Variant report

Variant	esv2759398
Chromosome Location	chr5:179534477-179729944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3123)
CpG islands
(count:5007)
Chromatin interactive
region (count:201)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:21)

(count:3123 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179724661-179724980	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:179720477-179720778	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:179717554-179717711	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:179628552-179628562	K562	blood:	n/a	n/a
5	ARID3A	chr5:179720502-179720795	K562	blood:	n/a	n/a
6	ATF1	chr5:179601223-179601365	K562	blood:	n/a	n/a
7	ATF2	chr5:179720348-179720900	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:179720267-179720956	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr5:179563820-179563990	K562	blood:	n/a	n/a
10	ATF3	chr5:179720392-179720963	A549	lung:	n/a	n/a
11	BACH1	chr5:179636266-179636486	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:179561454-179561491	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:179553967-179554302	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr5:179698237-179698477	GM12878	blood:	n/a	n/a
15	BATF	chr5:179634042-179634284	GM12878	blood:	n/a	n/a
16	BATF	chr5:179630216-179630472	GM12878	blood:	n/a	chr5:179630303-179630314
17	BCL3	chr5:179601267-179601897	GM12878	blood:	n/a	chr5:179601663-179601676
18	BCL3	chr5:179720340-179721023	A549	lung:	n/a	n/a
19	BCL3	chr5:179601323-179601671	GM12878	blood:	n/a	n/a
20	BCLAF1	chr5:179720327-179720896	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:179718950-179719809	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:179600029-179600349	HepG2	liver:	n/a	n/a
23	BHLHE40	chr5:179554169-179554355	K562	blood:	n/a	n/a
24	BHLHE40	chr5:179630351-179630386	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:179628400-179628520	K562	blood:	n/a	n/a
26	BHLHE40	chr5:179720495-179720872	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:179635456-179635812	K562	blood:	n/a	chr5:179635762-179635778
28	BHLHE40	chr5:179569016-179569216	K562	blood:	n/a	chr5:179569061-179569082 chr5:179569068-179569077
29	BHLHE40	chr5:179640139-179640313	K562	blood:	n/a	chr5:179640170-179640179 chr5:179640170-179640179 chr5:179640171-179640180
30	BHLHE40	chr5:179604518-179604553	K562	blood:	n/a	n/a
31	BHLHE40	chr5:179636064-179636339	HepG2	liver:	n/a	n/a
32	BHLHE40	chr5:179563858-179564016	K562	blood:	n/a	n/a
33	BHLHE40	chr5:179636135-179636335	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:179636050-179636406	K562	blood:	n/a	chr5:179636361-179636377
35	BHLHE40	chr5:179601408-179601608	K562	blood:	n/a	n/a
36	BHLHE40	chr5:179719365-179719686	K562	blood:	n/a	n/a
37	BHLHE40	chr5:179720388-179720831	K562	blood:	n/a	n/a
38	BRCA1	chr5:179720366-179720851	HepG2	liver:	n/a	n/a
39	BRCA1	chr5:179720396-179720674	GM12878	blood:	n/a	n/a
40	BRCA1	chr5:179719185-179719237	HepG2	liver:	n/a	n/a
41	BRCA1	chr5:179720359-179720856	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr5:179660112-179660400	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr5:179544235-179544409	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr5:179628437-179628462	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr5:179544320-179544323	HepG2	liver:	n/a	n/a
46	BRCA1	chr5:179719675-179719818	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr5:179680442-179680695	K562	blood:	n/a	n/a
48	CBX3	chr5:179680359-179680786	HCT-116	colon:	n/a	n/a
49	CBX3	chr5:179635449-179635868	K562	blood:	n/a	n/a
50	CBX3	chr5:179701704-179702034	K562	blood:	n/a	n/a

(count:5007 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179640174-179640224	AG04450	lung:	fetal
2	chr5:179719199-179719249	AG10803	skin:	n/a
3	chr5:179621502-179621552	SK-N-MC	brain:	n/a
4	chr5:179563745-179563795	T-47D	breast:	n/a
5	chr5:179717478-179717528	A549	lung:	n/a
6	chr5:179640174-179640224	AG04450	lung:	fetal
7	chr5:179719199-179719249	AG10803	skin:	n/a
8	chr5:179621502-179621552	SK-N-MC	brain:	n/a
9	chr5:179563745-179563795	T-47D	breast:	n/a
10	chr5:179717478-179717528	A549	lung:	n/a
11	chr5:179554555-179554605	H1-hESC	embryonic stem cell:	embryo
12	chr5:179554466-179554516	GM06990	blood:	n/a
13	chr5:179554555-179554605	HepG2	liver:	n/a
14	chr5:179636443-179636493	AG04450	lung:	fetal
15	chr5:179565349-179565399	Jurkat	blood:	n/a
16	chr5:179606623-179606673	HNPCEpiC	eye:	n/a
17	chr5:179557008-179557058	HRE	kidney:	n/a
18	chr5:179557008-179557058	SK-N-SH	brain:	n/a
19	chr5:179557008-179557058	SAEC	small airway:	n/a
20	chr5:179715673-179715723	NHBE	bronchial:	n/a
21	chr5:179591070-179591120	HCM	heart:	n/a
22	chr5:179569583-179569633	HepG2	liver:	n/a
23	chr5:179634383-179634433	HRCEpiC	kidney:	n/a
24	chr5:179606623-179606673	NHBE	bronchial:	n/a
25	chr5:179621734-179621784	PFSK-1	brain:	n/a
26	chr5:179621502-179621552	HMEC	breast:	n/a
27	chr5:179635979-179636029	HCM	heart:	n/a
28	chr5:179569583-179569633	MCF10A-Er-Src	breast:	n/a
29	chr5:179634383-179634433	PrEC	prostate:	n/a
30	chr5:179718531-179718581	NT2-D1	testis:	n/a
31	chr5:179588673-179588723	K562	blood:	n/a
32	chr5:179569548-179569598	HMEC	breast:	n/a
33	chr5:179643755-179643805	PrEC	prostate:	n/a
34	chr5:179588440-179588490	HEK293	kidney:	embryo
35	chr5:179587950-179588000	HUVEC	blood vessel:	n/a
36	chr5:179554555-179554605	CMK	blood:	n/a
37	chr5:179566792-179566842	Hepatocyte	liver:	n/a
38	chr5:179621502-179621552	H1-hESC	embryonic stem cell:	embryo
39	chr5:179563896-179563946	SK-N-SH	brain:	n/a
40	chr5:179621734-179621784	NB4	blood:	n/a
41	chr5:179643528-179643578	GM19239	blood:	n/a
42	chr5:179636422-179636472	SAEC	small airway:	n/a
43	chr5:179598884-179598934	BE2_C	brain:	n/a
44	chr5:179563200-179563250	U87	brain:	n/a
45	chr5:179563866-179563916	HCM	heart:	n/a
46	chr5:179719756-179719806	AG04450	lung:	fetal
47	chr5:179640174-179640224	IMR90	lung:	fetal
48	chr5:179636443-179636493	H1-hESC	embryonic stem cell:	embryo
49	chr5:179636617-179636667	H1-hESC	embryonic stem cell:	embryo
50	chr5:179636422-179636472	HIPEpiC	eye:	n/a

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr5:179568439..179571185-chr5:179571573..179574464,2	K562	blood:
2	chr5:179553629..179554257-chr5:179627968..179628886,2	MCF-7	breast:
3	chr5:179715141..179717166-chr5:179896710..179898786,2	MCF-7	breast:
4	chr5:179692679..179694795-chr5:179697303..179699548,2	K562	blood:
5	chr5:179661961..179665660-chr5:179666627..179671316,5	K562	blood:
6	chr5:179660175..179662984-chr5:180235591..180238303,2	MCF-7	breast:
7	chr5:179675041..179677707-chr5:179682161..179684985,2	K562	blood:
8	chr5:179720585..179721111-chr5:179742335..179742892,2	K562	blood:
9	chr5:179638635..179640906-chr5:179719445..179721732,2	K562	blood:
10	chr5:179603344..179605727-chr5:179894143..179896109,2	K562	blood:
11	chr5:179497086..179499283-chr5:179543542..179545830,3	MCF-7	breast:
12	chr5:179544196..179547081-chr5:179550763..179552798,2	MCF-7	breast:
13	chr5:179699041..179700703-chr5:179717946..179720199,2	MCF-7	breast:
14	chr5:179546334..179548220-chr5:179553814..179555869,2	MCF-7	breast:
15	chr5:179551435..179553864-chr5:179559199..179562159,2	K562	blood:
16	chr5:179716091..179718097-chr5:179718228..179720650,3	MCF-7	breast:
17	chr5:179656618..179658945-chr5:179717672..179719756,2	MCF-7	breast:
18	chr5:179588724..179589352-chr5:179627753..179628617,2	MCF-7	breast:
19	chr5:179720392..179721373-chr5:179895885..179896410,2	MCF-7	breast:
20	chr5:179693858..179696723-chr5:179696767..179698335,2	K562	blood:
21	chr5:179633062..179635561-chr5:179636902..179639752,2	MCF-7	breast:
22	chr5:179714082..179715807-chr5:179741478..179743115,2	MCF-7	breast:
23	chr5:179673735..179676191-chr5:179686105..179688393,2	MCF-7	breast:
24	chr5:179695378..179697431-chr5:179716689..179720620,4	K562	blood:
25	chr5:179679213..179680799-chr5:179687875..179689576,2	K562	blood:
26	chr5:179517772..179520759-chr5:179536622..179539248,2	MCF-7	breast:
27	chr5:179698719..179700980-chr5:179701613..179704938,3	MCF-7	breast:
28	chr2:175494696..175495196-chr5:179714935..179715700,2	MCF-7	breast:
29	chr17:11900847..11902529-chr5:179633459..179635305,2	MCF-7	breast:
30	chr5:179297336..179298161-chr5:179635822..179636672,3	K562	blood:
31	chr5:179707659..179712077-chr5:179712622..179717997,8	MCF-7	breast:
32	chr5:179556597..179557163-chr5:179565658..179566414,2	MCF-7	breast:
33	chr5:179716629..179721643-chr5:179722540..179727897,10	K562	blood:
34	chr5:179523738..179525811-chr5:179544274..179545923,2	MCF-7	breast:
35	chr5:179724635..179726412-chr5:179729293..179731756,2	MCF-7	breast:
36	chr5:179727104..179728705-chr5:179740247..179742971,2	MCF-7	breast:
37	chr5:179544274..179545099-chr5:179553728..179554648,2	MCF-7	breast:
38	chr5:179636340..179638403-chr5:179650637..179652737,2	K562	blood:
39	chr5:179712494..179714081-chr5:179717178..179718692,2	K562	blood:
40	chr5:179543851..179544407-chr5:179635297..179636277,2	MCF-7	breast:
41	chr5:179553629..179554257-chr5:179627968..179628886,2	MCF-7	breast:
42	chr5:179554536..179556521-chr5:179716236..179718994,2	MCF-7	breast:
43	chr5:179562265..179564254-chr5:179568163..179570454,2	K562	blood:
44	chr5:179555641..179558112-chr5:179558686..179561172,2	K562	blood:
45	chr5:179601654..179603372-chr5:179739320..179741770,2	MCF-7	breast:
46	chr5:179718262..179720717-chr5:180237170..180239607,2	MCF-7	breast:
47	chr5:179628129..179628639-chr5:179720355..179721073,2	MCF-7	breast:
48	chr5:179646868..179648525-chr5:179656321..179659011,2	K562	blood:
49	chr20:26189362..26189868-chr5:179709812..179710312,2	MCF-7	breast:
50	chr5:179555641..179558112-chr5:179558686..179561172,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6-4	chr5:179719195-179719481	XLOC_004678
2	lnc-CNOT6-4	chr5:179719184-179722539	NONHSAT105673
3	lnc-RASGEF1C-1	chr5:179639411-179639638	expReg_chr5_10974_-
4	lnc-CNOT6-4	chr5:179720245-179720418	XLOC_004678
5	lnc-CNOT6-9	chr5:179684680-179685366	NONHSAT105672
6	lnc-CNOT6-4	chr5:179722035-179722215	XLOC_004678
7	lnc-CNOT6-4	chr5:179722035-179722253	XLOC_004678

No data

(count:21 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GFPT2	hsa-miR-101-3p	chr5:179728272-179728293
2	GFPT2	hsa-miR-128-3p	chr5:179728276-179728270
3	GFPT2	hsa-miR-32-5p	chr5:179728301-179728322
4	MAPK9	hsa-miR-27b-3p	chr5:179674232-179674253
5	MAPK9	hsa-miR-106b-5p	chr5:179663022-179663016
6	GFPT2	hsa-miR-30b-5p	chr5:179728346-179728339
7	GFPT2	hsa-miR-124-3p	chr5:179728427-179728421
8	MAPK9	hsa-miR-93-5p	chr5:179663022-179663016
9	MAPK9	hsa-miR-17-5p	chr5:179663016-179663038
10	GFPT2	hsa-miR-32-5p	chr5:179728307-179728300
11	MAPK9	hsa-miR-20a-5p	chr5:179663022-179663016
12	MAPK9	hsa-miR-106b-5p	chr5:179663016-179663036
13	MAPK9	hsa-miR-17-5p	chr5:179663022-179663016
14	GFPT2	hsa-miR-101-3p	chr5:179728387-179728408
15	MAPK9	hsa-miR-7-5p	chr5:179663485-179663514
16	MAPK9	hsa-miR-20a-5p	chr5:179663016-179663038
17	GFPT2	hsa-miR-30b-5p	chr5:179728340-179728362
18	MAPK9	hsa-miR-27b-3p	chr5:179661888-179661908
19	MAPK9	hsa-miR-93-5p	chr5:179663016-179663038
20	MAPK9	hsa-miR-141-3p	chr5:179673497-179673517
21	GFPT2	hsa-miR-124-3p	chr5:179728421-179728440

Variant related genes	Relation type
RASGEF1C	TF binding region
ENSG00000229721	TF binding region
ENSG00000248367	TF binding region
ENSG00000253908	TF binding region
MAPK9	TF binding region
RASGEF1C	CpG island
ENSG00000229721	CpG island
ENSG00000248367	CpG island
ENSG00000253908	CpG island
MAPK9	CpG island
ENSG00000253908	chromatin interactions
ENSG00000229721	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000197226	chromatin interactions
ENSG00000131459	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000115935	chromatin interactions
ENSG00000146090	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000248367	chromatin interactions
ENSG00000113269	chromatin interactions
ENSG00000227195	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000113300	chromatin interactions
ENSG00000267073	chromatin interactions
TGFBR1	miRNA target sites

Extended variants
information (count: 8472 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:8472 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560692587	chr5:179534522-179534523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540710116	chr5:179534539-179534540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572891061	chr5:179534553-179534554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140774432	chr5:179534591-179534592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555506602	chr5:179534599-179534600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564417114	chr5:179534614-179534615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564093210	chr5:179534683-179534684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531775883	chr5:179534688-179534689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549882971	chr5:179534717-179534718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545083556	chr5:179534723-179534724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568045068	chr5:179534797-179534798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535374592	chr5:179534805-179534806	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs572069407	chr5:179534824-179534825	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs375747683	chr5:179534832-179534833	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs183201895	chr5:179534841-179534842	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs565541444	chr5:179534845-179534846	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs564973784	chr5:179534852-179534853	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs539216476	chr5:179534875-179534876	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs557882691	chr5:179534907-179534908	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs576035087	chr5:179535001-179535002	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs537084526	chr5:179535008-179535009	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs144605190	chr5:179535032-179535033	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs573654160	chr5:179535144-179535145	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs188262061	chr5:179535185-179535186	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs202061405	chr5:179535193-179535194	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs78670887	chr5:179535195-179535196	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs200380852	chr5:179535201-179535202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201715413	chr5:179535204-179535205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554375399	chr5:179535205-179535206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199907933	chr5:179535207-179535208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114017961	chr5:179535208-179535209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142588464	chr5:179535219-179535220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546075246	chr5:179535264-179535265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564630006	chr5:179535283-179535284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531693933	chr5:179535326-179535327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550211474	chr5:179535357-179535358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533483442	chr5:179535379-179535380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529203619	chr5:179535402-179535403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547297503	chr5:179535422-179535423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111920341	chr5:179535462-179535463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565627037	chr5:179535478-179535479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561405408	chr5:179535483-179535484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376677152	chr5:179535490-179535491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138505737	chr5:179535492-179535493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530455559	chr5:179535500-179535501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551272032	chr5:179535501-179535502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569798379	chr5:179535522-179535523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536768834	chr5:179535533-179535534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531529837	chr5:179535569-179535570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370224363	chr5:179535570-179535571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:4295 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179518400-179542800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr5:179528400-179538400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:179534800-179535200	ZNF genes & repeats	Fetal Brain Female	brain
4	chr5:179535600-179536000	ZNF genes & repeats	Fetal Brain Female	brain
5	chr5:179536000-179543600	Weak transcription	Fetal Brain Female	brain
6	chr5:179536200-179537800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:179536200-179554200	Weak transcription	Brain Germinal Matrix	brain
8	chr5:179536400-179536800	Weak transcription	Brain Hippocampus Middle	brain
9	chr5:179536600-179538800	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr5:179537000-179538200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:179537000-179538400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:179537200-179538200	Enhancers	Primary hematopoietic stem cells	blood
13	chr5:179537600-179537800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr5:179537800-179538800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:179537800-179546000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:179538400-179538600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:179538600-179539000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr5:179538600-179539200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr5:179538600-179541200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:179538800-179542600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:179538800-179543000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:179539000-179539200	Active TSS	Spleen	Spleen
23	chr5:179539000-179545000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr5:179539200-179543000	Weak transcription	Spleen	Spleen
25	chr5:179539400-179539600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
26	chr5:179540200-179543200	Weak transcription	Brain Angular Gyrus	brain
27	chr5:179541200-179541400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr5:179541400-179541800	Enhancers	K562	blood
29	chr5:179541400-179542000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:179541800-179542000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:179541800-179543400	Weak transcription	K562	blood
32	chr5:179542000-179543000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:179542000-179543000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:179542400-179542600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr5:179542600-179543400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr5:179542600-179544000	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr5:179542800-179543000	Enhancers	Brain Cingulate Gyrus	brain
38	chr5:179542800-179543200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr5:179542800-179543800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:179542800-179543800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr5:179543000-179543200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:179543000-179543200	Bivalent Enhancer	Fetal Stomach	stomach
43	chr5:179543000-179543200	Enhancers	Spleen	Spleen
44	chr5:179543000-179543400	Weak transcription	Brain Cingulate Gyrus	brain
45	chr5:179543000-179543800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:179543000-179543800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:179543000-179544000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr5:179543000-179544000	Enhancers	Brain Hippocampus Middle	brain
49	chr5:179543000-179544000	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr5:179543000-179544400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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