chr10:834953..835643,3	MCF-7	breast:
41	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
42	chr10:634748..636656-chr10:637964..639591,2	K562	blood:
43	chr10:593219..595264-chr10:597541..599754,3	MCF-7	breast:
44	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:
45	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
46	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
47	chr10:588040..589570-chr10:591232..593419,2	K562	blood:
48	chr10:625995..627810-chr10:664687..667494,2	K562	blood:
49	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
50	chr10:614375..617220-chr10:617772..620135,2	K562	blood:

No data

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

Extended variants
information (count: 3363 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3363 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11253082	chr10:588126-588127	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7071903	chr10:588141-588142	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575921856	chr10:588143-588144	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs117202264	chr10:588149-588150	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544476169	chr10:588150-588151	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs541559219	chr10:588160-588161	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs574553805	chr10:588172-588173	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs191669466	chr10:588176-588177	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs560088649	chr10:588187-588188	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs532388884	chr10:588189-588190	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs552578096	chr10:588205-588206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565027513	chr10:588206-588207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374263064	chr10:588216-588217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56670438	chr10:588245-588246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530872699	chr10:588249-588250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183776203	chr10:588275-588276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577880142	chr10:588280-588281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574803520	chr10:588307-588308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567470204	chr10:588318-588319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536323581	chr10:588345-588346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10904450	chr10:588406-588407	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs566604988	chr10:588415-588416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560787529	chr10:588416-588417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs200969640	chr10:588440-588441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs72774553	chr10:588458-588459	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185803929	chr10:588464-588465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575838838	chr10:588467-588468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538541675	chr10:588557-588558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375780943	chr10:588570-588571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11253087	chr10:588609-588610	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs114892863	chr10:588613-588614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540297978	chr10:588614-588615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560200941	chr10:588628-588629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576955648	chr10:588658-588659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112279810	chr10:588669-588670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374831343	chr10:588675-588676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562907887	chr10:588680-588681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530667505	chr10:588714-588715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190264968	chr10:588750-588751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201520642	chr10:588755-588756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182507018	chr10:588760-588761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs367897683	chr10:588764-588765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542926769	chr10:588774-588775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11253090	chr10:588779-588780	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs566568794	chr10:588789-588790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543376250	chr10:588818-588819	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538767153	chr10:588822-588823	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186657776	chr10:588824-588825	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192545481	chr10:588835-588836	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538129605	chr10:588837-588838	Weak transcription Enhancers Strong transcription	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:1553 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:582600-592600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr10:583200-592600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr10:583200-593000	Weak transcription	NH-A	brain
4	chr10:583200-604800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:583600-589000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr10:584800-589200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:585400-588800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:586000-593000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:586600-588200	Weak transcription	Brain Hippocampus Middle	brain
10	chr10:587000-589200	Enhancers	Right Ventricle	heart
11	chr10:587200-588400	Enhancers	Adipose Nuclei	Adipose
12	chr10:587200-588400	Enhancers	Gastric	stomach
13	chr10:587200-588400	Enhancers	Pancreas	Pancrea
14	chr10:587200-588400	Enhancers	Psoas Muscle	Psoas
15	chr10:587200-590200	Enhancers	Brain Germinal Matrix	brain
16	chr10:587200-590200	Enhancers	Esophagus	oesophagus
17	chr10:587400-588200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:587400-588200	Enhancers	Spleen	Spleen
19	chr10:587400-588400	Enhancers	Stomach Mucosa	stomach
20	chr10:587400-588400	Enhancers	GM12878-XiMat	blood
21	chr10:587400-588600	Enhancers	Fetal Muscle Trunk	muscle
22	chr10:587400-588600	Enhancers	Lung	lung
23	chr10:587400-588600	Enhancers	HepG2	liver
24	chr10:587400-589000	Enhancers	Brain Angular Gyrus	brain
25	chr10:587400-589200	Enhancers	Fetal Heart	heart
26	chr10:587400-589600	Enhancers	Ovary	ovary
27	chr10:587400-590200	Enhancers	Left Ventricle	heart
28	chr10:587600-588200	Enhancers	Duodenum Mucosa	Duodenum
29	chr10:587600-588200	Enhancers	Fetal Intestine Small	intestine
30	chr10:587600-588400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:587600-588400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr10:587600-588400	Enhancers	Fetal Intestine Large	intestine
33	chr10:587600-588400	Enhancers	Fetal Kidney	kidney
34	chr10:587600-588600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:587600-588600	Enhancers	Right Atrium	heart
36	chr10:587600-588800	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr10:587600-589000	Enhancers	Brain Anterior Caudate	brain
38	chr10:587600-589000	Enhancers	Brain Cingulate Gyrus	brain
39	chr10:587600-589000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr10:587600-590200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr10:587600-590200	Enhancers	Brain Substantia Nigra	brain
42	chr10:587600-590600	Enhancers	Fetal Brain Male	brain
43	chr10:587800-588200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:587800-588200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr10:587800-588200	Enhancers	Placenta	Placenta
46	chr10:587800-588200	Bivalent Enhancer	Fetal Stomach	stomach
47	chr10:587800-588200	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr10:587800-588400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr10:587800-588400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr10:587800-588600	Enhancers	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links