Variant report

Variant	nsv519077
Chromosome Location	chr5:111506751-111519018
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:111510730-111511070	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:111510692-111511049	K562	blood:	n/a	n/a
3	ATF1	chr5:111508263-111508448	K562	blood:	n/a	n/a
4	BHLHE40	chr5:111508874-111509074	HepG2	liver:	n/a	n/a
5	BHLHE40	chr5:111508824-111509113	K562	blood:	n/a	n/a
6	CHD2	chr5:111509013-111509030	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr5:111510840-111510990	AG04449	skin:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
8	CTCF	chr5:111510780-111510930	HA-sp	spinal cord:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
9	CTCF	chr5:111510780-111510930	HL-60	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
10	CTCF	chr5:111510709-111511023	ECC-1	luminal epithelium:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
11	CTCF	chr5:111510800-111510950	HCPEpiC	choroid plexus:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
12	CTCF	chr5:111515160-111515310	HEK293	kidney:	n/a	n/a
13	CTCF	chr5:111510800-111510950	GM12868	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
14	CTCF	chr5:111510800-111510950	NHDF-neo	bronchial:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
15	CTCF	chr5:111510800-111510950	HAc	cerebellar:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
16	CTCF	chr5:111510820-111510970	GM12801	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
17	CTCF	chr5:111510787-111510789	GM12892	blood:	n/a	n/a
18	CTCF	chr5:111510740-111510890	HFF-Myc	foreskin:	n/a	chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
19	CTCF	chr5:111510657-111511049	A549	lung:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
20	CTCF	chr5:111511720-111511870	WI-38	lung:	n/a	n/a
21	CTCF	chr5:111510800-111510950	AG10803	skin:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
22	CTCF	chr5:111510820-111510970	MCF-7	breast:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
23	CTCF	chr5:111510800-111510950	GM12870	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
24	CTCF	chr5:111510761-111511046	T-47D	breast:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
25	CTCF	chr5:111510703-111511049	H1-hESC	embryonic stem cell:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
26	CTCF	chr5:111510737-111511017	MCF-7	breast:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
27	CTCF	chr5:111510700-111510850	WI-38	lung:	n/a	n/a
28	CTCF	chr5:111510800-111510950	A549	lung:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
29	CTCF	chr5:111510800-111510950	AG04450	lung:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
30	CTCF	chr5:111510780-111510930	GM06990	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
31	CTCF	chr5:111510760-111510910	GM12875	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
32	CTCF	chr5:111510760-111510910	HepG2	liver:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
33	CTCF	chr5:111510771-111511001	Pancreas_OC	pancreas:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
34	CTCF	chr5:111515140-111515290	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr5:111510695-111511033	A549	lung:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
36	CTCF	chr5:111510529-111511199	HCT-116	colon:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
37	CTCF	chr5:111510800-111510950	HCFaa	heart:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
38	CTCF	chr5:111510780-111510930	GM12875	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
39	CTCF	chr5:111510820-111510970	AG09309	skin:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
40	CTCF	chr5:111510840-111510990	Caco-2	colon:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
41	CTCF	chr5:111510800-111510950	HEK293	kidney:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
42	CTCF	chr5:111510644-111511048	K562	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
43	CTCF	chr5:111510760-111510910	HA-sp	spinal cord:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
44	CTCF	chr5:111510760-111510910	HRPEpiC	eye:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
45	CTCF	chr5:111510800-111510950	HPF	lung:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
46	CTCF	chr5:111510820-111510970	HUVEC	blood vessel:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
47	CTCF	chr5:111510860-111511010	GM12874	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
48	CTCF	chr5:111510800-111510950	NHEK	skin:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
49	CTCF	chr5:111510505-111511221	HCT-116	colon:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881
50	CTCF	chr5:111510800-111510950	GM12872	blood:	n/a	chr5:111510871-111510892 chr5:111510870-111510886 chr5:111510872-111510885 chr5:111510869-111510887 chr5:111510872-111510881

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:111506984-111507034	MCF10A-Er-Src	breast:	n/a
2	chr5:111506984-111507034	GM12892	blood:	n/a
3	chr5:111506984-111507034	AG09309	skin:	n/a
4	chr5:111506984-111507034	HIPEpiC	eye:	n/a
5	chr5:111506984-111507034	AG04449	skin:	fetal
6	chr5:111506984-111507034	SAEC	small airway:	n/a
7	chr5:111506984-111507034	AoSMC	blood vessel:	n/a
8	chr5:111506984-111507034	ECC-1	luminal epithelium:	n/a
9	chr5:111506984-111507034	PrEC	prostate:	n/a
10	chr5:111506984-111507034	GM12878	blood:	n/a
11	chr5:111506984-111507034	H1-hESC	embryonic stem cell:	embryo
12	chr5:111506984-111507034	AG10803	skin:	n/a
13	chr5:111506984-111507034	Caco-2	colon:	n/a
14	chr5:111506984-111507034	ProgFib	skin:	n/a
15	chr5:111506984-111507034	HRE	kidney:	n/a
16	chr5:111506984-111507034	HEEpiC	esophagus:	n/a
17	chr5:111506984-111507034	K562	blood:	n/a
18	chr5:111506984-111507034	AG04450	lung:	fetal
19	chr5:111506984-111507034	NHBE	bronchial:	n/a
20	chr5:111506984-111507034	NH-A	brain:	n/a
21	chr5:111506984-111507034	CMK	blood:	n/a
22	chr5:111506984-111507034	LNCaP	prostate:	n/a
23	chr5:111506984-111507034	SK-N-MC	brain:	n/a
24	chr5:111506984-111507034	HRCEpiC	kidney:	n/a
25	chr5:111506984-111507034	HAEpiC	amniotic membrane:	n/a
26	chr5:111506984-111507034	HMEC	breast:	n/a
27	chr5:111506984-111507034	NHDF-neo	bronchial:	n/a
28	chr5:111506984-111507034	Hepatocyte	liver:	n/a
29	chr5:111506984-111507034	HUVEC	blood vessel:	n/a
30	chr5:111506984-111507034	Jurkat	blood:	n/a
31	chr5:111506984-111507034	HCT-116	colon:	n/a
32	chr5:111506984-111507034	SK-N-SH	brain:	n/a
33	chr5:111506984-111507034	A549	lung:	n/a
34	chr5:111506984-111507034	PFSK-1	brain:	n/a
35	chr5:111506984-111507034	U87	brain:	n/a
36	chr5:111506984-111507034	AG09319	gingival:	n/a
37	chr5:111506984-111507034	HCF	heart:	n/a
38	chr5:111506984-111507034	HNPCEpiC	eye:	n/a
39	chr5:111506984-111507034	GM19239	blood:	n/a
40	chr5:111506984-111507034	HEK293	kidney:	embryo
41	chr5:111506984-111507034	HRPEpiC	eye:	n/a
42	chr5:111506984-111507034	SKMC	muscle:	n/a
43	chr5:111506984-111507034	HCPEpiC	choroid plexus:	n/a
44	chr5:111506984-111507034	GM06990	blood:	n/a
45	chr5:111506984-111507034	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:111506984-111507034	MCF-7	breast:	n/a
47	chr5:111506984-111507034	BJ	skin:	n/a
48	chr5:111506984-111507034	BE2_C	brain:	n/a
49	chr5:111506984-111507034	SK-N-SH_RA	brain:	n/a
50	chr5:111506984-111507034	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:111504901..111509125-chr5:111533307..111535722,3	K562	blood:
2	chr5:111499476..111503077-chr5:111510420..111514419,5	MCF-7	breast:
3	chr5:111515172..111516726-chr5:111516880..111519743,2	K562	blood:
4	chr5:111510441..111511287-chr5:111827720..111828672,2	K562	blood:
5	chr5:111500735..111502979-chr5:111515229..111518240,3	K562	blood:
6	chr5:111510545..111511303-chr5:111755668..111756501,4	K562	blood:
7	chr5:111510679..111511249-chr5:111755846..111756377,2	MCF-7	breast:
8	chr5:111510501..111511275-chr5:111521767..111522782,4	MCF-7	breast:
9	chr5:111504802..111506899-chr5:111509148..111511328,2	MCF-7	breast:
10	chr5:111505441..111507205-chr5:111752251..111753989,2	K562	blood:
11	chr5:111514597..111516763-chr5:111520415..111522514,2	K562	blood:
12	chr5:111510526..111511304-chr5:111827701..111828275,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APC-5	chr5:111509267-111509385	ENSG00000250882.1
2	lnc-APC-5	chr5:111510908-111511245	ENSG00000250882.1

Variant related genes	Relation type
ENSG00000250882	TF binding region
ENSG00000250882	CpG island
ENSG00000129595	chromatin interactions
ENSG00000250882	chromatin interactions

Extended variants
information (count: 510 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17266771	chr5:111506751-111506752	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142223822	chr5:111506803-111506804	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574941354	chr5:111506823-111506824	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs542373669	chr5:111506827-111506828	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs563650785	chr5:111506866-111506867	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs531001692	chr5:111506868-111506869	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147418089	chr5:111506886-111506887	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188760995	chr5:111506969-111506970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564248020	chr5:111506977-111506978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528643446	chr5:111506984-111506985	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs547717114	chr5:111506996-111506997	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs565926475	chr5:111507001-111507002	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs547193271	chr5:111507048-111507049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368242082	chr5:111507077-111507078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536073944	chr5:111507094-111507095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139764364	chr5:111507195-111507196	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs193164118	chr5:111507245-111507246	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs569679646	chr5:111507248-111507249	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs377478510	chr5:111507252-111507253	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536735896	chr5:111507312-111507313	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs72663313	chr5:111507323-111507324	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs576428951	chr5:111507325-111507326	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs559574722	chr5:111507387-111507388	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs534275872	chr5:111507467-111507468	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs77783227	chr5:111507471-111507472	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs575047638	chr5:111507487-111507488	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs542083500	chr5:111507510-111507511	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs374227038	chr5:111507573-111507574	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs577401155	chr5:111507615-111507616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139331285	chr5:111507622-111507623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs386691153	chr5:111507623-111507624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374317549	chr5:111507625-111507626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs199670178	chr5:111507626-111507627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546315126	chr5:111507637-111507638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183300141	chr5:111507670-111507671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528506055	chr5:111507706-111507707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79796459	chr5:111507747-111507748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539962549	chr5:111507757-111507758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529980463	chr5:111507775-111507776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568921740	chr5:111507791-111507792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539516804	chr5:111507804-111507805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528408743	chr5:111507806-111507807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188353017	chr5:111507817-111507818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77689524	chr5:111507826-111507827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566574451	chr5:111507900-111507901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551861837	chr5:111507934-111507935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114939751	chr5:111507935-111507936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10068405	chr5:111507947-111507948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs10054719	chr5:111508008-111508009	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs191876327	chr5:111508027-111508028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Prostate cancer	22341455	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111497600-111538600	Weak transcription	Small Intestine	intestine
2	chr5:111498200-111518800	Weak transcription	Right Atrium	heart
3	chr5:111498400-111506800	Strong transcription	Adipose Nuclei	Adipose
4	chr5:111498800-111506800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:111498800-111507600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:111499600-111507200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:111499600-111510800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr5:111499800-111510600	Weak transcription	Colon Smooth Muscle	Colon
9	chr5:111500000-111510600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr5:111500200-111510600	Weak transcription	Brain Anterior Caudate	brain
11	chr5:111500400-111510600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:111500600-111508800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr5:111500800-111510600	Weak transcription	NHEK	skin
14	chr5:111501400-111546400	Weak transcription	Spleen	Spleen
15	chr5:111502200-111510600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:111502200-111510600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr5:111502200-111510600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr5:111502200-111511000	Weak transcription	Brain Substantia Nigra	brain
19	chr5:111502400-111510600	Weak transcription	Fetal Heart	heart
20	chr5:111502400-111510600	Weak transcription	K562	blood
21	chr5:111502400-111510600	Weak transcription	NH-A	brain
22	chr5:111502400-111518800	Weak transcription	Pancreas	Pancrea
23	chr5:111502400-111546400	Weak transcription	Aorta	Aorta
24	chr5:111502600-111507000	Weak transcription	HMEC	breast
25	chr5:111502600-111509600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr5:111502600-111510600	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr5:111502600-111510600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:111502600-111510600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr5:111502600-111510600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:111502600-111510600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr5:111502600-111510600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr5:111502800-111507200	Weak transcription	Brain Germinal Matrix	brain
33	chr5:111502800-111509800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr5:111502800-111510600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr5:111502800-111546000	Weak transcription	Ovary	ovary
36	chr5:111503000-111510400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr5:111503000-111510600	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr5:111503400-111508600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:111503600-111506800	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr5:111503600-111507000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr5:111503600-111510600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr5:111503600-111510600	Weak transcription	Brain Angular Gyrus	brain
43	chr5:111503600-111510600	Weak transcription	Fetal Intestine Small	intestine
44	chr5:111503600-111510600	Weak transcription	Dnd41	blood
45	chr5:111503600-111519000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr5:111503600-111527800	Weak transcription	Psoas Muscle	Psoas
47	chr5:111503600-111537400	Weak transcription	Lung	lung
48	chr5:111503800-111508600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr5:111503800-111508800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr5:111503800-111510600	Weak transcription	H1 Cell Line	embryonic stem cell

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