Variant report

Variant	nsv834384
Chromosome Location	chr2:134005229-134188648
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1319)
CpG islands
(count:1527)
Chromatin interactive
region (count:53)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1319 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:134175247-134175333	HepG2	liver:	n/a	n/a
2	BACH1	chr2:134097037-134097041	K562	blood:	n/a	n/a
3	BACH1	chr2:134022701-134024075	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:134005181-134005429	GM12878	blood:	n/a	n/a
5	BCL3	chr2:134084062-134084604	A549	lung:	n/a	chr2:134084326-134084335 chr2:134084327-134084336
6	BCL3	chr2:134023525-134024142	A549	lung:	n/a	n/a
7	BCL3	chr2:134104177-134104553	GM12878	blood:	n/a	n/a
8	BCL3	chr2:134023499-134024135	A549	lung:	n/a	n/a
9	BCL3	chr2:134182427-134182865	A549	lung:	n/a	chr2:134182682-134182691
10	BHLHE40	chr2:134178421-134178431	GM12878	blood:	n/a	n/a
11	BHLHE40	chr2:134069959-134070256	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:134173057-134173395	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:134119719-134119882	GM12878	blood:	n/a	n/a
14	BRCA1	chr2:134022507-134023986	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr2:134103274-134103787	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr2:134102290-134102899	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr2:134081191-134081206	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr2:134084130-134084724	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr2:134119678-134120195	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:134043975-134044199	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:134081859-134082203	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:134120886-134121183	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:134176307-134176600	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:134028771-134028886	A549	lung:	n/a	n/a
25	CEBPB	chr2:134179280-134179493	HepG2	liver:	n/a	chr2:134179420-134179433
26	CEBPB	chr2:134180543-134180995	A549	lung:	n/a	chr2:134180572-134180583
27	CEBPB	chr2:134043848-134044248	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:134180439-134180906	IMR90	lung:	n/a	chr2:134180572-134180583
29	CEBPB	chr2:134062054-134062195	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:134104232-134104595	A549	lung:	n/a	n/a
31	CEBPB	chr2:134161665-134161926	HepG2	liver:	n/a	chr2:134161818-134161829 chr2:134161819-134161830 chr2:134161818-134161831 chr2:134161861-134161874
32	CEBPB	chr2:134170046-134171171	Hela-S3	cervix:	n/a	chr2:134170438-134170451
33	CEBPB	chr2:134180445-134180899	A549	lung:	n/a	chr2:134180572-134180583
34	CEBPB	chr2:134053980-134054421	Hela-S3	cervix:	n/a	chr2:134054150-134054163 chr2:134054152-134054163 chr2:134054150-134054163
35	CEBPB	chr2:134043889-134044238	A549	lung:	n/a	n/a
36	CEBPB	chr2:134104155-134104720	IMR90	lung:	n/a	n/a
37	CEBPB	chr2:134084078-134084970	A549	lung:	n/a	n/a
38	CEBPB	chr2:134170306-134170630	A549	lung:	n/a	chr2:134170438-134170451
39	CEBPB	chr2:134011419-134011757	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:134081659-134082211	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr2:134043877-134044226	MCF-7	breast:	n/a	n/a
42	CEBPB	chr2:134045260-134045655	IMR90	lung:	n/a	n/a
43	CEBPB	chr2:134074709-134075358	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr2:134172108-134172326	IMR90	lung:	n/a	n/a
45	CEBPB	chr2:134104177-134104699	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr2:134062013-134062244	A549	lung:	n/a	n/a
47	CEBPB	chr2:134102267-134102854	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr2:134170352-134170525	IMR90	lung:	n/a	chr2:134170438-134170451
49	CEBPB	chr2:134043906-134044270	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:134095788-134096225	IMR90	lung:	n/a	chr2:134096054-134096065

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134024618-134024668	CMK	blood:	n/a
2	chr2:134024266-134024316	RPTEC	kidney:	n/a
3	chr2:134024618-134024668	CMK	blood:	n/a
4	chr2:134024266-134024316	RPTEC	kidney:	n/a
5	chr2:134068922-134068972	GM19239	blood:	n/a
6	chr2:134135267-134135317	HEEpiC	esophagus:	n/a
7	chr2:134169851-134169901	Hela-S3	cervix:	n/a
8	chr2:134024459-134024509	HRE	kidney:	n/a
9	chr2:134180028-134180078	HIPEpiC	eye:	n/a
10	chr2:134052012-134052062	SAEC	small airway:	n/a
11	chr2:134052012-134052062	PrEC	prostate:	n/a
12	chr2:134169851-134169901	AG09319	gingival:	n/a
13	chr2:134028440-134028490	GM06990	blood:	n/a
14	chr2:134020041-134020091	BJ	skin:	n/a
15	chr2:134163531-134163581	T-47D	breast:	n/a
16	chr2:134020041-134020091	HRE	kidney:	n/a
17	chr2:134127568-134127618	NHDF-neo	bronchial:	n/a
18	chr2:134169851-134169901	SKMC	muscle:	n/a
19	chr2:134024418-134024468	GM12878	blood:	n/a
20	chr2:134023210-134023260	SK-N-SH_RA	brain:	n/a
21	chr2:134169851-134169901	GM19239	blood:	n/a
22	chr2:134083495-134083545	PrEC	prostate:	n/a
23	chr2:134023210-134023260	GM12891	blood:	n/a
24	chr2:134020041-134020091	PrEC	prostate:	n/a
25	chr2:134163531-134163581	HEK293	kidney:	embryo
26	chr2:134028440-134028490	GM12878	blood:	n/a
27	chr2:134163531-134163581	GM19239	blood:	n/a
28	chr2:134180560-134180610	GM06990	blood:	n/a
29	chr2:134169851-134169901	GM06990	blood:	n/a
30	chr2:134010875-134010925	H1-hESC	embryonic stem cell:	embryo
31	chr2:134023210-134023260	HepG2	liver:	n/a
32	chr2:134020041-134020091	HCM	heart:	n/a
33	chr2:134023210-134023260	HIPEpiC	eye:	n/a
34	chr2:134135267-134135317	NH-A	brain:	n/a
35	chr2:134024266-134024316	AG09319	gingival:	n/a
36	chr2:134135267-134135317	NT2-D1	testis:	n/a
37	chr2:134024093-134024143	AG04449	skin:	fetal
38	chr2:134180028-134180078	AG04450	lung:	fetal
39	chr2:134075125-134075175	U87	brain:	n/a
40	chr2:134163531-134163581	GM12891	blood:	n/a
41	chr2:134010875-134010925	MCF10A-Er-Src	breast:	n/a
42	chr2:134024418-134024468	HMEC	breast:	n/a
43	chr2:134127568-134127618	AG04450	lung:	fetal
44	chr2:134083495-134083545	SK-N-SH	brain:	n/a
45	chr2:134024266-134024316	K562	blood:	n/a
46	chr2:134180028-134180078	H1-hESC	embryonic stem cell:	embryo
47	chr2:134182001-134182051	SKMC	muscle:	n/a
48	chr2:134075125-134075175	ProgFib	skin:	n/a
49	chr2:134180028-134180078	HRE	kidney:	n/a
50	chr2:134099762-134099812	SK-N-MC	brain:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:134083491..134086031-chr2:134262913..134265457,2	MCF-7	breast:
2	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
3	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
4	chr2:134154022..134156001-chr2:134158455..134161393,2	MCF-7	breast:
5	chr2:134101590..134103181-chr2:134107237..134110074,2	K562	blood:
6	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
7	chr2:134020255..134021142-chr2:134318343..134319277,2	MCF-7	breast:
8	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
9	chr2:134031322..134033202-chr2:134041949..134044223,2	MCF-7	breast:
10	chr2:134086116..134088912-chr2:134093493..134094997,2	MCF-7	breast:
11	chr2:134089010..134089877-chr2:134262426..134263057,3	MCF-7	breast:
12	chr2:134020041..134020759-chr2:134398921..134399467,2	MCF-7	breast:
13	chr2:134101590..134103181-chr2:134107237..134110074,2	K562	blood:
14	chr2:134179232..134182620-chr2:134183188..134186859,3	MCF-7	breast:
15	chr2:134020179..134020906-chr2:134601878..134602419,2	MCF-7	breast:
16	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
17	chr1:154946346..154946996-chr2:134023337..134024323,2	Hela-S3	cervix:
18	chr2:134148626..134150845-chr2:134154535..134156780,2	MCF-7	breast:
19	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
20	chr2:134033733..134036491-chr2:134192911..134194605,2	MCF-7	breast:
21	chr19:18793804..18794673-chr2:134023005..134023895,2	Hela-S3	cervix:
22	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
23	chr2:134168124..134170815-chr2:134171824..134174647,2	K562	blood:
24	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
25	chr2:134035082..134037430-chr2:134042512..134044195,2	MCF-7	breast:
26	chr2:134003474..134006247-chr2:134007339..134011249,3	MCF-7	breast:
27	chr2:134084453..134086561-chr2:134089070..134091697,3	MCF-7	breast:
28	chr2:134019056..134021492-chr2:134262374..134264487,2	MCF-7	breast:
29	chr2:134072524..134074621-chr2:134077160..134080145,2	K562	blood:
30	chr2:134020208..134021163-chr2:134537454..134538295,5	MCF-7	breast:
31	chr16:30709997..30710818-chr2:134023319..134023932,2	Hela-S3	cervix:
32	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
33	chr2:134179093..134179648-chr2:134601629..134602249,2	MCF-7	breast:
34	chr2:134088967..134089889-chr2:134250249..134251166,2	MCF-7	breast:
35	chr2:134020760..134021325-chr2:134537400..134538161,2	K562	blood:
36	chr2:134015404..134018015-chr2:134019119..134021924,2	MCF-7	breast:
37	chr2:134154022..134156001-chr2:134158455..134161393,2	MCF-7	breast:
38	chr2:134086116..134088912-chr2:134093493..134094997,2	MCF-7	breast:
39	chr2:134089345..134089856-chr2:134262223..134263005,2	MCF-7	breast:
40	chr2:134019393..134021124-chr2:134030265..134032879,2	K562	blood:
41	chr2:134028269..134031265-chr2:134033002..134035310,2	MCF-7	breast:
42	chr2:134073505..134075455-chr2:134080739..134083280,2	MCF-7	breast:
43	chr2:134179232..134182620-chr2:134183188..134186859,3	MCF-7	breast:
44	chr2:133999579..134001370-chr2:134029081..134031077,2	K562	blood:
45	chr2:134020528..134022424-chr2:134324632..134327514,2	MCF-7	breast:
46	chr2:134159517..134161483-chr2:134169565..134171940,2	MCF-7	breast:
47	chr2:134147354..134149666-chr2:134150601..134153236,2	K562	blood:
48	chr2:134072524..134074621-chr2:134077160..134080145,2	K562	blood:
49	chr2:134038890..134041623-chr2:134041735..134044144,2	MCF-7	breast:
50	chr2:134178712..134179890-chr2:134318289..134319234,5	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
2	lnc-LYPD1-4	chr2:134148681-134148970	NONHSAT074547
3	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953.3
4	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953
5	lnc-GPR39-4	chr2:134023767-134023868	ENSG00000226953
6	lnc-GPR39-4	chr2:134042267-134042330	NR_110294
7	lnc-GPR39-4	chr2:134025928-134026014	NR_110294
8	lnc-GPR39-4	chr2:134023814-134024008	ENSG00000226953.3
9	lnc-GPR39-4	chr2:134026488-134026613	ENSG00000226953.3
10	lnc-GPR39-4	chr2:134026488-134026613	NR_110294
11	lnc-GPR39-4	chr2:134023767-134023868	NR_110294
12	lnc-GPR39-4	chr2:134042267-134042334	ENSG00000226953
13	lnc-GPR39-4	chr2:134024845-134024996	NR_110294
14	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953
15	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953.3
16	lnc-GPR39-4	chr2:134025928-134026014	ENSG00000226953
17	lnc-GPR39-4	chr2:134022540-134022674	ENSG00000226953
18	lnc-GPR39-4	chr2:134024845-134024996	ENSG00000226953
19	lnc-GPR39-4	chr2:134026488-134026582	ENSG00000226953

No data

Variant related genes	Relation type
RNU6-579P	TF binding region
RN7SKP154	TF binding region
ENSG00000226953	TF binding region
RNU6-579P	CpG island
RN7SKP154	CpG island
ENSG00000226953	CpG island
ENSG00000080603	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000176771	chromatin interactions
ENSG00000252688	chromatin interactions
ENSG00000222068	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000105662	chromatin interactions
CALU	miRNA target sites
KIF23	miRNA target sites
SMCR7L	miRNA target sites
TNFSF10	miRNA target sites
IQCB1	miRNA target sites
FNTA	miRNA target sites
NFKB1	miRNA target sites
LRIG1	miRNA target sites
ATOX1	miRNA target sites

Extended variants
information (count: 6576 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:6576 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112962114	chr2:134005254-134005255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555164079	chr2:134005282-134005283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181029896	chr2:134005290-134005291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529906150	chr2:134005306-134005307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548048958	chr2:134005309-134005310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs569989019	chr2:134005364-134005365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78452496	chr2:134005380-134005381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572046075	chr2:134005427-134005428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550236396	chr2:134005436-134005437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189379753	chr2:134005460-134005461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs16822568	chr2:134005514-134005515	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs547874229	chr2:134005519-134005520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs80192542	chr2:134005532-134005533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536871559	chr2:134005549-134005550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10496702	chr2:134005569-134005570	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
16	rs576362031	chr2:134005612-134005613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115260356	chr2:134005664-134005665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558174769	chr2:134005681-134005682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs72985667	chr2:134005689-134005690	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs181347624	chr2:134005699-134005700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs77401611	chr2:134005841-134005842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76353342	chr2:134005853-134005854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372338922	chr2:134005948-134005949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542039426	chr2:134005960-134005961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540372532	chr2:134005977-134005978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563460516	chr2:134006003-134006004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530867269	chr2:134006006-134006007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552496406	chr2:134006008-134006009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564327415	chr2:134006019-134006020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532548797	chr2:134006034-134006035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547446791	chr2:134006096-134006097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566191143	chr2:134006167-134006168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs536333213	chr2:134006178-134006179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562252638	chr2:134006197-134006198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139970543	chr2:134006200-134006201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149999595	chr2:134006222-134006223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377378510	chr2:134006252-134006253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537198471	chr2:134006295-134006296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558331000	chr2:134006380-134006381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370815435	chr2:134006398-134006399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185957567	chr2:134006419-134006420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190774795	chr2:134006450-134006451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534636925	chr2:134006458-134006459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552674017	chr2:134006480-134006481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574512290	chr2:134006501-134006502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541554468	chr2:134006518-134006519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571815463	chr2:134006545-134006546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563521679	chr2:134006548-134006549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538909407	chr2:134006562-134006563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144237166	chr2:134006600-134006601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	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
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1657 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133991600-134005400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:133994000-134023600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:133998400-134005800	Weak transcription	Left Ventricle	heart
4	chr2:133998800-134013000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:133998800-134014800	Weak transcription	Fetal Stomach	stomach
6	chr2:133999200-134005400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:133999200-134007800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:133999400-134005400	Weak transcription	Ovary	ovary
9	chr2:133999400-134005800	Weak transcription	Lung	lung
10	chr2:134000200-134005400	Weak transcription	NHLF	lung
11	chr2:134001200-134005800	Weak transcription	Right Ventricle	heart
12	chr2:134003600-134006000	Enhancers	Fetal Lung	lung
13	chr2:134003600-134006400	Enhancers	Brain Substantia Nigra	brain
14	chr2:134003800-134005600	Weak transcription	Brain Hippocampus Middle	brain
15	chr2:134003800-134006200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:134003800-134010400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:134004200-134007400	Enhancers	Brain Anterior Caudate	brain
18	chr2:134004400-134005600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr2:134004600-134006200	Enhancers	Brain Angular Gyrus	brain
20	chr2:134004600-134021200	Weak transcription	Fetal Brain Male	brain
21	chr2:134004800-134005600	Weak transcription	Fetal Heart	heart
22	chr2:134005000-134006000	Enhancers	Primary B cells from peripheral blood	blood
23	chr2:134005000-134006000	Enhancers	NHDF-Ad	bronchial
24	chr2:134005000-134006200	Enhancers	Psoas Muscle	Psoas
25	chr2:134005200-134005600	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr2:134005200-134006200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:134005200-134006200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr2:134005200-134006200	Enhancers	Fetal Muscle Leg	muscle
29	chr2:134005200-134006400	Enhancers	Brain Cingulate Gyrus	brain
30	chr2:134005200-134008000	Enhancers	HUVEC	blood vessel
31	chr2:134005400-134005800	Enhancers	NHLF	lung
32	chr2:134005400-134006000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:134005400-134006200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr2:134005400-134006200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:134005400-134006400	Enhancers	Ovary	ovary
36	chr2:134005600-134006200	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr2:134005600-134006400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr2:134005600-134006400	Enhancers	Fetal Heart	heart
39	chr2:134005600-134006600	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr2:134005600-134006800	Enhancers	Brain Hippocampus Middle	brain
41	chr2:134005800-134006200	Enhancers	Placenta	Placenta
42	chr2:134005800-134006200	Enhancers	Right Ventricle	heart
43	chr2:134005800-134006400	Enhancers	Left Ventricle	heart
44	chr2:134005800-134006400	Enhancers	Lung	lung
45	chr2:134005800-134011000	Weak transcription	NHLF	lung
46	chr2:134006000-134006400	Enhancers	Adipose Nuclei	Adipose
47	chr2:134006000-134006400	Enhancers	Right Atrium	heart
48	chr2:134006000-134006600	Enhancers	Liver	Liver
49	chr2:134006000-134007800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:134006200-134007200	Weak transcription	Fetal Muscle Leg	muscle

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