Variant report

Variant	esv1804048
Chromosome Location	chr1:145066917-145104261
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1593)
CpG islands
(count:1710)
Chromatin interactive
region (count:93)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145091964-145092746	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:145098092-145098776	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:145089768-145090509	K562	blood:	n/a	n/a
4	ARID3A	chr1:145083440-145084471	K562	blood:	n/a	n/a
5	ARID3A	chr1:145096149-145096769	HepG2	liver:	n/a	n/a
6	ATF1	chr1:145078844-145078995	K562	blood:	n/a	n/a
7	ATF1	chr1:145069602-145070170	K562	blood:	n/a	n/a
8	ATF1	chr1:145090189-145090575	K562	blood:	n/a	n/a
9	ATF1	chr1:145083579-145084451	K562	blood:	n/a	n/a
10	ATF1	chr1:145086819-145087312	K562	blood:	n/a	n/a
11	ATF1	chr1:145073353-145074236	K562	blood:	n/a	n/a
12	ATF1	chr1:145082093-145082887	K562	blood:	n/a	n/a
13	ATF1	chr1:145096190-145096629	K562	blood:	n/a	n/a
14	ATF1	chr1:145098857-145100009	K562	blood:	n/a	n/a
15	ATF1	chr1:145068286-145068723	K562	blood:	n/a	n/a
16	ATF1	chr1:145077527-145078634	K562	blood:	n/a	n/a
17	ATF1	chr1:145080812-145081067	K562	blood:	n/a	n/a
18	ATF1	chr1:145070839-145072121	K562	blood:	n/a	n/a
19	ATF1	chr1:145074748-145075398	K562	blood:	n/a	n/a
20	ATF2	chr1:145092143-145092822	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr1:145092073-145092999	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr1:145096133-145096595	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr1:145096141-145096582	GM12878	blood:	n/a	n/a
24	ATF2	chr1:145096082-145096678	GM12878	blood:	n/a	n/a
25	ATF3	chr1:145096106-145096616	K562	blood:	n/a	n/a
26	BACH1	chr1:145074517-145076497	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr1:145083544-145084558	K562	blood:	n/a	n/a
28	BACH1	chr1:145079514-145080018	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr1:145074575-145075384	K562	blood:	n/a	n/a
30	BACH1	chr1:145080726-145081101	K562	blood:	n/a	n/a
31	BACH1	chr1:145091823-145092943	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr1:145096205-145096592	GM12878	blood:	n/a	n/a
33	BCL11A	chr1:145092578-145092840	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL3	chr1:145096072-145096636	A549	lung:	n/a	chr1:145096478-145096487
35	BCL3	chr1:145096195-145096579	A549	lung:	n/a	chr1:145096478-145096487
36	BCLAF1	chr1:145096014-145096670	K562	blood:	n/a	chr1:145096478-145096487
37	BCLAF1	chr1:145096061-145096778	GM12878	blood:	n/a	chr1:145096478-145096487
38	BCLAF1	chr1:145096125-145096707	K562	blood:	n/a	chr1:145096478-145096487
39	BCLAF1	chr1:145096075-145096673	GM12878	blood:	n/a	chr1:145096478-145096487
40	BDP1	chr1:145101360-145101992	Hela-S3	cervix:	n/a	n/a
41	BDP1	chr1:145097566-145098291	Hela-S3	cervix:	n/a	n/a
42	BDP1	chr1:145079575-145080056	Hela-S3	cervix:	n/a	n/a
43	BDP1	chr1:145102664-145103015	Hela-S3	cervix:	n/a	n/a
44	BDP1	chr1:145073525-145074027	Hela-S3	cervix:	n/a	n/a
45	BDP1	chr1:145103483-145103885	Hela-S3	cervix:	n/a	n/a
46	BDP1	chr1:145069865-145070376	Hela-S3	cervix:	n/a	n/a
47	BDP1	chr1:145085862-145086083	Hela-S3	cervix:	n/a	n/a
48	BDP1	chr1:145081634-145083761	Hela-S3	cervix:	n/a	n/a
49	BDP1	chr1:145083969-145084366	Hela-S3	cervix:	n/a	n/a
50	BDP1	chr1:145087358-145087975	Hela-S3	cervix:	n/a	n/a

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145096375-145096425	RPTEC	kidney:	n/a
2	chr1:145096723-145096773	PrEC	prostate:	n/a
3	chr1:145096375-145096425	RPTEC	kidney:	n/a
4	chr1:145096723-145096773	PrEC	prostate:	n/a
5	chr1:145096479-145096529	Caco-2	colon:	n/a
6	chr1:145096479-145096529	GM12878	blood:	n/a
7	chr1:145075538-145075588	T-47D	breast:	n/a
8	chr1:145079447-145079497	Hepatocyte	liver:	n/a
9	chr1:145076239-145076289	ECC-1	luminal epithelium:	n/a
10	chr1:145095965-145096015	NHBE	bronchial:	n/a
11	chr1:145096125-145096175	PFSK-1	brain:	n/a
12	chr1:145096723-145096773	ProgFib	skin:	n/a
13	chr1:145089017-145089067	BE2_C	brain:	n/a
14	chr1:145096602-145096652	RPTEC	kidney:	n/a
15	chr1:145100564-145100614	CMK	blood:	n/a
16	chr1:145076221-145076271	NB4	blood:	n/a
17	chr1:145075831-145075881	Jurkat	blood:	n/a
18	chr1:145092330-145092380	AoSMC	blood vessel:	n/a
19	chr1:145096125-145096175	GM12892	blood:	n/a
20	chr1:145096403-145096453	H1-hESC	embryonic stem cell:	embryo
21	chr1:145073743-145073793	Caco-2	colon:	n/a
22	chr1:145096236-145096286	SK-N-SH_RA	brain:	n/a
23	chr1:145092485-145092535	A549	lung:	n/a
24	chr1:145073743-145073793	Jurkat	blood:	n/a
25	chr1:145096723-145096773	H1-hESC	embryonic stem cell:	embryo
26	chr1:145095965-145096015	SK-N-SH_RA	brain:	n/a
27	chr1:145076221-145076271	HMEC	breast:	n/a
28	chr1:145097220-145097270	GM19239	blood:	n/a
29	chr1:145096236-145096286	SK-N-MC	brain:	n/a
30	chr1:145076221-145076271	GM06990	blood:	n/a
31	chr1:145096849-145096899	AG09319	gingival:	n/a
32	chr1:145096479-145096529	GM19239	blood:	n/a
33	chr1:145096723-145096773	PANC-1	pancreas:	n/a
34	chr1:145079447-145079497	HIPEpiC	eye:	n/a
35	chr1:145075349-145075399	HCF	heart:	n/a
36	chr1:145096375-145096425	HEK293	kidney:	embryo
37	chr1:145076221-145076271	NHDF-neo	bronchial:	n/a
38	chr1:145089017-145089067	K562	blood:	n/a
39	chr1:145095823-145095873	ProgFib	skin:	n/a
40	chr1:145095823-145095873	HCF	heart:	n/a
41	chr1:145095823-145095873	HEEpiC	esophagus:	n/a
42	chr1:145096321-145096371	HNPCEpiC	eye:	n/a
43	chr1:145075538-145075588	GM06990	blood:	n/a
44	chr1:145095965-145096015	ECC-1	luminal epithelium:	n/a
45	chr1:145097220-145097270	SK-N-SH_RA	brain:	n/a
46	chr1:145092485-145092535	IMR90	lung:	fetal
47	chr1:145092330-145092380	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:145073743-145073793	PrEC	prostate:	n/a
49	chr1:145096236-145096286	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:145073743-145073793	HAEpiC	amniotic membrane:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:145076371..145079610-chr1:145081907..145086657,4	K562	blood:
2	chr1:145032581..145034474-chr1:145068467..145071383,2	MCF-7	breast:
3	chr1:6844414..6845389-chr1:145096592..145097171,2	Hela-S3	cervix:
4	chr1:144988330..144990331-chr1:145096274..145097862,2	MCF-7	breast:
5	chr1:145070825..145073370-chr1:145075606..145078023,2	K562	blood:
6	chr1:144532343..144534218-chr1:145080801..145083620,2	K562	blood:
7	chr1:145096105..145096704-chr8:56685316..56686162,2	Hela-S3	cervix:
8	chr1:145043001..145044851-chr1:145077921..145079924,2	K562	blood:
9	chr1:145082537..145085433-chr1:145102296..145104665,3	MCF-7	breast:
10	chr1:145073673..145075611-chr1:145098058..145100166,2	MCF-7	breast:
11	chr1:144930691..144932405-chr1:145101538..145103976,2	MCF-7	breast:
12	chr1:120480674..120483081-chr1:145098868..145100829,2	MCF-7	breast:
13	chr1:145096224..145096777-chr2:143635158..143635659,2	Hela-S3	cervix:
14	chr1:145096397..145097357-chr5:168006463..168007379,2	Hela-S3	cervix:
15	chr1:145077663..145080122-chr1:145080911..145082669,2	MCF-7	breast:
16	chr1:145073673..145075611-chr1:145098058..145100166,2	MCF-7	breast:
17	chr1:145057641..145059158-chr1:145100599..145102878,2	MCF-7	breast:
18	chr1:144932003..144934560-chr1:145095329..145097401,2	MCF-7	breast:
19	chr1:144532668..144535961-chr1:145101125..145103299,5	K562	blood:
20	chr1:145068824..145071051-chr1:145086179..145089112,2	K562	blood:
21	chr1:145096186..145098889-chr12:66522673..66525529,2	MCF-7	breast:
22	chr1:145038465..145040335-chr1:145073529..145077328,4	MCF-7	breast:
23	chr1:144888141..144890870-chr1:145070504..145072082,2	K562	blood:
24	chr1:145079205..145081578-chr1:145083280..145086175,3	K562	blood:
25	chr1:145076679..145079296-chr1:145102825..145104399,2	MCF-7	breast:
26	chr1:144930933..144933900-chr1:145065814..145068964,3	MCF-7	breast:
27	chr1:145076679..145079296-chr1:145102825..145104399,2	MCF-7	breast:
28	chr1:145081885..145085259-chr1:145087352..145090342,5	K562	blood:
29	chr1:145021531..145024475-chr1:145100250..145102590,2	K562	blood:
30	chr1:145073942..145076773-chr1:145095058..145097883,2	K562	blood:
31	chr1:144988068..144990900-chr1:145065609..145067811,2	K562	blood:
32	chr1:145079205..145081578-chr1:145083280..145086175,3	K562	blood:
33	chr1:145073999..145076164-chr1:145381316..145383485,2	MCF-7	breast:
34	chr1:145070476..145072137-chr10:116063962..116066541,2	MCF-7	breast:
35	chr1:144533700..144535665-chr1:145063411..145067268,4	K562	blood:
36	chr1:145070476..145072647-chr1:145097716..145099798,2	K562	blood:
37	chr1:145054217..145054913-chr1:145103284..145104051,2	K562	blood:
38	chr1:145052557..145054250-chr1:145070398..145072943,2	K562	blood:
39	chr1:145069551..145072010-chr1:145087296..145089112,2	K562	blood:
40	chr1:144534089..144535693-chr1:145093143..145095512,2	K562	blood:
41	chr1:145095997..145096821-chr11:66384044..66384600,2	NB4	blood:
42	chr1:145068951..145071595-chr1:145074959..145076825,3	MCF-7	breast:
43	chr1:145073676..145075206-chr1:145114434..145117325,2	MCF-7	breast:
44	chr1:145082967..145085592-chr2:99952422..99954371,2	MCF-7	breast:
45	chr1:144986699..144988777-chr1:145068454..145070664,2	K562	blood:
46	chr1:145045315..145047510-chr1:145064968..145067113,2	K562	blood:
47	chr1:145069959..145072647-chr1:145097335..145099798,3	K562	blood:
48	chr1:144916772..144918364-chr1:145096684..145098671,2	MCF-7	breast:
49	chr1:145014851..145016441-chr1:145076191..145078114,2	K562	blood:
50	chr1:144532674..144534262-chr1:145089036..145091259,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE4DIP-5	chr1:145088039-145088567	NONHSAT005874

No data

Variant related genes	Relation type
SEC22B	TF binding region
PDE4DIP	TF binding region
ENSG00000271546	TF binding region
SEC22B	CpG island
PDE4DIP	CpG island
ENSG00000271546	CpG island
ENSG00000202408	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000239335	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000139233	chromatin interactions
ENSG00000167904	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000248643	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000115919	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000169129	chromatin interactions
ENSG00000271546	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000237436	chromatin interactions
ENSG00000171735	chromatin interactions
ENSG00000225362	chromatin interactions
ENSG00000137574	chromatin interactions
ENSG00000120137	chromatin interactions
ENSG00000239306	chromatin interactions

Extended variants
information (count: 1548 )
Associated
traits (count: 179 )

Variant overlapped rSNPs/rCNVs (count:1548 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1778761	chr1:145066917-145066918	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587770044	chr1:145066921-145066922	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs587666234	chr1:145066922-145066923	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs587742189	chr1:145066963-145066964	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs374704612	chr1:145066995-145066996	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs587615461	chr1:145066996-145066997	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs587676819	chr1:145067041-145067042	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs587710734	chr1:145067091-145067092	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs57204573	chr1:145067093-145067094	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs1778760	chr1:145067094-145067095	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs6692256	chr1:145067103-145067104	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs587726262	chr1:145067159-145067160	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs12239071	chr1:145067163-145067164	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs587660969	chr1:145067204-145067205	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs111482941	chr1:145067235-145067236	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs113633392	chr1:145067242-145067243	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs587739054	chr1:145067263-145067264	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs6682934	chr1:145067292-145067293	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs6692483	chr1:145067307-145067308	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs587616141	chr1:145067308-145067309	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587689178	chr1:145067333-145067334	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2985366	chr1:145067349-145067350	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs60325679	chr1:145067354-145067355	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs112233312	chr1:145067369-145067370	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs587735451	chr1:145067370-145067371	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs587626852	chr1:145067379-145067380	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375857947	chr1:145067391-145067392	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs1778759	chr1:145067444-145067445	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs373793750	chr1:145067451-145067452	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs587776150	chr1:145067477-145067478	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs587662044	chr1:145067499-145067500	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587721373	chr1:145067511-145067512	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs2590084	chr1:145067512-145067513	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs587772438	chr1:145067585-145067586	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs587659985	chr1:145067611-145067612	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs587712009	chr1:145067629-145067630	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs587598782	chr1:145067709-145067710	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs587645478	chr1:145067718-145067719	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs587702826	chr1:145067720-145067721	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs587606322	chr1:145067731-145067732	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs7555417	chr1:145067792-145067793	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs587661115	chr1:145067835-145067836	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587741039	chr1:145067887-145067888	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs11811257	chr1:145067910-145067911	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2590083	chr1:145067994-145067995	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587603413	chr1:145067998-145067999	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs587678210	chr1:145068008-145068009	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs587732058	chr1:145068030-145068031	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs10910731	chr1:145068035-145068036	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2590082	chr1:145068055-145068056	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:179)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Autism	22543975	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145061000-145068200	Weak transcription	Brain Angular Gyrus	brain
2	chr1:145061000-145071200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:145062800-145068400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:145062800-145069000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:145063400-145072400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr1:145065600-145067000	ZNF genes & repeats	Osteobl	bone
7	chr1:145065600-145068600	ZNF genes & repeats	NHDF-Ad	bronchial
8	chr1:145065800-145067000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:145065800-145067200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:145065800-145067200	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
11	chr1:145066000-145067600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr1:145066200-145067600	ZNF genes & repeats	Primary T cells from cord blood	blood
13	chr1:145066800-145067800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:145067000-145067400	Weak transcription	Osteobl	bone
15	chr1:145067200-145069800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:145067200-145071400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr1:145067200-145071600	Weak transcription	Brain Anterior Caudate	brain
18	chr1:145067400-145067600	Strong transcription	Osteobl	bone
19	chr1:145067400-145069600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr1:145067600-145067800	Weak transcription	Osteobl	bone
21	chr1:145067600-145071200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:145067600-145073800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:145067800-145068000	Strong transcription	Osteobl	bone
24	chr1:145068000-145068200	ZNF genes & repeats	Osteobl	bone
25	chr1:145068200-145068600	ZNF genes & repeats	Brain Angular Gyrus	brain
26	chr1:145068200-145069600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:145068200-145074600	Weak transcription	Osteobl	bone
28	chr1:145068400-145068600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:145068400-145068600	ZNF genes & repeats	HSMM	muscle
30	chr1:145068400-145069600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr1:145068600-145069600	Weak transcription	Brain Angular Gyrus	brain
32	chr1:145068600-145069600	Weak transcription	HSMM	muscle
33	chr1:145068600-145069600	Weak transcription	NHDF-Ad	bronchial
34	chr1:145068600-145069800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:145069000-145070200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:145069600-145069800	Enhancers	Brain Angular Gyrus	brain
37	chr1:145069600-145069800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:145069600-145070000	Genic enhancers	Brain Cingulate Gyrus	brain
39	chr1:145069600-145070000	ZNF genes & repeats	HSMM	muscle
40	chr1:145069600-145070000	ZNF genes & repeats	NHDF-Ad	bronchial
41	chr1:145069600-145070200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:145069800-145070000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:145069800-145070000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
44	chr1:145069800-145070000	ZNF genes & repeats	NHLF	lung
45	chr1:145069800-145071000	Weak transcription	Brain Angular Gyrus	brain
46	chr1:145069800-145071200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr1:145070000-145071000	Weak transcription	NHDF-Ad	bronchial
48	chr1:145070000-145071200	Weak transcription	Brain Cingulate Gyrus	brain
49	chr1:145070000-145074600	Weak transcription	NHLF	lung
50	chr1:145070200-145071600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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