Variant report

Variant	esv2757161
Chromosome Location	chr6:31251360-31335707
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1316)
CpG islands
(count:5070)
Chromatin interactive
region (count:45)
LncRNA
region (count:16)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1316 , 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	ATF1	chr6:31334724-31334995	K562	blood:	n/a	n/a
2	ATF1	chr6:31272445-31272772	K562	blood:	n/a	n/a
3	ATF1	chr6:31324888-31325183	K562	blood:	n/a	n/a
4	ATF2	chr6:31272379-31272838	GM12878	blood:	n/a	n/a
5	ATF2	chr6:31318444-31319386	GM12878	blood:	n/a	n/a
6	ATF2	chr6:31318632-31319385	GM12878	blood:	n/a	n/a
7	ATF2	chr6:31300449-31301004	GM12878	blood:	n/a	n/a
8	ATF2	chr6:31319512-31321668	GM12878	blood:	n/a	n/a
9	ATF2	chr6:31334664-31335022	GM12878	blood:	n/a	n/a
10	ATF2	chr6:31334516-31335091	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:31326062-31326576	GM12878	blood:	n/a	n/a
12	ATF2	chr6:31319422-31321748	GM12878	blood:	n/a	n/a
13	ATF2	chr6:31324794-31325350	GM12878	blood:	n/a	n/a
14	ATF2	chr6:31300411-31301086	GM12878	blood:	n/a	n/a
15	ATF2	chr6:31272219-31272895	GM12878	blood:	n/a	n/a
16	BACH1	chr6:31276089-31276266	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:31334685-31334994	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:31324449-31325316	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr6:31326056-31326411	GM12878	blood:	n/a	chr6:31326271-31326280
20	BATF	chr6:31300427-31300985	GM12878	blood:	n/a	n/a
21	BATF	chr6:31300476-31300903	GM12878	blood:	n/a	n/a
22	BATF	chr6:31326107-31326458	GM12878	blood:	n/a	chr6:31326271-31326280
23	BATF	chr6:31334694-31334977	GM12878	blood:	n/a	n/a
24	BATF	chr6:31325045-31325412	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:31318775-31319206	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:31326086-31326349	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:31320393-31320678	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:31319413-31321023	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:31300656-31300925	GM12878	blood:	n/a	n/a
30	BCL11A	chr6:31326082-31326510	GM12878	blood:	n/a	n/a
31	BCL3	chr6:31319812-31321116	GM12878	blood:	n/a	n/a
32	BCL3	chr6:31324702-31325296	GM12878	blood:	n/a	n/a
33	BCL3	chr6:31319415-31320898	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:31322776-31323862	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:31300404-31300834	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:31334586-31335058	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:31318701-31319362	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:31324267-31325663	GM12878	blood:	n/a	n/a
39	BCLAF1	chr6:31321125-31321669	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
40	BCLAF1	chr6:31322218-31322709	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:31319409-31321119	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:31319416-31321907	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
43	BCLAF1	chr6:31324713-31325348	GM12878	blood:	n/a	n/a
44	BCLAF1	chr6:31318925-31319357	GM12878	blood:	n/a	n/a
45	BCLAF1	chr6:31322541-31323765	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:31324260-31324641	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:31326283-31326390	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:31324382-31324473	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:31324888-31325236	GM12878	blood:	n/a	n/a
50	BHLHE40	chr6:31320567-31320928	GM12878	blood:	n/a	n/a

(count:5070 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31324280-31324330	HEEpiC	esophagus:	n/a
2	chr6:31275741-31275791	HCM	heart:	n/a
3	chr6:31325136-31325186	HIPEpiC	eye:	n/a
4	chr6:31322926-31322976	Caco-2	colon:	n/a
5	chr6:31323506-31323556	HCF	heart:	n/a
6	chr6:31276797-31276847	BE2_C	brain:	n/a
7	chr6:31275267-31275317	SAEC	small airway:	n/a
8	chr6:31324280-31324330	HEEpiC	esophagus:	n/a
9	chr6:31275741-31275791	HCM	heart:	n/a
10	chr6:31325136-31325186	HIPEpiC	eye:	n/a
11	chr6:31322926-31322976	Caco-2	colon:	n/a
12	chr6:31323506-31323556	HCF	heart:	n/a
13	chr6:31276797-31276847	BE2_C	brain:	n/a
14	chr6:31275267-31275317	SAEC	small airway:	n/a
15	chr6:31325817-31325867	HEEpiC	esophagus:	n/a
16	chr6:31324972-31325022	SK-N-MC	brain:	n/a
17	chr6:31322121-31322171	NB4	blood:	n/a
18	chr6:31327376-31327426	U87	brain:	n/a
19	chr6:31275267-31275317	HNPCEpiC	eye:	n/a
20	chr6:31325136-31325186	Hela-S3	cervix:	n/a
21	chr6:31324962-31325012	HCPEpiC	choroid plexus:	n/a
22	chr6:31322996-31323046	HNPCEpiC	eye:	n/a
23	chr6:31275664-31275714	NB4	blood:	n/a
24	chr6:31276088-31276138	HAEpiC	amniotic membrane:	n/a
25	chr6:31276212-31276262	HIPEpiC	eye:	n/a
26	chr6:31276664-31276714	SK-N-MC	brain:	n/a
27	chr6:31322996-31323046	MCF-7	breast:	n/a
28	chr6:31324319-31324369	AoSMC	blood vessel:	n/a
29	chr6:31276434-31276484	ECC-1	luminal epithelium:	n/a
30	chr6:31325003-31325053	SK-N-SH_RA	brain:	n/a
31	chr6:31276653-31276703	GM12891	blood:	n/a
32	chr6:31324684-31324734	HAEpiC	amniotic membrane:	n/a
33	chr6:31326324-31326374	RPTEC	kidney:	n/a
34	chr6:31325058-31325108	BE2_C	brain:	n/a
35	chr6:31323677-31323727	PrEC	prostate:	n/a
36	chr6:31275666-31275716	PANC-1	pancreas:	n/a
37	chr6:31324269-31324319	GM19239	blood:	n/a
38	chr6:31324565-31324615	GM12891	blood:	n/a
39	chr6:31275666-31275716	NB4	blood:	n/a
40	chr6:31323253-31323303	HNPCEpiC	eye:	n/a
41	chr6:31322577-31322627	HRPEpiC	eye:	n/a
42	chr6:31276212-31276262	AG09309	skin:	n/a
43	chr6:31325085-31325135	AG09309	skin:	n/a
44	chr6:31275791-31275841	HRPEpiC	eye:	n/a
45	chr6:31325058-31325108	GM12892	blood:	n/a
46	chr6:31322926-31322976	HAEpiC	amniotic membrane:	n/a
47	chr6:31323284-31323334	NB4	blood:	n/a
48	chr6:31324916-31324966	AG10803	skin:	n/a
49	chr6:31322577-31322627	GM19239	blood:	n/a
50	chr6:31324491-31324541	HCPEpiC	choroid plexus:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31241176..31243692-chr6:31324996..31327759,3	MCF-7	breast:
2	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:
3	chr6:31164078..31167331-chr6:31260118..31263696,3	K562	blood:
4	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:
5	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
6	chr6:31274576..31277552-chr6:31281409..31285159,3	MCF-7	breast:
7	chr6:31260315..31262066-chr6:31270612..31272546,2	MCF-7	breast:
8	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
9	chr6:31260315..31262066-chr6:31270612..31272546,2	MCF-7	breast:
10	chr6:31274551..31276643-chr6:31277971..31279738,2	MCF-7	breast:
11	chr6:31256122..31258941-chr6:31260246..31262615,2	MCF-7	breast:
12	chr6:31283440..31285991-chr6:31367270..31369843,2	K562	blood:
13	chr6:29759731..29760249-chr6:31324546..31325250,2	HCT-116	colon:
14	chr6:31164078..31166363-chr6:31260745..31263696,2	K562	blood:
15	chr6:31262379..31263887-chr6:31264452..31266692,2	MCF-7	breast:
16	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
17	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
18	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
19	chr6:31272067..31274682-chr6:31275532..31277366,2	MCF-7	breast:
20	chr6:31262379..31263887-chr6:31264452..31266692,2	MCF-7	breast:
21	chr6:31164428..31165295-chr6:31333347..31334316,2	MCF-7	breast:
22	chr6:29855116..29856102-chr6:31324046..31324566,2	Hela-S3	cervix:
23	chr6:31195002..31197168-chr6:31331435..31333390,2	K562	blood:
24	chr6:31274011..31276374-chr6:31277383..31280033,2	K562	blood:
25	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:
26	chr6:31104961..31105839-chr6:31334399..31335415,6	K562	blood:
27	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
28	chr6:31260319..31263250-chr6:31266330..31267976,2	K562	blood:
29	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
30	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
31	chr6:31163696..31166940-chr6:31333321..31336541,7	MCF-7	breast:
32	chr6:31260319..31263250-chr6:31266330..31267976,2	K562	blood:
33	chr6:31272998..31275186-chr6:31333057..31335314,2	K562	blood:
34	chr6:29689852..29692667-chr6:31324164..31326641,2	K562	blood:
35	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
36	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
37	chr6:31129596..31132185-chr6:31285768..31288675,2	MCF-7	breast:
38	chr6:31238976..31240351-chr6:31324393..31325523,6	HCT-116	colon:
39	chr6:31251382..31252914-chr6:31343854..31345706,2	MCF-7	breast:
40	chr6:31164797..31165692-chr6:31334361..31335283,4	K562	blood:
41	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
42	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
43	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
44	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
45	chr6:31239600..31240303-chr6:31325089..31325595,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-C-3	chr6:31253395-31253655	NONHSAT108749
2	lnc-HLA-C-1	chr6:31261992-31262072	ENSG00000256166
3	lnc-HLA-C-2	chr6:31321649-31322073	NONHSAT108752
4	lnc-MICA-9	chr6:31324424-31325414	NONHSAT108757
5	lnc-HLA-C-4	chr6:31276254-31276326	NONHSAT108751
6	lnc-HLA-C-2	chr6:31322256-31322303	NONHSAT108753
7	lnc-MICA-9	chr6:31324466-31324734	NONHSAT108756
8	lnc-MICA-9	chr6:31323945-31324219	NONHSAT108756
9	lnc-HLA-C-4	chr6:31275592-31275824	NONHSAT108751
10	lnc-HLA-C-2	chr6:31322256-31322303	NONHSAT108747
11	lnc-HLA-C-1	chr6:31269249-31269419	ENSG00000256166
12	lnc-HLA-C-1	chr6:31262721-31262790	ENSG00000256166
13	lnc-HLA-C-2	chr6:31322410-31322853	NONHSAT108753
14	lnc-HLA-C-2	chr6:31321649-31322073	NONHSAT108753
15	lnc-HLA-C-2	chr6:31322256-31322583	NONHSAT108752
16	lnc-HLA-C-1	chr6:31261685-31261898	ENSG00000256166

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6891-3p	chr6:31323005-31323025	MIMAT0027683
hsa-miR-6891-5p	chr6:31323074-31323092	MIMAT0027682

No data

Variant related genes	Relation type
RNU6-283P	TF binding region
ENSG00000229836	TF binding region
DHFRP2	TF binding region
ENSG00000271581	TF binding region
HLA-B	TF binding region
WASF5P	TF binding region
ENSG00000256166	TF binding region
RNU6-283P	CpG island
ENSG00000229836	CpG island
DHFRP2	CpG island
ENSG00000271581	CpG island
HLA-B	CpG island
WASF5P	CpG island
ENSG00000256166	CpG island
ENSG00000206344	chromatin interactions
ENSG00000225864	chromatin interactions
ENSG00000181126	chromatin interactions
ENSG00000204525	chromatin interactions
ENSG00000206341	chromatin interactions
ENSG00000214892	chromatin interactions
ENSG00000231402	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000228432	chromatin interactions
ENSG00000204642	chromatin interactions
ENSG00000206337	chromatin interactions
ENSG00000204540	chromatin interactions
ENSG00000230994	chromatin interactions
ENSG00000229836	chromatin interactions
ENSG00000272501	chromatin interactions

Extended variants
information (count: 4073 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:4073 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201329657	chr6:31251415-31251416	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs533481967	chr6:31251416-31251417	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2253842	chr6:31251418-31251419	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs2394963	chr6:31251462-31251463	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs6942360	chr6:31251474-31251475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2853938	chr6:31251477-31251478	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs542018931	chr6:31251478-31251479	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs557177084	chr6:31251507-31251508	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs12660083	chr6:31251523-31251524	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2394964	chr6:31251542-31251543	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs191360976	chr6:31251544-31251545	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2894206	chr6:31251558-31251559	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs556625716	chr6:31251560-31251561	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2524058	chr6:31251569-31251570	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
15	rs2844602	chr6:31251576-31251577	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2394965	chr6:31251581-31251582	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs138033234	chr6:31251596-31251597	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184002515	chr6:31251611-31251612	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs9461682	chr6:31251622-31251623	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs143944172	chr6:31251634-31251635	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs6899660	chr6:31251643-31251644	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs9468918	chr6:31251662-31251663	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
23	rs9461683	chr6:31251667-31251668	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs139371734	chr6:31251700-31251701	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs144205454	chr6:31251715-31251716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543030993	chr6:31251740-31251741	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs76737289	chr6:31251760-31251761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560704815	chr6:31251782-31251783	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs117477942	chr6:31251788-31251789	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369587681	chr6:31251822-31251823	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs117652729	chr6:31251841-31251842	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2524057	chr6:31251895-31251896	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs567503940	chr6:31251912-31251913	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12189871	chr6:31251924-31251925	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs114529772	chr6:31251937-31251938	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs115182712	chr6:31251954-31251955	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114020623	chr6:31251962-31251963	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553515832	chr6:31251968-31251969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563347568	chr6:31251992-31251993	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs565559794	chr6:31252019-31252020	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189035471	chr6:31252023-31252024	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs552305620	chr6:31252025-31252026	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs114652772	chr6:31252026-31252027	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs115699806	chr6:31252031-31252032	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114108198	chr6:31252033-31252034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543402650	chr6:31252075-31252076	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370568329	chr6:31252080-31252081	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558614126	chr6:31252105-31252106	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545792261	chr6:31252198-31252199	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2524056	chr6:31252216-31252217	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1089 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31252600-31254200	Enhancers	Primary hematopoietic stem cells	blood
2	chr6:31252600-31254600	Enhancers	Thymus	Thymus
3	chr6:31253000-31254200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:31253000-31254400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:31253000-31254600	Enhancers	Fetal Thymus	thymus
6	chr6:31253600-31254400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:31254000-31254400	Enhancers	Adipose Nuclei	Adipose
8	chr6:31255400-31255600	Enhancers	Right Atrium	heart
9	chr6:31257200-31257800	Enhancers	GM12878-XiMat	blood
10	chr6:31257600-31258000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:31258000-31260400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:31258200-31259200	Enhancers	Brain Substantia Nigra	brain
13	chr6:31258600-31259000	Enhancers	Brain Hippocampus Middle	brain
14	chr6:31267400-31268800	Enhancers	HepG2	liver
15	chr6:31269200-31269400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:31272400-31272800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr6:31272600-31272800	Enhancers	GM12878-XiMat	blood
18	chr6:31272800-31273800	Bivalent Enhancer	K562	blood
19	chr6:31273200-31273400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
20	chr6:31274000-31276200	Weak transcription	Right Atrium	heart
21	chr6:31275200-31275400	Weak transcription	GM12878-XiMat	blood
22	chr6:31275200-31275600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
23	chr6:31275200-31276800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
24	chr6:31275400-31275600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:31275400-31275600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
26	chr6:31275400-31275600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr6:31275400-31275600	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr6:31275400-31275600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
29	chr6:31275400-31275600	Bivalent/Poised TSS	Placenta Amnion	Placenta Amnion
30	chr6:31275400-31275800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr6:31275400-31275800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:31275400-31275800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:31275400-31275800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
34	chr6:31275400-31276200	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr6:31275400-31276400	Active TSS	H1 Cell Line	embryonic stem cell
36	chr6:31275400-31276600	Bivalent/Poised TSS	Right Ventricle	heart
37	chr6:31275400-31277000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
38	chr6:31275400-31277000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
39	chr6:31275600-31275800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:31275600-31275800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr6:31275600-31275800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
42	chr6:31275600-31275800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr6:31275600-31275800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:31275600-31275800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:31275600-31275800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:31275600-31275800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
47	chr6:31275600-31275800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
48	chr6:31275600-31275800	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
49	chr6:31275600-31276000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr6:31275600-31276000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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