Variant report

Variant	nsv524007
Chromosome Location	chr1:247098587-247162658
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:512)
CpG islands
(count:247)
Chromatin interactive
region (count:39)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:247123214-247123710	K562	blood:	n/a	n/a
2	ARID3A	chr1:247110706-247110906	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:247134751-247134857	HepG2	liver:	n/a	n/a
4	ATF1	chr1:247123316-247123705	K562	blood:	n/a	n/a
5	ATF2	chr1:247125667-247126071	GM12878	blood:	n/a	n/a
6	BACH1	chr1:247123309-247123710	K562	blood:	n/a	n/a
7	BATF	chr1:247125685-247126106	GM12878	blood:	n/a	n/a
8	BATF	chr1:247134750-247134944	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:247134725-247134937	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:247123207-247123210	K562	blood:	n/a	n/a
11	BHLHE40	chr1:247123261-247123622	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:247113475-247113478	K562	blood:	n/a	n/a
13	BHLHE40	chr1:247123542-247123742	K562	blood:	n/a	n/a
14	CBX3	chr1:247131709-247132145	K562	blood:	n/a	n/a
15	CBX3	chr1:247149994-247151026	K562	blood:	n/a	n/a
16	CBX3	chr1:247151634-247151960	K562	blood:	n/a	n/a
17	CBX3	chr1:247134562-247135051	K562	blood:	n/a	n/a
18	CBX3	chr1:247131794-247132102	K562	blood:	n/a	n/a
19	CBX3	chr1:247150129-247150801	K562	blood:	n/a	n/a
20	CBX3	chr1:247151598-247152049	K562	blood:	n/a	n/a
21	CBX3	chr1:247134728-247134995	K562	blood:	n/a	n/a
22	CCNT2	chr1:247123295-247123721	K562	blood:	n/a	n/a
23	CEBPB	chr1:247141630-247141951	HepG2	liver:	n/a	chr1:247141770-247141781
24	CEBPB	chr1:247105193-247105422	A549	lung:	n/a	chr1:247105338-247105349
25	CEBPB	chr1:247105185-247105428	Hela-S3	cervix:	n/a	chr1:247105338-247105349
26	CEBPB	chr1:247141588-247141951	IMR90	lung:	n/a	chr1:247141770-247141781
27	CEBPB	chr1:247147927-247147987	K562	blood:	n/a	chr1:247147941-247147952
28	CEBPB	chr1:247111859-247112182	K562	blood:	n/a	chr1:247112011-247112020 chr1:247112009-247112020 chr1:247112011-247112022
29	CEBPB	chr1:247105230-247105442	H1-hESC	embryonic stem cell:	n/a	chr1:247105338-247105349
30	CEBPB	chr1:247159223-247159333	K562	blood:	n/a	n/a
31	CEBPB	chr1:247125807-247125992	HepG2	liver:	n/a	chr1:247125952-247125963
32	CEBPB	chr1:247105183-247105522	IMR90	lung:	n/a	chr1:247105338-247105349
33	CEBPB	chr1:247105179-247105433	K562	blood:	n/a	chr1:247105338-247105349
34	CEBPB	chr1:247158287-247158490	HepG2	liver:	n/a	n/a
35	CEBPB	chr1:247113361-247113420	K562	blood:	n/a	n/a
36	CEBPB	chr1:247141602-247141915	K562	blood:	n/a	chr1:247141770-247141781
37	CEBPB	chr1:247105167-247105444	HepG2	liver:	n/a	chr1:247105338-247105349
38	CEBPB	chr1:247114333-247114470	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:247141630-247141920	A549	lung:	n/a	chr1:247141770-247141781
40	CEBPB	chr1:247147865-247147976	HepG2	liver:	n/a	chr1:247147941-247147952
41	CEBPB	chr1:247123209-247123650	K562	blood:	n/a	chr1:247123341-247123354
42	CEBPB	chr1:247111869-247112148	HepG2	liver:	n/a	chr1:247112011-247112020 chr1:247112009-247112020 chr1:247112011-247112022
43	CEBPB	chr1:247109294-247109363	K562	blood:	n/a	chr1:247109324-247109337
44	CHD2	chr1:247123442-247123594	GM12878	blood:	n/a	n/a
45	CTCF	chr1:247134714-247134992	GM12892	blood:	n/a	n/a
46	CTCF	chr1:247134780-247134930	HMF	breast:	n/a	n/a
47	CTCF	chr1:247134780-247134930	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr1:247123480-247123630	HL-60	blood:	n/a	n/a
49	CTCF	chr1:247123500-247123650	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr1:247134780-247134930	GM12871	blood:	n/a	n/a

(count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:247150106-247150156	AG09319	gingival:	n/a
2	chr1:247150106-247150156	GM12892	blood:	n/a
3	chr1:247112228-247112278	ovcar-3	ovarian:	n/a
4	chr1:247150106-247150156	AG09319	gingival:	n/a
5	chr1:247150106-247150156	GM12892	blood:	n/a
6	chr1:247112228-247112278	ovcar-3	ovarian:	n/a
7	chr1:247150106-247150156	HEK293	kidney:	embryo
8	chr1:247112228-247112278	BE2_C	brain:	n/a
9	chr1:247109089-247109139	A549	lung:	n/a
10	chr1:247109089-247109139	IMR90	lung:	fetal
11	chr1:247109025-247109075	NHBE	bronchial:	n/a
12	chr1:247109025-247109075	NHDF-neo	bronchial:	n/a
13	chr1:247109089-247109139	HEK293	kidney:	embryo
14	chr1:247109025-247109075	HMEC	breast:	n/a
15	chr1:247109025-247109075	GM12878	blood:	n/a
16	chr1:247109089-247109139	GM12878	blood:	n/a
17	chr1:247109025-247109075	AG09309	skin:	n/a
18	chr1:247109089-247109139	BE2_C	brain:	n/a
19	chr1:247109089-247109139	NH-A	brain:	n/a
20	chr1:247109025-247109075	SKMC	muscle:	n/a
21	chr1:247112228-247112278	MCF10A-Er-Src	breast:	n/a
22	chr1:247109089-247109139	HIPEpiC	eye:	n/a
23	chr1:247109089-247109139	HAEpiC	amniotic membrane:	n/a
24	chr1:247112228-247112278	HAEpiC	amniotic membrane:	n/a
25	chr1:247112228-247112278	NT2-D1	testis:	n/a
26	chr1:247112228-247112278	NB4	blood:	n/a
27	chr1:247150106-247150156	HCM	heart:	n/a
28	chr1:247150106-247150156	AG10803	skin:	n/a
29	chr1:247112228-247112278	HRE	kidney:	n/a
30	chr1:247109089-247109139	GM06990	blood:	n/a
31	chr1:247150106-247150156	GM19239	blood:	n/a
32	chr1:247109089-247109139	GM12892	blood:	n/a
33	chr1:247150106-247150156	HRCEpiC	kidney:	n/a
34	chr1:247109089-247109139	HNPCEpiC	eye:	n/a
35	chr1:247150106-247150156	PrEC	prostate:	n/a
36	chr1:247150106-247150156	ProgFib	skin:	n/a
37	chr1:247109089-247109139	NT2-D1	testis:	n/a
38	chr1:247150106-247150156	NHDF-neo	bronchial:	n/a
39	chr1:247112228-247112278	NH-A	brain:	n/a
40	chr1:247109025-247109075	ProgFib	skin:	n/a
41	chr1:247112228-247112278	HIPEpiC	eye:	n/a
42	chr1:247109025-247109075	SAEC	small airway:	n/a
43	chr1:247109025-247109075	HIPEpiC	eye:	n/a
44	chr1:247109089-247109139	U87	brain:	n/a
45	chr1:247112228-247112278	AoSMC	blood vessel:	n/a
46	chr1:247150106-247150156	NT2-D1	testis:	n/a
47	chr1:247150106-247150156	A549	lung:	n/a
48	chr1:247109025-247109075	U87	brain:	n/a
49	chr1:247150106-247150156	HAEpiC	amniotic membrane:	n/a
50	chr1:247150106-247150156	HL-60	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:247094518..247097018-chr1:247145719..247148664,2	MCF-7	breast:
2	chr1:247094081..247096260-chr1:247101445..247103602,2	MCF-7	breast:
3	chr1:247137339..247140267-chr1:247140866..247143086,4	K562	blood:
4	chr1:247093751..247096422-chr1:247117733..247120065,2	K562	blood:
5	chr1:247099451..247101729-chr1:247109483..247112346,2	K562	blood:
6	chr1:247140226..247142417-chr1:247149478..247152457,2	K562	blood:
7	chr1:247150077..247152155-chr1:247154277..247156770,2	K562	blood:
8	chr1:247093661..247096867-chr1:247100699..247105477,5	K562	blood:
9	chr1:247106858..247108880-chr1:247109823..247112372,2	MCF-7	breast:
10	chr1:247111510..247113379-chr1:247137669..247139614,2	K562	blood:
11	chr1:247033154..247036008-chr1:247106994..247108758,2	MCF-7	breast:
12	chr1:247140883..247143696-chr1:247267943..247270450,3	MCF-7	breast:
13	chr1:247112074..247113587-chr1:247113622..247116618,2	MCF-7	breast:
14	chr1:247114794..247117413-chr1:247121906..247123599,2	K562	blood:
15	chr1:247099451..247101729-chr1:247109483..247112346,2	K562	blood:
16	chr1:246946643..246948588-chr1:247104112..247106785,2	K562	blood:
17	chr1:247158690..247160814-chr11:10829475..10831701,2	MCF-7	breast:
18	chr1:247138215..247140006-chr1:247242158..247244457,2	K562	blood:
19	chr1:247162509..247164222-chr1:247168923..247171107,2	MCF-7	breast:
20	chr1:247094890..247097025-chr1:247137891..247140739,2	K562	blood:
21	chr1:247114794..247117413-chr1:247121906..247123599,2	K562	blood:
22	chr1:247093366..247095419-chr1:247122181..247124867,2	K562	blood:
23	chr1:247140498..247143013-chr1:247145266..247147665,2	K562	blood:
24	chr1:247093611..247096664-chr1:247097317..247101445,6	MCF-7	breast:
25	chr1:247150077..247152155-chr1:247154277..247156770,2	K562	blood:
26	chr1:247106858..247108880-chr1:247109823..247112372,2	MCF-7	breast:
27	chr1:247140226..247142417-chr1:247149478..247152457,2	K562	blood:
28	chr1:247134027..247135891-chr1:247168950..247171611,2	K562	blood:
29	chr1:247112074..247113587-chr1:247113622..247116618,2	MCF-7	breast:
30	chr1:247136099..247140606-chr1:247141190..247144010,6	K562	blood:
31	chr1:247145097..247146678-chr1:247148555..247150310,2	K562	blood:
32	chr1:247145097..247146678-chr1:247148555..247150310,2	K562	blood:
33	chr1:247095350..247097520-chr1:247156671..247158364,2	K562	blood:
34	chr1:247134263..247136085-chr1:247241844..247243624,2	K562	blood:
35	chr1:247095732..247098585-chr1:247108516..247110039,2	K562	blood:
36	chr1:247136099..247140606-chr1:247141190..247144010,6	K562	blood:
37	chr1:247140498..247143013-chr1:247145266..247147665,2	K562	blood:
38	chr1:247111510..247113379-chr1:247137669..247139614,2	K562	blood:
39	chr1:247137339..247140267-chr1:247140866..247143086,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHCTF1-3	chr1:247108980-247109129	NONHSAT010746
2	lnc-AHCTF1-3	chr1:247130997-247131094	NR_037892
3	lnc-AHCTF1-3	chr1:247151423-247151557	NONHSAT010746
4	lnc-AHCTF1-3	chr1:247130997-247131094	NONHSAT010746
5	lnc-AHCTF1-3	chr1:247108849-247109129	NR_037892
6	lnc-AHCTF1-3	chr1:247108849-247109129	NR_037894
7	lnc-AHCTF1-3	chr1:247143142-247143306	NR_037894
8	lnc-AHCTF1-3	chr1:247130997-247131094	NR_037894
9	lnc-AHCTF1-3	chr1:247162650-247162742	NR_037894
10	lnc-AHCTF1-3	chr1:247151423-247151557	NR_037892
11	lnc-AHCTF1-3	chr1:247151423-247151557	NR_037894
12	lnc-AHCTF1-3	chr1:247162650-247162742	NR_037892

No data

Variant related genes	Relation type
AHCTF1	TF binding region
AHCTF1	CpG island
ENSG00000153207	chromatin interactions
ENSG00000246308	chromatin interactions
ENSG00000197472	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000135747	chromatin interactions

Extended variants
information (count: 2760 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2760 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4971278	chr1:247098587-247098588	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112301800	chr1:247098611-247098612	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565420810	chr1:247098617-247098618	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs575482623	chr1:247098618-247098619	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548665404	chr1:247098625-247098626	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs544394665	chr1:247098650-247098651	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561058080	chr1:247098665-247098666	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530087228	chr1:247098678-247098679	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs74737151	chr1:247098705-247098706	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs142454419	chr1:247098725-247098726	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs560501445	chr1:247098873-247098874	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs181511165	chr1:247098909-247098910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs186106402	chr1:247099073-247099074	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535640293	chr1:247099106-247099107	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569170608	chr1:247099108-247099109	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531576676	chr1:247099110-247099111	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369250380	chr1:247099120-247099121	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548362844	chr1:247099131-247099132	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs146601463	chr1:247099148-247099149	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs115927525	chr1:247099154-247099155	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190072664	chr1:247099172-247099173	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs570458304	chr1:247099191-247099192	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539061703	chr1:247099226-247099227	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs558864472	chr1:247099231-247099232	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575495135	chr1:247099288-247099289	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs182811244	chr1:247099299-247099300	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554713344	chr1:247099319-247099320	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547615952	chr1:247099335-247099336	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185934480	chr1:247099336-247099337	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372603678	chr1:247099337-247099338	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs540753280	chr1:247099366-247099367	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs60311679	chr1:247099374-247099375	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs575759083	chr1:247099382-247099383	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs545866226	chr1:247099386-247099387	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs74152763	chr1:247099476-247099477	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs376508264	chr1:247099514-247099515	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191133217	chr1:247099569-247099570	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs183812237	chr1:247099599-247099600	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568296370	chr1:247099608-247099609	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377244914	chr1:247099610-247099611	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs188927184	chr1:247099612-247099613	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547518296	chr1:247099657-247099658	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570447252	chr1:247099660-247099661	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369865451	chr1:247099686-247099687	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370526092	chr1:247099692-247099693	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs2800223	chr1:247099693-247099694	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs200388962	chr1:247099758-247099759	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs372870660	chr1:247099770-247099771	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs143047863	chr1:247099802-247099803	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538113570	chr1:247099848-247099849	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Bipolar disorder	19114987	CNVD
Lung adenocarcinoma	21935476	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Lobular carcinoma	20658264	CNVD
Malaria	21633513	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:727 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:247095800-247124800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:247096000-247101600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:247096000-247101800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:247096000-247101800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr1:247096000-247101800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr1:247096000-247102000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:247096000-247104600	Weak transcription	Fetal Brain Female	brain
8	chr1:247096000-247110600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr1:247096000-247110800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr1:247096000-247110800	Weak transcription	Right Atrium	heart
11	chr1:247096000-247114600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:247096000-247121000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:247096000-247121800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:247096000-247125000	Weak transcription	Brain Germinal Matrix	brain
15	chr1:247096000-247130400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:247096000-247131600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr1:247096000-247131800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:247096200-247098600	Weak transcription	Brain Anterior Caudate	brain
19	chr1:247096200-247101800	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr1:247096200-247101800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:247096200-247102000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:247096200-247106800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr1:247096200-247106800	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:247096200-247109800	Weak transcription	HUVEC	blood vessel
25	chr1:247096200-247110000	Weak transcription	HepG2	liver
26	chr1:247096200-247110600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:247096200-247112000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr1:247096200-247112200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr1:247096200-247117400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:247096200-247123000	Weak transcription	K562	blood
31	chr1:247096200-247128400	Weak transcription	Fetal Stomach	stomach
32	chr1:247096400-247101800	Weak transcription	Dnd41	blood
33	chr1:247096400-247102000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:247096400-247110600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr1:247097000-247102000	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr1:247097800-247099000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr1:247098000-247098600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr1:247098600-247098800	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr1:247098600-247099000	Enhancers	Brain Anterior Caudate	brain
40	chr1:247101800-247102400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr1:247101800-247102800	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr1:247101800-247102800	Strong transcription	Cortex derived primary cultured neurospheres	brain
43	chr1:247101800-247102800	Strong transcription	Dnd41	blood
44	chr1:247101800-247103000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:247101800-247103200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr1:247102000-247102800	Strong transcription	H9 Cell Line	embryonic stem cell
47	chr1:247102000-247102800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:247102000-247103000	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr1:247102000-247103000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:247102400-247123000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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