Variant report

Variant	nsv877519
Chromosome Location	chr3:136035737-136279390
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1481)
CpG islands
(count:428)
Chromatin interactive
region (count:82)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1481 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:136264594-136264721	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:136219790-136219934	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:136110571-136110781	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:136070881-136071004	K562	blood:	n/a	n/a
5	ARID3A	chr3:136265535-136265813	K562	blood:	n/a	n/a
6	ARID3A	chr3:136221984-136222240	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:136217754-136218232	HepG2	liver:	n/a	n/a
8	ATF1	chr3:136049764-136050130	K562	blood:	n/a	n/a
9	ATF1	chr3:136227712-136227915	K562	blood:	n/a	n/a
10	BACH1	chr3:136082189-136082234	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr3:136072401-136072734	GM12878	blood:	n/a	n/a
12	BATF	chr3:136072399-136072681	GM12878	blood:	n/a	n/a
13	BCLAF1	chr3:136110406-136110854	GM12878	blood:	n/a	n/a
14	BCLAF1	chr3:136266136-136266529	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:136266318-136266353	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:136217855-136218178	HepG2	liver:	n/a	n/a
17	BRCA1	chr3:136271579-136271619	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr3:136207496-136207508	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr3:136174937-136175405	K562	blood:	n/a	n/a
20	CBX3	chr3:136175073-136175489	HCT-116	colon:	n/a	n/a
21	CBX3	chr3:136251284-136251617	K562	blood:	n/a	n/a
22	CBX3	chr3:136176200-136176544	K562	blood:	n/a	n/a
23	CBX3	chr3:136175060-136175369	K562	blood:	n/a	n/a
24	CCNT2	chr3:136153373-136153573	K562	blood:	n/a	n/a
25	CCNT2	chr3:136155958-136156415	K562	blood:	n/a	n/a
26	CCNT2	chr3:136062628-136063030	K562	blood:	n/a	n/a
27	CEBPB	chr3:136111448-136111691	HepG2	liver:	n/a	chr3:136111559-136111570
28	CEBPB	chr3:136263402-136263741	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:136085138-136085456	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:136125721-136126097	K562	blood:	n/a	chr3:136125860-136125873 chr3:136125924-136125935
31	CEBPB	chr3:136262231-136262562	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:136062692-136063434	IMR90	lung:	n/a	chr3:136063313-136063324 chr3:136063311-136063322
33	CEBPB	chr3:136195217-136195495	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr3:136063231-136063411	HepG2	liver:	n/a	chr3:136063313-136063324 chr3:136063311-136063322
35	CEBPB	chr3:136171262-136171415	Hela-S3	cervix:	n/a	chr3:136171356-136171367
36	CEBPB	chr3:136171217-136171413	H1-hESC	embryonic stem cell:	n/a	chr3:136171356-136171367
37	CEBPB	chr3:136195120-136195455	MCF-7	breast:	n/a	n/a
38	CEBPB	chr3:136153226-136153572	K562	blood:	n/a	n/a
39	CEBPB	chr3:136221930-136222301	HepG2	liver:	n/a	chr3:136222114-136222125 chr3:136222112-136222123 chr3:136222114-136222123
40	CEBPB	chr3:136125735-136126114	Hela-S3	cervix:	n/a	chr3:136125860-136125873 chr3:136125924-136125935
41	CEBPB	chr3:136111498-136111599	HepG2	liver:	n/a	chr3:136111559-136111570
42	CEBPB	chr3:136051558-136051884	IMR90	lung:	n/a	n/a
43	CEBPB	chr3:136125727-136126112	K562	blood:	n/a	chr3:136125860-136125873 chr3:136125924-136125935
44	CEBPB	chr3:136133390-136133658	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:136260862-136261149	IMR90	lung:	n/a	n/a
46	CEBPB	chr3:136111453-136111640	MCF-7	breast:	n/a	chr3:136111559-136111570
47	CEBPB	chr3:136111450-136111678	Hela-S3	cervix:	n/a	chr3:136111559-136111570
48	CEBPB	chr3:136260874-136261157	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:136238094-136238382	HepG2	liver:	n/a	chr3:136238219-136238232 chr3:136238219-136238230
50	CEBPB	chr3:136195174-136195526	A549	lung:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:136231858-136231908	SK-N-SH_RA	brain:	n/a
2	chr3:136231858-136231908	SK-N-SH_RA	brain:	n/a
3	chr3:136062740-136062790	IMR90	lung:	fetal
4	chr3:136069371-136069421	ECC-1	luminal epithelium:	n/a
5	chr3:136069371-136069421	SKMC	muscle:	n/a
6	chr3:136069371-136069421	AG09319	gingival:	n/a
7	chr3:136231858-136231908	BJ	skin:	n/a
8	chr3:136062740-136062790	LNCaP	prostate:	n/a
9	chr3:136194317-136194367	HUVEC	blood vessel:	n/a
10	chr3:136069371-136069421	MCF-7	breast:	n/a
11	chr3:136062740-136062790	GM12892	blood:	n/a
12	chr3:136194317-136194367	GM19239	blood:	n/a
13	chr3:136194317-136194367	Jurkat	blood:	n/a
14	chr3:136192388-136192438	ovcar-3	ovarian:	n/a
15	chr3:136192388-136192438	NB4	blood:	n/a
16	chr3:136056056-136056106	AG09309	skin:	n/a
17	chr3:136192388-136192438	NH-A	brain:	n/a
18	chr3:136231858-136231908	HCT-116	colon:	n/a
19	chr3:136056056-136056106	H1-hESC	embryonic stem cell:	embryo
20	chr3:136052698-136052748	HUVEC	blood vessel:	n/a
21	chr3:136231858-136231908	AG10803	skin:	n/a
22	chr3:136056056-136056106	HMEC	breast:	n/a
23	chr3:136052698-136052748	ovcar-3	ovarian:	n/a
24	chr3:136192388-136192438	AoSMC	blood vessel:	n/a
25	chr3:136052698-136052748	Hepatocyte	liver:	n/a
26	chr3:136192388-136192438	HepG2	liver:	n/a
27	chr3:136231858-136231908	HEK293	kidney:	embryo
28	chr3:136194317-136194367	HCM	heart:	n/a
29	chr3:136062740-136062790	Hepatocyte	liver:	n/a
30	chr3:136231858-136231908	HMEC	breast:	n/a
31	chr3:136231858-136231908	A549	lung:	n/a
32	chr3:136192388-136192438	K562	blood:	n/a
33	chr3:136069371-136069421	NH-A	brain:	n/a
34	chr3:136069371-136069421	NB4	blood:	n/a
35	chr3:136192388-136192438	SK-N-MC	brain:	n/a
36	chr3:136069371-136069421	HCM	heart:	n/a
37	chr3:136062740-136062790	SAEC	small airway:	n/a
38	chr3:136056056-136056106	IMR90	lung:	fetal
39	chr3:136194317-136194367	BE2_C	brain:	n/a
40	chr3:136052698-136052748	GM19239	blood:	n/a
41	chr3:136192388-136192438	GM12892	blood:	n/a
42	chr3:136194317-136194367	MCF-7	breast:	n/a
43	chr3:136062740-136062790	SK-N-SH	brain:	n/a
44	chr3:136194317-136194367	HMEC	breast:	n/a
45	chr3:136194317-136194367	HAEpiC	amniotic membrane:	n/a
46	chr3:136192388-136192438	BJ	skin:	n/a
47	chr3:136052698-136052748	HepG2	liver:	n/a
48	chr3:136194317-136194367	AoSMC	blood vessel:	n/a
49	chr3:136069371-136069421	Jurkat	blood:	n/a
50	chr3:136052698-136052748	HCM	heart:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:136111355..136112233-chr3:136471072..136471651,2	MCF-7	breast:
2	chr3:135913544..135916307-chr3:136066201..136068318,4	MCF-7	breast:
3	chr3:136264546..136265090-chr3:136732553..136733310,2	MCF-7	breast:
4	chr3:136044505..136047310-chr3:136053454..136056821,3	MCF-7	breast:
5	chr3:136049332..136050837-chr3:136449297..136451050,2	MCF-7	breast:
6	chr3:136264257..136265039-chr3:136470501..136471464,2	MCF-7	breast:
7	chr3:136257749..136260401-chr3:136264258..136266069,2	MCF-7	breast:
8	chr3:135793932..135794670-chr3:136110487..136111189,2	MCF-7	breast:
9	chr3:136062780..136064469-chr3:136066543..136068055,2	K562	blood:
10	chr3:136048349..136049959-chr3:136063905..136066760,2	K562	blood:
11	chr3:136056019..136058370-chr3:136058786..136061509,2	K562	blood:
12	chr3:136208388..136211090-chr3:136467197..136470066,2	K562	blood:
13	chr3:136223066..136225762-chr3:136237795..136239369,2	MCF-7	breast:
14	chr3:136056870..136058632-chr3:136058786..136060783,2	K562	blood:
15	chr3:136262930..136265454-chr3:136470250..136473086,3	K562	blood:
16	chr3:136166580..136169214-chr3:136176961..136178739,2	MCF-7	breast:
17	chr3:136263091..136265454-chr3:136470690..136473476,4	K562	blood:
18	chr3:136237342..136239151-chr3:136470510..136472888,2	MCF-7	breast:
19	chr3:136162413..136165672-chr3:136470682..136473383,3	MCF-7	breast:
20	chr3:135967729..135968689-chr3:136062451..136063319,2	MCF-7	breast:
21	chr3:136056019..136058370-chr3:136058786..136061509,2	K562	blood:
22	chr3:136050884..136053004-chr3:136057100..136060594,3	K562	blood:
23	chr3:136033614..136036060-chr3:136051639..136053164,2	MCF-7	breast:
24	chr3:136233567..136235148-chr3:136468458..136469958,2	K562	blood:
25	chr3:136081787..136083945-chr3:136470263..136471870,2	MCF-7	breast:
26	chr3:136085761..136088566-chr3:136470764..136472314,2	K562	blood:
27	chr3:136224749..136227067-chr3:136470099..136472380,2	K562	blood:
28	chr3:136061498..136064773-chr3:136469426..136473116,3	MCF-7	breast:
29	chr3:136166580..136169214-chr3:136176961..136178739,2	MCF-7	breast:
30	chr3:135915139..135916754-chr3:136035024..136037890,2	K562	blood:
31	chr3:136050884..136053004-chr3:136057100..136060594,3	K562	blood:
32	chr3:135914307..135917128-chr3:136060550..136064409,7	MCF-7	breast:
33	chr3:136226210..136226915-chr3:136470643..136471376,2	MCF-7	breast:
34	chr3:136264021..136266298-chr3:136470657..136471752,36	MCF-7	breast:
35	chr3:136261604..136263396-chr3:136467886..136469461,2	K562	blood:
36	chr3:136279189..136281857-chr3:136298738..136300966,2	MCF-7	breast:
37	chr3:136264451..136265000-chr3:136732487..136733381,2	MCF-7	breast:
38	chr3:136029722..136031537-chr3:136047190..136050098,2	MCF-7	breast:
39	chr3:136069906..136072188-chr3:136072294..136075006,2	MCF-7	breast:
40	chr3:136257749..136260401-chr3:136264258..136266069,2	MCF-7	breast:
41	chr3:136247859..136250822-chr3:136470944..136473511,2	K562	blood:
42	chr3:136268066..136271170-chr3:136469546..136471486,3	MCF-7	breast:
43	chr3:135793753..135796262-chr3:136127645..136129401,2	K562	blood:
44	chr3:136069906..136072188-chr3:136072294..136075006,2	MCF-7	breast:
45	chr3:136056870..136058632-chr3:136058786..136060783,2	K562	blood:
46	chr3:136174603..136175192-chr3:136470736..136471549,2	MCF-7	breast:
47	chr3:136263152..136267364-chr3:136469698..136472182,6	MCF-7	breast:
48	chr3:136110218..136111115-chr3:136470727..136471338,4	MCF-7	breast:
49	chr3:135914471..135916410-chr3:136223365..136225971,2	MCF-7	breast:
50	chr3:136062780..136064469-chr3:136066543..136068055,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PCCB	hsa-miR-378a-3p	chr3:136046062-136046084

Variant related genes	Relation type
STAG1	TF binding region
RNU6-1284P	TF binding region
STAG1	CpG island
RNU6-1284P	CpG island
ENSG00000261758	chromatin interactions
ENSG00000118007	chromatin interactions
ENSG00000114054	chromatin interactions
ENSG00000200571	chromatin interactions
ENSG00000174579	chromatin interactions

Extended variants
information (count: 9704 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:9704 , 50 per page) page: 1 2 3 4 5 6 7 ... 195

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9833162	chr3:136035737-136035738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77495412	chr3:136035741-136035742	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs377048891	chr3:136035743-136035744	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs560080578	chr3:136035754-136035755	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377660729	chr3:136035795-136035796	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370504998	chr3:136035796-136035797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375282859	chr3:136035798-136035799	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367662015	chr3:136035801-136035802	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370304541	chr3:136035818-136035819	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375456332	chr3:136035819-136035820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528745130	chr3:136035855-136035856	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548780280	chr3:136035945-136035946	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533632504	chr3:136035973-136035974	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531047779	chr3:136036007-136036008	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550767110	chr3:136036026-136036027	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4317048	chr3:136036031-136036032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs397694948	chr3:136036075-136036076	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150034447	chr3:136036086-136036087	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186107946	chr3:136036107-136036108	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs521775	chr3:136036121-136036122	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553563456	chr3:136036127-136036128	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146136716	chr3:136036180-136036181	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553497092	chr3:136036188-136036189	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558462074	chr3:136036189-136036190	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138853479	chr3:136036200-136036201	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141485325	chr3:136036214-136036215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1291921	chr3:136036226-136036227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs61574458	chr3:136036255-136036256	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574518826	chr3:136036283-136036284	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542089819	chr3:136036294-136036295	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs543508370	chr3:136036314-136036315	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150815298	chr3:136036329-136036330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111319187	chr3:136036336-136036337	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115607602	chr3:136036342-136036343	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs863900	chr3:136036404-136036405	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543722760	chr3:136036469-136036470	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560119913	chr3:136036488-136036489	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575803989	chr3:136036490-136036491	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544901696	chr3:136036512-136036513	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528777526	chr3:136036523-136036524	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529426928	chr3:136036541-136036542	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs190621714	chr3:136036563-136036564	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530958995	chr3:136036569-136036570	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551062676	chr3:136036617-136036618	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570845944	chr3:136036640-136036641	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182450063	chr3:136036644-136036645	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546567863	chr3:136036672-136036673	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs79753610	chr3:136036688-136036689	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186148836	chr3:136036737-136036738	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs377027426	chr3:136036754-136036755	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18511947	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:4384 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135970600-136039400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr3:135981200-136052000	Weak transcription	NH-A	brain
3	chr3:135998000-136040200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr3:135999800-136038200	Weak transcription	Fetal Brain Male	brain
5	chr3:135999800-136061200	Weak transcription	Hela-S3	cervix
6	chr3:136000200-136038200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr3:136014200-136040000	Weak transcription	Small Intestine	intestine
8	chr3:136015000-136038800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr3:136016400-136038400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:136016800-136045600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr3:136017000-136040000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr3:136018200-136051400	Weak transcription	A549	lung
13	chr3:136019000-136038600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:136020200-136036400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:136020200-136039000	Weak transcription	Colon Smooth Muscle	Colon
16	chr3:136020200-136040200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr3:136020200-136045200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr3:136020400-136038400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr3:136020400-136045200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:136020400-136045200	Weak transcription	Colonic Mucosa	Colon
21	chr3:136020600-136035800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr3:136020600-136035800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:136020600-136035800	Weak transcription	Aorta	Aorta
24	chr3:136020600-136035800	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr3:136020600-136036000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr3:136020600-136036200	Weak transcription	Lung	lung
27	chr3:136020600-136036400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:136020600-136038000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr3:136020600-136038200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr3:136020600-136045000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr3:136020600-136045200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr3:136020800-136035800	Weak transcription	Fetal Lung	lung
33	chr3:136020800-136035800	Weak transcription	Ovary	ovary
34	chr3:136020800-136036200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:136020800-136037400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr3:136020800-136040200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr3:136020800-136040200	Weak transcription	Esophagus	oesophagus
38	chr3:136020800-136042200	Weak transcription	Placenta	Placenta
39	chr3:136020800-136043000	Weak transcription	HSMM	muscle
40	chr3:136020800-136045000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr3:136021000-136035800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr3:136021000-136035800	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr3:136021000-136036000	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr3:136021000-136036000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr3:136021000-136036200	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr3:136021000-136036200	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr3:136021000-136036400	Weak transcription	Rectal Smooth Muscle	rectum
48	chr3:136021000-136036600	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr3:136021000-136038600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr3:136021000-136038600	Weak transcription	Right Ventricle	heart

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