Variant report

Variant	nsv1051595
Chromosome Location	chr10:112730022-112789048
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:8)
Mature miRNA
region (count: 2)
miRNA target
sites (count:5)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr10:112756107-112756365	A549	lung:	n/a	chr10:112756236-112756247
2	CEBPB	chr10:112731448-112731763	IMR90	lung:	n/a	chr10:112731603-112731612 chr10:112731602-112731613 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612
3	CEBPB	chr10:112731495-112731703	Hela-S3	cervix:	n/a	chr10:112731603-112731612 chr10:112731602-112731613 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612
4	CEBPB	chr10:112752808-112753222	IMR90	lung:	n/a	chr10:112753183-112753194
5	CEBPB	chr10:112731432-112731782	K562	blood:	n/a	chr10:112731603-112731612 chr10:112731602-112731613 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612
6	CEBPB	chr10:112731424-112731758	HepG2	liver:	n/a	chr10:112731603-112731612 chr10:112731602-112731613 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612
7	CEBPB	chr10:112756130-112756363	IMR90	lung:	n/a	chr10:112756236-112756247
8	CEBPB	chr10:112756159-112756390	K562	blood:	n/a	chr10:112756236-112756247
9	CEBPB	chr10:112774974-112775275	Hela-S3	cervix:	n/a	chr10:112775133-112775144
10	CEBPB	chr10:112756172-112756306	HepG2	liver:	n/a	chr10:112756236-112756247
11	CEBPB	chr10:112731468-112731737	H1-hESC	embryonic stem cell:	n/a	chr10:112731603-112731612 chr10:112731602-112731613 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612
12	CEBPB	chr10:112775676-112775917	A549	lung:	n/a	n/a
13	CEBPB	chr10:112756084-112756345	HepG2	liver:	n/a	chr10:112756236-112756247
14	CEBPB	chr10:112756104-112756396	H1-hESC	embryonic stem cell:	n/a	chr10:112756236-112756247
15	CEBPB	chr10:112775029-112775215	IMR90	lung:	n/a	chr10:112775133-112775144
16	CEBPB	chr10:112731467-112731736	A549	lung:	n/a	chr10:112731603-112731612 chr10:112731602-112731613 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612 chr10:112731601-112731614 chr10:112731603-112731612
17	CEBPB	chr10:112737629-112738120	IMR90	lung:	n/a	chr10:112738058-112738066
18	CEBPB	chr10:112748793-112749154	IMR90	lung:	n/a	n/a
19	CEBPB	chr10:112775001-112775257	A549	lung:	n/a	chr10:112775133-112775144
20	CHD2	chr10:112782705-112783106	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr10:112783511-112783711	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr10:112785160-112785310	GM12873	blood:	n/a	n/a
23	CTCF	chr10:112785100-112785250	HMF	breast:	n/a	n/a
24	CTCF	chr10:112785120-112785270	NHEK	skin:	n/a	n/a
25	CTCF	chr10:112785020-112785170	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr10:112785100-112785247	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr10:112785080-112785230	HMF	breast:	n/a	n/a
28	CTCF	chr10:112785100-112785250	AG04449	skin:	n/a	n/a
29	CTCF	chr10:112785040-112785190	HCM	heart:	n/a	n/a
30	CTCF	chr10:112785200-112785350	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr10:112785120-112785270	AG10803	skin:	n/a	n/a
32	CTCF	chr10:112785120-112785270	HMEC	breast:	n/a	n/a
33	CTCF	chr10:112785100-112785250	HFF	foreskin:	n/a	n/a
34	CTCF	chr10:112785060-112785210	AG04450	lung:	n/a	n/a
35	CTCF	chr10:112785120-112785270	RPTEC	kidney:	n/a	n/a
36	CTCF	chr10:112785100-112785250	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr10:112785040-112785190	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr10:112785020-112785170	HCT-116	colon:	n/a	n/a
39	CTCF	chr10:112785100-112785250	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr10:112785160-112785310	HVMF	connective:	n/a	n/a
41	CTCF	chr10:112785080-112785230	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr10:112785080-112785230	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:112785060-112785210	AG09319	gingival:	n/a	n/a
44	E2F4	chr10:112783352-112783552	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F6	chr10:112782422-112783271	H1-hESC	embryonic stem cell:	n/a	n/a
46	E2F6	chr10:112783723-112784168	H1-hESC	embryonic stem cell:	n/a	n/a
47	EP300	chr10:112752922-112753226	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr10:112777009-112777116	GM12878	blood:	n/a	chr10:112777061-112777075
49	FAM48A	chr10:112780374-112780565	GM12878	blood:	n/a	n/a
50	FOS	chr10:112752874-112753223	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:112772261-112772311	GM12891	blood:	n/a
2	chr10:112772261-112772311	ECC-1	luminal epithelium:	n/a
3	chr10:112772261-112772311	HNPCEpiC	eye:	n/a
4	chr10:112772261-112772311	NHDF-neo	bronchial:	n/a
5	chr10:112772261-112772311	NT2-D1	testis:	n/a
6	chr10:112772261-112772311	Caco-2	colon:	n/a
7	chr10:112772261-112772311	HEK293	kidney:	embryo
8	chr10:112772261-112772311	HRPEpiC	eye:	n/a
9	chr10:112772261-112772311	NH-A	brain:	n/a
10	chr10:112772261-112772311	HMEC	breast:	n/a
11	chr10:112772261-112772311	AoSMC	blood vessel:	n/a
12	chr10:112772261-112772311	SK-N-MC	brain:	n/a
13	chr10:112772261-112772311	HUVEC	blood vessel:	n/a
14	chr10:112772261-112772311	U87	brain:	n/a
15	chr10:112772261-112772311	K562	blood:	n/a
16	chr10:112772261-112772311	HepG2	liver:	n/a
17	chr10:112772261-112772311	CMK	blood:	n/a
18	chr10:112772261-112772311	HIPEpiC	eye:	n/a
19	chr10:112772261-112772311	RPTEC	kidney:	n/a
20	chr10:112772261-112772311	HEEpiC	esophagus:	n/a
21	chr10:112772261-112772311	AG04450	lung:	fetal
22	chr10:112772261-112772311	HCPEpiC	choroid plexus:	n/a
23	chr10:112772261-112772311	ovcar-3	ovarian:	n/a
24	chr10:112772261-112772311	HCF	heart:	n/a
25	chr10:112772261-112772311	NB4	blood:	n/a
26	chr10:112772261-112772311	AG09319	gingival:	n/a
27	chr10:112772261-112772311	HCM	heart:	n/a
28	chr10:112772261-112772311	NHBE	bronchial:	n/a
29	chr10:112772261-112772311	SAEC	small airway:	n/a
30	chr10:112772261-112772311	AG09309	skin:	n/a
31	chr10:112772261-112772311	GM06990	blood:	n/a
32	chr10:112772261-112772311	SKMC	muscle:	n/a
33	chr10:112772261-112772311	GM12878	blood:	n/a
34	chr10:112772261-112772311	BJ	skin:	n/a
35	chr10:112772261-112772311	HAEpiC	amniotic membrane:	n/a
36	chr10:112772261-112772311	HRE	kidney:	n/a
37	chr10:112772261-112772311	GM19239	blood:	n/a
38	chr10:112772261-112772311	PrEC	prostate:	n/a
39	chr10:112772261-112772311	IMR90	lung:	fetal
40	chr10:112772261-112772311	MCF-7	breast:	n/a
41	chr10:112772261-112772311	A549	lung:	n/a
42	chr10:112772261-112772311	MCF10A-Er-Src	breast:	n/a
43	chr10:112772261-112772311	ProgFib	skin:	n/a
44	chr10:112772261-112772311	LNCaP	prostate:	n/a
45	chr10:112772261-112772311	Hepatocyte	liver:	n/a
46	chr10:112772261-112772311	H1-hESC	embryonic stem cell:	embryo
47	chr10:112772261-112772311	Hela-S3	cervix:	n/a
48	chr10:112772261-112772311	AG04449	skin:	fetal
49	chr10:112772261-112772311	HCT-116	colon:	n/a
50	chr10:112772261-112772311	T-47D	breast:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:112746021..112748310-chr10:112757696..112760493,2	MCF-7	breast:
2	chr10:112728533..112731147-chr10:112731609..112733166,2	K562	blood:
3	chr10:112784890..112786956-chr10:112789080..112792697,3	K562	blood:
4	chr10:112778849..112781525-chr10:112783454..112785651,2	K562	blood:
5	chr10:112744001..112747517-chr10:112750803..112753417,3	MCF-7	breast:
6	chr10:112737444..112739132-chr10:112747044..112749128,2	K562	blood:
7	chr10:112776495..112778257-chr10:112780884..112782883,2	K562	blood:
8	chr10:112693592..112695425-chr10:112736222..112738778,2	MCF-7	breast:
9	chr10:112778849..112781525-chr10:112783454..112785651,2	K562	blood:
10	chr10:112677980..112679509-chr10:112776501..112778401,2	MCF-7	breast:
11	chr10:112746021..112748310-chr10:112757696..112760493,2	MCF-7	breast:
12	chr10:112722598..112724957-chr10:112728650..112731118,2	MCF-7	breast:
13	chr10:112677567..112680899-chr10:112734313..112738120,3	MCF-7	breast:
14	chr10:112776495..112778257-chr10:112780884..112782883,2	K562	blood:
15	chr10:112677043..112678843-chr10:112736477..112738600,2	MCF-7	breast:
16	chr10:112763502..112765745-chr10:112775415..112777948,2	MCF-7	breast:
17	chr10:112768505..112770915-chr10:112771228..112772833,2	K562	blood:
18	chr10:112728533..112731147-chr10:112731609..112733166,2	K562	blood:
19	chr10:112770762..112772712-chr10:112775005..112777166,2	K562	blood:
20	chr10:112747542..112749737-chr10:112770146..112772624,2	K562	blood:
21	chr10:112773361..112773861-chr7:2758450..2759306,2	MCF-7	breast:
22	chr10:112770762..112772712-chr10:112775005..112777166,2	K562	blood:
23	chr10:112754379..112754899-chr3:63098936..63099654,2	MCF-7	breast:
24	chr10:112763502..112765745-chr10:112775415..112777948,2	MCF-7	breast:
25	chr10:112725818..112728345-chr10:112732470..112734478,2	K562	blood:
26	chr10:112744001..112747517-chr10:112750803..112753417,3	MCF-7	breast:
27	chr10:112677296..112679780-chr10:112780580..112783275,2	MCF-7	breast:
28	chr10:112768505..112770915-chr10:112771228..112772833,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHOC2-2	chr10:112779678-112779747	XLOC_008614
2	lnc-SHOC2-2	chr10:112782246-112782449	XLOC_008614
3	lnc-SHOC2-1	chr10:112778764-112782745	NONHSAT016379
4	lnc-ADRA2A-4	chr10:112765815-112767131	l_376_chr10:112765430-112769802_testes
5	lnc-SHOC2-1	chr10:112776578-112777141	XLOC_008613
6	lnc-SHOC2-1	chr10:112779635-112779659	XLOC_008613
7	lnc-ADRA2A-4	chr10:112769625-112769802	l_376_chr10:112765430-112769802_testes
8	lnc-ADRA2A-4	chr10:112765431-112765801	l_376_chr10:112765430-112769802_testes

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548e-5p	chr10:112748698-112748719	MIMAT0026736
hsa-miR-548e-3p	chr10:112748736-112748757	MIMAT0005874

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SHOC2	hsa-miR-16-5p	chr10:112772691-112772711
2	SHOC2	hsa-miR-16-5p	chr10:112772704-112772710
3	SHOC2	hsa-miR-335-5p	chr10:112773037-112773060
4	SHOC2	hsa-miR-16-5p	chr10:112773034-112773058
5	SHOC2	hsa-miR-92a-3p	chr10:112772563-112772584

Variant related genes	Relation type
MIR548E	TF binding region
MIR548E	CpG island
ENSG00000214413	chromatin interactions
ENSG00000221214	chromatin interactions
ENSG00000108061	chromatin interactions
MIPOL1	miRNA target sites

Extended variants
information (count: 2044 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2044 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192283544	chr10:112730023-112730024	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs532795477	chr10:112730042-112730043	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185882200	chr10:112730046-112730047	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs34255229	chr10:112730145-112730146	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs566471949	chr10:112730149-112730150	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372274938	chr10:112730263-112730264	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548794443	chr10:112730291-112730292	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs567146918	chr10:112730297-112730298	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs137971776	chr10:112730397-112730398	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556391038	chr10:112730409-112730410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12762659	chr10:112730425-112730426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs142609050	chr10:112730464-112730465	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs56760151	chr10:112730488-112730489	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs78000451	chr10:112730500-112730501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566463144	chr10:112730503-112730504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535750978	chr10:112730527-112730528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs190207412	chr10:112730586-112730587	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550522067	chr10:112730594-112730595	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568951472	chr10:112730602-112730603	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542534807	chr10:112730617-112730618	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs11195392	chr10:112730678-112730679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs576572657	chr10:112730738-112730739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182023648	chr10:112730802-112730803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562492458	chr10:112730888-112730889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532934245	chr10:112730919-112730920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544640881	chr10:112730933-112730934	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559994226	chr10:112730957-112730958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs531410491	chr10:112730989-112730990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184410840	chr10:112730998-112730999	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548882180	chr10:112731019-112731020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369482336	chr10:112731023-112731024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs558004687	chr10:112731080-112731081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146088175	chr10:112731108-112731109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188753747	chr10:112731131-112731132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181356766	chr10:112731153-112731154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77379279	chr10:112731171-112731172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185636316	chr10:112731186-112731187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566097668	chr10:112731326-112731327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562881419	chr10:112731370-112731371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116075249	chr10:112731412-112731413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199936286	chr10:112731415-112731416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141402941	chr10:112731499-112731500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576577312	chr10:112731513-112731514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs557581124	chr10:112731567-112731568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375417427	chr10:112731571-112731572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556210000	chr10:112731580-112731581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs7088524	chr10:112731659-112731660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs544726755	chr10:112731675-112731676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559685127	chr10:112731690-112731691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs117188530	chr10:112731702-112731703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myxofibrosarcoma	16751306	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	16616336	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Sezary syndrome	18413736	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1143 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:112682000-112732400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr10:112692600-112732400	Weak transcription	Fetal Intestine Large	intestine
3	chr10:112697200-112740200	Weak transcription	Thymus	Thymus
4	chr10:112697200-112745400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr10:112700600-112764000	Weak transcription	Placenta	Placenta
6	chr10:112702400-112754800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr10:112705200-112789800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:112707200-112732200	Weak transcription	Pancreas	Pancrea
9	chr10:112707200-112732200	Weak transcription	NHEK	skin
10	chr10:112707200-112732400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr10:112707200-112737600	Weak transcription	Psoas Muscle	Psoas
12	chr10:112707200-112738800	Weak transcription	NH-A	brain
13	chr10:112707200-112755000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr10:112707200-112784200	Weak transcription	Left Ventricle	heart
15	chr10:112709000-112760000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr10:112710000-112736400	Weak transcription	HSMM	muscle
17	chr10:112711800-112735600	Weak transcription	Fetal Intestine Small	intestine
18	chr10:112712200-112732400	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr10:112712600-112732400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:112712600-112732400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr10:112712600-112732400	Weak transcription	Esophagus	oesophagus
22	chr10:112712600-112737200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr10:112712600-112737600	Weak transcription	HSMMtube	muscle
24	chr10:112712600-112737800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:112712600-112751200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr10:112712600-112755000	Weak transcription	Fetal Thymus	thymus
27	chr10:112712800-112736600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:112712800-112738000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr10:112712800-112751600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr10:112719400-112760800	Weak transcription	Fetal Muscle Leg	muscle
31	chr10:112719600-112732000	Weak transcription	A549	lung
32	chr10:112719800-112735800	Weak transcription	Fetal Stomach	stomach
33	chr10:112719800-112737600	Weak transcription	Rectal Smooth Muscle	rectum
34	chr10:112719800-112759200	Weak transcription	Fetal Lung	lung
35	chr10:112720800-112737600	Weak transcription	Ovary	ovary
36	chr10:112721600-112737600	Weak transcription	Fetal Heart	heart
37	chr10:112722600-112732400	Weak transcription	Brain Substantia Nigra	brain
38	chr10:112722800-112730600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr10:112722800-112736600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:112723200-112730800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr10:112723200-112783000	Weak transcription	Small Intestine	intestine
42	chr10:112723400-112732400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr10:112723600-112732600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr10:112724400-112737000	Weak transcription	Right Atrium	heart
45	chr10:112724400-112737800	Weak transcription	Stomach Mucosa	stomach
46	chr10:112724600-112748600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr10:112724800-112730600	Weak transcription	Brain Hippocampus Middle	brain
48	chr10:112724800-112738200	Weak transcription	Primary T cells from cord blood	blood
49	chr10:112724800-112739600	Weak transcription	Aorta	Aorta
50	chr10:112724800-112746600	Weak transcription	Primary monocytes fromperipheralblood	blood

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