Variant report

Variant	nsv515935
Chromosome Location	chr10:5820394-5869839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1341)
CpG islands
(count:611)
Chromatin interactive
region (count:118)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1341 , 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	chr10:5859616-5859936	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5851728-5852045	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5853087-5853351	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5855208-5855911	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5853061-5853443	K562	blood:	n/a	n/a
6	ARID3A	chr10:5848847-5849121	HepG2	liver:	n/a	n/a
7	ATF2	chr10:5854306-5854623	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr10:5861865-5862270	GM12878	blood:	n/a	n/a
9	ATF2	chr10:5855101-5856170	GM12878	blood:	n/a	n/a
10	ATF2	chr10:5855091-5856407	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr10:5855071-5855832	GM12878	blood:	n/a	n/a
12	ATF2	chr10:5859203-5859707	GM12878	blood:	n/a	n/a
13	ATF2	chr10:5859131-5859731	GM12878	blood:	n/a	n/a
14	ATF2	chr10:5855957-5856744	GM12878	blood:	n/a	n/a
15	ATF3	chr10:5855595-5855908	HepG2	liver:	n/a	chr10:5855642-5855651
16	BACH1	chr10:5855278-5856507	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:5856199-5856484	K562	blood:	n/a	n/a
18	BATF	chr10:5861887-5862254	GM12878	blood:	n/a	n/a
19	BATF	chr10:5859290-5859648	GM12878	blood:	n/a	n/a
20	BATF	chr10:5861790-5862457	GM12878	blood:	n/a	n/a
21	BCL11A	chr10:5859293-5859701	GM12878	blood:	n/a	n/a
22	BCL3	chr10:5855119-5855976	GM12878	blood:	n/a	chr10:5855137-5855150 chr10:5855451-5855464 chr10:5855323-5855332
23	BCL3	chr10:5855461-5856535	A549	lung:	n/a	chr10:5856027-5856036
24	BCLAF1	chr10:5857918-5858595	GM12878	blood:	n/a	n/a
25	BCLAF1	chr10:5855060-5856452	GM12878	blood:	n/a	chr10:5855137-5855150 chr10:5856027-5856036 chr10:5855451-5855464 chr10:5855323-5855332
26	BCLAF1	chr10:5859222-5859645	GM12878	blood:	n/a	n/a
27	BCLAF1	chr10:5854703-5856527	GM12878	blood:	n/a	chr10:5855137-5855150 chr10:5856027-5856036 chr10:5855451-5855464 chr10:5855323-5855332
28	BCLAF1	chr10:5859249-5859745	GM12878	blood:	n/a	n/a
29	BHLHE40	chr10:5853122-5853620	GM12878	blood:	n/a	n/a
30	BHLHE40	chr10:5859299-5859634	GM12878	blood:	n/a	n/a
31	BHLHE40	chr10:5858215-5858422	GM12878	blood:	n/a	n/a
32	BHLHE40	chr10:5855546-5855972	A549	lung:	n/a	n/a
33	BHLHE40	chr10:5855559-5855973	HepG2	liver:	n/a	n/a
34	BHLHE40	chr10:5854904-5856510	K562	blood:	n/a	chr10:5856331-5856340 chr10:5855115-5855131 chr10:5855131-5855147 chr10:5856325-5856346 chr10:5855450-5855466 chr10:5856331-5856340
35	BHLHE40	chr10:5855115-5856469	HepG2	liver:	n/a	chr10:5856331-5856340 chr10:5855115-5855131 chr10:5855131-5855147 chr10:5856325-5856346 chr10:5855450-5855466 chr10:5856331-5856340
36	BHLHE40	chr10:5855001-5856586	GM12878	blood:	n/a	chr10:5856331-5856340 chr10:5855115-5855131 chr10:5855131-5855147 chr10:5856325-5856346 chr10:5855450-5855466 chr10:5856331-5856340
37	BHLHE40	chr10:5854345-5854763	GM12878	blood:	n/a	n/a
38	BRCA1	chr10:5855193-5855954	GM12878	blood:	n/a	chr10:5855561-5855570
39	BRCA1	chr10:5855254-5856272	Hela-S3	cervix:	n/a	chr10:5855561-5855570
40	BRCA1	chr10:5855346-5856458	H1-hESC	embryonic stem cell:	n/a	chr10:5855561-5855570
41	BRCA1	chr10:5854603-5854800	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr10:5855223-5856033	HepG2	liver:	n/a	chr10:5855561-5855570
43	CBX3	chr10:5855698-5856485	K562	blood:	n/a	n/a
44	CBX3	chr10:5855130-5856534	K562	blood:	n/a	n/a
45	CCNT2	chr10:5854612-5856176	K562	blood:	n/a	chr10:5855150-5855159 chr10:5854874-5854883
46	CCNT2	chr10:5856544-5856744	K562	blood:	n/a	chr10:5856555-5856564
47	CEBPB	chr10:5829484-5829806	IMR90	lung:	n/a	n/a
48	CEBPB	chr10:5856543-5856945	H1-hESC	embryonic stem cell:	n/a	chr10:5856662-5856673 chr10:5856663-5856674
49	CEBPB	chr10:5855923-5856102	K562	blood:	n/a	n/a
50	CEBPB	chr10:5828060-5828312	K562	blood:	n/a	chr10:5828189-5828200

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5855588-5855638	MCF-7	breast:	n/a
2	chr10:5855588-5855638	MCF-7	breast:	n/a
3	chr10:5855475-5855525	HAEpiC	amniotic membrane:	n/a
4	chr10:5851600-5851650	K562	blood:	n/a
5	chr10:5855585-5855635	ovcar-3	ovarian:	n/a
6	chr10:5855675-5855725	SKMC	muscle:	n/a
7	chr10:5859460-5859510	GM19239	blood:	n/a
8	chr10:5855992-5856042	GM19239	blood:	n/a
9	chr10:5859460-5859510	HRE	kidney:	n/a
10	chr10:5855588-5855638	T-47D	breast:	n/a
11	chr10:5859460-5859510	NHDF-neo	bronchial:	n/a
12	chr10:5855588-5855638	ProgFib	skin:	n/a
13	chr10:5855475-5855525	ProgFib	skin:	n/a
14	chr10:5853447-5853497	Hepatocyte	liver:	n/a
15	chr10:5855475-5855525	MCF-7	breast:	n/a
16	chr10:5855992-5856042	K562	blood:	n/a
17	chr10:5855170-5855220	HIPEpiC	eye:	n/a
18	chr10:5855675-5855725	HEK293	kidney:	embryo
19	chr10:5855585-5855635	U87	brain:	n/a
20	chr10:5859460-5859510	HCPEpiC	choroid plexus:	n/a
21	chr10:5855009-5855059	IMR90	lung:	fetal
22	chr10:5859460-5859510	GM12892	blood:	n/a
23	chr10:5853447-5853497	HEK293	kidney:	embryo
24	chr10:5855585-5855635	NB4	blood:	n/a
25	chr10:5851600-5851650	GM12892	blood:	n/a
26	chr10:5859460-5859510	Hela-S3	cervix:	n/a
27	chr10:5851600-5851650	HRPEpiC	eye:	n/a
28	chr10:5855475-5855525	K562	blood:	n/a
29	chr10:5851600-5851650	SK-N-SH	brain:	n/a
30	chr10:5855675-5855725	U87	brain:	n/a
31	chr10:5855009-5855059	AG10803	skin:	n/a
32	chr10:5855588-5855638	BE2_C	brain:	n/a
33	chr10:5855009-5855059	H1-hESC	embryonic stem cell:	embryo
34	chr10:5855170-5855220	NHBE	bronchial:	n/a
35	chr10:5855675-5855725	SK-N-SH_RA	brain:	n/a
36	chr10:5859460-5859510	ECC-1	luminal epithelium:	n/a
37	chr10:5855992-5856042	AoSMC	blood vessel:	n/a
38	chr10:5853447-5853497	HNPCEpiC	eye:	n/a
39	chr10:5855475-5855525	H1-hESC	embryonic stem cell:	embryo
40	chr10:5859460-5859510	CMK	blood:	n/a
41	chr10:5855009-5855059	HRCEpiC	kidney:	n/a
42	chr10:5853447-5853497	H1-hESC	embryonic stem cell:	embryo
43	chr10:5855585-5855635	K562	blood:	n/a
44	chr10:5855170-5855220	NH-A	brain:	n/a
45	chr10:5859460-5859510	HepG2	liver:	n/a
46	chr10:5855170-5855220	GM06990	blood:	n/a
47	chr10:5855675-5855725	HCT-116	colon:	n/a
48	chr10:5859460-5859510	HIPEpiC	eye:	n/a
49	chr10:5855992-5856042	AG04450	lung:	fetal
50	chr10:5855475-5855525	NB4	blood:	n/a

(count:118 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:5840247..5841943-chr10:6244082..6246169,2	MCF-7	breast:
2	chr10:5849264..5850852-chr10:5930459..5932960,2	MCF-7	breast:
3	chr10:5864529..5867284-chr10:5869249..5871114,2	K562	blood:
4	chr10:5769286..5771166-chr10:5852816..5855046,2	K562	blood:
5	chr10:5708441..5709982-chr10:5853880..5856185,2	K562	blood:
6	chr10:5855392..5856073-chr16:57480920..57481571,2	HCT-116	colon:
7	chr10:5836323..5837944-chr10:5932347..5934576,2	K562	blood:
8	chr10:5833873..5836597-chr10:5841720..5845063,3	K562	blood:
9	chr10:5852595..5861125-chr10:5921136..5936216,31	MCF-7	breast:
10	chr10:5672014..5674575-chr10:5854060..5856479,2	MCF-7	breast:
11	chr10:5835592..5837932-chr10:5853752..5856634,3	K562	blood:
12	chr10:5822061..5824683-chr10:5847855..5850406,3	K562	blood:
13	chr10:5855140..5855745-chr6:26157980..26158656,2	Hela-S3	cervix:
14	chr10:5854450..5857183-chr10:5867124..5872976,6	MCF-7	breast:
15	chr10:5833873..5836597-chr10:5841720..5845063,3	K562	blood:
16	chr10:5841031..5843716-chr10:5843918..5845552,2	MCF-7	breast:
17	chr10:5725427..5729550-chr10:5853446..5856157,4	MCF-7	breast:
18	chr10:5814904..5817152-chr10:5861494..5864135,2	K562	blood:
19	chr10:5851570..5858995-chr10:5881654..5887342,9	K562	blood:
20	chr10:5854507..5855433-chr14:96968652..96969152,2	Hela-S3	cervix:
21	chr10:5728149..5729932-chr10:5839231..5841919,2	K562	blood:
22	chr10:5809558..5811083-chr10:5837217..5839027,2	MCF-7	breast:
23	chr10:5852473..5857853-chr10:5880942..5888645,8	MCF-7	breast:
24	chr10:5830187..5831718-chr10:5849725..5851751,2	K562	blood:
25	chr10:5839916..5843685-chr10:5848628..5853676,5	K562	blood:
26	chr10:5864529..5867284-chr10:5869249..5871114,2	K562	blood:
27	chr10:5809711..5811648-chr10:5855446..5857250,2	K562	blood:
28	chr10:5841980..5844348-chr10:5846040..5847807,2	MCF-7	breast:
29	chr10:5813790..5816403-chr10:5853643..5855335,2	MCF-7	breast:
30	chr10:5857210..5863651-chr10:5869000..5872361,6	MCF-7	breast:
31	chr10:5832214..5833980-chr10:5854681..5856521,2	MCF-7	breast:
32	chr10:5830218..5833166-chr10:5848485..5851225,2	K562	blood:
33	chr10:5841980..5844348-chr10:5846040..5847807,2	MCF-7	breast:
34	chr10:5841240..5842768-chr10:5845770..5847273,2	K562	blood:
35	chr10:5805727..5811403-chr10:5852267..5856532,7	MCF-7	breast:
36	chr10:5860095..5862542-chr10:5886681..5888594,2	MCF-7	breast:
37	chr10:5828777..5831652-chr10:5835784..5837888,2	K562	blood:
38	chr10:5867636..5869273-chr10:5869585..5872452,2	K562	blood:
39	chr10:5831817..5834005-chr10:5852525..5854271,2	K562	blood:
40	chr10:5831817..5834005-chr10:5852525..5854271,2	K562	blood:
41	chr10:5854666..5855862-chr15:65588031..65589114,3	Hela-S3	cervix:
42	chr10:5842019..5844066-chr10:5854494..5856804,2	K562	blood:
43	chr10:5844325..5846252-chr10:5848114..5849873,2	K562	blood:
44	chr10:5804502..5807044-chr10:5833917..5836570,2	K562	blood:
45	chr10:5867768..5870710-chr10:5870936..5873255,3	MCF-7	breast:
46	chr10:5850191..5852972-chr10:5915096..5916950,2	K562	blood:
47	chr10:5855076..5855594-chr5:43514799..43515487,2	Hela-S3	cervix:
48	chr10:5795617..5797655-chr10:5843237..5845319,2	K562	blood:
49	chr10:5854680..5855483-chr9:130486469..130487269,2	Hela-S3	cervix:
50	chr10:5835385..5837024-chr10:5893151..5895747,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM208B-5	chr10:5856190-5856404	ENSG00000272764.1
2	lnc-FAM208B-5	chr10:5855948-5856008	ENSG00000272764.1

No data

Variant related genes	Relation type
ENSG00000272764	TF binding region
GDI2	TF binding region
ENSG00000272764	CpG island
GDI2	CpG island
ENSG00000260806	chromatin interactions
ENSG00000169398	chromatin interactions
ENSG00000213994	chromatin interactions
ENSG00000240577	chromatin interactions
ENSG00000005194	chromatin interactions
ENSG00000228685	chromatin interactions
ENSG00000141934	chromatin interactions
ENSG00000187024	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000240180	chromatin interactions
ENSG00000170525	chromatin interactions
ENSG00000196372	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000088682	chromatin interactions
ENSG00000134470	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000108021	chromatin interactions
ENSG00000167384	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000203499	chromatin interactions
ENSG00000134452	chromatin interactions
ENSG00000248240	chromatin interactions
ENSG00000272764	chromatin interactions
ENSG00000270427	chromatin interactions
ENSG00000134461	chromatin interactions

Extended variants
information (count: 2088 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2088 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4748916	chr10:5820394-5820395	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72772362	chr10:5820395-5820396	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575281013	chr10:5820402-5820403	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs536924514	chr10:5820440-5820441	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs558845324	chr10:5820474-5820475	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs201771584	chr10:5820577-5820578	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs200421415	chr10:5820578-5820579	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs576926011	chr10:5820676-5820677	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs541240726	chr10:5820678-5820679	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs559147210	chr10:5820687-5820688	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs574578872	chr10:5820706-5820707	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs1567708	chr10:5820741-5820742	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189001200	chr10:5820767-5820768	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs530556589	chr10:5820786-5820787	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs149385456	chr10:5820827-5820828	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs138378243	chr10:5820832-5820833	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs564824495	chr10:5820885-5820886	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs144745727	chr10:5820886-5820887	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs10795544	chr10:5820897-5820898	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs182559052	chr10:5820927-5820928	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs368051541	chr10:5820989-5820990	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs148499673	chr10:5821004-5821005	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187171634	chr10:5821022-5821023	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539460778	chr10:5821023-5821024	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192094998	chr10:5821026-5821027	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570724358	chr10:5821033-5821034	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9702384	chr10:5821061-5821062	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577519633	chr10:5821082-5821083	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs180892711	chr10:5821141-5821142	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145356250	chr10:5821154-5821155	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574714654	chr10:5821166-5821167	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538410548	chr10:5821180-5821181	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs72772365	chr10:5821202-5821203	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs147733586	chr10:5821203-5821204	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35386932	chr10:5821231-5821232	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184971429	chr10:5821245-5821246	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190216695	chr10:5821286-5821287	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117203792	chr10:5821328-5821329	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182478918	chr10:5821339-5821340	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540616467	chr10:5821386-5821387	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141069797	chr10:5821395-5821396	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529477774	chr10:5821426-5821427	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112922889	chr10:5821428-5821429	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114311827	chr10:5821455-5821456	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114176145	chr10:5821460-5821461	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79047368	chr10:5821473-5821474	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs118076128	chr10:5821475-5821476	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4237365	chr10:5821484-5821485	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs566802539	chr10:5821519-5821520	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560054071	chr10:5821524-5821525	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2001 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5762600-5843400	Strong transcription	Dnd41	blood
2	chr10:5762800-5843000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr10:5768000-5849400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:5796000-5822400	Strong transcription	Fetal Intestine Large	intestine
5	chr10:5797400-5847400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr10:5798000-5842800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:5798200-5843000	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr10:5798600-5842800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr10:5805000-5843200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr10:5807400-5821800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:5808400-5826400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr10:5808800-5825800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr10:5809000-5824400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr10:5810400-5824800	Weak transcription	Ovary	ovary
15	chr10:5811800-5824400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr10:5812000-5823800	Weak transcription	Fetal Kidney	kidney
17	chr10:5812000-5824000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:5812400-5821600	Weak transcription	Brain Germinal Matrix	brain
19	chr10:5814600-5822600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr10:5817200-5831200	Weak transcription	Pancreas	Pancrea
21	chr10:5817400-5821000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr10:5817800-5821800	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr10:5817800-5825000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr10:5817800-5826200	Weak transcription	HMEC	breast
25	chr10:5818000-5824600	Weak transcription	Colonic Mucosa	Colon
26	chr10:5818000-5824600	Weak transcription	Gastric	stomach
27	chr10:5818000-5826400	Weak transcription	Esophagus	oesophagus
28	chr10:5818000-5854200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr10:5818200-5823600	Weak transcription	Placenta	Placenta
30	chr10:5818200-5824200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr10:5818200-5824200	Weak transcription	Fetal Brain Male	brain
32	chr10:5818200-5824800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr10:5818400-5820400	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr10:5818400-5820400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr10:5818400-5821600	Weak transcription	Fetal Stomach	stomach
36	chr10:5818400-5821800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr10:5818400-5821800	Weak transcription	Left Ventricle	heart
38	chr10:5818400-5821800	Weak transcription	Lung	lung
39	chr10:5818400-5822400	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr10:5818400-5823600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr10:5818400-5823800	Weak transcription	Fetal Muscle Trunk	muscle
42	chr10:5818400-5824000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr10:5818400-5824000	Weak transcription	Brain Anterior Caudate	brain
44	chr10:5818400-5824000	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr10:5818400-5824200	Weak transcription	Fetal Brain Female	brain
46	chr10:5818400-5824600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr10:5818400-5826200	Weak transcription	Hela-S3	cervix
48	chr10:5818400-5826400	Weak transcription	Aorta	Aorta
49	chr10:5818400-5826400	Weak transcription	Spleen	Spleen
50	chr10:5818400-5842800	Strong transcription	Duodenum Mucosa	Duodenum

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