Variant report

Variant	nsv975816
Chromosome Location	chr10:99344579-99354694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr10:99344884-99345251	HepG2	liver:	n/a	chr10:99345024-99345037
2	BHLHE40	chr10:99344873-99345110	K562	blood:	n/a	chr10:99345024-99345037
3	BRCA1	chr10:99346591-99346673	HepG2	liver:	n/a	n/a
4	CEBPB	chr10:99348246-99348525	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:99348281-99348455	HepG2	liver:	n/a	n/a
6	CTCF	chr10:99346154-99346281	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr10:99346191-99346290	MCF-7	breast:	n/a	n/a
8	CTCF	chr10:99346440-99346590	GM12867	blood:	n/a	n/a
9	CTCF	chr10:99346189-99346285	H1-hESC	embryonic stem cell:	n/a	n/a
10	E2F6	chr10:99344924-99345159	K562	blood:	n/a	chr10:99345052-99345063
11	E2F6	chr10:99344907-99345153	K562	blood:	n/a	chr10:99345052-99345063
12	E2F6	chr10:99344877-99345206	K562	blood:	n/a	chr10:99345052-99345063
13	EBF1	chr10:99350958-99351164	GM12878	blood:	n/a	chr10:99351083-99351094
14	EBF1	chr10:99350177-99350377	GM12878	blood:	n/a	n/a
15	EP300	chr10:99350243-99350350	GM12878	blood:	n/a	n/a
16	ESR1	chr10:99345131-99345517	T-47D	breast:	n/a	n/a
17	FOXA2	chr10:99344767-99345116	HepG2	liver:	n/a	n/a
18	GATA3	chr10:99344020-99344659	MCF-7	breast:	n/a	n/a
19	HDAC2	chr10:99348175-99348495	HepG2	liver:	n/a	n/a
20	HEY1	chr10:99343761-99344581	HepG2	liver:	n/a	n/a
21	HEY1	chr10:99343665-99344673	HepG2	liver:	n/a	n/a
22	HNF4A	chr10:99348211-99348499	HepG2	liver:	n/a	chr10:99348368-99348383
23	HNF4A	chr10:99348238-99348506	HepG2	liver:	n/a	chr10:99348368-99348383
24	HNF4G	chr10:99348201-99348478	HepG2	liver:	n/a	chr10:99348369-99348384
25	MAX	chr10:99344671-99345657	HepG2	liver:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
26	MAX	chr10:99344459-99345598	HepG2	liver:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
27	MAX	chr10:99349929-99350092	K562	blood:	n/a	n/a
28	MAX	chr10:99345013-99345102	GM12878	blood:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
29	MAX	chr10:99344884-99345175	HepG2	liver:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
30	MAX	chr10:99344849-99345177	K562	blood:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
31	MAX	chr10:99344844-99345135	K562	blood:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
32	MAX	chr10:99344932-99345084	K562	blood:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
33	MXI1	chr10:99344856-99345165	HepG2	liver:	n/a	chr10:99345025-99345034
34	MYC	chr10:99344957-99345056	K562	blood:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
35	MYC	chr10:99345002-99345066	HepG2	liver:	n/a	chr10:99345024-99345037 chr10:99345026-99345035 chr10:99345026-99345035
36	MYC	chr10:99350325-99350390	GM12878	blood:	n/a	n/a
37	NFIC	chr10:99349371-99349843	ECC-1	luminal epithelium:	n/a	n/a
38	NFIC	chr10:99350332-99350920	ECC-1	luminal epithelium:	n/a	n/a
39	NFIC	chr10:99353133-99353674	SK-N-SH	brain:	n/a	n/a
40	NR3C1	chr10:99344804-99345265	A549	lung:	n/a	chr10:99345073-99345087 chr10:99345071-99345088
41	PAX5	chr10:99350178-99350447	GM12878	blood:	n/a	n/a
42	PBX3	chr10:99353227-99353630	SK-N-SH	brain:	n/a	n/a
43	PBX3	chr10:99350155-99350310	GM12878	blood:	n/a	n/a
44	POLR2A	chr10:99343689-99345015	HepG2	liver:	n/a	n/a
45	POLR2A	chr10:99346147-99346213	HepG2	liver:	n/a	n/a
46	POLR2A	chr10:99345451-99345502	HepG2	liver:	n/a	n/a
47	POLR2A	chr10:99345697-99345852	HepG2	liver:	n/a	n/a
48	POLR2A	chr10:99343629-99344628	HepG2	liver:	n/a	n/a
49	RUNX3	chr10:99350158-99350387	GM12878	blood:	n/a	n/a
50	RXRA	chr10:99348226-99348476	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99348862-99348912	HRPEpiC	eye:	n/a
2	chr10:99350484-99350534	AoSMC	blood vessel:	n/a
3	chr10:99348862-99348912	H1-hESC	embryonic stem cell:	embryo
4	chr10:99350484-99350534	H1-hESC	embryonic stem cell:	embryo
5	chr10:99349003-99349053	AG04450	lung:	fetal
6	chr10:99350484-99350534	HEEpiC	esophagus:	n/a
7	chr10:99350484-99350534	GM12878	blood:	n/a
8	chr10:99349003-99349053	ovcar-3	ovarian:	n/a
9	chr10:99350484-99350534	HEK293	kidney:	embryo
10	chr10:99349003-99349053	HEK293	kidney:	embryo
11	chr10:99344969-99345019	AG09319	gingival:	n/a
12	chr10:99349361-99349411	GM19239	blood:	n/a
13	chr10:99349003-99349053	K562	blood:	n/a
14	chr10:99349361-99349411	GM06990	blood:	n/a
15	chr10:99350484-99350534	GM19239	blood:	n/a
16	chr10:99348862-99348912	LNCaP	prostate:	n/a
17	chr10:99348244-99348294	K562	blood:	n/a
18	chr10:99349003-99349053	Jurkat	blood:	n/a
19	chr10:99350484-99350534	HRCEpiC	kidney:	n/a
20	chr10:99349395-99349445	RPTEC	kidney:	n/a
21	chr10:99348244-99348294	SKMC	muscle:	n/a
22	chr10:99344969-99345019	T-47D	breast:	n/a
23	chr10:99348244-99348294	AG10803	skin:	n/a
24	chr10:99349361-99349411	T-47D	breast:	n/a
25	chr10:99348244-99348294	ProgFib	skin:	n/a
26	chr10:99344969-99345019	GM19239	blood:	n/a
27	chr10:99344969-99345019	AG04450	lung:	fetal
28	chr10:99349003-99349053	SK-N-MC	brain:	n/a
29	chr10:99349003-99349053	Hepatocyte	liver:	n/a
30	chr10:99349361-99349411	HCT-116	colon:	n/a
31	chr10:99344969-99345019	GM12891	blood:	n/a
32	chr10:99348862-99348912	HepG2	liver:	n/a
33	chr10:99348862-99348912	GM19239	blood:	n/a
34	chr10:99349395-99349445	SAEC	small airway:	n/a
35	chr10:99350484-99350534	BE2_C	brain:	n/a
36	chr10:99349395-99349445	HAEpiC	amniotic membrane:	n/a
37	chr10:99344969-99345019	HepG2	liver:	n/a
38	chr10:99349003-99349053	HCM	heart:	n/a
39	chr10:99348862-99348912	HNPCEpiC	eye:	n/a
40	chr10:99348244-99348294	T-47D	breast:	n/a
41	chr10:99348244-99348294	AG04450	lung:	fetal
42	chr10:99344969-99345019	PFSK-1	brain:	n/a
43	chr10:99349003-99349053	AG10803	skin:	n/a
44	chr10:99344969-99345019	SAEC	small airway:	n/a
45	chr10:99344969-99345019	K562	blood:	n/a
46	chr10:99349003-99349053	Caco-2	colon:	n/a
47	chr10:99348244-99348294	HEEpiC	esophagus:	n/a
48	chr10:99344969-99345019	HCF	heart:	n/a
49	chr10:99348244-99348294	Hela-S3	cervix:	n/a
50	chr10:99349003-99349053	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:99331139..99331795-chr10:99344716..99345483,2	MCF-7	breast:
2	chr10:99257383..99259278-chr10:99348125..99351802,3	MCF-7	breast:
3	chr10:99342912..99345937-chr10:99348140..99351473,3	K562	blood:
4	chr10:99342912..99345937-chr10:99348140..99351473,3	K562	blood:
5	chr10:99351412..99353396-chr10:99355023..99357817,2	K562	blood:
6	chr10:99345242..99348489-chr10:99349078..99351813,3	K562	blood:
7	chr10:99256457..99259169-chr10:99354656..99356211,2	MCF-7	breast:
8	chr10:99331295..99331846-chr10:99344716..99345312,2	MCF-7	breast:
9	chr10:99329733..99337149-chr10:99338392..99346753,19	MCF-7	breast:

Variant related genes	Relation type
C10orf62	TF binding region
HOGA1	TF binding region
C10orf62	CpG island
HOGA1	CpG island
ENSG00000165887	chromatin interactions
ENSG00000165886	chromatin interactions
ENSG00000249967	chromatin interactions
ENSG00000203942	chromatin interactions
ENSG00000241935	chromatin interactions
ENSG00000155229	chromatin interactions

Extended variants
information (count: 454 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141993402	chr10:99344628-99344629	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs150812556	chr10:99344645-99344646	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs369191992	chr10:99344660-99344661	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs267606763	chr10:99344669-99344670	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs372517912	chr10:99344685-99344686	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs552420631	chr10:99344691-99344692	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs202120436	chr10:99344700-99344701	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs201467858	chr10:99344709-99344710	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs558461907	chr10:99344745-99344746	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs184422949	chr10:99344798-99344799	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs568727907	chr10:99344809-99344810	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs536191408	chr10:99344816-99344817	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs564982505	chr10:99344836-99344837	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs548005955	chr10:99344865-99344866	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs530671049	chr10:99344874-99344875	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs189080771	chr10:99344882-99344883	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs533868366	chr10:99344901-99344902	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs558332992	chr10:99344954-99344955	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576892615	chr10:99344968-99344969	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs537401733	chr10:99344978-99344979	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs145064884	chr10:99344993-99344994	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs574382173	chr10:99345031-99345032	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs193196090	chr10:99345043-99345044	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs535595090	chr10:99345054-99345055	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs184754458	chr10:99345069-99345070	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs572183181	chr10:99345104-99345105	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs189959611	chr10:99345121-99345122	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs372060175	chr10:99345131-99345132	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs564398966	chr10:99345138-99345139	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs367584578	chr10:99345174-99345175	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs372379879	chr10:99345182-99345183	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs532819493	chr10:99345288-99345289	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs531839856	chr10:99345302-99345303	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs180806836	chr10:99345337-99345338	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs562109497	chr10:99345346-99345347	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs559013802	chr10:99345350-99345351	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs7070104	chr10:99345406-99345407	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs566545553	chr10:99345415-99345416	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs548141065	chr10:99345444-99345445	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs376597244	chr10:99345448-99345449	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs372130392	chr10:99345468-99345469	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs148312219	chr10:99345479-99345480	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs140305178	chr10:99345486-99345487	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs185147970	chr10:99345510-99345511	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs150347184	chr10:99345514-99345515	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs537590316	chr10:99345519-99345520	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555737856	chr10:99345548-99345549	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs138112590	chr10:99345581-99345582	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs189229451	chr10:99345618-99345619	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs181894287	chr10:99345628-99345629	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:219 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99336000-99348800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr10:99342600-99345200	Enhancers	Fetal Muscle Trunk	muscle
3	chr10:99343000-99346600	Enhancers	Fetal Heart	heart
4	chr10:99343200-99345600	Enhancers	Fetal Muscle Leg	muscle
5	chr10:99343400-99344600	Enhancers	Psoas Muscle	Psoas
6	chr10:99343400-99344800	Enhancers	Fetal Intestine Large	intestine
7	chr10:99343400-99345400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr10:99343400-99345400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:99343400-99345400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr10:99343400-99345600	Enhancers	NHEK	skin
11	chr10:99343400-99346400	Enhancers	Adipose Nuclei	Adipose
12	chr10:99343400-99346600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr10:99343600-99344600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:99343600-99344600	Flanking Active TSS	Brain Hippocampus Middle	brain
15	chr10:99343600-99344800	Enhancers	Fetal Intestine Small	intestine
16	chr10:99343600-99345000	Flanking Active TSS	A549	lung
17	chr10:99343600-99345600	Flanking Active TSS	HepG2	liver
18	chr10:99343600-99345600	Enhancers	NHDF-Ad	bronchial
19	chr10:99343600-99345800	Enhancers	Placenta	Placenta
20	chr10:99343800-99345200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr10:99343800-99345400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr10:99344000-99344600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr10:99344000-99345000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:99344000-99345000	Weak transcription	Lung	lung
25	chr10:99344000-99349000	Weak transcription	Fetal Stomach	stomach
26	chr10:99344200-99344600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr10:99344200-99344600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr10:99344200-99344600	Enhancers	Osteobl	bone
29	chr10:99344200-99345200	Active TSS	Left Ventricle	heart
30	chr10:99344200-99345200	Active TSS	Right Ventricle	heart
31	chr10:99344200-99345400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr10:99344200-99345400	Flanking Active TSS	Hela-S3	cervix
33	chr10:99344200-99345600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr10:99344200-99346600	Flanking Active TSS	Liver	Liver
35	chr10:99344200-99347000	Enhancers	Right Atrium	heart
36	chr10:99344200-99348800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr10:99344400-99344600	Enhancers	Pancreas	Pancrea
38	chr10:99344400-99344800	Flanking Active TSS	Brain Angular Gyrus	brain
39	chr10:99344400-99344800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
40	chr10:99344400-99345000	Flanking Active TSS	Brain Anterior Caudate	brain
41	chr10:99344400-99345000	Enhancers	Brain Cingulate Gyrus	brain
42	chr10:99344400-99345000	Flanking Active TSS	Brain Substantia Nigra	brain
43	chr10:99344600-99344800	Flanking Active TSS	Pancreas	Pancrea
44	chr10:99344600-99345000	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr10:99344600-99345200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr10:99344600-99345400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr10:99344600-99346400	Active TSS	Fetal Kidney	kidney
48	chr10:99344600-99346800	Enhancers	Brain Hippocampus Middle	brain
49	chr10:99344800-99345200	Active TSS	Pancreas	Pancrea
50	chr10:99344800-99346200	Enhancers	Brain Inferior Temporal Lobe	brain

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