Variant report

Variant	nsv1004693
Chromosome Location	chr2:179933683-180265288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2741)
CpG islands
(count:611)
Chromatin interactive
region (count:85)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:2741 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:180129321-180130164	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:180083747-180084075	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:180136821-180137690	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:180127655-180128278	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:180126156-180126501	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:180208774-180209700	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:180205491-180205811	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:180103469-180105057	HepG2	liver:	n/a	chr2:180104020-180104036
9	ARID3A	chr2:180138150-180138733	HepG2	liver:	n/a	chr2:180138538-180138554
10	ARID3A	chr2:180105511-180105719	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:180197727-180198019	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:179971271-179972019	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:180058459-180058657	HepG2	liver:	n/a	n/a
14	ARID3A	chr2:180038980-180039282	HepG2	liver:	n/a	n/a
15	ARID3A	chr2:180097397-180097407	HepG2	liver:	n/a	n/a
16	ARID3A	chr2:179994512-179994681	HepG2	liver:	n/a	n/a
17	ATF1	chr2:180261968-180262362	K562	blood:	n/a	n/a
18	ATF1	chr2:179971376-179971690	K562	blood:	n/a	n/a
19	ATF1	chr2:180098919-180099109	K562	blood:	n/a	n/a
20	ATF2	chr2:180103903-180104351	GM12878	blood:	n/a	n/a
21	ATF2	chr2:179971273-179971999	GM12878	blood:	n/a	n/a
22	ATF2	chr2:180132917-180133336	GM12878	blood:	n/a	n/a
23	ATF2	chr2:180132865-180133290	GM12878	blood:	n/a	n/a
24	ATF2	chr2:180044931-180045459	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr2:180044989-180045412	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr2:179971230-179971779	GM12878	blood:	n/a	n/a
27	ATF3	chr2:179971183-179971847	HCT-116	colon:	n/a	n/a
28	ATF3	chr2:179971378-179971740	K562	blood:	n/a	n/a
29	ATF3	chr2:179971224-179971786	HCT-116	colon:	n/a	n/a
30	ATF3	chr2:179971312-179971863	A549	lung:	n/a	n/a
31	BACH1	chr2:180209168-180209565	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr2:180128320-180128520	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr2:180129343-180129796	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr2:180022603-180022624	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr2:180128833-180129052	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr2:180209211-180209504	K562	blood:	n/a	n/a
37	BACH1	chr2:180133419-180133619	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr2:179972520-179972798	GM12878	blood:	n/a	n/a
39	BATF	chr2:180119834-180120242	GM12878	blood:	n/a	n/a
40	BATF	chr2:180103968-180104241	GM12878	blood:	n/a	chr2:180104091-180104102
41	BATF	chr2:180103988-180104180	GM12878	blood:	n/a	chr2:180104091-180104102
42	BATF	chr2:180133010-180133329	GM12878	blood:	n/a	n/a
43	BATF	chr2:180133009-180133382	GM12878	blood:	n/a	n/a
44	BATF	chr2:179962975-179963390	GM12878	blood:	n/a	n/a
45	BATF	chr2:179994289-179994529	GM12878	blood:	n/a	chr2:179994389-179994400
46	BATF	chr2:179971354-179971672	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:180132947-180133351	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:180045026-180045361	H1-hESC	embryonic stem cell:	n/a	n/a
49	BCL11A	chr2:179971329-179971874	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:180045033-180045282	H1-hESC	embryonic stem cell:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180125932-180125982	NT2-D1	testis:	n/a
2	chr2:180125932-180125982	NT2-D1	testis:	n/a
3	chr2:180128889-180128939	HRE	kidney:	n/a
4	chr2:180202670-180202720	NHBE	bronchial:	n/a
5	chr2:179974586-179974636	AG09319	gingival:	n/a
6	chr2:180128889-180128939	RPTEC	kidney:	n/a
7	chr2:180128889-180128939	SK-N-SH_RA	brain:	n/a
8	chr2:179974586-179974636	H1-hESC	embryonic stem cell:	embryo
9	chr2:180128490-180128540	BJ	skin:	n/a
10	chr2:180129612-180129662	NH-A	brain:	n/a
11	chr2:180125932-180125982	HCT-116	colon:	n/a
12	chr2:180129612-180129662	HEK293	kidney:	embryo
13	chr2:180128490-180128540	BE2_C	brain:	n/a
14	chr2:180129612-180129662	HCF	heart:	n/a
15	chr2:180202670-180202720	HCF	heart:	n/a
16	chr2:180128490-180128540	MCF10A-Er-Src	breast:	n/a
17	chr2:180200208-180200258	HUVEC	blood vessel:	n/a
18	chr2:180046003-180046053	HCM	heart:	n/a
19	chr2:180202670-180202720	GM12891	blood:	n/a
20	chr2:180046003-180046053	HMEC	breast:	n/a
21	chr2:180125932-180125982	BE2_C	brain:	n/a
22	chr2:180130081-180130131	IMR90	lung:	fetal
23	chr2:180202670-180202720	HRCEpiC	kidney:	n/a
24	chr2:180128889-180128939	PANC-1	pancreas:	n/a
25	chr2:180128889-180128939	HIPEpiC	eye:	n/a
26	chr2:180128889-180128939	HRCEpiC	kidney:	n/a
27	chr2:180129612-180129662	SK-N-MC	brain:	n/a
28	chr2:180130081-180130131	NT2-D1	testis:	n/a
29	chr2:180128490-180128540	HCPEpiC	choroid plexus:	n/a
30	chr2:180202670-180202720	ovcar-3	ovarian:	n/a
31	chr2:180128490-180128540	SK-N-MC	brain:	n/a
32	chr2:180202670-180202720	Caco-2	colon:	n/a
33	chr2:180125932-180125982	HEK293	kidney:	embryo
34	chr2:180129612-180129662	HAEpiC	amniotic membrane:	n/a
35	chr2:180128907-180128957	NB4	blood:	n/a
36	chr2:180128889-180128939	Caco-2	colon:	n/a
37	chr2:180200208-180200258	HIPEpiC	eye:	n/a
38	chr2:179974586-179974636	HL-60	blood:	n/a
39	chr2:180130081-180130131	HRPEpiC	eye:	n/a
40	chr2:180128490-180128540	MCF-7	breast:	n/a
41	chr2:180128889-180128939	HPAEpiC	pulmonary alveolar:	n/a
42	chr2:180202670-180202720	GM12892	blood:	n/a
43	chr2:180129612-180129662	AoSMC	blood vessel:	n/a
44	chr2:179974586-179974636	SK-N-SH	brain:	n/a
45	chr2:180129612-180129662	SK-N-SH_RA	brain:	n/a
46	chr2:180125932-180125982	GM12878	blood:	n/a
47	chr2:180129612-180129662	NHDF-neo	bronchial:	n/a
48	chr2:180128889-180128939	ovcar-3	ovarian:	n/a
49	chr2:180202670-180202720	PANC-1	pancreas:	n/a
50	chr2:180128907-180128957	AG04450	lung:	fetal

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:179983325..179985286-chr2:179986584..179988899,2	K562	blood:
2	chr2:180128256..180129810-chr2:180207695..180210396,2	MCF-7	breast:
3	chr2:180115892..180117617-chr2:180123291..180126152,2	K562	blood:
4	chr2:180083456..180084009-chr2:180615655..180616482,2	MCF-7	breast:
5	chr2:180027947..180030148-chr2:180031681..180034023,3	MCF-7	breast:
6	chr2:180045016..180046890-chr2:180047637..180050152,2	K562	blood:
7	chr2:179962282..179964737-chr2:179968470..179970797,2	MCF-7	breast:
8	chr2:180005225..180008035-chr2:180008843..180011202,2	K562	blood:
9	chr2:122288038..122288614-chr2:180219711..180220231,2	Hela-S3	cervix:
10	chr2:180091710..180093707-chr2:180097296..180099649,3	MCF-7	breast:
11	chr2:180099965..180101717-chr2:180103234..180105570,2	K562	blood:
12	chr2:180039372..180041323-chr2:180056705..180058266,2	MCF-7	breast:
13	chr2:180114644..180119395-chr2:180127594..180130471,4	MCF-7	breast:
14	chr2:179965713..179967518-chr2:179989741..179992075,2	K562	blood:
15	chr2:180127231..180129754-chr2:180137790..180140822,6	MCF-7	breast:
16	chr2:180091710..180093707-chr2:180097296..180099649,3	MCF-7	breast:
17	chr2:179315142..179317025-chr2:180127825..180130038,2	MCF-7	breast:
18	chr2:179990644..179992721-chr2:180003873..180005520,2	K562	blood:
19	chr2:180127590..180133149-chr2:180134052..180141026,12	MCF-7	breast:
20	chr2:180115892..180117617-chr2:180123291..180126152,2	K562	blood:
21	chr2:180148874..180150969-chr2:180153037..180154846,2	K562	blood:
22	chr2:180114550..180116150-chr2:180123274..180125911,2	MCF-7	breast:
23	chr2:180138330..180140789-chr2:180141084..180143785,2	MCF-7	breast:
24	chr2:180083560..180084369-chr2:180205061..180206359,5	MCF-7	breast:
25	chr2:180083391..180084449-chr2:180205175..180206192,5	MCF-7	breast:
26	chr2:180114654..180117674-chr2:180127724..180131363,3	MCF-7	breast:
27	chr2:180118975..180121494-chr2:180124484..180126493,2	K562	blood:
28	chr2:180068360..180070223-chr2:180071616..180074057,2	K562	blood:
29	chr2:180122860..180124976-chr2:180127824..180130891,3	MCF-7	breast:
30	chr2:179966762..179969783-chr2:179969877..179973075,3	K562	blood:
31	chr2:180005469..180007805-chr2:180127766..180130374,2	MCF-7	breast:
32	chr2:179660514..179661453-chr2:179994101..179994985,3	MCF-7	breast:
33	chr2:179966762..179969783-chr2:179969877..179973075,3	K562	blood:
34	chr2:180115733..180117570-chr2:180124952..180126888,2	MCF-7	breast:
35	chr2:180084814..180086461-chr2:180088409..180090009,2	K562	blood:
36	chr2:180115733..180117570-chr2:180124952..180126888,2	MCF-7	breast:
37	chr2:180129872..180132234-chr2:180132866..180134594,2	K562	blood:
38	chr2:180083866..180084412-chr2:180305093..180305735,3	K562	blood:
39	chr2:179628215..179630011-chr2:180014131..180016832,2	MCF-7	breast:
40	chr2:179967469..179969783-chr2:179970648..179973075,2	K562	blood:
41	chr2:180099014..180101971-chr2:180103448..180105283,2	MCF-7	breast:
42	chr2:179983325..179985286-chr2:179986584..179988899,2	K562	blood:
43	chr2:180239709..180241583-chr5:140042637..140044682,2	MCF-7	breast:
44	chr13:27745918..27746778-chr2:180129319..180129887,2	HCT-116	colon:
45	chr2:180083391..180084449-chr2:180205175..180206192,5	MCF-7	breast:
46	chr2:180083493..180084369-chr2:180219016..180219973,3	MCF-7	breast:
47	chr2:180099014..180101971-chr2:180103448..180105283,2	MCF-7	breast:
48	chr2:180127349..180129790-chr2:180202340..180204483,2	MCF-7	breast:
49	chr2:180083839..180084369-chr2:180763413..180764243,2	K562	blood:
50	chr2:179988043..179990926-chr2:179994238..179996343,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHA3-18	chr2:180209221-180209682	NONHSAT075828
2	lnc-PLEKHA3-7	chr2:180138822-180138851	XLOC_001771
3	lnc-CCDC141-1	chr2:179967007-179969211	NONHSAT075824
4	lnc-PLEKHA3-7	chr2:180138558-180138855	XLOC_001771
5	lnc-PLEKHA3-18	chr2:180216558-180220164	NONHSAT075828
6	lnc-PLEKHA3-7	chr2:180150181-180150391	XLOC_001771
7	lnc-PLEKHA3-7	chr2:180150181-180150434	XLOC_001771

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SESTD1	hsa-miR-148a-3p	chr2:179974388-179974413
2	SESTD1	hsa-miR-148b-3p	chr2:179974394-179974387
3	SESTD1	hsa-miR-130b-3p	chr2:179974389-179974410
4	SESTD1	hsa-miR-148b-3p	chr2:179974388-179974413
5	SESTD1	hsa-miR-148a-3p	chr2:179974394-179974387
6	SESTD1	hsa-miR-130b-3p	chr2:179974395-179974389
7	SESTD1	hsa-miR-21-5p	chr2:179974332-179974326

Variant related genes	Relation type
ENSG00000237477	TF binding region
SESTD1	TF binding region
ENSG00000238339	TF binding region
ENSG00000237477	CpG island
SESTD1	CpG island
ENSG00000238339	CpG island
ENSG00000180228	chromatin interactions
ENSG00000152484	chromatin interactions
ENSG00000204311	chromatin interactions
ENSG00000230641	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000187231	chromatin interactions
ENSG00000237477	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000238339	chromatin interactions
ENSG00000120314	chromatin interactions
ERRFI1	miRNA target sites
PTPRD	miRNA target sites

Extended variants
information (count: 11050 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:11050 , 50 per page) page: 1 2 3 4 5 6 7 ... 221

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367766287	chr2:179933692-179933693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs78359977	chr2:179933695-179933696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569467192	chr2:179933729-179933730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550387007	chr2:179933765-179933766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538837436	chr2:179933795-179933796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs7578521	chr2:179933815-179933816	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373803441	chr2:179933869-179933870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558374705	chr2:179933871-179933872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572355478	chr2:179933872-179933873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs578119008	chr2:179933879-179933880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181737215	chr2:179933891-179933892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562267395	chr2:179933892-179933893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575712114	chr2:179933906-179933907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532909310	chr2:179933911-179933912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551409483	chr2:179933924-179933925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs28636399	chr2:179933963-179933964	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138544506	chr2:179933994-179933995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144147592	chr2:179934017-179934018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547378265	chr2:179934018-179934019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs386653146	chr2:179934023-179934024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7605060	chr2:179934024-179934025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs377424453	chr2:179934091-179934092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs72535744	chr2:179934101-179934102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397830545	chr2:179934102-179934103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200083536	chr2:179934103-179934104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549918377	chr2:179934105-179934106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570190642	chr2:179934118-179934119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535935214	chr2:179934130-179934131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7578961	chr2:179934175-179934176	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs112104110	chr2:179934188-179934189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534978758	chr2:179934267-179934268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558185662	chr2:179934269-179934270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7579263	chr2:179934274-179934275	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34443218	chr2:179934286-179934287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537277642	chr2:179934366-179934367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78807548	chr2:179934414-179934415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377066924	chr2:179934494-179934495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs137943125	chr2:179934515-179934516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs11893153	chr2:179934543-179934544	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs200889924	chr2:179934558-179934559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11903793	chr2:179934583-179934584	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs187162387	chr2:179934608-179934609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11883598	chr2:179934609-179934610	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs564245129	chr2:179934611-179934612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11883599	chr2:179934613-179934614	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs372940870	chr2:179934614-179934615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543674218	chr2:179934635-179934636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563460760	chr2:179934636-179934637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190600526	chr2:179934644-179934645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6732629	chr2:179934663-179934664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Schizophrenia	19348701	CNVD
Muscular dystrophy	17160897	CNVD
Cardiomyopathy	17576883	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:4066 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179923600-179933800	Weak transcription	Gastric	stomach
2	chr2:179932000-179937000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:179933400-179934000	Enhancers	Stomach Mucosa	stomach
4	chr2:179933400-179934200	Enhancers	Fetal Heart	heart
5	chr2:179933800-179934600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr2:179933800-179934600	Enhancers	Gastric	stomach
7	chr2:179933800-179934600	Enhancers	HepG2	liver
8	chr2:179933800-179934800	Enhancers	Left Ventricle	heart
9	chr2:179934800-179942800	Weak transcription	Left Ventricle	heart
10	chr2:179935400-179936800	Weak transcription	Small Intestine	intestine
11	chr2:179935600-179936000	Enhancers	Fetal Muscle Leg	muscle
12	chr2:179935600-179937800	Enhancers	Dnd41	blood
13	chr2:179935600-179938200	Enhancers	Fetal Thymus	thymus
14	chr2:179936600-179937000	Enhancers	Primary T cells from cord blood	blood
15	chr2:179936600-179937200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr2:179936600-179938600	Enhancers	Thymus	Thymus
17	chr2:179936800-179937000	Enhancers	Small Intestine	intestine
18	chr2:179936800-179937200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr2:179937000-179937200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:179937200-179947600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:179937800-179938800	ZNF genes & repeats	Dnd41	blood
22	chr2:179939200-179939400	Enhancers	Thymus	Thymus
23	chr2:179947000-179948000	Enhancers	HepG2	liver
24	chr2:179947200-179947400	Enhancers	Pancreas	Pancrea
25	chr2:179947600-179947800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:179947800-179948000	Enhancers	Fetal Heart	heart
27	chr2:179950000-179950800	Enhancers	Fetal Heart	heart
28	chr2:179959800-179963000	Enhancers	Primary B cells from cord blood	blood
29	chr2:179960000-179962000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr2:179960000-179962800	Enhancers	Primary B cells from peripheral blood	blood
31	chr2:179960200-179961400	Enhancers	Thymus	Thymus
32	chr2:179960200-179961800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr2:179960400-179960600	Enhancers	GM12878-XiMat	blood
34	chr2:179960400-179961600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr2:179960400-179961600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr2:179960400-179961600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr2:179960400-179961800	Enhancers	Primary T cells from cord blood	blood
38	chr2:179960400-179961800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr2:179960400-179962000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr2:179960600-179960800	Enhancers	HMEC	breast
41	chr2:179960600-179961200	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr2:179960600-179961200	Enhancers	Dnd41	blood
43	chr2:179960600-179961200	Flanking Active TSS	GM12878-XiMat	blood
44	chr2:179960600-179961400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr2:179960600-179961600	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr2:179960600-179961600	Enhancers	Primary T cells fromperipheralblood	blood
47	chr2:179960600-179961600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr2:179960600-179961800	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr2:179960600-179962000	Enhancers	Primary hematopoietic stem cells	blood
50	chr2:179960600-179962000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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