Variant report

Variant	esv2580719
Chromosome Location	chr22:29759273-29816494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1402)
CpG islands
(count:1039)
Chromatin interactive
region (count:71)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1402 , 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	chr22:29784598-29784803	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:29790955-29791320	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:29778868-29779190	K562	blood:	n/a	n/a
4	ARID3A	chr22:29784494-29784815	K562	blood:	n/a	n/a
5	ATF1	chr22:29797555-29797746	K562	blood:	n/a	n/a
6	ATF1	chr22:29760207-29760407	K562	blood:	n/a	n/a
7	ATF2	chr22:29784482-29784966	GM12878	blood:	n/a	n/a
8	ATF2	chr22:29765407-29765735	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr22:29765433-29765705	H1-hESC	embryonic stem cell:	n/a	chr22:29765575-29765589
10	BATF	chr22:29808804-29809035	GM12878	blood:	n/a	n/a
11	BATF	chr22:29810856-29811337	GM12878	blood:	n/a	n/a
12	BATF	chr22:29763694-29763993	GM12878	blood:	n/a	chr22:29763867-29763878
13	BCL11A	chr22:29801979-29802220	GM12878	blood:	n/a	n/a
14	BCL11A	chr22:29760070-29760322	GM12878	blood:	n/a	chr22:29760190-29760199
15	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
16	BCLAF1	chr22:29781657-29782228	GM12878	blood:	n/a	chr22:29781963-29781972
17	BCLAF1	chr22:29784355-29784799	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
18	BCLAF1	chr22:29784167-29784915	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
19	BHLHE40	chr22:29783782-29784846	GM12878	blood:	n/a	chr22:29784290-29784306
20	BHLHE40	chr22:29783767-29784854	K562	blood:	n/a	chr22:29784290-29784306
21	BHLHE40	chr22:29807666-29807691	GM12878	blood:	n/a	n/a
22	BHLHE40	chr22:29784305-29784732	HepG2	liver:	n/a	n/a
23	BHLHE40	chr22:29779081-29779149	K562	blood:	n/a	n/a
24	BHLHE40	chr22:29816277-29816626	K562	blood:	n/a	n/a
25	BHLHE40	chr22:29765504-29765531	HepG2	liver:	n/a	n/a
26	BHLHE40	chr22:29816228-29816602	GM12878	blood:	n/a	n/a
27	BHLHE40	chr22:29810866-29811343	GM12878	blood:	n/a	n/a
28	BRCA1	chr22:29791082-29791132	HepG2	liver:	n/a	n/a
29	BRCA1	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
31	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
32	CCNT2	chr22:29778935-29779230	K562	blood:	n/a	n/a
33	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
34	CEBPB	chr22:29771478-29771805	K562	blood:	n/a	n/a
35	CEBPB	chr22:29805051-29805224	K562	blood:	n/a	chr22:29805152-29805163
36	CEBPB	chr22:29784432-29784838	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr22:29765399-29765731	K562	blood:	n/a	n/a
38	CEBPB	chr22:29771466-29771819	IMR90	lung:	n/a	n/a
39	CEBPB	chr22:29773211-29773460	MCF-7	breast:	n/a	n/a
40	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr22:29804956-29805312	K562	blood:	n/a	chr22:29805152-29805163
42	CEBPB	chr22:29784560-29784804	K562	blood:	n/a	n/a
43	CEBPB	chr22:29805000-29805273	HepG2	liver:	n/a	chr22:29805152-29805163
44	CEBPB	chr22:29771588-29771690	A549	lung:	n/a	n/a
45	CEBPB	chr22:29791176-29791249	K562	blood:	n/a	n/a
46	CEBPB	chr22:29804972-29805323	K562	blood:	n/a	chr22:29805152-29805163
47	CEBPB	chr22:29805089-29805202	IMR90	lung:	n/a	chr22:29805152-29805163
48	CEBPB	chr22:29765707-29765808	HepG2	liver:	n/a	n/a
49	CEBPB	chr22:29773807-29774448	MCF-7	breast:	n/a	n/a
50	CEBPB	chr22:29805054-29805264	MCF-7	breast:	n/a	chr22:29805152-29805163

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29784644-29784694	AG10803	skin:	n/a
2	chr22:29784644-29784694	K562	blood:	n/a
3	chr22:29784644-29784694	AG10803	skin:	n/a
4	chr22:29784644-29784694	K562	blood:	n/a
5	chr22:29784441-29784491	ovcar-3	ovarian:	n/a
6	chr22:29783861-29783911	SK-N-SH	brain:	n/a
7	chr22:29778415-29778465	MCF10A-Er-Src	breast:	n/a
8	chr22:29784697-29784747	BJ	skin:	n/a
9	chr22:29784237-29784287	MCF10A-Er-Src	breast:	n/a
10	chr22:29778415-29778465	GM06990	blood:	n/a
11	chr22:29778415-29778465	ECC-1	luminal epithelium:	n/a
12	chr22:29784697-29784747	NHDF-neo	bronchial:	n/a
13	chr22:29785355-29785405	LNCaP	prostate:	n/a
14	chr22:29783861-29783911	MCF10A-Er-Src	breast:	n/a
15	chr22:29781841-29781891	PFSK-1	brain:	n/a
16	chr22:29778415-29778465	GM12891	blood:	n/a
17	chr22:29781841-29781891	Hepatocyte	liver:	n/a
18	chr22:29784237-29784287	GM12892	blood:	n/a
19	chr22:29784624-29784674	HNPCEpiC	eye:	n/a
20	chr22:29784441-29784491	AG09309	skin:	n/a
21	chr22:29778415-29778465	Hela-S3	cervix:	n/a
22	chr22:29785355-29785405	ProgFib	skin:	n/a
23	chr22:29781841-29781891	SAEC	small airway:	n/a
24	chr22:29784237-29784287	HCF	heart:	n/a
25	chr22:29784441-29784491	HPAEpiC	pulmonary alveolar:	n/a
26	chr22:29785355-29785405	Caco-2	colon:	n/a
27	chr22:29778415-29778465	HCPEpiC	choroid plexus:	n/a
28	chr22:29782753-29782803	GM12878	blood:	n/a
29	chr22:29785355-29785405	Hela-S3	cervix:	n/a
30	chr22:29784813-29784863	K562	blood:	n/a
31	chr22:29784692-29784742	HIPEpiC	eye:	n/a
32	chr22:29787625-29787675	AG04449	skin:	fetal
33	chr22:29784813-29784863	NHDF-neo	bronchial:	n/a
34	chr22:29784694-29784744	ovcar-3	ovarian:	n/a
35	chr22:29784694-29784744	K562	blood:	n/a
36	chr22:29784237-29784287	LNCaP	prostate:	n/a
37	chr22:29784697-29784747	K562	blood:	n/a
38	chr22:29778415-29778465	HIPEpiC	eye:	n/a
39	chr22:29784624-29784674	NHBE	bronchial:	n/a
40	chr22:29787625-29787675	MCF10A-Er-Src	breast:	n/a
41	chr22:29784813-29784863	GM12878	blood:	n/a
42	chr22:29784441-29784491	HL-60	blood:	n/a
43	chr22:29784644-29784694	HCF	heart:	n/a
44	chr22:29784671-29784721	HRE	kidney:	n/a
45	chr22:29784644-29784694	NH-A	brain:	n/a
46	chr22:29784692-29784742	NHDF-neo	bronchial:	n/a
47	chr22:29784813-29784863	BE2_C	brain:	n/a
48	chr22:29784671-29784721	SKMC	muscle:	n/a
49	chr22:29787625-29787675	HUVEC	blood vessel:	n/a
50	chr22:29784697-29784747	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
2	chr22:29704102..29706466-chr22:29771552..29773376,2	MCF-7	breast:
3	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
4	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:
5	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
6	chr22:29775197..29780621-chr22:29782246..29785885,8	K562	blood:
7	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
8	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
9	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
10	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
11	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
12	chr22:29773835..29774566-chr22:29913414..29914007,2	MCF-7	breast:
13	chr22:29771733..29774744-chr22:29774993..29776760,3	MCF-7	breast:
14	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
15	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
16	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
17	chr22:29770398..29771976-chr22:29778753..29780431,2	K562	blood:
18	chr22:29704896..29707829-chr22:29780262..29782390,2	MCF-7	breast:
19	chr22:29787252..29790791-chr22:29920718..29924086,3	MCF-7	breast:
20	chr22:29781578..29782726-chr22:29877337..29878344,7	MCF-7	breast:
21	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
22	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
23	chr22:29777011..29779930-chr22:29821335..29822984,2	K562	blood:
24	chr22:29760830..29763484-chr22:29765100..29766942,2	K562	blood:
25	chr22:29209443..29210342-chr22:29781715..29782736,4	MCF-7	breast:
26	chr22:29781864..29782673-chr22:29877575..29878342,2	MCF-7	breast:
27	chr22:29702455..29704377-chr22:29769522..29771265,2	MCF-7	breast:
28	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
29	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
30	chr22:29770782..29772689-chr22:29780811..29782872,2	K562	blood:
31	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
32	chr22:29771731..29774347-chr22:29784237..29785863,2	MCF-7	breast:
33	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
34	chr22:29771983..29774340-chr22:29774881..29776429,2	K562	blood:
35	chr22:29774141..29774748-chr22:29913128..29913945,5	MCF-7	breast:
36	chr22:29778467..29780035-chr22:29782839..29784624,2	MCF-7	breast:
37	chr22:29701804..29704290-chr22:29781998..29785634,5	MCF-7	breast:
38	chr22:29762328..29763973-chr22:29771513..29774228,2	MCF-7	breast:
39	chr22:29739232..29740930-chr22:29780922..29783404,2	MCF-7	breast:
40	chr22:29801402..29803143-chr22:32549344..32551299,2	K562	blood:
41	chr22:29780907..29784157-chr22:29912302..29916422,4	MCF-7	breast:
42	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
43	chr22:29780492..29782846-chr22:29865528..29867159,2	MCF-7	breast:
44	chr22:29764682..29767147-chr22:29767285..29770224,2	MCF-7	breast:
45	chr22:29760830..29763484-chr22:29765100..29766942,2	K562	blood:
46	chr22:29781890..29782717-chr22:29913055..29913918,8	MCF-7	breast:
47	chr22:29784194..29786218-chr22:29789472..29791131,2	K562	blood:
48	chr22:29792519..29794058-chr22:29864789..29867115,2	MCF-7	breast:
49	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
50	chr22:29781329..29782720-chr22:29913118..29914020,4	MCF-7	breast:

No data

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

Extended variants
information (count: 1912 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1912 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558856831	chr22:29759306-29759307	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577348176	chr22:29759318-29759319	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541399583	chr22:29759327-29759328	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557276097	chr22:29759348-29759349	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs188927338	chr22:29759367-29759368	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs146541795	chr22:29759393-29759394	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542203909	chr22:29759404-29759405	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558168682	chr22:29759413-29759414	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs376007850	chr22:29759414-29759415	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546254821	chr22:29759421-29759422	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs564159116	chr22:29759433-29759434	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs174769	chr22:29759444-29759445	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs546539329	chr22:29759471-29759472	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567970266	chr22:29759506-29759507	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542992388	chr22:29759507-29759508	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559981520	chr22:29759508-29759509	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550127143	chr22:29759524-29759525	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112776192	chr22:29759526-29759527	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539187386	chr22:29759561-29759562	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150811545	chr22:29759583-29759584	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376476092	chr22:29759594-29759595	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544629033	chr22:29759614-29759615	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571002994	chr22:29759618-29759619	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535172017	chr22:29759619-29759620	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113169955	chr22:29759626-29759627	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181678538	chr22:29759650-29759651	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375515295	chr22:29759691-29759692	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs185310273	chr22:29759712-29759713	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs370911263	chr22:29759742-29759743	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113565322	chr22:29759756-29759757	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557417941	chr22:29759766-29759767	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149320651	chr22:29759782-29759783	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546023300	chr22:29759801-29759802	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs540550646	chr22:29759827-29759828	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs116388887	chr22:29759832-29759833	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540000890	chr22:29759883-29759884	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561664010	chr22:29759886-29759887	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs374207796	chr22:29759927-29759928	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs397832710	chr22:29760011-29760012	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191438589	chr22:29760012-29760013	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs7289528	chr22:29760064-29760065	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568795993	chr22:29760079-29760080	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs532937966	chr22:29760081-29760082	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs180757257	chr22:29760096-29760097	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186143606	chr22:29760106-29760107	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs378720	chr22:29760139-29760140	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs379061	chr22:29760236-29760237	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs553573363	chr22:29760259-29760260	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568646234	chr22:29760291-29760292	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536187033	chr22:29760313-29760314	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	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:2168 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29722000-29759800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr22:29722200-29759800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr22:29723000-29765000	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr22:29739000-29762800	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr22:29741000-29782800	Weak transcription	Hela-S3	cervix
6	chr22:29741800-29760200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr22:29745000-29765200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr22:29745600-29763400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr22:29750600-29765200	Weak transcription	NHDF-Ad	bronchial
10	chr22:29750600-29766800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr22:29750800-29760000	Weak transcription	K562	blood
12	chr22:29750800-29764400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr22:29753000-29777600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr22:29754600-29770400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr22:29754800-29759600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr22:29754800-29765200	Weak transcription	HSMM	muscle
17	chr22:29755000-29759400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr22:29755000-29765200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr22:29755000-29772200	Weak transcription	Aorta	Aorta
20	chr22:29755000-29783800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr22:29755200-29765000	Weak transcription	NH-A	brain
22	chr22:29755200-29773800	Weak transcription	Stomach Mucosa	stomach
23	chr22:29755200-29781000	Weak transcription	Fetal Brain Male	brain
24	chr22:29755200-29782800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr22:29755400-29759600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr22:29755400-29762000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr22:29755400-29764600	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr22:29755400-29765400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr22:29755400-29783600	Weak transcription	Fetal Kidney	kidney
30	chr22:29755600-29762000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr22:29755600-29763800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr22:29755600-29763800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr22:29755600-29771400	Weak transcription	Psoas Muscle	Psoas
34	chr22:29755600-29778600	Weak transcription	Fetal Lung	lung
35	chr22:29755800-29776600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr22:29756000-29759400	Weak transcription	Fetal Muscle Trunk	muscle
37	chr22:29756000-29759800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr22:29756000-29760800	Weak transcription	Duodenum Mucosa	Duodenum
39	chr22:29756000-29762000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr22:29756000-29762000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr22:29756000-29762000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr22:29756000-29762000	Weak transcription	Brain Hippocampus Middle	brain
43	chr22:29756000-29762000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr22:29756000-29762000	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr22:29756000-29763000	Strong transcription	Fetal Intestine Small	intestine
46	chr22:29756000-29764000	Weak transcription	Brain Substantia Nigra	brain
47	chr22:29756000-29764200	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr22:29756000-29764400	Weak transcription	Brain Angular Gyrus	brain
49	chr22:29756000-29764400	Weak transcription	NHEK	skin
50	chr22:29756000-29764600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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