Variant report

Variant	nsv538183
Chromosome Location	chr6:31277798-31337397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1185)
CpG islands
(count:3361)
Chromatin interactive
region (count:31)
LncRNA
region (count:9)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr6:31324888-31325183	K562	blood:	n/a	n/a
3	ATF2	chr6:31326062-31326576	GM12878	blood:	n/a	n/a
4	ATF2	chr6:31300411-31301086	GM12878	blood:	n/a	n/a
5	ATF2	chr6:31319512-31321668	GM12878	blood:	n/a	n/a
6	ATF2	chr6:31324794-31325350	GM12878	blood:	n/a	n/a
7	ATF2	chr6:31318444-31319386	GM12878	blood:	n/a	n/a
8	ATF2	chr6:31334664-31335022	GM12878	blood:	n/a	n/a
9	ATF2	chr6:31300449-31301004	GM12878	blood:	n/a	n/a
10	ATF2	chr6:31334516-31335091	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:31318632-31319385	GM12878	blood:	n/a	n/a
12	ATF2	chr6:31319422-31321748	GM12878	blood:	n/a	n/a
13	BACH1	chr6:31324449-31325316	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:31334685-31334994	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:31300427-31300985	GM12878	blood:	n/a	n/a
16	BATF	chr6:31326056-31326411	GM12878	blood:	n/a	chr6:31326271-31326280
17	BATF	chr6:31325045-31325412	GM12878	blood:	n/a	n/a
18	BATF	chr6:31300476-31300903	GM12878	blood:	n/a	n/a
19	BATF	chr6:31326107-31326458	GM12878	blood:	n/a	chr6:31326271-31326280
20	BATF	chr6:31334694-31334977	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:31318775-31319206	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:31320393-31320678	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:31326086-31326349	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:31319413-31321023	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:31326082-31326510	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:31300656-31300925	GM12878	blood:	n/a	n/a
27	BCL3	chr6:31324702-31325296	GM12878	blood:	n/a	n/a
28	BCL3	chr6:31319812-31321116	GM12878	blood:	n/a	n/a
29	BCL3	chr6:31319415-31320898	GM12878	blood:	n/a	n/a
30	BCLAF1	chr6:31318701-31319362	GM12878	blood:	n/a	n/a
31	BCLAF1	chr6:31300404-31300834	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:31324267-31325663	GM12878	blood:	n/a	n/a
33	BCLAF1	chr6:31319409-31321119	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:31324260-31324641	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:31324713-31325348	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:31322776-31323862	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:31321125-31321669	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
38	BCLAF1	chr6:31322218-31322709	GM12878	blood:	n/a	n/a
39	BCLAF1	chr6:31318925-31319357	GM12878	blood:	n/a	n/a
40	BCLAF1	chr6:31334586-31335058	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:31322541-31323765	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:31319416-31321907	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
43	BHLHE40	chr6:31324888-31325236	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:31326283-31326390	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:31334682-31335021	K562	blood:	n/a	n/a
46	BHLHE40	chr6:31320567-31320928	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:31323948-31324053	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:31318412-31318711	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:31324382-31324473	GM12878	blood:	n/a	n/a
50	BHLHE40	chr6:31319623-31320237	GM12878	blood:	n/a	n/a

(count:3361 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31325817-31325867	U87	brain:	n/a
2	chr6:31324259-31324309	A549	lung:	n/a
3	chr6:31324684-31324734	HEK293	kidney:	embryo
4	chr6:31323397-31323447	Hepatocyte	liver:	n/a
5	chr6:31323985-31324035	AG09319	gingival:	n/a
6	chr6:31324941-31324991	ProgFib	skin:	n/a
7	chr6:31325817-31325867	U87	brain:	n/a
8	chr6:31324259-31324309	A549	lung:	n/a
9	chr6:31324684-31324734	HEK293	kidney:	embryo
10	chr6:31323397-31323447	Hepatocyte	liver:	n/a
11	chr6:31323985-31324035	AG09319	gingival:	n/a
12	chr6:31324941-31324991	ProgFib	skin:	n/a
13	chr6:31321433-31321483	HCT-116	colon:	n/a
14	chr6:31324252-31324302	AG04449	skin:	fetal
15	chr6:31324319-31324369	Hela-S3	cervix:	n/a
16	chr6:31325427-31325477	HCM	heart:	n/a
17	chr6:31323677-31323727	Hela-S3	cervix:	n/a
18	chr6:31323397-31323447	A549	lung:	n/a
19	chr6:31322914-31322964	MCF10A-Er-Src	breast:	n/a
20	chr6:31323506-31323556	ECC-1	luminal epithelium:	n/a
21	chr6:31324916-31324966	K562	blood:	n/a
22	chr6:31324565-31324615	HAEpiC	amniotic membrane:	n/a
23	chr6:31322577-31322627	K562	blood:	n/a
24	chr6:31323261-31323311	MCF10A-Er-Src	breast:	n/a
25	chr6:31323397-31323447	AG10803	skin:	n/a
26	chr6:31322766-31322816	Caco-2	colon:	n/a
27	chr6:31324684-31324734	LNCaP	prostate:	n/a
28	chr6:31322926-31322976	GM12891	blood:	n/a
29	chr6:31324997-31325047	MCF10A-Er-Src	breast:	n/a
30	chr6:31323253-31323303	SK-N-SH_RA	brain:	n/a
31	chr6:31322348-31322398	IMR90	lung:	fetal
32	chr6:31322914-31322964	SK-N-SH	brain:	n/a
33	chr6:31325136-31325186	HPAEpiC	pulmonary alveolar:	n/a
34	chr6:31322348-31322398	HCPEpiC	choroid plexus:	n/a
35	chr6:31325003-31325053	Hela-S3	cervix:	n/a
36	chr6:31323985-31324035	HEK293	kidney:	embryo
37	chr6:31323253-31323303	HEK293	kidney:	embryo
38	chr6:31324627-31324677	GM19239	blood:	n/a
39	chr6:31322298-31322348	NT2-D1	testis:	n/a
40	chr6:31322926-31322976	HepG2	liver:	n/a
41	chr6:31325063-31325113	GM12892	blood:	n/a
42	chr6:31323261-31323311	T-47D	breast:	n/a
43	chr6:31324551-31324601	BJ	skin:	n/a
44	chr6:31323677-31323727	GM12891	blood:	n/a
45	chr6:31324500-31324550	HIPEpiC	eye:	n/a
46	chr6:31322914-31322964	HEEpiC	esophagus:	n/a
47	chr6:31324621-31324671	HEK293	kidney:	embryo
48	chr6:31325085-31325135	SK-N-SH_RA	brain:	n/a
49	chr6:31323856-31323906	GM12892	blood:	n/a
50	chr6:31325000-31325050	NHDF-neo	bronchial:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
2	chr6:31104961..31105839-chr6:31334399..31335415,6	K562	blood:
3	chr6:31195002..31197168-chr6:31331435..31333390,2	K562	blood:
4	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
5	chr6:31164428..31165295-chr6:31333347..31334316,2	MCF-7	breast:
6	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
7	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
8	chr6:31274576..31277552-chr6:31281409..31285159,3	MCF-7	breast:
9	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
10	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
11	chr6:31238976..31240351-chr6:31324393..31325523,6	HCT-116	colon:
12	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
13	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
14	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
15	chr6:31164797..31165692-chr6:31334361..31335283,4	K562	blood:
16	chr6:31239600..31240303-chr6:31325089..31325595,2	Hela-S3	cervix:
17	chr6:31241176..31243692-chr6:31324996..31327759,3	MCF-7	breast:
18	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:
19	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
20	chr6:29759731..29760249-chr6:31324546..31325250,2	HCT-116	colon:
21	chr6:29689852..29692667-chr6:31324164..31326641,2	K562	blood:
22	chr6:31274011..31276374-chr6:31277383..31280033,2	K562	blood:
23	chr6:29855116..29856102-chr6:31324046..31324566,2	Hela-S3	cervix:
24	chr6:31283440..31285991-chr6:31367270..31369843,2	K562	blood:
25	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
26	chr6:31274551..31276643-chr6:31277971..31279738,2	MCF-7	breast:
27	chr6:31129596..31132185-chr6:31285768..31288675,2	MCF-7	breast:
28	chr6:31164859..31165402-chr6:31336129..31336993,3	MCF-7	breast:
29	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:
30	chr6:31163696..31166940-chr6:31333321..31336541,7	MCF-7	breast:
31	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-C-2	chr6:31322256-31322583	NONHSAT108752
2	lnc-HLA-C-2	chr6:31321649-31322073	NONHSAT108753
3	lnc-MICA-9	chr6:31323945-31324219	NONHSAT108756
4	lnc-MICA-9	chr6:31324466-31324734	NONHSAT108756
5	lnc-HLA-C-2	chr6:31322256-31322303	NONHSAT108753
6	lnc-HLA-C-2	chr6:31322256-31322303	NONHSAT108747
7	lnc-MICA-9	chr6:31324424-31325414	NONHSAT108757
8	lnc-HLA-C-2	chr6:31322410-31322853	NONHSAT108753
9	lnc-HLA-C-2	chr6:31321649-31322073	NONHSAT108752

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

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
RNU6-283P	CpG island
ENSG00000229836	CpG island
DHFRP2	CpG island
ENSG00000271581	CpG island
HLA-B	CpG island
ENSG00000206344	chromatin interactions
ENSG00000181126	chromatin interactions
ENSG00000204642	chromatin interactions
ENSG00000272501	chromatin interactions
ENSG00000206337	chromatin interactions
ENSG00000214892	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000206341	chromatin interactions
ENSG00000204540	chromatin interactions
ENSG00000204525	chromatin interactions
ENSG00000225864	chromatin interactions
ENSG00000229836	chromatin interactions

Extended variants
information (count: 3168 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:3168 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73730053	chr6:31277826-31277827	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541621584	chr6:31277885-31277886	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs559747304	chr6:31277889-31277890	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs185747258	chr6:31277928-31277929	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs566574411	chr6:31277942-31277943	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189439138	chr6:31277956-31277957	Inactive region	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7755852	chr6:31277988-31277989	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs573838951	chr6:31278077-31278078	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538028615	chr6:31278079-31278080	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556543017	chr6:31278095-31278096	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73396806	chr6:31278177-31278178	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs545419389	chr6:31278178-31278179	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181808018	chr6:31278182-31278183	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572506024	chr6:31278198-31278199	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184548673	chr6:31278210-31278211	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs149964596	chr6:31278327-31278328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145087951	chr6:31278338-31278339	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549941947	chr6:31278375-31278376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149148792	chr6:31278378-31278379	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1634754	chr6:31278398-31278399	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs9264969	chr6:31278415-31278416	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
22	rs9264970	chr6:31278449-31278450	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs552389902	chr6:31278465-31278466	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs9264971	chr6:31278472-31278473	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549138180	chr6:31278479-31278480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs143544407	chr6:31278492-31278493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538065694	chr6:31278505-31278506	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs5028535	chr6:31278562-31278563	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs1614015	chr6:31278605-31278606	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370504048	chr6:31278620-31278621	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374086181	chr6:31278625-31278626	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538511542	chr6:31278658-31278659	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs567986758	chr6:31278714-31278715	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12197373	chr6:31278722-31278723	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs572243496	chr6:31278727-31278728	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181335505	chr6:31278734-31278735	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
37	rs5013807	chr6:31278785-31278786	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs394051	chr6:31278794-31278795	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs201091263	chr6:31278808-31278809	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs186455495	chr6:31278815-31278816	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576114822	chr6:31278824-31278825	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs9468947	chr6:31278864-31278865	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs141033336	chr6:31278912-31278913	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532841205	chr6:31278913-31278914	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7742981	chr6:31278956-31278957	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs559984825	chr6:31278958-31278959	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs13194426	chr6:31278987-31278988	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs28732119	chr6:31279001-31279002	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs7764976	chr6:31279009-31279010	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs413119	chr6:31279087-31279088	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:902 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31280800-31282400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:31282000-31284000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:31282400-31283000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:31283000-31284200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:31289200-31290000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:31295400-31297000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr6:31299400-31301200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:31300000-31301000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr6:31300000-31301200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:31300000-31301200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr6:31300000-31301600	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr6:31300200-31301000	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr6:31300200-31301000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:31300200-31301200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr6:31300400-31301200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr6:31300400-31301200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:31300400-31301200	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr6:31300600-31301200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr6:31300600-31301200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr6:31300800-31301200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:31303600-31307400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:31304200-31305200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr6:31304200-31305600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:31304400-31305200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
25	chr6:31307200-31307600	Enhancers	Primary B cells from peripheral blood	blood
26	chr6:31311400-31312800	Enhancers	Primary B cells from peripheral blood	blood
27	chr6:31311600-31311800	Bivalent Enhancer	NHDF-Ad	bronchial
28	chr6:31312000-31313000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr6:31312400-31313000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr6:31312600-31312800	Enhancers	Primary T cells fromperipheralblood	blood
31	chr6:31312600-31313000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr6:31312600-31313200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr6:31312800-31313000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:31312800-31317800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr6:31313000-31313400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:31313000-31315600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr6:31313200-31316000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr6:31313400-31313600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr6:31313600-31315200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr6:31314200-31315600	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr6:31315000-31315600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:31315200-31315600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr6:31315600-31315800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr6:31315600-31315800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:31315600-31316400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:31315600-31316600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr6:31315600-31322800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:31315800-31316000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr6:31315800-31316400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:31315800-31316600	Weak transcription	H1 Cell Line	embryonic stem cell

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