Variant report

Variant	nsv1064350
Chromosome Location	chr22:30724148-30742125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:328)
CpG islands
(count:183)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30723854-30724440	K562	blood:	n/a	n/a
2	CCNT2	chr22:30724080-30724254	K562	blood:	n/a	n/a
3	CEBPB	chr22:30724015-30724323	IMR90	lung:	n/a	chr22:30724181-30724192
4	CEBPB	chr22:30732790-30733107	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr22:30724099-30724328	Hela-S3	cervix:	n/a	chr22:30724181-30724192
6	CEBPB	chr22:30732817-30733014	HepG2	liver:	n/a	n/a
7	CEBPB	chr22:30724027-30724343	HepG2	liver:	n/a	chr22:30724181-30724192
8	CEBPB	chr22:30724054-30724331	K562	blood:	n/a	chr22:30724181-30724192
9	CEBPB	chr22:30723951-30724319	H1-hESC	embryonic stem cell:	n/a	chr22:30724181-30724192
10	CEBPB	chr22:30724009-30724382	K562	blood:	n/a	chr22:30724181-30724192
11	CEBPB	chr22:30723929-30724341	K562	blood:	n/a	chr22:30724181-30724192
12	CEBPB	chr22:30733656-30733667	HepG2	liver:	n/a	n/a
13	CTCF	chr22:30725380-30725423	GM10266	blood:	n/a	n/a
14	CTCF	chr22:30723679-30724186	MCF-7	breast:	n/a	n/a
15	CTCF	chr22:30728771-30728784	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr22:30723753-30724188	MCF-7	breast:	n/a	n/a
17	CTCF	chr22:30733610-30733642	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr22:30723491-30724302	HCT-116	colon:	n/a	n/a
19	CTCF	chr22:30723701-30724367	A549	lung:	n/a	n/a
20	EBF1	chr22:30731351-30731519	GM12878	blood:	n/a	chr22:30731421-30731431 chr22:30731421-30731430
21	EBF1	chr22:30731304-30731528	GM12878	blood:	n/a	chr22:30731421-30731431 chr22:30731421-30731430
22	EP300	chr22:30739954-30739991	HepG2	liver:	n/a	n/a
23	EP300	chr22:30726683-30727050	T-47D	breast:	n/a	n/a
24	EP300	chr22:30723920-30724385	K562	blood:	n/a	n/a
25	FOXA2	chr22:30730635-30731007	HepG2	liver:	n/a	n/a
26	GATA3	chr22:30726805-30727106	T-47D	breast:	n/a	n/a
27	GATA3	chr22:30726708-30727164	T-47D	breast:	n/a	n/a
28	GATA3	chr22:30726697-30727392	MCF-7	breast:	n/a	n/a
29	GATA3	chr22:30726685-30727164	MCF-7	breast:	n/a	n/a
30	GATA3	chr22:30726723-30727294	SK-N-SH	brain:	n/a	n/a
31	GATA3	chr22:30726889-30727120	MCF-7	breast:	n/a	n/a
32	JUND	chr22:30723923-30724333	K562	blood:	n/a	n/a
33	MYC	chr22:30723923-30724340	K562	blood:	n/a	n/a
34	POLR2A	chr22:30728897-30729184	K562	blood:	n/a	n/a
35	POLR2A	chr22:30732069-30732456	HepG2	liver:	n/a	n/a
36	POLR2A	chr22:30736190-30736778	GM12892	blood:	n/a	n/a
37	POLR2A	chr22:30729460-30729465	MCF-7	breast:	n/a	n/a
38	POLR2A	chr22:30733510-30733641	GM12878	blood:	n/a	n/a
39	POLR2A	chr22:30729651-30729658	GM12878	blood:	n/a	n/a
40	POLR2A	chr22:30724273-30724972	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr22:30733154-30733317	HepG2	liver:	n/a	n/a
42	POLR2A	chr22:30728689-30728986	MCF-7	breast:	n/a	n/a
43	POLR2A	chr22:30732530-30733104	GM12878	blood:	n/a	n/a
44	POLR2A	chr22:30724186-30724225	HepG2	liver:	n/a	n/a
45	POLR2A	chr22:30722284-30724180	GM12891	blood:	n/a	n/a
46	POLR2A	chr22:30736194-30736683	K562	blood:	n/a	n/a
47	POLR2A	chr22:30723863-30724174	HepG2	liver:	n/a	n/a
48	POLR2A	chr22:30729215-30729631	U87	brain:	n/a	n/a
49	POLR2A	chr22:30729525-30729534	MCF-7	breast:	n/a	n/a
50	POLR2A	chr22:30730796-30731130	PFSK-1	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30736610-30736660	HCPEpiC	choroid plexus:	n/a
2	chr22:30725357-30725407	BE2_C	brain:	n/a
3	chr22:30728510-30728560	BJ	skin:	n/a
4	chr22:30728510-30728560	HRCEpiC	kidney:	n/a
5	chr22:30728510-30728560	PFSK-1	brain:	n/a
6	chr22:30728510-30728560	HCF	heart:	n/a
7	chr22:30728510-30728560	SK-N-SH_RA	brain:	n/a
8	chr22:30728510-30728560	HepG2	liver:	n/a
9	chr22:30736610-30736660	HCT-116	colon:	n/a
10	chr22:30725357-30725407	SK-N-SH	brain:	n/a
11	chr22:30736610-30736660	GM06990	blood:	n/a
12	chr22:30736610-30736660	NT2-D1	testis:	n/a
13	chr22:30728510-30728560	HCM	heart:	n/a
14	chr22:30725357-30725407	ProgFib	skin:	n/a
15	chr22:30736610-30736660	HAEpiC	amniotic membrane:	n/a
16	chr22:30725357-30725407	NHDF-neo	bronchial:	n/a
17	chr22:30736610-30736660	Jurkat	blood:	n/a
18	chr22:30725357-30725407	HCPEpiC	choroid plexus:	n/a
19	chr22:30736610-30736660	AG10803	skin:	n/a
20	chr22:30725357-30725407	NHBE	bronchial:	n/a
21	chr22:30728510-30728560	AG04450	lung:	fetal
22	chr22:30725357-30725407	HCF	heart:	n/a
23	chr22:30736610-30736660	AG04450	lung:	fetal
24	chr22:30728510-30728560	Caco-2	colon:	n/a
25	chr22:30728510-30728560	PrEC	prostate:	n/a
26	chr22:30736610-30736660	HEK293	kidney:	embryo
27	chr22:30736610-30736660	HRPEpiC	eye:	n/a
28	chr22:30736610-30736660	HL-60	blood:	n/a
29	chr22:30725357-30725407	HRE	kidney:	n/a
30	chr22:30725357-30725407	HRCEpiC	kidney:	n/a
31	chr22:30725357-30725407	GM19239	blood:	n/a
32	chr22:30736610-30736660	NB4	blood:	n/a
33	chr22:30736610-30736660	MCF-7	breast:	n/a
34	chr22:30736610-30736660	MCF10A-Er-Src	breast:	n/a
35	chr22:30736610-30736660	ECC-1	luminal epithelium:	n/a
36	chr22:30728510-30728560	U87	brain:	n/a
37	chr22:30728510-30728560	T-47D	breast:	n/a
38	chr22:30736610-30736660	HMEC	breast:	n/a
39	chr22:30728510-30728560	HL-60	blood:	n/a
40	chr22:30736610-30736660	SKMC	muscle:	n/a
41	chr22:30736610-30736660	HUVEC	blood vessel:	n/a
42	chr22:30736610-30736660	PrEC	prostate:	n/a
43	chr22:30725357-30725407	AG10803	skin:	n/a
44	chr22:30725357-30725407	HRPEpiC	eye:	n/a
45	chr22:30728510-30728560	SKMC	muscle:	n/a
46	chr22:30725357-30725407	IMR90	lung:	fetal
47	chr22:30725357-30725407	AG04449	skin:	fetal
48	chr22:30736610-30736660	HPAEpiC	pulmonary alveolar:	n/a
49	chr22:30725357-30725407	HAEpiC	amniotic membrane:	n/a
50	chr22:30728510-30728560	SK-N-MC	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30733324..30735003-chr22:30738407..30740999,2	MCF-7	breast:
2	chr22:30720496..30722809-chr22:30723809..30726893,3	MCF-7	breast:
3	chr22:30679226..30682000-chr22:30723679..30728534,4	K562	blood:
4	chr22:30726026..30729085-chr22:30749869..30754191,5	MCF-7	breast:
5	chr22:30721941..30724645-chr22:30725200..30726744,2	K562	blood:
6	chr22:30684944..30687538-chr22:30739118..30741799,2	MCF-7	breast:
7	chr22:30732544..30735281-chr22:30742253..30745088,2	MCF-7	breast:
8	chr22:30710168..30712716-chr22:30726036..30728244,2	MCF-7	breast:
9	chr22:30692849..30696422-chr22:30721996..30724187,4	MCF-7	breast:
10	chr22:30721434..30723843-chr22:30737479..30740425,2	K562	blood:
11	chr22:30641352..30643505-chr22:30721621..30724253,3	MCF-7	breast:
12	chr22:30722860..30724693-chr22:30742029..30744821,2	K562	blood:
13	chr22:30733497..30738627-chr22:30739549..30742352,7	K562	blood:
14	chr22:30723090..30724854-chr22:30725952..30728416,2	K562	blood:
15	chr22:30722829..30724775-chr22:30819297..30822266,2	MCF-7	breast:
16	chr22:30722006..30724246-chr22:30752442..30754508,2	K562	blood:
17	chr22:30733324..30735003-chr22:30738407..30740999,2	MCF-7	breast:
18	chr22:30736285..30738543-chr22:30751447..30754136,3	K562	blood:
19	chr22:30730281..30734311-chr22:30742898..30745201,3	MCF-7	breast:
20	chr22:30722860..30724693-chr22:30742029..30744821,2	K562	blood:
21	chr22:30681692..30688141-chr22:30720232..30725114,19	MCF-7	breast:
22	chr22:30729301..30730817-chr22:30750203..30752944,2	K562	blood:
23	chr22:30736285..30738437-chr22:30751447..30754136,2	K562	blood:
24	chr22:30710430..30716803-chr22:30717996..30724228,10	MCF-7	breast:
25	chr22:30683311..30684720-chr22:30723282..30724915,12	MCF-7	breast:
26	chr22:30683778..30684535-chr22:30723476..30724412,5	MCF-7	breast:
27	chr22:30732348..30737677-chr22:30750921..30755238,7	MCF-7	breast:
28	chr22:30723840..30727994-chr22:30728827..30733130,4	K562	blood:
29	chr22:30723090..30724854-chr22:30725952..30728416,2	K562	blood:
30	chr22:30733302..30736055-chr22:30750553..30752956,2	K562	blood:
31	chr22:30683831..30686273-chr22:30722432..30724567,2	K562	blood:
32	chr22:30740000..30742543-chr22:30750600..30752817,3	MCF-7	breast:
33	chr22:30679955..30682000-chr22:30725118..30726971,2	K562	blood:
34	chr22:30692473..30695111-chr22:30722676..30724964,2	K562	blood:
35	chr22:30656777..30659153-chr22:30723216..30725905,2	MCF-7	breast:
36	chr22:30733497..30738627-chr22:30739549..30742352,7	K562	blood:
37	chr22:30701046..30703997-chr22:30721368..30724437,4	K562	blood:
38	chr22:30728274..30730328-chr22:30731097..30733421,3	MCF-7	breast:
39	chr22:30728274..30730328-chr22:30731097..30733421,3	MCF-7	breast:
40	chr22:30723840..30727994-chr22:30728827..30733130,4	K562	blood:
41	chr22:30721780..30724167-chr22:30728041..30729954,3	MCF-7	breast:
42	chr22:30721494..30724747-chr22:30781448..30784941,5	MCF-7	breast:
43	chr22:30719395..30724233-chr22:30750032..30754717,7	MCF-7	breast:
44	chr22:30733497..30736082-chr22:30739249..30742350,4	K562	blood:
45	chr22:30722006..30725049-chr22:30749886..30754508,5	K562	blood:
46	chr22:30720936..30724991-chr22:30750350..30754449,10	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SF3A1	hsa-miR-193b-3p	chr22:30728223-30728246

Variant related genes	Relation type
SF3A1	TF binding region
TBC1D10A	TF binding region
SF3A1	CpG island
TBC1D10A	CpG island
ENSG00000187860	chromatin interactions
ENSG00000128342	chromatin interactions
ENSG00000099995	chromatin interactions
ENSG00000242114	chromatin interactions
ENSG00000268812	chromatin interactions
ENSG00000239282	chromatin interactions
ENSG00000099999	chromatin interactions
ENSG00000099992	chromatin interactions
ENSG00000248751	chromatin interactions

Extended variants
information (count: 708 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187054023	chr22:30724166-30724167	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs576655653	chr22:30724261-30724262	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs537517854	chr22:30724291-30724292	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs73881440	chr22:30724351-30724352	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs577192892	chr22:30724362-30724363	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs541021740	chr22:30724374-30724375	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs192342208	chr22:30724409-30724410	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs560476090	chr22:30724431-30724432	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs574635550	chr22:30724459-30724460	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs139843551	chr22:30724519-30724520	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs541669814	chr22:30724550-30724551	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs183244969	chr22:30724565-30724566	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs79416124	chr22:30724594-30724595	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs111821224	chr22:30724633-30724634	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs532344325	chr22:30724652-30724653	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs374204153	chr22:30724699-30724700	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs187167650	chr22:30724746-30724747	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs144039145	chr22:30724748-30724749	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs11704510	chr22:30724784-30724785	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs79422377	chr22:30724828-30724829	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs377228077	chr22:30724837-30724838	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs113741566	chr22:30724847-30724848	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs566401921	chr22:30724862-30724863	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs147322481	chr22:30724890-30724891	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs548825644	chr22:30724911-30724912	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs570245146	chr22:30724921-30724922	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs537616705	chr22:30724928-30724929	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs559015501	chr22:30724942-30724943	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs570818935	chr22:30724960-30724961	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs376524117	chr22:30724978-30724979	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs535060444	chr22:30724983-30724984	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs190037049	chr22:30724993-30724994	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs367765118	chr22:30725018-30725019	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs182624958	chr22:30725042-30725043	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs71328839	chr22:30725078-30725079	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
36	rs187082073	chr22:30725102-30725103	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541705956	chr22:30725175-30725176	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs191138113	chr22:30725203-30725204	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs556803155	chr22:30725235-30725236	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs575118476	chr22:30725236-30725237	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs737751	chr22:30725274-30725275	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs564217336	chr22:30725281-30725282	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs737750	chr22:30725302-30725303	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs540267191	chr22:30725303-30725304	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182231864	chr22:30725304-30725305	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs530450140	chr22:30725313-30725314	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs35868625	chr22:30725335-30725336	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs548912953	chr22:30725357-30725358	Weak transcription Enhancers Strong transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs4597639	chr22:30725396-30725397	Weak transcription Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188589896	chr22:30725409-30725410	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
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
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
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD

Chromatin state (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30722200-30724400	Active TSS	Rectal Smooth Muscle	rectum
2	chr22:30723000-30728400	Weak transcription	Small Intestine	intestine
3	chr22:30723200-30724200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
4	chr22:30723200-30724200	Flanking Active TSS	K562	blood
5	chr22:30723400-30724200	Enhancers	Fetal Lung	lung
6	chr22:30723400-30725000	Enhancers	HSMM	muscle
7	chr22:30723400-30725200	Enhancers	HSMMtube	muscle
8	chr22:30723400-30726400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr22:30723400-30726400	Weak transcription	Left Ventricle	heart
10	chr22:30723400-30726400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr22:30723400-30726600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr22:30723400-30726600	Weak transcription	Brain Substantia Nigra	brain
13	chr22:30723400-30726600	Weak transcription	Gastric	stomach
14	chr22:30723400-30726600	Weak transcription	Lung	lung
15	chr22:30723400-30727400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr22:30723400-30728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr22:30723400-30728600	Weak transcription	Esophagus	oesophagus
18	chr22:30723400-30728600	Weak transcription	Right Ventricle	heart
19	chr22:30723400-30728800	Weak transcription	Ovary	ovary
20	chr22:30723400-30729400	Weak transcription	Psoas Muscle	Psoas
21	chr22:30723400-30732600	Weak transcription	Right Atrium	heart
22	chr22:30723600-30724200	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr22:30723600-30724200	Enhancers	Primary B cells from peripheral blood	blood
24	chr22:30723600-30724200	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr22:30723600-30724200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr22:30723600-30724200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr22:30723600-30724200	Flanking Active TSS	GM12878-XiMat	blood
28	chr22:30723600-30724200	Enhancers	Hela-S3	cervix
29	chr22:30723600-30724200	Enhancers	NH-A	brain
30	chr22:30723600-30724400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr22:30723600-30724400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr22:30723600-30724400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr22:30723600-30724400	Enhancers	A549	lung
34	chr22:30723600-30724600	Enhancers	Fetal Intestine Large	intestine
35	chr22:30723600-30724600	Enhancers	Fetal Intestine Small	intestine
36	chr22:30723600-30724600	Weak transcription	Osteobl	bone
37	chr22:30723600-30724800	Enhancers	Stomach Mucosa	stomach
38	chr22:30723600-30724800	Enhancers	Stomach Smooth Muscle	stomach
39	chr22:30723600-30725000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr22:30723600-30725000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr22:30723600-30725200	Weak transcription	Fetal Muscle Leg	muscle
42	chr22:30723600-30725200	Enhancers	Placenta Amnion	Placenta Amnion
43	chr22:30723600-30725400	Weak transcription	Fetal Muscle Trunk	muscle
44	chr22:30723600-30725400	Weak transcription	Fetal Stomach	stomach
45	chr22:30723600-30725600	Enhancers	Placenta	Placenta
46	chr22:30723600-30725800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr22:30723600-30726400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr22:30723600-30726400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr22:30723600-30726400	Weak transcription	Adipose Nuclei	Adipose
50	chr22:30723600-30726600	Weak transcription	H9 Cell Line	embryonic stem cell

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