Variant report

Variant	esv1823205
Chromosome Location	chr1:144036737-144471989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1893)
CpG islands
(count:244)
Chromatin interactive
region (count:0)
LncRNA
region (count:71)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144091634-144091915	GM12878	blood:	n/a	n/a
2	BATF	chr1:144312324-144312589	GM12878	blood:	n/a	n/a
3	BATF	chr1:144389055-144389404	GM12878	blood:	n/a	chr1:144389254-144389265
4	BATF	chr1:144322789-144323057	GM12878	blood:	n/a	n/a
5	BATF	chr1:144309943-144310144	GM12878	blood:	n/a	n/a
6	BATF	chr1:144068660-144069151	GM12878	blood:	n/a	chr1:144068921-144068932
7	BATF	chr1:144343242-144343436	GM12878	blood:	n/a	n/a
8	BATF	chr1:144068682-144069090	GM12878	blood:	n/a	chr1:144068921-144068932
9	BATF	chr1:144078682-144078883	GM12878	blood:	n/a	n/a
10	BATF	chr1:144333842-144334072	GM12878	blood:	n/a	n/a
11	BATF	chr1:144383867-144384453	GM12878	blood:	n/a	n/a
12	BATF	chr1:144339194-144339724	GM12878	blood:	n/a	n/a
13	BATF	chr1:144379807-144380075	GM12878	blood:	n/a	n/a
14	BATF	chr1:144383897-144384409	GM12878	blood:	n/a	n/a
15	BATF	chr1:144379834-144380086	GM12878	blood:	n/a	n/a
16	BATF	chr1:144310931-144311678	GM12878	blood:	n/a	n/a
17	BATF	chr1:144384899-144385095	GM12878	blood:	n/a	n/a
18	BATF	chr1:144340377-144340881	GM12878	blood:	n/a	n/a
19	BATF	chr1:144335044-144335280	GM12878	blood:	n/a	n/a
20	BATF	chr1:144383148-144383357	GM12878	blood:	n/a	n/a
21	BATF	chr1:144325736-144326116	GM12878	blood:	n/a	n/a
22	BATF	chr1:144157512-144157961	GM12878	blood:	n/a	chr1:144157741-144157749
23	BATF	chr1:144355376-144355716	GM12878	blood:	n/a	n/a
24	BATF	chr1:144339109-144341237	GM12878	blood:	n/a	n/a
25	BATF	chr1:144157508-144157950	GM12878	blood:	n/a	chr1:144157741-144157749
26	BATF	chr1:144333140-144333410	GM12878	blood:	n/a	n/a
27	BATF	chr1:144327210-144327464	GM12878	blood:	n/a	n/a
28	BATF	chr1:144389062-144389424	GM12878	blood:	n/a	chr1:144389254-144389265
29	BATF	chr1:144326880-144327091	GM12878	blood:	n/a	n/a
30	BATF	chr1:144310715-144311748	GM12878	blood:	n/a	n/a
31	BATF	chr1:144336769-144337135	GM12878	blood:	n/a	n/a
32	BATF	chr1:144383148-144383389	GM12878	blood:	n/a	n/a
33	BATF	chr1:144314152-144314409	GM12878	blood:	n/a	n/a
34	BATF	chr1:144327848-144328102	GM12878	blood:	n/a	n/a
35	BATF	chr1:144338647-144338871	GM12878	blood:	n/a	n/a
36	BATF	chr1:144067068-144067372	GM12878	blood:	n/a	chr1:144067195-144067206
37	BATF	chr1:144094411-144095211	GM12878	blood:	n/a	chr1:144094595-144094605
38	BATF	chr1:144321363-144321837	GM12878	blood:	n/a	n/a
39	BATF	chr1:144320981-144321799	GM12878	blood:	n/a	chr1:144321317-144321326
40	BATF	chr1:144328845-144329056	GM12878	blood:	n/a	n/a
41	BATF	chr1:144146857-144147088	GM12878	blood:	n/a	n/a
42	BATF	chr1:144067020-144067334	GM12878	blood:	n/a	chr1:144067195-144067206
43	BATF	chr1:144036890-144037115	GM12878	blood:	n/a	n/a
44	BATF	chr1:144355401-144355740	GM12878	blood:	n/a	n/a
45	BATF	chr1:144341397-144342307	GM12878	blood:	n/a	n/a
46	BATF	chr1:144335102-144335314	GM12878	blood:	n/a	n/a
47	BATF	chr1:144094860-144095134	GM12878	blood:	n/a	n/a
48	BATF	chr1:144341526-144342037	GM12878	blood:	n/a	n/a
49	BATF	chr1:144393889-144394266	GM12878	blood:	n/a	chr1:144393981-144393992 chr1:144394139-144394149
50	BATF	chr1:144393767-144394272	GM12878	blood:	n/a	chr1:144393981-144393992 chr1:144394139-144394149

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144340103-144340153	AG10803	skin:	n/a
2	chr1:144340103-144340153	PANC-1	pancreas:	n/a
3	chr1:144340103-144340153	SK-N-SH	brain:	n/a
4	chr1:144340161-144340211	NHBE	bronchial:	n/a
5	chr1:144340161-144340211	IMR90	lung:	fetal
6	chr1:144044138-144044188	SK-N-SH_RA	brain:	n/a
7	chr1:144340161-144340211	Hepatocyte	liver:	n/a
8	chr1:144340161-144340211	H1-hESC	embryonic stem cell:	embryo
9	chr1:144044138-144044188	PANC-1	pancreas:	n/a
10	chr1:144340103-144340153	GM12891	blood:	n/a
11	chr1:144340251-144340301	Hepatocyte	liver:	n/a
12	chr1:144044138-144044188	A549	lung:	n/a
13	chr1:144044138-144044188	HNPCEpiC	eye:	n/a
14	chr1:144340103-144340153	Caco-2	colon:	n/a
15	chr1:144340251-144340301	SK-N-SH	brain:	n/a
16	chr1:144044138-144044188	ProgFib	skin:	n/a
17	chr1:144340103-144340153	HMEC	breast:	n/a
18	chr1:144044138-144044188	HUVEC	blood vessel:	n/a
19	chr1:144340161-144340211	ECC-1	luminal epithelium:	n/a
20	chr1:144340251-144340301	NHDF-neo	bronchial:	n/a
21	chr1:144340103-144340153	U87	brain:	n/a
22	chr1:144340251-144340301	BE2_C	brain:	n/a
23	chr1:144340161-144340211	AG09319	gingival:	n/a
24	chr1:144044138-144044188	PFSK-1	brain:	n/a
25	chr1:144340251-144340301	MCF-7	breast:	n/a
26	chr1:144340103-144340153	HCPEpiC	choroid plexus:	n/a
27	chr1:144340161-144340211	SK-N-MC	brain:	n/a
28	chr1:144340103-144340153	SKMC	muscle:	n/a
29	chr1:144340161-144340211	GM06990	blood:	n/a
30	chr1:144044138-144044188	CMK	blood:	n/a
31	chr1:144044138-144044188	SK-N-MC	brain:	n/a
32	chr1:144340251-144340301	AoSMC	blood vessel:	n/a
33	chr1:144340103-144340153	K562	blood:	n/a
34	chr1:144340161-144340211	Jurkat	blood:	n/a
35	chr1:144044138-144044188	NH-A	brain:	n/a
36	chr1:144340161-144340211	HepG2	liver:	n/a
37	chr1:144340103-144340153	HCF	heart:	n/a
38	chr1:144340161-144340211	NH-A	brain:	n/a
39	chr1:144340251-144340301	HRPEpiC	eye:	n/a
40	chr1:144044138-144044188	ovcar-3	ovarian:	n/a
41	chr1:144340251-144340301	NH-A	brain:	n/a
42	chr1:144340161-144340211	PrEC	prostate:	n/a
43	chr1:144340103-144340153	AG09319	gingival:	n/a
44	chr1:144340251-144340301	HepG2	liver:	n/a
45	chr1:144044138-144044188	Jurkat	blood:	n/a
46	chr1:144340103-144340153	NH-A	brain:	n/a
47	chr1:144340161-144340211	SK-N-SH_RA	brain:	n/a
48	chr1:144044138-144044188	GM06990	blood:	n/a
49	chr1:144044138-144044188	AoSMC	blood vessel:	n/a
50	chr1:144340161-144340211	SK-N-SH	brain:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPIAL4B-1	chr1:144340526-144340593	ENSG00000235398
2	lnc-PPIAL4B-1	chr1:144280730-144280868	ENSG00000235398
3	lnc-RP3-377D14.1.1-10	chr1:144401304-144401978	expReg_chr1_15531_+
4	lnc-PPIAL4B-1	chr1:144326026-144326185	ENSG00000235398
5	lnc-PPIAL4B-1	chr1:144341670-144341756	ENSG00000235398.4
6	lnc-PPIAL4B-1	chr1:144340526-144340623	NONHSAT005782
7	lnc-PPIAL4B-1	chr1:144340851-144341057	ENSG00000235398
8	lnc-FAM72D-1	chr1:144091810-144091946	ENSG00000224363
9	lnc-PPIAL4B-1	chr1:144336229-144336254	ENSG00000235398
10	lnc-PPIAL4B-1	chr1:144325839-144326185	ENSG00000235398
11	lnc-FAM72D-1	chr1:144089281-144089406	NONHSAT005767
12	lnc-FAM72D-3	chr1:144086700-144086911	NONHSAT005763
13	lnc-FAM72D-1	chr1:144093413-144093719	NONHSAT005766
14	lnc-PPIAL4B-1	chr1:144340526-144340623	ENSG00000235398
15	lnc-PPIAL4B-1	chr1:144300512-144300755	NR_109754
16	lnc-FAM72D-1	chr1:144089058-144089129	NONHSAT005765
17	lnc-PPIAL4B-3	chr1:144392143-144392429	NONHSAT005791
18	lnc-PPIAL4B-1	chr1:144301190-144301536	NONHSAT005782
19	lnc-AL592284.1-3	chr1:144214429-144214601	NONHSAT005770
20	lnc-PPIAL4B-1	chr1:144341670-144341755	NR_024584
21	lnc-FAM72D-1	chr1:144087684-144087804	NONHSAT005766
22	lnc-PPIAL4B-4	chr1:144297622-144297896	expRegAs_chr1_13930_-
23	lnc-PPIAL4B-1	chr1:144301190-144301536	ENSG00000235398
24	lnc-AL592284.1-4	chr1:144166564-144166933	NONHSAT005769
25	lnc-FAM72D-2	chr1:144085156-144086051	ucscGeneNc_uc001enh_1
26	lnc-PPIAL4B-1	chr1:144340526-144340671	ENSG00000235398
27	lnc-PPIAL4B-1	chr1:144301326-144301536	ENSG00000235398.4
28	lnc-FAM72D-1	chr1:144093413-144093754	NONHSAT005764
29	lnc-PPIAL4B-1	chr1:144281066-144281169	ENSG00000235398
30	lnc-PPIAL4B-1	chr1:144300514-144300755	NONHSAT005782
31	lnc-FAM72D-3	chr1:144083445-144085155	ucscGeneNc_uc001eng_1
32	lnc-PPIAL4B-1	chr1:144326026-144326185	ENSG00000235398
33	lnc-PPIAL4B-1	chr1:144300512-144300755	NONHSAT005780
34	lnc-FAM72D-1	chr1:144088374-144088668	NONHSAT005765
35	lnc-FAM72D-1	chr1:144087901-144088049	NONHSAT005764
36	lnc-AL592284.1-4	chr1:144167648-144167711	NONHSAT005769
37	lnc-PPIAL4B-1	chr1:144340526-144340773	NR_109754
38	lnc-AL592284.1-3	chr1:144215316-144215424	NONHSAT005770
39	lnc-PPIAL4B-1	chr1:144340526-144340736	ENSG00000235398
40	lnc-PPIAL4B-1	chr1:144300512-144300755	ENSG00000235398
41	lnc-PPIAL4B-1	chr1:144341670-144341755	NONHSAT005782
42	lnc-PPIAL4B-1	chr1:144301190-144301536	NONHSAT005780
43	lnc-PPIAL4B-1	chr1:144300512-144301536	NONHSAT005781
44	lnc-FAM72D-1	chr1:144088374-144088668	NONHSAT005766
45	lnc-PPIAL4B-1	chr1:144300515-144301536	ENSG00000235398
46	lnc-PPIAL4B-1	chr1:144325552-144325673	ENSG00000235398
47	lnc-PPIAL4B-2	chr1:144460973-144461111	ENSG00000236943.1
48	lnc-PPIAL4B-1	chr1:144301325-144301536	ENSG00000235398
49	lnc-PPIAL4B-1	chr1:144301350-144301536	NR_109754
50	lnc-FAM72D-1	chr1:144087524-144087804	NONHSAT005765

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	NBPF15	hsa-let-7b-5p	chr1:144174551-144174571
2	NBPF15	hsa-let-7b-5p	chr1:144166620-144166640
3	NBPF15	hsa-let-7b-5p	chr1:144199965-144199985

Variant related genes	Relation type
ENSG00000236943	TF binding region
PPIAL4B	TF binding region
ENSG00000271223	TF binding region
RNVU1-4	TF binding region
ENSG00000271644	TF binding region
ENSG00000231360	TF binding region
ENSG00000224363	TF binding region
NBPF8	TF binding region
LINC00623	TF binding region
ENSG00000236943	CpG island
PPIAL4B	CpG island
ENSG00000271223	CpG island
RNVU1-4	CpG island
ENSG00000271644	CpG island
ENSG00000231360	CpG island
ENSG00000224363	CpG island
NBPF8	CpG island
LINC00623	CpG island

Extended variants
information (count: 1626 )
Associated
traits (count: 178 )

Variant overlapped rSNPs/rCNVs (count:1626 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587766963	chr1:144036738-144036739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs587635052	chr1:144036748-144036749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587719177	chr1:144036760-144036761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs58833103	chr1:144036786-144036787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs199842523	chr1:144036799-144036800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587599720	chr1:144036840-144036841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587673650	chr1:144036857-144036858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs61378419	chr1:144036882-144036883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587708078	chr1:144036921-144036922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587606596	chr1:144036980-144036981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587661059	chr1:144037002-144037003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs587734090	chr1:144037017-144037018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs587594115	chr1:144037019-144037020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146046885	chr1:144037023-144037024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587663523	chr1:144037051-144037052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138533843	chr1:144037063-144037064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587747673	chr1:144037070-144037071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587641957	chr1:144037104-144037105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs587721685	chr1:144037145-144037146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1622502	chr1:144037211-144037212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587756125	chr1:144037232-144037233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587651982	chr1:144037240-144037241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs479196	chr1:144037265-144037266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181098482	chr1:144037273-144037274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1739157	chr1:144037301-144037302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1739156	chr1:144037371-144037372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs587761075	chr1:144037427-144037428	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs1754477	chr1:144037431-144037432	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs587642042	chr1:144037432-144037433	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs375130646	chr1:144037438-144037439	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs587755532	chr1:144037456-144037457	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs587650989	chr1:144037494-144037495	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs1754476	chr1:144037498-144037499	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs6671470	chr1:144037533-144037534	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs587707991	chr1:144037553-144037554	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs61822936	chr1:144037564-144037565	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs587606562	chr1:144037566-144037567	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs587628925	chr1:144037597-144037598	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs2987950	chr1:144037620-144037621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1754474	chr1:144037642-144037643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11284626	chr1:144037662-144037663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs587714618	chr1:144037680-144037681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs587608438	chr1:144037687-144037688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587667041	chr1:144037710-144037711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587742464	chr1:144037712-144037713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185745507	chr1:144037727-144037728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587698903	chr1:144037745-144037746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587754086	chr1:144037748-144037749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6663498	chr1:144037755-144037756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587651839	chr1:144037815-144037816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:178)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Schizophrenia	19197363	CNVD
Dyslexia	22102821	CNVD
Breast cancer	22522925	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	19805367	CNVD
Lung adenocarcinoma	21935476	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Autism	20841430	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144016800-144037200	Weak transcription	A549	lung
2	chr1:144017600-144037000	Weak transcription	Fetal Stomach	stomach
3	chr1:144017600-144037200	Weak transcription	Adipose Nuclei	Adipose
4	chr1:144019200-144037200	Weak transcription	HepG2	liver
5	chr1:144019400-144037200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:144019400-144038600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:144019400-144048600	Weak transcription	Brain Hippocampus Middle	brain
8	chr1:144019600-144037800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:144029200-144038800	Weak transcription	NH-A	brain
10	chr1:144029600-144037200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr1:144029600-144037400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:144029600-144038000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:144029600-144039800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:144029600-144044400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:144029600-144044800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:144029600-144046600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:144029600-144060200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr1:144030200-144053000	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr1:144031800-144037200	Weak transcription	Hela-S3	cervix
20	chr1:144034200-144054000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:144036000-144036800	Enhancers	Right Atrium	heart
22	chr1:144036000-144037600	Enhancers	Fetal Heart	heart
23	chr1:144036400-144037600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:144036400-144037600	Enhancers	HSMMtube	muscle
25	chr1:144036400-144037800	Enhancers	Fetal Muscle Leg	muscle
26	chr1:144036600-144037200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:144037200-144037400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:144037200-144037400	Enhancers	Fetal Stomach	stomach
29	chr1:144037200-144037400	Enhancers	A549	lung
30	chr1:144037200-144037600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:144037200-144037600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:144037200-144037600	Enhancers	Adipose Nuclei	Adipose
33	chr1:144037200-144037600	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr1:144037200-144037600	Enhancers	Hela-S3	cervix
35	chr1:144037200-144037600	Enhancers	HepG2	liver
36	chr1:144037200-144037600	Enhancers	HSMM	muscle
37	chr1:144037400-144037600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr1:144037600-144048400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:144043600-144044400	Weak transcription	NH-A	brain
40	chr1:144043800-144044200	Active TSS	Placenta	Placenta
41	chr1:144044000-144044400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr1:144044000-144044400	Enhancers	Right Atrium	heart
43	chr1:144044000-144044600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr1:144044000-144045000	Enhancers	Brain Germinal Matrix	brain
45	chr1:144044000-144045600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr1:144044200-144044400	Enhancers	Placenta	Placenta
47	chr1:144044200-144044400	Enhancers	Left Ventricle	heart
48	chr1:144044200-144044400	Enhancers	Right Ventricle	heart
49	chr1:144044200-144044600	Enhancers	Gastric	stomach
50	chr1:144044200-144045600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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