Variant report

Variant	nsv834472
Chromosome Location	chr2:180091670-180220448
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1613)
CpG islands
(count:488)
Chromatin interactive
region (count:47)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:180138150-180138733	HepG2	liver:	n/a	chr2:180138538-180138554
2	ARID3A	chr2:180103469-180105057	HepG2	liver:	n/a	chr2:180104020-180104036
3	ARID3A	chr2:180097397-180097407	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:180136821-180137690	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:180208774-180209700	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:180197727-180198019	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:180205491-180205811	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:180105511-180105719	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:180129321-180130164	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:180127655-180128278	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:180126156-180126501	HepG2	liver:	n/a	n/a
12	ATF1	chr2:180098919-180099109	K562	blood:	n/a	n/a
13	ATF2	chr2:180132917-180133336	GM12878	blood:	n/a	n/a
14	ATF2	chr2:180132865-180133290	GM12878	blood:	n/a	n/a
15	ATF2	chr2:180103903-180104351	GM12878	blood:	n/a	n/a
16	BACH1	chr2:180129343-180129796	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr2:180209168-180209565	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr2:180133419-180133619	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:180128833-180129052	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr2:180209211-180209504	K562	blood:	n/a	n/a
21	BACH1	chr2:180128320-180128520	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr2:180103968-180104241	GM12878	blood:	n/a	chr2:180104091-180104102
23	BATF	chr2:180133010-180133329	GM12878	blood:	n/a	n/a
24	BATF	chr2:180103988-180104180	GM12878	blood:	n/a	chr2:180104091-180104102
25	BATF	chr2:180119834-180120242	GM12878	blood:	n/a	n/a
26	BATF	chr2:180133009-180133382	GM12878	blood:	n/a	n/a
27	BCL11A	chr2:180132947-180133351	GM12878	blood:	n/a	n/a
28	BCL3	chr2:180132984-180133317	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:180137156-180137744	HepG2	liver:	n/a	n/a
30	BHLHE40	chr2:180128003-180128702	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:180123251-180123570	GM12878	blood:	n/a	n/a
32	BHLHE40	chr2:180129188-180129549	GM12878	blood:	n/a	chr2:180129245-180129261
33	BHLHE40	chr2:180104626-180104759	HepG2	liver:	n/a	n/a
34	BHLHE40	chr2:180124419-180124597	GM12878	blood:	n/a	n/a
35	BRCA1	chr2:180153555-180153741	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr2:180127895-180128575	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr2:180096213-180096413	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr2:180138324-180138328	GM12878	blood:	n/a	n/a
39	BRCA1	chr2:180137670-180138158	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr2:180103827-180104447	HCT-116	colon:	n/a	n/a
41	CCNT2	chr2:180128600-180129961	K562	blood:	n/a	chr2:180129649-180129658
42	CEBPB	chr2:180133029-180133378	A549	lung:	n/a	n/a
43	CEBPB	chr2:180093015-180093346	HepG2	liver:	n/a	chr2:180093164-180093175
44	CEBPB	chr2:180127607-180129046	Hela-S3	cervix:	n/a	chr2:180127867-180127880 chr2:180128847-180128858 chr2:180128845-180128856 chr2:180128845-180128858 chr2:180127719-180127731 chr2:180128847-180128856
45	CEBPB	chr2:180103159-180103516	HepG2	liver:	n/a	chr2:180103341-180103352 chr2:180103343-180103354
46	CEBPB	chr2:180129888-180130267	K562	blood:	n/a	chr2:180130075-180130088
47	CEBPB	chr2:180198811-180199027	HepG2	liver:	n/a	chr2:180198876-180198887 chr2:180198835-180198846
48	CEBPB	chr2:180187095-180187345	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:180136985-180138015	Hela-S3	cervix:	n/a	chr2:180137601-180137614
50	CEBPB	chr2:180127804-180127968	HepG2	liver:	n/a	chr2:180127867-180127880

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180200208-180200258	NHBE	bronchial:	n/a
2	chr2:180129612-180129662	Jurkat	blood:	n/a
3	chr2:180128889-180128939	GM12892	blood:	n/a
4	chr2:180130081-180130131	HepG2	liver:	n/a
5	chr2:180130081-180130131	ovcar-3	ovarian:	n/a
6	chr2:180128490-180128540	HCT-116	colon:	n/a
7	chr2:180128490-180128540	LNCaP	prostate:	n/a
8	chr2:180130081-180130131	K562	blood:	n/a
9	chr2:180130081-180130131	GM12878	blood:	n/a
10	chr2:180129612-180129662	LNCaP	prostate:	n/a
11	chr2:180202670-180202720	AG04450	lung:	fetal
12	chr2:180202670-180202720	HMEC	breast:	n/a
13	chr2:180129612-180129662	Caco-2	colon:	n/a
14	chr2:180202670-180202720	NT2-D1	testis:	n/a
15	chr2:180128907-180128957	GM06990	blood:	n/a
16	chr2:180125932-180125982	SAEC	small airway:	n/a
17	chr2:180200208-180200258	T-47D	breast:	n/a
18	chr2:180125932-180125982	BJ	skin:	n/a
19	chr2:180200208-180200258	IMR90	lung:	fetal
20	chr2:180202670-180202720	BJ	skin:	n/a
21	chr2:180130081-180130131	AG04449	skin:	fetal
22	chr2:180129612-180129662	HMEC	breast:	n/a
23	chr2:180128907-180128957	K562	blood:	n/a
24	chr2:180130081-180130131	H1-hESC	embryonic stem cell:	embryo
25	chr2:180130081-180130131	PFSK-1	brain:	n/a
26	chr2:180128907-180128957	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:180130081-180130131	HRPEpiC	eye:	n/a
28	chr2:180202670-180202720	HNPCEpiC	eye:	n/a
29	chr2:180200208-180200258	HIPEpiC	eye:	n/a
30	chr2:180128490-180128540	AG09309	skin:	n/a
31	chr2:180130081-180130131	AG09319	gingival:	n/a
32	chr2:180130081-180130131	Jurkat	blood:	n/a
33	chr2:180128490-180128540	SKMC	muscle:	n/a
34	chr2:180128889-180128939	SK-N-SH	brain:	n/a
35	chr2:180200208-180200258	SK-N-SH_RA	brain:	n/a
36	chr2:180128889-180128939	A549	lung:	n/a
37	chr2:180128889-180128939	NHDF-neo	bronchial:	n/a
38	chr2:180129612-180129662	HCM	heart:	n/a
39	chr2:180128907-180128957	HUVEC	blood vessel:	n/a
40	chr2:180129612-180129662	HPAEpiC	pulmonary alveolar:	n/a
41	chr2:180128907-180128957	ECC-1	luminal epithelium:	n/a
42	chr2:180125932-180125982	HMEC	breast:	n/a
43	chr2:180200208-180200258	HRCEpiC	kidney:	n/a
44	chr2:180202670-180202720	Hepatocyte	liver:	n/a
45	chr2:180128490-180128540	MCF-7	breast:	n/a
46	chr2:180129612-180129662	SK-N-MC	brain:	n/a
47	chr2:180125932-180125982	GM12892	blood:	n/a
48	chr2:180128889-180128939	Jurkat	blood:	n/a
49	chr2:180200208-180200258	RPTEC	kidney:	n/a
50	chr2:180200208-180200258	HCF	heart:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:180114550..180116150-chr2:180123274..180125911,2	MCF-7	breast:
2	chr2:180116382..180118315-chr2:180123410..180126262,2	MCF-7	breast:
3	chr2:180127590..180133149-chr2:180134052..180141026,12	MCF-7	breast:
4	chr2:180129872..180132234-chr2:180132866..180134594,2	K562	blood:
5	chr2:180128113..180129614-chr2:180196214..180198013,2	MCF-7	breast:
6	chr2:180091158..180092678-chr2:180127658..180130558,2	MCF-7	breast:
7	chr2:180116382..180118315-chr2:180123410..180126262,2	MCF-7	breast:
8	chr2:180099014..180101971-chr2:180103448..180105283,2	MCF-7	breast:
9	chr2:122288038..122288614-chr2:180219711..180220231,2	Hela-S3	cervix:
10	chr2:180127983..180129556-chr2:180176387..180178694,3	MCF-7	breast:
11	chr2:180107067..180109133-chr2:180128125..180129799,2	MCF-7	breast:
12	chr2:180083493..180084369-chr2:180219016..180219973,3	MCF-7	breast:
13	chr2:180120526..180124742-chr2:180127021..180129947,5	K562	blood:
14	chr2:180127590..180133149-chr2:180134052..180141026,12	MCF-7	breast:
15	chr2:180091649..180092168-chr20:53297444..53298069,2	MCF-7	breast:
16	chr2:180099014..180101971-chr2:180103448..180105283,2	MCF-7	breast:
17	chr2:180136977..180138919-chr2:180139042..180142671,5	MCF-7	breast:
18	chr2:180114654..180117674-chr2:180127724..180131363,3	MCF-7	breast:
19	chr2:180127231..180129754-chr2:180137790..180140822,6	MCF-7	breast:
20	chr2:180148874..180150969-chr2:180153037..180154846,2	K562	blood:
21	chr2:180127349..180129790-chr2:180202340..180204483,2	MCF-7	breast:
22	chr2:180115892..180117617-chr2:180123291..180126152,2	K562	blood:
23	chr2:180091710..180093707-chr2:180097296..180099649,3	MCF-7	breast:
24	chr2:180127197..180131104-chr2:180131643..180133525,5	MCF-7	breast:
25	chr2:180099965..180101717-chr2:180103234..180105570,2	K562	blood:
26	chr2:180138330..180140789-chr2:180141084..180143785,2	MCF-7	breast:
27	chr2:180115733..180117570-chr2:180124952..180126888,2	MCF-7	breast:
28	chr2:180118975..180121494-chr2:180124484..180126493,2	K562	blood:
29	chr2:180128170..180130191-chr2:180204875..180207349,3	MCF-7	breast:
30	chr2:180114550..180116150-chr2:180123274..180125911,2	MCF-7	breast:
31	chr2:180128256..180129810-chr2:180207695..180210396,2	MCF-7	breast:
32	chr2:180129872..180132234-chr2:180132866..180134594,2	K562	blood:
33	chr2:180099965..180101717-chr2:180103234..180105570,2	K562	blood:
34	chr2:180132248..180134762-chr2:180137452..180139078,2	MCF-7	breast:
35	chr2:180118975..180121494-chr2:180124484..180126493,2	K562	blood:
36	chr2:180083560..180084369-chr2:180205061..180206359,5	MCF-7	breast:
37	chr2:180111560..180114126-chr2:180128041..180130307,2	MCF-7	breast:
38	chr2:180083391..180084449-chr2:180205175..180206192,5	MCF-7	breast:
39	chr2:180127231..180129754-chr2:180137790..180140822,6	MCF-7	breast:
40	chr13:27745918..27746778-chr2:180129319..180129887,2	HCT-116	colon:
41	chr2:180122860..180124976-chr2:180127824..180130891,3	MCF-7	breast:
42	chr2:180114644..180119395-chr2:180127594..180130471,4	MCF-7	breast:
43	chr2:179315142..179317025-chr2:180127825..180130038,2	MCF-7	breast:
44	chr2:180115733..180117570-chr2:180124952..180126888,2	MCF-7	breast:
45	chr2:180148874..180150969-chr2:180153037..180154846,2	K562	blood:
46	chr2:180091710..180093707-chr2:180097296..180099649,3	MCF-7	breast:
47	chr2:180115892..180117617-chr2:180123291..180126152,2	K562	blood:

(count:6 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 4341 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4341 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373114412	chr2:180091677-180091678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141733807	chr2:180091712-180091713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573751897	chr2:180091745-180091746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs559443738	chr2:180091763-180091764	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs11898291	chr2:180091794-180091795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs150151486	chr2:180091885-180091886	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572777434	chr2:180091890-180091891	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs145568893	chr2:180091895-180091896	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544947088	chr2:180091965-180091966	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564885108	chr2:180092012-180092013	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs187935164	chr2:180092019-180092020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544249043	chr2:180092047-180092048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs193230830	chr2:180092084-180092085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185296642	chr2:180092103-180092104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138750968	chr2:180092129-180092130	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112389996	chr2:180092143-180092144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560715339	chr2:180092184-180092185	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532845907	chr2:180092207-180092208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552913848	chr2:180092249-180092250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs569185877	chr2:180092285-180092286	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553349945	chr2:180092290-180092291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs13029239	chr2:180092330-180092331	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190099274	chr2:180092344-180092345	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568448983	chr2:180092345-180092346	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371058643	chr2:180092354-180092355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534056904	chr2:180092356-180092357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181343203	chr2:180092367-180092368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75493136	chr2:180092391-180092392	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572739870	chr2:180092417-180092418	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538502068	chr2:180092432-180092433	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558575428	chr2:180092435-180092436	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183974796	chr2:180092446-180092447	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs562198960	chr2:180092459-180092460	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs146292122	chr2:180092567-180092568	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188650084	chr2:180092586-180092587	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74540663	chr2:180092620-180092621	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534478014	chr2:180092664-180092665	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs139525291	chr2:180092698-180092699	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560629592	chr2:180092717-180092718	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532756379	chr2:180092744-180092745	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200853974	chr2:180092794-180092795	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181076994	chr2:180092800-180092801	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs118164305	chr2:180092808-180092809	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149576065	chr2:180092831-180092832	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532068386	chr2:180092866-180092867	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs548268768	chr2:180092876-180092877	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144283955	chr2:180092892-180092893	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568487082	chr2:180092927-180092928	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185235137	chr2:180092937-180092938	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547492933	chr2:180092965-180092966	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2057 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180067600-180097600	Weak transcription	Primary B cells from cord blood	blood
2	chr2:180067600-180104600	Weak transcription	Fetal Kidney	kidney
3	chr2:180068000-180103800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr2:180068400-180092800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:180083800-180092000	Weak transcription	Aorta	Aorta
6	chr2:180083800-180102200	Weak transcription	HMEC	breast
7	chr2:180087200-180097600	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr2:180087400-180094800	Weak transcription	Osteobl	bone
9	chr2:180087600-180095800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:180088400-180093000	Enhancers	Brain Cingulate Gyrus	brain
11	chr2:180088600-180092200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:180088800-180098400	Weak transcription	Spleen	Spleen
13	chr2:180089000-180091800	Enhancers	Brain Angular Gyrus	brain
14	chr2:180089000-180093000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:180089000-180093000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr2:180089000-180093000	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr2:180089000-180093400	Enhancers	Brain Anterior Caudate	brain
18	chr2:180089200-180092400	Weak transcription	Ovary	ovary
19	chr2:180089600-180092000	Weak transcription	Primary B cells from peripheral blood	blood
20	chr2:180089600-180095000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr2:180089600-180115200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:180089800-180095000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr2:180089800-180095000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr2:180089800-180100200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:180089800-180100200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr2:180089800-180102000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr2:180090000-180092600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr2:180090000-180093800	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr2:180090000-180098400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:180090000-180102000	Weak transcription	Fetal Muscle Leg	muscle
31	chr2:180090200-180092200	Enhancers	Brain Germinal Matrix	brain
32	chr2:180090400-180091800	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr2:180090400-180092600	Enhancers	Liver	Liver
34	chr2:180090400-180092800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr2:180090400-180093000	Enhancers	Adipose Nuclei	Adipose
36	chr2:180090600-180102000	Weak transcription	Psoas Muscle	Psoas
37	chr2:180090600-180102400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr2:180091000-180091800	Enhancers	Fetal Brain Male	brain
39	chr2:180091000-180091800	Enhancers	Small Intestine	intestine
40	chr2:180091000-180092000	Weak transcription	Stomach Smooth Muscle	stomach
41	chr2:180091000-180092800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr2:180091000-180093400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:180091200-180091800	Enhancers	Fetal Heart	heart
44	chr2:180091200-180091800	Enhancers	Rectal Smooth Muscle	rectum
45	chr2:180091200-180092000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:180091200-180092400	Weak transcription	Pancreas	Pancrea
47	chr2:180091200-180092800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:180091200-180102400	Weak transcription	Left Ventricle	heart
49	chr2:180091200-180104600	Weak transcription	Right Ventricle	heart
50	chr2:180091400-180091800	Enhancers	Fetal Brain Female	brain

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