Variant report

Variant	nsv1042004
Chromosome Location	chr10:27607185-27691799
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	chr10:27629946-27630482	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27672857-27673169	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:27649547-27649808	K562	blood:	n/a	n/a
4	ATF1	chr10:27649531-27649804	K562	blood:	n/a	n/a
5	BATF	chr10:27633841-27634192	GM12878	blood:	n/a	n/a
6	BATF	chr10:27649564-27649764	GM12878	blood:	n/a	n/a
7	BATF	chr10:27643692-27643988	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:27643658-27644039	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:27643724-27643987	GM12878	blood:	n/a	n/a
10	BCL3	chr10:27672617-27673252	A549	lung:	n/a	n/a
11	BCLAF1	chr10:27643572-27643923	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:27649517-27649830	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:27646116-27646388	K562	blood:	n/a	chr10:27646219-27646232 chr10:27646221-27646230 chr10:27646222-27646231 chr10:27646221-27646230
14	BHLHE40	chr10:27649567-27649799	K562	blood:	n/a	n/a
15	BHLHE40	chr10:27633890-27634818	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:27672558-27673044	HepG2	liver:	n/a	n/a
17	BRCA1	chr10:27672817-27673127	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr10:27681617-27681837	K562	blood:	n/a	n/a
19	CBX3	chr10:27681602-27681815	K562	blood:	n/a	n/a
20	CCNT2	chr10:27649596-27649806	K562	blood:	n/a	n/a
21	CCNT2	chr10:27639061-27639239	K562	blood:	n/a	n/a
22	CEBPB	chr10:27608935-27609364	ECC-1	luminal epithelium:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
23	CEBPB	chr10:27672755-27673183	A549	lung:	n/a	n/a
24	CEBPB	chr10:27634350-27634708	IMR90	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
25	CEBPB	chr10:27649533-27649818	A549	lung:	n/a	chr10:27649675-27649686
26	CEBPB	chr10:27649513-27649869	IMR90	lung:	n/a	chr10:27649675-27649686
27	CEBPB	chr10:27677739-27678016	HepG2	liver:	n/a	chr10:27677849-27677860
28	CEBPB	chr10:27609103-27609337	HepG2	liver:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
29	CEBPB	chr10:27655050-27655300	K562	blood:	n/a	chr10:27655162-27655173 chr10:27655161-27655172 chr10:27655161-27655174
30	CEBPB	chr10:27680208-27680388	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr10:27608939-27609321	ECC-1	luminal epithelium:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
32	CEBPB	chr10:27662820-27663067	HepG2	liver:	n/a	chr10:27662910-27662921
33	CEBPB	chr10:27609089-27609311	A549	lung:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
34	CEBPB	chr10:27608518-27609427	Hela-S3	cervix:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
35	CEBPB	chr10:27677736-27678037	IMR90	lung:	n/a	chr10:27677849-27677860
36	CEBPB	chr10:27677675-27678050	Hela-S3	cervix:	n/a	chr10:27677849-27677860
37	CEBPB	chr10:27653947-27654086	K562	blood:	n/a	n/a
38	CEBPB	chr10:27672818-27673157	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:27649575-27649846	HepG2	liver:	n/a	chr10:27649675-27649686
40	CEBPB	chr10:27634311-27634682	A549	lung:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
41	CEBPB	chr10:27634266-27634780	HepG2	liver:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
42	CEBPB	chr10:27634283-27634772	Hela-S3	cervix:	n/a	chr10:27634411-27634420 chr10:27634411-27634422
43	CEBPB	chr10:27608871-27609380	MCF-7	breast:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
44	CEBPB	chr10:27659541-27659772	HepG2	liver:	n/a	chr10:27659628-27659639 chr10:27659627-27659638 chr10:27659627-27659640
45	CEBPB	chr10:27609087-27609339	K562	blood:	n/a	chr10:27609272-27609283 chr10:27609201-27609212 chr10:27609124-27609137
46	CEBPB	chr10:27649503-27649883	K562	blood:	n/a	chr10:27649675-27649686
47	CEBPB	chr10:27669848-27670363	HepG2	liver:	n/a	chr10:27669887-27669899
48	CEBPB	chr10:27679600-27679898	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr10:27662837-27663055	K562	blood:	n/a	chr10:27662910-27662921
50	CEBPB	chr10:27672728-27673265	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27607960-27608010	NH-A	brain:	n/a
2	chr10:27609163-27609213	Hepatocyte	liver:	n/a
3	chr10:27607960-27608010	NH-A	brain:	n/a
4	chr10:27609163-27609213	Hepatocyte	liver:	n/a
5	chr10:27608703-27608753	NHBE	bronchial:	n/a
6	chr10:27634719-27634769	BE2_C	brain:	n/a
7	chr10:27609163-27609213	GM12892	blood:	n/a
8	chr10:27609163-27609213	ovcar-3	ovarian:	n/a
9	chr10:27609333-27609383	BJ	skin:	n/a
10	chr10:27609286-27609336	Hepatocyte	liver:	n/a
11	chr10:27609163-27609213	ECC-1	luminal epithelium:	n/a
12	chr10:27639156-27639206	AoSMC	blood vessel:	n/a
13	chr10:27639156-27639206	HRCEpiC	kidney:	n/a
14	chr10:27608703-27608753	HCF	heart:	n/a
15	chr10:27608703-27608753	T-47D	breast:	n/a
16	chr10:27633745-27633795	BE2_C	brain:	n/a
17	chr10:27609310-27609360	H1-hESC	embryonic stem cell:	embryo
18	chr10:27608719-27608769	HNPCEpiC	eye:	n/a
19	chr10:27634719-27634769	Caco-2	colon:	n/a
20	chr10:27634719-27634769	GM12878	blood:	n/a
21	chr10:27608703-27608753	GM19239	blood:	n/a
22	chr10:27633745-27633795	NHBE	bronchial:	n/a
23	chr10:27633745-27633795	HCT-116	colon:	n/a
24	chr10:27639136-27639186	AG09319	gingival:	n/a
25	chr10:27609163-27609213	SK-N-MC	brain:	n/a
26	chr10:27609163-27609213	Jurkat	blood:	n/a
27	chr10:27609286-27609336	H1-hESC	embryonic stem cell:	embryo
28	chr10:27609163-27609213	HCF	heart:	n/a
29	chr10:27633745-27633795	HepG2	liver:	n/a
30	chr10:27608719-27608769	HRPEpiC	eye:	n/a
31	chr10:27634719-27634769	BJ	skin:	n/a
32	chr10:27609163-27609213	AG09319	gingival:	n/a
33	chr10:27633745-27633795	GM06990	blood:	n/a
34	chr10:27607960-27608010	SK-N-SH	brain:	n/a
35	chr10:27639136-27639186	CMK	blood:	n/a
36	chr10:27609286-27609336	HCPEpiC	choroid plexus:	n/a
37	chr10:27639156-27639206	BE2_C	brain:	n/a
38	chr10:27608719-27608769	NHBE	bronchial:	n/a
39	chr10:27609286-27609336	BE2_C	brain:	n/a
40	chr10:27639156-27639206	Jurkat	blood:	n/a
41	chr10:27609163-27609213	NHDF-neo	bronchial:	n/a
42	chr10:27633745-27633795	K562	blood:	n/a
43	chr10:27607960-27608010	HRPEpiC	eye:	n/a
44	chr10:27639156-27639206	MCF10A-Er-Src	breast:	n/a
45	chr10:27639156-27639206	HPAEpiC	pulmonary alveolar:	n/a
46	chr10:27607960-27608010	RPTEC	kidney:	n/a
47	chr10:27608703-27608753	HL-60	blood:	n/a
48	chr10:27633745-27633795	SK-N-SH	brain:	n/a
49	chr10:27639156-27639206	NHDF-neo	bronchial:	n/a
50	chr10:27639136-27639186	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
2	chr10:27529763..27532096-chr10:27643724..27645777,2	MCF-7	breast:
3	chr10:27530526..27532390-chr10:27644695..27646372,2	MCF-7	breast:
4	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
5	chr10:27684512..27686768-chr10:27700849..27702736,2	K562	blood:
6	chr10:27441984..27445191-chr10:27642152..27645235,3	MCF-7	breast:
7	chr10:27609103..27610966-chr10:27614340..27616128,2	K562	blood:
8	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
9	chr10:27669052..27671269-chr10:27683257..27685068,2	K562	blood:
10	chr10:26984968..26988044-chr10:27607336..27609040,6	MCF-7	breast:
11	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
12	chr10:27659175..27661663-chr10:27792060..27794224,2	MCF-7	breast:
13	chr10:26985474..26987624-chr10:27607358..27610341,4	MCF-7	breast:
14	chr10:27531028..27532588-chr10:27647976..27649755,2	K562	blood:
15	chr10:27640371..27642415-chr10:27644846..27646556,2	K562	blood:
16	chr10:27607489..27609150-chr10:27638206..27640628,2	MCF-7	breast:
17	chr10:27609103..27610966-chr10:27614340..27616128,2	K562	blood:
18	chr10:27681780..27685010-chr10:27685683..27688279,3	K562	blood:
19	chr10:27527860..27530153-chr10:27647076..27648802,2	MCF-7	breast:
20	chr10:27659927..27662822-chr10:27662832..27664720,3	K562	blood:
21	chr10:26985698..26986799-chr10:27608358..27609419,4	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTCHD3-2	chr10:27636298-27636725	l_277_chr10:27627368-27636725_testes
2	lnc-PTCHD3-2	chr10:27634694-27635239	l_277_chr10:27627368-27636725_testes
3	lnc-MASTL-2	chr10:27632365-27633580	ENSG00000260151.1
4	lnc-MASTL-2	chr10:27633668-27633846	ENSG00000260151.1
5	lnc-PTCHD3-2	chr10:27627369-27627692	l_277_chr10:27627368-27636725_testes
6	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
FAM210CP	TF binding region
ENSG00000260151	TF binding region
TRIAP1P1	TF binding region
RNU6-452P	TF binding region
ENSG00000215409	TF binding region
FAM210CP	CpG island
ENSG00000260151	CpG island
TRIAP1P1	CpG island
RNU6-452P	CpG island
ENSG00000215409	CpG island
ENSG00000136758	chromatin interactions
ENSG00000107897	chromatin interactions
ENSG00000148459	chromatin interactions
ENSG00000099246	chromatin interactions
ENSG00000213770	chromatin interactions
ENSG00000262412	chromatin interactions
ENSG00000120539	chromatin interactions

Extended variants
information (count: 2467 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:2467 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17476860	chr10:27607185-27607186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564956068	chr10:27607205-27607206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530686905	chr10:27607221-27607222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs17476874	chr10:27607226-27607227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs188457129	chr10:27607230-27607231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192687166	chr10:27607250-27607251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546599234	chr10:27607266-27607267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116666280	chr10:27607271-27607272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532116644	chr10:27607303-27607304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544658249	chr10:27607344-27607345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs150022756	chr10:27607348-27607349	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571750779	chr10:27607363-27607364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs76221128	chr10:27607365-27607366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567088837	chr10:27607433-27607434	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184522211	chr10:27607469-27607470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529473969	chr10:27607493-27607494	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570729278	chr10:27607524-27607525	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs557070829	chr10:27607571-27607572	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376111863	chr10:27607574-27607575	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs3864846	chr10:27607622-27607623	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs188974466	chr10:27607691-27607692	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs377729610	chr10:27607696-27607697	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536696898	chr10:27607709-27607710	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544980934	chr10:27607815-27607816	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs565150006	chr10:27607865-27607866	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs575389261	chr10:27607867-27607868	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370219710	chr10:27607874-27607875	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs367762762	chr10:27607875-27607876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs237600	chr10:27607884-27607885	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs71386995	chr10:27607885-27607886	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs237601	chr10:27607905-27607906	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs546683061	chr10:27607915-27607916	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112462937	chr10:27607961-27607962	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113176734	chr10:27607977-27607978	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs375619746	chr10:27607979-27607980	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552205271	chr10:27608002-27608003	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs237602	chr10:27608013-27608014	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs369619329	chr10:27608043-27608044	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs559432052	chr10:27608048-27608049	Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567453696	chr10:27608203-27608204	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536370990	chr10:27608207-27608208	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs539524308	chr10:27608240-27608241	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs184567145	chr10:27608273-27608274	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs552622404	chr10:27608274-27608275	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs77893908	chr10:27608294-27608295	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139003012	chr10:27608332-27608333	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs189259729	chr10:27608357-27608358	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs181626153	chr10:27608404-27608405	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs141859147	chr10:27608418-27608419	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs561082703	chr10:27608425-27608426	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS	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:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27605000-27608000	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr10:27608000-27608200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr10:27608000-27608200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
4	chr10:27608000-27608400	Enhancers	GM12878-XiMat	blood
5	chr10:27608000-27608400	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr10:27608000-27608600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr10:27608000-27608600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
8	chr10:27608200-27608400	Enhancers	Primary B cells from cord blood	blood
9	chr10:27608200-27608400	Enhancers	Primary hematopoietic stem cells	blood
10	chr10:27608200-27608400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr10:27608200-27608400	Bivalent Enhancer	Brain Hippocampus Middle	brain
12	chr10:27608200-27608600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr10:27608200-27608600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr10:27608200-27608600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr10:27608200-27608600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:27608200-27608600	Enhancers	Fetal Intestine Large	intestine
17	chr10:27608200-27608600	Enhancers	Left Ventricle	heart
18	chr10:27608200-27608600	Enhancers	Right Ventricle	heart
19	chr10:27608200-27608800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr10:27608200-27609200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:27608200-27609200	Enhancers	Primary B cells from peripheral blood	blood
22	chr10:27608200-27609200	Enhancers	Fetal Brain Male	brain
23	chr10:27608200-27609400	Enhancers	Esophagus	oesophagus
24	chr10:27608200-27609800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr10:27608400-27608600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr10:27608400-27608600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr10:27608400-27608600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr10:27608400-27608600	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr10:27608400-27608600	Enhancers	Fetal Muscle Trunk	muscle
30	chr10:27608400-27608600	Enhancers	Hela-S3	cervix
31	chr10:27608400-27608600	Enhancers	HMEC	breast
32	chr10:27608400-27608800	Enhancers	Stomach Mucosa	stomach
33	chr10:27608400-27609000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr10:27608400-27609000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr10:27608400-27609000	Flanking Active TSS	Primary B cells from cord blood	blood
36	chr10:27608400-27609000	Active TSS	Fetal Kidney	kidney
37	chr10:27608400-27609000	Flanking Active TSS	GM12878-XiMat	blood
38	chr10:27608400-27609200	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr10:27608400-27609200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
40	chr10:27608400-27609200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
41	chr10:27608400-27609200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr10:27608400-27609200	Flanking Active TSS	Primary hematopoietic stem cells	blood
43	chr10:27608400-27609200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:27608400-27609200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
45	chr10:27608400-27609200	Active TSS	A549	lung
46	chr10:27608400-27609200	Flanking Active TSS	HUVEC	blood vessel
47	chr10:27608400-27609200	Active TSS	NH-A	brain
48	chr10:27608400-27609400	Enhancers	Fetal Heart	heart
49	chr10:27608400-27609400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr10:27608600-27608800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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