Variant report

Variant	nsv10817
Chromosome Location	chr6:31252221-31319757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:495)
CpG islands
(count:1712)
Chromatin interactive
region (count:32)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:31272445-31272772	K562	blood:	n/a	n/a
2	ATF2	chr6:31272219-31272895	GM12878	blood:	n/a	n/a
3	ATF2	chr6:31272379-31272838	GM12878	blood:	n/a	n/a
4	ATF2	chr6:31318444-31319386	GM12878	blood:	n/a	n/a
5	ATF2	chr6:31300411-31301086	GM12878	blood:	n/a	n/a
6	ATF2	chr6:31300449-31301004	GM12878	blood:	n/a	n/a
7	ATF2	chr6:31318632-31319385	GM12878	blood:	n/a	n/a
8	ATF2	chr6:31319512-31321668	GM12878	blood:	n/a	n/a
9	ATF2	chr6:31319422-31321748	GM12878	blood:	n/a	n/a
10	BACH1	chr6:31276089-31276266	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr6:31300427-31300985	GM12878	blood:	n/a	n/a
12	BATF	chr6:31300476-31300903	GM12878	blood:	n/a	n/a
13	BCL11A	chr6:31319413-31321023	GM12878	blood:	n/a	n/a
14	BCL11A	chr6:31300656-31300925	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:31318775-31319206	GM12878	blood:	n/a	n/a
16	BCL3	chr6:31319415-31320898	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:31318925-31319357	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:31319416-31321907	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
19	BCLAF1	chr6:31319409-31321119	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:31300404-31300834	GM12878	blood:	n/a	n/a
21	BCLAF1	chr6:31318701-31319362	GM12878	blood:	n/a	n/a
22	BHLHE40	chr6:31319623-31320237	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:31318412-31318711	GM12878	blood:	n/a	n/a
24	BRCA1	chr6:31319716-31319729	GM12878	blood:	n/a	n/a
25	CBX3	chr6:31308066-31308395	K562	blood:	n/a	n/a
26	CBX3	chr6:31272647-31272911	K562	blood:	n/a	n/a
27	CBX3	chr6:31296085-31296471	K562	blood:	n/a	n/a
28	CBX3	chr6:31304557-31305309	HCT-116	colon:	n/a	n/a
29	CBX3	chr6:31308059-31308327	K562	blood:	n/a	n/a
30	CBX3	chr6:31296053-31296562	HCT-116	colon:	n/a	n/a
31	CBX3	chr6:31296167-31296435	K562	blood:	n/a	n/a
32	CBX3	chr6:31304563-31305062	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:31308020-31308398	HCT-116	colon:	n/a	n/a
34	CBX3	chr6:31273672-31273874	K562	blood:	n/a	n/a
35	CEBPB	chr6:31298472-31298769	HepG2	liver:	n/a	chr6:31298602-31298613
36	CEBPB	chr6:31300483-31301054	GM12878	blood:	n/a	n/a
37	CEBPB	chr6:31298538-31298651	K562	blood:	n/a	chr6:31298602-31298613
38	CEBPB	chr6:31277693-31277960	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:31253836-31254077	A549	lung:	n/a	chr6:31253908-31253917
40	CEBPB	chr6:31277750-31277899	A549	lung:	n/a	n/a
41	CEBPB	chr6:31253886-31253955	K562	blood:	n/a	chr6:31253908-31253917
42	CEBPB	chr6:31298464-31298742	IMR90	lung:	n/a	chr6:31298602-31298613
43	CEBPB	chr6:31253791-31254077	HepG2	liver:	n/a	chr6:31253908-31253917
44	CEBPB	chr6:31253830-31254055	IMR90	lung:	n/a	chr6:31253908-31253917
45	CEBPB	chr6:31319547-31321170	GM12878	blood:	n/a	n/a
46	CEBPB	chr6:31298559-31298674	A549	lung:	n/a	chr6:31298602-31298613
47	CHD2	chr6:31275791-31276113	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr6:31319633-31320032	GM12878	blood:	n/a	n/a
49	CHD2	chr6:31318939-31318986	GM12878	blood:	n/a	n/a
50	CREB1	chr6:31272355-31272934	GM12878	blood:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31276187-31276237	GM06990	blood:	n/a
2	chr6:31276667-31276717	BE2_C	brain:	n/a
3	chr6:31275666-31275716	HAEpiC	amniotic membrane:	n/a
4	chr6:31276146-31276196	PrEC	prostate:	n/a
5	chr6:31276187-31276237	GM06990	blood:	n/a
6	chr6:31276667-31276717	BE2_C	brain:	n/a
7	chr6:31275666-31275716	HAEpiC	amniotic membrane:	n/a
8	chr6:31276146-31276196	PrEC	prostate:	n/a
9	chr6:31275551-31275601	NHBE	bronchial:	n/a
10	chr6:31275267-31275317	HRE	kidney:	n/a
11	chr6:31275666-31275716	ECC-1	luminal epithelium:	n/a
12	chr6:31276653-31276703	RPTEC	kidney:	n/a
13	chr6:31275875-31275925	HRCEpiC	kidney:	n/a
14	chr6:31276437-31276487	GM06990	blood:	n/a
15	chr6:31276664-31276714	NHDF-neo	bronchial:	n/a
16	chr6:31276669-31276719	AG09319	gingival:	n/a
17	chr6:31275551-31275601	H1-hESC	embryonic stem cell:	embryo
18	chr6:31275767-31275817	HMEC	breast:	n/a
19	chr6:31275148-31275198	IMR90	lung:	fetal
20	chr6:31276797-31276847	GM19239	blood:	n/a
21	chr6:31272449-31272499	U87	brain:	n/a
22	chr6:31276504-31276554	AG10803	skin:	n/a
23	chr6:31276146-31276196	NH-A	brain:	n/a
24	chr6:31275664-31275714	ovcar-3	ovarian:	n/a
25	chr6:31276653-31276703	BJ	skin:	n/a
26	chr6:31275718-31275768	AG10803	skin:	n/a
27	chr6:31276212-31276262	PANC-1	pancreas:	n/a
28	chr6:31276418-31276468	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:31276653-31276703	NT2-D1	testis:	n/a
30	chr6:31275664-31275714	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:31275551-31275601	Hela-S3	cervix:	n/a
32	chr6:31276664-31276714	HepG2	liver:	n/a
33	chr6:31275767-31275817	CMK	blood:	n/a
34	chr6:31275807-31275857	ECC-1	luminal epithelium:	n/a
35	chr6:31275767-31275817	NT2-D1	testis:	n/a
36	chr6:31275807-31275857	A549	lung:	n/a
37	chr6:31275881-31275931	PrEC	prostate:	n/a
38	chr6:31275148-31275198	PFSK-1	brain:	n/a
39	chr6:31276667-31276717	HCM	heart:	n/a
40	chr6:31276434-31276484	GM19239	blood:	n/a
41	chr6:31275741-31275791	ECC-1	luminal epithelium:	n/a
42	chr6:31276667-31276717	A549	lung:	n/a
43	chr6:31275643-31275693	HCPEpiC	choroid plexus:	n/a
44	chr6:31275807-31275857	HAEpiC	amniotic membrane:	n/a
45	chr6:31276667-31276717	ECC-1	luminal epithelium:	n/a
46	chr6:31275718-31275768	CMK	blood:	n/a
47	chr6:31276212-31276262	GM19239	blood:	n/a
48	chr6:31276664-31276714	NHBE	bronchial:	n/a
49	chr6:31275643-31275693	SK-N-SH_RA	brain:	n/a
50	chr6:31275551-31275601	HPAEpiC	pulmonary alveolar:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
2	chr6:31262379..31263887-chr6:31264452..31266692,2	MCF-7	breast:
3	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
4	chr6:31272998..31275186-chr6:31333057..31335314,2	K562	blood:
5	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
6	chr6:31283440..31285991-chr6:31367270..31369843,2	K562	blood:
7	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
8	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
9	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
10	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
11	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:
12	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
13	chr6:31272067..31274682-chr6:31275532..31277366,2	MCF-7	breast:
14	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
15	chr6:31262379..31263887-chr6:31264452..31266692,2	MCF-7	breast:
16	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:
17	chr6:31251382..31252914-chr6:31343854..31345706,2	MCF-7	breast:
18	chr6:31274551..31276643-chr6:31277971..31279738,2	MCF-7	breast:
19	chr6:31274011..31276374-chr6:31277383..31280033,2	K562	blood:
20	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
21	chr6:31260315..31262066-chr6:31270612..31272546,2	MCF-7	breast:
22	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
23	chr6:31260315..31262066-chr6:31270612..31272546,2	MCF-7	breast:
24	chr6:31256122..31258941-chr6:31260246..31262615,2	MCF-7	breast:
25	chr6:31129596..31132185-chr6:31285768..31288675,2	MCF-7	breast:
26	chr6:31274576..31277552-chr6:31281409..31285159,3	MCF-7	breast:
27	chr6:31260319..31263250-chr6:31266330..31267976,2	K562	blood:
28	chr6:31164078..31166363-chr6:31260745..31263696,2	K562	blood:
29	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
30	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
31	chr6:31260319..31263250-chr6:31266330..31267976,2	K562	blood:
32	chr6:31164078..31167331-chr6:31260118..31263696,3	K562	blood:

(count:7 , 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	chr6:31269249-31269419	ENSG00000256166
3	lnc-HLA-C-1	chr6:31261992-31262072	ENSG00000256166
4	lnc-HLA-C-1	chr6:31261685-31261898	ENSG00000256166
5	lnc-HLA-C-4	chr6:31276254-31276326	NONHSAT108751
6	lnc-HLA-C-4	chr6:31275592-31275824	NONHSAT108751
7	lnc-HLA-C-1	chr6:31262721-31262790	ENSG00000256166

No data

Variant related genes	Relation type
ENSG00000271581	TF binding region
ENSG00000229836	TF binding region
WASF5P	TF binding region
ENSG00000256166	TF binding region
ENSG00000271581	CpG island
ENSG00000229836	CpG island
WASF5P	CpG island
ENSG00000256166	CpG island
ENSG00000230994	chromatin interactions
ENSG00000206337	chromatin interactions
ENSG00000229836	chromatin interactions
ENSG00000231402	chromatin interactions
ENSG00000228432	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000272501	chromatin interactions

Extended variants
information (count: 2721 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:2721 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373127861	chr6:31252230-31252231	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs377402380	chr6:31252231-31252232	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2524055	chr6:31252237-31252238	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs539648586	chr6:31252243-31252244	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192977656	chr6:31252266-31252267	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573346967	chr6:31252372-31252373	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114115450	chr6:31252388-31252389	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2524054	chr6:31252396-31252397	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
9	rs115931507	chr6:31252406-31252407	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191981693	chr6:31252457-31252458	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs386568878	chr6:31252469-31252470	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371173717	chr6:31252512-31252513	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115862431	chr6:31252521-31252522	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs116281893	chr6:31252527-31252528	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2853937	chr6:31252569-31252570	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs564348804	chr6:31252571-31252572	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547488697	chr6:31252589-31252590	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs116838750	chr6:31252641-31252642	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540165736	chr6:31252645-31252646	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536438924	chr6:31252667-31252668	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529265656	chr6:31252668-31252669	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143609752	chr6:31252671-31252672	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs367736640	chr6:31252672-31252673	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs140086525	chr6:31252676-31252677	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569154718	chr6:31252704-31252705	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555968073	chr6:31252722-31252723	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs386622031	chr6:31252747-31252748	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149805428	chr6:31252778-31252779	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs534102760	chr6:31252832-31252833	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556108581	chr6:31252835-31252836	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567914682	chr6:31252868-31252869	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576938885	chr6:31252882-31252883	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534659501	chr6:31252893-31252894	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs117116032	chr6:31252909-31252910	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12191877	chr6:31252925-31252926	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
36	rs116350468	chr6:31252951-31252952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188765396	chr6:31252992-31252993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561354037	chr6:31253030-31253031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115727572	chr6:31253034-31253035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561657890	chr6:31253049-31253050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145758722	chr6:31253052-31253053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148990928	chr6:31253067-31253068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs28367591	chr6:31253097-31253098	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs564888318	chr6:31253109-31253110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35857242	chr6:31253121-31253122	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs191783278	chr6:31253128-31253129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143740418	chr6:31253142-31253143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183862848	chr6:31253238-31253239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188298333	chr6:31253239-31253240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559794967	chr6:31253246-31253247	Enhancers	n/a	n/a	Overlapped CNVs	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:311 , 50 per page) page: 1 2 3 4 5 6 7

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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