Variant report

Variant	nsv1045404
Chromosome Location	chr10:224406-520269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3396)
CpG islands
(count:14302)
Chromatin interactive
region (count:190)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:3396 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:285265-285305	K562	blood:	n/a	n/a
2	ARID3A	chr10:327960-327969	K562	blood:	n/a	n/a
3	ARID3A	chr10:419183-419192	HepG2	liver:	n/a	n/a
4	ATF1	chr10:375453-375999	K562	blood:	n/a	n/a
5	ATF1	chr10:519286-519676	K562	blood:	n/a	n/a
6	ATF2	chr10:329685-330303	GM12878	blood:	n/a	n/a
7	ATF2	chr10:329652-330120	GM12878	blood:	n/a	n/a
8	BACH1	chr10:337886-338129	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:476617-476752	K562	blood:	n/a	n/a
10	BACH1	chr10:299777-299833	K562	blood:	n/a	n/a
11	BACH1	chr10:247184-247226	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr10:313072-313372	GM12878	blood:	n/a	chr10:313257-313268
13	BATF	chr10:470848-471468	GM12878	blood:	n/a	n/a
14	BATF	chr10:310207-311382	GM12878	blood:	n/a	n/a
15	BATF	chr10:310253-311303	GM12878	blood:	n/a	n/a
16	BATF	chr10:329741-330161	GM12878	blood:	n/a	n/a
17	BATF	chr10:369900-370264	GM12878	blood:	n/a	chr10:370082-370093 chr10:370087-370097
18	BATF	chr10:369880-370229	GM12878	blood:	n/a	chr10:370082-370093 chr10:370087-370097
19	BATF	chr10:497160-497443	GM12878	blood:	n/a	n/a
20	BATF	chr10:266943-267203	GM12878	blood:	n/a	n/a
21	BATF	chr10:470788-471665	GM12878	blood:	n/a	n/a
22	BATF	chr10:228818-229091	GM12878	blood:	n/a	chr10:228957-228965
23	BATF	chr10:228892-229099	GM12878	blood:	n/a	chr10:228957-228965
24	BATF	chr10:329758-330365	GM12878	blood:	n/a	n/a
25	BCL11A	chr10:379590-379962	GM12878	blood:	n/a	n/a
26	BCL11A	chr10:392313-392549	GM12878	blood:	n/a	n/a
27	BCL11A	chr10:329716-330184	GM12878	blood:	n/a	chr10:329975-329984
28	BCL11A	chr10:393213-393521	GM12878	blood:	n/a	n/a
29	BCL11A	chr10:470785-471490	GM12878	blood:	n/a	n/a
30	BCL11A	chr10:310813-310984	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:471026-471238	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:369918-370151	GM12878	blood:	n/a	chr10:370085-370094
33	BCL11A	chr10:392745-392995	GM12878	blood:	n/a	n/a
34	BCL11A	chr10:497201-497455	GM12878	blood:	n/a	n/a
35	BCL3	chr10:494945-495169	GM12878	blood:	n/a	n/a
36	BCL3	chr10:370037-370277	GM12878	blood:	n/a	chr10:370085-370094
37	BCL3	chr10:393628-394091	GM12878	blood:	n/a	n/a
38	BCL3	chr10:285845-286102	GM12878	blood:	n/a	n/a
39	BCL3	chr10:350434-350934	GM12878	blood:	n/a	n/a
40	BCL3	chr10:393148-393491	GM12878	blood:	n/a	n/a
41	BCL3	chr10:470630-471011	GM12878	blood:	n/a	n/a
42	BCL3	chr10:471217-471750	GM12878	blood:	n/a	n/a
43	BCL3	chr10:457507-457860	GM12878	blood:	n/a	chr10:457805-457812
44	BCL3	chr10:457469-457868	GM12878	blood:	n/a	chr10:457805-457812
45	BCL3	chr10:393666-394045	GM12878	blood:	n/a	n/a
46	BCL3	chr10:471285-471748	GM12878	blood:	n/a	n/a
47	BCL3	chr10:494959-495195	GM12878	blood:	n/a	n/a
48	BCL3	chr10:351043-351410	GM12878	blood:	n/a	n/a
49	BCL3	chr10:470666-471026	GM12878	blood:	n/a	n/a
50	BCL3	chr10:350431-351274	GM12878	blood:	n/a	n/a

(count:14302 , 50 per page) page: 1 2 3 4 5 6 7 ... 287

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:394333-394383	HEEpiC	esophagus:	n/a
2	chr10:386708-386758	T-47D	breast:	n/a
3	chr10:405362-405412	HCF	heart:	n/a
4	chr10:453318-453368	HIPEpiC	eye:	n/a
5	chr10:441309-441359	AoSMC	blood vessel:	n/a
6	chr10:405362-405412	SK-N-SH_RA	brain:	n/a
7	chr10:332271-332321	AG09319	gingival:	n/a
8	chr10:423907-423957	HRE	kidney:	n/a
9	chr10:459908-459958	Hepatocyte	liver:	n/a
10	chr10:438317-438367	T-47D	breast:	n/a
11	chr10:466338-466388	LNCaP	prostate:	n/a
12	chr10:357370-357420	AoSMC	blood vessel:	n/a
13	chr10:468755-468805	NHDF-neo	bronchial:	n/a
14	chr10:327533-327583	GM12891	blood:	n/a
15	chr10:295087-295137	T-47D	breast:	n/a
16	chr10:435953-436003	HEK293	kidney:	embryo
17	chr10:323809-323859	A549	lung:	n/a
18	chr10:518210-518260	HMEC	breast:	n/a
19	chr10:384286-384336	A549	lung:	n/a
20	chr10:457264-457314	AG10803	skin:	n/a
21	chr10:436477-436527	MCF10A-Er-Src	breast:	n/a
22	chr10:407721-407771	AoSMC	blood vessel:	n/a
23	chr10:327132-327182	A549	lung:	n/a
24	chr10:498333-498383	CMK	blood:	n/a
25	chr10:403653-403703	H1-hESC	embryonic stem cell:	embryo
26	chr10:397923-397973	K562	blood:	n/a
27	chr10:395292-395342	BE2_C	brain:	n/a
28	chr10:453149-453199	PANC-1	pancreas:	n/a
29	chr10:394333-394383	HEEpiC	esophagus:	n/a
30	chr10:386708-386758	T-47D	breast:	n/a
31	chr10:405362-405412	HCF	heart:	n/a
32	chr10:453318-453368	HIPEpiC	eye:	n/a
33	chr10:441309-441359	AoSMC	blood vessel:	n/a
34	chr10:405362-405412	SK-N-SH_RA	brain:	n/a
35	chr10:332271-332321	AG09319	gingival:	n/a
36	chr10:423907-423957	HRE	kidney:	n/a
37	chr10:459908-459958	Hepatocyte	liver:	n/a
38	chr10:438317-438367	T-47D	breast:	n/a
39	chr10:466338-466388	LNCaP	prostate:	n/a
40	chr10:357370-357420	AoSMC	blood vessel:	n/a
41	chr10:468755-468805	NHDF-neo	bronchial:	n/a
42	chr10:327533-327583	GM12891	blood:	n/a
43	chr10:295087-295137	T-47D	breast:	n/a
44	chr10:435953-436003	HEK293	kidney:	embryo
45	chr10:323809-323859	A549	lung:	n/a
46	chr10:518210-518260	HMEC	breast:	n/a
47	chr10:384286-384336	A549	lung:	n/a
48	chr10:457264-457314	AG10803	skin:	n/a
49	chr10:436477-436527	MCF10A-Er-Src	breast:	n/a
50	chr10:407721-407771	AoSMC	blood vessel:	n/a

(count:190 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr10:241555..243319-chr10:245606..248591,2	K562	blood:
2	chr10:407263..407805-chr10:482123..482764,2	MCF-7	breast:
3	chr10:257536..259107-chr10:276996..279515,2	MCF-7	breast:
4	chr10:378234..380248-chr10:380796..382303,2	MCF-7	breast:
5	chr10:461858..462407-chr10:481646..482609,2	MCF-7	breast:
6	chr10:334420..336052-chr10:388078..389597,2	MCF-7	breast:
7	chr10:290658..294570-chr10:295479..299395,6	MCF-7	breast:
8	chr10:259460..261096-chr10:265646..267645,2	K562	blood:
9	chr10:359838..363980-chr10:372787..377005,5	MCF-7	breast:
10	chr10:334360..337128-chr10:339804..341421,2	K562	blood:
11	chr10:450799..453680-chr10:480575..483479,3	MCF-7	breast:
12	chr10:461634..462240-chr10:481924..482823,2	MCF-7	breast:
13	chr10:285181..287900-chr10:288868..291206,2	K562	blood:
14	chr10:268763..271224-chr10:275247..277353,2	K562	blood:
15	chr10:300746..302265-chr10:307288..309222,2	MCF-7	breast:
16	chr10:119668..120194-chr10:254902..255569,2	MCF-7	breast:
17	chr10:322972..326718-chr10:480117..482387,3	MCF-7	breast:
18	chr10:180488..183115-chr10:414614..416196,2	MCF-7	breast:
19	chr10:229531..231342-chr10:232780..235682,2	K562	blood:
20	chr10:243958..245643-chr10:246215..248277,2	MCF-7	breast:
21	chr10:396298..399033-chr10:399080..401152,2	MCF-7	breast:
22	chr10:414936..417865-chr10:461204..463108,2	MCF-7	breast:
23	chr10:180649..183609-chr10:237438..240674,3	MCF-7	breast:
24	chr10:329515..331543-chr10:346847..348584,2	MCF-7	breast:
25	chr10:240760..243336-chr10:243989..247106,3	K562	blood:
26	chr10:352441..354760-chr10:358582..361541,3	MCF-7	breast:
27	chr10:273796..276925-chr10:278951..281573,3	K562	blood:
28	chr10:317070..320401-chr10:332484..334993,3	K562	blood:
29	chr10:181155..183094-chr10:255528..258839,3	MCF-7	breast:
30	chr10:354319..356536-chr10:361569..363521,3	MCF-7	breast:
31	chr10:411310..414863-chr10:418751..420766,3	MCF-7	breast:
32	chr10:352835..354904-chr10:383242..385492,2	MCF-7	breast:
33	chr10:417156..419779-chr10:480813..483517,2	MCF-7	breast:
34	chr10:450799..453680-chr10:480575..483479,3	MCF-7	breast:
35	chr10:414936..417865-chr10:461204..463108,2	MCF-7	breast:
36	chr10:485797..489382-chr10:492522..494449,3	MCF-7	breast:
37	chr10:329515..331543-chr10:346847..348584,2	MCF-7	breast:
38	chr10:368780..371728-chr10:384825..386792,2	MCF-7	breast:
39	chr10:359212..361579-chr10:361961..364084,3	MCF-7	breast:
40	chr10:418529..420977-chr10:423875..425608,2	MCF-7	breast:
41	chr10:461779..462665-chr10:840464..841138,2	MCF-7	breast:
42	chr10:352835..354904-chr10:383242..385492,2	MCF-7	breast:
43	chr10:267548..269172-chr10:272326..274711,2	K562	blood:
44	chr10:267548..269172-chr10:272326..274711,2	K562	blood:
45	chr10:180161..182379-chr10:231060..233421,2	K562	blood:
46	chr10:454564..456430-chr10:464308..466702,2	MCF-7	breast:
47	chr10:375592..377558-chr10:407112..409225,2	MCF-7	breast:
48	chr10:461634..462240-chr10:481924..482823,2	MCF-7	breast:
49	chr10:236283..239568-chr10:240498..242911,3	MCF-7	breast:
50	chr10:384657..385391-chr10:407116..407713,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZMYND11-2	chr10:383723-383927	NONHSAT010856
2	lnc-ZMYND11-2	chr10:383079-383236	NONHSAT010856
3	lnc-ZMYND11-1	chr10:483501-483855	ENSG00000233021.2
4	lnc-DIP2C-1	chr10:289686-290565	predAs_engstrom06_BU902898_1
5	lnc-ZMYND11-1	chr10:486908-487110	ENSG00000233021.2
6	lnc-LARP4B-4	chr10:476181-476444	NONHSAT010858

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ZMYND11	hsa-miR-27b-3p	chr10:300275-300295
2	DIP2C	hsa-miR-375	chr10:320428-320449
3	ZMYND11	hsa-miR-192-5p	chr10:300337-300358
4	ZMYND11	hsa-miR-27b-3p	chr10:299829-299850
5	DIP2C	hsa-miR-375	chr10:322372-322393
6	DIP2C	hsa-miR-335-5p	chr10:428374-428397
7	DIP2C	hsa-miR-375	chr10:320433-320427
8	ZMYND11	hsa-miR-215-5p	chr10:300337-300358

Variant related genes	Relation type
RNA5SP298	TF binding region
ENSG00000233021	TF binding region
DIP2C	TF binding region
RN7SL754P	TF binding region
ENSG00000264248	TF binding region
ZMYND11	TF binding region
RNA5SP298	CpG island
ENSG00000233021	CpG island
DIP2C	CpG island
RN7SL754P	CpG island
ENSG00000264248	CpG island
ZMYND11	CpG island
ENSG00000015171	chromatin interactions
ENSG00000233021	chromatin interactions
ENSG00000005073	chromatin interactions
ENSG00000151240	chromatin interactions
ENSG00000264248	chromatin interactions
ENSG00000268081	chromatin interactions
ENSG00000239822	chromatin interactions
ENSG00000201861	chromatin interactions
ENSG00000173876	chromatin interactions

Extended variants
information (count: 15557 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:15557 , 50 per page) page: 1 2 3 4 5 6 7 ... 312

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145521623	chr10:224422-224423	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs185624412	chr10:224456-224457	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554866386	chr10:224459-224460	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563868132	chr10:224464-224465	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571458436	chr10:224477-224478	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs117956295	chr10:224497-224498	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550454406	chr10:224505-224506	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs566949678	chr10:224507-224508	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs145247055	chr10:224544-224545	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs137861626	chr10:224559-224560	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs572869601	chr10:224578-224579	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs538865296	chr10:224680-224681	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs375352325	chr10:224687-224688	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs190782224	chr10:224699-224700	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs575739676	chr10:224711-224712	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544969972	chr10:224759-224760	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143106089	chr10:224782-224783	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs574900177	chr10:224849-224850	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540604549	chr10:224852-224853	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs560385221	chr10:224858-224859	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs532596128	chr10:224922-224923	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11250718	chr10:224961-224962	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs565131958	chr10:224962-224963	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530594910	chr10:224990-224991	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs372274468	chr10:224992-224993	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs550497840	chr10:225000-225001	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs193064594	chr10:225064-225065	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145162185	chr10:225108-225109	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs532145657	chr10:225116-225117	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs185475915	chr10:225131-225132	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148358640	chr10:225145-225146	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs114872010	chr10:225154-225155	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558367631	chr10:225167-225168	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs141514744	chr10:225170-225171	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549165655	chr10:225263-225264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555322543	chr10:225269-225270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs34349855	chr10:225324-225325	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534657779	chr10:225346-225347	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs559797083	chr10:225475-225476	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540639653	chr10:225480-225481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554176249	chr10:225496-225497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528445330	chr10:225505-225506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs546304131	chr10:225523-225524	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs151273482	chr10:225527-225528	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs57748257	chr10:225546-225547	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530636146	chr10:225588-225589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543976780	chr10:225590-225591	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs2448364	chr10:225659-225660	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs78596996	chr10:225711-225712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546569204	chr10:225714-225715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:7918 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:194200-228200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr10:200000-228000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:200400-226800	Weak transcription	HSMM	muscle
4	chr10:200400-230400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:207200-226800	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr10:208200-293000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr10:209800-225800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr10:209800-226600	Weak transcription	Liver	Liver
9	chr10:210800-224800	Weak transcription	Ovary	ovary
10	chr10:212800-226400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr10:213800-226000	Weak transcription	Dnd41	blood
12	chr10:215200-237600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr10:215400-227000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:215600-226600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr10:216200-227800	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr10:217600-226000	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr10:217800-225800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr10:218200-227000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr10:218200-227200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr10:218200-238000	Weak transcription	Pancreas	Pancrea
21	chr10:218200-242800	Weak transcription	Fetal Brain Male	brain
22	chr10:218600-226400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr10:218600-227400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr10:219000-226000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr10:219400-225800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr10:219600-226200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr10:220000-226600	Weak transcription	Brain Anterior Caudate	brain
28	chr10:220200-227400	Weak transcription	HUVEC	blood vessel
29	chr10:220400-224600	Weak transcription	Fetal Heart	heart
30	chr10:220600-280800	Weak transcription	Gastric	stomach
31	chr10:222200-225800	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr10:222200-226200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr10:222600-226800	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr10:223000-229400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr10:223000-237800	Weak transcription	Psoas Muscle	Psoas
36	chr10:223200-224600	Weak transcription	Brain Angular Gyrus	brain
37	chr10:223200-224800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr10:223200-227000	Weak transcription	Fetal Muscle Leg	muscle
39	chr10:223400-224600	Weak transcription	Brain Hippocampus Middle	brain
40	chr10:223400-228000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr10:223600-225800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr10:223600-242800	Weak transcription	Aorta	Aorta
43	chr10:224000-226400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:224000-226600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr10:224200-226400	Weak transcription	Fetal Intestine Large	intestine
46	chr10:224200-226600	Weak transcription	A549	lung
47	chr10:224200-227200	Weak transcription	Primary T cells from cord blood	blood
48	chr10:224200-227200	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr10:224200-227800	Weak transcription	Brain Germinal Matrix	brain
50	chr10:224200-228000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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