Variant report

Variant	esv2761620
Chromosome Location	chr10:98047045-98089749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:764)
CpG islands
(count:489)
Chromatin interactive
region (count:26)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:98047390-98048001	HepG2	liver:	n/a	n/a
2	ATF2	chr10:98047333-98048554	GM12878	blood:	n/a	n/a
3	ATF2	chr10:98050115-98051002	GM12878	blood:	n/a	n/a
4	ATF2	chr10:98050141-98051092	GM12878	blood:	n/a	n/a
5	ATF2	chr10:98046965-98048607	GM12878	blood:	n/a	n/a
6	ATF2	chr10:98085631-98086220	GM12878	blood:	n/a	n/a
7	BACH1	chr10:98079826-98080300	H1-hESC	embryonic stem cell:	n/a	chr10:98080069-98080083
8	BACH1	chr10:98079899-98080293	K562	blood:	n/a	chr10:98080069-98080083
9	BATF	chr10:98085457-98086312	GM12878	blood:	n/a	n/a
10	BATF	chr10:98047524-98047795	GM12878	blood:	n/a	n/a
11	BATF	chr10:98048007-98048317	GM12878	blood:	n/a	n/a
12	BATF	chr10:98050369-98050912	GM12878	blood:	n/a	n/a
13	BATF	chr10:98085759-98086131	GM12878	blood:	n/a	n/a
14	BATF	chr10:98047833-98048425	GM12878	blood:	n/a	chr10:98047861-98047869
15	BATF	chr10:98050470-98050858	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:98050486-98050892	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:98047933-98048439	GM12878	blood:	n/a	chr10:98048307-98048316
18	BCL11A	chr10:98047436-98047807	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:98085702-98086059	GM12878	blood:	n/a	n/a
20	BCL3	chr10:98050487-98050949	GM12878	blood:	n/a	n/a
21	BCLAF1	chr10:98050141-98050955	GM12878	blood:	n/a	n/a
22	BCLAF1	chr10:98047174-98048413	GM12878	blood:	n/a	chr10:98048307-98048316
23	BCLAF1	chr10:98050148-98050894	GM12878	blood:	n/a	n/a
24	BCLAF1	chr10:98052964-98053449	GM12878	blood:	n/a	n/a
25	BCLAF1	chr10:98047036-98048584	GM12878	blood:	n/a	chr10:98048307-98048316
26	BHLHE40	chr10:98049074-98049399	GM12878	blood:	n/a	chr10:98049157-98049166 chr10:98049151-98049172 chr10:98049155-98049168 chr10:98049157-98049166 chr10:98049158-98049167
27	BHLHE40	chr10:98047630-98047800	HepG2	liver:	n/a	n/a
28	BHLHE40	chr10:98050328-98050906	GM12878	blood:	n/a	n/a
29	BHLHE40	chr10:98047075-98048559	GM12878	blood:	n/a	n/a
30	BRCA1	chr10:98063262-98063377	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr10:98053515-98053533	GM12878	blood:	n/a	n/a
32	CEBPB	chr10:98069561-98070114	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr10:98086003-98086070	HepG2	liver:	n/a	chr10:98086045-98086056
34	CEBPB	chr10:98049249-98049711	MCF-7	breast:	n/a	n/a
35	CEBPB	chr10:98050106-98051070	GM12878	blood:	n/a	n/a
36	CEBPB	chr10:98088645-98088727	HepG2	liver:	n/a	chr10:98088666-98088675 chr10:98088664-98088675
37	CEBPB	chr10:98047428-98047906	MCF-7	breast:	n/a	chr10:98047704-98047717
38	CEBPB	chr10:98046999-98048603	GM12878	blood:	n/a	chr10:98047704-98047717
39	CEBPB	chr10:98047475-98047892	HepG2	liver:	n/a	chr10:98047704-98047717
40	CEBPB	chr10:98067907-98068181	Hela-S3	cervix:	n/a	chr10:98068060-98068073 chr10:98068062-98068073 chr10:98068060-98068073 chr10:98068060-98068073 chr10:98068062-98068073
41	CEBPB	chr10:98085979-98086087	IMR90	lung:	n/a	chr10:98086045-98086056
42	CHD1	chr10:98047089-98048577	GM12878	blood:	n/a	n/a
43	CHD1	chr10:98050323-98050788	GM12878	blood:	n/a	n/a
44	CHD2	chr10:98069657-98070215	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr10:98047083-98048455	GM12878	blood:	n/a	n/a
46	CREB1	chr10:98047437-98048512	GM12878	blood:	n/a	n/a
47	CTBP2	chr10:98069668-98069953	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr10:98053172-98053338	ProgFib	skin:	n/a	chr10:98053205-98053226
49	CTCF	chr10:98084419-98084508	A549	lung:	n/a	n/a
50	CTCF	chr10:98077322-98077464	Hela-S3	cervix:	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	chr10:98063999-98064049	Hepatocyte	liver:	n/a
2	chr10:98063999-98064049	Hepatocyte	liver:	n/a
3	chr10:98069610-98069660	HCT-116	colon:	n/a
4	chr10:98061530-98061580	SAEC	small airway:	n/a
5	chr10:98062687-98062737	Hepatocyte	liver:	n/a
6	chr10:98069610-98069660	HUVEC	blood vessel:	n/a
7	chr10:98064175-98064225	AG09319	gingival:	n/a
8	chr10:98063967-98064017	PrEC	prostate:	n/a
9	chr10:98064362-98064412	IMR90	lung:	fetal
10	chr10:98063999-98064049	HepG2	liver:	n/a
11	chr10:98062747-98062797	IMR90	lung:	fetal
12	chr10:98062687-98062737	AG09319	gingival:	n/a
13	chr10:98063999-98064049	SK-N-SH_RA	brain:	n/a
14	chr10:98062747-98062797	HRE	kidney:	n/a
15	chr10:98064362-98064412	NHBE	bronchial:	n/a
16	chr10:98063967-98064017	PFSK-1	brain:	n/a
17	chr10:98062687-98062737	HNPCEpiC	eye:	n/a
18	chr10:98062747-98062797	GM19239	blood:	n/a
19	chr10:98064362-98064412	NT2-D1	testis:	n/a
20	chr10:98069610-98069660	GM12878	blood:	n/a
21	chr10:98064175-98064225	HL-60	blood:	n/a
22	chr10:98064362-98064412	GM12892	blood:	n/a
23	chr10:98062747-98062797	BE2_C	brain:	n/a
24	chr10:98062747-98062797	HCPEpiC	choroid plexus:	n/a
25	chr10:98061530-98061580	HCM	heart:	n/a
26	chr10:98064175-98064225	SK-N-MC	brain:	n/a
27	chr10:98063967-98064017	HIPEpiC	eye:	n/a
28	chr10:98061530-98061580	ovcar-3	ovarian:	n/a
29	chr10:98069610-98069660	HL-60	blood:	n/a
30	chr10:98063967-98064017	HNPCEpiC	eye:	n/a
31	chr10:98063999-98064049	MCF-7	breast:	n/a
32	chr10:98061530-98061580	K562	blood:	n/a
33	chr10:98062687-98062737	GM12892	blood:	n/a
34	chr10:98061530-98061580	HCPEpiC	choroid plexus:	n/a
35	chr10:98069610-98069660	ovcar-3	ovarian:	n/a
36	chr10:98063967-98064017	HL-60	blood:	n/a
37	chr10:98063967-98064017	HepG2	liver:	n/a
38	chr10:98063967-98064017	SK-N-MC	brain:	n/a
39	chr10:98064175-98064225	AG04450	lung:	fetal
40	chr10:98064362-98064412	GM19239	blood:	n/a
41	chr10:98069610-98069660	GM06990	blood:	n/a
42	chr10:98061530-98061580	HL-60	blood:	n/a
43	chr10:98062747-98062797	SKMC	muscle:	n/a
44	chr10:98062747-98062797	BJ	skin:	n/a
45	chr10:98062747-98062797	PFSK-1	brain:	n/a
46	chr10:98062687-98062737	GM06990	blood:	n/a
47	chr10:98063967-98064017	LNCaP	prostate:	n/a
48	chr10:98064175-98064225	NB4	blood:	n/a
49	chr10:98062747-98062797	HPAEpiC	pulmonary alveolar:	n/a
50	chr10:98061530-98061580	HMEC	breast:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:97993410..97995538-chr10:98048766..98051029,2	MCF-7	breast:
2	chr10:98067037..98069492-chr10:98071586..98073914,2	K562	blood:
3	chr10:98046170..98047854-chr10:98073375..98075159,2	MCF-7	breast:
4	chr10:97989046..97989956-chr10:98052486..98053488,8	MCF-7	breast:
5	chr10:98062204..98064987-chr10:98065467..98068204,2	K562	blood:
6	chr10:97802874..97804849-chr10:98083936..98085539,2	MCF-7	breast:
7	chr10:98088637..98090186-chr10:98091371..98093641,2	K562	blood:
8	chr10:97890578..97892383-chr10:98073643..98076276,2	MCF-7	breast:
9	chr10:97988988..97989760-chr10:98048810..98049411,2	MCF-7	breast:
10	chr10:98062862..98065652-chr10:98072222..98073783,2	MCF-7	breast:
11	chr10:98067037..98069492-chr10:98071586..98073914,2	K562	blood:
12	chr10:97989212..97989943-chr10:98075931..98076672,2	MCF-7	breast:
13	chr10:97996830..97998741-chr10:98049014..98051338,2	MCF-7	breast:
14	chr10:97988968..97989965-chr10:98052754..98053801,25	MCF-7	breast:
15	chr10:97776929..97777676-chr10:98052758..98053580,3	MCF-7	breast:
16	chr10:98046170..98047854-chr10:98073375..98075159,2	MCF-7	breast:
17	chr10:97776596..97777595-chr10:98052760..98053742,4	K562	blood:
18	chr10:98054173..98056503-chr10:98059907..98061674,2	K562	blood:
19	chr10:97889408..97891756-chr10:98048251..98051356,3	MCF-7	breast:
20	chr10:98024012..98025766-chr10:98077469..98079823,2	K562	blood:
21	chr10:98042724..98044710-chr10:98045849..98048382,2	K562	blood:
22	chr10:97989131..97989863-chr10:98050597..98051298,2	MCF-7	breast:
23	chr10:97802271..97805251-chr10:98083540..98085523,3	MCF-7	breast:
24	chr10:97803583..97805560-chr10:98074679..98076235,2	MCF-7	breast:
25	chr10:98062204..98064987-chr10:98065467..98068204,2	K562	blood:
26	chr10:98054173..98056503-chr10:98059907..98061674,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLNK-3	chr10:98060020-98060106	ENSG00000229418.2
2	lnc-BLNK-3	chr10:98060020-98060106	NONHSAT015809
3	lnc-BLNK-3	chr10:98054639-98054724	NONHSAT015809
4	lnc-DNTT-1	chr10:98054639-98054724	ENSG00000229418.1
5	lnc-DNTT-1	chr10:98066266-98066452	ENSG00000229418.1
6	lnc-BLNK-3	chr10:98054639-98054724	ENSG00000229418.2
7	lnc-DNTT-1	chr10:98053537-98054000	ENSG00000229418.1
8	lnc-BLNK-3	chr10:98066266-98066460	NONHSAT015809
9	lnc-DNTT-1	chr10:98060020-98060106	ENSG00000229418.1
10	lnc-BLNK-3	chr10:98052442-98054005	NONHSAT015809
11	lnc-BLNK-3	chr10:98066266-98066452	ENSG00000229418.2
12	lnc-BLNK-3	chr10:98052442-98054005	ENSG00000229418.2

No data

Variant related genes	Relation type
ENSG00000229418	TF binding region
DNTT	TF binding region
ENSG00000229418	CpG island
DNTT	CpG island
ENSG00000226688	chromatin interactions
ENSG00000177853	chromatin interactions
ENSG00000107447	chromatin interactions
ENSG00000107443	chromatin interactions
ENSG00000229418	chromatin interactions

Extended variants
information (count: 1635 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1635 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574891980	chr10:98047047-98047048	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs147187612	chr10:98047114-98047115	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs140660552	chr10:98047148-98047149	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs577185442	chr10:98047228-98047229	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs545712604	chr10:98047234-98047235	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs185796088	chr10:98047314-98047315	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs572920866	chr10:98047321-98047322	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs537448405	chr10:98047362-98047363	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs79380165	chr10:98047392-98047393	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs554137274	chr10:98047395-98047396	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs142214561	chr10:98047416-98047417	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs574435099	chr10:98047460-98047461	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530463275	chr10:98047504-98047505	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs550156074	chr10:98047511-98047512	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs75675755	chr10:98047528-98047529	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs532826838	chr10:98047539-98047540	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs78097027	chr10:98047575-98047576	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs566285466	chr10:98047612-98047613	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs188482359	chr10:98047628-98047629	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs548675790	chr10:98047633-98047634	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs560118969	chr10:98047689-98047690	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs11188696	chr10:98047696-98047697	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs568558735	chr10:98047750-98047751	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs537491368	chr10:98047772-98047773	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs72520090	chr10:98047783-98047784	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs576992035	chr10:98047784-98047785	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs17111560	chr10:98047785-98047786	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs570822874	chr10:98047787-98047788	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs5787177	chr10:98047793-98047794	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs151145100	chr10:98047829-98047830	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs552942020	chr10:98047878-98047879	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs565389189	chr10:98047884-98047885	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs117219667	chr10:98047959-98047960	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs2146391	chr10:98047990-98047991	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs555088135	chr10:98048015-98048016	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs181966713	chr10:98048054-98048055	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574971644	chr10:98048113-98048114	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs114665727	chr10:98048144-98048145	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs138985301	chr10:98048178-98048179	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs117699776	chr10:98048265-98048266	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77253426	chr10:98048268-98048269	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559757757	chr10:98048299-98048300	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs371230924	chr10:98048300-98048301	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7896766	chr10:98048322-98048323	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs78698659	chr10:98048360-98048361	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs397830789	chr10:98048368-98048369	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567016865	chr10:98048378-98048379	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577708102	chr10:98048379-98048380	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs78573017	chr10:98048411-98048412	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs186709601	chr10:98048431-98048432	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	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
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98032400-98047200	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr10:98043400-98047400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr10:98044800-98047200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr10:98044800-98047400	Enhancers	Primary B cells from peripheral blood	blood
5	chr10:98044800-98047400	Enhancers	Fetal Intestine Large	intestine
6	chr10:98045000-98047400	Enhancers	Sigmoid Colon	Sigmoid Colon
7	chr10:98045200-98047200	Enhancers	Liver	Liver
8	chr10:98045200-98047400	Enhancers	Fetal Intestine Small	intestine
9	chr10:98045400-98048000	Weak transcription	Gastric	stomach
10	chr10:98045400-98048200	Enhancers	Colonic Mucosa	Colon
11	chr10:98045600-98047200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:98045600-98047600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr10:98045600-98049800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr10:98045600-98052800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr10:98045600-98053000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr10:98046200-98047400	Enhancers	Pancreas	Pancrea
17	chr10:98046200-98048400	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr10:98046400-98047400	Flanking Active TSS	GM12878-XiMat	blood
19	chr10:98046400-98047600	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr10:98046400-98047600	Enhancers	Stomach Mucosa	stomach
21	chr10:98046400-98047800	Enhancers	Colon Smooth Muscle	Colon
22	chr10:98046400-98048600	Enhancers	Dnd41	blood
23	chr10:98046600-98047200	Weak transcription	Spleen	Spleen
24	chr10:98046600-98047400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr10:98046600-98047600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr10:98046600-98048200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr10:98046600-98050800	Enhancers	Fetal Thymus	thymus
28	chr10:98046800-98047400	Enhancers	Primary hematopoietic stem cells	blood
29	chr10:98046800-98047400	Enhancers	Thymus	Thymus
30	chr10:98046800-98049400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:98047000-98047200	Flanking Active TSS	Fetal Kidney	kidney
32	chr10:98047000-98047200	Enhancers	HepG2	liver
33	chr10:98047000-98047400	Enhancers	Esophagus	oesophagus
34	chr10:98047000-98047400	Enhancers	Fetal Stomach	stomach
35	chr10:98047000-98047400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr10:98047000-98047400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr10:98047000-98047600	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr10:98047000-98047600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr10:98047000-98047600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:98047000-98047600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr10:98047000-98047600	Flanking Active TSS	Duodenum Mucosa	Duodenum
42	chr10:98047000-98047600	Enhancers	Small Intestine	intestine
43	chr10:98047000-98047800	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr10:98047000-98048000	Enhancers	Rectal Smooth Muscle	rectum
45	chr10:98047000-98048200	Enhancers	Fetal Lung	lung
46	chr10:98047000-98048200	Enhancers	NHEK	skin
47	chr10:98047000-98048400	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr10:98047000-98048400	Enhancers	HMEC	breast
49	chr10:98047000-98048600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr10:98047000-98050400	Enhancers	Placenta	Placenta

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