Variant report

Variant	esv1798973
Chromosome Location	chr10:26968171-27001814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:934)
CpG islands
(count:612)
Chromatin interactive
region (count:30)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:26973565-26973899	K562	blood:	n/a	n/a
2	ARID3A	chr10:26986523-26986820	HepG2	liver:	n/a	n/a
3	BACH1	chr10:26985861-26986287	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:26987934-26988097	K562	blood:	n/a	n/a
5	BACH1	chr10:26973707-26973757	K562	blood:	n/a	n/a
6	BACH1	chr10:26986551-26986751	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:26973677-26973926	GM12878	blood:	n/a	n/a
8	BCLAF1	chr10:26986011-26987039	GM12878	blood:	n/a	chr10:26986432-26986445 chr10:26986483-26986496
9	BCLAF1	chr10:26985935-26986722	GM12878	blood:	n/a	chr10:26986432-26986445 chr10:26986483-26986496
10	BHLHE40	chr10:26985803-26987387	GM12878	blood:	n/a	chr10:26986481-26986497
11	BHLHE40	chr10:26985922-26987049	HepG2	liver:	n/a	chr10:26986481-26986497
12	BHLHE40	chr10:26985767-26987417	K562	blood:	n/a	chr10:26986481-26986497
13	BHLHE40	chr10:26986673-26986949	HepG2	liver:	n/a	n/a
14	BHLHE40	chr10:26980191-26980254	K562	blood:	n/a	n/a
15	BHLHE40	chr10:26973734-26973939	K562	blood:	n/a	n/a
16	CBX3	chr10:26985862-26986661	K562	blood:	n/a	n/a
17	CCNT2	chr10:26986274-26987047	K562	blood:	n/a	n/a
18	CCNT2	chr10:26994723-26994882	K562	blood:	n/a	n/a
19	CEBPB	chr10:26972520-26972834	IMR90	lung:	n/a	chr10:26972694-26972705
20	CEBPB	chr10:26985852-26986335	ECC-1	luminal epithelium:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
21	CEBPB	chr10:26985767-26986942	Hela-S3	cervix:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
22	CEBPB	chr10:26972539-26972809	K562	blood:	n/a	chr10:26972694-26972705
23	CEBPB	chr10:26985687-26986324	K562	blood:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
24	CEBPB	chr10:26985830-26986253	IMR90	lung:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
25	CEBPB	chr10:26985874-26986194	H1-hESC	embryonic stem cell:	n/a	chr10:26986010-26986021 chr10:26985938-26985949 chr10:26986086-26986099
26	CEBPB	chr10:26985841-26986411	K562	blood:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
27	CEBPB	chr10:26985933-26986221	ECC-1	luminal epithelium:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
28	CEBPB	chr10:26985733-26986594	A549	lung:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
29	CEBPB	chr10:26985832-26986242	A549	lung:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
30	CEBPB	chr10:26972547-26972840	HepG2	liver:	n/a	chr10:26972694-26972705
31	CEBPB	chr10:26985871-26986170	K562	blood:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
32	CEBPB	chr10:26985956-26986164	HepG2	liver:	n/a	chr10:26986086-26986099 chr10:26986010-26986021
33	CEBPB	chr10:26985911-26986182	A549	lung:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
34	CEBPB	chr10:26985786-26986434	MCF-7	breast:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
35	CEBPB	chr10:26985839-26986455	MCF-7	breast:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
36	CEBPB	chr10:26985887-26986485	GM12878	blood:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
37	CEBPB	chr10:26985836-26986329	HepG2	liver:	n/a	chr10:26986086-26986099 chr10:26986010-26986021 chr10:26985938-26985949
38	CEBPB	chr10:26995171-26995387	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:26972612-26972824	A549	lung:	n/a	chr10:26972694-26972705
40	CEBPB	chr10:26995173-26995482	K562	blood:	n/a	n/a
41	CEBPD	chr10:26986429-26987144	HepG2	liver:	n/a	n/a
42	CEBPD	chr10:26986310-26986769	K562	blood:	n/a	n/a
43	CHD1	chr10:26986428-26986558	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr10:26993963-26994017	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr10:26985972-26986894	GM12878	blood:	n/a	n/a
46	CHD2	chr10:26985946-26987436	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr10:26986709-26986949	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr10:26986050-26987222	GM12878	blood:	n/a	n/a
49	CHD2	chr10:26986272-26987319	HepG2	liver:	n/a	n/a
50	CHD2	chr10:26986338-26986935	K562	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:26986380-26986430	GM19239	blood:	n/a
2	chr10:26985910-26985960	MCF-7	breast:	n/a
3	chr10:26986380-26986430	GM19239	blood:	n/a
4	chr10:26985910-26985960	MCF-7	breast:	n/a
5	chr10:26986312-26986362	PANC-1	pancreas:	n/a
6	chr10:26983600-26983650	NHBE	bronchial:	n/a
7	chr10:26983600-26983650	H1-hESC	embryonic stem cell:	embryo
8	chr10:26989581-26989631	GM06990	blood:	n/a
9	chr10:26989581-26989631	HepG2	liver:	n/a
10	chr10:26986590-26986640	HL-60	blood:	n/a
11	chr10:26987120-26987170	IMR90	lung:	fetal
12	chr10:26986380-26986430	ovcar-3	ovarian:	n/a
13	chr10:26986380-26986430	PrEC	prostate:	n/a
14	chr10:26986384-26986434	HMEC	breast:	n/a
15	chr10:26987087-26987137	AoSMC	blood vessel:	n/a
16	chr10:26986380-26986430	NB4	blood:	n/a
17	chr10:26985910-26985960	Hepatocyte	liver:	n/a
18	chr10:26986380-26986430	SAEC	small airway:	n/a
19	chr10:26989581-26989631	GM12878	blood:	n/a
20	chr10:26989581-26989631	AG04450	lung:	fetal
21	chr10:26983600-26983650	AG04449	skin:	fetal
22	chr10:26986312-26986362	Jurkat	blood:	n/a
23	chr10:26985759-26985809	RPTEC	kidney:	n/a
24	chr10:26985910-26985960	AG04450	lung:	fetal
25	chr10:26989581-26989631	BE2_C	brain:	n/a
26	chr10:26985759-26985809	IMR90	lung:	fetal
27	chr10:26986380-26986430	SKMC	muscle:	n/a
28	chr10:26985910-26985960	PrEC	prostate:	n/a
29	chr10:26987087-26987137	HL-60	blood:	n/a
30	chr10:26987087-26987137	NB4	blood:	n/a
31	chr10:26989581-26989631	H1-hESC	embryonic stem cell:	embryo
32	chr10:26986380-26986430	AG09319	gingival:	n/a
33	chr10:26987120-26987170	GM06990	blood:	n/a
34	chr10:26983600-26983650	A549	lung:	n/a
35	chr10:26987120-26987170	SK-N-SH_RA	brain:	n/a
36	chr10:26985759-26985809	AG04450	lung:	fetal
37	chr10:26983600-26983650	PrEC	prostate:	n/a
38	chr10:26985910-26985960	HepG2	liver:	n/a
39	chr10:26986590-26986640	BE2_C	brain:	n/a
40	chr10:26985910-26985960	ovcar-3	ovarian:	n/a
41	chr10:26987087-26987137	NHDF-neo	bronchial:	n/a
42	chr10:26985759-26985809	BJ	skin:	n/a
43	chr10:26985910-26985960	HNPCEpiC	eye:	n/a
44	chr10:26986312-26986362	GM12891	blood:	n/a
45	chr10:26987087-26987137	A549	lung:	n/a
46	chr10:26989581-26989631	GM12891	blood:	n/a
47	chr10:26985910-26985960	HMEC	breast:	n/a
48	chr10:26983600-26983650	Caco-2	colon:	n/a
49	chr10:26987120-26987170	HL-60	blood:	n/a
50	chr10:26985759-26985809	SK-N-SH	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
2	chr10:26968705..26971277-chr10:26973238..26975564,2	K562	blood:
3	chr10:26986018..26986729-chr5:147763063..147763851,2	MCF-7	breast:
4	chr10:26986066..26987689-chr10:27148181..27149962,2	K562	blood:
5	chr10:26986021..26987940-chr10:27149008..27151636,2	MCF-7	breast:
6	chr10:26968705..26971277-chr10:26973238..26975564,2	K562	blood:
7	chr10:26961383..26963009-chr10:26967023..26968974,2	K562	blood:
8	chr10:26973781..26976716-chr10:26986143..26988490,2	K562	blood:
9	chr10:26895319..26895931-chr10:26973740..26974253,2	K562	blood:
10	chr10:26997066..27000236-chr10:27001137..27005066,4	K562	blood:
11	chr10:26952451..26954548-chr10:26967592..26969154,2	K562	blood:
12	chr10:26985323..26988042-chr10:27148387..27150466,3	MCF-7	breast:
13	chr10:26895094..26895872-chr10:26973347..26973911,2	MCF-7	breast:
14	chr10:26979944..26983109-chr10:26984592..26988021,5	MCF-7	breast:
15	chr10:26985157..26986871-chr10:26995628..26997533,2	MCF-7	breast:
16	chr10:26995580..26998397-chr10:27011031..27013187,2	K562	blood:
17	chr10:26985918..26987566-chr10:27148462..27151237,2	K562	blood:
18	chr10:26985752..26988058-chr10:26992017..26994907,3	MCF-7	breast:
19	chr10:26954305..26956450-chr10:26987430..26988975,2	K562	blood:
20	chr10:26996672..26998643-chr10:27000088..27002341,2	MCF-7	breast:
21	chr10:26988675..26990300-chr10:27168290..27169944,2	K562	blood:
22	chr10:26986198..26989615-chr10:27022506..27024765,3	MCF-7	breast:
23	chr10:26985640..26986465-chr5:82372961..82373834,2	Hela-S3	cervix:
24	chr10:26996672..26998643-chr10:27000088..27002341,2	MCF-7	breast:
25	chr10:26985057..26986781-chr10:27006850..27009579,2	K562	blood:
26	chr10:26985752..26988058-chr10:26992017..26994907,3	MCF-7	breast:
27	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:
28	chr10:26972585..26978071-chr10:26984536..26988033,8	MCF-7	breast:
29	chr10:26965108..26970102-chr10:26984839..26987979,6	K562	blood:
30	chr10:26986774..26988762-chr10:27020723..27023686,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI1-7	chr10:26984020-26986554	NONHSAT011856
2	lnc-PDSS1-5	chr10:26972163-26972531	NONHSAT011852
3	lnc-PDSS1-5	chr10:26973849-26973951	NONHSAT011852
4	lnc-PDSS1-3	chr10:26979489-26979726	NONHSAT011853
5	lnc-PDSS1-3	chr10:26979489-26979592	NONHSAT011855
6	lnc-ABI1-6	chr10:26993141-26993327	NONHSAT011857
7	lnc-PDSS1-3	chr10:26976921-26977217	NONHSAT011853
8	lnc-ABI1-6	chr10:26997342-26997429	NONHSAT011857
9	lnc-PDSS1-3	chr10:26982000-26982389	NONHSAT011854
10	lnc-PDSS1-3	chr10:26978326-26978528	NONHSAT011853
11	lnc-PDSS1-3	chr10:26977035-26977217	NONHSAT011854
12	lnc-PDSS1-3	chr10:26982000-26982381	NONHSAT011853
13	lnc-PDSS1-3	chr10:26977886-26977985	NONHSAT011853
14	lnc-PDSS1-3	chr10:26978326-26978528	NONHSAT011854
15	lnc-PDSS1-3	chr10:26979489-26979592	NONHSAT011854
16	lnc-PDSS1-3	chr10:26982000-26982046	NONHSAT011855
17	lnc-PDSS1-3	chr10:26978267-26978528	NONHSAT011855

No data

Variant related genes	Relation type
ENSG00000235843	TF binding region
HSPA8P3	TF binding region
ENSG00000227932	TF binding region
PDSS1	TF binding region
ENSG00000235843	CpG island
HSPA8P3	CpG island
ENSG00000227932	CpG island
PDSS1	CpG island
ENSG00000234788	chromatin interactions
ENSG00000152422	chromatin interactions
ENSG00000145868	chromatin interactions
ENSG00000136754	chromatin interactions
ENSG00000148459	chromatin interactions
ENSG00000174695	chromatin interactions
ENSG00000247199	chromatin interactions

Extended variants
information (count: 1512 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:1512 , 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	rs12252298	chr10:26968171-26968172	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530576900	chr10:26968180-26968181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs150145589	chr10:26968183-26968184	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78552426	chr10:26968191-26968192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs12252358	chr10:26968206-26968207	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs1677715	chr10:26968215-26968216	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs12252368	chr10:26968268-26968269	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374995847	chr10:26968277-26968278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs200692343	chr10:26968299-26968300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112231090	chr10:26968302-26968303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566336518	chr10:26968308-26968309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370335063	chr10:26968338-26968339	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528798561	chr10:26968445-26968446	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145578562	chr10:26968454-26968455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs1677714	chr10:26968456-26968457	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs372488029	chr10:26968465-26968466	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550644737	chr10:26968472-26968473	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs1677713	chr10:26968515-26968516	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs182715391	chr10:26968537-26968538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536619037	chr10:26968542-26968543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553105508	chr10:26968631-26968632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573050476	chr10:26968647-26968648	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141914265	chr10:26968714-26968715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375712598	chr10:26968715-26968716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558942048	chr10:26968718-26968719	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536651921	chr10:26968725-26968726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs539639874	chr10:26968743-26968744	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375616641	chr10:26968744-26968745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs6143835	chr10:26968745-26968746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534435101	chr10:26968746-26968747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373734673	chr10:26968747-26968748	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544454743	chr10:26968836-26968837	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560944702	chr10:26968853-26968854	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs574471603	chr10:26968857-26968858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12263262	chr10:26968904-26968905	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192779288	chr10:26968921-26968922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111821092	chr10:26968932-26968933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs551777233	chr10:26968951-26968952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs183206814	chr10:26968958-26968959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12261754	chr10:26968994-26968995	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550781953	chr10:26969031-26969032	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs567386191	chr10:26969090-26969091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369121705	chr10:26969120-26969121	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs536355089	chr10:26969138-26969139	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs138389893	chr10:26969171-26969172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374290672	chr10:26969209-26969210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566752928	chr10:26969223-26969224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539066910	chr10:26969234-26969235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368326085	chr10:26969235-26969236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558877742	chr10:26969245-26969246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:43)

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
small cell lung cancer	20016488	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
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26963400-26969400	Weak transcription	Thymus	Thymus
2	chr10:26965600-26969400	Weak transcription	Fetal Thymus	thymus
3	chr10:26967000-26973800	Weak transcription	K562	blood
4	chr10:26969400-26969800	ZNF genes & repeats	Fetal Thymus	thymus
5	chr10:26969400-26969800	Enhancers	Thymus	Thymus
6	chr10:26969400-26972200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr10:26969600-26971800	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr10:26969600-26973000	Enhancers	Dnd41	blood
9	chr10:26969600-26974800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr10:26969800-26970600	Weak transcription	Fetal Thymus	thymus
11	chr10:26969800-26972000	Weak transcription	Thymus	Thymus
12	chr10:26970000-26970800	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr10:26970200-26970600	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr10:26970600-26971000	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr10:26970600-26971000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:26970600-26971200	Enhancers	Fetal Thymus	thymus
17	chr10:26970600-26972000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr10:26970600-26973800	Enhancers	Primary T cells from cord blood	blood
19	chr10:26970600-26974200	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr10:26970600-26974400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr10:26970800-26973800	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr10:26971000-26971200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr10:26971000-26971400	Enhancers	HMEC	breast
24	chr10:26971000-26971800	Enhancers	A549	lung
25	chr10:26971000-26974400	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr10:26971000-26974400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr10:26971000-26974400	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr10:26971200-26971600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr10:26971200-26972600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr10:26971200-26972600	Weak transcription	Fetal Thymus	thymus
31	chr10:26971200-26973000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr10:26971600-26973400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr10:26971800-26973800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr10:26972000-26973200	Enhancers	Thymus	Thymus
35	chr10:26972000-26973800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:26972200-26973800	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr10:26972600-26973200	Enhancers	Fetal Thymus	thymus
38	chr10:26972600-26973600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr10:26973000-26973400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr10:26973000-26978000	Weak transcription	Dnd41	blood
41	chr10:26973200-26973600	Weak transcription	Fetal Thymus	thymus
42	chr10:26973200-26973600	Weak transcription	Thymus	Thymus
43	chr10:26973400-26974400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr10:26973600-26973800	Enhancers	Fetal Thymus	thymus
45	chr10:26973600-26973800	Enhancers	Thymus	Thymus
46	chr10:26973800-26974000	Enhancers	Primary T cells fromperipheralblood	blood
47	chr10:26973800-26974000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr10:26973800-26974000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:26973800-26974000	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr10:26973800-26974000	Flanking Active TSS	Thymus	Thymus

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