Variant report

Variant	nsv914965
Chromosome Location	chr22:30086144-30112226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:605)
CpG islands
(count:122)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30100619-30100836	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:30097434-30097985	HepG2	liver:	n/a	n/a
3	BCL3	chr22:30101958-30102330	GM12878	blood:	n/a	n/a
4	CEBPB	chr22:30087998-30088064	IMR90	lung:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
5	CEBPB	chr22:30087842-30088200	H1-hESC	embryonic stem cell:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
6	CEBPB	chr22:30087950-30088067	Hela-S3	cervix:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
7	CEBPB	chr22:30106956-30107195	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr22:30099063-30099290	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr22:30087982-30088055	K562	blood:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
10	CHD2	chr22:30106924-30107562	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr22:30102501-30102765	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr22:30098635-30099768	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr22:30097360-30097510	HCT-116	colon:	n/a	n/a
14	CTCF	chr22:30100620-30100770	HepG2	liver:	n/a	n/a
15	CTCF	chr22:30097280-30097430	HEEpiC	esophagus:	n/a	n/a
16	CTCF	chr22:30097280-30097430	GM12872	blood:	n/a	n/a
17	CTCF	chr22:30097360-30097510	AoAF	blood vessel:	n/a	n/a
18	CTCF	chr22:30085210-30086606	SK-N-SH	brain:	n/a	chr22:30085998-30086007 chr22:30085997-30086018 chr22:30085995-30086013 chr22:30085998-30086011 chr22:30085996-30086012
19	CTCF	chr22:30097366-30097455	GM10248	blood:	n/a	n/a
20	CTCF	chr22:30097360-30097510	AG04450	lung:	n/a	n/a
21	CTCF	chr22:30097300-30097450	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr22:30098420-30098570	HPAF	blood vessel:	n/a	chr22:30098464-30098473
23	CTCF	chr22:30097420-30097570	HL-60	blood:	n/a	n/a
24	CTCF	chr22:30097280-30097430	AG09309	skin:	n/a	n/a
25	CTCF	chr22:30098400-30098550	HMF	breast:	n/a	chr22:30098464-30098473
26	CTCF	chr22:30098360-30098510	HMEC	breast:	n/a	chr22:30098464-30098473
27	CTCF	chr22:30098400-30098550	HFF	foreskin:	n/a	chr22:30098464-30098473
28	CTCF	chr22:30098380-30098530	AG10803	skin:	n/a	chr22:30098464-30098473
29	CTCF	chr22:30098340-30098490	HMEC	breast:	n/a	chr22:30098464-30098473
30	CTCF	chr22:30097300-30097450	RPTEC	kidney:	n/a	n/a
31	CTCF	chr22:30098400-30098550	HEEpiC	esophagus:	n/a	chr22:30098464-30098473
32	CTCF	chr22:30097303-30097504	T-47D	breast:	n/a	n/a
33	CTCF	chr22:30097347-30097498	GM19240	blood:	n/a	n/a
34	CTCF	chr22:30097320-30097470	GM12871	blood:	n/a	n/a
35	CTCF	chr22:30098400-30098550	HEK293	kidney:	n/a	chr22:30098464-30098473
36	CTCF	chr22:30097320-30097470	GM12865	blood:	n/a	n/a
37	CTCF	chr22:30098421-30098497	HepG2	liver:	n/a	chr22:30098464-30098473
38	CTCF	chr22:30096300-30096450	K562	blood:	n/a	n/a
39	CTCF	chr22:30098418-30098482	Fibrobl	skin:	n/a	chr22:30098464-30098473
40	CTCF	chr22:30098434-30098459	ProgFib	skin:	n/a	n/a
41	CTCF	chr22:30091296-30091449	NHEK	skin:	n/a	n/a
42	CTCF	chr22:30097140-30097290	GM12871	blood:	n/a	n/a
43	CTCF	chr22:30097105-30097868	HCT-116	colon:	n/a	n/a
44	CTCF	chr22:30097128-30097596	MCF-7	breast:	n/a	n/a
45	CTCF	chr22:30097305-30097525	MCF-7	breast:	n/a	n/a
46	CTCF	chr22:30097280-30097430	HCT-116	colon:	n/a	n/a
47	CTCF	chr22:30085800-30086144	SK-N-SH_RA	brain:	n/a	chr22:30085998-30086007 chr22:30085997-30086018 chr22:30085995-30086013 chr22:30085998-30086011 chr22:30085996-30086012
48	CTCF	chr22:30097325-30097508	GM12892	blood:	n/a	n/a
49	CTCF	chr22:30097320-30097470	MCF-7	breast:	n/a	n/a
50	CTCF	chr22:30097340-30097490	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30107178-30107228	MCF-7	breast:	n/a
2	chr22:30107178-30107228	SKMC	muscle:	n/a
3	chr22:30107178-30107228	T-47D	breast:	n/a
4	chr22:30107178-30107228	GM19239	blood:	n/a
5	chr22:30091734-30091784	PFSK-1	brain:	n/a
6	chr22:30107178-30107228	SK-N-MC	brain:	n/a
7	chr22:30107178-30107228	SK-N-SH	brain:	n/a
8	chr22:30091734-30091784	HepG2	liver:	n/a
9	chr22:30107178-30107228	PANC-1	pancreas:	n/a
10	chr22:30091734-30091784	GM19239	blood:	n/a
11	chr22:30107178-30107228	HCF	heart:	n/a
12	chr22:30091734-30091784	SK-N-MC	brain:	n/a
13	chr22:30091734-30091784	HRCEpiC	kidney:	n/a
14	chr22:30107178-30107228	K562	blood:	n/a
15	chr22:30091734-30091784	NT2-D1	testis:	n/a
16	chr22:30107178-30107228	ECC-1	luminal epithelium:	n/a
17	chr22:30091734-30091784	BE2_C	brain:	n/a
18	chr22:30091734-30091784	GM06990	blood:	n/a
19	chr22:30091734-30091784	HEEpiC	esophagus:	n/a
20	chr22:30107178-30107228	IMR90	lung:	fetal
21	chr22:30091734-30091784	HEK293	kidney:	embryo
22	chr22:30091734-30091784	IMR90	lung:	fetal
23	chr22:30091734-30091784	Jurkat	blood:	n/a
24	chr22:30107178-30107228	SAEC	small airway:	n/a
25	chr22:30091734-30091784	Hela-S3	cervix:	n/a
26	chr22:30107178-30107228	RPTEC	kidney:	n/a
27	chr22:30107178-30107228	A549	lung:	n/a
28	chr22:30107178-30107228	HepG2	liver:	n/a
29	chr22:30091734-30091784	AG09319	gingival:	n/a
30	chr22:30107178-30107228	NHDF-neo	bronchial:	n/a
31	chr22:30107178-30107228	GM12878	blood:	n/a
32	chr22:30091734-30091784	A549	lung:	n/a
33	chr22:30091734-30091784	HCM	heart:	n/a
34	chr22:30091734-30091784	H1-hESC	embryonic stem cell:	embryo
35	chr22:30107178-30107228	Hepatocyte	liver:	n/a
36	chr22:30107178-30107228	HIPEpiC	eye:	n/a
37	chr22:30107178-30107228	HRE	kidney:	n/a
38	chr22:30107178-30107228	HUVEC	blood vessel:	n/a
39	chr22:30091734-30091784	HPAEpiC	pulmonary alveolar:	n/a
40	chr22:30091734-30091784	HL-60	blood:	n/a
41	chr22:30091734-30091784	CMK	blood:	n/a
42	chr22:30107178-30107228	H1-hESC	embryonic stem cell:	embryo
43	chr22:30091734-30091784	HIPEpiC	eye:	n/a
44	chr22:30091734-30091784	LNCaP	prostate:	n/a
45	chr22:30107178-30107228	AG09319	gingival:	n/a
46	chr22:30091734-30091784	SAEC	small airway:	n/a
47	chr22:30107178-30107228	HRPEpiC	eye:	n/a
48	chr22:30091734-30091784	AG10803	skin:	n/a
49	chr22:30107178-30107228	BE2_C	brain:	n/a
50	chr22:30107178-30107228	HRCEpiC	kidney:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30092151..30092731-chr22:30484958..30485506,2	K562	blood:
2	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
3	chr22:30086150..30087724-chr22:30089523..30091656,2	K562	blood:
4	chr22:30086550..30091376-chr22:30091742..30099600,10	MCF-7	breast:
5	chr22:30097300..30097855-chr22:30400940..30401466,2	K562	blood:
6	chr22:30086150..30087724-chr22:30089523..30091656,2	K562	blood:
7	chr22:30086357..30088684-chr22:30160929..30163029,2	MCF-7	breast:
8	chr22:30098350..30101826-chr22:30195223..30196896,3	MCF-7	breast:
9	chr22:30097693..30098380-chr22:30484799..30485447,2	MCF-7	breast:
10	chr22:30091150..30094109-chr22:30098424..30101093,2	K562	blood:
11	chr22:30098089..30098947-chr22:30484640..30485526,4	MCF-7	breast:
12	chr22:30085928..30087473-chr22:30162751..30164903,2	MCF-7	breast:
13	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
14	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
15	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
16	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
17	chr22:30091889..30092650-chr22:30194897..30195405,2	MCF-7	breast:
18	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
19	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
20	chr22:30091150..30094109-chr22:30098424..30101093,2	K562	blood:
21	chr22:30085941..30086486-chr22:30484564..30485178,2	K562	blood:
22	chr22:30091841..30093848-chr22:30094919..30097302,3	MCF-7	breast:
23	chr22:30097244..30097815-chr22:30485015..30485549,2	MCF-7	breast:
24	chr22:30085509..30086792-chr22:30400990..30401964,4	MCF-7	breast:
25	chr22:30094321..30096563-chr22:30160914..30162763,2	MCF-7	breast:
26	chr22:30096098..30098972-chr22:30384609..30387065,2	MCF-7	breast:
27	chr22:30086550..30091376-chr22:30091742..30099600,10	MCF-7	breast:
28	chr22:30091841..30093848-chr22:30094919..30097302,3	MCF-7	breast:
29	chr22:30085501..30086471-chr22:30400885..30401468,2	K562	blood:
30	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
31	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
32	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
33	chr22:30079243..30081163-chr22:30089735..30091351,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZMAT5-1	chr22:30107809-30107906	XLOC_014338
2	lnc-ZMAT5-1	chr22:30101245-30101418	XLOC_014338
3	lnc-ZMAT5-1	chr22:30107802-30107984	XLOC_014338
4	lnc-ZMAT5-1	chr22:30102120-30102223	XLOC_014338

No data

Variant related genes	Relation type
CABP7	TF binding region
CABP7	CpG island
ENSG00000100319	chromatin interactions
ENSG00000184076	chromatin interactions
ENSG00000100325	chromatin interactions
NHLRC3	miRNA target sites

Extended variants
information (count: 987 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs756053	chr22:30086144-30086145	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546078417	chr22:30086202-30086203	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs369942892	chr22:30086227-30086228	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs147741152	chr22:30086297-30086298	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs538292938	chr22:30086338-30086339	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs149202264	chr22:30086357-30086358	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561950555	chr22:30086409-30086410	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371990586	chr22:30086470-30086471	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs528919474	chr22:30086483-30086484	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs143339501	chr22:30086498-30086499	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs550280580	chr22:30086581-30086582	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs183465323	chr22:30086706-30086707	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568282331	chr22:30086717-30086718	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs6006226	chr22:30086758-30086759	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs551004726	chr22:30086769-30086770	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376091595	chr22:30086772-30086773	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs9625852	chr22:30086846-30086847	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs78670297	chr22:30086952-30086953	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs201834185	chr22:30086965-30086966	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141472217	chr22:30087056-30087057	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs145671937	chr22:30087061-30087062	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs188186760	chr22:30087103-30087104	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs554022637	chr22:30087134-30087135	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375229774	chr22:30087145-30087146	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs115983371	chr22:30087159-30087160	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576819704	chr22:30087170-30087171	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575848174	chr22:30087184-30087185	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs539071671	chr22:30087262-30087263	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138235136	chr22:30087279-30087280	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564531928	chr22:30087299-30087300	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573038859	chr22:30087311-30087312	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142750685	chr22:30087396-30087397	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs181769493	chr22:30087532-30087533	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs377567451	chr22:30087617-30087618	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529056484	chr22:30087638-30087639	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550219214	chr22:30087716-30087717	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556077303	chr22:30087730-30087731	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562236012	chr22:30087731-30087732	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113270432	chr22:30087761-30087762	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558563407	chr22:30087762-30087763	Enhancers Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs527612583	chr22:30087858-30087859	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs370837183	chr22:30087859-30087860	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185766283	chr22:30087884-30087885	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532909316	chr22:30087885-30087886	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs374345123	chr22:30087951-30087952	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551069285	chr22:30087998-30087999	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566499373	chr22:30088000-30088001	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs190490457	chr22:30088027-30088028	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2267151	chr22:30088039-30088040	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs181761823	chr22:30088098-30088099	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	1 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
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
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30020800-30097000	Weak transcription	Stomach Mucosa	stomach
2	chr22:30050400-30093000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr22:30053400-30087400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr22:30054000-30094800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr22:30055400-30095200	Strong transcription	Fetal Intestine Small	intestine
6	chr22:30056000-30094800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr22:30060200-30093600	Strong transcription	Fetal Thymus	thymus
8	chr22:30063400-30094600	Strong transcription	Primary T cells from cord blood	blood
9	chr22:30072800-30088200	Weak transcription	Right Atrium	heart
10	chr22:30075000-30087000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr22:30075000-30087800	Weak transcription	K562	blood
12	chr22:30075400-30097400	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr22:30076800-30096400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr22:30077800-30096400	Weak transcription	Small Intestine	intestine
15	chr22:30079600-30097000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr22:30079600-30097400	Weak transcription	Hela-S3	cervix
17	chr22:30080000-30097000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr22:30080200-30089600	Weak transcription	Colonic Mucosa	Colon
19	chr22:30080200-30098800	Weak transcription	GM12878-XiMat	blood
20	chr22:30080400-30087000	Weak transcription	Right Ventricle	heart
21	chr22:30081000-30096400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr22:30081200-30088000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr22:30081200-30088000	Weak transcription	Pancreas	Pancrea
24	chr22:30081200-30096400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr22:30081400-30089000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr22:30082000-30088800	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr22:30083200-30090000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr22:30083400-30086400	Weak transcription	Primary B cells from peripheral blood	blood
29	chr22:30083400-30089000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr22:30083800-30087200	Weak transcription	Esophagus	oesophagus
31	chr22:30083800-30087400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr22:30083800-30087800	Enhancers	Placenta Amnion	Placenta Amnion
33	chr22:30083800-30088200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr22:30083800-30088200	Weak transcription	Ovary	ovary
35	chr22:30083800-30088400	Weak transcription	Primary B cells from cord blood	blood
36	chr22:30083800-30088400	Weak transcription	Fetal Intestine Large	intestine
37	chr22:30084000-30089400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr22:30084000-30090000	Weak transcription	Aorta	Aorta
39	chr22:30084200-30088800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr22:30084400-30086200	Weak transcription	Adipose Nuclei	Adipose
41	chr22:30084400-30086600	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr22:30084400-30086800	Enhancers	Fetal Muscle Leg	muscle
43	chr22:30084400-30086800	Weak transcription	HepG2	liver
44	chr22:30084400-30088600	Weak transcription	Left Ventricle	heart
45	chr22:30084400-30089000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr22:30084400-30089000	Weak transcription	HUVEC	blood vessel
47	chr22:30084400-30089600	Weak transcription	HMEC	breast
48	chr22:30084400-30090400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr22:30084600-30086400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr22:30084600-30086600	Weak transcription	Liver	Liver

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