Variant report

Variant	nsv550275
Chromosome Location	chr10:27645731-27705855
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	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
7	BHLHE40	chr10:27649567-27649799	K562	blood:	n/a	n/a
8	BHLHE40	chr10:27649517-27649830	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:27646116-27646388	K562	blood:	n/a	chr10:27646219-27646232 chr10:27646221-27646230 chr10:27646222-27646231 chr10:27646221-27646230
10	BRCA1	chr10:27672817-27673127	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr10:27681602-27681815	K562	blood:	n/a	n/a
12	CBX3	chr10:27681617-27681837	K562	blood:	n/a	n/a
13	CCNT2	chr10:27649596-27649806	K562	blood:	n/a	n/a
14	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
15	CEBPB	chr10:27672658-27673316	A549	lung:	n/a	n/a
16	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
17	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
18	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686
19	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
20	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr10:27672803-27673162	MCF-7	breast:	n/a	n/a
22	CEBPB	chr10:27684721-27685002	Hela-S3	cervix:	n/a	chr10:27684883-27684896
23	CEBPB	chr10:27655035-27655235	HepG2	liver:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
24	CEBPB	chr10:27672754-27673203	A549	lung:	n/a	n/a
25	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
27	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
28	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
29	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860
30	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
31	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
32	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
33	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
34	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
36	CEBPB	chr10:27677693-27677915	MCF-7	breast:	n/a	chr10:27677849-27677860
37	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
38	CHD2	chr10:27672857-27673148	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr10:27660335-27660679	K562	blood:	n/a	n/a
40	CTCF	chr10:27649563-27649818	HepG2	liver:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
41	CTCF	chr10:27649541-27649855	A549	lung:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
42	CTCF	chr10:27649640-27649790	AG09319	gingival:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
43	CTCF	chr10:27658860-27659010	HRE	kidney:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
44	CTCF	chr10:27658876-27659061	HUVEC	blood vessel:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962
45	CTCF	chr10:27649600-27649750	HMEC	breast:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
46	CTCF	chr10:27649620-27649770	GM12873	blood:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
47	CTCF	chr10:27649553-27649844	Lung_OC	lung:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
48	CTCF	chr10:27649640-27649790	HMF	breast:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
49	CTCF	chr10:27649640-27649790	HMEC	breast:	n/a	chr10:27649687-27649700 chr10:27649680-27649701 chr10:27649686-27649702 chr10:27649685-27649703
50	CTCF	chr10:27658880-27659030	HPAF	blood vessel:	n/a	chr10:27658945-27658961 chr10:27658946-27658967 chr10:27658944-27658962

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27703329-27703379	HCM	heart:	n/a
2	chr10:27703377-27703427	IMR90	lung:	fetal
3	chr10:27698606-27698656	PANC-1	pancreas:	n/a
4	chr10:27703547-27703597	RPTEC	kidney:	n/a
5	chr10:27703247-27703297	HRE	kidney:	n/a
6	chr10:27698606-27698656	NH-A	brain:	n/a
7	chr10:27698606-27698656	GM12878	blood:	n/a
8	chr10:27703289-27703339	BJ	skin:	n/a
9	chr10:27703247-27703297	HRCEpiC	kidney:	n/a
10	chr10:27703336-27703386	GM12878	blood:	n/a
11	chr10:27703486-27703536	HEEpiC	esophagus:	n/a
12	chr10:27703247-27703297	K562	blood:	n/a
13	chr10:27703289-27703339	NB4	blood:	n/a
14	chr10:27705739-27705789	HUVEC	blood vessel:	n/a
15	chr10:27703336-27703386	GM19239	blood:	n/a
16	chr10:27703486-27703536	HepG2	liver:	n/a
17	chr10:27703377-27703427	GM19239	blood:	n/a
18	chr10:27704592-27704642	SKMC	muscle:	n/a
19	chr10:27705739-27705789	A549	lung:	n/a
20	chr10:27702528-27702578	GM12878	blood:	n/a
21	chr10:27703247-27703297	HCF	heart:	n/a
22	chr10:27702309-27702359	MCF10A-Er-Src	breast:	n/a
23	chr10:27703329-27703379	HCF	heart:	n/a
24	chr10:27702309-27702359	GM12878	blood:	n/a
25	chr10:27703362-27703412	MCF-7	breast:	n/a
26	chr10:27704762-27704812	NT2-D1	testis:	n/a
27	chr10:27704762-27704812	Hela-S3	cervix:	n/a
28	chr10:27703547-27703597	PFSK-1	brain:	n/a
29	chr10:27703336-27703386	CMK	blood:	n/a
30	chr10:27703289-27703339	HCT-116	colon:	n/a
31	chr10:27703486-27703536	NHBE	bronchial:	n/a
32	chr10:27703377-27703427	HepG2	liver:	n/a
33	chr10:27705739-27705789	Caco-2	colon:	n/a
34	chr10:27703486-27703536	SK-N-SH	brain:	n/a
35	chr10:27702774-27702824	AG04450	lung:	fetal
36	chr10:27703247-27703297	NB4	blood:	n/a
37	chr10:27702309-27702359	GM06990	blood:	n/a
38	chr10:27704592-27704642	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:27704762-27704812	PANC-1	pancreas:	n/a
40	chr10:27703329-27703379	SAEC	small airway:	n/a
41	chr10:27698606-27698656	HRCEpiC	kidney:	n/a
42	chr10:27703377-27703427	HL-60	blood:	n/a
43	chr10:27703336-27703386	GM12891	blood:	n/a
44	chr10:27705739-27705789	BE2_C	brain:	n/a
45	chr10:27704762-27704812	HRE	kidney:	n/a
46	chr10:27702309-27702359	HNPCEpiC	eye:	n/a
47	chr10:27702309-27702359	HIPEpiC	eye:	n/a
48	chr10:27704762-27704812	Jurkat	blood:	n/a
49	chr10:27705739-27705789	HEEpiC	esophagus:	n/a
50	chr10:27703289-27703339	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27659175..27661663-chr10:27792060..27794224,2	MCF-7	breast:
2	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
3	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
4	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
5	chr10:27694442..27697083-chr10:27703247..27705702,3	K562	blood:
6	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
7	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
8	chr10:27530526..27532390-chr10:27644695..27646372,2	MCF-7	breast:
9	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
10	chr10:27529763..27532096-chr10:27643724..27645777,2	MCF-7	breast:
11	chr10:27531028..27532588-chr10:27647976..27649755,2	K562	blood:
12	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
13	chr10:27527860..27530153-chr10:27647076..27648802,2	MCF-7	breast:
14	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
15	chr10:27659927..27662822-chr10:27662832..27664720,3	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
ENSG00000262412	chromatin interactions
ENSG00000182077	chromatin interactions
ENSG00000099246	chromatin interactions
ENSG00000107897	chromatin interactions

Extended variants
information (count: 1529 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11015717	chr10:27645731-27645732	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185145654	chr10:27645762-27645763	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs375780584	chr10:27645777-27645778	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs545577549	chr10:27645780-27645781	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs147687035	chr10:27645797-27645798	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs117339611	chr10:27645812-27645813	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369251550	chr10:27645814-27645815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531192657	chr10:27645828-27645829	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140751591	chr10:27645837-27645838	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539651588	chr10:27645855-27645856	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs11015718	chr10:27645897-27645898	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs144636623	chr10:27645914-27645915	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs547226421	chr10:27645943-27645944	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs539216666	chr10:27645945-27645946	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567062942	chr10:27645975-27645976	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs189855053	chr10:27646006-27646007	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs552371492	chr10:27646022-27646023	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576249595	chr10:27646029-27646030	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs114786220	chr10:27646036-27646037	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs12571165	chr10:27646037-27646038	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs117312555	chr10:27646083-27646084	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs574400237	chr10:27646092-27646093	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147869753	chr10:27646093-27646094	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs553597207	chr10:27646112-27646113	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs182130405	chr10:27646157-27646158	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs149020512	chr10:27646177-27646178	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541209113	chr10:27646198-27646199	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs140606024	chr10:27646206-27646207	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556000770	chr10:27646216-27646217	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs367576318	chr10:27646226-27646227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs150472334	chr10:27646235-27646236	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs369612521	chr10:27646236-27646237	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs541464874	chr10:27646260-27646261	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561628473	chr10:27646272-27646273	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188965169	chr10:27646294-27646295	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs193213229	chr10:27646313-27646314	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs145375517	chr10:27646318-27646319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs149190876	chr10:27646366-27646367	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552695259	chr10:27646442-27646443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569277246	chr10:27646443-27646444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145383162	chr10:27646446-27646447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548328678	chr10:27646491-27646492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560876790	chr10:27646539-27646540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530001163	chr10:27646586-27646587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568093770	chr10:27646605-27646606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533880724	chr10:27646624-27646625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543321234	chr10:27646651-27646652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553641026	chr10:27646701-27646702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570373374	chr10:27646714-27646715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539259716	chr10:27646767-27646768	Weak transcription	n/a	n/a	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:150 , 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	chr10:27643400-27645800	Weak transcription	Pancreas	Pancrea
3	chr10:27645200-27649600	Weak transcription	Right Ventricle	heart
4	chr10:27645400-27648800	Weak transcription	Fetal Muscle Leg	muscle
5	chr10:27645600-27646000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:27645800-27646000	Enhancers	Pancreas	Pancrea
7	chr10:27648800-27649400	Enhancers	Fetal Muscle Leg	muscle
8	chr10:27648800-27649600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:27649600-27649800	Enhancers	Fetal Kidney	kidney
10	chr10:27649600-27649800	Enhancers	Right Ventricle	heart
11	chr10:27653000-27653200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:27654200-27656600	Enhancers	GM12878-XiMat	blood
13	chr10:27655200-27655600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr10:27659000-27659200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr10:27659000-27659400	Enhancers	Hela-S3	cervix
16	chr10:27659000-27659600	Enhancers	Fetal Brain Female	brain
17	chr10:27659000-27660000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr10:27659200-27659400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr10:27659400-27661000	Weak transcription	Hela-S3	cervix
20	chr10:27659600-27660800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:27660000-27660400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr10:27660400-27661200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:27660800-27661800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr10:27661000-27661800	Enhancers	NHDF-Ad	bronchial
25	chr10:27661000-27663200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr10:27661200-27661400	Enhancers	Hela-S3	cervix
27	chr10:27661200-27661600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:27661200-27661600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:27661200-27663200	Enhancers	NHEK	skin
30	chr10:27661200-27663400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:27661600-27662600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr10:27661600-27662800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr10:27662600-27662800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr10:27669200-27670600	Enhancers	HepG2	liver
35	chr10:27669400-27671200	Enhancers	Adipose Nuclei	Adipose
36	chr10:27669600-27671000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr10:27669800-27670000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr10:27669800-27670000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
39	chr10:27670600-27672600	Weak transcription	HepG2	liver
40	chr10:27671000-27672600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:27672200-27673600	Enhancers	Hela-S3	cervix
42	chr10:27672600-27672800	Enhancers	Thymus	Thymus
43	chr10:27672600-27672800	Flanking Active TSS	HUVEC	blood vessel
44	chr10:27672600-27673000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr10:27672600-27673200	Enhancers	HepG2	liver
46	chr10:27672600-27673200	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr10:27672600-27673400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr10:27672600-27673400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr10:27672600-27673400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr10:27672600-27673400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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