Variant report

Variant	nsv601687
Chromosome Location	chr6:31283297-31351442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1390)
CpG islands
(count:3421)
Chromatin interactive
region (count:31)
LncRNA
region (count:12)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1390 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

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	chr6:31318444-31319386	GM12878	blood:	n/a	n/a
5	ATF2	chr6:31318632-31319385	GM12878	blood:	n/a	n/a
6	ATF2	chr6:31334664-31335022	GM12878	blood:	n/a	n/a
7	ATF2	chr6:31324794-31325350	GM12878	blood:	n/a	n/a
8	ATF2	chr6:31319422-31321748	GM12878	blood:	n/a	n/a
9	ATF2	chr6:31319512-31321668	GM12878	blood:	n/a	n/a
10	ATF2	chr6:31300449-31301004	GM12878	blood:	n/a	n/a
11	ATF2	chr6:31334516-31335091	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:31300411-31301086	GM12878	blood:	n/a	n/a
13	BACH1	chr6:31334685-31334994	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:31324449-31325316	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:31326056-31326411	GM12878	blood:	n/a	chr6:31326271-31326280
16	BATF	chr6:31300427-31300985	GM12878	blood:	n/a	n/a
17	BATF	chr6:31300476-31300903	GM12878	blood:	n/a	n/a
18	BATF	chr6:31325045-31325412	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	chr6:31300656-31300925	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:31326082-31326510	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:31326086-31326349	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:31320393-31320678	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:31319413-31321023	GM12878	blood:	n/a	n/a
27	BCL3	chr6:31319415-31320898	GM12878	blood:	n/a	n/a
28	BCL3	chr6:31324702-31325296	GM12878	blood:	n/a	n/a
29	BCL3	chr6:31319812-31321116	GM12878	blood:	n/a	n/a
30	BCLAF1	chr6:31321125-31321669	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
31	BCLAF1	chr6:31318925-31319357	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:31319409-31321119	GM12878	blood:	n/a	n/a
33	BCLAF1	chr6:31322218-31322709	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:31324260-31324641	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:31300404-31300834	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:31324267-31325663	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:31322776-31323862	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:31324713-31325348	GM12878	blood:	n/a	n/a
39	BCLAF1	chr6:31334586-31335058	GM12878	blood:	n/a	n/a
40	BCLAF1	chr6:31322541-31323765	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:31318701-31319362	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:31319416-31321907	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
43	BHLHE40	chr6:31323948-31324053	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:31320567-31320928	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:31326283-31326390	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:31334679-31335011	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:31318412-31318711	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:31324927-31325138	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:31324382-31324473	GM12878	blood:	n/a	n/a
50	BHLHE40	chr6:31334682-31335021	K562	blood:	n/a	n/a

(count:3421 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31325141-31325191	AG09309	skin:	n/a
2	chr6:31324962-31325012	ovcar-3	ovarian:	n/a
3	chr6:31323677-31323727	AG04449	skin:	fetal
4	chr6:31323677-31323727	GM12891	blood:	n/a
5	chr6:31325455-31325505	GM06990	blood:	n/a
6	chr6:31325141-31325191	AG09309	skin:	n/a
7	chr6:31324962-31325012	ovcar-3	ovarian:	n/a
8	chr6:31323677-31323727	AG04449	skin:	fetal
9	chr6:31323677-31323727	GM12891	blood:	n/a
10	chr6:31325455-31325505	GM06990	blood:	n/a
11	chr6:31324259-31324309	LNCaP	prostate:	n/a
12	chr6:31324252-31324302	NT2-D1	testis:	n/a
13	chr6:31325003-31325053	SAEC	small airway:	n/a
14	chr6:31323284-31323334	HRE	kidney:	n/a
15	chr6:31325000-31325050	NB4	blood:	n/a
16	chr6:31322348-31322398	SK-N-MC	brain:	n/a
17	chr6:31325003-31325053	HPAEpiC	pulmonary alveolar:	n/a
18	chr6:31324972-31325022	HMEC	breast:	n/a
19	chr6:31325455-31325505	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:31325058-31325108	MCF10A-Er-Src	breast:	n/a
21	chr6:31324252-31324302	HMEC	breast:	n/a
22	chr6:31324500-31324550	Caco-2	colon:	n/a
23	chr6:31322577-31322627	ovcar-3	ovarian:	n/a
24	chr6:31321433-31321483	Jurkat	blood:	n/a
25	chr6:31323253-31323303	Caco-2	colon:	n/a
26	chr6:31325085-31325135	PANC-1	pancreas:	n/a
27	chr6:31325000-31325050	T-47D	breast:	n/a
28	chr6:31322996-31323046	IMR90	lung:	fetal
29	chr6:31324921-31324971	Hepatocyte	liver:	n/a
30	chr6:31324227-31324277	LNCaP	prostate:	n/a
31	chr6:31323677-31323727	K562	blood:	n/a
32	chr6:31324319-31324369	K562	blood:	n/a
33	chr6:31321433-31321483	NHDF-neo	bronchial:	n/a
34	chr6:31334836-31334886	HCT-116	colon:	n/a
35	chr6:31325136-31325186	HIPEpiC	eye:	n/a
36	chr6:31324621-31324671	MCF-7	breast:	n/a
37	chr6:31324962-31325012	HCF	heart:	n/a
38	chr6:31322766-31322816	ovcar-3	ovarian:	n/a
39	chr6:31324491-31324541	HEEpiC	esophagus:	n/a
40	chr6:31324269-31324319	BE2_C	brain:	n/a
41	chr6:31321433-31321483	AG04449	skin:	fetal
42	chr6:31323998-31324048	ovcar-3	ovarian:	n/a
43	chr6:31323261-31323311	HCPEpiC	choroid plexus:	n/a
44	chr6:31323760-31323810	ovcar-3	ovarian:	n/a
45	chr6:31324252-31324302	PANC-1	pancreas:	n/a
46	chr6:31324941-31324991	NB4	blood:	n/a
47	chr6:31323261-31323311	GM12891	blood:	n/a
48	chr6:31321433-31321483	ProgFib	skin:	n/a
49	chr6:31327376-31327426	AG09309	skin:	n/a
50	chr6:31322996-31323046	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type
1	chr6:29759731..29760249-chr6:31324546..31325250,2	HCT-116	colon:
2	chr6:31195002..31197168-chr6:31331435..31333390,2	K562	blood:
3	chr6:29855116..29856102-chr6:31324046..31324566,2	Hela-S3	cervix:
4	chr6:29689852..29692667-chr6:31324164..31326641,2	K562	blood:
5	chr6:31274576..31277552-chr6:31281409..31285159,3	MCF-7	breast:
6	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
7	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:
8	chr6:31346282..31347893-chr6:31349953..31352420,2	K562	blood:
9	chr6:31238976..31240351-chr6:31324393..31325523,6	HCT-116	colon:
10	chr6:31239600..31240303-chr6:31325089..31325595,2	Hela-S3	cervix:
11	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
12	chr6:31164428..31165295-chr6:31333347..31334316,2	MCF-7	breast:
13	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
14	chr6:31283440..31285991-chr6:31367270..31369843,2	K562	blood:
15	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
16	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
17	chr6:31241176..31243692-chr6:31324996..31327759,3	MCF-7	breast:
18	chr6:31129596..31132185-chr6:31285768..31288675,2	MCF-7	breast:
19	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
20	chr6:31343886..31345657-chr6:31346957..31349841,2	MCF-7	breast:
21	chr6:31163696..31166940-chr6:31333321..31336541,7	MCF-7	breast:
22	chr6:31343886..31345657-chr6:31346957..31349841,2	MCF-7	breast:
23	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
24	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
25	chr6:31164859..31165402-chr6:31336129..31336993,3	MCF-7	breast:
26	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
27	chr6:31104961..31105839-chr6:31334399..31335415,6	K562	blood:
28	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
29	chr6:31164797..31165692-chr6:31334361..31335283,4	K562	blood:
30	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
31	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MICA-7	chr6:31348188-31348616	NONHSAT108761
2	lnc-MICA-9	chr6:31324424-31325414	NONHSAT108757
3	lnc-HLA-C-2	chr6:31321649-31322073	NONHSAT108753
4	lnc-MICA-9	chr6:31323945-31324219	NONHSAT108756
5	lnc-HLA-C-2	chr6:31322256-31322583	NONHSAT108752
6	lnc-HLA-C-2	chr6:31322256-31322303	NONHSAT108747
7	lnc-HLA-C-2	chr6:31322256-31322303	NONHSAT108753
8	lnc-HLA-C-2	chr6:31322410-31322853	NONHSAT108753
9	lnc-HLA-B-1	chr6:31350626-31350967	NONHSAT108764
10	lnc-MICA-9	chr6:31324466-31324734	NONHSAT108756
11	lnc-MICA-6	chr6:31350312-31351479	NONHSAT108763
12	lnc-HLA-C-2	chr6:31321649-31322073	NONHSAT108752

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
FGFR3P1	TF binding region
ENSG00000271581	TF binding region
RNU6-283P	TF binding region
HLA-B	TF binding region
HLA-S	TF binding region
ZDHHC20P2	TF binding region
ENSG00000265294	TF binding region
DHFRP2	TF binding region
FGFR3P1	CpG island
ENSG00000271581	CpG island
RNU6-283P	CpG island
HLA-B	CpG island
HLA-S	CpG island
ZDHHC20P2	CpG island
ENSG00000265294	CpG island
DHFRP2	CpG island
ENSG00000206337	chromatin interactions
ENSG00000214892	chromatin interactions
ENSG00000225851	chromatin interactions
ENSG00000204540	chromatin interactions
ENSG00000206341	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000181126	chromatin interactions
ENSG00000204642	chromatin interactions
ENSG00000230994	chromatin interactions
ENSG00000225864	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000223702	chromatin interactions
ENSG00000272501	chromatin interactions
ENSG00000204525	chromatin interactions
ENSG00000229836	chromatin interactions

Extended variants
information (count: 3591 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:3591 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1634785	chr6:31283297-31283298	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs111404112	chr6:31283301-31283302	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1634744	chr6:31283317-31283318	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1634784	chr6:31283318-31283319	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs116105379	chr6:31283329-31283330	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs116152469	chr6:31283330-31283331	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114854895	chr6:31283342-31283343	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9264988	chr6:31283392-31283393	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs9264989	chr6:31283409-31283410	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs144327082	chr6:31283428-31283429	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs549205199	chr6:31283445-31283446	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs9264990	chr6:31283446-31283447	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs72856821	chr6:31283481-31283482	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs59474238	chr6:31283482-31283483	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs538663058	chr6:31283524-31283525	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs58242580	chr6:31283567-31283568	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs149203328	chr6:31283603-31283604	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs1634783	chr6:31283604-31283605	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs184932840	chr6:31283618-31283619	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs1634743	chr6:31283651-31283652	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs543971688	chr6:31283681-31283682	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1634782	chr6:31283687-31283688	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs34768512	chr6:31283700-31283701	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs532364203	chr6:31283743-31283744	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547834150	chr6:31283749-31283750	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201660546	chr6:31283763-31283764	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs9264995	chr6:31283764-31283765	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs1634742	chr6:31283793-31283794	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs539240031	chr6:31283831-31283832	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569745431	chr6:31283849-31283850	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs1634741	chr6:31283886-31283887	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs9394060	chr6:31283890-31283891	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs1634740	chr6:31283928-31283929	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs1634739	chr6:31283932-31283933	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs9380245	chr6:31283968-31283969	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs547395581	chr6:31284078-31284079	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs147646792	chr6:31284092-31284093	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565774677	chr6:31284103-31284104	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs143322157	chr6:31284108-31284109	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs9394061	chr6:31284109-31284110	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs3132477	chr6:31284121-31284122	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs2524167	chr6:31284136-31284137	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs117789106	chr6:31284157-31284158	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577617462	chr6:31284163-31284164	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565392551	chr6:31284174-31284175	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560080372	chr6:31284220-31284221	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs151331159	chr6:31284290-31284291	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559760772	chr6:31284310-31284311	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs114455662	chr6:31284326-31284327	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs3132476	chr6:31284344-31284345	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31282000-31284000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:31283000-31284200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:31289200-31290000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:31295400-31297000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:31299400-31301200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:31300000-31301000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr6:31300000-31301200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:31300000-31301200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr6:31300000-31301600	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr6:31300200-31301000	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr6:31300200-31301000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:31300200-31301200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
13	chr6:31300400-31301200	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr6:31300400-31301200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:31300400-31301200	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr6:31300600-31301200	Enhancers	Primary T cells fromperipheralblood	blood
17	chr6:31300600-31301200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr6:31300800-31301200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr6:31303600-31307400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:31304200-31305200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:31304200-31305600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:31304400-31305200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
23	chr6:31307200-31307600	Enhancers	Primary B cells from peripheral blood	blood
24	chr6:31311400-31312800	Enhancers	Primary B cells from peripheral blood	blood
25	chr6:31311600-31311800	Bivalent Enhancer	NHDF-Ad	bronchial
26	chr6:31312000-31313000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr6:31312400-31313000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:31312600-31312800	Enhancers	Primary T cells fromperipheralblood	blood
29	chr6:31312600-31313000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:31312600-31313200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr6:31312800-31313000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr6:31312800-31317800	Weak transcription	Primary B cells from peripheral blood	blood
33	chr6:31313000-31313400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:31313000-31315600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr6:31313200-31316000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr6:31313400-31313600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr6:31313600-31315200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr6:31314200-31315600	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr6:31315000-31315600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:31315200-31315600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:31315600-31315800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr6:31315600-31315800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:31315600-31316400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:31315600-31316600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr6:31315600-31322800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr6:31315800-31316000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr6:31315800-31316400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr6:31315800-31316600	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr6:31315800-31323400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr6:31316000-31316200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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