Variant report

Variant	nsv466889
Chromosome Location	chr10:45210690-45359483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1362)
CpG islands
(count:734)
Chromatin interactive
region (count:70)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:45353231-45353390	K562	blood:	n/a	n/a
2	ATF1	chr10:45284313-45284641	K562	blood:	n/a	n/a
3	ATF2	chr10:45353031-45353569	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:45305172-45305309	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:45299606-45299615	K562	blood:	n/a	n/a
6	BACH1	chr10:45353406-45353571	K562	blood:	n/a	n/a
7	BACH1	chr10:45320128-45320341	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:45353142-45353592	H1-hESC	embryonic stem cell:	n/a	chr10:45353244-45353258
9	BATF	chr10:45220940-45221158	GM12878	blood:	n/a	n/a
10	BATF	chr10:45220327-45220549	GM12878	blood:	n/a	chr10:45220487-45220497
11	BATF	chr10:45220907-45221196	GM12878	blood:	n/a	n/a
12	BCL11A	chr10:45353248-45353459	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr10:45353153-45353511	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:45353269-45353487	K562	blood:	n/a	n/a
15	BHLHE40	chr10:45316768-45317065	HepG2	liver:	n/a	n/a
16	BHLHE40	chr10:45316732-45317038	K562	blood:	n/a	n/a
17	BHLHE40	chr10:45281024-45281155	K562	blood:	n/a	chr10:45281073-45281082 chr10:45281071-45281080 chr10:45281072-45281081 chr10:45281066-45281087 chr10:45281072-45281081 chr10:45281070-45281083
18	BHLHE40	chr10:45320033-45320161	K562	blood:	n/a	n/a
19	BHLHE40	chr10:45263065-45263128	K562	blood:	n/a	n/a
20	BHLHE40	chr10:45353265-45353562	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:45284232-45284511	K562	blood:	n/a	n/a
22	BRCA1	chr10:45317191-45317198	HepG2	liver:	n/a	n/a
23	BRCA1	chr10:45353094-45353455	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr10:45323848-45323869	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr10:45240019-45240107	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:45323362-45323726	HepG2	liver:	n/a	n/a
27	CEBPB	chr10:45294297-45294572	A549	lung:	n/a	chr10:45294421-45294432
28	CEBPB	chr10:45220810-45221187	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:45248264-45248775	IMR90	lung:	n/a	chr10:45248346-45248358
30	CEBPB	chr10:45308030-45308247	A549	lung:	n/a	chr10:45308145-45308156
31	CEBPB	chr10:45308006-45308303	IMR90	lung:	n/a	chr10:45308145-45308156
32	CEBPB	chr10:45281919-45282355	IMR90	lung:	n/a	n/a
33	CEBPB	chr10:45284290-45284604	K562	blood:	n/a	n/a
34	CEBPB	chr10:45291597-45291775	K562	blood:	n/a	chr10:45291656-45291667
35	CEBPB	chr10:45276653-45276925	IMR90	lung:	n/a	n/a
36	CEBPB	chr10:45346038-45346267	A549	lung:	n/a	chr10:45346135-45346144 chr10:45346135-45346144 chr10:45346134-45346145 chr10:45346135-45346144 chr10:45346133-45346144 chr10:45346133-45346146 chr10:45346135-45346144
37	CEBPB	chr10:45251683-45252022	IMR90	lung:	n/a	n/a
38	CEBPB	chr10:45220843-45221155	K562	blood:	n/a	n/a
39	CEBPB	chr10:45294263-45294553	IMR90	lung:	n/a	chr10:45294421-45294432
40	CEBPB	chr10:45248271-45248670	MCF-7	breast:	n/a	chr10:45248346-45248358
41	CEBPB	chr10:45305184-45305384	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr10:45351884-45352061	K562	blood:	n/a	chr10:45352018-45352029 chr10:45352018-45352029
43	CEBPB	chr10:45266517-45266742	K562	blood:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
44	CEBPB	chr10:45353142-45353614	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr10:45266543-45266695	HepG2	liver:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
46	CEBPB	chr10:45284306-45284404	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:45277676-45277830	HepG2	liver:	n/a	chr10:45277784-45277795
48	CEBPB	chr10:45291507-45291802	HepG2	liver:	n/a	chr10:45291656-45291667
49	CEBPB	chr10:45308055-45308266	HepG2	liver:	n/a	chr10:45308145-45308156
50	CEBPB	chr10:45323342-45323756	MCF-7	breast:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45298460-45298510	HUVEC	blood vessel:	n/a
2	chr10:45306728-45306778	HRCEpiC	kidney:	n/a
3	chr10:45298460-45298510	HUVEC	blood vessel:	n/a
4	chr10:45306728-45306778	HRCEpiC	kidney:	n/a
5	chr10:45306728-45306778	U87	brain:	n/a
6	chr10:45353344-45353394	NHBE	bronchial:	n/a
7	chr10:45357075-45357125	AG09309	skin:	n/a
8	chr10:45324653-45324703	NH-A	brain:	n/a
9	chr10:45306728-45306778	SK-N-SH_RA	brain:	n/a
10	chr10:45352772-45352822	T-47D	breast:	n/a
11	chr10:45357075-45357125	Jurkat	blood:	n/a
12	chr10:45282107-45282157	HCF	heart:	n/a
13	chr10:45282107-45282157	AG10803	skin:	n/a
14	chr10:45352772-45352822	PFSK-1	brain:	n/a
15	chr10:45270290-45270340	U87	brain:	n/a
16	chr10:45324999-45325049	NH-A	brain:	n/a
17	chr10:45298460-45298510	CMK	blood:	n/a
18	chr10:45219814-45219864	SK-N-SH_RA	brain:	n/a
19	chr10:45211116-45211166	SKMC	muscle:	n/a
20	chr10:45270290-45270340	HEEpiC	esophagus:	n/a
21	chr10:45357075-45357125	T-47D	breast:	n/a
22	chr10:45219814-45219864	BE2_C	brain:	n/a
23	chr10:45211116-45211166	NHBE	bronchial:	n/a
24	chr10:45282107-45282157	PrEC	prostate:	n/a
25	chr10:45270290-45270340	AG09309	skin:	n/a
26	chr10:45324653-45324703	AG04449	skin:	fetal
27	chr10:45324999-45325049	Hepatocyte	liver:	n/a
28	chr10:45324999-45325049	MCF-7	breast:	n/a
29	chr10:45306728-45306778	Hepatocyte	liver:	n/a
30	chr10:45270290-45270340	AG10803	skin:	n/a
31	chr10:45282107-45282157	SAEC	small airway:	n/a
32	chr10:45219814-45219864	AG04449	skin:	fetal
33	chr10:45324999-45325049	A549	lung:	n/a
34	chr10:45211116-45211166	SK-N-SH_RA	brain:	n/a
35	chr10:45282107-45282157	GM12878	blood:	n/a
36	chr10:45219814-45219864	HCM	heart:	n/a
37	chr10:45357075-45357125	HRPEpiC	eye:	n/a
38	chr10:45306728-45306778	HepG2	liver:	n/a
39	chr10:45298460-45298510	IMR90	lung:	fetal
40	chr10:45270290-45270340	AoSMC	blood vessel:	n/a
41	chr10:45270290-45270340	MCF10A-Er-Src	breast:	n/a
42	chr10:45211116-45211166	HRE	kidney:	n/a
43	chr10:45352772-45352822	NH-A	brain:	n/a
44	chr10:45248889-45248939	HepG2	liver:	n/a
45	chr10:45211116-45211166	HAEpiC	amniotic membrane:	n/a
46	chr10:45306728-45306778	NHDF-neo	bronchial:	n/a
47	chr10:45324999-45325049	NHDF-neo	bronchial:	n/a
48	chr10:45219814-45219864	U87	brain:	n/a
49	chr10:45353344-45353394	HPAEpiC	pulmonary alveolar:	n/a
50	chr10:45306728-45306778	GM12892	blood:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
2	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
3	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
4	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
5	chr10:44166788..44167692-chr10:45352916..45353842,3	K562	blood:
6	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
7	chr10:45348502..45349200-chr7:103463744..103464468,2	MCF-7	breast:
8	chr10:45315653..45316627-chr10:45360108..45360667,2	MCF-7	breast:
9	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
10	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
11	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
12	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
13	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
14	chr10:44889278..44891908-chr10:45358859..45361394,2	MCF-7	breast:
15	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
16	chr10:44806565..44809195-chr10:45358624..45361285,2	MCF-7	breast:
17	chr10:44881926..44882676-chr10:45348263..45349209,2	MCF-7	breast:
18	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
19	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
20	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
21	chr10:45359136..45362011-chr10:45365608..45368022,2	MCF-7	breast:
22	chr10:44838214..44839988-chr10:45358990..45361761,2	MCF-7	breast:
23	chr10:45359058..45361978-chr10:45470827..45473686,2	K562	blood:
24	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
25	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
26	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
27	chr10:45336364..45339014-chr10:45360151..45362117,2	MCF-7	breast:
28	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
29	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
30	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
31	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
32	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
33	chr10:45220517..45222297-chr10:45222405..45225320,2	MCF-7	breast:
34	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
35	chr10:45358806..45362184-chr10:45374031..45377195,7	MCF-7	breast:
36	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
37	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
38	chr10:45216057..45218772-chr10:45222677..45225036,2	K562	blood:
39	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
40	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
41	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
42	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
43	chr10:45225689..45228283-chr10:45230513..45233134,2	K562	blood:
44	chr10:45226792..45229457-chr10:45322793..45324637,2	MCF-7	breast:
45	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
46	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:
47	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
48	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
49	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
50	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812.2
2	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812
3	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812.2
4	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812
5	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812
6	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812
7	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812.2
8	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812
9	lnc-C10orf10-2	chr10:45324023-45324287	NONHSAT013044
10	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812.2
11	lnc-C10orf10-2	chr10:45322733-45324287	NONHSAT013043
12	lnc-C10orf10-2	chr10:45321600-45321818	ENSG00000224812
13	lnc-C10orf10-2	chr10:45324620-45324729	NONHSAT013044
14	lnc-C10orf10-5	chr10:45270071-45272253	ucscGeneNc_uc001jcf_1
15	lnc-TMEM72-2	chr10:45301891-45303671	NONHSAT013040
16	lnc-C10orf10-2	chr10:45321600-45321816	ENSG00000224812.2
17	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812.2

No data

Variant related genes	Relation type
EIF2AP4	TF binding region
EIF2AP4	CpG island
ENSG00000107562	chromatin interactions
YOD1	miRNA target sites
MALT1	miRNA target sites

Extended variants
information (count: 5768 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5768 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7097094	chr10:45210690-45210691	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184815277	chr10:45210719-45210720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534919625	chr10:45210747-45210748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546872842	chr10:45210752-45210753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571276493	chr10:45210759-45210760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76093803	chr10:45210779-45210780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557120448	chr10:45210799-45210800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575282639	chr10:45210800-45210801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536485179	chr10:45210818-45210819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555142412	chr10:45210845-45210846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs573310845	chr10:45210847-45210848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369408944	chr10:45210857-45210858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188526646	chr10:45210859-45210860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146586082	chr10:45210870-45210871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576851459	chr10:45210913-45210914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs12570392	chr10:45210926-45210927	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs562678642	chr10:45210970-45210971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569671685	chr10:45211100-45211101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114665315	chr10:45211108-45211109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548344794	chr10:45211116-45211117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556919152	chr10:45211119-45211120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561143850	chr10:45211208-45211209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377495864	chr10:45211210-45211211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370975885	chr10:45211225-45211226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546934221	chr10:45211234-45211235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571544607	chr10:45211266-45211267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532178031	chr10:45211274-45211275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550584674	chr10:45211301-45211302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141212381	chr10:45211335-45211336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536351502	chr10:45211337-45211338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538786663	chr10:45211359-45211360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564991722	chr10:45211366-45211367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78747167	chr10:45211398-45211399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567070507	chr10:45211444-45211445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112560364	chr10:45211461-45211462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558853985	chr10:45211490-45211491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577108491	chr10:45211532-45211533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs59604881	chr10:45211556-45211557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116047046	chr10:45211560-45211561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574700367	chr10:45211589-45211590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2199906	chr10:45211610-45211611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540977357	chr10:45211643-45211644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542322789	chr10:45211669-45211670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560354177	chr10:45211709-45211710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568592674	chr10:45211737-45211738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184925270	chr10:45211763-45211764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114860081	chr10:45211781-45211782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532444416	chr10:45211808-45211809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550845853	chr10:45211814-45211815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145021826	chr10:45211815-45211816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Glioblastoma multiforme	22122801	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45207000-45212600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr10:45208400-45211200	Enhancers	Fetal Muscle Leg	muscle
3	chr10:45208400-45211400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:45208400-45211400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr10:45208800-45211600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:45209400-45211200	Enhancers	Fetal Muscle Trunk	muscle
7	chr10:45210000-45211200	Enhancers	NH-A	brain
8	chr10:45210000-45211400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:45210000-45211600	Enhancers	Osteobl	bone
10	chr10:45210000-45211800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:45210200-45211400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr10:45210400-45211000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr10:45210400-45211200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:45210600-45210800	Enhancers	Colon Smooth Muscle	Colon
15	chr10:45210600-45211000	Enhancers	HMEC	breast
16	chr10:45210600-45211200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr10:45211000-45212000	Weak transcription	HMEC	breast
18	chr10:45211400-45211800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr10:45211400-45211800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr10:45211400-45218000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr10:45211800-45212400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr10:45211800-45212400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr10:45211800-45212600	Enhancers	Fetal Lung	lung
24	chr10:45212000-45212600	Enhancers	HMEC	breast
25	chr10:45214800-45219200	Weak transcription	Aorta	Aorta
26	chr10:45217400-45219800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr10:45217800-45221400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr10:45218000-45218400	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr10:45218000-45221400	Enhancers	Primary B cells from peripheral blood	blood
30	chr10:45218000-45221400	Enhancers	NHDF-Ad	bronchial
31	chr10:45218000-45221600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr10:45218200-45219400	Enhancers	Primary hematopoietic stem cells	blood
33	chr10:45218200-45220200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:45218200-45221400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr10:45218200-45221400	Enhancers	Osteobl	bone
36	chr10:45218200-45221600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr10:45218400-45218600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr10:45218400-45218800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
39	chr10:45218400-45220400	Enhancers	Primary B cells from cord blood	blood
40	chr10:45218400-45220400	Enhancers	Fetal Muscle Leg	muscle
41	chr10:45218400-45221400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr10:45218600-45220000	Enhancers	GM12878-XiMat	blood
43	chr10:45218600-45221200	Enhancers	NH-A	brain
44	chr10:45218600-45221400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr10:45218800-45220000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr10:45218800-45220000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr10:45219000-45219200	Enhancers	HSMMtube	muscle
48	chr10:45219000-45219400	Enhancers	Placenta Amnion	Placenta Amnion
49	chr10:45219000-45220200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr10:45219000-45220200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links