Variant report

Variant	nsv571819
Chromosome Location	chr16:30158757-30215621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1860)
CpG islands
(count:1281)
Chromatin interactive
region (count:41)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1860 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

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	ARID3A	chr16:30182291-30182531	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:30182745-30182862	HepG2	liver:	n/a	n/a
4	ATF1	chr16:30198455-30198718	K562	blood:	n/a	n/a
5	ATF2	chr16:30194769-30195107	GM12878	blood:	n/a	n/a
6	ATF2	chr16:30177517-30177990	GM12878	blood:	n/a	n/a
7	ATF2	chr16:30177440-30178013	GM12878	blood:	n/a	n/a
8	ATF2	chr16:30198423-30199069	GM12878	blood:	n/a	n/a
9	ATF2	chr16:30193876-30194374	GM12878	blood:	n/a	n/a
10	ATF2	chr16:30196503-30197466	GM12878	blood:	n/a	n/a
11	ATF2	chr16:30198083-30199160	GM12878	blood:	n/a	n/a
12	ATF2	chr16:30195156-30197910	GM12878	blood:	n/a	n/a
13	ATF2	chr16:30195759-30196132	GM12878	blood:	n/a	n/a
14	BACH1	chr16:30198003-30198007	K562	blood:	n/a	n/a
15	BACH1	chr16:30198528-30198904	K562	blood:	n/a	n/a
16	BACH1	chr16:30198613-30198914	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr16:30204418-30205489	GM12878	blood:	n/a	n/a
18	BATF	chr16:30177505-30177828	GM12878	blood:	n/a	n/a
19	BCL11A	chr16:30177528-30177966	GM12878	blood:	n/a	n/a
20	BCL11A	chr16:30177543-30177899	GM12878	blood:	n/a	n/a
21	BCL11A	chr16:30203419-30203820	GM12878	blood:	n/a	n/a
22	BCL11A	chr16:30203933-30205250	GM12878	blood:	n/a	n/a
23	BCL11A	chr16:30202309-30202711	GM12878	blood:	n/a	n/a
24	BCL11A	chr16:30204786-30205053	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:30197818-30198265	GM12878	blood:	n/a	n/a
26	BCL3	chr16:30198207-30199080	A549	lung:	n/a	n/a
27	BCL3	chr16:30195266-30195671	GM12878	blood:	n/a	chr16:30195642-30195655
28	BCLAF1	chr16:30195097-30199113	GM12878	blood:	n/a	chr16:30195642-30195655 chr16:30197167-30197180
29	BCLAF1	chr16:30194548-30199158	GM12878	blood:	n/a	chr16:30195642-30195655 chr16:30197167-30197180 chr16:30194870-30194879 chr16:30194825-30194838
30	BCLAF1	chr16:30194550-30195085	GM12878	blood:	n/a	chr16:30194870-30194879 chr16:30194825-30194838
31	BCLAF1	chr16:30177489-30178005	GM12878	blood:	n/a	n/a
32	BCLAF1	chr16:30177501-30177945	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:30196426-30197505	GM12878	blood:	n/a	chr16:30197435-30197451
34	BHLHE40	chr16:30210902-30211673	HepG2	liver:	n/a	n/a
35	BHLHE40	chr16:30205607-30205898	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:30193847-30194404	GM12878	blood:	n/a	n/a
37	BHLHE40	chr16:30177509-30177916	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:30182399-30182672	HepG2	liver:	n/a	n/a
39	BHLHE40	chr16:30204722-30205224	HepG2	liver:	n/a	n/a
40	BHLHE40	chr16:30182321-30182749	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:30198454-30198956	K562	blood:	n/a	n/a
42	BHLHE40	chr16:30177645-30177846	K562	blood:	n/a	n/a
43	BHLHE40	chr16:30182386-30182725	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:30194857-30194946	K562	blood:	n/a	n/a
45	BHLHE40	chr16:30197995-30198979	GM12878	blood:	n/a	n/a
46	BHLHE40	chr16:30204184-30204453	HepG2	liver:	n/a	n/a
47	BHLHE40	chr16:30194613-30195046	GM12878	blood:	n/a	n/a
48	BHLHE40	chr16:30195302-30196027	GM12878	blood:	n/a	n/a
49	BHLHE40	chr16:30189943-30190272	HepG2	liver:	n/a	n/a
50	BHLHE40	chr16:30198633-30198880	HepG2	liver:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30197211-30197261	HUVEC	blood vessel:	n/a
2	chr16:30197211-30197261	MCF10A-Er-Src	breast:	n/a
3	chr16:30198509-30198559	RPTEC	kidney:	n/a
4	chr16:30206076-30206126	Hepatocyte	liver:	n/a
5	chr16:30195067-30195117	PFSK-1	brain:	n/a
6	chr16:30209202-30209252	Hepatocyte	liver:	n/a
7	chr16:30194903-30194953	HEEpiC	esophagus:	n/a
8	chr16:30198370-30198420	BJ	skin:	n/a
9	chr16:30194815-30194865	H1-hESC	embryonic stem cell:	embryo
10	chr16:30194717-30194767	HPAEpiC	pulmonary alveolar:	n/a
11	chr16:30194886-30194936	HepG2	liver:	n/a
12	chr16:30194886-30194936	AG09319	gingival:	n/a
13	chr16:30194484-30194534	IMR90	lung:	fetal
14	chr16:30195318-30195368	A549	lung:	n/a
15	chr16:30194886-30194936	HEK293	kidney:	embryo
16	chr16:30194484-30194534	AG10803	skin:	n/a
17	chr16:30198509-30198559	HCT-116	colon:	n/a
18	chr16:30206076-30206126	HL-60	blood:	n/a
19	chr16:30206073-30206123	BE2_C	brain:	n/a
20	chr16:30194416-30194466	NHBE	bronchial:	n/a
21	chr16:30194717-30194767	HL-60	blood:	n/a
22	chr16:30194717-30194767	PFSK-1	brain:	n/a
23	chr16:30197211-30197261	GM19239	blood:	n/a
24	chr16:30194717-30194767	HEK293	kidney:	embryo
25	chr16:30194903-30194953	AoSMC	blood vessel:	n/a
26	chr16:30194903-30194953	PANC-1	pancreas:	n/a
27	chr16:30194815-30194865	NHBE	bronchial:	n/a
28	chr16:30206046-30206096	SKMC	muscle:	n/a
29	chr16:30197211-30197261	T-47D	breast:	n/a
30	chr16:30196023-30196073	GM12891	blood:	n/a
31	chr16:30194888-30194938	PFSK-1	brain:	n/a
32	chr16:30194416-30194466	H1-hESC	embryonic stem cell:	embryo
33	chr16:30194484-30194534	NHDF-neo	bronchial:	n/a
34	chr16:30198505-30198555	SK-N-SH	brain:	n/a
35	chr16:30198509-30198559	HRPEpiC	eye:	n/a
36	chr16:30206076-30206126	AG09319	gingival:	n/a
37	chr16:30196023-30196073	SK-N-SH_RA	brain:	n/a
38	chr16:30209202-30209252	HMEC	breast:	n/a
39	chr16:30198505-30198555	SK-N-SH_RA	brain:	n/a
40	chr16:30194903-30194953	SKMC	muscle:	n/a
41	chr16:30195318-30195368	LNCaP	prostate:	n/a
42	chr16:30194717-30194767	NT2-D1	testis:	n/a
43	chr16:30198370-30198420	T-47D	breast:	n/a
44	chr16:30192587-30192637	NHDF-neo	bronchial:	n/a
45	chr16:30194903-30194953	SAEC	small airway:	n/a
46	chr16:30206073-30206123	A549	lung:	n/a
47	chr16:30209202-30209252	BE2_C	brain:	n/a
48	chr16:30206046-30206096	AG09319	gingival:	n/a
49	chr16:30194815-30194865	GM12892	blood:	n/a
50	chr16:30194888-30194938	H1-hESC	embryonic stem cell:	embryo

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30159556..30162388-chr16:30677070..30678638,2	K562	blood:
2	chr16:30132897..30136323-chr16:30193309..30196336,5	MCF-7	breast:
3	chr16:30087286..30089339-chr16:30194884..30196555,2	MCF-7	breast:
4	chr16:30173126..30174657-chr16:30193076..30195048,2	MCF-7	breast:
5	chr16:30164181..30165686-chr16:30171890..30174652,2	K562	blood:
6	chr11:60691741..60692731-chr16:30194046..30194929,2	HCT-116	colon:
7	chr16:30099194..30104975-chr16:30193189..30199409,9	MCF-7	breast:
8	chr16:29815002..29817643-chr16:30193444..30196373,3	MCF-7	breast:
9	chr16:30077452..30079715-chr16:30197226..30200095,2	MCF-7	breast:
10	chr16:30102283..30103884-chr16:30194608..30196819,2	MCF-7	breast:
11	chr16:30197384..30200120-chr16:30417665..30420072,2	K562	blood:
12	chr16:30134390..30135940-chr16:30193438..30196422,2	MCF-7	breast:
13	chr16:30185936..30188220-chr16:30197826..30199753,2	MCF-7	breast:
14	chr16:30122445..30125435-chr16:30197147..30198801,2	K562	blood:
15	chr16:30086324..30089424-chr16:30196059..30198552,4	MCF-7	breast:
16	chr16:30132759..30134974-chr16:30196981..30199413,2	MCF-7	breast:
17	chr16:30075696..30078954-chr16:30197360..30200413,3	K562	blood:
18	chr16:30198315..30198870-chr16:30420884..30421401,2	MCF-7	breast:
19	chr16:30079070..30081233-chr16:30194915..30196655,2	MCF-7	breast:
20	chr16:30076811..30079031-chr16:30197360..30200413,3	K562	blood:
21	chr16:30073832..30076686-chr16:30197424..30199809,3	MCF-7	breast:
22	chr16:30121828..30124583-chr16:30196625..30198544,2	MCF-7	breast:
23	chr16:30075111..30080393-chr16:30194482..30199026,7	MCF-7	breast:
24	chr1:12399202..12400121-chr16:30198326..30198844,2	K562	blood:
25	chr16:30123508..30126853-chr16:30193449..30196569,3	MCF-7	breast:
26	chr16:30197379..30199709-chr16:30708853..30710594,2	MCF-7	breast:
27	chr16:30127849..30129805-chr16:30193188..30195789,2	MCF-7	breast:
28	chr16:30194030..30196796-chr16:30455949..30457567,2	K562	blood:
29	chr16:30122202..30125558-chr16:30192872..30196155,3	MCF-7	breast:
30	chr16:30196751..30201052-chr16:30379113..30382636,3	MCF-7	breast:
31	chr16:30124210..30124751-chr16:30198102..30199056,2	MCF-7	breast:
32	chr16:30102992..30106412-chr16:30196223..30199425,3	K562	blood:
33	chr16:30080041..30082622-chr16:30171672..30174574,2	MCF-7	breast:
34	chr16:30194484..30196796-chr16:30455955..30457567,2	K562	blood:
35	chr16:30102992..30108322-chr16:30194679..30199860,7	K562	blood:
36	chr16:30105196..30108316-chr16:30196676..30200078,3	MCF-7	breast:
37	chr16:30194759..30196474-chr16:30708321..30710929,2	K562	blood:
38	chr16:30197720..30200168-chr16:30772376..30774510,2	MCF-7	breast:
39	chr16:30164181..30165686-chr16:30171890..30174652,2	K562	blood:
40	chr16:30122556..30125865-chr16:30196040..30198997,3	K562	blood:
41	chr16:30193615..30195273-chr16:30388746..30390987,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SULT1A3.1-1	chr16:30208591-30208724	NONHSAT141721
2	lnc-SULT1A3.1-1	chr16:30208758-30208851	NONHSAT141720
3	lnc-BOLA2B-1	chr16:30195383-30195740	ENSG00000261416.1
4	lnc-BOLA2B-1	chr16:30196153-30196278	ENSG00000261416.1
5	lnc-BOLA2B-1	chr16:30195825-30195860	ENSG00000261416.1
6	lnc-SULT1A3.1-1	chr16:30207633-30208678	NONHSAT141720
7	lnc-SLX1A-1	chr16:30200005-30200575	NONHSAT141716
8	lnc-SULT1A3.1-1	chr16:30214329-30214825	NONHSAT141723
9	lnc-SULT1A3.1-1	chr16:30207979-30208422	NONHSAT141721

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
ENSG00000102886	chromatin interactions
ENSG00000196118	chromatin interactions
ENSG00000006118	chromatin interactions
ENSG00000179965	chromatin interactions
ENSG00000103549	chromatin interactions
ENSG00000169221	chromatin interactions
ENSG00000103495	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000090238	chromatin interactions
ENSG00000102879	chromatin interactions
ENSG00000156860	chromatin interactions
ENSG00000149923	chromatin interactions
ENSG00000149922	chromatin interactions
ENSG00000102882	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000250616	chromatin interactions
ENSG00000080603	chromatin interactions

Extended variants
information (count: 1457 )
Associated
traits (count: 129 )

Variant overlapped rSNPs/rCNVs (count:1457 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7199462	chr16:30158757-30158758	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535250317	chr16:30158774-30158775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371753376	chr16:30158852-30158853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560874839	chr16:30158855-30158856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532713814	chr16:30158857-30158858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551116197	chr16:30158925-30158926	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569116395	chr16:30158964-30158965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530473799	chr16:30158980-30158981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150153045	chr16:30158988-30158989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534647578	chr16:30158989-30158990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552970340	chr16:30159012-30159013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138583533	chr16:30159052-30159053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538566742	chr16:30159056-30159057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs202162232	chr16:30159075-30159076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12919578	chr16:30159107-30159108	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs575557301	chr16:30159110-30159111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543137103	chr16:30159127-30159128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555136584	chr16:30159202-30159203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573136885	chr16:30159217-30159218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532614045	chr16:30159239-30159240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146794057	chr16:30159240-30159241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540590438	chr16:30159273-30159274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565147761	chr16:30159335-30159336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192004377	chr16:30159364-30159365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577423974	chr16:30159386-30159387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375523983	chr16:30159479-30159480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544580113	chr16:30159492-30159493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562739534	chr16:30159523-30159524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530269411	chr16:30159533-30159534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147478084	chr16:30159563-30159564	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11645626	chr16:30159590-30159591	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139949617	chr16:30159648-30159649	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528190565	chr16:30159678-30159679	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184691403	chr16:30159679-30159680	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs571160355	chr16:30159715-30159716	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538922031	chr16:30159775-30159776	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550937417	chr16:30159822-30159823	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs57842455	chr16:30159839-30159840	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201453553	chr16:30159841-30159842	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368810095	chr16:30159843-30159844	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560263381	chr16:30159845-30159846	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs184266005	chr16:30159968-30159969	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs79468307	chr16:30159975-30159976	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558863807	chr16:30159980-30159981	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs527518764	chr16:30160136-30160137	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577212421	chr16:30160166-30160167	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189313832	chr16:30160168-30160169	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562875388	chr16:30160211-30160212	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368913522	chr16:30160224-30160225	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs574670477	chr16:30160388-30160389	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:129)

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
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30157000-30160200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr16:30157200-30162800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr16:30158200-30160600	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr16:30158200-30162200	Enhancers	Primary B cells from cord blood	blood
5	chr16:30158600-30159000	Weak transcription	Hela-S3	cervix
6	chr16:30159000-30159600	Enhancers	Hela-S3	cervix
7	chr16:30160200-30160600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr16:30160600-30161000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr16:30160600-30161200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr16:30161000-30161800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr16:30161200-30161600	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr16:30161600-30161800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr16:30161600-30162000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr16:30161600-30162800	Enhancers	HepG2	liver
15	chr16:30161800-30163200	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr16:30161800-30163200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr16:30162400-30163200	Enhancers	Primary B cells from peripheral blood	blood
18	chr16:30162800-30163000	Bivalent Enhancer	HepG2	liver
19	chr16:30162800-30165200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr16:30163000-30163200	Flanking Bivalent TSS/Enh	HepG2	liver
21	chr16:30163200-30163400	Bivalent Enhancer	HepG2	liver
22	chr16:30163200-30165400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr16:30165200-30165600	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr16:30165400-30165600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr16:30165800-30167000	Enhancers	HepG2	liver
26	chr16:30167000-30168200	Weak transcription	HepG2	liver
27	chr16:30168200-30168800	Enhancers	HepG2	liver
28	chr16:30168800-30171000	Weak transcription	HepG2	liver
29	chr16:30170000-30170400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr16:30170000-30170400	Enhancers	Placenta	Placenta
31	chr16:30171000-30171400	Enhancers	HepG2	liver
32	chr16:30171400-30182200	Weak transcription	HepG2	liver
33	chr16:30171600-30172000	Enhancers	Fetal Brain Male	brain
34	chr16:30172000-30174800	Weak transcription	Fetal Brain Male	brain
35	chr16:30172400-30172600	Enhancers	Primary T cells fromperipheralblood	blood
36	chr16:30172600-30173600	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr16:30173200-30173400	Active TSS	Gastric	stomach
38	chr16:30173600-30179000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr16:30174200-30179000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr16:30174600-30175000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr16:30174600-30175200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr16:30174800-30175000	Enhancers	Primary T cells from cord blood	blood
43	chr16:30174800-30175000	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr16:30174800-30175000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr16:30174800-30175000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr16:30174800-30175200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr16:30174800-30175200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr16:30174800-30175200	Enhancers	Fetal Brain Male	brain
49	chr16:30174800-30177600	Enhancers	GM12878-XiMat	blood
50	chr16:30175000-30175200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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