Variant report

Variant	nsv821257
Chromosome Location	chr22:29783172-29794087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:706)
CpG islands
(count:855)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	ARID3A	chr22:29790955-29791320	HepG2	liver:	n/a	n/a
4	ATF2	chr22:29784482-29784966	GM12878	blood:	n/a	n/a
5	BCL3	chr22:29784461-29785020	GM12878	blood:	n/a	chr22:29784573-29784582 chr22:29784685-29784698 chr22:29784546-29784555
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	chr22:29784487-29784668	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr22:29784309-29784324	HepG2	liver:	n/a	n/a
13	BRCA1	chr22:29791082-29791132	HepG2	liver:	n/a	n/a
14	CBX3	chr22:29784370-29784766	K562	blood:	n/a	n/a
15	CCNT2	chr22:29784213-29784825	K562	blood:	n/a	n/a
16	CEBPB	chr22:29784560-29784804	K562	blood:	n/a	n/a
17	CEBPB	chr22:29791176-29791249	K562	blood:	n/a	n/a
18	CEBPB	chr22:29784432-29784838	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr22:29784541-29784752	HepG2	liver:	n/a	n/a
20	CEBPB	chr22:29784634-29784925	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPD	chr22:29784249-29784577	HepG2	liver:	n/a	n/a
22	CHD1	chr22:29784047-29784690	GM12878	blood:	n/a	chr22:29784363-29784373
23	CHD2	chr22:29784311-29784747	Hela-S3	cervix:	n/a	chr22:29784363-29784373
24	CHD2	chr22:29783991-29784944	GM12878	blood:	n/a	chr22:29784363-29784373
25	CHD2	chr22:29791078-29791089	HepG2	liver:	n/a	n/a
26	CHD2	chr22:29784280-29784804	H1-hESC	embryonic stem cell:	n/a	chr22:29784363-29784373
27	CHD2	chr22:29790975-29791296	GM12878	blood:	n/a	n/a
28	CHD2	chr22:29784690-29784742	K562	blood:	n/a	n/a
29	CHD2	chr22:29784755-29784887	HepG2	liver:	n/a	n/a
30	CREB1	chr22:29784307-29784902	GM12878	blood:	n/a	n/a
31	CREB1	chr22:29784344-29784793	A549	lung:	n/a	n/a
32	CREB1	chr22:29784315-29784717	ECC-1	luminal epithelium:	n/a	n/a
33	CREB1	chr22:29784199-29784929	HepG2	liver:	n/a	n/a
34	CTCF	chr22:29791060-29791210	HMEC	breast:	n/a	chr22:29791127-29791143
35	CTCF	chr22:29790740-29790890	K562	blood:	n/a	n/a
36	CTCF	chr22:29790966-29791380	H1-hESC	embryonic stem cell:	n/a	chr22:29791127-29791143
37	CTCF	chr22:29784395-29784682	K562	blood:	n/a	n/a
38	CTCF	chr22:29791040-29791190	GM12875	blood:	n/a	chr22:29791127-29791143
39	CTCF	chr22:29791060-29791210	HCPEpiC	choroid plexus:	n/a	chr22:29791127-29791143
40	CTCF	chr22:29784400-29784550	Caco-2	colon:	n/a	n/a
41	CTCF	chr22:29791060-29791210	HAc	cerebellar:	n/a	chr22:29791127-29791143
42	CTCF	chr22:29791080-29791230	GM12869	blood:	n/a	chr22:29791127-29791143
43	CTCF	chr22:29791060-29791210	GM12865	blood:	n/a	chr22:29791127-29791143
44	CTCF	chr22:29791023-29791243	GM20000	blood:	n/a	chr22:29791127-29791143
45	CTCF	chr22:29790951-29791317	HepG2	liver:	n/a	chr22:29791127-29791143
46	CTCF	chr22:29791520-29791670	HEK293	kidney:	n/a	chr22:29791572-29791585
47	CTCF	chr22:29791017-29791252	HepG2	liver:	n/a	chr22:29791127-29791143
48	CTCF	chr22:29791080-29791230	AG04450	lung:	n/a	chr22:29791127-29791143
49	CTCF	chr22:29790984-29791319	Spleen_OC	spleen:	n/a	chr22:29791127-29791143
50	CTCF	chr22:29790740-29790890	AG04449	skin:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29784694-29784744	HCT-116	colon:	n/a
2	chr22:29784694-29784744	HCT-116	colon:	n/a
3	chr22:29784436-29784486	HL-60	blood:	n/a
4	chr22:29787625-29787675	SK-N-MC	brain:	n/a
5	chr22:29784671-29784721	GM06990	blood:	n/a
6	chr22:29784697-29784747	Jurkat	blood:	n/a
7	chr22:29784671-29784721	AoSMC	blood vessel:	n/a
8	chr22:29784694-29784744	AoSMC	blood vessel:	n/a
9	chr22:29784237-29784287	LNCaP	prostate:	n/a
10	chr22:29784778-29784828	HNPCEpiC	eye:	n/a
11	chr22:29787625-29787675	GM12891	blood:	n/a
12	chr22:29785355-29785405	ProgFib	skin:	n/a
13	chr22:29783861-29783911	IMR90	lung:	fetal
14	chr22:29784778-29784828	GM12892	blood:	n/a
15	chr22:29784644-29784694	GM12892	blood:	n/a
16	chr22:29784778-29784828	BJ	skin:	n/a
17	chr22:29784694-29784744	HNPCEpiC	eye:	n/a
18	chr22:29784436-29784486	Jurkat	blood:	n/a
19	chr22:29784441-29784491	SKMC	muscle:	n/a
20	chr22:29785355-29785405	HEEpiC	esophagus:	n/a
21	chr22:29784441-29784491	T-47D	breast:	n/a
22	chr22:29784237-29784287	HPAEpiC	pulmonary alveolar:	n/a
23	chr22:29784813-29784863	HL-60	blood:	n/a
24	chr22:29787625-29787675	NH-A	brain:	n/a
25	chr22:29784694-29784744	K562	blood:	n/a
26	chr22:29784778-29784828	HCT-116	colon:	n/a
27	chr22:29784813-29784863	MCF-7	breast:	n/a
28	chr22:29784624-29784674	AG09309	skin:	n/a
29	chr22:29784671-29784721	PrEC	prostate:	n/a
30	chr22:29784697-29784747	MCF-7	breast:	n/a
31	chr22:29784697-29784747	HCM	heart:	n/a
32	chr22:29784694-29784744	HRPEpiC	eye:	n/a
33	chr22:29784671-29784721	PANC-1	pancreas:	n/a
34	chr22:29784624-29784674	RPTEC	kidney:	n/a
35	chr22:29784441-29784491	Caco-2	colon:	n/a
36	chr22:29784644-29784694	HMEC	breast:	n/a
37	chr22:29784697-29784747	SKMC	muscle:	n/a
38	chr22:29787625-29787675	AG10803	skin:	n/a
39	chr22:29784778-29784828	SK-N-SH	brain:	n/a
40	chr22:29787625-29787675	HIPEpiC	eye:	n/a
41	chr22:29784778-29784828	AG04449	skin:	fetal
42	chr22:29784813-29784863	NHDF-neo	bronchial:	n/a
43	chr22:29784671-29784721	GM12878	blood:	n/a
44	chr22:29784694-29784744	NHBE	bronchial:	n/a
45	chr22:29785355-29785405	NHDF-neo	bronchial:	n/a
46	chr22:29784778-29784828	HRE	kidney:	n/a
47	chr22:29784692-29784742	Caco-2	colon:	n/a
48	chr22:29784813-29784863	H1-hESC	embryonic stem cell:	embryo
49	chr22:29784624-29784674	GM06990	blood:	n/a
50	chr22:29784697-29784747	GM12878	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
2	chr22:29790720..29791562-chr22:29920209..29921282,4	MCF-7	breast:
3	chr22:29787252..29790791-chr22:29920718..29924086,3	MCF-7	breast:
4	chr22:29784630..29786169-chr22:29786224..29787893,2	K562	blood:
5	chr22:29771666..29773871-chr22:29789734..29792185,2	MCF-7	breast:
6	chr22:29701804..29704290-chr22:29781998..29785634,5	MCF-7	breast:
7	chr22:29782601..29785697-chr22:29975164..29978533,5	MCF-7	breast:
8	chr22:29771898..29775582-chr22:29781742..29783845,4	MCF-7	breast:
9	chr22:29739232..29740930-chr22:29780922..29783404,2	MCF-7	breast:
10	chr22:29780907..29784157-chr22:29912302..29916422,4	MCF-7	breast:
11	chr22:29790656..29791686-chr22:29920171..29921137,10	MCF-7	breast:
12	chr22:29792519..29794058-chr22:29864789..29867115,2	MCF-7	breast:
13	chr22:29791047..29793663-chr22:29794223..29797120,2	MCF-7	breast:
14	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
15	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
16	chr22:29784558..29786360-chr22:29786552..29791390,4	MCF-7	breast:
17	chr22:29783150..29785946-chr22:29944649..29946343,2	MCF-7	breast:
18	chr22:29781675..29783812-chr22:29788035..29790235,2	MCF-7	breast:
19	chr22:29792125..29793668-chr22:29802474..29805006,2	K562	blood:
20	chr22:29708527..29710108-chr22:29782946..29784507,2	K562	blood:
21	chr22:29786384..29789088-chr22:29790926..29793690,2	K562	blood:
22	chr22:29783197..29785326-chr22:29874558..29877420,2	MCF-7	breast:
23	chr22:29784194..29786218-chr22:29789472..29791131,2	K562	blood:
24	chr22:29712026..29714411-chr22:29782149..29784555,3	K562	blood:

No data

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

Extended variants
information (count: 387 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547225363	chr22:29783281-29783282	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs369078165	chr22:29783294-29783295	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs80020683	chr22:29783312-29783313	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs77661714	chr22:29783313-29783314	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs71196659	chr22:29783314-29783315	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs561794469	chr22:29783384-29783385	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs192529576	chr22:29783388-29783389	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs112924188	chr22:29783400-29783401	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs113813971	chr22:29783423-29783424	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs557215503	chr22:29783442-29783443	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	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
12	rs568986385	chr22:29783473-29783474	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs184438457	chr22:29783483-29783484	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	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
15	rs551302386	chr22:29783511-29783512	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs190502858	chr22:29783541-29783542	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs371737327	chr22:29783565-29783566	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs533844431	chr22:29783619-29783620	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs146150435	chr22:29783658-29783659	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs567308623	chr22:29783669-29783670	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs535860554	chr22:29783677-29783678	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs182028339	chr22:29783678-29783679	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs556169651	chr22:29783707-29783708	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs556311101	chr22:29783740-29783741	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs138994153	chr22:29783761-29783762	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs142144694	chr22:29783766-29783767	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs576367813	chr22:29783789-29783790	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs77131175	chr22:29783973-29783974	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs695416	chr22:29783978-29783979	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs695506	chr22:29783981-29783982	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs695556	chr22:29783982-29783983	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs695585	chr22:29783983-29783984	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs376699948	chr22:29784003-29784004	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs573381527	chr22:29784020-29784021	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs369387676	chr22:29784031-29784032	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs200965446	chr22:29784042-29784043	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs202102342	chr22:29784043-29784044	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs540612310	chr22:29784060-29784061	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs375909120	chr22:29784079-29784080	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs577562377	chr22:29784118-29784119	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs529275946	chr22:29784149-29784150	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs544221089	chr22:29784150-29784151	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs76890695	chr22:29784170-29784171	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs558431209	chr22:29784197-29784198	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs533273821	chr22:29784198-29784199	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs551803184	chr22:29784235-29784236	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs566594407	chr22:29784263-29784264	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs5997470	chr22:29784289-29784290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs695429	chr22:29784292-29784293	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs549328126	chr22:29784297-29784298	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	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:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29755000-29783800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr22:29755400-29783600	Weak transcription	Fetal Kidney	kidney
3	chr22:29756000-29783600	Weak transcription	Right Ventricle	heart
4	chr22:29756000-29783800	Weak transcription	Ovary	ovary
5	chr22:29765400-29783600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr22:29765600-29783600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr22:29765600-29783600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr22:29766200-29783600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr22:29767200-29783600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr22:29767400-29783400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr22:29767400-29783600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr22:29768000-29783600	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr22:29768000-29783800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr22:29769200-29783600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr22:29772600-29783400	Weak transcription	HSMMtube	muscle
16	chr22:29773600-29783600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr22:29773600-29783600	Weak transcription	HSMM	muscle
18	chr22:29774000-29783600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr22:29774200-29783600	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr22:29774200-29784000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr22:29776400-29783600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr22:29777000-29783400	Weak transcription	Right Atrium	heart
23	chr22:29777000-29783600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr22:29778400-29783600	Enhancers	HepG2	liver
25	chr22:29779000-29783600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr22:29779000-29783800	Weak transcription	Aorta	Aorta
27	chr22:29779200-29783400	Weak transcription	Fetal Heart	heart
28	chr22:29779200-29783600	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr22:29779200-29783800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr22:29780000-29783200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr22:29780000-29783800	Weak transcription	Lung	lung
32	chr22:29780200-29783600	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr22:29780200-29783600	Enhancers	Stomach Mucosa	stomach
34	chr22:29780400-29783600	Enhancers	Pancreas	Pancrea
35	chr22:29780400-29783600	Weak transcription	Thymus	Thymus
36	chr22:29780800-29785200	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr22:29781000-29783800	Enhancers	Fetal Brain Male	brain
38	chr22:29781000-29784200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr22:29781200-29783600	Enhancers	Primary hematopoietic stem cells	blood
40	chr22:29781400-29783200	Flanking Active TSS	GM12878-XiMat	blood
41	chr22:29781400-29783600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr22:29781400-29783800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr22:29781600-29783400	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr22:29781600-29783400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr22:29781600-29783400	Weak transcription	Fetal Muscle Leg	muscle
46	chr22:29781600-29783600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr22:29781600-29783600	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr22:29781600-29783600	Enhancers	Brain Angular Gyrus	brain
49	chr22:29781600-29783600	Weak transcription	Brain Substantia Nigra	brain
50	chr22:29781600-29783600	Weak transcription	Fetal Muscle Trunk	muscle

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