Variant report

Variant	esv16579
Chromosome Location	chr6:31285646-31351653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1387)
CpG islands
(count:3423)
Chromatin interactive
region (count:29)
LncRNA
region (count:12)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1387 , 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	chr6:31324888-31325183	K562	blood:	n/a	n/a
2	ATF1	chr6:31334724-31334995	K562	blood:	n/a	n/a
3	ATF2	chr6:31334516-31335091	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:31324794-31325350	GM12878	blood:	n/a	n/a
5	ATF2	chr6:31318444-31319386	GM12878	blood:	n/a	n/a
6	ATF2	chr6:31319422-31321748	GM12878	blood:	n/a	n/a
7	ATF2	chr6:31300411-31301086	GM12878	blood:	n/a	n/a
8	ATF2	chr6:31326062-31326576	GM12878	blood:	n/a	n/a
9	ATF2	chr6:31319512-31321668	GM12878	blood:	n/a	n/a
10	ATF2	chr6:31318632-31319385	GM12878	blood:	n/a	n/a
11	ATF2	chr6:31300449-31301004	GM12878	blood:	n/a	n/a
12	ATF2	chr6:31334664-31335022	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	chr6:31326107-31326458	GM12878	blood:	n/a	chr6:31326271-31326280
16	BATF	chr6:31300427-31300985	GM12878	blood:	n/a	n/a
17	BATF	chr6:31334694-31334977	GM12878	blood:	n/a	n/a
18	BATF	chr6:31300476-31300903	GM12878	blood:	n/a	n/a
19	BATF	chr6:31326056-31326411	GM12878	blood:	n/a	chr6:31326271-31326280
20	BATF	chr6:31325045-31325412	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:31318775-31319206	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:31326082-31326510	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:31320393-31320678	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:31326086-31326349	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:31319413-31321023	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	chr6:31318925-31319357	GM12878	blood:	n/a	n/a
31	BCLAF1	chr6:31322776-31323862	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:31318701-31319362	GM12878	blood:	n/a	n/a
33	BCLAF1	chr6:31322541-31323765	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:31322218-31322709	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:31319409-31321119	GM12878	blood:	n/a	n/a
36	BCLAF1	chr6:31324267-31325663	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:31324260-31324641	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:31321125-31321669	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
39	BCLAF1	chr6:31319416-31321907	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
40	BCLAF1	chr6:31324713-31325348	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:31300404-31300834	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:31334586-31335058	GM12878	blood:	n/a	n/a
43	BHLHE40	chr6:31324382-31324473	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:31323948-31324053	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:31318412-31318711	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:31334679-31335011	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:31326283-31326390	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:31319623-31320237	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:31334682-31335021	K562	blood:	n/a	n/a
50	BHLHE40	chr6:31320567-31320928	GM12878	blood:	n/a	n/a

(count:3423 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31334836-31334886	GM19239	blood:	n/a
2	chr6:31325314-31325364	LNCaP	prostate:	n/a
3	chr6:31325817-31325867	SAEC	small airway:	n/a
4	chr6:31324252-31324302	NB4	blood:	n/a
5	chr6:31324627-31324677	HAEpiC	amniotic membrane:	n/a
6	chr6:31324269-31324319	NHDF-neo	bronchial:	n/a
7	chr6:31325455-31325505	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:31334836-31334886	GM19239	blood:	n/a
9	chr6:31325314-31325364	LNCaP	prostate:	n/a
10	chr6:31325817-31325867	SAEC	small airway:	n/a
11	chr6:31324252-31324302	NB4	blood:	n/a
12	chr6:31324627-31324677	HAEpiC	amniotic membrane:	n/a
13	chr6:31324269-31324319	NHDF-neo	bronchial:	n/a
14	chr6:31325455-31325505	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:31325000-31325050	NB4	blood:	n/a
16	chr6:31321433-31321483	AoSMC	blood vessel:	n/a
17	chr6:31323506-31323556	AG04450	lung:	fetal
18	chr6:31324252-31324302	GM06990	blood:	n/a
19	chr6:31324259-31324309	GM12891	blood:	n/a
20	chr6:31324259-31324309	ECC-1	luminal epithelium:	n/a
21	chr6:31322766-31322816	HRE	kidney:	n/a
22	chr6:31324962-31325012	HL-60	blood:	n/a
23	chr6:31323261-31323311	AG10803	skin:	n/a
24	chr6:31324259-31324309	HMEC	breast:	n/a
25	chr6:31324500-31324550	AG04449	skin:	fetal
26	chr6:31324252-31324302	BE2_C	brain:	n/a
27	chr6:31323985-31324035	BJ	skin:	n/a
28	chr6:31324024-31324074	MCF10A-Er-Src	breast:	n/a
29	chr6:31324227-31324277	GM12878	blood:	n/a
30	chr6:31324621-31324671	HCPEpiC	choroid plexus:	n/a
31	chr6:31324512-31324562	HEEpiC	esophagus:	n/a
32	chr6:31325000-31325050	A549	lung:	n/a
33	chr6:31322996-31323046	NH-A	brain:	n/a
34	chr6:31323284-31323334	HCF	heart:	n/a
35	chr6:31324627-31324677	GM12878	blood:	n/a
36	chr6:31324024-31324074	A549	lung:	n/a
37	chr6:31323998-31324048	NH-A	brain:	n/a
38	chr6:31322348-31322398	NHDF-neo	bronchial:	n/a
39	chr6:31347802-31347852	GM12878	blood:	n/a
40	chr6:31322298-31322348	MCF-7	breast:	n/a
41	chr6:31322298-31322348	SK-N-SH_RA	brain:	n/a
42	chr6:31324916-31324966	HEEpiC	esophagus:	n/a
43	chr6:31323284-31323334	AG04450	lung:	fetal
44	chr6:31325427-31325477	HCF	heart:	n/a
45	chr6:31324916-31324966	ECC-1	luminal epithelium:	n/a
46	chr6:31324491-31324541	A549	lung:	n/a
47	chr6:31323253-31323303	GM19239	blood:	n/a
48	chr6:31323253-31323303	HCPEpiC	choroid plexus:	n/a
49	chr6:31323253-31323303	HCM	heart:	n/a
50	chr6:31325427-31325477	Hela-S3	cervix:	n/a

(count:29 , 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	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
4	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
5	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
6	chr6:31343886..31345657-chr6:31346957..31349841,2	MCF-7	breast:
7	chr6:29855116..29856102-chr6:31324046..31324566,2	Hela-S3	cervix:
8	chr6:31195002..31197168-chr6:31331435..31333390,2	K562	blood:
9	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
10	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:
11	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
12	chr6:31104961..31105839-chr6:31334399..31335415,6	K562	blood:
13	chr6:31239600..31240303-chr6:31325089..31325595,2	Hela-S3	cervix:
14	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
15	chr6:31283440..31285991-chr6:31367270..31369843,2	K562	blood:
16	chr6:31164797..31165692-chr6:31334361..31335283,4	K562	blood:
17	chr6:31163696..31166940-chr6:31333321..31336541,7	MCF-7	breast:
18	chr6:31164428..31165295-chr6:31333347..31334316,2	MCF-7	breast:
19	chr6:29759731..29760249-chr6:31324546..31325250,2	HCT-116	colon:
20	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
21	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
22	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
23	chr6:31164859..31165402-chr6:31336129..31336993,3	MCF-7	breast:
24	chr6:31129596..31132185-chr6:31285768..31288675,2	MCF-7	breast:
25	chr6:29689852..29692667-chr6:31324164..31326641,2	K562	blood:
26	chr6:31238976..31240351-chr6:31324393..31325523,6	HCT-116	colon:
27	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
28	chr6:31343886..31345657-chr6:31346957..31349841,2	MCF-7	breast:
29	chr6:31346282..31347893-chr6:31349953..31352420,2	K562	blood:

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

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

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
ENSG00000206341	chromatin interactions
ENSG00000223702	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000204540	chromatin interactions
ENSG00000181126	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000225851	chromatin interactions
ENSG00000225864	chromatin interactions
ENSG00000272501	chromatin interactions
ENSG00000230994	chromatin interactions
ENSG00000214892	chromatin interactions
ENSG00000204525	chromatin interactions
ENSG00000204642	chromatin interactions
ENSG00000206337	chromatin interactions

Extended variants
information (count: 3478 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:3478 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9265028	chr6:31285648-31285649	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs9265029	chr6:31285651-31285652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs9265030	chr6:31285652-31285653	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs9265031	chr6:31285660-31285661	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs9265032	chr6:31285667-31285668	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs9265033	chr6:31285669-31285670	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs370543357	chr6:31285684-31285685	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9265034	chr6:31285696-31285697	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534350749	chr6:31285703-31285704	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs189790930	chr6:31285711-31285712	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535157644	chr6:31285731-31285732	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs9265035	chr6:31285748-31285749	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs28542438	chr6:31285749-31285750	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs78225537	chr6:31285768-31285769	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573138482	chr6:31285817-31285818	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs28367721	chr6:31285842-31285843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs539793836	chr6:31285843-31285844	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs9265037	chr6:31285865-31285866	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs533379588	chr6:31285872-31285873	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs9265038	chr6:31285876-31285877	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557960138	chr6:31285889-31285890	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs186162934	chr6:31285900-31285901	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9265039	chr6:31285932-31285933	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs76861632	chr6:31285943-31285944	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs9265041	chr6:31285967-31285968	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9265166	chr6:31289242-31289243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555316522	chr6:31289245-31289246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs9265167	chr6:31289255-31289256	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs386699027	chr6:31289271-31289272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9265170	chr6:31289284-31289285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531285921	chr6:31289309-31289310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9281332	chr6:31289315-31289316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9265171	chr6:31289349-31289350	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs189877359	chr6:31289362-31289363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9265172	chr6:31289364-31289365	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs9265173	chr6:31289394-31289395	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs560872099	chr6:31289395-31289396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs386699028	chr6:31289449-31289450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs28752782	chr6:31289451-31289452	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
40	rs566005474	chr6:31289455-31289456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs386699029	chr6:31289460-31289461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs9265181	chr6:31289478-31289479	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs9265182	chr6:31289484-31289485	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs9265183	chr6:31289517-31289518	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs9265184	chr6:31289535-31289536	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs556506203	chr6:31289541-31289542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs9265185	chr6:31289548-31289549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs202213669	chr6:31289563-31289564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs386699030	chr6:31289564-31289565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9265187	chr6:31289565-31289566	Enhancers	n/a	n/a	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:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31289200-31290000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:31295400-31297000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:31299400-31301200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:31300000-31301000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:31300000-31301200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr6:31300000-31301200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
7	chr6:31300000-31301600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr6:31300200-31301000	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr6:31300200-31301000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:31300200-31301200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr6:31300400-31301200	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr6:31300400-31301200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr6:31300400-31301200	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr6:31300600-31301200	Enhancers	Primary T cells fromperipheralblood	blood
15	chr6:31300600-31301200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr6:31300800-31301200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:31303600-31307400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:31304200-31305200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr6:31304200-31305600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:31304400-31305200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr6:31307200-31307600	Enhancers	Primary B cells from peripheral blood	blood
22	chr6:31311400-31312800	Enhancers	Primary B cells from peripheral blood	blood
23	chr6:31311600-31311800	Bivalent Enhancer	NHDF-Ad	bronchial
24	chr6:31312000-31313000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:31312400-31313000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:31312600-31312800	Enhancers	Primary T cells fromperipheralblood	blood
27	chr6:31312600-31313000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr6:31312600-31313200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:31312800-31313000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr6:31312800-31317800	Weak transcription	Primary B cells from peripheral blood	blood
31	chr6:31313000-31313400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:31313000-31315600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr6:31313200-31316000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr6:31313400-31313600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:31313600-31315200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:31314200-31315600	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr6:31315000-31315600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:31315200-31315600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr6:31315600-31315800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr6:31315600-31315800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr6:31315600-31316400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:31315600-31316600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:31315600-31322800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:31315800-31316000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr6:31315800-31316400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr6:31315800-31316600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr6:31315800-31323400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:31316000-31316200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:31316000-31316600	Enhancers	HepG2	liver
50	chr6:31316200-31316400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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