Variant report

Variant	nsv894969
Chromosome Location	chr10:25345720-25395579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:995)
CpG islands
(count:184)
Chromatin interactive
region (count:63)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:995 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:25349037-25349247	K562	blood:	n/a	n/a
2	ARID3A	chr10:25367422-25368533	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:25371398-25372030	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:25350560-25351729	K562	blood:	n/a	n/a
5	ARID3A	chr10:25349028-25349245	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:25369916-25370267	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:25391463-25391574	K562	blood:	n/a	n/a
8	ARID3A	chr10:25351365-25351716	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:25369889-25370231	K562	blood:	n/a	n/a
10	ATF1	chr10:25357320-25357627	K562	blood:	n/a	n/a
11	ATF1	chr10:25365656-25366064	K562	blood:	n/a	n/a
12	ATF1	chr10:25350728-25351739	K562	blood:	n/a	n/a
13	ATF2	chr10:25357189-25357600	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr10:25351288-25351785	K562	blood:	n/a	n/a
15	ATF3	chr10:25351381-25351746	K562	blood:	n/a	n/a
16	ATF3	chr10:25348898-25349344	K562	blood:	n/a	n/a
17	ATF3	chr10:25349000-25349280	K562	blood:	n/a	n/a
18	BACH1	chr10:25350626-25351684	K562	blood:	n/a	n/a
19	BACH1	chr10:25370118-25370135	K562	blood:	n/a	n/a
20	BATF	chr10:25357156-25357476	GM12878	blood:	n/a	chr10:25357432-25357445 chr10:25357318-25357327
21	BATF	chr10:25352365-25352714	GM12878	blood:	n/a	chr10:25352563-25352574
22	BHLHE40	chr10:25369837-25370263	K562	blood:	n/a	n/a
23	BHLHE40	chr10:25365610-25366191	K562	blood:	n/a	n/a
24	BHLHE40	chr10:25392671-25393053	K562	blood:	n/a	n/a
25	BHLHE40	chr10:25351006-25351743	HepG2	liver:	n/a	n/a
26	BHLHE40	chr10:25350527-25351837	K562	blood:	n/a	n/a
27	BHLHE40	chr10:25351356-25351683	A549	lung:	n/a	n/a
28	BHLHE40	chr10:25349186-25349285	K562	blood:	n/a	n/a
29	BHLHE40	chr10:25369836-25370202	GM12878	blood:	n/a	n/a
30	BRCA1	chr10:25348995-25349471	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr10:25383573-25383835	K562	blood:	n/a	n/a
32	CBX3	chr10:25383526-25383825	K562	blood:	n/a	n/a
33	CBX3	chr10:25350677-25351934	K562	blood:	n/a	n/a
34	CBX3	chr10:25369779-25370295	K562	blood:	n/a	n/a
35	CBX3	chr10:25351123-25351936	HCT-116	colon:	n/a	n/a
36	CCNT2	chr10:25370016-25370363	K562	blood:	n/a	n/a
37	CCNT2	chr10:25351359-25351787	K562	blood:	n/a	chr10:25351586-25351606
38	CCNT2	chr10:25350662-25351072	K562	blood:	n/a	n/a
39	CEBPB	chr10:25374422-25375169	A549	lung:	n/a	chr10:25375031-25375040 chr10:25374829-25374840 chr10:25375029-25375042 chr10:25375029-25375040 chr10:25375030-25375041 chr10:25375029-25375042
40	CEBPB	chr10:25348979-25349348	HepG2	liver:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
41	CEBPB	chr10:25348902-25349419	A549	lung:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
42	CEBPB	chr10:25348559-25349460	HCT-116	colon:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
43	CEBPB	chr10:25348845-25349379	MCF-7	breast:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
44	CEBPB	chr10:25374861-25375093	HepG2	liver:	n/a	chr10:25375031-25375040 chr10:25375029-25375042 chr10:25375029-25375040 chr10:25375030-25375041 chr10:25375029-25375042
45	CEBPB	chr10:25367655-25368221	HepG2	liver:	n/a	n/a
46	CEBPB	chr10:25367651-25368348	A549	lung:	n/a	n/a
47	CEBPB	chr10:25367661-25367861	K562	blood:	n/a	n/a
48	CEBPB	chr10:25349086-25349239	HepG2	liver:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
49	CEBPB	chr10:25348936-25349386	ECC-1	luminal epithelium:	n/a	chr10:25349162-25349173 chr10:25349161-25349174
50	CEBPB	chr10:25348039-25348208	K562	blood:	n/a	chr10:25348117-25348128

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:25371488-25371538	HRE	kidney:	n/a
2	chr10:25371488-25371538	HRE	kidney:	n/a
3	chr10:25371488-25371538	SK-N-SH	brain:	n/a
4	chr10:25357368-25357418	MCF-7	breast:	n/a
5	chr10:25371488-25371538	HIPEpiC	eye:	n/a
6	chr10:25357368-25357418	Jurkat	blood:	n/a
7	chr10:25357368-25357418	GM12892	blood:	n/a
8	chr10:25350802-25350852	U87	brain:	n/a
9	chr10:25350802-25350852	HL-60	blood:	n/a
10	chr10:25371488-25371538	BJ	skin:	n/a
11	chr10:25371488-25371538	ovcar-3	ovarian:	n/a
12	chr10:25357368-25357418	PFSK-1	brain:	n/a
13	chr10:25371488-25371538	PrEC	prostate:	n/a
14	chr10:25371488-25371538	H1-hESC	embryonic stem cell:	embryo
15	chr10:25357368-25357418	HNPCEpiC	eye:	n/a
16	chr10:25350802-25350852	HEEpiC	esophagus:	n/a
17	chr10:25350802-25350852	Hela-S3	cervix:	n/a
18	chr10:25350802-25350852	ProgFib	skin:	n/a
19	chr10:25350802-25350852	GM12891	blood:	n/a
20	chr10:25350802-25350852	PFSK-1	brain:	n/a
21	chr10:25371488-25371538	Jurkat	blood:	n/a
22	chr10:25350802-25350852	HAEpiC	amniotic membrane:	n/a
23	chr10:25357368-25357418	HCF	heart:	n/a
24	chr10:25350802-25350852	AG04450	lung:	fetal
25	chr10:25350802-25350852	HPAEpiC	pulmonary alveolar:	n/a
26	chr10:25357368-25357418	NHBE	bronchial:	n/a
27	chr10:25357368-25357418	PANC-1	pancreas:	n/a
28	chr10:25371488-25371538	HRPEpiC	eye:	n/a
29	chr10:25371488-25371538	U87	brain:	n/a
30	chr10:25357368-25357418	CMK	blood:	n/a
31	chr10:25350802-25350852	AG04449	skin:	fetal
32	chr10:25371488-25371538	PFSK-1	brain:	n/a
33	chr10:25357368-25357418	SK-N-SH_RA	brain:	n/a
34	chr10:25371488-25371538	Caco-2	colon:	n/a
35	chr10:25350802-25350852	AG10803	skin:	n/a
36	chr10:25371488-25371538	AG09319	gingival:	n/a
37	chr10:25371488-25371538	BE2_C	brain:	n/a
38	chr10:25350802-25350852	HRPEpiC	eye:	n/a
39	chr10:25371488-25371538	MCF-7	breast:	n/a
40	chr10:25350802-25350852	PANC-1	pancreas:	n/a
41	chr10:25357368-25357418	HIPEpiC	eye:	n/a
42	chr10:25371488-25371538	HUVEC	blood vessel:	n/a
43	chr10:25357368-25357418	A549	lung:	n/a
44	chr10:25357368-25357418	H1-hESC	embryonic stem cell:	embryo
45	chr10:25350802-25350852	ECC-1	luminal epithelium:	n/a
46	chr10:25357368-25357418	LNCaP	prostate:	n/a
47	chr10:25350802-25350852	BJ	skin:	n/a
48	chr10:25350802-25350852	SK-N-SH	brain:	n/a
49	chr10:25357368-25357418	BJ	skin:	n/a
50	chr10:25371488-25371538	HCM	heart:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:25306123..25307821-chr10:25350955..25353147,2	MCF-7	breast:
2	chr10:25239858..25243208-chr10:25347592..25352504,4	K562	blood:
3	chr10:25384858..25387044-chr10:25387748..25390557,2	K562	blood:
4	chr10:25011194..25013594-chr10:25390011..25392696,2	K562	blood:
5	chr10:25306319..25307953-chr10:25346499..25349389,2	MCF-7	breast:
6	chr10:25345062..25348953-chr10:25349936..25353027,4	K562	blood:
7	chr10:25350138..25352241-chr10:25355108..25357944,2	MCF-7	breast:
8	chr10:25315371..25316092-chr10:25369588..25370596,3	K562	blood:
9	chr10:25016699..25017443-chr10:25369664..25370556,4	K562	blood:
10	chr10:25344528..25346562-chr10:25350767..25353027,3	K562	blood:
11	chr10:25305403..25308444-chr10:25369519..25373361,4	MCF-7	breast:
12	chr10:25372240..25374997-chr10:25377094..25379582,2	K562	blood:
13	chr10:25345062..25348953-chr10:25349936..25353027,4	K562	blood:
14	chr10:24854730..24857189-chr10:25359782..25362279,2	K562	blood:
15	chr10:25304278..25309002-chr10:25368191..25372754,5	K562	blood:
16	chr10:25356543..25358700-chr10:25359934..25363281,3	K562	blood:
17	chr10:25349510..25351855-chr10:25352161..25354821,2	MCF-7	breast:
18	chr10:25362224..25363937-chr10:25363978..25365901,2	K562	blood:
19	chr10:25304800..25307444-chr10:25366624..25371121,4	MCF-7	breast:
20	chr10:25343371..25346299-chr10:25346762..25349074,2	K562	blood:
21	chr10:24931513..24932500-chr10:25369531..25370644,4	K562	blood:
22	chr10:25340489..25343849-chr10:25349173..25351054,3	K562	blood:
23	chr10:25369500..25372471-chr10:25373482..25376338,3	MCF-7	breast:
24	chr10:25344134..25348116-chr10:25349607..25352644,3	MCF-7	breast:
25	chr10:25369500..25372471-chr10:25373482..25376338,3	MCF-7	breast:
26	chr10:25357593..25359343-chr10:25368933..25370472,2	K562	blood:
27	chr10:25343578..25346366-chr10:25349000..25351556,3	MCF-7	breast:
28	chr10:25341537..25343849-chr10:25349173..25350705,2	K562	blood:
29	chr10:25307575..25310244-chr10:25349571..25352250,2	MCF-7	breast:
30	chr10:25308766..25310925-chr10:25358161..25359867,2	K562	blood:
31	chr10:25315173..25316027-chr10:25369505..25370579,6	MCF-7	breast:
32	chr10:25343371..25346299-chr10:25346762..25349074,2	K562	blood:
33	chr10:25079435..25081057-chr10:25368417..25370064,2	K562	blood:
34	chr10:25372240..25374997-chr10:25377094..25379582,2	K562	blood:
35	chr10:25384858..25387044-chr10:25387748..25390557,2	K562	blood:
36	chr10:25303827..25307133-chr10:25349437..25354097,8	K562	blood:
37	chr10:25356543..25358700-chr10:25359934..25363281,3	K562	blood:
38	chr10:25315162..25315967-chr10:25369953..25370895,6	MCF-7	breast:
39	chr10:25011013..25013160-chr10:25345003..25347658,2	K562	blood:
40	chr10:25304955..25307281-chr10:25348708..25354586,7	MCF-7	breast:
41	chr10:25352997..25355657-chr10:25355970..25357954,2	K562	blood:
42	chr10:25303695..25307800-chr10:25367762..25370827,4	K562	blood:
43	chr10:25369667..25370602-chr10:25971300..25972009,2	MCF-7	breast:
44	chr10:25304592..25306407-chr10:25373363..25375162,2	MCF-7	breast:
45	chr10:25344528..25346562-chr10:25350767..25353027,3	K562	blood:
46	chr10:25334592..25336921-chr10:25350299..25353033,2	K562	blood:
47	chr10:25329304..25331383-chr10:25344755..25346865,2	K562	blood:
48	chr10:25357593..25359343-chr10:25368933..25370472,2	K562	blood:
49	chr10:25239725..25241588-chr10:25374362..25376183,2	K562	blood:
50	chr10:25343578..25346366-chr10:25349000..25351556,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000266069	TF binding region
ENSG00000266069	CpG island
ENSG00000107863	chromatin interactions
ENSG00000151023	chromatin interactions
ENSG00000273107	chromatin interactions
ENSG00000099256	chromatin interactions
ENSG00000185875	chromatin interactions

Extended variants
information (count: 1680 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:1680 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11014365	chr10:25345720-25345721	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183761356	chr10:25345721-25345722	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531203898	chr10:25345747-25345748	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs190472305	chr10:25345799-25345800	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150009466	chr10:25345834-25345835	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529827254	chr10:25345868-25345869	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs182138249	chr10:25346017-25346018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560149874	chr10:25346039-25346040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370350481	chr10:25346047-25346048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145273454	chr10:25346067-25346068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs186855248	chr10:25346086-25346087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568825291	chr10:25346129-25346130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537731062	chr10:25346159-25346160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550587888	chr10:25346190-25346191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs533861275	chr10:25346208-25346209	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs530154953	chr10:25346213-25346214	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139515865	chr10:25346310-25346311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76956370	chr10:25346355-25346356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs57431152	chr10:25346357-25346358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs386370954	chr10:25346358-25346359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35895381	chr10:25346359-25346360	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs569826081	chr10:25346371-25346372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553201384	chr10:25346395-25346396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146787763	chr10:25346449-25346450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538883399	chr10:25346455-25346456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538799449	chr10:25346476-25346477	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374035438	chr10:25346486-25346487	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559162091	chr10:25346573-25346574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191642462	chr10:25346575-25346576	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs544900875	chr10:25346583-25346584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560915716	chr10:25346613-25346614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs372247597	chr10:25346614-25346615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574344611	chr10:25346644-25346645	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11014366	chr10:25346673-25346674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs552374097	chr10:25346698-25346699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560010810	chr10:25346710-25346711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368541853	chr10:25346749-25346750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12241035	chr10:25346802-25346803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143981638	chr10:25346867-25346868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs7894458	chr10:25346876-25346877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs372693946	chr10:25346902-25346903	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113791548	chr10:25346962-25346963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181704418	chr10:25346968-25346969	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562328925	chr10:25346979-25346980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs531541274	chr10:25346982-25346983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs563891729	chr10:25347014-25347015	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs568298688	chr10:25347016-25347017	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs536259692	chr10:25347020-25347021	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566328543	chr10:25347035-25347036	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs140693971	chr10:25347054-25347055	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25337400-25348200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:25337600-25348200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:25338200-25348400	Weak transcription	Duodenum Mucosa	Duodenum
4	chr10:25341200-25345800	Weak transcription	Liver	Liver
5	chr10:25345200-25349400	Enhancers	Fetal Intestine Small	intestine
6	chr10:25345600-25346000	Genic enhancers	K562	blood
7	chr10:25345600-25350600	Enhancers	Fetal Intestine Large	intestine
8	chr10:25345800-25346000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:25345800-25347200	Enhancers	Liver	Liver
10	chr10:25346000-25347200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr10:25346000-25349200	Enhancers	K562	blood
12	chr10:25346400-25347400	Enhancers	Stomach Mucosa	stomach
13	chr10:25346400-25347400	Enhancers	HUVEC	blood vessel
14	chr10:25347000-25347200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr10:25347000-25347200	Enhancers	Gastric	stomach
16	chr10:25347000-25347200	Enhancers	HepG2	liver
17	chr10:25347000-25347600	Enhancers	A549	lung
18	chr10:25347200-25347400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr10:25347200-25350600	Weak transcription	Liver	Liver
20	chr10:25347200-25350600	Weak transcription	Gastric	stomach
21	chr10:25347200-25350800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr10:25347400-25348200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:25347400-25348400	Weak transcription	Stomach Mucosa	stomach
24	chr10:25347400-25348400	Weak transcription	HepG2	liver
25	chr10:25347400-25348400	Weak transcription	HUVEC	blood vessel
26	chr10:25347600-25348000	Weak transcription	A549	lung
27	chr10:25347600-25348800	Enhancers	Hela-S3	cervix
28	chr10:25348000-25348400	Enhancers	A549	lung
29	chr10:25348200-25350600	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr10:25348200-25351200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr10:25348200-25351600	Enhancers	Placenta Amnion	Placenta Amnion
32	chr10:25348200-25352200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr10:25348400-25348600	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr10:25348400-25348800	Enhancers	NHEK	skin
35	chr10:25348400-25349000	Enhancers	Lung	lung
36	chr10:25348400-25349000	Enhancers	Small Intestine	intestine
37	chr10:25348400-25349600	Enhancers	Duodenum Mucosa	Duodenum
38	chr10:25348400-25349600	Flanking Active TSS	A549	lung
39	chr10:25348400-25349800	Enhancers	Placenta	Placenta
40	chr10:25348400-25350800	Enhancers	HepG2	liver
41	chr10:25348400-25351000	Enhancers	HMEC	breast
42	chr10:25348400-25351200	Enhancers	HUVEC	blood vessel
43	chr10:25348400-25351600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr10:25348400-25352200	Enhancers	Stomach Mucosa	stomach
45	chr10:25348400-25352800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr10:25348600-25348800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr10:25348600-25348800	Enhancers	Aorta	Aorta
48	chr10:25348600-25348800	Enhancers	Colonic Mucosa	Colon
49	chr10:25348600-25349200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr10:25348600-25349600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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