Variant report

Variant	nsv946242
Chromosome Location	chr1:144588546-144622111
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:936)
CpG islands
(count:976)
Chromatin interactive
region (count:10)
LncRNA
region (count:90)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:936 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144618572-144618830	GM12878	blood:	n/a	n/a
2	BATF	chr1:144614551-144615001	GM12878	blood:	n/a	n/a
3	BATF	chr1:144594146-144594619	GM12878	blood:	n/a	n/a
4	BATF	chr1:144614537-144614797	GM12878	blood:	n/a	n/a
5	BATF	chr1:144618840-144619109	GM12878	blood:	n/a	n/a
6	BATF	chr1:144604582-144604786	GM12878	blood:	n/a	n/a
7	BATF	chr1:144593349-144593687	GM12878	blood:	n/a	n/a
8	BATF	chr1:144615131-144615468	GM12878	blood:	n/a	n/a
9	BATF	chr1:144621396-144621792	GM12878	blood:	n/a	n/a
10	BATF	chr1:144618285-144618435	GM12878	blood:	n/a	n/a
11	BATF	chr1:144615010-144615375	GM12878	blood:	n/a	n/a
12	BATF	chr1:144594992-144595236	GM12878	blood:	n/a	n/a
13	BATF	chr1:144617485-144617685	GM12878	blood:	n/a	n/a
14	BCL11A	chr1:144615162-144615415	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:144594216-144594609	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:144593207-144593737	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:144588906-144589083	GM12878	blood:	n/a	n/a
18	BCL11A	chr1:144620110-144620305	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:144618887-144619298	GM12878	blood:	n/a	n/a
20	BCL11A	chr1:144616137-144616391	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:144594234-144594691	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:144614491-144614868	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:144593251-144593513	GM12878	blood:	n/a	n/a
24	BCL11A	chr1:144614565-144614849	GM12878	blood:	n/a	n/a
25	BCL11A	chr1:144621190-144621435	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:144592484-144592707	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:144594908-144595186	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:144618530-144618828	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:144618876-144619331	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:144593128-144593433	HepG2	liver:	n/a	n/a
31	BHLHE40	chr1:144618560-144618873	HepG2	liver:	n/a	n/a
32	BHLHE40	chr1:144621538-144621780	HepG2	liver:	n/a	n/a
33	BHLHE40	chr1:144593618-144593811	HepG2	liver:	n/a	n/a
34	BRCA1	chr1:144594141-144594142	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr1:144593049-144594111	K562	blood:	n/a	n/a
36	CEBPB	chr1:144594027-144595012	GM12878	blood:	n/a	n/a
37	CEBPB	chr1:144593562-144593941	K562	blood:	n/a	n/a
38	CEBPB	chr1:144593686-144593779	Hela-S3	cervix:	n/a	n/a
39	CEBPD	chr1:144603624-144604138	K562	blood:	n/a	n/a
40	CEBPD	chr1:144593418-144593967	K562	blood:	n/a	n/a
41	CEBPD	chr1:144593600-144593851	HepG2	liver:	n/a	n/a
42	CHD2	chr1:144593678-144594302	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:144621403-144621735	A549	lung:	n/a	n/a
44	CTCF	chr1:144615075-144615250	IMR90	lung:	n/a	n/a
45	CTCF	chr1:144593862-144593919	GM19239	blood:	n/a	n/a
46	CTCF	chr1:144593536-144593651	GM10248	blood:	n/a	n/a
47	CTCF	chr1:144615140-144615290	GM12870	blood:	n/a	n/a
48	CTCF	chr1:144593640-144593790	BE2_C	brain:	n/a	n/a
49	CTCF	chr1:144593480-144593688	GM12892	blood:	n/a	n/a
50	CTCF	chr1:144593511-144593691	NHEK	skin:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144594085-144594135	CMK	blood:	n/a
2	chr1:144593341-144593391	HCM	heart:	n/a
3	chr1:144612358-144612408	PFSK-1	brain:	n/a
4	chr1:144612358-144612408	HUVEC	blood vessel:	n/a
5	chr1:144593903-144593953	NH-A	brain:	n/a
6	chr1:144612646-144612696	ovcar-3	ovarian:	n/a
7	chr1:144594107-144594157	Jurkat	blood:	n/a
8	chr1:144592392-144592442	HEEpiC	esophagus:	n/a
9	chr1:144594085-144594135	HUVEC	blood vessel:	n/a
10	chr1:144594259-144594309	HepG2	liver:	n/a
11	chr1:144592392-144592442	HCPEpiC	choroid plexus:	n/a
12	chr1:144594259-144594309	RPTEC	kidney:	n/a
13	chr1:144595718-144595768	BE2_C	brain:	n/a
14	chr1:144615272-144615322	HIPEpiC	eye:	n/a
15	chr1:144594006-144594056	PFSK-1	brain:	n/a
16	chr1:144612646-144612696	SKMC	muscle:	n/a
17	chr1:144619354-144619404	RPTEC	kidney:	n/a
18	chr1:144594259-144594309	AG04449	skin:	fetal
19	chr1:144594006-144594056	GM19239	blood:	n/a
20	chr1:144594259-144594309	AG10803	skin:	n/a
21	chr1:144594006-144594056	HEEpiC	esophagus:	n/a
22	chr1:144593343-144593393	AG04449	skin:	fetal
23	chr1:144594259-144594309	SK-N-SH_RA	brain:	n/a
24	chr1:144592392-144592442	U87	brain:	n/a
25	chr1:144612646-144612696	Caco-2	colon:	n/a
26	chr1:144615272-144615322	HMEC	breast:	n/a
27	chr1:144595718-144595768	HIPEpiC	eye:	n/a
28	chr1:144592392-144592442	SK-N-SH_RA	brain:	n/a
29	chr1:144592392-144592442	Hela-S3	cervix:	n/a
30	chr1:144593343-144593393	HCM	heart:	n/a
31	chr1:144620428-144620478	SKMC	muscle:	n/a
32	chr1:144595718-144595768	SAEC	small airway:	n/a
33	chr1:144612358-144612408	NH-A	brain:	n/a
34	chr1:144619354-144619404	PANC-1	pancreas:	n/a
35	chr1:144594259-144594309	Hepatocyte	liver:	n/a
36	chr1:144596061-144596111	HRCEpiC	kidney:	n/a
37	chr1:144593903-144593953	AoSMC	blood vessel:	n/a
38	chr1:144596061-144596111	ovcar-3	ovarian:	n/a
39	chr1:144612358-144612408	HAEpiC	amniotic membrane:	n/a
40	chr1:144594107-144594157	AG09309	skin:	n/a
41	chr1:144592392-144592442	AG04449	skin:	fetal
42	chr1:144596061-144596111	H1-hESC	embryonic stem cell:	embryo
43	chr1:144593343-144593393	BJ	skin:	n/a
44	chr1:144619354-144619404	NH-A	brain:	n/a
45	chr1:144619354-144619404	MCF-7	breast:	n/a
46	chr1:144594085-144594135	PFSK-1	brain:	n/a
47	chr1:144619354-144619404	LNCaP	prostate:	n/a
48	chr1:144615272-144615322	GM19239	blood:	n/a
49	chr1:144594006-144594056	GM12878	blood:	n/a
50	chr1:144594107-144594157	HCPEpiC	choroid plexus:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144593856..144595655-chr1:148555098..148556798,2	MCF-7	breast:
2	chr1:144590335..144591846-chr1:148550727..148552604,2	MCF-7	breast:
3	chr1:144593716..144594289-chr1:148555892..148556883,2	MCF-7	breast:
4	chr1:144532845..144535745-chr1:144588641..144591361,2	K562	blood:
5	chr1:144590246..144591117-chr1:148550866..148551429,2	MCF-7	breast:
6	chr1:144589128..144591973-chr1:144594157..144597024,2	MCF-7	breast:
7	chr1:144594105..144596972-chr1:148555192..148558576,3	MCF-7	breast:
8	chr1:144594107..144594639-chr1:148556298..148556816,2	Hela-S3	cervix:
9	chr1:144593744..144594609-chr1:148555862..148556622,3	HCT-116	colon:
10	chr1:144589128..144591973-chr1:144594157..144597024,2	MCF-7	breast:

(count:90 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-1	chr1:144606369-144606510	ENSG00000225241
2	lnc-AL592284.1-1	chr1:144606369-144606510	NONHSAT005823
3	lnc-AL592284.1-1	chr1:144598512-144598780	NONHSAT005825
4	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102404
5	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
6	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
7	lnc-AL592284.1-1	chr1:144604478-144604508	ENSG00000225241
8	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
9	lnc-AL592284.1-1	chr1:144618082-144618296	NR_102404
10	lnc-AL592284.1-1	chr1:144621447-144621655	ENSG00000225241
11	lnc-AL592284.1-1	chr1:144596281-144596473	NONHSAT005824
12	lnc-AL592284.1-1	chr1:144596281-144596473	NONHSAT005823
13	lnc-AL592284.1-1	chr1:144593907-144593936	ENSG00000225241
14	lnc-AL592284.1-1	chr1:144598391-144598780	NONHSAT005826
15	lnc-AL592284.1-1	chr1:144619347-144619419	NR_102405
16	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
17	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102405
18	lnc-AL592284.1-1	chr1:144606369-144606510	NONHSAT005822
19	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
20	lnc-AL592284.1-1	chr1:144612349-144612599	ENSG00000225241
21	lnc-AL592284.1-1	chr1:144619347-144619419	NR_102404
22	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
23	lnc-AL592284.1-1	chr1:144614388-144614998	ENSG00000225241
24	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
25	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
26	lnc-AL592284.1-1	chr1:144606938-144607061	ENSG00000225241
27	lnc-AL592284.1-1	chr1:144598614-144598780	ENSG00000225241
28	lnc-AL592284.1-1	chr1:144598512-144598780	ENSG00000225241
29	lnc-AL592284.1-1	chr1:144598512-144598780	NONHSAT005823
30	lnc-AL592284.1-1	chr1:144614959-144615303	NR_102405
31	lnc-AL592284.1-1	chr1:144619883-144620039	ENSG00000225241
32	lnc-AL592284.1-1	chr1:144614892-144615303	NONHSAT139893
33	lnc-AL592284.1-1	chr1:144618082-144618296	NR_102405
34	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102404
35	lnc-AL592284.1-1	chr1:144598512-144598780	ENSG00000225241
36	lnc-AL592284.1-1	chr1:144614532-144614993	ENSG00000225241
37	lnc-AL592284.1-1	chr1:144618513-144618663	ENSG00000225241
38	lnc-AL592284.1-1	chr1:144606838-144607342	NONHSAT005826
39	lnc-AL592284.1-1	chr1:144606369-144606510	ENSG00000225241
40	lnc-AL592284.1-1	chr1:144614959-144615303	NR_102404
41	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
42	lnc-AL592284.1-1	chr1:144621447-144621656	ENSG00000225241
43	lnc-AL592284.1-1	chr1:144604417-144604508	ENSG00000225241
44	lnc-AL592284.1-1	chr1:144614840-144614993	ENSG00000225241
45	lnc-AL592284.1-1	chr1:144617150-144617208	NONHSAT139893
46	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
47	lnc-AL592284.1-1	chr1:144606369-144606562	NONHSAT005824
48	lnc-AL592284.1-1	chr1:144606129-144606278	ENSG00000225241
49	lnc-AL592284.1-1	chr1:144612349-144612562	NONHSAT005823
50	lnc-AL592284.1-1	chr1:144604410-144604508	ENSG00000225241

No data

Variant related genes	Relation type
ENSG00000225241	TF binding region
PFN1P2	TF binding region
ENSG00000225241	CpG island
PFN1P2	CpG island
ENSG00000201699	chromatin interactions
ENSG00000243452	chromatin interactions

Extended variants
information (count: 1665 )
Associated
traits (count: 167 )

Variant overlapped rSNPs/rCNVs (count:1665 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148989244	chr1:144588656-144588657	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs587705442	chr1:144588705-144588706	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143751903	chr1:144588823-144588824	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587666405	chr1:144588828-144588829	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148172341	chr1:144588836-144588837	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs113858659	chr1:144588895-144588896	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587745970	chr1:144588898-144588899	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587619288	chr1:144588902-144588903	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189756005	chr1:144588908-144588909	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs587716811	chr1:144588919-144588920	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs587593780	chr1:144588945-144588946	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs74651662	chr1:144588958-144588959	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs587732768	chr1:144589009-144589010	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs368057093	chr1:144589028-144589029	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs200129306	chr1:144589038-144589039	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs61806561	chr1:144589061-144589062	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112491781	chr1:144589062-144589063	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs587663199	chr1:144589187-144589188	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587742796	chr1:144589223-144589224	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs199649699	chr1:144589247-144589248	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs182703960	chr1:144589248-144589249	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114453813	chr1:144589252-144589253	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs587623079	chr1:144589262-144589263	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200406724	chr1:144589264-144589265	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs587713244	chr1:144589323-144589324	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201249373	chr1:144589400-144589401	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs587776149	chr1:144589431-144589432	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs1630277	chr1:144589468-144589469	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs587664481	chr1:144589549-144589550	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201225948	chr1:144589593-144589594	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs1699824	chr1:144589596-144589597	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs587744122	chr1:144589614-144589615	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371382984	chr1:144589851-144589852	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs587637952	chr1:144589854-144589855	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587709941	chr1:144589855-144589856	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2019347	chr1:144589869-144589870	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587594155	chr1:144589909-144589910	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs587668000	chr1:144589987-144589988	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587710059	chr1:144589990-144589991	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369160656	chr1:144590002-144590003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587608055	chr1:144590008-144590009	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587662998	chr1:144590030-144590031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587747032	chr1:144590051-144590052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587598453	chr1:144590061-144590062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587675974	chr1:144590076-144590077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376836662	chr1:144590122-144590123	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs71229036	chr1:144590136-144590137	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs1698574	chr1:144590210-144590211	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs587727952	chr1:144590274-144590275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587635967	chr1:144590314-144590315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:167)

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
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	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
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144589000-144590000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:144589200-144589400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr1:144589800-144590000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:144589800-144590600	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr1:144590000-144593200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:144590600-144593200	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr1:144592800-144593200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:144593000-144593200	Enhancers	Dnd41	blood
9	chr1:144593000-144593800	Active TSS	Primary hematopoietic stem cells	blood
10	chr1:144593000-144594200	Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr1:144593000-144595400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:144593200-144593400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
13	chr1:144593200-144593400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
14	chr1:144593200-144593400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
15	chr1:144593200-144593400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr1:144593200-144593400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:144593200-144593400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:144593200-144593400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:144593200-144593400	Flanking Active TSS	Thymus	Thymus
20	chr1:144593200-144593400	Flanking Active TSS	Dnd41	blood
21	chr1:144593200-144593400	Flanking Active TSS	HMEC	breast
22	chr1:144593200-144593400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr1:144593200-144593400	Flanking Active TSS	NH-A	brain
24	chr1:144593200-144593600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:144593200-144593600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
26	chr1:144593200-144593600	Enhancers	Placenta	Placenta
27	chr1:144593200-144593800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
28	chr1:144593200-144593800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:144593200-144593800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:144593200-144594000	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr1:144593200-144594000	Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr1:144593200-144594000	Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr1:144593200-144594000	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr1:144593200-144594000	Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr1:144593200-144594000	Active TSS	Primary B cells from cord blood	blood
36	chr1:144593200-144594000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr1:144593200-144594000	Active TSS	Adipose Nuclei	Adipose
38	chr1:144593200-144594000	Active TSS	Duodenum Mucosa	Duodenum
39	chr1:144593200-144594000	Active TSS	Fetal Thymus	thymus
40	chr1:144593200-144594000	Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr1:144593200-144594200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:144593200-144594200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr1:144593200-144594200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:144593200-144594200	Active TSS	Primary monocytes fromperipheralblood	blood
45	chr1:144593200-144594200	Active TSS	Primary B cells from peripheral blood	blood
46	chr1:144593200-144594200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
47	chr1:144593200-144594200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:144593200-144594200	Active TSS	Fetal Muscle Leg	muscle
49	chr1:144593200-144594200	Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr1:144593200-144594200	Active TSS	K562	blood

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