Variant report

Variant	nsv1012188
Chromosome Location	chr2:172855923-172928891
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1225)
CpG islands
(count:611)
Chromatin interactive
region (count:182)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1225 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:172864563-172865226	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:172893071-172893460	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:172916809-172917967	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:172910679-172911423	K562	blood:	n/a	n/a
5	ARID3A	chr2:172913048-172913814	K562	blood:	n/a	n/a
6	ARID3A	chr2:172914584-172914892	K562	blood:	n/a	n/a
7	ARID3A	chr2:172927551-172927788	K562	blood:	n/a	n/a
8	ATF1	chr2:172886054-172886409	K562	blood:	n/a	n/a
9	ATF1	chr2:172892239-172892343	K562	blood:	n/a	n/a
10	ATF1	chr2:172873713-172873935	K562	blood:	n/a	n/a
11	ATF1	chr2:172910780-172911229	K562	blood:	n/a	n/a
12	ATF2	chr2:172864646-172865225	GM12878	blood:	n/a	n/a
13	ATF2	chr2:172864728-172865248	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr2:172864737-172865279	GM12878	blood:	n/a	n/a
15	ATF2	chr2:172876621-172877079	GM12878	blood:	n/a	n/a
16	ATF2	chr2:172864623-172865200	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:172876754-172877091	GM12878	blood:	n/a	n/a
18	ATF3	chr2:172864544-172865213	A549	lung:	n/a	n/a
19	ATF3	chr2:172873552-172873961	K562	blood:	n/a	n/a
20	ATF3	chr2:172864644-172865024	HepG2	liver:	n/a	n/a
21	ATF3	chr2:172873487-172873987	HCT-116	colon:	n/a	n/a
22	ATF3	chr2:172864752-172864967	GM12878	blood:	n/a	n/a
23	ATF3	chr2:172873499-172873996	HCT-116	colon:	n/a	n/a
24	ATF3	chr2:172864649-172865119	GM12878	blood:	n/a	n/a
25	ATF3	chr2:172864542-172865008	K562	blood:	n/a	n/a
26	ATF3	chr2:172864669-172865265	A549	lung:	n/a	n/a
27	BACH1	chr2:172864526-172865251	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr2:172878446-172878732	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr2:172876834-172877071	GM12878	blood:	n/a	n/a
30	BCL11A	chr2:172878376-172878694	GM12878	blood:	n/a	chr2:172878378-172878387
31	BCL3	chr2:172864767-172865174	GM12878	blood:	n/a	n/a
32	BCL3	chr2:172864390-172865401	A549	lung:	n/a	n/a
33	BCLAF1	chr2:172864552-172865212	GM12878	blood:	n/a	n/a
34	BCLAF1	chr2:172864465-172865197	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:172878397-172878805	GM12878	blood:	n/a	n/a
36	BHLHE40	chr2:172873771-172873832	K562	blood:	n/a	n/a
37	BHLHE40	chr2:172886489-172886720	K562	blood:	n/a	n/a
38	BHLHE40	chr2:172864516-172865252	GM12878	blood:	n/a	chr2:172864823-172864839
39	BHLHE40	chr2:172927314-172927514	K562	blood:	n/a	n/a
40	BHLHE40	chr2:172876767-172877034	GM12878	blood:	n/a	n/a
41	BHLHE40	chr2:172864395-172865422	K562	blood:	n/a	chr2:172864823-172864839
42	BHLHE40	chr2:172864708-172865249	A549	lung:	n/a	chr2:172864823-172864839
43	BHLHE40	chr2:172887079-172887212	K562	blood:	n/a	n/a
44	BHLHE40	chr2:172892991-172893393	HepG2	liver:	n/a	n/a
45	BHLHE40	chr2:172893182-172893336	K562	blood:	n/a	n/a
46	BHLHE40	chr2:172864537-172865321	HepG2	liver:	n/a	chr2:172864823-172864839
47	BRCA1	chr2:172864499-172865359	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr2:172864551-172864621	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr2:172864649-172865115	HepG2	liver:	n/a	n/a
50	CBX3	chr2:172873529-172874075	HCT-116	colon:	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	chr2:172916330-172916380	PANC-1	pancreas:	n/a
2	chr2:172916330-172916380	PANC-1	pancreas:	n/a
3	chr2:172916330-172916380	H1-hESC	embryonic stem cell:	embryo
4	chr2:172912454-172912504	BJ	skin:	n/a
5	chr2:172887136-172887186	HRCEpiC	kidney:	n/a
6	chr2:172912454-172912504	HIPEpiC	eye:	n/a
7	chr2:172878103-172878153	SK-N-SH_RA	brain:	n/a
8	chr2:172864273-172864323	ProgFib	skin:	n/a
9	chr2:172912454-172912504	CMK	blood:	n/a
10	chr2:172916330-172916380	HCM	heart:	n/a
11	chr2:172887136-172887186	NB4	blood:	n/a
12	chr2:172864273-172864323	Hela-S3	cervix:	n/a
13	chr2:172887136-172887186	SK-N-SH	brain:	n/a
14	chr2:172864273-172864323	GM12891	blood:	n/a
15	chr2:172878103-172878153	PANC-1	pancreas:	n/a
16	chr2:172916330-172916380	AG04450	lung:	fetal
17	chr2:172864273-172864323	HAEpiC	amniotic membrane:	n/a
18	chr2:172878103-172878153	BE2_C	brain:	n/a
19	chr2:172864014-172864064	BE2_C	brain:	n/a
20	chr2:172887136-172887186	MCF10A-Er-Src	breast:	n/a
21	chr2:172912454-172912504	PrEC	prostate:	n/a
22	chr2:172864014-172864064	RPTEC	kidney:	n/a
23	chr2:172864014-172864064	HMEC	breast:	n/a
24	chr2:172864014-172864064	NH-A	brain:	n/a
25	chr2:172864014-172864064	AG10803	skin:	n/a
26	chr2:172887136-172887186	HCPEpiC	choroid plexus:	n/a
27	chr2:172916330-172916380	HEEpiC	esophagus:	n/a
28	chr2:172916330-172916380	SK-N-MC	brain:	n/a
29	chr2:172864976-172865026	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:172912454-172912504	GM12892	blood:	n/a
31	chr2:172912454-172912504	HUVEC	blood vessel:	n/a
32	chr2:172864014-172864064	HRPEpiC	eye:	n/a
33	chr2:172887136-172887186	NH-A	brain:	n/a
34	chr2:172916330-172916380	HUVEC	blood vessel:	n/a
35	chr2:172878103-172878153	GM12892	blood:	n/a
36	chr2:172864337-172864387	Caco-2	colon:	n/a
37	chr2:172916330-172916380	SK-N-SH_RA	brain:	n/a
38	chr2:172887136-172887186	GM12878	blood:	n/a
39	chr2:172864976-172865026	HUVEC	blood vessel:	n/a
40	chr2:172864273-172864323	BE2_C	brain:	n/a
41	chr2:172864337-172864387	CMK	blood:	n/a
42	chr2:172878103-172878153	HNPCEpiC	eye:	n/a
43	chr2:172864614-172864664	NHDF-neo	bronchial:	n/a
44	chr2:172864273-172864323	HEK293	kidney:	embryo
45	chr2:172861329-172861379	GM12878	blood:	n/a
46	chr2:172916330-172916380	AG09319	gingival:	n/a
47	chr2:172864337-172864387	HCF	heart:	n/a
48	chr2:172887136-172887186	Caco-2	colon:	n/a
49	chr2:172916330-172916380	HCF	heart:	n/a
50	chr2:172864976-172865026	AG10803	skin:	n/a

(count:182 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr2:172861569..172867068-chr2:172965912..172971063,13	K562	blood:
2	chr2:172814398..172816773-chr2:172897088..172899114,2	MCF-7	breast:
3	chr2:172863189..172870519-chr2:172946500..172952655,22	K562	blood:
4	chr2:172863381..172865132-chr2:172924958..172927915,2	MCF-7	breast:
5	chr2:172872127..172874571-chr2:172915848..172917626,2	MCF-7	breast:
6	chr2:172900249..172901946-chr2:172954569..172956583,2	MCF-7	breast:
7	chr16:1104912..1105605-chr2:172921758..172922343,2	MCF-7	breast:
8	chr2:172914690..172917285-chr2:172958653..172961540,2	MCF-7	breast:
9	chr2:172908370..172912601-chr2:172912982..172915334,3	K562	blood:
10	chr2:172859684..172862159-chr2:172863026..172866256,3	MCF-7	breast:
11	chr2:172856619..172859628-chr2:172864292..172866200,3	MCF-7	breast:
12	chr2:172906506..172908883-chr2:172947128..172949722,2	MCF-7	breast:
13	chr2:172910524..172912386-chr2:172915560..172917116,2	K562	blood:
14	chr2:172864183..172866309-chr2:172899245..172901678,2	K562	blood:
15	chr2:172920303..172928510-chr2:172947424..172952310,9	K562	blood:
16	chr2:172863226..172865802-chr2:172966081..172969208,5	MCF-7	breast:
17	chr2:172919420..172922156-chr2:172937386..172939240,3	MCF-7	breast:
18	chr2:172897089..172900010-chr2:172909839..172912586,2	K562	blood:
19	chr2:172872941..172875027-chr2:172948561..172950206,2	MCF-7	breast:
20	chr2:172903562..172906519-chr2:172947983..172949880,2	K562	blood:
21	chr2:172922530..172925310-chr2:172938096..172940236,2	MCF-7	breast:
22	chr2:172777448..172780686-chr2:172863264..172866650,5	K562	blood:
23	chr2:172864878..172867088-chr2:172885343..172888601,3	MCF-7	breast:
24	chr2:172863850..172866643-chr2:172902053..172905217,4	MCF-7	breast:
25	chr2:172910524..172912386-chr2:172915560..172917116,2	K562	blood:
26	chr2:172909670..172912609-chr2:172916665..172919120,2	MCF-7	breast:
27	chr2:172892888..172895304-chr2:172895689..172897604,2	K562	blood:
28	chr2:172909159..172912131-chr2:172917033..172919851,3	MCF-7	breast:
29	chr2:172872334..172876033-chr2:172959738..172961363,3	MCF-7	breast:
30	chr2:172913443..172915901-chr2:172963690..172966629,2	MCF-7	breast:
31	chr2:172915830..172918019-chr2:172965851..172967372,2	MCF-7	breast:
32	chr2:172857904..172859439-chr2:172876035..172878668,2	K562	blood:
33	chr2:172911212..172913559-chr2:172957702..172960003,2	MCF-7	breast:
34	chr2:172923032..172925626-chr2:172949094..172951045,3	MCF-7	breast:
35	chr2:172902218..172904158-chr2:172948537..172951197,2	K562	blood:
36	chr2:172905200..172906777-chr2:172909127..172910851,3	K562	blood:
37	chr2:172867998..172870491-chr2:172948122..172949809,2	MCF-7	breast:
38	chr2:172901825..172905111-chr2:172958470..172962198,5	MCF-7	breast:
39	chr2:172864500..172866706-chr2:172879081..172880840,2	K562	blood:
40	chr2:172870841..172873802-chr2:172876022..172878107,2	MCF-7	breast:
41	chr2:172860607..172867322-chr2:172946572..172954768,24	MCF-7	breast:
42	chr2:172894190..172896473-chr2:172910929..172913288,2	K562	blood:
43	chr2:172895941..172897535-chr2:172913713..172916052,2	K562	blood:
44	chr2:172863680..172867220-chr2:172914121..172918663,4	MCF-7	breast:
45	chr2:172862481..172869340-chr2:172872333..172878575,9	MCF-7	breast:
46	chr2:172909670..172912609-chr2:172916665..172919120,2	MCF-7	breast:
47	chr2:172895941..172897535-chr2:172913713..172916052,2	K562	blood:
48	chr2:172866585..172869561-chr2:172915980..172919427,3	K562	blood:
49	chr2:172860017..172861984-chr2:172875793..172878198,2	K562	blood:
50	chr2:172900542..172905634-chr2:172946761..172951890,10	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HAT1-1	chr2:172928439-172929142	NONHSAT075484
2	lnc-HAT1-1	chr2:172886703-172886771	NONHSAT075486
3	lnc-HAT1-1	chr2:172864862-172864916	NONHSAT075485
4	lnc-HAT1-1	chr2:172926226-172926383	NONHSAT075486
5	lnc-HAT1-1	chr2:172926226-172926383	NONHSAT075484
6	lnc-METAP1D-2	chr2:172902321-172902351	l_1987_chr2:172825346-172897114_testes
7	lnc-HAT1-1	chr2:172864850-172864916	NONHSAT075484
8	lnc-METAP1D-2	chr2:172896324-172897114	l_1987_chr2:172825346-172897114_testes
9	lnc-HAT1-1	chr2:172926226-172926722	NONHSAT075485
10	lnc-HAT1-1	chr2:172928439-172928478	NONHSAT075486
11	lnc-METAP1D-2	chr2:172874105-172874190	l_1987_chr2:172825346-172897114_testes

No data

Variant related genes	Relation type
METAP1D	TF binding region
SLC25A12	TF binding region
METAP1D	CpG island
SLC25A12	CpG island
ENSG00000251562	chromatin interactions
ENSG00000168883	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000115844	chromatin interactions
ENSG00000115840	chromatin interactions
ENSG00000172878	chromatin interactions
ENSG00000115827	chromatin interactions
ENSG00000123600	chromatin interactions
ENSG00000071967	chromatin interactions
ENSG00000236651	chromatin interactions
ENSG00000144355	chromatin interactions
ENSG00000115806	chromatin interactions
ENSG00000128708	chromatin interactions
VCL	miRNA target sites
TSPAN9	miRNA target sites

Extended variants
information (count: 2667 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:2667 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543524284	chr2:172855970-172855971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561703444	chr2:172856003-172856004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573695171	chr2:172856032-172856033	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs76040648	chr2:172856041-172856042	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72890858	chr2:172856130-172856131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs144418473	chr2:172856202-172856203	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184654718	chr2:172856203-172856204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs189975722	chr2:172856207-172856208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs146594898	chr2:172856226-172856227	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141431393	chr2:172856268-172856269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs543235737	chr2:172856271-172856272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs567386106	chr2:172856272-172856273	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561465089	chr2:172856352-172856353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145161155	chr2:172856371-172856372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs192112765	chr2:172856417-172856418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570299248	chr2:172856450-172856451	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539318410	chr2:172856458-172856459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373548067	chr2:172856469-172856470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528134963	chr2:172856481-172856482	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138745684	chr2:172856486-172856487	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148924635	chr2:172856527-172856528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs575781444	chr2:172856548-172856549	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs184706539	chr2:172856576-172856577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547897864	chr2:172856600-172856601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576651110	chr2:172856603-172856604	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148119320	chr2:172856622-172856623	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs143893854	chr2:172856735-172856736	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs11676484	chr2:172856874-172856875	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs576877416	chr2:172856885-172856886	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs147985041	chr2:172856914-172856915	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs577905270	chr2:172856933-172856934	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs545264705	chr2:172856960-172856961	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs563371442	chr2:172856988-172856989	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs376061798	chr2:172857030-172857031	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs74648245	chr2:172857032-172857033	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs75645419	chr2:172857033-172857034	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs58572868	chr2:172857047-172857048	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs73976542	chr2:172857056-172857057	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs189272306	chr2:172857061-172857062	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs561048067	chr2:172857104-172857105	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs138777298	chr2:172857140-172857141	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs557153923	chr2:172857243-172857244	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546726516	chr2:172857263-172857264	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs113324552	chr2:172857331-172857332	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs35079645	chr2:172857354-172857355	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs66927171	chr2:172857355-172857356	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs199891876	chr2:172857356-172857357	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs61474915	chr2:172857358-172857359	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs201212442	chr2:172857359-172857360	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs539000396	chr2:172857383-172857384	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:48)

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
Cancer	20164919	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
small cell lung cancer	20016488	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Prostate cancer	16573809	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Donnai-Barrow syndrome	21085971	CNVD
Breast cancer	21045282	CNVD
Limb abnormalities	22140379	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1123 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172810000-172862600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:172813000-172859200	Weak transcription	Fetal Brain Male	brain
3	chr2:172821000-172862800	Weak transcription	Brain Angular Gyrus	brain
4	chr2:172824000-172857800	Weak transcription	Brain Anterior Caudate	brain
5	chr2:172824000-172857800	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:172840800-172857600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:172844200-172857200	Weak transcription	Brain Germinal Matrix	brain
8	chr2:172844400-172857400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr2:172845200-172857600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr2:172846000-172857600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr2:172847400-172864000	Weak transcription	HSMM	muscle
12	chr2:172847800-172857600	Weak transcription	Ovary	ovary
13	chr2:172848000-172863200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:172848400-172856000	Weak transcription	K562	blood
15	chr2:172849200-172856600	Weak transcription	Left Ventricle	heart
16	chr2:172849200-172857200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:172849200-172857400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr2:172849600-172863800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr2:172850400-172860600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr2:172851000-172856800	Weak transcription	Dnd41	blood
21	chr2:172851600-172857600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr2:172855600-172856400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr2:172855600-172856400	Enhancers	Fetal Heart	heart
24	chr2:172856000-172856600	Enhancers	K562	blood
25	chr2:172856600-172863200	Weak transcription	K562	blood
26	chr2:172857200-172857400	Enhancers	Brain Germinal Matrix	brain
27	chr2:172857200-172857600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr2:172857400-172857600	Flanking Active TSS	Brain Germinal Matrix	brain
29	chr2:172857400-172858000	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:172857400-172858800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr2:172857600-172857800	Active TSS	Brain Germinal Matrix	brain
32	chr2:172857600-172858000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:172857600-172858000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr2:172857600-172858000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:172857600-172858000	Enhancers	Ovary	ovary
36	chr2:172857600-172858400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:172857800-172858000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:172857800-172858000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:172857800-172858000	Enhancers	Brain Anterior Caudate	brain
40	chr2:172857800-172858000	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr2:172857800-172858200	Enhancers	Brain Hippocampus Middle	brain
42	chr2:172858000-172858200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:172858000-172858200	Active TSS	Brain Germinal Matrix	brain
44	chr2:172858000-172858600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr2:172858000-172859600	Weak transcription	Ovary	ovary
46	chr2:172858000-172860400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:172858200-172860000	Enhancers	Brain Germinal Matrix	brain
48	chr2:172858600-172863200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:172858800-172859000	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr2:172859000-172859400	Enhancers	Cortex derived primary cultured neurospheres	brain

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