Variant report

Variant	nsv1063136
Chromosome Location	chr19:52231449-52350896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1792)
CpG islands
(count:1404)
Chromatin interactive
region (count:102)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1792 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:52299117-52300997	K562	blood:	n/a	n/a
2	ARID3A	chr19:52306606-52307609	K562	blood:	n/a	n/a
3	ARID3A	chr19:52281095-52281512	K562	blood:	n/a	n/a
4	ARID3A	chr19:52302554-52302890	K562	blood:	n/a	n/a
5	ARID3A	chr19:52237226-52237413	K562	blood:	n/a	n/a
6	ARID3A	chr19:52274862-52275001	K562	blood:	n/a	n/a
7	ARID3A	chr19:52288166-52289145	K562	blood:	n/a	n/a
8	ARID3A	chr19:52310240-52311002	K562	blood:	n/a	n/a
9	ARID3A	chr19:52307809-52308459	K562	blood:	n/a	n/a
10	ARID3A	chr19:52298176-52298372	K562	blood:	n/a	n/a
11	ARID3A	chr19:52311894-52312194	K562	blood:	n/a	n/a
12	ARID3A	chr19:52313645-52313812	HepG2	liver:	n/a	n/a
13	ARID3A	chr19:52313557-52313692	K562	blood:	n/a	n/a
14	ARID3A	chr19:52303443-52304384	K562	blood:	n/a	n/a
15	ARID3A	chr19:52286712-52286989	K562	blood:	n/a	n/a
16	ARID3A	chr19:52308170-52308456	HepG2	liver:	n/a	n/a
17	ARID3A	chr19:52333617-52333822	K562	blood:	n/a	n/a
18	ATF1	chr19:52325702-52325884	K562	blood:	n/a	n/a
19	ATF1	chr19:52299358-52299816	K562	blood:	n/a	n/a
20	ATF1	chr19:52308082-52308473	K562	blood:	n/a	n/a
21	ATF1	chr19:52286699-52286989	K562	blood:	n/a	n/a
22	ATF1	chr19:52303528-52304254	K562	blood:	n/a	n/a
23	ATF1	chr19:52313567-52313801	K562	blood:	n/a	n/a
24	ATF1	chr19:52290370-52290609	K562	blood:	n/a	n/a
25	ATF1	chr19:52243137-52243393	K562	blood:	n/a	n/a
26	ATF1	chr19:52302531-52302910	K562	blood:	n/a	n/a
27	ATF1	chr19:52282997-52283290	K562	blood:	n/a	n/a
28	ATF1	chr19:52288144-52288776	K562	blood:	n/a	n/a
29	ATF1	chr19:52310327-52310825	K562	blood:	n/a	n/a
30	ATF1	chr19:52239296-52239871	K562	blood:	n/a	n/a
31	ATF1	chr19:52237092-52237389	K562	blood:	n/a	n/a
32	ATF3	chr19:52302515-52302919	K562	blood:	n/a	n/a
33	BACH1	chr19:52306462-52306629	K562	blood:	n/a	n/a
34	BACH1	chr19:52282939-52282950	K562	blood:	n/a	n/a
35	BACH1	chr19:52303550-52304264	K562	blood:	n/a	n/a
36	BACH1	chr19:52237319-52237585	K562	blood:	n/a	n/a
37	BATF	chr19:52314564-52314896	GM12878	blood:	n/a	chr19:52314743-52314754
38	BATF	chr19:52288291-52288627	GM12878	blood:	n/a	n/a
39	BATF	chr19:52314611-52314850	GM12878	blood:	n/a	chr19:52314743-52314754
40	BATF	chr19:52288219-52288683	GM12878	blood:	n/a	n/a
41	BHLHE40	chr19:52308159-52308429	K562	blood:	n/a	n/a
42	BHLHE40	chr19:52288349-52288645	GM12878	blood:	n/a	n/a
43	BHLHE40	chr19:52246078-52246278	K562	blood:	n/a	n/a
44	BHLHE40	chr19:52239301-52239565	K562	blood:	n/a	n/a
45	BHLHE40	chr19:52299393-52299860	K562	blood:	n/a	n/a
46	BHLHE40	chr19:52271420-52271644	K562	blood:	n/a	n/a
47	BHLHE40	chr19:52242921-52243268	K562	blood:	n/a	chr19:52243075-52243096
48	BHLHE40	chr19:52310320-52310864	K562	blood:	n/a	n/a
49	BHLHE40	chr19:52306949-52307111	K562	blood:	n/a	n/a
50	BHLHE40	chr19:52311826-52312099	K562	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:52253373-52253423	SAEC	small airway:	n/a
2	chr19:52253373-52253423	SAEC	small airway:	n/a
3	chr19:52266295-52266345	BE2_C	brain:	n/a
4	chr19:52302551-52302601	HCT-116	colon:	n/a
5	chr19:52249171-52249221	HPAEpiC	pulmonary alveolar:	n/a
6	chr19:52266642-52266692	HCT-116	colon:	n/a
7	chr19:52256460-52256510	IMR90	lung:	fetal
8	chr19:52254222-52254272	GM12891	blood:	n/a
9	chr19:52253373-52253423	T-47D	breast:	n/a
10	chr19:52266295-52266345	SAEC	small airway:	n/a
11	chr19:52264413-52264463	HCT-116	colon:	n/a
12	chr19:52268814-52268864	Jurkat	blood:	n/a
13	chr19:52302551-52302601	ovcar-3	ovarian:	n/a
14	chr19:52272839-52272889	IMR90	lung:	fetal
15	chr19:52266295-52266345	HL-60	blood:	n/a
16	chr19:52255673-52255723	MCF-7	breast:	n/a
17	chr19:52297519-52297569	HPAEpiC	pulmonary alveolar:	n/a
18	chr19:52297519-52297569	HCM	heart:	n/a
19	chr19:52264411-52264461	PANC-1	pancreas:	n/a
20	chr19:52253373-52253423	SK-N-SH_RA	brain:	n/a
21	chr19:52302551-52302601	CMK	blood:	n/a
22	chr19:52266482-52266532	HMEC	breast:	n/a
23	chr19:52327441-52327491	SK-N-MC	brain:	n/a
24	chr19:52266482-52266532	AG09319	gingival:	n/a
25	chr19:52254222-52254272	GM12878	blood:	n/a
26	chr19:52262969-52263019	RPTEC	kidney:	n/a
27	chr19:52255413-52255463	HAEpiC	amniotic membrane:	n/a
28	chr19:52268814-52268864	SK-N-MC	brain:	n/a
29	chr19:52255673-52255723	HUVEC	blood vessel:	n/a
30	chr19:52249599-52249649	SK-N-SH_RA	brain:	n/a
31	chr19:52327441-52327491	NHBE	bronchial:	n/a
32	chr19:52266295-52266345	HRPEpiC	eye:	n/a
33	chr19:52249171-52249221	NHBE	bronchial:	n/a
34	chr19:52249599-52249649	HRCEpiC	kidney:	n/a
35	chr19:52302551-52302601	BJ	skin:	n/a
36	chr19:52266295-52266345	Caco-2	colon:	n/a
37	chr19:52264413-52264463	AG09319	gingival:	n/a
38	chr19:52297519-52297569	HCF	heart:	n/a
39	chr19:52297968-52298018	AoSMC	blood vessel:	n/a
40	chr19:52268814-52268864	GM12892	blood:	n/a
41	chr19:52262969-52263019	HepG2	liver:	n/a
42	chr19:52327441-52327491	K562	blood:	n/a
43	chr19:52249171-52249221	MCF-7	breast:	n/a
44	chr19:52249599-52249649	RPTEC	kidney:	n/a
45	chr19:52272839-52272889	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:52264429-52264479	HEEpiC	esophagus:	n/a
47	chr19:52328110-52328160	NH-A	brain:	n/a
48	chr19:52265748-52265798	NHBE	bronchial:	n/a
49	chr19:52249599-52249649	GM12892	blood:	n/a
50	chr19:52297968-52298018	HEK293	kidney:	embryo

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr19:52327504..52330084-chr19:52332158..52334716,2	K562	blood:
2	chr19:52283826..52285939-chr19:52290295..52292684,2	K562	blood:
3	chr19:52246232..52248265-chr19:52275684..52277593,2	K562	blood:
4	chr19:52164333..52164883-chr19:52286275..52287235,2	K562	blood:
5	chr19:52281378..52282199-chr19:52310053..52311134,3	MCF-7	breast:
6	chr19:52302303..52304352-chr19:52308836..52310824,2	K562	blood:
7	chr19:52213445..52215561-chr19:52311102..52312961,2	MCF-7	breast:
8	chr19:52237851..52239794-chr19:52278357..52281103,2	K562	blood:
9	chr19:52350825..52353378-chr19:52353698..52357895,4	K562	blood:
10	chr19:52264566..52267681-chr19:52268997..52272339,3	K562	blood:
11	chr19:52229702..52232519-chr19:52243094..52246090,2	K562	blood:
12	chr19:52213474..52218033-chr19:52227253..52233222,6	K562	blood:
13	chr19:52325388..52327096-chr19:52332762..52335331,2	K562	blood:
14	chr19:52288417..52292749-chr19:52303564..52308075,7	MCF-7	breast:
15	chr19:52286503..52287282-chr19:52313444..52314004,2	MCF-7	breast:
16	chr19:52339899..52342041-chr19:52352045..52353775,2	K562	blood:
17	chr19:52288793..52290684-chr19:52309015..52310845,2	MCF-7	breast:
18	chr19:51925248..51925915-chr19:52333639..52334203,3	K562	blood:
19	chr19:51976250..51976763-chr19:52286398..52287255,2	MCF-7	breast:
20	chr19:52286428..52287255-chr19:52311675..52312485,2	K562	blood:
21	chr19:52266346..52268006-chr19:52288638..52290358,2	K562	blood:
22	chr19:52311117..52313803-chr19:52333610..52335464,2	MCF-7	breast:
23	chr19:52306935..52308670-chr19:52309140..52312015,2	K562	blood:
24	chr19:52293197..52295427-chr19:52302350..52304718,2	K562	blood:
25	chr19:52053557..52056461-chr19:52303271..52305092,2	K562	blood:
26	chr19:52216020..52218332-chr19:52241843..52243372,2	MCF-7	breast:
27	chr19:52110881..52111404-chr19:52311887..52312611,2	K562	blood:
28	chr19:52211595..52213921-chr19:52286963..52288731,2	MCF-7	breast:
29	chr19:52277252..52280164-chr19:52282818..52285281,2	K562	blood:
30	chr19:52279714..52282274-chr19:52309726..52312482,2	MCF-7	breast:
31	chr19:52325388..52327096-chr19:52332762..52335331,2	K562	blood:
32	chr19:52215836..52216573-chr19:52280774..52281726,5	MCF-7	breast:
33	chr19:52246232..52248265-chr19:52275684..52277593,2	K562	blood:
34	chr19:52216500..52217173-chr19:52286806..52287310,2	MCF-7	breast:
35	chr19:52288499..52290197-chr19:52294981..52296482,2	MCF-7	breast:
36	chr19:51870824..51872343-chr19:52285701..52288482,2	MCF-7	breast:
37	chr19:52160319..52160911-chr19:52311474..52312517,3	K562	blood:
38	chr19:52310543..52312207-chr19:52772236..52773979,2	MCF-7	breast:
39	chr19:52229702..52232519-chr19:52243094..52246090,2	K562	blood:
40	chr19:52283826..52285939-chr19:52290295..52292684,2	K562	blood:
41	chr19:52286760..52288347-chr19:52288825..52290368,2	MCF-7	breast:
42	chr19:52299823..52301344-chr19:52301707..52303402,2	K562	blood:
43	chr19:52344484..52346538-chr19:52349352..52351510,2	K562	blood:
44	chr19:52344484..52346538-chr19:52349352..52351510,2	K562	blood:
45	chr19:52311117..52313803-chr19:52333610..52335464,2	MCF-7	breast:
46	chr19:52213474..52215839-chr19:52229447..52232151,2	K562	blood:
47	chr19:52276673..52280164-chr19:52282818..52285281,3	K562	blood:
48	chr19:52199590..52202022-chr19:52311266..52313737,2	MCF-7	breast:
49	chr19:52276673..52280164-chr19:52282818..52285281,3	K562	blood:
50	chr19:52171972..52176073-chr19:52299212..52302483,3	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF577-3	chr19:52314710-52314992	NONHSAT067478
2	lnc-ZNF577-3	chr19:52307980-52308507	NONHSAT067477
3	lnc-FPR1-1	chr19:52282890-52283234	XLOC_013388
4	lnc-FPR1-1	chr19:52284430-52284578	XLOC_013388
5	lnc-ZNF577-2	chr19:52346074-52346166	ENSG00000269483.1
6	lnc-ZNF577-2	chr19:52346442-52346577	ENSG00000269483.1
7	lnc-ZNF577-2	chr19:52343177-52343370	ENSG00000269483.1
8	lnc-FPR1-1	chr19:52286673-52286772	NONHSAT067476
9	lnc-ZNF577-2	chr19:52342867-52343370	NONHSAT067482
10	lnc-ZNF577-2	chr19:52343146-52343370	NONHSAT067481
11	lnc-ZNF577-2	chr19:52343756-52344198	ENSG00000268316.1
12	lnc-ZNF577-2	chr19:52343024-52343132	ENSG00000268316.1
13	lnc-ZNF577-3	chr19:52314710-52314992	NONHSAT067477
14	lnc-ZNF577-2	chr19:52346074-52346186	NONHSAT067482
15	lnc-ZNF577-2	chr19:52317206-52317230	NONHSAT067481
16	lnc-FPR1-1	chr19:52283028-52283234	NONHSAT067476
17	lnc-FPR1-1	chr19:52284430-52284599	NONHSAT067476
18	lnc-ZNF577-2	chr19:52346074-52346168	NONHSAT067481
19	lnc-ZNF577-3	chr19:52307980-52308424	NONHSAT067478

No data

Variant related genes	Relation type
HAS1	TF binding region
ENSG00000268316	TF binding region
FPR1	TF binding region
FPR2	TF binding region
ENSG00000269483	TF binding region
FPR3	TF binding region
HAS1	CpG island
ENSG00000268316	CpG island
FPR1	CpG island
FPR2	CpG island
ENSG00000269483	CpG island
FPR3	CpG island
ENSG00000171051	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000105509	chromatin interactions
ENSG00000182310	chromatin interactions
ENSG00000171049	chromatin interactions
ENSG00000269403	chromatin interactions
ENSG00000198093	chromatin interactions
ENSG00000160318	chromatin interactions
ENSG00000238486	chromatin interactions
ENSG00000187474	chromatin interactions
ENSG00000196214	chromatin interactions
ENSG00000161551	chromatin interactions
HIF1A	miRNA target sites
YTHDC2	miRNA target sites
GIGYF1	miRNA target sites
CAMTA1	miRNA target sites

Extended variants
information (count: 4662 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4662 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12971652	chr19:52231449-52231450	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539003158	chr19:52231473-52231474	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs557747639	chr19:52231481-52231482	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs576024808	chr19:52231565-52231566	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs543530548	chr19:52231592-52231593	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs144795580	chr19:52231648-52231649	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs573819135	chr19:52231653-52231654	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs73934294	chr19:52231667-52231668	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs559584862	chr19:52231683-52231684	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs79212058	chr19:52231706-52231707	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs189781784	chr19:52231744-52231745	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs573477038	chr19:52231770-52231771	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs546184525	chr19:52231799-52231800	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs564528037	chr19:52231816-52231817	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138456945	chr19:52231871-52231872	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs180747529	chr19:52231884-52231885	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs568552931	chr19:52231897-52231898	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529493074	chr19:52231922-52231923	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369808088	chr19:52231949-52231950	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs8112223	chr19:52231976-52231977	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs186276966	chr19:52232015-52232016	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs190745207	chr19:52232029-52232030	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551065432	chr19:52232044-52232045	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs569665733	chr19:52232049-52232050	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536736510	chr19:52232080-52232081	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555484840	chr19:52232085-52232086	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs573781951	chr19:52232147-52232148	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs8112259	chr19:52232151-52232152	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79771542	chr19:52232156-52232157	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200740776	chr19:52232158-52232159	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200818172	chr19:52232159-52232160	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs147368724	chr19:52232212-52232213	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577978679	chr19:52232308-52232309	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs8112373	chr19:52232324-52232325	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs73056853	chr19:52232325-52232326	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555393273	chr19:52232332-52232333	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs73568350	chr19:52232367-52232368	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs562254718	chr19:52232409-52232410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529335097	chr19:52232442-52232443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547616094	chr19:52232463-52232464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559496198	chr19:52232475-52232476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs533463633	chr19:52232488-52232489	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540793275	chr19:52232506-52232507	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7259578	chr19:52232525-52232526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs11880762	chr19:52232545-52232546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537098601	chr19:52232597-52232598	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs548693016	chr19:52232619-52232620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs184027594	chr19:52232624-52232625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534685308	chr19:52232649-52232650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553226286	chr19:52232654-52232655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20531469	CNVD

Chromatin state (count:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52228600-52233800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr19:52229400-52231600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr19:52229400-52231800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr19:52229400-52232000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:52230000-52231600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr19:52230000-52231600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr19:52230000-52231600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr19:52230000-52231800	Weak transcription	K562	blood
9	chr19:52230000-52232000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr19:52230200-52231800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr19:52230800-52231800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr19:52230800-52231800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
13	chr19:52230800-52232000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr19:52230800-52232800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr19:52231000-52232800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr19:52231000-52232800	Weak transcription	NHDF-Ad	bronchial
17	chr19:52231000-52232800	Weak transcription	Osteobl	bone
18	chr19:52231000-52233000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr19:52231000-52233400	Weak transcription	HSMM	muscle
20	chr19:52231200-52233200	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr19:52231200-52233400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr19:52231600-52231800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
23	chr19:52231600-52232400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr19:52231600-52232400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr19:52231600-52233400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr19:52231800-52232000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr19:52231800-52232000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr19:52231800-52232400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr19:52231800-52233600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr19:52231800-52233600	Enhancers	K562	blood
31	chr19:52232000-52232200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr19:52232000-52232200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:52232000-52233200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:52232000-52233400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr19:52232200-52233200	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr19:52232400-52233200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr19:52232400-52236800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr19:52232800-52233600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr19:52232800-52233600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr19:52232800-52233800	Enhancers	NHDF-Ad	bronchial
41	chr19:52232800-52233800	Enhancers	Osteobl	bone
42	chr19:52233000-52233400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:52233200-52233400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr19:52233200-52233600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr19:52233200-52234000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:52233400-52233600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr19:52233400-52233600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr19:52233400-52233600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr19:52233400-52233800	Bivalent Enhancer	Adipose Nuclei	Adipose
50	chr19:52233400-52233800	Enhancers	HSMM	muscle

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