Variant report

Variant	esv1802274
Chromosome Location	chr22:29781844-29790912
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:976)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29784494-29784815	K562	blood:	n/a	n/a
2	ARID3A	chr22:29784598-29784803	HepG2	liver:	n/a	n/a
3	ATF2	chr22:29784482-29784966	GM12878	blood:	n/a	n/a
4	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
5	BCLAF1	chr22:29781657-29782228	GM12878	blood:	n/a	chr22:29781963-29781972
6	BCLAF1	chr22:29784167-29784915	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
7	BCLAF1	chr22:29784355-29784799	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
8	BHLHE40	chr22:29783767-29784854	K562	blood:	n/a	chr22:29784290-29784306
9	BHLHE40	chr22:29783782-29784846	GM12878	blood:	n/a	chr22:29784290-29784306
10	BHLHE40	chr22:29784305-29784732	HepG2	liver:	n/a	n/a
11	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
12	BRCA1	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
14	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
15	CEBPB	chr22:29784432-29784838	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr22:29784560-29784804	K562	blood:	n/a	n/a
17	CEBPB	chr22:29784541-29784752	HepG2	liver:	n/a	n/a
18	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPD	chr22:29784249-29784577	HepG2	liver:	n/a	n/a
20	CHD1	chr22:29784047-29784690	GM12878	blood:	n/a	chr22:29784363-29784373
21	CHD2	chr22:29784755-29784887	HepG2	liver:	n/a	n/a
22	CHD2	chr22:29784311-29784747	Hela-S3	cervix:	n/a	chr22:29784363-29784373
23	CHD2	chr22:29783991-29784944	GM12878	blood:	n/a	chr22:29784363-29784373
24	CHD2	chr22:29784280-29784804	H1-hESC	embryonic stem cell:	n/a	chr22:29784363-29784373
25	CHD2	chr22:29784690-29784742	K562	blood:	n/a	n/a
26	CREB1	chr22:29784307-29784902	GM12878	blood:	n/a	n/a
27	CREB1	chr22:29784315-29784717	ECC-1	luminal epithelium:	n/a	n/a
28	CREB1	chr22:29784199-29784929	HepG2	liver:	n/a	n/a
29	CREB1	chr22:29784344-29784793	A549	lung:	n/a	n/a
30	CTCF	chr22:29790770-29790844	Medullo	brain:	n/a	n/a
31	CTCF	chr22:29784120-29784270	GM12878	blood:	n/a	n/a
32	CTCF	chr22:29790612-29791606	SK-N-SH	brain:	n/a	chr22:29791127-29791143 chr22:29791572-29791585 chr22:29791391-29791404
33	CTCF	chr22:29784600-29784750	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr22:29790897-29791384	A549	lung:	n/a	chr22:29791127-29791143
35	CTCF	chr22:29784520-29784670	GM12878	blood:	n/a	n/a
36	CTCF	chr22:29790825-29790858	GM19238	blood:	n/a	n/a
37	CTCF	chr22:29784200-29784350	GM12871	blood:	n/a	n/a
38	CTCF	chr22:29782040-29782190	GM12865	blood:	n/a	n/a
39	CTCF	chr22:29784480-29784630	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr22:29784504-29784664	Lung_OC	lung:	n/a	n/a
41	CTCF	chr22:29790740-29790890	K562	blood:	n/a	n/a
42	CTCF	chr22:29783060-29783210	GM12873	blood:	n/a	n/a
43	CTCF	chr22:29783900-29784050	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr22:29790908-29791332	T-47D	breast:	n/a	chr22:29791127-29791143
45	CTCF	chr22:29784420-29784570	GM12865	blood:	n/a	n/a
46	CTCF	chr22:29784060-29784210	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr22:29790720-29791429	A549	lung:	n/a	chr22:29791127-29791143 chr22:29791391-29791404
48	CTCF	chr22:29784180-29784330	GM12865	blood:	n/a	n/a
49	CTCF	chr22:29790706-29791422	HCT-116	colon:	n/a	chr22:29791127-29791143 chr22:29791391-29791404
50	CTCF	chr22:29784100-29784250	AG04450	lung:	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	chr22:29784694-29784744	PFSK-1	brain:	n/a
2	chr22:29784694-29784744	PrEC	prostate:	n/a
3	chr22:29783861-29783911	AG04450	lung:	fetal
4	chr22:29785355-29785405	K562	blood:	n/a
5	chr22:29782753-29782803	MCF10A-Er-Src	breast:	n/a
6	chr22:29785355-29785405	HEK293	kidney:	embryo
7	chr22:29784644-29784694	PrEC	prostate:	n/a
8	chr22:29784237-29784287	AG09319	gingival:	n/a
9	chr22:29784778-29784828	SKMC	muscle:	n/a
10	chr22:29785355-29785405	GM12891	blood:	n/a
11	chr22:29783861-29783911	MCF10A-Er-Src	breast:	n/a
12	chr22:29784694-29784744	ovcar-3	ovarian:	n/a
13	chr22:29784778-29784828	ProgFib	skin:	n/a
14	chr22:29783861-29783911	PrEC	prostate:	n/a
15	chr22:29784644-29784694	AG10803	skin:	n/a
16	chr22:29784813-29784863	ProgFib	skin:	n/a
17	chr22:29784697-29784747	HRPEpiC	eye:	n/a
18	chr22:29784697-29784747	NHBE	bronchial:	n/a
19	chr22:29784692-29784742	IMR90	lung:	fetal
20	chr22:29784813-29784863	AG09319	gingival:	n/a
21	chr22:29781841-29781891	AG04449	skin:	fetal
22	chr22:29782753-29782803	A549	lung:	n/a
23	chr22:29784813-29784863	GM12878	blood:	n/a
24	chr22:29784237-29784287	PANC-1	pancreas:	n/a
25	chr22:29784237-29784287	Hepatocyte	liver:	n/a
26	chr22:29787625-29787675	HCT-116	colon:	n/a
27	chr22:29784671-29784721	ECC-1	luminal epithelium:	n/a
28	chr22:29784697-29784747	HepG2	liver:	n/a
29	chr22:29784237-29784287	SK-N-MC	brain:	n/a
30	chr22:29784441-29784491	RPTEC	kidney:	n/a
31	chr22:29784697-29784747	BE2_C	brain:	n/a
32	chr22:29783861-29783911	SK-N-MC	brain:	n/a
33	chr22:29784441-29784491	K562	blood:	n/a
34	chr22:29785355-29785405	SKMC	muscle:	n/a
35	chr22:29784778-29784828	HRPEpiC	eye:	n/a
36	chr22:29784237-29784287	MCF-7	breast:	n/a
37	chr22:29781841-29781891	SK-N-SH_RA	brain:	n/a
38	chr22:29783861-29783911	HepG2	liver:	n/a
39	chr22:29784813-29784863	NHBE	bronchial:	n/a
40	chr22:29784441-29784491	ProgFib	skin:	n/a
41	chr22:29784778-29784828	RPTEC	kidney:	n/a
42	chr22:29784671-29784721	CMK	blood:	n/a
43	chr22:29784441-29784491	PANC-1	pancreas:	n/a
44	chr22:29784624-29784674	Hepatocyte	liver:	n/a
45	chr22:29784813-29784863	GM06990	blood:	n/a
46	chr22:29784644-29784694	HL-60	blood:	n/a
47	chr22:29785355-29785405	ECC-1	luminal epithelium:	n/a
48	chr22:29784778-29784828	AoSMC	blood vessel:	n/a
49	chr22:29782753-29782803	GM19239	blood:	n/a
50	chr22:29785355-29785405	SK-N-MC	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29781310..29782787-chr22:29913055..29914130,15	MCF-7	breast:
2	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
3	chr22:29780907..29784157-chr22:29912302..29916422,4	MCF-7	breast:
4	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
5	chr22:29781864..29782673-chr22:29877575..29878342,2	MCF-7	breast:
6	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
7	chr22:29739232..29740930-chr22:29780922..29783404,2	MCF-7	breast:
8	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
9	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
10	chr22:29704896..29707829-chr22:29780262..29782390,2	MCF-7	breast:
11	chr22:29774091..29774727-chr22:29781651..29782814,5	MCF-7	breast:
12	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
13	chr22:29782601..29785697-chr22:29975164..29978533,5	MCF-7	breast:
14	chr22:29781890..29782717-chr22:29913055..29913918,8	MCF-7	breast:
15	chr22:29783197..29785326-chr22:29874558..29877420,2	MCF-7	breast:
16	chr22:29780492..29782846-chr22:29865528..29867159,2	MCF-7	breast:
17	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
18	chr22:29784558..29786360-chr22:29786552..29791390,4	MCF-7	breast:
19	chr22:29784194..29786218-chr22:29789472..29791131,2	K562	blood:
20	chr22:29787252..29790791-chr22:29920718..29924086,3	MCF-7	breast:
21	chr22:29701804..29704290-chr22:29781998..29785634,5	MCF-7	breast:
22	chr22:29209443..29210342-chr22:29781715..29782736,4	MCF-7	breast:
23	chr22:29781329..29782720-chr22:29913118..29914020,4	MCF-7	breast:
24	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
25	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:
26	chr22:29781578..29782726-chr22:29877337..29878344,7	MCF-7	breast:
27	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
28	chr22:29708527..29710108-chr22:29782946..29784507,2	K562	blood:
29	chr22:29774109..29774727-chr22:29781778..29782854,8	MCF-7	breast:
30	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
31	chr22:29770782..29772689-chr22:29780811..29782872,2	K562	blood:

No data

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

Extended variants
information (count: 296 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142180482	chr22:29781960-29781961	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565453028	chr22:29781972-29781973	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531121328	chr22:29781979-29781980	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552871151	chr22:29781996-29781997	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537573091	chr22:29782005-29782006	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564606732	chr22:29782007-29782008	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528756683	chr22:29782022-29782023	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs546695818	chr22:29782035-29782036	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368468429	chr22:29782083-29782084	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568073684	chr22:29782090-29782091	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535559052	chr22:29782183-29782184	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs192344478	chr22:29782339-29782340	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372666217	chr22:29782381-29782382	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs715494	chr22:29782433-29782434	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs551163846	chr22:29782473-29782474	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200470279	chr22:29782524-29782525	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539241255	chr22:29782544-29782545	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs558059408	chr22:29782584-29782585	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184147456	chr22:29782622-29782623	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs145910280	chr22:29782634-29782635	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs117087212	chr22:29782643-29782644	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs187223271	chr22:29782709-29782710	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs571067766	chr22:29782758-29782759	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs5763187	chr22:29782768-29782769	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138748755	chr22:29782769-29782770	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs562556971	chr22:29782858-29782859	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs140160683	chr22:29782868-29782869	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs367559003	chr22:29783066-29783067	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs150306570	chr22:29783074-29783075	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs371599328	chr22:29783112-29783113	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs547225363	chr22:29783281-29783282	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs369078165	chr22:29783294-29783295	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs80020683	chr22:29783312-29783313	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs77661714	chr22:29783313-29783314	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs71196659	chr22:29783314-29783315	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs561794469	chr22:29783384-29783385	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs192529576	chr22:29783388-29783389	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs112924188	chr22:29783400-29783401	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs113813971	chr22:29783423-29783424	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs557215503	chr22:29783442-29783443	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs61295298	chr22:29783445-29783446	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs568986385	chr22:29783473-29783474	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs184438457	chr22:29783483-29783484	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs6006117	chr22:29783498-29783499	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551302386	chr22:29783511-29783512	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs190502858	chr22:29783541-29783542	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs371737327	chr22:29783565-29783566	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs533844431	chr22:29783619-29783620	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs146150435	chr22:29783658-29783659	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs567308623	chr22:29783669-29783670	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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

Chromatin state (count:778 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29741000-29782800	Weak transcription	Hela-S3	cervix
2	chr22:29755000-29783800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr22:29755200-29782800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr22:29755400-29783600	Weak transcription	Fetal Kidney	kidney
5	chr22:29756000-29783600	Weak transcription	Right Ventricle	heart
6	chr22:29756000-29783800	Weak transcription	Ovary	ovary
7	chr22:29756400-29782600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr22:29765400-29782600	Weak transcription	Colon Smooth Muscle	Colon
9	chr22:29765400-29783600	Weak transcription	Rectal Smooth Muscle	rectum
10	chr22:29765600-29783600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr22:29765600-29783600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr22:29765800-29782800	Weak transcription	NHDF-Ad	bronchial
13	chr22:29766200-29783600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr22:29767200-29783600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr22:29767400-29783400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr22:29767400-29783600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr22:29768000-29783600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr22:29768000-29783800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr22:29769200-29783600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr22:29770400-29782600	Strong transcription	Primary T cells from cord blood	blood
21	chr22:29772400-29783000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr22:29772600-29782400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr22:29772600-29783400	Weak transcription	HSMMtube	muscle
24	chr22:29772800-29782800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr22:29773600-29783600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr22:29773600-29783600	Weak transcription	HSMM	muscle
27	chr22:29774000-29783600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr22:29774200-29782000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr22:29774200-29783000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr22:29774200-29783600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr22:29774200-29784000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr22:29774600-29782200	Weak transcription	Psoas Muscle	Psoas
33	chr22:29776200-29782000	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr22:29776400-29783600	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr22:29776800-29782800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr22:29777000-29782200	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr22:29777000-29782800	Weak transcription	Esophagus	oesophagus
38	chr22:29777000-29783400	Weak transcription	Right Atrium	heart
39	chr22:29777000-29783600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr22:29777200-29782200	Weak transcription	HMEC	breast
41	chr22:29777600-29782000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr22:29778000-29782600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr22:29778000-29783000	Enhancers	Liver	Liver
44	chr22:29778400-29783600	Enhancers	HepG2	liver
45	chr22:29779000-29783600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr22:29779000-29783800	Weak transcription	Aorta	Aorta
47	chr22:29779200-29782400	Weak transcription	A549	lung
48	chr22:29779200-29783000	Weak transcription	Fetal Lung	lung
49	chr22:29779200-29783400	Weak transcription	Fetal Heart	heart
50	chr22:29779200-29783600	Enhancers	Primary monocytes fromperipheralblood	blood

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