Variant report

Variant	nsv914961
Chromosome Location	chr22:29755888-29817506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1443)
CpG islands
(count:1099)
Chromatin interactive
region (count:75)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1443 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29790955-29791320	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:29784494-29784815	K562	blood:	n/a	n/a
3	ARID3A	chr22:29784598-29784803	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:29778868-29779190	K562	blood:	n/a	n/a
5	ATF1	chr22:29760207-29760407	K562	blood:	n/a	n/a
6	ATF1	chr22:29797555-29797746	K562	blood:	n/a	n/a
7	ATF2	chr22:29765407-29765735	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr22:29784482-29784966	GM12878	blood:	n/a	n/a
9	BACH1	chr22:29765433-29765705	H1-hESC	embryonic stem cell:	n/a	chr22:29765575-29765589
10	BATF	chr22:29810856-29811337	GM12878	blood:	n/a	n/a
11	BATF	chr22:29763694-29763993	GM12878	blood:	n/a	chr22:29763867-29763878
12	BATF	chr22:29808804-29809035	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:29760070-29760322	GM12878	blood:	n/a	chr22:29760190-29760199
14	BCL11A	chr22:29801979-29802220	GM12878	blood:	n/a	n/a
15	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
16	BCLAF1	chr22:29784355-29784799	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
17	BCLAF1	chr22:29784167-29784915	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
18	BCLAF1	chr22:29781657-29782228	GM12878	blood:	n/a	chr22:29781963-29781972
19	BHLHE40	chr22:29816277-29816626	K562	blood:	n/a	n/a
20	BHLHE40	chr22:29783767-29784854	K562	blood:	n/a	chr22:29784290-29784306
21	BHLHE40	chr22:29784305-29784732	HepG2	liver:	n/a	n/a
22	BHLHE40	chr22:29807666-29807691	GM12878	blood:	n/a	n/a
23	BHLHE40	chr22:29810866-29811343	GM12878	blood:	n/a	n/a
24	BHLHE40	chr22:29765504-29765531	HepG2	liver:	n/a	n/a
25	BHLHE40	chr22:29783782-29784846	GM12878	blood:	n/a	chr22:29784290-29784306
26	BHLHE40	chr22:29779081-29779149	K562	blood:	n/a	n/a
27	BHLHE40	chr22:29816228-29816602	GM12878	blood:	n/a	n/a
28	BRCA1	chr22:29791082-29791132	HepG2	liver:	n/a	n/a
29	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
30	BRCA1	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
32	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
33	CCNT2	chr22:29778935-29779230	K562	blood:	n/a	n/a
34	CEBPB	chr22:29765399-29765731	K562	blood:	n/a	n/a
35	CEBPB	chr22:29765427-29765877	A549	lung:	n/a	n/a
36	CEBPB	chr22:29765315-29765680	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr22:29805000-29805273	HepG2	liver:	n/a	chr22:29805152-29805163
38	CEBPB	chr22:29771466-29771819	IMR90	lung:	n/a	n/a
39	CEBPB	chr22:29765357-29765938	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr22:29771478-29771805	K562	blood:	n/a	n/a
41	CEBPB	chr22:29805054-29805264	MCF-7	breast:	n/a	chr22:29805152-29805163
42	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr22:29771539-29771762	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr22:29791176-29791249	K562	blood:	n/a	n/a
45	CEBPB	chr22:29773811-29774403	MCF-7	breast:	n/a	n/a
46	CEBPB	chr22:29781370-29781510	HepG2	liver:	n/a	n/a
47	CEBPB	chr22:29804956-29805312	K562	blood:	n/a	chr22:29805152-29805163
48	CEBPB	chr22:29771588-29771690	A549	lung:	n/a	n/a
49	CEBPB	chr22:29765292-29765790	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr22:29784541-29784752	HepG2	liver:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29784692-29784742	NB4	blood:	n/a
2	chr22:29784692-29784742	NB4	blood:	n/a
3	chr22:29784692-29784742	AG04449	skin:	fetal
4	chr22:29784671-29784721	HNPCEpiC	eye:	n/a
5	chr22:29784624-29784674	Jurkat	blood:	n/a
6	chr22:29784624-29784674	NB4	blood:	n/a
7	chr22:29784237-29784287	HCF	heart:	n/a
8	chr22:29783861-29783911	HRE	kidney:	n/a
9	chr22:29784697-29784747	HCM	heart:	n/a
10	chr22:29784441-29784491	IMR90	lung:	fetal
11	chr22:29784813-29784863	HAEpiC	amniotic membrane:	n/a
12	chr22:29784697-29784747	NB4	blood:	n/a
13	chr22:29781841-29781891	HCPEpiC	choroid plexus:	n/a
14	chr22:29784436-29784486	Hela-S3	cervix:	n/a
15	chr22:29784624-29784674	LNCaP	prostate:	n/a
16	chr22:29787625-29787675	AG04449	skin:	fetal
17	chr22:29784813-29784863	GM06990	blood:	n/a
18	chr22:29782753-29782803	HMEC	breast:	n/a
19	chr22:29784692-29784742	HCF	heart:	n/a
20	chr22:29784624-29784674	U87	brain:	n/a
21	chr22:29784624-29784674	HMEC	breast:	n/a
22	chr22:29785355-29785405	SAEC	small airway:	n/a
23	chr22:29784694-29784744	HRCEpiC	kidney:	n/a
24	chr22:29783861-29783911	HRCEpiC	kidney:	n/a
25	chr22:29778415-29778465	PANC-1	pancreas:	n/a
26	chr22:29784436-29784486	AG09309	skin:	n/a
27	chr22:29784436-29784486	PFSK-1	brain:	n/a
28	chr22:29784813-29784863	HCM	heart:	n/a
29	chr22:29781841-29781891	HRCEpiC	kidney:	n/a
30	chr22:29784436-29784486	GM12892	blood:	n/a
31	chr22:29784671-29784721	HMEC	breast:	n/a
32	chr22:29784813-29784863	HCT-116	colon:	n/a
33	chr22:29781841-29781891	NB4	blood:	n/a
34	chr22:29778415-29778465	HL-60	blood:	n/a
35	chr22:29778415-29778465	AG04450	lung:	fetal
36	chr22:29755863-29755913	ProgFib	skin:	n/a
37	chr22:29784624-29784674	NT2-D1	testis:	n/a
38	chr22:29785355-29785405	U87	brain:	n/a
39	chr22:29784697-29784747	NT2-D1	testis:	n/a
40	chr22:29785355-29785405	GM12891	blood:	n/a
41	chr22:29784436-29784486	AG04449	skin:	fetal
42	chr22:29784813-29784863	HEEpiC	esophagus:	n/a
43	chr22:29784778-29784828	AG04450	lung:	fetal
44	chr22:29784436-29784486	HRE	kidney:	n/a
45	chr22:29784237-29784287	AG10803	skin:	n/a
46	chr22:29784644-29784694	Jurkat	blood:	n/a
47	chr22:29784671-29784721	CMK	blood:	n/a
48	chr22:29784671-29784721	AG10803	skin:	n/a
49	chr22:29784624-29784674	PANC-1	pancreas:	n/a
50	chr22:29784436-29784486	SK-N-SH	brain:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:29780492..29782846-chr22:29865528..29867159,2	MCF-7	breast:
2	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
3	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
4	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
5	chr22:29760830..29763484-chr22:29765100..29766942,2	K562	blood:
6	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:
7	chr22:29801402..29803143-chr22:32549344..32551299,2	K562	blood:
8	chr22:29707397..29709984-chr22:29754201..29756527,2	MCF-7	breast:
9	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
10	chr22:29764682..29767147-chr22:29767285..29770224,2	MCF-7	breast:
11	chr22:29774141..29774748-chr22:29913157..29913945,3	MCF-7	breast:
12	chr22:29739232..29740930-chr22:29780922..29783404,2	MCF-7	breast:
13	chr22:29781864..29782673-chr22:29877575..29878342,2	MCF-7	breast:
14	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
15	chr22:29770398..29771976-chr22:29778753..29780431,2	K562	blood:
16	chr22:29776140..29778611-chr22:29995991..29998407,2	K562	blood:
17	chr22:29783197..29785326-chr22:29874558..29877420,2	MCF-7	breast:
18	chr22:29762328..29763973-chr22:29771513..29774228,2	MCF-7	breast:
19	chr22:29749186..29751153-chr22:29753987..29756178,2	K562	blood:
20	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
21	chr22:29774141..29774748-chr22:29913128..29913945,5	MCF-7	breast:
22	chr22:29771733..29774744-chr22:29774993..29776760,3	MCF-7	breast:
23	chr22:29787252..29790791-chr22:29920718..29924086,3	MCF-7	breast:
24	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
25	chr22:29782601..29785697-chr22:29975164..29978533,5	MCF-7	breast:
26	chr22:29701853..29704489-chr22:29754340..29756996,2	MCF-7	breast:
27	chr22:29775197..29780621-chr22:29782246..29785885,8	K562	blood:
28	chr22:29770398..29771976-chr22:29778753..29780431,2	K562	blood:
29	chr22:29704896..29707829-chr22:29780262..29782390,2	MCF-7	breast:
30	chr22:29771733..29774744-chr22:29774993..29776760,3	MCF-7	breast:
31	chr22:29773835..29774566-chr22:29913414..29914007,2	MCF-7	breast:
32	chr22:29781890..29782717-chr22:29913055..29913918,8	MCF-7	breast:
33	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
34	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
35	chr22:29708527..29710108-chr22:29782946..29784507,2	K562	blood:
36	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
37	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
38	chr22:29701804..29704290-chr22:29781998..29785634,5	MCF-7	breast:
39	chr22:29760830..29763484-chr22:29765100..29766942,2	K562	blood:
40	chr22:29704102..29706466-chr22:29771552..29773376,2	MCF-7	breast:
41	chr22:29774954..29777707-chr22:29779123..29781815,2	K562	blood:
42	chr22:29702455..29704377-chr22:29769522..29771265,2	MCF-7	breast:
43	chr22:29781578..29782726-chr22:29877337..29878344,7	MCF-7	breast:
44	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
45	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
46	chr22:29774954..29777707-chr22:29779123..29781815,2	K562	blood:
47	chr22:29794548..29795126-chr22:29913333..29914116,2	MCF-7	breast:
48	chr22:29209443..29210342-chr22:29781715..29782736,4	MCF-7	breast:
49	chr22:29700727..29703108-chr22:29758204..29760542,2	MCF-7	breast:
50	chr22:29778467..29780035-chr22:29782839..29784624,2	MCF-7	breast:

No data

Variant related genes	Relation type
AP1B1	TF binding region
AP1B1	CpG island
ENSG00000273216	chromatin interactions
ENSG00000184117	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000100285	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000100296	chromatin interactions
ENSG00000185340	chromatin interactions
ENSG00000100280	chromatin interactions

Extended variants
information (count: 2117 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2117 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2072051	chr22:29755888-29755889	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368021350	chr22:29755891-29755892	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567108618	chr22:29755909-29755910	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371485364	chr22:29755912-29755913	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375299154	chr22:29755963-29755964	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs181127377	chr22:29755964-29755965	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs373208542	chr22:29755974-29755975	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs376680107	chr22:29755996-29755997	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555313194	chr22:29756030-29756031	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573675826	chr22:29756081-29756082	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373784954	chr22:29756098-29756099	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537983140	chr22:29756116-29756117	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs114966167	chr22:29756170-29756171	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577804979	chr22:29756220-29756221	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs575734985	chr22:29756261-29756262	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs113576653	chr22:29756277-29756278	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553125122	chr22:29756312-29756313	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs78972756	chr22:29756332-29756333	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs79332733	chr22:29756333-29756334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs9613874	chr22:29756349-29756350	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555478467	chr22:29756370-29756371	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs545139937	chr22:29756479-29756480	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150865628	chr22:29756480-29756481	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185656888	chr22:29756496-29756497	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542282249	chr22:29756529-29756530	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560899429	chr22:29756530-29756531	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376983448	chr22:29756571-29756572	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541577720	chr22:29756574-29756575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138410726	chr22:29756589-29756590	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs549943352	chr22:29756632-29756633	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190749836	chr22:29756636-29756637	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182890995	chr22:29756650-29756651	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192505039	chr22:29756654-29756655	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551912106	chr22:29756670-29756671	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567073368	chr22:29756698-29756699	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs147254444	chr22:29756714-29756715	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140690986	chr22:29756726-29756727	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565708724	chr22:29756727-29756728	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567361878	chr22:29756758-29756759	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs5997466	chr22:29756836-29756837	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs556238487	chr22:29756847-29756848	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs578014095	chr22:29756855-29756856	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538468760	chr22:29756870-29756871	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553906466	chr22:29756915-29756916	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs416358	chr22:29756948-29756949	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs192379314	chr22:29756971-29756972	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371626422	chr22:29756982-29756983	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs578231767	chr22:29756987-29756988	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576154388	chr22:29756997-29756998	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543395886	chr22:29757021-29757022	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2301 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29721800-29756800	Strong transcription	Primary T cells from cord blood	blood
2	chr22:29722000-29759200	Strong transcription	Dnd41	blood
3	chr22:29722000-29759800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr22:29722200-29756400	Strong transcription	Thymus	Thymus
5	chr22:29722200-29756600	Strong transcription	Rectal Mucosa Donor 29	rectum
6	chr22:29722200-29759800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr22:29722400-29756800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr22:29722400-29758400	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr22:29722600-29756000	Strong transcription	Primary T helper cells PMA-I stimulated	--
10	chr22:29722600-29757200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr22:29722600-29758000	Strong transcription	Primary B cells from peripheral blood	blood
12	chr22:29722600-29758800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr22:29723000-29758800	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr22:29723000-29765000	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr22:29725400-29756200	Strong transcription	Primary B cells from cord blood	blood
16	chr22:29727400-29756200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr22:29728000-29756200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr22:29739000-29762800	Strong transcription	Primary neutrophils fromperipheralblood	blood
19	chr22:29739800-29757200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr22:29740200-29756400	Strong transcription	Fetal Thymus	thymus
21	chr22:29740600-29759000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr22:29740800-29756000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr22:29740800-29759000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr22:29741000-29782800	Weak transcription	Hela-S3	cervix
25	chr22:29741800-29756200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr22:29741800-29757200	Strong transcription	Primary hematopoietic stem cells	blood
27	chr22:29741800-29760200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr22:29742000-29756000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
29	chr22:29742000-29756000	Strong transcription	NHEK	skin
30	chr22:29742000-29757000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr22:29742200-29756200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr22:29742200-29756200	Strong transcription	Lung	lung
33	chr22:29742400-29756000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr22:29743200-29756000	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr22:29743600-29756000	Strong transcription	Brain Germinal Matrix	brain
36	chr22:29744000-29756600	Strong transcription	Fetal Brain Female	brain
37	chr22:29745000-29765200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr22:29745600-29763400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr22:29747800-29756000	Strong transcription	Pancreas	Pancrea
40	chr22:29749200-29756000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr22:29750400-29756200	Strong transcription	Brain Anterior Caudate	brain
42	chr22:29750600-29765200	Weak transcription	NHDF-Ad	bronchial
43	chr22:29750600-29766800	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr22:29750800-29760000	Weak transcription	K562	blood
45	chr22:29750800-29764400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr22:29752000-29756400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr22:29753000-29777600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr22:29754000-29756000	Strong transcription	HMEC	breast
49	chr22:29754000-29756000	Strong transcription	NHLF	lung
50	chr22:29754000-29756200	Strong transcription	H9 Cell Line	embryonic stem cell

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