Variant report

Variant	nsv552021
Chromosome Location	chr10:97053404-97071334
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:648)
CpG islands
(count:489)
Chromatin interactive
region (count:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:97068524-97068760	K562	blood:	n/a	n/a
2	ARID3A	chr10:97057146-97057530	K562	blood:	n/a	n/a
3	ARID3A	chr10:97067726-97068262	K562	blood:	n/a	n/a
4	ATF1	chr10:97057155-97057590	K562	blood:	n/a	n/a
5	ATF1	chr10:97068491-97068818	K562	blood:	n/a	n/a
6	ATF2	chr10:97057118-97057632	GM12878	blood:	n/a	n/a
7	ATF2	chr10:97069736-97070274	GM12878	blood:	n/a	n/a
8	ATF2	chr10:97054583-97055465	GM12878	blood:	n/a	n/a
9	ATF2	chr10:97054517-97055806	GM12878	blood:	n/a	n/a
10	ATF3	chr10:97068463-97068901	K562	blood:	n/a	n/a
11	ATF3	chr10:97068438-97068927	A549	lung:	n/a	n/a
12	BACH1	chr10:97064080-97064082	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:97055022-97055539	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr10:97068563-97068860	GM12878	blood:	n/a	n/a
15	BCL11A	chr10:97054859-97055306	GM12878	blood:	n/a	n/a
16	BCL3	chr10:97068316-97069037	A549	lung:	n/a	n/a
17	BCL3	chr10:97068090-97069004	A549	lung:	n/a	n/a
18	BCL3	chr10:97054696-97055391	GM12878	blood:	n/a	n/a
19	BCLAF1	chr10:97054602-97055731	GM12878	blood:	n/a	n/a
20	BCLAF1	chr10:97052711-97053466	GM12878	blood:	n/a	n/a
21	BCLAF1	chr10:97054286-97055575	GM12878	blood:	n/a	n/a
22	BCLAF1	chr10:97052832-97053538	GM12878	blood:	n/a	chr10:97053528-97053537
23	BHLHE40	chr10:97054877-97055398	K562	blood:	n/a	n/a
24	BHLHE40	chr10:97052865-97053577	GM12878	blood:	n/a	n/a
25	BHLHE40	chr10:97054746-97055725	GM12878	blood:	n/a	n/a
26	BHLHE40	chr10:97057108-97057611	K562	blood:	n/a	n/a
27	BHLHE40	chr10:97068266-97068735	K562	blood:	n/a	n/a
28	BRCA1	chr10:97068559-97068832	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr10:97063255-97063695	K562	blood:	n/a	n/a
30	CBX3	chr10:97054897-97055314	K562	blood:	n/a	n/a
31	CBX3	chr10:97057091-97057604	K562	blood:	n/a	n/a
32	CBX3	chr10:97068184-97069037	HCT-116	colon:	n/a	n/a
33	CCNT2	chr10:97057082-97057531	K562	blood:	n/a	n/a
34	CCNT2	chr10:97068471-97068730	K562	blood:	n/a	n/a
35	CCNT2	chr10:97063237-97063707	K562	blood:	n/a	n/a
36	CCNT2	chr10:97054813-97055466	K562	blood:	n/a	n/a
37	CEBPB	chr10:97064867-97065028	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:97067459-97067762	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr10:97068104-97068835	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:97064889-97064915	K562	blood:	n/a	n/a
41	CEBPB	chr10:97054948-97055373	GM12878	blood:	n/a	n/a
42	CEBPB	chr10:97068536-97068876	A549	lung:	n/a	n/a
43	CEBPB	chr10:97054303-97055902	GM12878	blood:	n/a	n/a
44	CEBPB	chr10:97068478-97069032	A549	lung:	n/a	n/a
45	CEBPB	chr10:97068422-97068866	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr10:97064786-97065107	A549	lung:	n/a	n/a
47	CEBPB	chr10:97052854-97053611	GM12878	blood:	n/a	n/a
48	CEBPB	chr10:97068263-97068968	ECC-1	luminal epithelium:	n/a	n/a
49	CHD1	chr10:97054414-97055693	GM12878	blood:	n/a	n/a
50	CHD2	chr10:97054660-97055621	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:97056219-97056269	NB4	blood:	n/a
2	chr10:97056219-97056269	NB4	blood:	n/a
3	chr10:97056219-97056269	IMR90	lung:	fetal
4	chr10:97056219-97056269	HMEC	breast:	n/a
5	chr10:97054967-97055017	HRE	kidney:	n/a
6	chr10:97064500-97064550	BJ	skin:	n/a
7	chr10:97055282-97055332	H1-hESC	embryonic stem cell:	embryo
8	chr10:97068696-97068746	LNCaP	prostate:	n/a
9	chr10:97054967-97055017	HNPCEpiC	eye:	n/a
10	chr10:97056219-97056269	SAEC	small airway:	n/a
11	chr10:97056219-97056269	AG04450	lung:	fetal
12	chr10:97056219-97056269	Hela-S3	cervix:	n/a
13	chr10:97056219-97056269	NHBE	bronchial:	n/a
14	chr10:97055150-97055200	Hepatocyte	liver:	n/a
15	chr10:97056219-97056269	GM06990	blood:	n/a
16	chr10:97058531-97058581	HPAEpiC	pulmonary alveolar:	n/a
17	chr10:97058531-97058581	GM12891	blood:	n/a
18	chr10:97055439-97055489	HRE	kidney:	n/a
19	chr10:97056219-97056269	AG10803	skin:	n/a
20	chr10:97055439-97055489	ProgFib	skin:	n/a
21	chr10:97055439-97055489	A549	lung:	n/a
22	chr10:97054967-97055017	SK-N-MC	brain:	n/a
23	chr10:97058531-97058581	Hepatocyte	liver:	n/a
24	chr10:97054967-97055017	AG09309	skin:	n/a
25	chr10:97068696-97068746	NHBE	bronchial:	n/a
26	chr10:97055439-97055489	MCF-7	breast:	n/a
27	chr10:97055150-97055200	NT2-D1	testis:	n/a
28	chr10:97054967-97055017	Caco-2	colon:	n/a
29	chr10:97055439-97055489	HCPEpiC	choroid plexus:	n/a
30	chr10:97055439-97055489	HRPEpiC	eye:	n/a
31	chr10:97054967-97055017	PrEC	prostate:	n/a
32	chr10:97054967-97055017	SK-N-SH	brain:	n/a
33	chr10:97054967-97055017	ovcar-3	ovarian:	n/a
34	chr10:97055150-97055200	IMR90	lung:	fetal
35	chr10:97055150-97055200	HRPEpiC	eye:	n/a
36	chr10:97055439-97055489	AG09319	gingival:	n/a
37	chr10:97054967-97055017	HMEC	breast:	n/a
38	chr10:97055150-97055200	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:97054967-97055017	MCF-7	breast:	n/a
40	chr10:97055150-97055200	Jurkat	blood:	n/a
41	chr10:97068696-97068746	AG10803	skin:	n/a
42	chr10:97055282-97055332	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:97054967-97055017	GM12892	blood:	n/a
44	chr10:97056219-97056269	AoSMC	blood vessel:	n/a
45	chr10:97055150-97055200	SAEC	small airway:	n/a
46	chr10:97055282-97055332	ovcar-3	ovarian:	n/a
47	chr10:97055439-97055489	SKMC	muscle:	n/a
48	chr10:97068696-97068746	SK-N-MC	brain:	n/a
49	chr10:97055150-97055200	HAEpiC	amniotic membrane:	n/a
50	chr10:97068696-97068746	Jurkat	blood:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:97063353..97065156-chr10:97068953..97071321,2	MCF-7	breast:
2	chr10:97021192..97022891-chr10:97052326..97054601,2	K562	blood:
3	chr10:97071047..97076253-chr10:97076532..97079541,6	K562	blood:
4	chr10:97055273..97057323-chr10:97068658..97070274,2	K562	blood:
5	chr10:97046965..97049082-chr10:97066729..97068931,2	K562	blood:
6	chr10:97049651..97052657-chr10:97053278..97056357,3	MCF-7	breast:
7	chr10:97051927..97054727-chr10:97113861..97115578,2	K562	blood:
8	chr10:97049641..97052402-chr10:97061641..97064043,3	K562	blood:
9	chr10:97055273..97057323-chr10:97068658..97070274,2	K562	blood:
10	chr10:97058437..97060123-chr10:97062143..97063800,2	K562	blood:
11	chr10:97057079..97058801-chr10:97061706..97063249,2	K562	blood:
12	chr10:97054860..97057387-chr10:97070796..97073546,2	K562	blood:
13	chr10:97047645..97051954-chr10:97061072..97065962,7	MCF-7	breast:
14	chr10:97065717..97068641-chr10:97084315..97087112,2	K562	blood:
15	chr10:97063353..97065156-chr10:97068953..97071321,2	MCF-7	breast:
16	chr10:97038835..97040878-chr10:97054289..97056491,2	K562	blood:
17	chr10:97063446..97065363-chr10:97067014..97069636,2	K562	blood:
18	chr10:97055747..97058721-chr10:97058965..97061918,2	MCF-7	breast:
19	chr10:97054091..97056343-chr10:97062077..97064550,2	K562	blood:
20	chr10:97057079..97058801-chr10:97061706..97063249,2	K562	blood:
21	chr10:97054091..97056343-chr10:97062077..97064550,2	K562	blood:
22	chr10:97048197..97050132-chr10:97070905..97072692,2	MCF-7	breast:
23	chr10:97067527..97069717-chr10:97074996..97076961,2	MCF-7	breast:
24	chr10:97049242..97050860-chr10:97068797..97070801,3	MCF-7	breast:
25	chr10:97047325..97053107-chr10:97053232..97056483,6	MCF-7	breast:
26	chr10:97055600..97058139-chr10:97065773..97067717,2	K562	blood:
27	chr10:97067141..97070104-chr10:97084315..97087296,2	K562	blood:
28	chr10:97053251..97055097-chr10:97056727..97058389,2	K562	blood:
29	chr10:97067391..97069707-chr10:97088772..97090844,2	MCF-7	breast:
30	chr10:97036138..97037977-chr10:97055615..97058500,2	K562	blood:
31	chr10:97063446..97065566-chr10:97068136..97069871,2	K562	blood:
32	chr10:97055747..97058721-chr10:97058965..97061918,2	MCF-7	breast:
33	chr10:97055600..97058139-chr10:97065773..97067717,2	K562	blood:
34	chr10:97064103..97065891-chr2:12251209..12253913,2	MCF-7	breast:
35	chr10:97049641..97053849-chr10:97062543..97067097,4	K562	blood:
36	chr10:97058437..97060123-chr10:97062143..97063800,2	K562	blood:
37	chr10:97063446..97065363-chr10:97067014..97069636,2	K562	blood:
38	chr10:97053251..97055097-chr10:97056727..97058389,2	K562	blood:
39	chr10:97054860..97057387-chr10:97070796..97073546,2	K562	blood:
40	chr10:97065210..97065763-chr7:126649354..126650093,2	MCF-7	breast:
41	chr10:96975681..96977490-chr10:97052151..97054934,2	K562	blood:
42	chr10:97063446..97065566-chr10:97068136..97069871,2	K562	blood:

No data

Variant related genes	Relation type
PDLIM1	TF binding region
PDLIM1	CpG island
ENSG00000107438	chromatin interactions

Extended variants
information (count: 695 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11599166	chr10:97053404-97053405	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546761036	chr10:97053456-97053457	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs117992313	chr10:97053489-97053490	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs535311876	chr10:97053719-97053720	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548732565	chr10:97053740-97053741	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs568819274	chr10:97053756-97053757	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs76591659	chr10:97053769-97053770	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557379409	chr10:97053770-97053771	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs1328599	chr10:97053775-97053776	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs190167470	chr10:97053794-97053795	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548738940	chr10:97053801-97053802	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553567667	chr10:97053817-97053818	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs567877509	chr10:97053842-97053843	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs377730912	chr10:97053848-97053849	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs552449741	chr10:97053849-97053850	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs113967751	chr10:97053906-97053907	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183115534	chr10:97053922-97053923	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566941450	chr10:97053949-97053950	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11188265	chr10:97054006-97054007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11382783	chr10:97054050-97054051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372091175	chr10:97054068-97054069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34570294	chr10:97054069-97054070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373441299	chr10:97054092-97054093	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562226064	chr10:97054111-97054112	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs188249460	chr10:97054117-97054118	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544909114	chr10:97054121-97054122	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs564535881	chr10:97054122-97054123	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192980731	chr10:97054128-97054129	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs148593867	chr10:97054200-97054201	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546944691	chr10:97054303-97054304	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs560397518	chr10:97054310-97054311	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs529305715	chr10:97054313-97054314	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs80002058	chr10:97054318-97054319	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs183492281	chr10:97054331-97054332	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12784371	chr10:97054366-97054367	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs372648185	chr10:97054397-97054398	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147679038	chr10:97054416-97054417	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561860654	chr10:97054423-97054424	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7918340	chr10:97054442-97054443	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs187898502	chr10:97054451-97054452	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs74880976	chr10:97054471-97054472	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs78222667	chr10:97054474-97054475	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573665157	chr10:97054497-97054498	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554421717	chr10:97054536-97054537	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs544980391	chr10:97054544-97054545	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs536309052	chr10:97054562-97054563	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs374815982	chr10:97054582-97054583	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs575888679	chr10:97054605-97054606	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs544945940	chr10:97054664-97054665	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75622655	chr10:97054701-97054702	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Prostate cancer	16573809	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	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
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97050600-97054600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr10:97051200-97054400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:97051200-97054400	Weak transcription	NHLF	lung
4	chr10:97051200-97054600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:97051200-97054600	Weak transcription	Aorta	Aorta
6	chr10:97051200-97054600	Weak transcription	Liver	Liver
7	chr10:97051200-97054600	Weak transcription	Colon Smooth Muscle	Colon
8	chr10:97051200-97054600	Weak transcription	Lung	lung
9	chr10:97051200-97054600	Weak transcription	Psoas Muscle	Psoas
10	chr10:97051200-97054600	Weak transcription	Right Atrium	heart
11	chr10:97051200-97054800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:97051200-97054800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr10:97051200-97054800	Weak transcription	HSMM	muscle
14	chr10:97051200-97055000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr10:97051200-97056800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr10:97051400-97054200	Weak transcription	HMEC	breast
17	chr10:97051400-97054200	Weak transcription	NHEK	skin
18	chr10:97051400-97054400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr10:97051400-97054400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr10:97051400-97054400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr10:97051400-97054400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr10:97051400-97054400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr10:97051400-97054400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:97051400-97054400	Weak transcription	Colonic Mucosa	Colon
25	chr10:97051400-97054400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr10:97051400-97054400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr10:97051400-97054400	Weak transcription	Osteobl	bone
28	chr10:97051400-97054600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:97051400-97054600	Enhancers	Primary B cells from peripheral blood	blood
30	chr10:97051400-97054600	Weak transcription	Esophagus	oesophagus
31	chr10:97051400-97054600	Weak transcription	Left Ventricle	heart
32	chr10:97051400-97054600	Weak transcription	Pancreas	Pancrea
33	chr10:97051400-97054600	Weak transcription	Rectal Smooth Muscle	rectum
34	chr10:97051400-97054600	Weak transcription	HUVEC	blood vessel
35	chr10:97051600-97054200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr10:97051600-97054400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr10:97051600-97054400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr10:97051600-97054400	Weak transcription	A549	lung
39	chr10:97051600-97054600	Weak transcription	Right Ventricle	heart
40	chr10:97051600-97054600	Weak transcription	NH-A	brain
41	chr10:97051600-97055000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr10:97051800-97054600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:97051800-97054600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr10:97051800-97054600	Weak transcription	Fetal Heart	heart
45	chr10:97052000-97054400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr10:97052000-97054400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr10:97052000-97054400	Weak transcription	HepG2	liver
48	chr10:97052600-97053600	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr10:97052600-97053800	Enhancers	Fetal Intestine Small	intestine
50	chr10:97052600-97054600	Weak transcription	Spleen	Spleen

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