Variant report

Variant	nsv1002955
Chromosome Location	chr2:133440142-133743211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:942)
CpG islands
(count:610)
Chromatin interactive
region (count:59)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:942 , 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	ARID3A	chr2:133617193-133617424	HepG2	liver:	n/a	n/a
2	BACH1	chr2:133573784-133574146	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr2:133653618-133653917	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:133736400-133736844	GM12878	blood:	n/a	n/a
5	BCL11A	chr2:133711370-133711688	GM12878	blood:	n/a	n/a
6	BCL3	chr2:133515343-133515697	GM12878	blood:	n/a	n/a
7	BCL3	chr2:133515389-133515606	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:133694444-133694688	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:133727257-133727412	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:133512674-133512966	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:133736509-133736513	GM12878	blood:	n/a	n/a
12	BRCA1	chr2:133573154-133573439	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr2:133676696-133676742	K562	blood:	n/a	n/a
14	CCNT2	chr2:133559502-133559520	K562	blood:	n/a	n/a
15	CEBPB	chr2:133735747-133736076	IMR90	lung:	n/a	n/a
16	CEBPB	chr2:133510137-133510396	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:133488270-133488544	A549	lung:	n/a	n/a
18	CEBPB	chr2:133479544-133479875	Hela-S3	cervix:	n/a	chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479708-133479721
19	CEBPB	chr2:133594728-133594998	Hela-S3	cervix:	n/a	chr2:133594876-133594887
20	CEBPB	chr2:133488239-133488578	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:133479537-133479893	HepG2	liver:	n/a	chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479708-133479721
22	CEBPB	chr2:133490770-133491039	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:133690013-133690065	HepG2	liver:	n/a	chr2:133690026-133690039 chr2:133690028-133690039 chr2:133690026-133690037
24	CEBPB	chr2:133479575-133479815	K562	blood:	n/a	chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479708-133479721
25	CEBPB	chr2:133659336-133659561	HepG2	liver:	n/a	chr2:133659455-133659466
26	CEBPB	chr2:133573054-133573611	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:133617805-133618112	IMR90	lung:	n/a	chr2:133617955-133617968 chr2:133617956-133617967
28	CEBPB	chr2:133689986-133690100	IMR90	lung:	n/a	chr2:133690026-133690039 chr2:133690028-133690039 chr2:133690026-133690037
29	CEBPB	chr2:133594714-133595027	IMR90	lung:	n/a	chr2:133594876-133594887
30	CEBPB	chr2:133490761-133491064	A549	lung:	n/a	n/a
31	CEBPB	chr2:133488406-133488528	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:133510118-133510373	A549	lung:	n/a	n/a
33	CEBPB	chr2:133505271-133505352	HepG2	liver:	n/a	n/a
34	CEBPB	chr2:133462736-133462779	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:133479614-133479773	H1-hESC	embryonic stem cell:	n/a	chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479708-133479721
36	CEBPB	chr2:133594780-133594971	H1-hESC	embryonic stem cell:	n/a	chr2:133594876-133594887
37	CEBPB	chr2:133641865-133642307	A549	lung:	n/a	chr2:133642044-133642055
38	CEBPB	chr2:133488400-133488477	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr2:133490852-133490972	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:133527279-133527434	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:133594699-133595011	A549	lung:	n/a	chr2:133594876-133594887
42	CEBPB	chr2:133599567-133599777	Hela-S3	cervix:	n/a	chr2:133599720-133599737
43	CEBPB	chr2:133461057-133461293	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:133723194-133723273	HepG2	liver:	n/a	chr2:133723220-133723231
45	CEBPB	chr2:133482542-133482626	IMR90	lung:	n/a	chr2:133482558-133482571
46	CEBPB	chr2:133448568-133448902	IMR90	lung:	n/a	n/a
47	CEBPB	chr2:133527238-133527420	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:133617159-133617359	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:133479555-133479897	A549	lung:	n/a	chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479710-133479719 chr2:133479708-133479721
50	CEBPB	chr2:133459453-133459633	IMR90	lung:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133670347-133670397	AoSMC	blood vessel:	n/a
2	chr2:133587191-133587241	HRE	kidney:	n/a
3	chr2:133670347-133670397	Jurkat	blood:	n/a
4	chr2:133587191-133587241	HCF	heart:	n/a
5	chr2:133508993-133509043	SAEC	small airway:	n/a
6	chr2:133630172-133630222	IMR90	lung:	fetal
7	chr2:133561787-133561837	AoSMC	blood vessel:	n/a
8	chr2:133672682-133672732	NHDF-neo	bronchial:	n/a
9	chr2:133561787-133561837	HRPEpiC	eye:	n/a
10	chr2:133695582-133695632	Hepatocyte	liver:	n/a
11	chr2:133635152-133635202	HepG2	liver:	n/a
12	chr2:133733241-133733291	Jurkat	blood:	n/a
13	chr2:133695582-133695632	HCF	heart:	n/a
14	chr2:133587191-133587241	U87	brain:	n/a
15	chr2:133672682-133672732	BE2_C	brain:	n/a
16	chr2:133630172-133630222	Caco-2	colon:	n/a
17	chr2:133635152-133635202	NH-A	brain:	n/a
18	chr2:133635152-133635202	HRE	kidney:	n/a
19	chr2:133514793-133514843	U87	brain:	n/a
20	chr2:133670347-133670397	Caco-2	colon:	n/a
21	chr2:133733241-133733291	HUVEC	blood vessel:	n/a
22	chr2:133514793-133514843	HRCEpiC	kidney:	n/a
23	chr2:133508993-133509043	PANC-1	pancreas:	n/a
24	chr2:133672682-133672732	SK-N-SH	brain:	n/a
25	chr2:133514793-133514843	NT2-D1	testis:	n/a
26	chr2:133695582-133695632	AG04450	lung:	fetal
27	chr2:133733241-133733291	BE2_C	brain:	n/a
28	chr2:133733241-133733291	CMK	blood:	n/a
29	chr2:133587191-133587241	HMEC	breast:	n/a
30	chr2:133672682-133672732	HMEC	breast:	n/a
31	chr2:133514793-133514843	RPTEC	kidney:	n/a
32	chr2:133672682-133672732	ECC-1	luminal epithelium:	n/a
33	chr2:133508993-133509043	PFSK-1	brain:	n/a
34	chr2:133508993-133509043	IMR90	lung:	fetal
35	chr2:133561787-133561837	HepG2	liver:	n/a
36	chr2:133672682-133672732	HEEpiC	esophagus:	n/a
37	chr2:133508993-133509043	HCPEpiC	choroid plexus:	n/a
38	chr2:133508993-133509043	SK-N-SH_RA	brain:	n/a
39	chr2:133587191-133587241	HIPEpiC	eye:	n/a
40	chr2:133733241-133733291	Caco-2	colon:	n/a
41	chr2:133561787-133561837	SKMC	muscle:	n/a
42	chr2:133514793-133514843	PANC-1	pancreas:	n/a
43	chr2:133672682-133672732	SK-N-MC	brain:	n/a
44	chr2:133635152-133635202	PFSK-1	brain:	n/a
45	chr2:133672682-133672732	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:133508993-133509043	H1-hESC	embryonic stem cell:	embryo
47	chr2:133561787-133561837	NHDF-neo	bronchial:	n/a
48	chr2:133514793-133514843	GM12878	blood:	n/a
49	chr2:133733241-133733291	HMEC	breast:	n/a
50	chr2:133587191-133587241	IMR90	lung:	fetal

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:133536409..133537927-chr2:133542677..133544641,2	K562	blood:
2	chr2:133473952..133476092-chr2:133482509..133484612,2	K562	blood:
3	chr2:133466983..133469956-chr2:133475273..133477903,2	K562	blood:
4	chr2:133551089..133552887-chr2:133586655..133588378,2	K562	blood:
5	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:
6	chr2:133395639..133398146-chr2:133561635..133563516,2	K562	blood:
7	chr2:133339874..133340573-chr2:133634427..133634936,2	MCF-7	breast:
8	chr2:133473952..133476092-chr2:133482509..133484612,2	K562	blood:
9	chr2:133426777..133428941-chr2:133439028..133441096,3	MCF-7	breast:
10	chr2:133542405..133544813-chr2:133545944..133548855,2	K562	blood:
11	chr2:133556846..133559424-chr2:133561319..133562974,2	MCF-7	breast:
12	chr2:133530106..133532173-chr2:133536887..133539675,2	K562	blood:
13	chr2:133474076..133476809-chr2:133480916..133483257,3	MCF-7	breast:
14	chr2:133474076..133476809-chr2:133480916..133483257,3	MCF-7	breast:
15	chr2:133605601..133608289-chr2:133610152..133612436,2	K562	blood:
16	chr19:11489081..11491625-chr2:133446373..133449058,2	MCF-7	breast:
17	chr2:133529831..133532826-chr2:133534612..133536132,2	K562	blood:
18	chr2:133525565..133527270-chr2:133534502..133536629,2	K562	blood:
19	chr2:133722484..133724496-chr2:133727279..133729057,2	K562	blood:
20	chr2:133605601..133608289-chr2:133610152..133612436,2	K562	blood:
21	chr2:133661857..133663730-chr2:133665052..133667903,2	K562	blood:
22	chr2:133632988..133635026-chr2:133635332..133637813,2	MCF-7	breast:
23	chr2:133408590..133409186-chr2:133610447..133611309,2	MCF-7	breast:
24	chr2:133529831..133532826-chr2:133534612..133536132,2	K562	blood:
25	chr2:133556846..133559424-chr2:133561319..133562974,2	MCF-7	breast:
26	chr2:133466983..133469956-chr2:133475273..133477903,2	K562	blood:
27	chr2:133710364..133712250-chr2:133715085..133717070,2	K562	blood:
28	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
29	chr2:133339765..133340550-chr2:133641463..133642066,3	MCF-7	breast:
30	chr12:96424203..96424877-chr2:133616548..133617287,2	MCF-7	breast:
31	chr2:133551089..133552887-chr2:133586655..133588378,2	K562	blood:
32	chr2:133542405..133544813-chr2:133545944..133548855,2	K562	blood:
33	chr2:133427176..133428915-chr2:133615683..133617868,2	MCF-7	breast:
34	chr2:133607951..133610816-chr2:133632079..133634420,2	MCF-7	breast:
35	chr2:133581642..133584243-chr2:133588053..133589989,2	K562	blood:
36	chr2:133595520..133597238-chr2:133598348..133600832,2	K562	blood:
37	chr2:133661857..133663730-chr2:133665052..133667903,2	K562	blood:
38	chr2:133519220..133521835-chr2:133522921..133525265,2	MCF-7	breast:
39	chr2:133339874..133340573-chr2:133634427..133635308,3	MCF-7	breast:
40	chr2:133550880..133552525-chr2:133559488..133561560,2	MCF-7	breast:
41	chr2:133737097..133739714-chr2:133742077..133743742,2	MCF-7	breast:
42	chr2:133632988..133635026-chr2:133635332..133637813,2	MCF-7	breast:
43	chr2:133737230..133740275-chr2:133741296..133743711,3	K562	blood:
44	chr2:133519220..133521835-chr2:133522921..133525265,2	MCF-7	breast:
45	chr2:133304259..133305229-chr2:133647133..133647703,2	MCF-7	breast:
46	chr2:133422076..133424197-chr2:133633337..133635605,2	MCF-7	breast:
47	chr2:133710364..133712250-chr2:133715085..133717070,2	K562	blood:
48	chr2:133525565..133527270-chr2:133534502..133536629,2	K562	blood:
49	chr2:133498325..133500281-chr2:133500580..133503062,2	MCF-7	breast:
50	chr2:133607951..133610816-chr2:133632079..133634420,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYPD1-2	chr2:133538625-133538802	NONHSAT074540
2	lnc-LYPD1-2	chr2:133539513-133539596	NONHSAT074540
3	lnc-GPR39-3	chr2:133673130-133673224	ENSG00000233729.1
4	lnc-GPR39-12	chr2:133741315-133741466	ucscGeneNc_uc002ttu_1
5	lnc-LYPD1-2	chr2:133489522-133489624	NONHSAT074540
6	lnc-GPR39-12	chr2:133742958-133743083	ucscGeneNc_uc002ttu_1
7	lnc-GPR39-12	chr2:133740284-133740478	ucscGeneNc_uc002ttu_1
8	lnc-GPR39-12	chr2:133742398-133742484	ucscGeneNc_uc002ttu_1
9	lnc-GPR39-3	chr2:133687452-133689067	ENSG00000233729.1

No data

Variant related genes	Relation type
ENSG00000228721	TF binding region
NCKAP5	TF binding region
ENSG00000233729	TF binding region
ENSG00000228721	CpG island
NCKAP5	CpG island
ENSG00000233729	CpG island
ENSG00000176771	chromatin interactions
ENSG00000150551	chromatin interactions

Extended variants
information (count: 11506 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:11506 , 50 per page) page: 1 2 3 4 5 6 7 ... 231

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565657438	chr2:133440204-133440205	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs533901813	chr2:133440205-133440206	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2709549	chr2:133440227-133440228	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs2566528	chr2:133440237-133440238	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544740082	chr2:133440245-133440246	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573028852	chr2:133440301-133440302	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs578150126	chr2:133440320-133440321	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185166141	chr2:133440321-133440322	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540570470	chr2:133440359-133440360	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2709548	chr2:133440362-133440363	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs528000699	chr2:133440374-133440375	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542596245	chr2:133440383-133440384	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574056886	chr2:133440411-133440412	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560984077	chr2:133440430-133440431	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201009406	chr2:133440460-133440461	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs116103137	chr2:133440466-133440467	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs56329807	chr2:133440490-133440491	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs564906376	chr2:133440503-133440504	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371180896	chr2:133440521-133440522	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547206576	chr2:133440526-133440527	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs544622222	chr2:133440550-133440551	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561666910	chr2:133440592-133440593	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139193358	chr2:133440605-133440606	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549108290	chr2:133440652-133440653	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567692530	chr2:133440660-133440661	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs562802099	chr2:133440690-133440691	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs149948976	chr2:133440706-133440707	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556647932	chr2:133440731-133440732	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs188359550	chr2:133440737-133440738	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181126478	chr2:133440746-133440747	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536331198	chr2:133440747-133440748	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145014242	chr2:133440760-133440761	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543344937	chr2:133440769-133440770	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs13424058	chr2:133440774-133440775	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs185869319	chr2:133440778-133440779	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs140455207	chr2:133440786-133440787	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs144313830	chr2:133440787-133440788	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191847722	chr2:133440788-133440789	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs77210852	chr2:133440797-133440798	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559172705	chr2:133440806-133440807	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529929883	chr2:133440824-133440825	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs548499103	chr2:133440837-133440838	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34784302	chr2:133440839-133440840	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs397758004	chr2:133440848-133440849	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374972076	chr2:133440859-133440860	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183559939	chr2:133440889-133440890	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187331594	chr2:133440924-133440925	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549915697	chr2:133440986-133440987	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs147794701	chr2:133441080-133441081	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539182628	chr2:133441135-133441136	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133430000-133444000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:133436400-133447000	Weak transcription	Hela-S3	cervix
3	chr2:133439400-133444000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:133440000-133441000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:133441000-133441400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:133441200-133454800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:133441400-133442400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:133441600-133462600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:133442400-133443400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:133443400-133447000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr2:133444000-133446600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:133446600-133447400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:133446800-133447000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr2:133447000-133447600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:133447000-133448200	Weak transcription	Fetal Stomach	stomach
16	chr2:133447000-133448800	Enhancers	Brain Hippocampus Middle	brain
17	chr2:133447200-133448200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr2:133447400-133450400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:133447600-133448000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:133447800-133448200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr2:133447800-133448600	Enhancers	Brain Substantia Nigra	brain
22	chr2:133447800-133448600	Enhancers	Stomach Smooth Muscle	stomach
23	chr2:133448000-133451200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr2:133448200-133448600	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr2:133448200-133448600	Enhancers	Fetal Stomach	stomach
26	chr2:133448200-133449000	Enhancers	HSMMtube	muscle
27	chr2:133448200-133449200	Enhancers	Osteobl	bone
28	chr2:133448200-133449600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr2:133448400-133448600	Enhancers	NHLF	lung
30	chr2:133448600-133450200	Weak transcription	NHLF	lung
31	chr2:133448600-133477000	Weak transcription	Fetal Stomach	stomach
32	chr2:133449000-133450400	Weak transcription	HSMMtube	muscle
33	chr2:133449200-133450200	Weak transcription	Osteobl	bone
34	chr2:133449600-133450000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:133450000-133451000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:133450200-133451000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr2:133450200-133451000	Enhancers	NHLF	lung
38	chr2:133450200-133451200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:133450200-133451200	Enhancers	Adipose Nuclei	Adipose
40	chr2:133450200-133451200	Enhancers	Osteobl	bone
41	chr2:133450400-133450600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:133450400-133450600	Enhancers	HSMMtube	muscle
43	chr2:133450400-133450800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:133450600-133450800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:133450800-133451600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:133450800-133454400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:133451000-133455000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:133451000-133455200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr2:133451200-133459200	Weak transcription	Osteobl	bone
50	chr2:133451200-133459400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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