Variant report

Variant	nsv876800
Chromosome Location	chr3:53038786-53113762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1807)
CpG islands
(count:794)
Chromatin interactive
region (count:71)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1807 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:53079923-53080078	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:53074378-53074816	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:53101853-53101925	K562	blood:	n/a	n/a
4	ARID3A	chr3:53090521-53090927	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:53106781-53106936	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:53066637-53066919	HepG2	liver:	n/a	n/a
7	ATF2	chr3:53106531-53107065	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:53106615-53107023	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:53080620-53080928	GM12878	blood:	n/a	n/a
10	ATF2	chr3:53080591-53080904	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:53085995-53086184	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:53078839-53078970	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:53079417-53081172	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:53106729-53106946	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:53065056-53065448	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCLAF1	chr3:53080452-53080983	GM12878	blood:	n/a	n/a
17	BCLAF1	chr3:53079955-53080354	GM12878	blood:	n/a	n/a
18	BCLAF1	chr3:53078329-53079258	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:53040502-53040694	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:53105956-53106407	K562	blood:	n/a	n/a
21	BHLHE40	chr3:53090633-53090756	K562	blood:	n/a	n/a
22	BHLHE40	chr3:53079792-53080082	K562	blood:	n/a	n/a
23	BHLHE40	chr3:53080388-53080805	K562	blood:	n/a	n/a
24	BHLHE40	chr3:53080387-53080740	A549	lung:	n/a	n/a
25	BHLHE40	chr3:53079770-53081260	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:53106663-53106995	GM12878	blood:	n/a	chr3:53106769-53106785
27	BHLHE40	chr3:53053064-53053368	K562	blood:	n/a	n/a
28	BHLHE40	chr3:53106791-53107608	K562	blood:	n/a	n/a
29	BRCA1	chr3:53105623-53105651	HepG2	liver:	n/a	n/a
30	BRCA1	chr3:53090665-53090674	HepG2	liver:	n/a	n/a
31	BRCA1	chr3:53106901-53106908	HepG2	liver:	n/a	n/a
32	CBX3	chr3:53106583-53106951	K562	blood:	n/a	n/a
33	CCNT2	chr3:53079023-53080645	K562	blood:	n/a	chr3:53080122-53080131
34	CEBPB	chr3:53084039-53084293	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:53060857-53060870	K562	blood:	n/a	n/a
36	CEBPB	chr3:53060779-53061025	HepG2	liver:	n/a	chr3:53060872-53060883
37	CEBPB	chr3:53112578-53112757	A549	lung:	n/a	chr3:53112708-53112719
38	CEBPB	chr3:53112597-53112805	Hela-S3	cervix:	n/a	chr3:53112708-53112719
39	CEBPB	chr3:53112563-53112796	HepG2	liver:	n/a	chr3:53112708-53112719
40	CEBPB	chr3:53056711-53057039	HepG2	liver:	n/a	chr3:53056861-53056872
41	CEBPB	chr3:53084000-53084311	HepG2	liver:	n/a	n/a
42	CEBPB	chr3:53074242-53074861	Hela-S3	cervix:	n/a	chr3:53074381-53074392 chr3:53074381-53074392
43	CEBPB	chr3:53042520-53042592	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr3:53067264-53067276	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr3:53106730-53106983	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:53073480-53073654	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:53084050-53084271	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:53074601-53074898	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:53056695-53057040	IMR90	lung:	n/a	chr3:53056861-53056872
50	CEBPB	chr3:53110932-53111219	HepG2	liver:	n/a	chr3:53111052-53111063

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:53084209-53084259	ovcar-3	ovarian:	n/a
2	chr3:53084209-53084259	ovcar-3	ovarian:	n/a
3	chr3:53078990-53079040	PFSK-1	brain:	n/a
4	chr3:53106725-53106775	AG04450	lung:	fetal
5	chr3:53080682-53080732	HepG2	liver:	n/a
6	chr3:53106725-53106775	SK-N-MC	brain:	n/a
7	chr3:53084209-53084259	AG09319	gingival:	n/a
8	chr3:53051694-53051744	HAEpiC	amniotic membrane:	n/a
9	chr3:53084209-53084259	NB4	blood:	n/a
10	chr3:53051694-53051744	BJ	skin:	n/a
11	chr3:53051694-53051744	AG10803	skin:	n/a
12	chr3:53080176-53080226	HIPEpiC	eye:	n/a
13	chr3:53075834-53075884	SK-N-SH	brain:	n/a
14	chr3:53079105-53079155	GM12892	blood:	n/a
15	chr3:53078218-53078268	GM06990	blood:	n/a
16	chr3:53042940-53042990	Caco-2	colon:	n/a
17	chr3:53051694-53051744	SAEC	small airway:	n/a
18	chr3:53080440-53080490	MCF10A-Er-Src	breast:	n/a
19	chr3:53078990-53079040	T-47D	breast:	n/a
20	chr3:53078990-53079040	AG10803	skin:	n/a
21	chr3:53042940-53042990	AoSMC	blood vessel:	n/a
22	chr3:53044901-53044951	HMEC	breast:	n/a
23	chr3:53044901-53044951	NB4	blood:	n/a
24	chr3:53080176-53080226	H1-hESC	embryonic stem cell:	embryo
25	chr3:53078218-53078268	T-47D	breast:	n/a
26	chr3:53084209-53084259	Hela-S3	cervix:	n/a
27	chr3:53051694-53051744	GM12891	blood:	n/a
28	chr3:53078990-53079040	Caco-2	colon:	n/a
29	chr3:53079796-53079846	SKMC	muscle:	n/a
30	chr3:53106725-53106775	LNCaP	prostate:	n/a
31	chr3:53078990-53079040	NHDF-neo	bronchial:	n/a
32	chr3:53084209-53084259	A549	lung:	n/a
33	chr3:53084209-53084259	GM12878	blood:	n/a
34	chr3:53078990-53079040	PANC-1	pancreas:	n/a
35	chr3:53042940-53042990	Hepatocyte	liver:	n/a
36	chr3:53084209-53084259	HRCEpiC	kidney:	n/a
37	chr3:53079105-53079155	T-47D	breast:	n/a
38	chr3:53044901-53044951	HAEpiC	amniotic membrane:	n/a
39	chr3:53084209-53084259	HRPEpiC	eye:	n/a
40	chr3:53079105-53079155	HRCEpiC	kidney:	n/a
41	chr3:53080682-53080732	NHDF-neo	bronchial:	n/a
42	chr3:53051694-53051744	HRCEpiC	kidney:	n/a
43	chr3:53042940-53042990	SK-N-SH_RA	brain:	n/a
44	chr3:53080682-53080732	MCF-7	breast:	n/a
45	chr3:53080682-53080732	U87	brain:	n/a
46	chr3:53044901-53044951	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:53075834-53075884	BE2_C	brain:	n/a
48	chr3:53075834-53075884	T-47D	breast:	n/a
49	chr3:53042940-53042990	ProgFib	skin:	n/a
50	chr3:53075834-53075884	NB4	blood:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:53047316..53051698-chr3:53056732..53062167,5	MCF-7	breast:
2	chr3:53056801..53057547-chr3:53179048..53179588,2	MCF-7	breast:
3	chr3:53068314..53070606-chr3:53078738..53080578,2	MCF-7	breast:
4	chr3:53091998..53093845-chr3:53107358..53110286,2	K562	blood:
5	chr3:53059584..53062030-chr3:53075790..53077753,2	K562	blood:
6	chr3:53105521..53108004-chr3:53109136..53111308,2	K562	blood:
7	chr3:53108616..53110693-chr3:53113648..53116561,3	K562	blood:
8	chr3:53045411..53048406-chr3:53050370..53052257,2	K562	blood:
9	chr3:52888069..52891024-chr3:53081330..53083131,2	K562	blood:
10	chr3:53106835..53109332-chr3:53109780..53113042,3	MCF-7	breast:
11	chr3:53054569..53056705-chr3:53106775..53108496,2	MCF-7	breast:
12	chr3:53072702..53076307-chr3:53077847..53082050,5	MCF-7	breast:
13	chr3:53079254..53083085-chr3:53089108..53091913,3	K562	blood:
14	chr3:53108616..53110693-chr3:53113648..53116561,3	K562	blood:
15	chr3:53060296..53062382-chr3:53075868..53077771,2	MCF-7	breast:
16	chr3:53078502..53082899-chr3:53088396..53093067,6	K562	blood:
17	chr3:52885301..52886003-chr3:53106363..53107313,2	K562	blood:
18	chr3:53089913..53093845-chr3:53106258..53110286,4	K562	blood:
19	chr3:53058305..53064318-chr3:53075790..53081540,9	K562	blood:
20	chr3:53037209..53039730-chr3:53079605..53081876,2	MCF-7	breast:
21	chr3:53099455..53102184-chr3:53105815..53107465,2	K562	blood:
22	chr3:53078061..53080828-chr3:53106166..53109030,2	K562	blood:
23	chr3:53061590..53065851-chr3:53079689..53082481,4	K562	blood:
24	chr3:53045411..53048406-chr3:53050370..53052257,2	K562	blood:
25	chr3:53069872..53071542-chr3:53073094..53075949,2	K562	blood:
26	chr3:53059584..53062030-chr3:53075790..53077753,2	K562	blood:
27	chr3:53099455..53102184-chr3:53105815..53107465,2	K562	blood:
28	chr3:52885415..52886070-chr3:53106396..53107102,2	MCF-7	breast:
29	chr3:53078034..53080828-chr3:53106166..53109030,3	K562	blood:
30	chr3:53060296..53062382-chr3:53075868..53077771,2	MCF-7	breast:
31	chr3:53047316..53051698-chr3:53056732..53062167,5	MCF-7	breast:
32	chr3:53085682..53086543-chr3:53106733..53107482,2	MCF-7	breast:
33	chr3:53054569..53056705-chr3:53106775..53108496,2	MCF-7	breast:
34	chr3:53111563..53113216-chr3:53114335..53116434,2	K562	blood:
35	chr3:53053108..53056030-chr3:53104834..53107226,3	K562	blood:
36	chr3:52964018..52964668-chr3:53072552..53073141,2	MCF-7	breast:
37	chr3:53105521..53108004-chr3:53109136..53111308,2	K562	blood:
38	chr3:53111263..53113792-chr3:53115613..53118566,2	MCF-7	breast:
39	chr3:53085682..53086543-chr3:53106733..53107482,2	MCF-7	breast:
40	chr3:53074151..53077350-chr3:53077899..53081125,4	K562	blood:
41	chr3:53056126..53058134-chr3:53061359..53063994,2	K562	blood:
42	chr3:53066267..53068975-chr3:53075224..53077291,2	K562	blood:
43	chr3:53053108..53056030-chr3:53104834..53107226,3	K562	blood:
44	chr3:53079254..53081173-chr3:53081236..53082757,2	MCF-7	breast:
45	chr3:52933827..52935933-chr3:53105479..53107077,2	K562	blood:
46	chr3:53058305..53060040-chr3:53077970..53080050,2	K562	blood:
47	chr3:53055176..53056730-chr3:53078490..53080404,2	MCF-7	breast:
48	chr3:52462587..52463429-chr3:53106363..53107313,2	K562	blood:
49	chr3:53106835..53109332-chr3:53109780..53113042,3	MCF-7	breast:
50	chr3:53106005..53108622-chr3:53188208..53190732,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFT1-2	chr3:53111718-53112173	NONHSAT089981
2	lnc-RFT1-5	chr3:53077152-53077270	NONHSAT089976
3	lnc-RFT1-5	chr3:53052102-53052244	NONHSAT089975
4	lnc-PRKCD-2	chr3:53080091-53082182	NONHSAT089977
5	lnc-RFT1-5	chr3:53080476-53080766	NONHSAT089975
6	lnc-SFMBT1-1	chr3:53096500-53096607	l_2369_chr3:53093657-53096607_testes
7	lnc-RFT1-5	chr3:53079832-53080073	NONHSAT089976
8	lnc-RFT1-3	chr3:53100873-53109103	NONHSAT089980
9	lnc-SFMBT1-2	chr3:53098299-53099107	NONHSAT089979
10	lnc-RFT1-2	chr3:53112985-53113038	NONHSAT089981
11	lnc-SFMBT1-1	chr3:53093658-53094908	l_2369_chr3:53093657-53096607_testes
12	lnc-RFT1-5	chr3:53077152-53077270	NONHSAT089975
13	lnc-RFT1-1	chr3:53112200-53112227	XLOC_003130

No data

Variant related genes	Relation type
SERBP1P3	TF binding region
ENSG00000266635	TF binding region
SFMBT1	TF binding region
SERBP1P3	CpG island
ENSG00000266635	CpG island
SFMBT1	CpG island
ENSG00000055955	chromatin interactions
ENSG00000163932	chromatin interactions
ENSG00000163935	chromatin interactions
ENSG00000267395	chromatin interactions
ENSG00000101019	chromatin interactions
E2F1	miRNA target sites

Extended variants
information (count: 2503 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2581795	chr3:53038786-53038787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188686200	chr3:53038802-53038803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532182493	chr3:53038853-53038854	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143222515	chr3:53038854-53038855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559371884	chr3:53038879-53038880	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs386508422	chr3:53038898-53038899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528525009	chr3:53038913-53038914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7628501	chr3:53038983-53038984	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs116655165	chr3:53038994-53038995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191798981	chr3:53039100-53039101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs550768914	chr3:53039116-53039117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184235955	chr3:53039130-53039131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187564505	chr3:53039131-53039132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553653873	chr3:53039142-53039143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs151171883	chr3:53039167-53039168	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs367729709	chr3:53039174-53039175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs141026959	chr3:53039181-53039182	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554155249	chr3:53039189-53039190	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191412717	chr3:53039190-53039191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543528653	chr3:53039194-53039195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563205825	chr3:53039200-53039201	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs372859802	chr3:53039203-53039204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs75897730	chr3:53039250-53039251	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs115979382	chr3:53039307-53039308	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570893797	chr3:53039319-53039320	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545657691	chr3:53039373-53039374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs34692375	chr3:53039408-53039409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559647212	chr3:53039421-53039422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs1529544	chr3:53039455-53039456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs150251686	chr3:53039472-53039473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373284469	chr3:53039587-53039588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115510335	chr3:53039588-53039589	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556742460	chr3:53039642-53039643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551087620	chr3:53039680-53039681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183905215	chr3:53039698-53039699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs117626810	chr3:53039735-53039736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546867769	chr3:53039746-53039747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145855466	chr3:53039770-53039771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141895881	chr3:53039794-53039795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555612918	chr3:53039797-53039798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568697868	chr3:53039854-53039855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370149717	chr3:53039878-53039879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567733462	chr3:53039924-53039925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201186374	chr3:53040107-53040108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536626696	chr3:53040154-53040155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147033247	chr3:53040157-53040158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576865131	chr3:53040163-53040164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568660729	chr3:53040165-53040166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73839646	chr3:53040172-53040173	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs186905620	chr3:53040218-53040219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Lung cancer	16618734	CNVD
Neuroblastoma	19686582	CNVD
Renal cell carcinoma	18765545	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1908 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52965000-53039800	Weak transcription	Left Ventricle	heart
2	chr3:53018000-53044200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:53018200-53045200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr3:53019000-53057200	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr3:53019200-53039600	Weak transcription	GM12878-XiMat	blood
6	chr3:53019600-53056400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr3:53019800-53044400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr3:53020600-53057000	Weak transcription	Dnd41	blood
9	chr3:53022600-53043000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr3:53022600-53050400	Weak transcription	Primary B cells from cord blood	blood
11	chr3:53025200-53039000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr3:53025600-53061600	Weak transcription	Lung	lung
13	chr3:53026200-53042400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr3:53026200-53044200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr3:53027200-53043400	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr3:53027600-53061600	Weak transcription	Liver	Liver
17	chr3:53027800-53051000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr3:53028400-53044200	Weak transcription	Adipose Nuclei	Adipose
19	chr3:53030200-53059400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:53030400-53052400	Weak transcription	Primary T cells from cord blood	blood
21	chr3:53030800-53050400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr3:53031000-53039800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr3:53032800-53041000	Weak transcription	Brain Germinal Matrix	brain
24	chr3:53032800-53051600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr3:53033000-53078400	Weak transcription	Aorta	Aorta
26	chr3:53033200-53044000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:53033200-53057000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr3:53033400-53043600	Weak transcription	Right Ventricle	heart
29	chr3:53033600-53056200	Weak transcription	Fetal Stomach	stomach
30	chr3:53033800-53039400	Weak transcription	Pancreas	Pancrea
31	chr3:53033800-53045200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:53033800-53052800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr3:53033800-53053800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr3:53033800-53060400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr3:53033800-53065000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr3:53035600-53039000	Weak transcription	HepG2	liver
37	chr3:53037000-53039800	Weak transcription	Fetal Intestine Large	intestine
38	chr3:53037000-53044200	Weak transcription	Psoas Muscle	Psoas
39	chr3:53037000-53065000	Weak transcription	Fetal Intestine Small	intestine
40	chr3:53037800-53038800	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr3:53038800-53044000	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr3:53039000-53039200	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr3:53039000-53041000	Enhancers	HepG2	liver
44	chr3:53039200-53043800	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr3:53039400-53039600	Enhancers	Pancreas	Pancrea
46	chr3:53039600-53040000	Weak transcription	Pancreas	Pancrea
47	chr3:53039600-53041200	Enhancers	GM12878-XiMat	blood
48	chr3:53039800-53040200	Enhancers	Left Ventricle	heart
49	chr3:53039800-53040200	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr3:53039800-53040400	Enhancers	Skeletal Muscle Male	skeletal muscle

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