Variant report

Variant	nsv905723
Chromosome Location	chr16:30187676-30205302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1323)
CpG islands
(count:1040)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1323 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:30194725-30194739	HepG2	liver:	n/a	n/a
2	ATF1	chr16:30198455-30198718	K562	blood:	n/a	n/a
3	ATF2	chr16:30194769-30195107	GM12878	blood:	n/a	n/a
4	ATF2	chr16:30198423-30199069	GM12878	blood:	n/a	n/a
5	ATF2	chr16:30198083-30199160	GM12878	blood:	n/a	n/a
6	ATF2	chr16:30195759-30196132	GM12878	blood:	n/a	n/a
7	ATF2	chr16:30196503-30197466	GM12878	blood:	n/a	n/a
8	ATF2	chr16:30195156-30197910	GM12878	blood:	n/a	n/a
9	ATF2	chr16:30193876-30194374	GM12878	blood:	n/a	n/a
10	BACH1	chr16:30198613-30198914	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:30198528-30198904	K562	blood:	n/a	n/a
12	BACH1	chr16:30198003-30198007	K562	blood:	n/a	n/a
13	BATF	chr16:30204418-30205489	GM12878	blood:	n/a	n/a
14	BCL11A	chr16:30203419-30203820	GM12878	blood:	n/a	n/a
15	BCL11A	chr16:30203933-30205250	GM12878	blood:	n/a	n/a
16	BCL11A	chr16:30204786-30205053	GM12878	blood:	n/a	n/a
17	BCL11A	chr16:30197818-30198265	GM12878	blood:	n/a	n/a
18	BCL11A	chr16:30202309-30202711	GM12878	blood:	n/a	n/a
19	BCL3	chr16:30198207-30199080	A549	lung:	n/a	n/a
20	BCL3	chr16:30195266-30195671	GM12878	blood:	n/a	chr16:30195642-30195655
21	BCLAF1	chr16:30195097-30199113	GM12878	blood:	n/a	chr16:30195642-30195655 chr16:30197167-30197180
22	BCLAF1	chr16:30194550-30195085	GM12878	blood:	n/a	chr16:30194870-30194879 chr16:30194825-30194838
23	BCLAF1	chr16:30194548-30199158	GM12878	blood:	n/a	chr16:30195642-30195655 chr16:30197167-30197180 chr16:30194870-30194879 chr16:30194825-30194838
24	BHLHE40	chr16:30197995-30198979	GM12878	blood:	n/a	n/a
25	BHLHE40	chr16:30189943-30190272	HepG2	liver:	n/a	n/a
26	BHLHE40	chr16:30194613-30195046	GM12878	blood:	n/a	n/a
27	BHLHE40	chr16:30196426-30197505	GM12878	blood:	n/a	chr16:30197435-30197451
28	BHLHE40	chr16:30193847-30194404	GM12878	blood:	n/a	n/a
29	BHLHE40	chr16:30198454-30198956	K562	blood:	n/a	n/a
30	BHLHE40	chr16:30204184-30204453	HepG2	liver:	n/a	n/a
31	BHLHE40	chr16:30195302-30196027	GM12878	blood:	n/a	n/a
32	BHLHE40	chr16:30198633-30198880	HepG2	liver:	n/a	n/a
33	BHLHE40	chr16:30204722-30205224	HepG2	liver:	n/a	n/a
34	BHLHE40	chr16:30194857-30194946	K562	blood:	n/a	n/a
35	BRCA1	chr16:30198502-30198547	HepG2	liver:	n/a	n/a
36	BRCA1	chr16:30195351-30195364	GM12878	blood:	n/a	n/a
37	CBX3	chr16:30198506-30198929	K562	blood:	n/a	n/a
38	CBX3	chr16:30204785-30205411	K562	blood:	n/a	n/a
39	CBX3	chr16:30198527-30198990	K562	blood:	n/a	n/a
40	CBX3	chr16:30204132-30205858	K562	blood:	n/a	n/a
41	CCNT2	chr16:30194744-30195127	K562	blood:	n/a	chr16:30194810-30194819
42	CCNT2	chr16:30198456-30198847	K562	blood:	n/a	n/a
43	CEBPB	chr16:30196985-30197319	K562	blood:	n/a	chr16:30197146-30197157
44	CEBPB	chr16:30196416-30197547	GM12878	blood:	n/a	chr16:30197146-30197157 chr16:30197421-30197434
45	CEBPB	chr16:30188440-30188614	A549	lung:	n/a	n/a
46	CEBPB	chr16:30204902-30205208	GM12878	blood:	n/a	chr16:30205120-30205128
47	CEBPB	chr16:30197833-30198427	GM12878	blood:	n/a	n/a
48	CEBPB	chr16:30197059-30197216	IMR90	lung:	n/a	chr16:30197146-30197157
49	CEBPB	chr16:30197082-30197270	GM12878	blood:	n/a	chr16:30197146-30197157
50	CEBPB	chr16:30188382-30188600	K562	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30192587-30192637	T-47D	breast:	n/a
2	chr16:30195318-30195368	GM06990	blood:	n/a
3	chr16:30198370-30198420	NHDF-neo	bronchial:	n/a
4	chr16:30192587-30192637	T-47D	breast:	n/a
5	chr16:30195318-30195368	GM06990	blood:	n/a
6	chr16:30198370-30198420	NHDF-neo	bronchial:	n/a
7	chr16:30192587-30192637	SK-N-SH	brain:	n/a
8	chr16:30194815-30194865	AG09309	skin:	n/a
9	chr16:30192587-30192637	HCT-116	colon:	n/a
10	chr16:30198517-30198567	HIPEpiC	eye:	n/a
11	chr16:30194815-30194865	HRE	kidney:	n/a
12	chr16:30196023-30196073	NT2-D1	testis:	n/a
13	chr16:30194484-30194534	HCPEpiC	choroid plexus:	n/a
14	chr16:30198370-30198420	BJ	skin:	n/a
15	chr16:30192587-30192637	BJ	skin:	n/a
16	chr16:30192587-30192637	HMEC	breast:	n/a
17	chr16:30195318-30195368	HCT-116	colon:	n/a
18	chr16:30196023-30196073	Hela-S3	cervix:	n/a
19	chr16:30195318-30195368	A549	lung:	n/a
20	chr16:30192587-30192637	HNPCEpiC	eye:	n/a
21	chr16:30198509-30198559	AG09309	skin:	n/a
22	chr16:30196023-30196073	RPTEC	kidney:	n/a
23	chr16:30194416-30194466	AG09319	gingival:	n/a
24	chr16:30195067-30195117	HCM	heart:	n/a
25	chr16:30198505-30198555	RPTEC	kidney:	n/a
26	chr16:30194815-30194865	ECC-1	luminal epithelium:	n/a
27	chr16:30194886-30194936	GM19239	blood:	n/a
28	chr16:30198509-30198559	CMK	blood:	n/a
29	chr16:30194888-30194938	BJ	skin:	n/a
30	chr16:30194888-30194938	CMK	blood:	n/a
31	chr16:30198509-30198559	HAEpiC	amniotic membrane:	n/a
32	chr16:30194776-30194826	GM06990	blood:	n/a
33	chr16:30196023-30196073	NHBE	bronchial:	n/a
34	chr16:30198509-30198559	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:30194888-30194938	Hepatocyte	liver:	n/a
36	chr16:30194776-30194826	ECC-1	luminal epithelium:	n/a
37	chr16:30197211-30197261	HPAEpiC	pulmonary alveolar:	n/a
38	chr16:30194886-30194936	HCF	heart:	n/a
39	chr16:30194776-30194826	HRE	kidney:	n/a
40	chr16:30194903-30194953	GM06990	blood:	n/a
41	chr16:30194886-30194936	GM06990	blood:	n/a
42	chr16:30195067-30195117	PrEC	prostate:	n/a
43	chr16:30194776-30194826	AG04449	skin:	fetal
44	chr16:30194886-30194936	HRE	kidney:	n/a
45	chr16:30194815-30194865	HCT-116	colon:	n/a
46	chr16:30197211-30197261	HepG2	liver:	n/a
47	chr16:30197211-30197261	RPTEC	kidney:	n/a
48	chr16:30198517-30198567	PrEC	prostate:	n/a
49	chr16:30194776-30194826	HRCEpiC	kidney:	n/a
50	chr16:30194776-30194826	GM12891	blood:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:29815002..29817643-chr16:30193444..30196373,3	MCF-7	breast:
2	chr16:30102283..30103884-chr16:30194608..30196819,2	MCF-7	breast:
3	chr16:30122445..30125435-chr16:30197147..30198801,2	K562	blood:
4	chr16:30124210..30124751-chr16:30198102..30199056,2	MCF-7	breast:
5	chr16:30073832..30076686-chr16:30197424..30199809,3	MCF-7	breast:
6	chr16:30194759..30196474-chr16:30708321..30710929,2	K562	blood:
7	chr16:30079070..30081233-chr16:30194915..30196655,2	MCF-7	breast:
8	chr16:30185936..30188220-chr16:30197826..30199753,2	MCF-7	breast:
9	chr11:60691741..60692731-chr16:30194046..30194929,2	HCT-116	colon:
10	chr16:30132897..30136323-chr16:30193309..30196336,5	MCF-7	breast:
11	chr16:30198315..30198870-chr16:30420884..30421401,2	MCF-7	breast:
12	chr16:30196751..30201052-chr16:30379113..30382636,3	MCF-7	breast:
13	chr16:30122556..30125865-chr16:30196040..30198997,3	K562	blood:
14	chr16:30075111..30080393-chr16:30194482..30199026,7	MCF-7	breast:
15	chr16:30099194..30104975-chr16:30193189..30199409,9	MCF-7	breast:
16	chr16:30076811..30079031-chr16:30197360..30200413,3	K562	blood:
17	chr16:30197379..30199709-chr16:30708853..30710594,2	MCF-7	breast:
18	chr16:30102992..30106412-chr16:30196223..30199425,3	K562	blood:
19	chr16:30105196..30108316-chr16:30196676..30200078,3	MCF-7	breast:
20	chr16:30102992..30108322-chr16:30194679..30199860,7	K562	blood:
21	chr16:30132759..30134974-chr16:30196981..30199413,2	MCF-7	breast:
22	chr16:30194484..30196796-chr16:30455955..30457567,2	K562	blood:
23	chr16:30121828..30124583-chr16:30196625..30198544,2	MCF-7	breast:
24	chr16:30127849..30129805-chr16:30193188..30195789,2	MCF-7	breast:
25	chr16:30197720..30200168-chr16:30772376..30774510,2	MCF-7	breast:
26	chr16:30193615..30195273-chr16:30388746..30390987,2	K562	blood:
27	chr16:30134390..30135940-chr16:30193438..30196422,2	MCF-7	breast:
28	chr16:30197384..30200120-chr16:30417665..30420072,2	K562	blood:
29	chr16:30123508..30126853-chr16:30193449..30196569,3	MCF-7	breast:
30	chr16:30194030..30196796-chr16:30455949..30457567,2	K562	blood:
31	chr16:30086324..30089424-chr16:30196059..30198552,4	MCF-7	breast:
32	chr16:30075696..30078954-chr16:30197360..30200413,3	K562	blood:
33	chr16:30077452..30079715-chr16:30197226..30200095,2	MCF-7	breast:
34	chr16:30122202..30125558-chr16:30192872..30196155,3	MCF-7	breast:
35	chr16:30087286..30089339-chr16:30194884..30196555,2	MCF-7	breast:
36	chr1:12399202..12400121-chr16:30198326..30198844,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLX1A-1	chr16:30200005-30200575	NONHSAT141716
2	lnc-BOLA2B-1	chr16:30196153-30196278	ENSG00000261416.1
3	lnc-BOLA2B-1	chr16:30195825-30195860	ENSG00000261416.1
4	lnc-BOLA2B-1	chr16:30195383-30195740	ENSG00000261416.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CORO1A	hsa-miR-24-3p	chr16:30198442-30198465

Variant related genes	Relation type
BOLA2B	TF binding region
SULT1A3	TF binding region
ENSG00000261416	TF binding region
SLX1A	TF binding region
CORO1A	TF binding region
SLX1A-SULT1A3	TF binding region
BOLA2B	CpG island
SULT1A3	CpG island
ENSG00000261416	CpG island
SLX1A	CpG island
CORO1A	CpG island
SLX1A-SULT1A3	CpG island
ENSG00000103549	chromatin interactions
ENSG00000196118	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000250616	chromatin interactions
ENSG00000102882	chromatin interactions
ENSG00000102886	chromatin interactions
ENSG00000102879	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000169221	chromatin interactions
ENSG00000103495	chromatin interactions
ENSG00000006118	chromatin interactions
ENSG00000179965	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000149923	chromatin interactions
ENSG00000090238	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000149922	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000180035	chromatin interactions

Extended variants
information (count: 470 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12373078	chr16:30187676-30187677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35308784	chr16:30187678-30187679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556307535	chr16:30187679-30187680	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369058703	chr16:30187709-30187710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144995728	chr16:30187729-30187730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566587057	chr16:30187733-30187734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376331347	chr16:30187777-30187778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542507064	chr16:30187778-30187779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558269573	chr16:30187799-30187800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11862691	chr16:30187851-30187852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs537793492	chr16:30187863-30187864	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377112695	chr16:30187888-30187889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560295640	chr16:30187909-30187910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545662994	chr16:30187982-30187983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547649706	chr16:30188006-30188007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140647398	chr16:30188013-30188014	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200339116	chr16:30188016-30188017	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372250820	chr16:30188017-30188018	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560182472	chr16:30188034-30188035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112323497	chr16:30188050-30188051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs199683095	chr16:30188059-30188060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572460842	chr16:30188065-30188066	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs552470650	chr16:30188070-30188071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs564373068	chr16:30188071-30188072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532013883	chr16:30188072-30188073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550521280	chr16:30188090-30188091	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187570079	chr16:30188120-30188121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs529472239	chr16:30188141-30188142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190603249	chr16:30188164-30188165	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369610214	chr16:30188254-30188255	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs554203955	chr16:30188259-30188260	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs533696018	chr16:30188289-30188290	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs150476277	chr16:30188326-30188327	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs570388715	chr16:30188390-30188391	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs538122518	chr16:30188477-30188478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556011884	chr16:30188479-30188480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374276690	chr16:30188514-30188515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138310571	chr16:30188634-30188635	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs182881115	chr16:30188638-30188639	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs377640316	chr16:30188659-30188660	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs553556369	chr16:30188796-30188797	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs201685092	chr16:30188821-30188822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572501718	chr16:30188880-30188881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187934744	chr16:30188962-30188963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572395525	chr16:30189012-30189013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374718659	chr16:30189078-30189079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564481866	chr16:30189090-30189091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576327578	chr16:30189103-30189104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs193000050	chr16:30189118-30189119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554874385	chr16:30189143-30189144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

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
Congenital diaphragmatic hernia	21525063	CNVD
Epilepsy	20502679	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	21346763	CNVD
autism	21731881	CNVD
Developmental delay	22909776	CNVD
speech impairment	22909776	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30179000-30188000	Weak transcription	Primary B cells from cord blood	blood
2	chr16:30179000-30188200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr16:30182600-30194200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:30183000-30188000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr16:30183000-30188200	Weak transcription	HepG2	liver
6	chr16:30185200-30194000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr16:30187000-30188200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr16:30187600-30189200	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr16:30188000-30188200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr16:30188000-30188800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr16:30188000-30189200	Enhancers	Primary B cells from cord blood	blood
12	chr16:30188200-30188400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr16:30188200-30188400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr16:30188200-30188400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr16:30188200-30189000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr16:30188200-30189200	Enhancers	HepG2	liver
17	chr16:30188400-30188600	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr16:30188400-30188600	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr16:30188400-30194000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr16:30188600-30188800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr16:30188600-30188800	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr16:30188600-30188800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
23	chr16:30188800-30189000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr16:30188800-30189800	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr16:30188800-30190200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr16:30188800-30194000	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr16:30189000-30193400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr16:30189000-30193600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr16:30189200-30189600	Weak transcription	HepG2	liver
30	chr16:30189200-30193200	Weak transcription	Primary B cells from cord blood	blood
31	chr16:30189200-30193400	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr16:30189600-30190800	Enhancers	Fetal Intestine Small	intestine
33	chr16:30189600-30192800	Enhancers	HepG2	liver
34	chr16:30189800-30190000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr16:30189800-30190000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr16:30189800-30190200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr16:30189800-30190200	Enhancers	Fetal Muscle Trunk	muscle
38	chr16:30189800-30190200	Enhancers	Fetal Muscle Leg	muscle
39	chr16:30189800-30190200	Enhancers	Gastric	stomach
40	chr16:30189800-30190200	Enhancers	Pancreas	Pancrea
41	chr16:30189800-30190200	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr16:30189800-30190200	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr16:30189800-30190200	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr16:30189800-30190400	Enhancers	Stomach Mucosa	stomach
45	chr16:30189800-30190800	Enhancers	Duodenum Mucosa	Duodenum
46	chr16:30189800-30190800	Enhancers	Fetal Intestine Large	intestine
47	chr16:30190000-30190200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:30190000-30190200	Enhancers	Colonic Mucosa	Colon
49	chr16:30190000-30190200	Enhancers	A549	lung
50	chr16:30190200-30192200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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