Variant report

Variant	esv35082
Chromosome Location	chr10:5665774-5716858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1275)
CpG islands
(count:1893)
Chromatin interactive
region (count:161)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5701790-5702333	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5710369-5710645	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5674430-5674670	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5687310-5687479	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5669701-5669799	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:5707453-5707725	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:5705962-5706115	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:5701164-5701572	HepG2	liver:	n/a	n/a
9	ATF3	chr10:5701883-5702096	K562	blood:	n/a	n/a
10	ATF3	chr10:5708602-5709006	A549	lung:	n/a	n/a
11	ATF3	chr10:5708504-5708755	HepG2	liver:	n/a	n/a
12	ATF3	chr10:5708448-5708805	K562	blood:	n/a	n/a
13	ATF3	chr10:5701787-5702111	K562	blood:	n/a	n/a
14	BACH1	chr10:5707878-5708540	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr10:5689892-5690986	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr10:5668087-5668358	GM12878	blood:	n/a	chr10:5668206-5668217
17	BATF	chr10:5670758-5671129	GM12878	blood:	n/a	n/a
18	BATF	chr10:5671298-5671685	GM12878	blood:	n/a	chr10:5671497-5671508
19	BATF	chr10:5701623-5702127	GM12878	blood:	n/a	n/a
20	BCL3	chr10:5708804-5709189	GM12878	blood:	n/a	n/a
21	BCL3	chr10:5708858-5709224	GM12878	blood:	n/a	n/a
22	BHLHE40	chr10:5701024-5702625	HepG2	liver:	n/a	n/a
23	BHLHE40	chr10:5707876-5708313	K562	blood:	n/a	n/a
24	BHLHE40	chr10:5701799-5702319	K562	blood:	n/a	n/a
25	BHLHE40	chr10:5701989-5702001	A549	lung:	n/a	n/a
26	BHLHE40	chr10:5674486-5674734	HepG2	liver:	n/a	n/a
27	BHLHE40	chr10:5707938-5708371	HepG2	liver:	n/a	n/a
28	BHLHE40	chr10:5708641-5709243	HepG2	liver:	n/a	n/a
29	BHLHE40	chr10:5711632-5711940	K562	blood:	n/a	n/a
30	BHLHE40	chr10:5708587-5709192	K562	blood:	n/a	n/a
31	BRCA1	chr10:5708541-5708817	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr10:5708655-5708931	HepG2	liver:	n/a	n/a
33	BRCA1	chr10:5701399-5701533	HepG2	liver:	n/a	n/a
34	CBX3	chr10:5716240-5716561	K562	blood:	n/a	n/a
35	CCNT2	chr10:5707836-5708803	K562	blood:	n/a	n/a
36	CCNT2	chr10:5711612-5711848	K562	blood:	n/a	n/a
37	CEBPB	chr10:5685566-5685753	K562	blood:	n/a	chr10:5685620-5685631
38	CEBPB	chr10:5707556-5708606	A549	lung:	n/a	chr10:5707632-5707643
39	CEBPB	chr10:5701386-5702563	MCF-7	breast:	n/a	n/a
40	CEBPB	chr10:5685475-5685681	HepG2	liver:	n/a	chr10:5685620-5685631
41	CEBPB	chr10:5707621-5708410	K562	blood:	n/a	chr10:5707632-5707643
42	CEBPB	chr10:5669464-5669914	HepG2	liver:	n/a	chr10:5669608-5669619
43	CEBPB	chr10:5674382-5674755	A549	lung:	n/a	n/a
44	CEBPB	chr10:5708056-5708323	K562	blood:	n/a	n/a
45	CEBPB	chr10:5674443-5674725	IMR90	lung:	n/a	n/a
46	CEBPB	chr10:5674408-5674656	HepG2	liver:	n/a	n/a
47	CEBPB	chr10:5701805-5702140	K562	blood:	n/a	n/a
48	CEBPB	chr10:5674330-5674853	HCT-116	colon:	n/a	n/a
49	CEBPB	chr10:5707682-5708415	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr10:5701572-5701675	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5683763-5683813	HEEpiC	esophagus:	n/a
2	chr10:5693432-5693482	AG09309	skin:	n/a
3	chr10:5683763-5683813	HEEpiC	esophagus:	n/a
4	chr10:5693432-5693482	AG09309	skin:	n/a
5	chr10:5688620-5688670	NH-A	brain:	n/a
6	chr10:5666739-5666789	HEEpiC	esophagus:	n/a
7	chr10:5681208-5681258	LNCaP	prostate:	n/a
8	chr10:5707981-5708031	HCM	heart:	n/a
9	chr10:5683916-5683966	HCF	heart:	n/a
10	chr10:5666739-5666789	AG09319	gingival:	n/a
11	chr10:5688620-5688670	HL-60	blood:	n/a
12	chr10:5667028-5667078	HRCEpiC	kidney:	n/a
13	chr10:5682262-5682312	HCF	heart:	n/a
14	chr10:5688470-5688520	PFSK-1	brain:	n/a
15	chr10:5688620-5688670	SKMC	muscle:	n/a
16	chr10:5693331-5693381	ECC-1	luminal epithelium:	n/a
17	chr10:5688515-5688565	HCPEpiC	choroid plexus:	n/a
18	chr10:5681092-5681142	Caco-2	colon:	n/a
19	chr10:5707799-5707849	SK-N-SH	brain:	n/a
20	chr10:5708797-5708847	PANC-1	pancreas:	n/a
21	chr10:5666739-5666789	U87	brain:	n/a
22	chr10:5682262-5682312	HRE	kidney:	n/a
23	chr10:5688515-5688565	AG09319	gingival:	n/a
24	chr10:5690971-5691021	K562	blood:	n/a
25	chr10:5683763-5683813	NHDF-neo	bronchial:	n/a
26	chr10:5682262-5682312	GM12878	blood:	n/a
27	chr10:5708327-5708377	GM19239	blood:	n/a
28	chr10:5708327-5708377	IMR90	lung:	fetal
29	chr10:5690914-5690964	HEK293	kidney:	embryo
30	chr10:5708674-5708724	SK-N-SH	brain:	n/a
31	chr10:5666739-5666789	HL-60	blood:	n/a
32	chr10:5710888-5710938	AG10803	skin:	n/a
33	chr10:5707799-5707849	U87	brain:	n/a
34	chr10:5666739-5666789	HepG2	liver:	n/a
35	chr10:5708765-5708815	SK-N-SH	brain:	n/a
36	chr10:5683916-5683966	GM12892	blood:	n/a
37	chr10:5688515-5688565	Hepatocyte	liver:	n/a
38	chr10:5688620-5688670	HIPEpiC	eye:	n/a
39	chr10:5693432-5693482	NT2-D1	testis:	n/a
40	chr10:5671107-5671157	HIPEpiC	eye:	n/a
41	chr10:5688620-5688670	GM12878	blood:	n/a
42	chr10:5708674-5708724	NT2-D1	testis:	n/a
43	chr10:5690971-5691021	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:5707981-5708031	RPTEC	kidney:	n/a
45	chr10:5683916-5683966	K562	blood:	n/a
46	chr10:5708327-5708377	Caco-2	colon:	n/a
47	chr10:5708797-5708847	BJ	skin:	n/a
48	chr10:5688620-5688670	T-47D	breast:	n/a
49	chr10:5690971-5691021	SKMC	muscle:	n/a
50	chr10:5682262-5682312	MCF10A-Er-Src	breast:	n/a

(count:161 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr10:5541719..5543881-chr10:5694869..5697799,2	MCF-7	breast:
2	chr10:5665389..5668245-chr10:5681455..5685230,3	MCF-7	breast:
3	chr10:5539704..5542101-chr10:5707355..5709721,2	MCF-7	breast:
4	chr10:5689201..5692930-chr10:5693365..5696384,5	MCF-7	breast:
5	chr10:5534278..5536175-chr10:5709413..5711333,2	MCF-7	breast:
6	chr10:5695046..5697803-chr10:5701163..5704178,3	K562	blood:
7	chr10:5483932..5485882-chr10:5690922..5692910,2	MCF-7	breast:
8	chr10:5696053..5698803-chr10:5727232..5729360,2	K562	blood:
9	chr10:5672469..5675172-chr10:5707074..5708649,2	K562	blood:
10	chr10:5533350..5536301-chr10:5674963..5676854,2	MCF-7	breast:
11	chr10:5673292..5677112-chr10:5724421..5727333,4	K562	blood:
12	chr10:5593662..5595801-chr10:5669870..5671896,3	MCF-7	breast:
13	chr10:5623488..5628108-chr10:5662504..5666628,7	MCF-7	breast:
14	chr10:5679760..5682702-chr10:5686083..5689402,3	MCF-7	breast:
15	chr10:5694967..5699050-chr10:5700246..5704500,5	K562	blood:
16	chr10:5708098..5708636-chr5:43483746..43484576,2	Hela-S3	cervix:
17	chr10:5589918..5590450-chr10:5701824..5702522,2	MCF-7	breast:
18	chr10:5685269..5687615-chr10:5700766..5703664,2	K562	blood:
19	chr10:5685269..5687615-chr10:5700766..5703664,2	K562	blood:
20	chr10:5670551..5672473-chr10:5683404..5685273,2	MCF-7	breast:
21	chr10:5667968..5670611-chr10:5726547..5729408,2	K562	blood:
22	chr10:5630058..5631900-chr10:5703072..5705315,2	MCF-7	breast:
23	chr10:5694967..5699050-chr10:5700246..5704500,5	K562	blood:
24	chr10:5486956..5489810-chr10:5700664..5703642,2	MCF-7	breast:
25	chr10:5693572..5694560-chr10:5701990..5702791,2	MCF-7	breast:
26	chr10:5687724..5689255-chr10:5700903..5703551,2	K562	blood:
27	chr10:5538324..5539171-chr10:5702082..5702946,2	MCF-7	breast:
28	chr10:5691710..5696017-chr10:5704918..5709884,5	K562	blood:
29	chr10:5586583..5591953-chr10:5698330..5703488,13	MCF-7	breast:
30	chr10:5681863..5687705-chr10:5689280..5694830,6	K562	blood:
31	chr10:5487091..5489925-chr10:5665112..5666919,2	K562	blood:
32	chr10:5708283..5708927-chr16:31470241..31471151,2	Hela-S3	cervix:
33	chr10:5491006..5493868-chr10:5664560..5666317,3	K562	blood:
34	chr10:5708070..5709600-chr10:5714196..5716454,2	K562	blood:
35	chr10:5706894..5712025-chr10:5724987..5728504,7	MCF-7	breast:
36	chr10:5688504..5689004-chr19:2050803..2051309,2	Hela-S3	cervix:
37	chr10:5538295..5539248-chr10:5701936..5702508,5	MCF-7	breast:
38	chr10:5672014..5674575-chr10:5854060..5856479,2	MCF-7	breast:
39	chr10:5679152..5681152-chr10:5682870..5684955,2	MCF-7	breast:
40	chr10:5672469..5675172-chr10:5707074..5708649,2	K562	blood:
41	chr10:5696591..5698219-chr10:5706106..5707832,2	K562	blood:
42	chr10:5530065..5530714-chr10:5701918..5702531,2	MCF-7	breast:
43	chr10:5694251..5695909-chr10:5704918..5707656,2	K562	blood:
44	chr10:5691457..5694675-chr10:5697614..5700530,3	K562	blood:
45	chr10:5664947..5667027-chr10:5854331..5857046,2	MCF-7	breast:
46	chr10:5668872..5673126-chr10:5707160..5709989,4	MCF-7	breast:
47	chr10:5595300..5599425-chr10:5700368..5703903,3	MCF-7	breast:
48	chr10:5686229..5688364-chr10:5688975..5690846,2	MCF-7	breast:
49	chr10:5488364..5489916-chr10:5672026..5673861,2	K562	blood:
50	chr10:5679095..5680812-chr10:5681190..5683010,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDI2-4	chr10:5698831-5699156	NONHSAT011172
2	lnc-ASB13-5	chr10:5677980-5678087	NONHSAT011162
3	lnc-GDI2-5	chr10:5692701-5692762	NONHSAT011171
4	lnc-GDI2-5	chr10:5691656-5691766	NONHSAT011171
5	lnc-FAM208B-7	chr10:5666587-5666905	NONHSAT011167
6	lnc-GDI2-4	chr10:5699900-5700130	NONHSAT011172
7	lnc-FAM208B-7	chr10:5667817-5667847	NONHSAT011167
8	lnc-FAM208B-6	chr10:5673426-5673716	NONHSAT011169
9	lnc-GDI2-5	chr10:5692283-5692405	NONHSAT011171
10	lnc-FAM208B-4	chr10:5707302-5707309	l_247_chr10:5707185-5708703_testes
11	lnc-FAM208B-4	chr10:5707186-5707298	l_247_chr10:5707185-5708703_testes
12	lnc-GDI2-5	chr10:5690444-5690700	NONHSAT011171
13	lnc-FAM208B-4	chr10:5707823-5708703	l_247_chr10:5707185-5708703_testes
14	lnc-GDI2-5	chr10:5692077-5692136	NONHSAT011171
15	lnc-GDI2-4	chr10:5699270-5699369	NONHSAT011172
16	lnc-ASB13-5	chr10:5677111-5677548	NONHSAT011162

No data

Variant related genes	Relation type
ASB13	TF binding region
ENSG00000228685	TF binding region
RN7SL445P	TF binding region
ASB13	CpG island
ENSG00000228685	CpG island
RN7SL445P	CpG island
ENSG00000134452	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000226647	chromatin interactions
ENSG00000228685	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000240577	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000099875	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000228951	chromatin interactions
ENSG00000178372	chromatin interactions
ENSG00000270427	chromatin interactions
ENSG00000134461	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000260267	chromatin interactions

Extended variants
information (count: 2336 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2336 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17141741	chr10:5665774-5665775	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
2	rs184099402	chr10:5665800-5665801	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs571805564	chr10:5665835-5665836	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs559386144	chr10:5665883-5665884	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs187014839	chr10:5665899-5665900	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs554429848	chr10:5665911-5665912	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs572618369	chr10:5665917-5665918	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs536270718	chr10:5665955-5665956	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs375816606	chr10:5665962-5665963	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs12771305	chr10:5665966-5665967	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs144479231	chr10:5666008-5666009	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs558656901	chr10:5666011-5666012	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs572173733	chr10:5666123-5666124	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs543505457	chr10:5666141-5666142	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs192267627	chr10:5666144-5666145	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs373133238	chr10:5666169-5666170	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs111248553	chr10:5666198-5666199	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs560416368	chr10:5666208-5666209	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs140393656	chr10:5666209-5666210	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs542651373	chr10:5666211-5666212	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs548189497	chr10:5666216-5666217	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs190065654	chr10:5666284-5666285	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs35369411	chr10:5666384-5666385	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs56243537	chr10:5666409-5666410	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs532755132	chr10:5666440-5666441	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs547648886	chr10:5666507-5666508	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs369268882	chr10:5666509-5666510	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs12777494	chr10:5666527-5666528	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs11255736	chr10:5666576-5666577	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs144356532	chr10:5666588-5666589	Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
31	rs115721162	chr10:5666610-5666611	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
32	rs551191497	chr10:5666612-5666613	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
33	rs534693428	chr10:5666654-5666655	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs553371986	chr10:5666656-5666657	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs558995338	chr10:5666673-5666674	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
36	rs570995096	chr10:5666710-5666711	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
37	rs185614164	chr10:5666711-5666712	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs545189139	chr10:5666735-5666736	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
39	rs147759294	chr10:5666738-5666739	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
40	rs148405353	chr10:5666739-5666740	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
41	rs114071621	chr10:5666744-5666745	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
42	rs542937381	chr10:5666760-5666761	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
43	rs113966377	chr10:5666776-5666777	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs189278038	chr10:5666779-5666780	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
45	rs142662477	chr10:5666783-5666784	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
46	rs76155720	chr10:5666804-5666805	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
47	rs565015552	chr10:5666845-5666846	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
48	rs532064506	chr10:5666854-5666855	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
49	rs180873283	chr10:5666872-5666873	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
50	rs140901092	chr10:5666914-5666915	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	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
Breast cancer	17133270	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
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Ovarian cancer	22355333	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2061 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5658000-5673600	Weak transcription	Left Ventricle	heart
2	chr10:5661600-5667800	Weak transcription	HSMMtube	muscle
3	chr10:5661600-5670000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:5661600-5670200	Weak transcription	Right Atrium	heart
5	chr10:5662200-5669800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:5662200-5670600	Weak transcription	Fetal Lung	lung
7	chr10:5662600-5668400	Weak transcription	NH-A	brain
8	chr10:5662800-5666600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:5662800-5667800	Weak transcription	Ovary	ovary
10	chr10:5663400-5669800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:5663800-5665800	Enhancers	Adipose Nuclei	Adipose
12	chr10:5664000-5665800	Enhancers	Fetal Muscle Leg	muscle
13	chr10:5664000-5670200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:5664400-5665800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:5664800-5666000	Enhancers	Fetal Muscle Trunk	muscle
16	chr10:5665000-5665800	Enhancers	Liver	Liver
17	chr10:5665000-5665800	Enhancers	Fetal Thymus	thymus
18	chr10:5665000-5665800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr10:5665000-5665800	Enhancers	Hela-S3	cervix
20	chr10:5665000-5666000	Enhancers	Fetal Intestine Large	intestine
21	chr10:5665200-5666400	Weak transcription	Spleen	Spleen
22	chr10:5665200-5667800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:5665200-5668400	Weak transcription	NHDF-Ad	bronchial
24	chr10:5665200-5670200	Weak transcription	Esophagus	oesophagus
25	chr10:5665200-5670200	Weak transcription	Osteobl	bone
26	chr10:5665200-5671800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr10:5665200-5681800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr10:5665400-5667800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr10:5665400-5668000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:5665400-5668400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr10:5665400-5670400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr10:5665400-5672600	Weak transcription	Lung	lung
33	chr10:5665400-5673800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr10:5665400-5680400	Weak transcription	Brain Hippocampus Middle	brain
35	chr10:5665400-5680600	Weak transcription	Fetal Brain Female	brain
36	chr10:5665600-5665800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr10:5665600-5665800	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr10:5665600-5666600	Weak transcription	Pancreas	Pancrea
39	chr10:5665600-5667800	Weak transcription	Psoas Muscle	Psoas
40	chr10:5665600-5667800	Weak transcription	HSMM	muscle
41	chr10:5665600-5668000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr10:5665600-5668000	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr10:5665600-5668000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr10:5665600-5668200	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr10:5665600-5668200	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr10:5665600-5668200	Weak transcription	Stomach Mucosa	stomach
47	chr10:5665600-5668400	Weak transcription	Gastric	stomach
48	chr10:5665600-5668400	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr10:5665600-5669800	Weak transcription	Aorta	Aorta
50	chr10:5665600-5669800	Weak transcription	Fetal Intestine Small	intestine

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