Variant report

Variant	nsv466847
Chromosome Location	chr10:27648069-27705855
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	ARID3A	chr10:27649547-27649808	K562	blood:	n/a	n/a
2	ARID3A	chr10:27672857-27673169	HepG2	liver:	n/a	n/a
3	ATF1	chr10:27649531-27649804	K562	blood:	n/a	n/a
4	BATF	chr10:27649564-27649764	GM12878	blood:	n/a	n/a
5	BCL3	chr10:27672617-27673252	A549	lung:	n/a	n/a
6	BHLHE40	chr10:27649567-27649799	K562	blood:	n/a	n/a
7	BHLHE40	chr10:27649517-27649830	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
9	BRCA1	chr10:27672817-27673127	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr10:27681602-27681815	K562	blood:	n/a	n/a
11	CBX3	chr10:27681617-27681837	K562	blood:	n/a	n/a
12	CCNT2	chr10:27649596-27649806	K562	blood:	n/a	n/a
13	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
14	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
15	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
16	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
17	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
18	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
20	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
21	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860
22	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
23	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
24	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
25	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860
26	CEBPB	chr10:27655035-27655235	HepG2	liver:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
27	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
28	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
29	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
30	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
31	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
32	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
33	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686
36	CEBPB	chr10:27672803-27673162	MCF-7	breast:	n/a	n/a
37	CHD2	chr10:27672857-27673148	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr10:27660335-27660679	K562	blood:	n/a	n/a
39	CTCF	chr10:27649600-27649750	GM12867	blood:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
40	CTCF	chr10:27649580-27649730	HEK293	kidney:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
41	CTCF	chr10:27658900-27659050	AoAF	blood vessel:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
42	CTCF	chr10:27658620-27658770	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr10:27658900-27659050	HCM	heart:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
44	CTCF	chr10:27649620-27649770	HEEpiC	esophagus:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
45	CTCF	chr10:27658900-27659050	A549	lung:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
46	CTCF	chr10:27649556-27649768	T-47D	breast:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
47	CTCF	chr10:27649620-27649770	HVMF	connective:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
48	CTCF	chr10:27704835-27704889	GM13976	blood:	n/a	n/a
49	CTCF	chr10:27702355-27702613	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr10:27658721-27659172	MCF-7	breast:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27703329-27703379	Hepatocyte	liver:	n/a
2	chr10:27703329-27703379	Hepatocyte	liver:	n/a
3	chr10:27703336-27703386	MCF10A-Er-Src	breast:	n/a
4	chr10:27703547-27703597	NH-A	brain:	n/a
5	chr10:27702309-27702359	NHBE	bronchial:	n/a
6	chr10:27702528-27702578	ECC-1	luminal epithelium:	n/a
7	chr10:27703377-27703427	T-47D	breast:	n/a
8	chr10:27703547-27703597	NB4	blood:	n/a
9	chr10:27703362-27703412	HRCEpiC	kidney:	n/a
10	chr10:27705739-27705789	AG10803	skin:	n/a
11	chr10:27703486-27703536	GM12878	blood:	n/a
12	chr10:27702528-27702578	SK-N-MC	brain:	n/a
13	chr10:27703486-27703536	BJ	skin:	n/a
14	chr10:27703289-27703339	AG04450	lung:	fetal
15	chr10:27705739-27705789	AG04449	skin:	fetal
16	chr10:27698606-27698656	SKMC	muscle:	n/a
17	chr10:27703377-27703427	SAEC	small airway:	n/a
18	chr10:27703329-27703379	HCPEpiC	choroid plexus:	n/a
19	chr10:27703336-27703386	HIPEpiC	eye:	n/a
20	chr10:27703377-27703427	Caco-2	colon:	n/a
21	chr10:27703336-27703386	CMK	blood:	n/a
22	chr10:27703289-27703339	NHBE	bronchial:	n/a
23	chr10:27704592-27704642	LNCaP	prostate:	n/a
24	chr10:27702528-27702578	Hepatocyte	liver:	n/a
25	chr10:27703247-27703297	GM12892	blood:	n/a
26	chr10:27703486-27703536	SK-N-MC	brain:	n/a
27	chr10:27705739-27705789	MCF10A-Er-Src	breast:	n/a
28	chr10:27704592-27704642	GM19239	blood:	n/a
29	chr10:27703329-27703379	HL-60	blood:	n/a
30	chr10:27703329-27703379	SKMC	muscle:	n/a
31	chr10:27704762-27704812	HMEC	breast:	n/a
32	chr10:27703486-27703536	Caco-2	colon:	n/a
33	chr10:27703362-27703412	PANC-1	pancreas:	n/a
34	chr10:27703247-27703297	GM19239	blood:	n/a
35	chr10:27703247-27703297	Hepatocyte	liver:	n/a
36	chr10:27702309-27702359	PANC-1	pancreas:	n/a
37	chr10:27703362-27703412	Caco-2	colon:	n/a
38	chr10:27702774-27702824	Caco-2	colon:	n/a
39	chr10:27702309-27702359	NT2-D1	testis:	n/a
40	chr10:27702528-27702578	Jurkat	blood:	n/a
41	chr10:27705739-27705789	T-47D	breast:	n/a
42	chr10:27703486-27703536	ProgFib	skin:	n/a
43	chr10:27703289-27703339	AG09319	gingival:	n/a
44	chr10:27704762-27704812	HCM	heart:	n/a
45	chr10:27698606-27698656	NHBE	bronchial:	n/a
46	chr10:27705739-27705789	NHBE	bronchial:	n/a
47	chr10:27703289-27703339	GM12891	blood:	n/a
48	chr10:27703289-27703339	HUVEC	blood vessel:	n/a
49	chr10:27703377-27703427	HepG2	liver:	n/a
50	chr10:27703486-27703536	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27531028..27532588-chr10:27647976..27649755,2	K562	blood:
2	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
3	chr10:27659175..27661663-chr10:27792060..27794224,2	MCF-7	breast:
4	chr10:27694442..27697083-chr10:27703247..27705702,3	K562	blood:
5	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
6	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
7	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
8	chr10:27527860..27530153-chr10:27647076..27648802,2	MCF-7	breast:
9	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
10	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
11	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
12	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTCHD3-1	chr10:27667067-27667291	NONHSAT011904

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTCHD3	hsa-miR-128-3p	chr10:27687123-27687143

Variant related genes	Relation type
TRIAP1P1	TF binding region
PTCHD3	TF binding region
TRIAP1P1	CpG island
PTCHD3	CpG island
ENSG00000099246	chromatin interactions
ENSG00000182077	chromatin interactions
ENSG00000107897	chromatin interactions
ENSG00000262412	chromatin interactions

Extended variants
information (count: 1429 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10829248	chr10:27648069-27648070	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190436078	chr10:27648070-27648071	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs550044039	chr10:27648087-27648088	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144605870	chr10:27648096-27648097	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs545968529	chr10:27648098-27648099	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549174556	chr10:27648099-27648100	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs80304539	chr10:27648166-27648167	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12242166	chr10:27648173-27648174	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs559370713	chr10:27648217-27648218	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs112239722	chr10:27648285-27648286	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs577563979	chr10:27648310-27648311	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs148182431	chr10:27648352-27648353	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs547632097	chr10:27648363-27648364	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs372542606	chr10:27648384-27648385	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367924489	chr10:27648399-27648400	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540721108	chr10:27648433-27648434	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs237559	chr10:27648452-27648453	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574510599	chr10:27648470-27648471	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs182215564	chr10:27648492-27648493	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs561911734	chr10:27648494-27648495	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs12414335	chr10:27648568-27648569	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs563220894	chr10:27648582-27648583	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs541103759	chr10:27648592-27648593	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs564368857	chr10:27648607-27648608	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532415686	chr10:27648615-27648616	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs533349515	chr10:27648616-27648617	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549864329	chr10:27648619-27648620	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs558010871	chr10:27648624-27648625	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs59555803	chr10:27648648-27648649	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs74555193	chr10:27648661-27648662	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs150796555	chr10:27648683-27648684	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549235905	chr10:27648691-27648692	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs565860520	chr10:27648715-27648716	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528127773	chr10:27648718-27648719	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541175705	chr10:27648750-27648751	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534757586	chr10:27648806-27648807	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs551448164	chr10:27648834-27648835	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75993134	chr10:27648856-27648857	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs559283718	chr10:27648891-27648892	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs537053791	chr10:27648892-27648893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs556655320	chr10:27648903-27648904	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570343477	chr10:27648904-27648905	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs535731664	chr10:27648917-27648918	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547741394	chr10:27648924-27648925	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs138048113	chr10:27648928-27648929	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs11015719	chr10:27648950-27648951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs74579373	chr10:27648959-27648960	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548365399	chr10:27648965-27648966	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs577997628	chr10:27648988-27648989	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs568655797	chr10:27649012-27649013	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:46)

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
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
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27633800-27655400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:27645200-27649600	Weak transcription	Right Ventricle	heart
3	chr10:27645400-27648800	Weak transcription	Fetal Muscle Leg	muscle
4	chr10:27648800-27649400	Enhancers	Fetal Muscle Leg	muscle
5	chr10:27648800-27649600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr10:27649600-27649800	Enhancers	Fetal Kidney	kidney
7	chr10:27649600-27649800	Enhancers	Right Ventricle	heart
8	chr10:27653000-27653200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:27654200-27656600	Enhancers	GM12878-XiMat	blood
10	chr10:27655200-27655600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr10:27659000-27659200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr10:27659000-27659400	Enhancers	Hela-S3	cervix
13	chr10:27659000-27659600	Enhancers	Fetal Brain Female	brain
14	chr10:27659000-27660000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:27659200-27659400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr10:27659400-27661000	Weak transcription	Hela-S3	cervix
17	chr10:27659600-27660800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr10:27660000-27660400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:27660400-27661200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr10:27660800-27661800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:27661000-27661800	Enhancers	NHDF-Ad	bronchial
22	chr10:27661000-27663200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr10:27661200-27661400	Enhancers	Hela-S3	cervix
24	chr10:27661200-27661600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr10:27661200-27661600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr10:27661200-27663200	Enhancers	NHEK	skin
27	chr10:27661200-27663400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr10:27661600-27662600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:27661600-27662800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr10:27662600-27662800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr10:27669200-27670600	Enhancers	HepG2	liver
32	chr10:27669400-27671200	Enhancers	Adipose Nuclei	Adipose
33	chr10:27669600-27671000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:27669800-27670000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr10:27669800-27670000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
36	chr10:27670600-27672600	Weak transcription	HepG2	liver
37	chr10:27671000-27672600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr10:27672200-27673600	Enhancers	Hela-S3	cervix
39	chr10:27672600-27672800	Enhancers	Thymus	Thymus
40	chr10:27672600-27672800	Flanking Active TSS	HUVEC	blood vessel
41	chr10:27672600-27673000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr10:27672600-27673200	Enhancers	HepG2	liver
43	chr10:27672600-27673200	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr10:27672600-27673400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr10:27672600-27673400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr10:27672600-27673400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr10:27672600-27673400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:27672600-27673400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr10:27672600-27673400	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr10:27672600-27673400	Enhancers	Lung	lung

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