Variant report

Variant	nsv982902
Chromosome Location	chr10:5872818-5889953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:494)
CpG islands
(count:552)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:494 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5888296-5888348	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5887078-5887316	K562	blood:	n/a	n/a
3	ARID3A	chr10:5882378-5882749	HepG2	liver:	n/a	n/a
4	ATF2	chr10:5882822-5883381	GM12878	blood:	n/a	n/a
5	ATF2	chr10:5885726-5886294	GM12878	blood:	n/a	n/a
6	ATF2	chr10:5888079-5888517	GM12878	blood:	n/a	n/a
7	ATF2	chr10:5885759-5886344	GM12878	blood:	n/a	n/a
8	ATF2	chr10:5882081-5882634	GM12878	blood:	n/a	n/a
9	ATF2	chr10:5872492-5872930	GM12878	blood:	n/a	n/a
10	ATF2	chr10:5882088-5883394	GM12878	blood:	n/a	n/a
11	ATF2	chr10:5887991-5888533	GM12878	blood:	n/a	n/a
12	ATF3	chr10:5887049-5887248	K562	blood:	n/a	chr10:5887191-5887200 chr10:5887191-5887211
13	BACH1	chr10:5883022-5883034	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr10:5888064-5888456	GM12878	blood:	n/a	n/a
15	BATF	chr10:5872639-5872854	GM12878	blood:	n/a	n/a
16	BATF	chr10:5888145-5888416	GM12878	blood:	n/a	n/a
17	BATF	chr10:5872567-5872931	GM12878	blood:	n/a	n/a
18	BATF	chr10:5882191-5882590	GM12878	blood:	n/a	chr10:5882324-5882334
19	BCL11A	chr10:5888140-5888401	GM12878	blood:	n/a	n/a
20	BCL11A	chr10:5885938-5886268	GM12878	blood:	n/a	n/a
21	BCL11A	chr10:5882963-5883335	GM12878	blood:	n/a	n/a
22	BCL11A	chr10:5882236-5882572	GM12878	blood:	n/a	n/a
23	BCL11A	chr10:5888070-5888508	GM12878	blood:	n/a	n/a
24	BCL11A	chr10:5882223-5882654	GM12878	blood:	n/a	n/a
25	BCL3	chr10:5888086-5888466	GM12878	blood:	n/a	n/a
26	BCL3	chr10:5882190-5882621	GM12878	blood:	n/a	n/a
27	BCLAF1	chr10:5888041-5888445	GM12878	blood:	n/a	n/a
28	BCLAF1	chr10:5886650-5887130	GM12878	blood:	n/a	n/a
29	BCLAF1	chr10:5885619-5886233	GM12878	blood:	n/a	n/a
30	BCLAF1	chr10:5882114-5882863	GM12878	blood:	n/a	n/a
31	BCLAF1	chr10:5882182-5883297	GM12878	blood:	n/a	n/a
32	BHLHE40	chr10:5888110-5888526	GM12878	blood:	n/a	n/a
33	BHLHE40	chr10:5882132-5883638	GM12878	blood:	n/a	chr10:5882998-5883014
34	BHLHE40	chr10:5885663-5886195	GM12878	blood:	n/a	n/a
35	BHLHE40	chr10:5872585-5872925	GM12878	blood:	n/a	n/a
36	BHLHE40	chr10:5886727-5887382	K562	blood:	n/a	chr10:5887189-5887202 chr10:5887201-5887217 chr10:5887185-5887206 chr10:5887191-5887200 chr10:5887192-5887201 chr10:5887190-5887199 chr10:5887191-5887200
37	BHLHE40	chr10:5886564-5887354	GM12878	blood:	n/a	chr10:5887189-5887202 chr10:5887201-5887217 chr10:5887185-5887206 chr10:5887191-5887200 chr10:5887192-5887201 chr10:5887190-5887199 chr10:5887191-5887200
38	BHLHE40	chr10:5883163-5883340	K562	blood:	n/a	n/a
39	BHLHE40	chr10:5882216-5883361	HepG2	liver:	n/a	chr10:5882998-5883014
40	BRCA1	chr10:5882900-5883263	GM12878	blood:	n/a	n/a
41	BRCA1	chr10:5882293-5882553	GM12878	blood:	n/a	n/a
42	CBX3	chr10:5877519-5877756	K562	blood:	n/a	n/a
43	CEBPB	chr10:5873633-5873822	K562	blood:	n/a	n/a
44	CEBPB	chr10:5882313-5882506	GM12878	blood:	n/a	n/a
45	CEBPB	chr10:5888660-5888839	IMR90	lung:	n/a	chr10:5888800-5888811
46	CEBPB	chr10:5877919-5877984	HepG2	liver:	n/a	chr10:5877970-5877983
47	CEBPB	chr10:5888759-5888958	A549	lung:	n/a	chr10:5888800-5888811
48	CEBPB	chr10:5886636-5886859	IMR90	lung:	n/a	n/a
49	CEBPB	chr10:5882112-5882804	GM12878	blood:	n/a	n/a
50	CEBPB	chr10:5888650-5888829	K562	blood:	n/a	chr10:5888800-5888811

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5884153-5884203	HMEC	breast:	n/a
2	chr10:5884061-5884111	SK-N-MC	brain:	n/a
3	chr10:5886111-5886161	IMR90	lung:	fetal
4	chr10:5884153-5884203	HMEC	breast:	n/a
5	chr10:5884061-5884111	SK-N-MC	brain:	n/a
6	chr10:5886111-5886161	IMR90	lung:	fetal
7	chr10:5882576-5882626	GM12891	blood:	n/a
8	chr10:5882576-5882626	H1-hESC	embryonic stem cell:	embryo
9	chr10:5884105-5884155	HAEpiC	amniotic membrane:	n/a
10	chr10:5882466-5882516	MCF-7	breast:	n/a
11	chr10:5884061-5884111	HCM	heart:	n/a
12	chr10:5884061-5884111	Hepatocyte	liver:	n/a
13	chr10:5882739-5882789	SK-N-MC	brain:	n/a
14	chr10:5886111-5886161	U87	brain:	n/a
15	chr10:5884105-5884155	Hepatocyte	liver:	n/a
16	chr10:5882304-5882354	HNPCEpiC	eye:	n/a
17	chr10:5882304-5882354	BJ	skin:	n/a
18	chr10:5884105-5884155	HL-60	blood:	n/a
19	chr10:5882466-5882516	SK-N-MC	brain:	n/a
20	chr10:5882739-5882789	AG09309	skin:	n/a
21	chr10:5884105-5884155	AG04450	lung:	fetal
22	chr10:5884105-5884155	SK-N-SH_RA	brain:	n/a
23	chr10:5884061-5884111	PFSK-1	brain:	n/a
24	chr10:5882304-5882354	HMEC	breast:	n/a
25	chr10:5884153-5884203	AoSMC	blood vessel:	n/a
26	chr10:5884061-5884111	SAEC	small airway:	n/a
27	chr10:5884105-5884155	PFSK-1	brain:	n/a
28	chr10:5882466-5882516	PANC-1	pancreas:	n/a
29	chr10:5882739-5882789	PrEC	prostate:	n/a
30	chr10:5884061-5884111	SK-N-SH	brain:	n/a
31	chr10:5882304-5882354	AG04450	lung:	fetal
32	chr10:5886111-5886161	HRE	kidney:	n/a
33	chr10:5882466-5882516	HCPEpiC	choroid plexus:	n/a
34	chr10:5879090-5879140	AG04450	lung:	fetal
35	chr10:5884105-5884155	SKMC	muscle:	n/a
36	chr10:5879090-5879140	GM19239	blood:	n/a
37	chr10:5879090-5879140	AG09309	skin:	n/a
38	chr10:5879090-5879140	Hela-S3	cervix:	n/a
39	chr10:5882466-5882516	HAEpiC	amniotic membrane:	n/a
40	chr10:5879090-5879140	Jurkat	blood:	n/a
41	chr10:5884105-5884155	HEEpiC	esophagus:	n/a
42	chr10:5884153-5884203	HUVEC	blood vessel:	n/a
43	chr10:5884153-5884203	CMK	blood:	n/a
44	chr10:5882576-5882626	HUVEC	blood vessel:	n/a
45	chr10:5882739-5882789	SK-N-SH	brain:	n/a
46	chr10:5882739-5882789	ECC-1	luminal epithelium:	n/a
47	chr10:5884061-5884111	NB4	blood:	n/a
48	chr10:5882576-5882626	AG04450	lung:	fetal
49	chr10:5886111-5886161	AG09319	gingival:	n/a
50	chr10:5882304-5882354	HIPEpiC	eye:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5854620..5857118-chr10:5886149..5888419,4	K562	blood:
2	chr10:5854265..5856578-chr10:5874847..5876421,2	MCF-7	breast:
3	chr10:5860095..5862542-chr10:5886681..5888594,2	MCF-7	breast:
4	chr10:5875866..5877647-chr10:5881023..5883616,2	K562	blood:
5	chr10:5870260..5872899-chr10:5873504..5877637,4	K562	blood:
6	chr10:5853267..5855548-chr10:5881785..5884894,3	MCF-7	breast:
7	chr10:5851570..5858995-chr10:5881654..5887342,9	K562	blood:
8	chr10:5873375..5874969-chr10:5930314..5932944,2	MCF-7	breast:
9	chr10:5889255..5891417-chr10:5903224..5906135,2	MCF-7	breast:
10	chr10:5876253..5877969-chr10:5881683..5883648,2	K562	blood:
11	chr10:5867768..5870710-chr10:5870936..5873255,3	MCF-7	breast:
12	chr10:5851448..5853265-chr10:5875008..5877610,2	MCF-7	breast:
13	chr10:5871204..5872899-chr10:5874747..5877637,3	K562	blood:
14	chr10:5876253..5877969-chr10:5881683..5883648,2	K562	blood:
15	chr10:5850869..5856128-chr10:5879241..5885807,8	K562	blood:
16	chr10:5869665..5872246-chr10:5873304..5875744,2	MCF-7	breast:
17	chr10:5872995..5874657-chr10:5893099..5894735,2	K562	blood:
18	chr10:5871204..5872899-chr10:5874747..5877637,3	K562	blood:
19	chr10:5868411..5871104-chr10:5884225..5887747,3	K562	blood:
20	chr10:5874603..5876795-chr10:5886014..5887751,3	MCF-7	breast:
21	chr10:5852473..5857853-chr10:5880942..5888645,8	MCF-7	breast:
22	chr10:5887234..5889271-chr10:5891738..5894895,3	K562	blood:
23	chr10:5852230..5858723-chr10:5874443..5879399,10	K562	blood:
24	chr10:5874889..5877951-chr10:5883018..5886610,3	MCF-7	breast:
25	chr10:5853933..5861862-chr10:5868343..5873668,10	K562	blood:
26	chr10:5857495..5859789-chr10:5881654..5883847,2	K562	blood:
27	chr10:5855088..5855608-chr10:5874999..5875621,2	MCF-7	breast:
28	chr10:5853712..5856413-chr10:5877125..5879138,3	MCF-7	breast:
29	chr10:5853739..5856663-chr10:5888964..5891448,2	MCF-7	breast:
30	chr10:5874603..5876795-chr10:5886014..5887751,3	MCF-7	breast:
31	chr10:5874179..5876350-chr10:5894206..5896113,2	K562	blood:
32	chr10:5854450..5857183-chr10:5867124..5872976,6	MCF-7	breast:
33	chr10:5858242..5861090-chr10:5872989..5875709,2	MCF-7	breast:
34	chr10:5875866..5877647-chr10:5881023..5883616,2	K562	blood:
35	chr10:5870260..5872899-chr10:5873504..5877637,4	K562	blood:
36	chr10:5886207..5890565-chr10:5893992..5897304,3	K562	blood:
37	chr10:5887749..5890618-chr10:5895657..5897180,2	K562	blood:

No data

Variant related genes	Relation type
GDI2	TF binding region
GDI2	CpG island
ENSG00000134461	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000240180	chromatin interactions
ENSG00000057608	chromatin interactions

Extended variants
information (count: 713 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574262427	chr10:5872878-5872879	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544867001	chr10:5872889-5872890	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs556611145	chr10:5872903-5872904	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs578040855	chr10:5872942-5872943	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs140419858	chr10:5872972-5872973	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs76733856	chr10:5872993-5872994	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs560305341	chr10:5873001-5873002	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs113554217	chr10:5873036-5873037	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112076472	chr10:5873037-5873038	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138472228	chr10:5873038-5873039	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs540117925	chr10:5873145-5873146	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs561673668	chr10:5873148-5873149	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs367695034	chr10:5873189-5873190	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs191554856	chr10:5873242-5873243	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs371257927	chr10:5873244-5873245	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs77838678	chr10:5873266-5873267	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs182489518	chr10:5873268-5873269	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143095059	chr10:5873273-5873274	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs373751526	chr10:5873288-5873289	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs72774109	chr10:5873360-5873361	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs566461041	chr10:5873446-5873447	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs116833613	chr10:5873554-5873555	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs145175229	chr10:5873561-5873562	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs7085071	chr10:5873577-5873578	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs186042339	chr10:5873606-5873607	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs556482092	chr10:5873623-5873624	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs4749407	chr10:5873696-5873697	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545184480	chr10:5873705-5873706	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs377035740	chr10:5873720-5873721	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375615672	chr10:5873735-5873736	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201638664	chr10:5873838-5873839	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs61832877	chr10:5873860-5873861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs143101664	chr10:5873862-5873863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs572083724	chr10:5873881-5873882	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs561568975	chr10:5873905-5873906	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs576667922	chr10:5873917-5873918	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs369341456	chr10:5873970-5873971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561611365	chr10:5873979-5873980	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs4749408	chr10:5873997-5873998	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544368412	chr10:5874047-5874048	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs55659521	chr10:5874073-5874074	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs533076109	chr10:5874091-5874092	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144471795	chr10:5874102-5874103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533644096	chr10:5874120-5874121	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs190504206	chr10:5874124-5874125	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs55834056	chr10:5874132-5874133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs527269997	chr10:5874136-5874137	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183114298	chr10:5874141-5874142	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs560134811	chr10:5874210-5874211	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs141624700	chr10:5874237-5874238	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5870200-5875000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:5872200-5873600	Enhancers	Primary B cells from peripheral blood	blood
3	chr10:5872400-5873400	Enhancers	Primary B cells from cord blood	blood
4	chr10:5872400-5873400	Enhancers	Fetal Thymus	thymus
5	chr10:5872400-5875600	Weak transcription	K562	blood
6	chr10:5872600-5873400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr10:5872600-5873400	Enhancers	GM12878-XiMat	blood
8	chr10:5872800-5873200	Active TSS	Spleen	Spleen
9	chr10:5872800-5873600	Flanking Active TSS	HepG2	liver
10	chr10:5873000-5873200	Enhancers	Primary T cells fromperipheralblood	blood
11	chr10:5873000-5873400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:5873200-5873400	Enhancers	Esophagus	oesophagus
13	chr10:5873200-5882400	Weak transcription	Spleen	Spleen
14	chr10:5873400-5873600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr10:5873400-5874400	Weak transcription	Esophagus	oesophagus
16	chr10:5873400-5875000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr10:5873400-5875600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr10:5873600-5875600	Enhancers	HepG2	liver
19	chr10:5874400-5875000	Weak transcription	Right Atrium	heart
20	chr10:5874400-5875200	Enhancers	Esophagus	oesophagus
21	chr10:5874600-5875000	Enhancers	Duodenum Mucosa	Duodenum
22	chr10:5874600-5875000	Enhancers	Placenta Amnion	Placenta Amnion
23	chr10:5874600-5875000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr10:5874600-5875200	Enhancers	Stomach Mucosa	stomach
25	chr10:5874600-5876400	Enhancers	Placenta	Placenta
26	chr10:5874800-5875400	Enhancers	Colonic Mucosa	Colon
27	chr10:5874800-5875400	Enhancers	Gastric	stomach
28	chr10:5874800-5876000	Enhancers	Fetal Heart	heart
29	chr10:5875000-5875200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr10:5875000-5875200	Genic enhancers	Right Atrium	heart
31	chr10:5875000-5875400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr10:5875000-5875400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr10:5875000-5875400	Active TSS	Duodenum Mucosa	Duodenum
34	chr10:5875000-5875400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr10:5875000-5876000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr10:5875000-5886600	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr10:5875200-5875400	Enhancers	Left Ventricle	heart
38	chr10:5875200-5875800	Weak transcription	Stomach Mucosa	stomach
39	chr10:5875200-5877600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:5875200-5882200	Weak transcription	Right Atrium	heart
41	chr10:5875400-5876000	Weak transcription	Left Ventricle	heart
42	chr10:5875400-5876200	Weak transcription	Gastric	stomach
43	chr10:5875600-5875800	Bivalent Enhancer	HepG2	liver
44	chr10:5875600-5876000	Flanking Active TSS	K562	blood
45	chr10:5875600-5876200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr10:5875800-5876000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr10:5875800-5876000	Enhancers	Stomach Mucosa	stomach
48	chr10:5875800-5876000	Flanking Bivalent TSS/Enh	HepG2	liver
49	chr10:5875800-5876600	Enhancers	Fetal Muscle Leg	muscle
50	chr10:5875800-5876600	Enhancers	Right Ventricle	heart

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