Variant report

Variant	nsv830714
Chromosome Location	chr1:98025090-98229416
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	BRCA1	chr1:98124459-98124526	GM12878	blood:	n/a	n/a
2	CEBPB	chr1:98211520-98211827	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:98049282-98049304	K562	blood:	n/a	n/a
4	CEBPB	chr1:98049246-98049365	H1-hESC	embryonic stem cell:	n/a	chr1:98049309-98049320
5	CEBPB	chr1:98198657-98198872	IMR90	lung:	n/a	chr1:98198701-98198714
6	CEBPB	chr1:98208137-98208487	IMR90	lung:	n/a	chr1:98208316-98208327
7	CEBPB	chr1:98177429-98177798	HepG2	liver:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
8	CEBPB	chr1:98031433-98031738	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:98038143-98038477	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:98133477-98133729	IMR90	lung:	n/a	chr1:98133577-98133588
11	CEBPB	chr1:98032993-98033294	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:98177450-98177788	K562	blood:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
13	CEBPB	chr1:98029529-98029805	MCF-7	breast:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
14	CEBPB	chr1:98067027-98067247	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:98156908-98156979	A549	lung:	n/a	n/a
16	CEBPB	chr1:98208214-98208462	Hela-S3	cervix:	n/a	chr1:98208316-98208327
17	CEBPB	chr1:98049201-98049463	IMR90	lung:	n/a	chr1:98049309-98049320
18	CEBPB	chr1:98221656-98222027	IMR90	lung:	n/a	chr1:98221861-98221870
19	CEBPB	chr1:98047808-98048044	HepG2	liver:	n/a	chr1:98047947-98047958
20	CEBPB	chr1:98029324-98029866	IMR90	lung:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
21	CEBPB	chr1:98177432-98177781	A549	lung:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
22	CEBPB	chr1:98029328-98029864	HepG2	liver:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
23	CEBPB	chr1:98208154-98208479	HepG2	liver:	n/a	chr1:98208316-98208327
24	CEBPB	chr1:98029511-98029813	H1-hESC	embryonic stem cell:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
25	CEBPB	chr1:98137133-98137371	HepG2	liver:	n/a	chr1:98137261-98137272 chr1:98137260-98137271 chr1:98137242-98137255 chr1:98137260-98137271 chr1:98137260-98137273
26	CEBPB	chr1:98193010-98193283	A549	lung:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
27	CEBPB	chr1:98039132-98039464	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:98177430-98177801	IMR90	lung:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
29	CEBPB	chr1:98064954-98065258	IMR90	lung:	n/a	chr1:98065102-98065113
30	CEBPB	chr1:98047844-98048025	A549	lung:	n/a	chr1:98047947-98047958
31	CEBPB	chr1:98134567-98134871	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:98039241-98039362	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:98049266-98049454	A549	lung:	n/a	chr1:98049309-98049320
34	CEBPB	chr1:98029335-98029853	Hela-S3	cervix:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
35	CEBPB	chr1:98140175-98140425	A549	lung:	n/a	chr1:98140277-98140288 chr1:98140279-98140288 chr1:98140277-98140288 chr1:98140279-98140288 chr1:98140277-98140290 chr1:98140277-98140290 chr1:98140279-98140288 chr1:98140279-98140288 chr1:98140277-98140290
36	CEBPB	chr1:98177451-98177785	H1-hESC	embryonic stem cell:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
37	CEBPB	chr1:98140134-98140417	IMR90	lung:	n/a	chr1:98140277-98140288 chr1:98140279-98140288 chr1:98140277-98140288 chr1:98140279-98140288 chr1:98140277-98140290 chr1:98140277-98140290 chr1:98140279-98140288 chr1:98140279-98140288 chr1:98140277-98140290
38	CEBPB	chr1:98047822-98048112	IMR90	lung:	n/a	chr1:98047947-98047958
39	CEBPB	chr1:98049168-98049482	HepG2	liver:	n/a	chr1:98049309-98049320
40	CEBPB	chr1:98133490-98133716	HepG2	liver:	n/a	chr1:98133577-98133588
41	CEBPB	chr1:98208209-98208432	H1-hESC	embryonic stem cell:	n/a	chr1:98208316-98208327
42	CEBPB	chr1:98064958-98065202	HepG2	liver:	n/a	chr1:98065102-98065113
43	CEBPB	chr1:98208142-98208499	A549	lung:	n/a	chr1:98208316-98208327
44	CEBPB	chr1:98039138-98039475	IMR90	lung:	n/a	n/a
45	CEBPB	chr1:98228781-98228989	HepG2	liver:	n/a	chr1:98228933-98228942 chr1:98228933-98228942 chr1:98228933-98228942 chr1:98228931-98228942 chr1:98228933-98228942 chr1:98228933-98228944
46	CEBPB	chr1:98177451-98177762	Hela-S3	cervix:	n/a	chr1:98177612-98177621 chr1:98177612-98177623 chr1:98177610-98177621 chr1:98177612-98177621 chr1:98177610-98177623 chr1:98177612-98177621 chr1:98177612-98177621 chr1:98177610-98177623
47	CEBPB	chr1:98029519-98029746	K562	blood:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685
48	CEBPB	chr1:98193045-98193294	HepG2	liver:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
49	CEBPB	chr1:98192995-98193291	IMR90	lung:	n/a	chr1:98193195-98193208 chr1:98193196-98193207
50	CEBPB	chr1:98029340-98029867	A549	lung:	n/a	chr1:98029675-98029684 chr1:98029675-98029684 chr1:98029500-98029509 chr1:98029500-98029509 chr1:98029675-98029684 chr1:98029673-98029686 chr1:98029674-98029685

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:98031839-98031889	ovcar-3	ovarian:	n/a
2	chr1:98031839-98031889	T-47D	breast:	n/a
3	chr1:98036695-98036745	PANC-1	pancreas:	n/a
4	chr1:98088314-98088364	T-47D	breast:	n/a
5	chr1:98036695-98036745	GM06990	blood:	n/a
6	chr1:98036695-98036745	HAEpiC	amniotic membrane:	n/a
7	chr1:98088314-98088364	NT2-D1	testis:	n/a
8	chr1:98036695-98036745	HCPEpiC	choroid plexus:	n/a
9	chr1:98031839-98031889	GM12878	blood:	n/a
10	chr1:98036695-98036745	SAEC	small airway:	n/a
11	chr1:98036695-98036745	HUVEC	blood vessel:	n/a
12	chr1:98088314-98088364	HEEpiC	esophagus:	n/a
13	chr1:98036695-98036745	HEK293	kidney:	embryo
14	chr1:98036695-98036745	HCF	heart:	n/a
15	chr1:98036695-98036745	HEEpiC	esophagus:	n/a
16	chr1:98036695-98036745	AG09309	skin:	n/a
17	chr1:98031839-98031889	HIPEpiC	eye:	n/a
18	chr1:98036695-98036745	AG09319	gingival:	n/a
19	chr1:98036695-98036745	HRE	kidney:	n/a
20	chr1:98031839-98031889	HepG2	liver:	n/a
21	chr1:98088314-98088364	AG09319	gingival:	n/a
22	chr1:98036695-98036745	RPTEC	kidney:	n/a
23	chr1:98031839-98031889	NHBE	bronchial:	n/a
24	chr1:98088314-98088364	MCF-7	breast:	n/a
25	chr1:98031839-98031889	PFSK-1	brain:	n/a
26	chr1:98031839-98031889	HNPCEpiC	eye:	n/a
27	chr1:98031839-98031889	LNCaP	prostate:	n/a
28	chr1:98036695-98036745	GM12891	blood:	n/a
29	chr1:98031839-98031889	AG04450	lung:	fetal
30	chr1:98031839-98031889	GM19239	blood:	n/a
31	chr1:98031839-98031889	PrEC	prostate:	n/a
32	chr1:98031839-98031889	HEK293	kidney:	embryo
33	chr1:98031839-98031889	AG04449	skin:	fetal
34	chr1:98088314-98088364	HCF	heart:	n/a
35	chr1:98036695-98036745	HNPCEpiC	eye:	n/a
36	chr1:98031839-98031889	SKMC	muscle:	n/a
37	chr1:98088314-98088364	Hela-S3	cervix:	n/a
38	chr1:98031839-98031889	SK-N-MC	brain:	n/a
39	chr1:98088314-98088364	RPTEC	kidney:	n/a
40	chr1:98036695-98036745	HRPEpiC	eye:	n/a
41	chr1:98088314-98088364	SAEC	small airway:	n/a
42	chr1:98036695-98036745	BJ	skin:	n/a
43	chr1:98031839-98031889	HCPEpiC	choroid plexus:	n/a
44	chr1:98031839-98031889	K562	blood:	n/a
45	chr1:98031839-98031889	SK-N-SH_RA	brain:	n/a
46	chr1:98088314-98088364	HNPCEpiC	eye:	n/a
47	chr1:98036695-98036745	CMK	blood:	n/a
48	chr1:98036695-98036745	NHDF-neo	bronchial:	n/a
49	chr1:98031839-98031889	HRE	kidney:	n/a
50	chr1:98031839-98031889	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:98139213..98141128-chr1:98143534..98146360,2	K562	blood:
2	chr1:98055252..98058071-chr1:98058495..98060527,2	K562	blood:
3	chr1:98123470..98125782-chr1:98130120..98131778,2	K562	blood:
4	chr1:98123470..98125782-chr1:98130120..98131778,2	K562	blood:
5	chr1:98215254..98218184-chr1:98219378..98221906,2	K562	blood:
6	chr1:98035531..98037801-chr1:98038552..98041185,2	K562	blood:
7	chr1:98215254..98218184-chr1:98219378..98221906,2	K562	blood:
8	chr1:98139213..98141128-chr1:98143534..98146360,2	K562	blood:
9	chr1:98035531..98037801-chr1:98038552..98041185,2	K562	blood:
10	chr1:97716792..97718843-chr1:98161897..98164294,2	K562	blood:
11	chr1:98228606..98230942-chr1:98231366..98234177,2	K562	blood:
12	chr1:98055044..98057543-chr1:98059775..98062568,2	MCF-7	breast:
13	chr1:98043717..98044559-chr1:114764772..114765348,2	Hela-S3	cervix:
14	chr1:98055252..98058071-chr1:98058495..98060527,2	K562	blood:
15	chr1:98055044..98057543-chr1:98059775..98062568,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPPR5.1-4	chr1:98213108-98213244	l_97_chr1:98213107-98217461
2	lnc-LPPR5.1-4	chr1:98229394-98229587	l_97_chr1:98213107-98217461
3	lnc-PTBP2-10	chr1:98051418-98051850	NONHSAT004717
4	lnc-LPPR5.1-4	chr1:98213403-98213506	l_97_chr1:98213107-98217461
5	lnc-LPPR5.1-4	chr1:98227401-98227713	l_97_chr1:98213107-98217461
6	lnc-LPPR5.1-4	chr1:98217399-98217461	l_97_chr1:98213107-98217461

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DPYD	hsa-miR-124-3p	chr1:98185550-98185569

Variant related genes	Relation type
DPYD	TF binding region
RPL26P9	TF binding region
DPYD	CpG island
RPL26P9	CpG island

Extended variants
information (count: 7225 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:7225 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538574946	chr1:98025111-98025112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569407256	chr1:98025119-98025120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542039203	chr1:98025144-98025145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7522200	chr1:98025195-98025196	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs142860494	chr1:98025208-98025209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558759027	chr1:98025219-98025220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7533929	chr1:98025242-98025243	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs186718540	chr1:98025259-98025260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191212190	chr1:98025275-98025276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572249781	chr1:98025344-98025345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75280548	chr1:98025357-98025358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536645590	chr1:98025367-98025368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556636338	chr1:98025427-98025428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576596003	chr1:98025464-98025465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545547961	chr1:98025490-98025491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565453565	chr1:98025507-98025508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35127872	chr1:98025540-98025541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2786537	chr1:98025592-98025593	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541672489	chr1:98025642-98025643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114733895	chr1:98025811-98025812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17377638	chr1:98025817-98025818	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs182366253	chr1:98025829-98025830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78015184	chr1:98025859-98025860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554610579	chr1:98025921-98025922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543359423	chr1:98025936-98025937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185149903	chr1:98025937-98025938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563145689	chr1:98025974-98025975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551874493	chr1:98026050-98026051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372196815	chr1:98026053-98026054	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149964104	chr1:98026061-98026062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377146536	chr1:98026114-98026115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs67653141	chr1:98026115-98026116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548416583	chr1:98026118-98026119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs61789184	chr1:98026134-98026135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74316989	chr1:98026140-98026141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75346203	chr1:98026142-98026143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539487149	chr1:98026154-98026155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146512228	chr1:98026175-98026176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12066229	chr1:98026230-98026231	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs189664401	chr1:98026257-98026258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570088332	chr1:98026285-98026286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568296745	chr1:98026369-98026370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558795040	chr1:98026400-98026401	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369682123	chr1:98026425-98026426	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565263985	chr1:98026442-98026443	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139939880	chr1:98026461-98026462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555183108	chr1:98026494-98026495	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183392876	chr1:98026514-98026515	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543731243	chr1:98026520-98026521	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547622406	chr1:98026560-98026561	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20803296	CNVD
Colorectal cancer	20653680	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97976600-98054200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:97976800-98051400	Weak transcription	Left Ventricle	heart
3	chr1:97996000-98037400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:97998600-98063800	Weak transcription	Right Ventricle	heart
5	chr1:97999400-98064600	Weak transcription	Psoas Muscle	Psoas
6	chr1:97999400-98074000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:98001200-98062400	Weak transcription	Fetal Lung	lung
8	chr1:98002000-98054600	Weak transcription	Lung	lung
9	chr1:98002000-98069400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr1:98002800-98058800	Weak transcription	Gastric	stomach
11	chr1:98004400-98058400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr1:98006400-98040600	Weak transcription	Pancreas	Pancrea
13	chr1:98007800-98058400	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr1:98007800-98075800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:98009800-98076800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr1:98009800-98112200	Weak transcription	HSMM	muscle
17	chr1:98012000-98054200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr1:98012200-98026400	Weak transcription	Aorta	Aorta
19	chr1:98012600-98036400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr1:98013400-98048600	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr1:98013600-98036400	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr1:98013600-98058800	Weak transcription	Esophagus	oesophagus
23	chr1:98015200-98038000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr1:98015200-98040200	Weak transcription	HSMMtube	muscle
25	chr1:98015200-98047000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:98015200-98054000	Weak transcription	Adipose Nuclei	Adipose
27	chr1:98015200-98058600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:98015200-98062000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr1:98015400-98038800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:98015600-98034600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr1:98015600-98058600	Weak transcription	Osteobl	bone
32	chr1:98017000-98036400	Weak transcription	NHDF-Ad	bronchial
33	chr1:98018400-98040400	Weak transcription	Small Intestine	intestine
34	chr1:98020000-98059000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr1:98020000-98060600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr1:98021600-98032600	Weak transcription	Stomach Smooth Muscle	stomach
37	chr1:98022800-98025200	Strong transcription	Primary B cells from cord blood	blood
38	chr1:98023200-98026000	Strong transcription	Primary hematopoietic stem cells	blood
39	chr1:98023200-98041000	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr1:98023200-98045400	Weak transcription	Fetal Intestine Small	intestine
41	chr1:98023600-98026200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr1:98023800-98036400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:98023800-98037200	Weak transcription	Primary T cells fromperipheralblood	blood
44	chr1:98023800-98053000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr1:98024200-98035200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr1:98024400-98035400	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr1:98024400-98038000	Weak transcription	Dnd41	blood
48	chr1:98024400-98039200	Weak transcription	Primary T cells from cord blood	blood
49	chr1:98025000-98031200	Strong transcription	Liver	Liver
50	chr1:98025200-98026200	Weak transcription	Primary B cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

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