Variant report

Variant	esv3394301
Chromosome Location	chr16:30426951-30431549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:435)
CpG islands
(count:427)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr16:30428959-30429727	GM12878	blood:	n/a	n/a
2	ATF2	chr16:30429004-30429714	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr16:30428993-30429544	A549	lung:	n/a	n/a
4	ATF3	chr16:30429243-30429715	A549	lung:	n/a	n/a
5	BACH1	chr16:30428737-30429960	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr16:30428831-30430251	A549	lung:	n/a	n/a
7	BCL3	chr16:30428581-30430071	A549	lung:	n/a	n/a
8	BCL3	chr16:30428799-30429766	GM12878	blood:	n/a	n/a
9	BCLAF1	chr16:30428798-30429821	GM12878	blood:	n/a	n/a
10	BCLAF1	chr16:30428948-30429666	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:30429085-30429646	A549	lung:	n/a	n/a
12	BHLHE40	chr16:30428817-30429663	GM12878	blood:	n/a	n/a
13	BRCA1	chr16:30429497-30429636	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr16:30429293-30429642	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr16:30429560-30429633	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr16:30429999-30430035	GM12878	blood:	n/a	n/a
17	CHD1	chr16:30429038-30429535	GM12878	blood:	n/a	n/a
18	CHD2	chr16:30429049-30429713	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr16:30429043-30429674	GM12878	blood:	n/a	n/a
20	CREB1	chr16:30428909-30429841	GM12878	blood:	n/a	n/a
21	CREB1	chr16:30428938-30429787	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr16:30428905-30429800	A549	lung:	n/a	n/a
23	CTBP2	chr16:30428847-30429617	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr16:30429480-30429630	BJ	skin:	n/a	n/a
25	CTCF	chr16:30429520-30429670	GM12873	blood:	n/a	n/a
26	CTCF	chr16:30429537-30429700	GM10248	blood:	n/a	n/a
27	CTCF	chr16:30429560-30429710	HRE	kidney:	n/a	n/a
28	CTCF	chr16:30429040-30429190	GM12868	blood:	n/a	n/a
29	CTCF	chr16:30429520-30429670	SAEC	small airway:	n/a	n/a
30	CTCF	chr16:30429520-30429670	GM12874	blood:	n/a	n/a
31	CTCF	chr16:30429409-30429415	GM12892	blood:	n/a	n/a
32	CTCF	chr16:30429560-30429710	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr16:30429458-30429759	GM12892	blood:	n/a	n/a
34	CTCF	chr16:30429500-30429650	HCM	heart:	n/a	n/a
35	CTCF	chr16:30429580-30429730	HPF	lung:	n/a	n/a
36	CTCF	chr16:30429462-30429759	GM19239	blood:	n/a	n/a
37	CTCF	chr16:30429540-30429690	GM12865	blood:	n/a	n/a
38	CTCF	chr16:30429500-30429650	BE2_C	brain:	n/a	n/a
39	CTCF	chr16:30429541-30429683	LNCaP	prostate:	n/a	n/a
40	CTCF	chr16:30429580-30429730	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr16:30429540-30429690	HEK293	kidney:	n/a	n/a
42	CTCF	chr16:30429520-30429670	GM12878	blood:	n/a	n/a
43	CTCF	chr16:30429540-30429690	GM12870	blood:	n/a	n/a
44	CTCF	chr16:30429098-30429812	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr16:30429420-30429570	GM12868	blood:	n/a	n/a
46	CTCF	chr16:30429480-30429630	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr16:30429485-30429721	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr16:30429490-30429729	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr16:30429600-30429750	GM12869	blood:	n/a	n/a
50	CTCF	chr16:30429580-30429730	GM12873	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30430148-30430198	NT2-D1	testis:	n/a
2	chr16:30429711-30429761	HRCEpiC	kidney:	n/a
3	chr16:30430089-30430139	HCM	heart:	n/a
4	chr16:30429837-30429887	HL-60	blood:	n/a
5	chr16:30430044-30430094	HRCEpiC	kidney:	n/a
6	chr16:30430044-30430094	SK-N-SH_RA	brain:	n/a
7	chr16:30430044-30430094	SKMC	muscle:	n/a
8	chr16:30428842-30428892	HRE	kidney:	n/a
9	chr16:30428842-30428892	ECC-1	luminal epithelium:	n/a
10	chr16:30429711-30429761	SAEC	small airway:	n/a
11	chr16:30430044-30430094	PANC-1	pancreas:	n/a
12	chr16:30428842-30428892	GM12891	blood:	n/a
13	chr16:30430044-30430094	AG10803	skin:	n/a
14	chr16:30429711-30429761	Hela-S3	cervix:	n/a
15	chr16:30430044-30430094	HepG2	liver:	n/a
16	chr16:30429837-30429887	HCT-116	colon:	n/a
17	chr16:30430148-30430198	Hela-S3	cervix:	n/a
18	chr16:30430089-30430139	U87	brain:	n/a
19	chr16:30429711-30429761	SK-N-MC	brain:	n/a
20	chr16:30429711-30429761	HEEpiC	esophagus:	n/a
21	chr16:30428842-30428892	HNPCEpiC	eye:	n/a
22	chr16:30430044-30430094	LNCaP	prostate:	n/a
23	chr16:30430148-30430198	AG04450	lung:	fetal
24	chr16:30430044-30430094	PFSK-1	brain:	n/a
25	chr16:30429711-30429761	HCF	heart:	n/a
26	chr16:30430148-30430198	K562	blood:	n/a
27	chr16:30429837-30429887	AG09319	gingival:	n/a
28	chr16:30429837-30429887	HPAEpiC	pulmonary alveolar:	n/a
29	chr16:30429711-30429761	AG10803	skin:	n/a
30	chr16:30429837-30429887	NH-A	brain:	n/a
31	chr16:30430044-30430094	RPTEC	kidney:	n/a
32	chr16:30428842-30428892	GM12892	blood:	n/a
33	chr16:30429204-30429254	Caco-2	colon:	n/a
34	chr16:30430089-30430139	HIPEpiC	eye:	n/a
35	chr16:30428842-30428892	T-47D	breast:	n/a
36	chr16:30430089-30430139	IMR90	lung:	fetal
37	chr16:30430089-30430139	Jurkat	blood:	n/a
38	chr16:30428842-30428892	HL-60	blood:	n/a
39	chr16:30430148-30430198	U87	brain:	n/a
40	chr16:30430044-30430094	AG09319	gingival:	n/a
41	chr16:30430089-30430139	GM12892	blood:	n/a
42	chr16:30430148-30430198	H1-hESC	embryonic stem cell:	embryo
43	chr16:30430089-30430139	MCF-7	breast:	n/a
44	chr16:30429711-30429761	HMEC	breast:	n/a
45	chr16:30430089-30430139	ECC-1	luminal epithelium:	n/a
46	chr16:30429711-30429761	MCF10A-Er-Src	breast:	n/a
47	chr16:30428842-30428892	GM12878	blood:	n/a
48	chr16:30428842-30428892	PANC-1	pancreas:	n/a
49	chr16:30430089-30430139	AG04450	lung:	fetal
50	chr16:30429837-30429887	ECC-1	luminal epithelium:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30428282..30430706-chr16:30650260..30652815,2	MCF-7	breast:
2	chr16:30122802..30125684-chr16:30426687..30428488,2	K562	blood:
3	chr16:30367168..30369191-chr16:30427259..30429781,3	MCF-7	breast:
4	chr16:30388796..30390827-chr16:30426623..30428713,2	MCF-7	breast:
5	chr16:30426230..30430771-chr16:30440207..30443266,5	K562	blood:
6	chr16:30378643..30380815-chr16:30427484..30429569,2	MCF-7	breast:
7	chr16:30428344..30430995-chr16:30535727..30539808,4	MCF-7	breast:
8	chr16:30430091..30431864-chr16:30536696..30538449,2	K562	blood:
9	chr16:30427799..30431834-chr16:30534294..30540593,7	MCF-7	breast:
10	chr16:30427103..30429593-chr16:30455374..30458526,5	MCF-7	breast:
11	chr16:30429086..30431594-chr16:30439120..30441728,2	MCF-7	breast:
12	chr16:30124184..30126989-chr16:30425859..30428488,3	K562	blood:
13	chr16:30428232..30430752-chr16:30661502..30664068,2	MCF-7	breast:
14	chr16:30427113..30429104-chr16:30669120..30671415,2	MCF-7	breast:
15	chr16:30430091..30432882-chr16:30536696..30538204,2	K562	blood:
16	chr16:30387643..30390000-chr16:30427735..30430082,2	MCF-7	breast:
17	chr16:30133035..30135349-chr16:30425863..30428832,2	MCF-7	breast:
18	chr16:30427757..30432109-chr16:30437396..30442167,10	MCF-7	breast:
19	chr16:30364489..30367608-chr16:30429426..30432189,3	K562	blood:
20	chr16:30428007..30431562-chr16:30708422..30711318,5	MCF-7	breast:
21	chr16:30427599..30430058-chr16:30620615..30623502,2	MCF-7	breast:
22	chr16:30100427..30103235-chr16:30427361..30429315,2	MCF-7	breast:
23	chr16:30427326..30429415-chr16:30670296..30671867,2	MCF-7	breast:
24	chr16:30428172..30431085-chr17:59475920..59478019,2	MCF-7	breast:
25	chr16:30382519..30385051-chr16:30425815..30427953,2	K562	blood:
26	chr16:30428527..30430623-chr16:30582267..30583993,2	MCF-7	breast:
27	chr16:30425958..30428339-chr16:30429435..30431595,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000199787	TF binding region
ENSG00000199787	CpG island
ENSG00000260219	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000102882	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000169221	chromatin interactions
ENSG00000102886	chromatin interactions
ENSG00000156858	chromatin interactions
ENSG00000156860	chromatin interactions
ENSG00000239791	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000229809	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000156853	chromatin interactions
ENSG00000179958	chromatin interactions
ENSG00000169217	chromatin interactions
ENSG00000199787	chromatin interactions
ENSG00000169957	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000149922	chromatin interactions
ENSG00000261840	chromatin interactions

Extended variants
information (count: 123 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:123 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542648555	chr16:30426981-30426982	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs561296745	chr16:30427065-30427066	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs528481779	chr16:30427074-30427075	Weak transcription Enhancers Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs540861779	chr16:30427119-30427120	Weak transcription Enhancers Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs546864072	chr16:30427165-30427166	Weak transcription Enhancers Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs141461517	chr16:30427193-30427194	Weak transcription Enhancers Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs566726172	chr16:30427431-30427432	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs532543217	chr16:30427443-30427444	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs184066939	chr16:30427464-30427465	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs569400955	chr16:30427527-30427528	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs537107055	chr16:30427554-30427555	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs548806314	chr16:30427615-30427616	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
13	rs567225074	chr16:30427644-30427645	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
14	rs534337615	chr16:30427660-30427661	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
15	rs553287846	chr16:30427738-30427739	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
16	rs145174360	chr16:30427823-30427824	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs538833701	chr16:30427901-30427902	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs557234679	chr16:30427925-30427926	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs113242480	chr16:30427929-30427930	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs138991023	chr16:30427974-30427975	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
21	rs543063175	chr16:30428039-30428040	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs148983772	chr16:30428045-30428046	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs573160400	chr16:30428047-30428048	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs540256310	chr16:30428074-30428075	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
25	rs4129614	chr16:30428076-30428077	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
26	rs143758982	chr16:30428117-30428118	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
27	rs148233051	chr16:30428120-30428121	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
28	rs552294334	chr16:30428126-30428127	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
29	rs544512128	chr16:30428137-30428138	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs374488233	chr16:30428148-30428149	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs377766614	chr16:30428213-30428214	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
32	rs34982677	chr16:30428241-30428242	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
33	rs188748918	chr16:30428271-30428272	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
34	rs565088059	chr16:30428336-30428337	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
35	rs192920412	chr16:30428343-30428344	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
36	rs79718222	chr16:30428380-30428381	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
37	rs571557210	chr16:30428390-30428391	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
38	rs185642653	chr16:30428391-30428392	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
39	rs557298063	chr16:30428456-30428457	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
40	rs569007288	chr16:30428618-30428619	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
41	rs536075666	chr16:30428663-30428664	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
42	rs190566905	chr16:30428671-30428672	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
43	rs573300529	chr16:30428700-30428701	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
44	rs202208289	chr16:30428735-30428736	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
45	rs558480922	chr16:30428761-30428762	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
46	rs576828842	chr16:30428869-30428870	Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
47	rs11541228	chr16:30428884-30428885	Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
48	rs544473661	chr16:30428899-30428900	Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
49	rs563054452	chr16:30428930-30428931	Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
50	rs11541227	chr16:30428932-30428933	Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30419200-30428800	Weak transcription	Small Intestine	intestine
2	chr16:30419600-30428600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr16:30419800-30428600	Weak transcription	Esophagus	oesophagus
4	chr16:30419800-30428800	Weak transcription	Gastric	stomach
5	chr16:30420000-30428800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr16:30421000-30427000	Weak transcription	GM12878-XiMat	blood
7	chr16:30421000-30428200	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr16:30421000-30428400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr16:30421200-30428200	Weak transcription	Primary B cells from cord blood	blood
10	chr16:30421200-30428200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr16:30421200-30428200	Weak transcription	Fetal Brain Male	brain
12	chr16:30421200-30428200	Weak transcription	Placenta	Placenta
13	chr16:30421200-30428200	Weak transcription	Spleen	Spleen
14	chr16:30421200-30428200	Weak transcription	NHDF-Ad	bronchial
15	chr16:30421200-30428400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr16:30421200-30428400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr16:30421200-30428400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr16:30421200-30428600	Weak transcription	Colonic Mucosa	Colon
19	chr16:30421200-30437600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr16:30421200-30437600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr16:30421400-30428200	Weak transcription	Primary B cells from peripheral blood	blood
22	chr16:30421400-30428200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr16:30421400-30428200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr16:30421400-30428200	Weak transcription	Colon Smooth Muscle	Colon
25	chr16:30421400-30428200	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr16:30421400-30428400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr16:30421400-30428400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr16:30421400-30428400	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr16:30421400-30428600	Weak transcription	Hela-S3	cervix
30	chr16:30421400-30428800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr16:30422000-30428400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr16:30422000-30428600	Weak transcription	Stomach Mucosa	stomach
33	chr16:30422200-30428200	Strong transcription	Fetal Stomach	stomach
34	chr16:30423200-30428600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr16:30423400-30428200	Weak transcription	Fetal Brain Female	brain
36	chr16:30423400-30428400	Weak transcription	Fetal Lung	lung
37	chr16:30423400-30428600	Weak transcription	Fetal Kidney	kidney
38	chr16:30423400-30428600	Weak transcription	Right Ventricle	heart
39	chr16:30423600-30427400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr16:30423600-30428200	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr16:30423600-30428200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr16:30423600-30428400	Weak transcription	HUVEC	blood vessel
43	chr16:30423600-30428600	Weak transcription	Aorta	Aorta
44	chr16:30423600-30428600	Weak transcription	HMEC	breast
45	chr16:30423800-30428000	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr16:30423800-30428400	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr16:30423800-30428400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr16:30423800-30428400	Weak transcription	Brain Cingulate Gyrus	brain
49	chr16:30423800-30428400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr16:30423800-30428600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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