Variant report

Variant	nsv598753
Chromosome Location	chr5:81031741-81491087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6273)
CpG islands
(count:2811)
Chromatin interactive
region (count:377)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6273 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:81047152-81047393	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:81204671-81204944	K562	blood:	n/a	n/a
3	ARID3A	chr5:81055533-81055748	K562	blood:	n/a	n/a
4	ARID3A	chr5:81057808-81058184	K562	blood:	n/a	n/a
5	ARID3A	chr5:81059347-81059740	K562	blood:	n/a	n/a
6	ARID3A	chr5:81461745-81462065	K562	blood:	n/a	n/a
7	ARID3A	chr5:81403142-81403371	K562	blood:	n/a	n/a
8	ARID3A	chr5:81149050-81149611	K562	blood:	n/a	n/a
9	ARID3A	chr5:81074562-81075067	K562	blood:	n/a	n/a
10	ARID3A	chr5:81049568-81051331	K562	blood:	n/a	n/a
11	ARID3A	chr5:81144264-81144508	K562	blood:	n/a	n/a
12	ARID3A	chr5:81056958-81057213	K562	blood:	n/a	n/a
13	ARID3A	chr5:81147301-81148022	K562	blood:	n/a	n/a
14	ARID3A	chr5:81059998-81060002	K562	blood:	n/a	n/a
15	ARID3A	chr5:81407108-81407356	K562	blood:	n/a	n/a
16	ARID3A	chr5:81266897-81267196	HepG2	liver:	n/a	n/a
17	ARID3A	chr5:81261048-81261303	K562	blood:	n/a	n/a
18	ARID3A	chr5:81149841-81151200	K562	blood:	n/a	chr5:81150291-81150307 chr5:81150415-81150431
19	ARID3A	chr5:81455026-81455045	K562	blood:	n/a	n/a
20	ARID3A	chr5:81267493-81268095	HepG2	liver:	n/a	n/a
21	ARID3A	chr5:81134311-81134719	K562	blood:	n/a	n/a
22	ARID3A	chr5:81115408-81115443	K562	blood:	n/a	n/a
23	ARID3A	chr5:81047100-81047417	K562	blood:	n/a	n/a
24	ARID3A	chr5:81250707-81250923	K562	blood:	n/a	n/a
25	ARID3A	chr5:81404945-81405115	HepG2	liver:	n/a	n/a
26	ARID3A	chr5:81461748-81462101	HepG2	liver:	n/a	n/a
27	ARID3A	chr5:81152725-81153030	K562	blood:	n/a	n/a
28	ARID3A	chr5:81048263-81048618	K562	blood:	n/a	n/a
29	ARID3A	chr5:81204448-81204457	K562	blood:	n/a	n/a
30	ARID3A	chr5:81054562-81054991	K562	blood:	n/a	n/a
31	ATF1	chr5:81469999-81470209	K562	blood:	n/a	n/a
32	ATF1	chr5:81150785-81150886	K562	blood:	n/a	n/a
33	ATF1	chr5:81204610-81204948	K562	blood:	n/a	n/a
34	ATF1	chr5:81250662-81250964	K562	blood:	n/a	n/a
35	ATF1	chr5:81267500-81268041	K562	blood:	n/a	n/a
36	ATF1	chr5:81147648-81148002	K562	blood:	n/a	n/a
37	ATF1	chr5:81407071-81407380	K562	blood:	n/a	n/a
38	ATF1	chr5:81461711-81462098	K562	blood:	n/a	n/a
39	ATF1	chr5:81451198-81451217	K562	blood:	n/a	n/a
40	ATF1	chr5:81167745-81167755	K562	blood:	n/a	n/a
41	ATF1	chr5:81194316-81194639	K562	blood:	n/a	n/a
42	ATF1	chr5:81057199-81058024	K562	blood:	n/a	n/a
43	ATF1	chr5:81046732-81047309	K562	blood:	n/a	n/a
44	ATF1	chr5:81078679-81078991	K562	blood:	n/a	n/a
45	ATF2	chr5:81469783-81470369	GM12878	blood:	n/a	n/a
46	ATF2	chr5:81461696-81462135	GM12878	blood:	n/a	n/a
47	ATF2	chr5:81267512-81268373	GM12878	blood:	n/a	n/a
48	ATF2	chr5:81147632-81148074	GM12878	blood:	n/a	n/a
49	ATF2	chr5:81461697-81462036	GM12878	blood:	n/a	n/a
50	ATF2	chr5:81461678-81462173	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2811 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:81160426-81160476	HIPEpiC	eye:	n/a
2	chr5:81046758-81046808	HMEC	breast:	n/a
3	chr5:81267935-81267985	SKMC	muscle:	n/a
4	chr5:81160426-81160476	SK-N-SH_RA	brain:	n/a
5	chr5:81051199-81051249	HIPEpiC	eye:	n/a
6	chr5:81160426-81160476	HIPEpiC	eye:	n/a
7	chr5:81046758-81046808	HMEC	breast:	n/a
8	chr5:81267935-81267985	SKMC	muscle:	n/a
9	chr5:81160426-81160476	SK-N-SH_RA	brain:	n/a
10	chr5:81051199-81051249	HIPEpiC	eye:	n/a
11	chr5:81043172-81043222	Hela-S3	cervix:	n/a
12	chr5:81047249-81047299	HIPEpiC	eye:	n/a
13	chr5:81160426-81160476	HCM	heart:	n/a
14	chr5:81147781-81147831	A549	lung:	n/a
15	chr5:81075060-81075110	IMR90	lung:	fetal
16	chr5:81047188-81047238	ProgFib	skin:	n/a
17	chr5:81047246-81047296	H1-hESC	embryonic stem cell:	embryo
18	chr5:81048305-81048355	ProgFib	skin:	n/a
19	chr5:81047249-81047299	AG04450	lung:	fetal
20	chr5:81269189-81269239	PrEC	prostate:	n/a
21	chr5:81048305-81048355	HRE	kidney:	n/a
22	chr5:81063103-81063153	HUVEC	blood vessel:	n/a
23	chr5:81045966-81046016	ECC-1	luminal epithelium:	n/a
24	chr5:81045418-81045468	PFSK-1	brain:	n/a
25	chr5:81267704-81267754	HCF	heart:	n/a
26	chr5:81047486-81047536	NT2-D1	testis:	n/a
27	chr5:81047184-81047234	HL-60	blood:	n/a
28	chr5:81267578-81267628	NH-A	brain:	n/a
29	chr5:81342312-81342362	Jurkat	blood:	n/a
30	chr5:81047486-81047536	PrEC	prostate:	n/a
31	chr5:81320947-81320997	ECC-1	luminal epithelium:	n/a
32	chr5:81267578-81267628	T-47D	breast:	n/a
33	chr5:81133592-81133642	K562	blood:	n/a
34	chr5:81047188-81047238	NH-A	brain:	n/a
35	chr5:81146787-81146837	AG09319	gingival:	n/a
36	chr5:81047184-81047234	HAEpiC	amniotic membrane:	n/a
37	chr5:81152212-81152262	GM12892	blood:	n/a
38	chr5:81149002-81149052	U87	brain:	n/a
39	chr5:81149002-81149052	LNCaP	prostate:	n/a
40	chr5:81269189-81269239	RPTEC	kidney:	n/a
41	chr5:81470056-81470106	HCPEpiC	choroid plexus:	n/a
42	chr5:81149002-81149052	Caco-2	colon:	n/a
43	chr5:81047246-81047296	HMEC	breast:	n/a
44	chr5:81082946-81082996	NB4	blood:	n/a
45	chr5:81452987-81453037	AoSMC	blood vessel:	n/a
46	chr5:81047246-81047296	AG04450	lung:	fetal
47	chr5:81267935-81267985	LNCaP	prostate:	n/a
48	chr5:81046408-81046458	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:81047249-81047299	HUVEC	blood vessel:	n/a
50	chr5:81046408-81046458	NHDF-neo	bronchial:	n/a

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Distal block	Cell Line	Cell type
1	chr5:81081244..81081894-chr5:81461502..81462199,2	MCF-7	breast:
2	chr14:78266259..78267034-chr5:81267621..81268405,2	Hela-S3	cervix:
3	chr5:81087872..81090171-chr5:81298580..81301554,2	K562	blood:
4	chr5:81041366..81043872-chr5:81148506..81150879,2	MCF-7	breast:
5	chr19:17829859..17830727-chr5:81268250..81268757,2	Hela-S3	cervix:
6	chr5:81111778..81114275-chr5:81117590..81119741,3	K562	blood:
7	chr5:81148447..81151496-chr5:81159857..81162688,3	K562	blood:
8	chr5:81045699..81050245-chr5:81142897..81150556,22	MCF-7	breast:
9	chr1:197170273..197170845-chr5:81268356..81268871,2	Hela-S3	cervix:
10	chr5:81267350..81269478-chr5:81326653..81329634,2	K562	blood:
11	chr5:81267902..81269890-chr5:81297469..81300441,2	K562	blood:
12	chr5:81047531..81050440-chr5:81268054..81269557,2	K562	blood:
13	chr5:81450171..81453125-chr5:81456829..81460107,3	K562	blood:
14	chr5:81121370..81123662-chr5:81126128..81128513,2	K562	blood:
15	chr5:81047090..81048060-chr5:81147785..81148575,2	NB4	blood:
16	chr5:81324799..81327472-chr5:81331097..81332975,2	K562	blood:
17	chr5:81080822..81081725-chr5:81150091..81150639,2	MCF-7	breast:
18	chr5:81369418..81371722-chr5:81372983..81374815,2	K562	blood:
19	chr5:81046850..81048241-chr5:81147402..81148427,4	Hela-S3	cervix:
20	chr5:81324799..81327472-chr5:81331097..81332975,2	K562	blood:
21	chr5:81122980..81125105-chr5:81265818..81268180,2	MCF-7	breast:
22	chr5:81149040..81150601-chr5:81152664..81154620,2	MCF-7	breast:
23	chr5:81153969..81156932-chr5:81161326..81164107,2	K562	blood:
24	chr5:81132026..81134746-chr5:81267997..81269668,2	MCF-7	breast:
25	chr5:81069624..81072338-chr5:81075602..81078025,2	K562	blood:
26	chr5:81470359..81473177-chr5:81473889..81476272,2	MCF-7	breast:
27	chr5:81087872..81090171-chr5:81298580..81301554,2	K562	blood:
28	chr5:81144274..81146832-chr5:81147802..81149692,2	K562	blood:
29	chr5:81163743..81165690-chr5:81182903..81184824,2	K562	blood:
30	chr5:81004548..81007464-chr5:81143257..81145481,2	K562	blood:
31	chr5:81450289..81453125-chr5:81456829..81458783,2	K562	blood:
32	chr5:81341617..81344926-chr5:81346112..81348915,3	K562	blood:
33	chr5:81073239..81075996-chr5:81079626..81082317,4	K562	blood:
34	chr10:52177751..52178388-chr5:81267152..81267908,2	Hela-S3	cervix:
35	chr5:81034741..81036819-chr5:81039221..81041707,2	K562	blood:
36	chr5:81045450..81049221-chr5:81128024..81131112,4	K562	blood:
37	chr5:81385087..81386605-chr5:81388427..81391205,2	K562	blood:
38	chr5:81266666..81268501-chr5:81347555..81349473,2	K562	blood:
39	chr5:81045891..81048139-chr5:81176444..81178228,2	K562	blood:
40	chr5:81029893..81032355-chr5:81038922..81041227,2	K562	blood:
41	chr5:81218775..81220722-chr5:81220823..81223756,3	K562	blood:
42	chr5:81053903..81057293-chr5:81057315..81060035,4	K562	blood:
43	chr5:81158992..81160951-chr5:81164614..81167325,2	MCF-7	breast:
44	chr5:81401474..81403838-chr5:81406719..81408810,2	K562	blood:
45	chr5:81470080..81473048-chr5:81572125..81574292,2	K562	blood:
46	chr5:81068024..81069829-chr5:81070706..81073662,2	MCF-7	breast:
47	chr5:81054557..81056248-chr5:81096931..81099616,2	MCF-7	breast:
48	chr5:81046777..81047952-chr5:81146745..81148237,8	MCF-7	breast:
49	chr13:75506708..75507325-chr5:81133617..81134458,2	MCF-7	breast:
50	chr1:197744364..197744977-chr5:81267510..81268258,2	HCT-116	colon:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG10-1	chr5:81196247-81196638	XLOC_004443
2	lnc-ATG10-1	chr5:81190738-81190868	XLOC_004443
3	lnc-RPS23-1	chr5:81368874-81369521	ENSG00000248192.1
4	lnc-ATG10-4	chr5:81188309-81188477	NONHSAT102471
5	lnc-SSBP2-1	chr5:81183117-81183334	uc_162_-
6	lnc-ATG10-4	chr5:81188501-81188540	NONHSAT102471
7	lnc-ATP6AP1L-1	chr5:81287814-81288300	ENSG00000236447.2
8	lnc-ATP6AP1L-7	chr5:81374246-81374541	NONHSAT102476
9	lnc-ATG10-5	chr5:81183117-81183334	uc_162_+
10	lnc-ATG10-3	chr5:81147420-81148020	ENSG00000249483

No data

Variant related genes	Relation type
ATG10-AS1	TF binding region
RN7SL378P	TF binding region
ENSG00000249483	TF binding region
ATG10-IT1	TF binding region
PPIAP11	TF binding region
SSBP2	TF binding region
SHFM1P1	TF binding region
ATG10	TF binding region
ENSG00000264142	TF binding region
ATG10-AS1	CpG island
RN7SL378P	CpG island
ENSG00000249483	CpG island
ATG10-IT1	CpG island
PPIAP11	CpG island
SSBP2	CpG island
SHFM1P1	CpG island
ATG10	CpG island
ENSG00000264142	CpG island
ENSG00000186468	chromatin interactions
ENSG00000182224	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000105855	chromatin interactions
ENSG00000231473	chromatin interactions
ENSG00000130479	chromatin interactions
ENSG00000145687	chromatin interactions
ENSG00000187514	chromatin interactions
ENSG00000264142	chromatin interactions
ENSG00000198964	chromatin interactions
ENSG00000213047	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000139687	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000249483	chromatin interactions
ENSG00000125835	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000120705	chromatin interactions
ENSG00000125505	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000265684	chromatin interactions
ENSG00000236447	chromatin interactions
ENSG00000134376	chromatin interactions
ENSG00000173171	chromatin interactions
ENSG00000163393	chromatin interactions
ENSG00000119969	chromatin interactions
ENSG00000183011	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000152348	chromatin interactions
ENSG00000183684	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000251495	chromatin interactions
ENSG00000130826	chromatin interactions
ENSG00000152413	chromatin interactions
ENSG00000110047	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000141552	chromatin interactions
ENSG00000158402	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000168237	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000063761	chromatin interactions
ENSG00000120709	chromatin interactions
ENSG00000248192	chromatin interactions

Extended variants
information (count: 14385 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:14385 , 50 per page) page: 1 2 3 4 5 6 7 ... 288

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6867759	chr5:81031741-81031742	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185081498	chr5:81031771-81031772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552515912	chr5:81031772-81031773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564474442	chr5:81031816-81031817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370303740	chr5:81031819-81031820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530266332	chr5:81031820-81031821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528553970	chr5:81031864-81031865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547105743	chr5:81031883-81031884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568618074	chr5:81031905-81031906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560247092	chr5:81031910-81031911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142760774	chr5:81031949-81031950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367849923	chr5:81031961-81031962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs402433	chr5:81031962-81031963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs58000137	chr5:81032003-81032004	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs72063392	chr5:81032006-81032007	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs66828331	chr5:81032007-81032008	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs58588638	chr5:81032008-81032009	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9293278	chr5:81032009-81032010	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370808718	chr5:81032062-81032063	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547120001	chr5:81032080-81032081	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200319874	chr5:81032084-81032085	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138635179	chr5:81032089-81032090	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs202214038	chr5:81032100-81032101	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368246147	chr5:81032143-81032144	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372153711	chr5:81032153-81032154	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181454450	chr5:81032174-81032175	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552624700	chr5:81032177-81032178	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs186189235	chr5:81032355-81032356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566932033	chr5:81032378-81032379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149331057	chr5:81032409-81032410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541972081	chr5:81032433-81032434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563357195	chr5:81032575-81032576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190109950	chr5:81032592-81032593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546127841	chr5:81032671-81032672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369571120	chr5:81032770-81032771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181417548	chr5:81032812-81032813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs417304	chr5:81032819-81032820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs186001482	chr5:81032962-81032963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562196741	chr5:81033047-81033048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150915753	chr5:81033114-81033115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558792448	chr5:81033132-81033133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79199405	chr5:81033133-81033134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557907553	chr5:81033144-81033145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529385763	chr5:81033164-81033165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190973612	chr5:81033267-81033268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115764872	chr5:81033293-81033294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540086834	chr5:81033327-81033328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184013625	chr5:81033330-81033331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571484939	chr5:81033377-81033378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144531561	chr5:81033384-81033385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Tetralogy of Fallot	22912587	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD
Basal cell lymphoma	17053054	CNVD

Chromatin state (count:6265 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80984200-81032000	Weak transcription	Esophagus	oesophagus
2	chr5:81008800-81044800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:81015800-81034600	Weak transcription	Left Ventricle	heart
4	chr5:81016000-81031800	Weak transcription	Ovary	ovary
5	chr5:81016000-81044800	Weak transcription	Fetal Stomach	stomach
6	chr5:81018600-81033800	Weak transcription	Thymus	Thymus
7	chr5:81018600-81038400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr5:81020800-81039200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr5:81021000-81033600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr5:81021600-81033600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr5:81022800-81036400	Weak transcription	Fetal Thymus	thymus
12	chr5:81023800-81031800	Weak transcription	Psoas Muscle	Psoas
13	chr5:81024000-81031800	Weak transcription	Brain Substantia Nigra	brain
14	chr5:81024000-81036400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr5:81028600-81044200	Weak transcription	Primary B cells from cord blood	blood
16	chr5:81028800-81035600	Weak transcription	Colon Smooth Muscle	Colon
17	chr5:81029200-81031800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr5:81029400-81038200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr5:81029800-81040800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr5:81030000-81032000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:81030200-81043000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr5:81030400-81035200	Weak transcription	Fetal Heart	heart
23	chr5:81030400-81039600	Weak transcription	Primary T cells from cord blood	blood
24	chr5:81030600-81031800	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr5:81031000-81032200	Enhancers	Fetal Brain Male	brain
26	chr5:81031200-81031800	Enhancers	Fetal Brain Female	brain
27	chr5:81031200-81033800	Enhancers	Dnd41	blood
28	chr5:81031400-81031800	Weak transcription	K562	blood
29	chr5:81031400-81033000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr5:81031600-81032000	Enhancers	Brain Angular Gyrus	brain
31	chr5:81031800-81032000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr5:81031800-81032000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr5:81031800-81032000	Enhancers	Brain Substantia Nigra	brain
34	chr5:81031800-81032000	Enhancers	K562	blood
35	chr5:81031800-81032200	Enhancers	Primary T helper cells PMA-I stimulated	--
36	chr5:81031800-81032200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:81031800-81032200	Enhancers	Ovary	ovary
38	chr5:81031800-81032200	Enhancers	Pancreas	Pancrea
39	chr5:81031800-81032200	Enhancers	Psoas Muscle	Psoas
40	chr5:81031800-81032200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr5:81031800-81032200	Enhancers	Small Intestine	intestine
42	chr5:81031800-81032200	Enhancers	Stomach Mucosa	stomach
43	chr5:81031800-81032200	Enhancers	A549	lung
44	chr5:81031800-81040400	Weak transcription	Fetal Brain Female	brain
45	chr5:81031800-81043000	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr5:81032000-81032200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:81032000-81032200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:81032000-81032200	Enhancers	Esophagus	oesophagus
49	chr5:81032000-81032200	Enhancers	Fetal Lung	lung
50	chr5:81032000-81033800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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