Variant report

Variant	nsv823818
Chromosome Location	chr6:109757222-109761294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:109761101-109761402	K562	blood:	n/a	n/a
2	CBX3	chr6:109761235-109762357	K562	blood:	n/a	n/a
3	CTCF	chr6:109758384-109758414	GM10266	blood:	n/a	n/a
4	CTCF	chr6:109758229-109758532	GM12878	blood:	n/a	chr6:109758475-109758488
5	CTCF	chr6:109758320-109758470	BE2_C	brain:	n/a	n/a
6	CTCF	chr6:109758280-109758430	NHEK	skin:	n/a	n/a
7	CTCF	chr6:109761140-109761290	AG10803	skin:	n/a	n/a
8	CTCF	chr6:109758300-109758450	GM12873	blood:	n/a	n/a
9	CTCF	chr6:109758260-109758410	GM12878	blood:	n/a	n/a
10	CTCF	chr6:109758320-109758454	K562	blood:	n/a	n/a
11	CTCF	chr6:109758320-109758470	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr6:109758321-109758452	HepG2	liver:	n/a	n/a
13	CTCF	chr6:109758140-109758290	HMEC	breast:	n/a	n/a
14	CTCF	chr6:109758360-109758510	HMEC	breast:	n/a	chr6:109758475-109758488
15	CTCF	chr6:109758256-109758549	K562	blood:	n/a	chr6:109758475-109758488
16	CTCF	chr6:109760880-109761030	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr6:109758332-109758432	Hela-S3	cervix:	n/a	n/a
18	E2F6	chr6:109761252-109762891	K562	blood:	n/a	chr6:109761583-109761593 chr6:109761855-109761864 chr6:109761875-109761884 chr6:109761453-109761462 chr6:109761577-109761586 chr6:109761563-109761572 chr6:109762207-109762216 chr6:109762209-109762219
19	E2F6	chr6:109761218-109762764	A549	lung:	n/a	chr6:109761583-109761593 chr6:109761855-109761864 chr6:109761875-109761884 chr6:109761453-109761462 chr6:109761577-109761586 chr6:109761563-109761572 chr6:109762207-109762216 chr6:109762209-109762219
20	E2F6	chr6:109761274-109762704	K562	blood:	n/a	chr6:109761583-109761593 chr6:109761855-109761864 chr6:109761875-109761884 chr6:109761453-109761462 chr6:109761577-109761586 chr6:109761563-109761572 chr6:109762207-109762216 chr6:109762209-109762219
21	EGR1	chr6:109761156-109762851	HCT-116	colon:	n/a	chr6:109761875-109761885 chr6:109761894-109761907 chr6:109761454-109761467 chr6:109761562-109761572 chr6:109761854-109761864 chr6:109761454-109761467 chr6:109761856-109761869
22	FOS	chr6:109760742-109761192	HUVEC	blood vessel:	n/a	n/a
23	FOSL1	chr6:109760679-109761003	K562	blood:	n/a	n/a
24	FOSL2	chr6:109760677-109761114	A549	lung:	n/a	n/a
25	GATA2	chr6:109761271-109762146	SH-SY5Y	brain:	n/a	chr6:109761383-109761392 chr6:109761383-109761390
26	GTF2F1	chr6:109760849-109761188	Hela-S3	cervix:	n/a	n/a
27	HCFC1	chr6:109761064-109762978	Hela-S3	cervix:	n/a	n/a
28	JUN	chr6:109760673-109761236	K562	blood:	n/a	n/a
29	JUND	chr6:109760662-109761105	Hela-S3	cervix:	n/a	n/a
30	JUND	chr6:109761276-109762746	K562	blood:	n/a	n/a
31	JUND	chr6:109760643-109761063	K562	blood:	n/a	n/a
32	JUND	chr6:109761149-109761319	H1-hESC	embryonic stem cell:	n/a	n/a
33	MAFK	chr6:109760403-109760534	HepG2	liver:	n/a	chr6:109760511-109760520
34	MAX	chr6:109761285-109762982	HCT-116	colon:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
35	MAX	chr6:109761182-109762928	A549	lung:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
36	MAX	chr6:109760974-109762799	K562	blood:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
37	MAX	chr6:109761257-109762845	SK-N-SH	brain:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
38	MAX	chr6:109761293-109762899	HepG2	liver:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
39	MAX	chr6:109761215-109762753	A549	lung:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
40	MAX	chr6:109760825-109762882	Hela-S3	cervix:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
41	MAX	chr6:109761267-109763135	HCT-116	colon:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
42	MAX	chr6:109761195-109762675	A549	lung:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
43	MAX	chr6:109761189-109761829	ECC-1	luminal epithelium:	n/a	chr6:109761564-109761574
44	MAZ	chr6:109761290-109763147	IMR90	lung:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
45	MXI1	chr6:109760621-109763112	SK-N-SH	brain:	n/a	chr6:109762145-109762160 chr6:109761832-109761847
46	MXI1	chr6:109761280-109762918	GM12878	blood:	n/a	chr6:109762145-109762160 chr6:109761832-109761847
47	MXI1	chr6:109760770-109762521	Hela-S3	cervix:	n/a	chr6:109762145-109762160 chr6:109761832-109761847
48	MYC	chr6:109761231-109761250	MCF10A-Er-Src	breast:	n/a	n/a
49	MYC	chr6:109761278-109762743	MCF10A-Er-Src	breast:	n/a	chr6:109761564-109761574 chr6:109762181-109762190
50	MYC	chr6:109760685-109762935	A549	lung:	n/a	chr6:109761564-109761574 chr6:109762181-109762190

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:109760819-109760869	Hepatocyte	liver:	n/a
2	chr6:109760819-109760869	LNCaP	prostate:	n/a
3	chr6:109760819-109760869	ovcar-3	ovarian:	n/a
4	chr6:109757646-109757696	AG09309	skin:	n/a
5	chr6:109757646-109757696	HCT-116	colon:	n/a
6	chr6:109757646-109757696	NHDF-neo	bronchial:	n/a
7	chr6:109760819-109760869	NHDF-neo	bronchial:	n/a
8	chr6:109760819-109760869	H1-hESC	embryonic stem cell:	embryo
9	chr6:109757646-109757696	PFSK-1	brain:	n/a
10	chr6:109760819-109760869	NT2-D1	testis:	n/a
11	chr6:109760819-109760869	GM12891	blood:	n/a
12	chr6:109760819-109760869	AG09309	skin:	n/a
13	chr6:109760831-109760881	HMEC	breast:	n/a
14	chr6:109760819-109760869	RPTEC	kidney:	n/a
15	chr6:109760831-109760881	AG10803	skin:	n/a
16	chr6:109760831-109760881	HCM	heart:	n/a
17	chr6:109760831-109760881	NHBE	bronchial:	n/a
18	chr6:109760831-109760881	GM12891	blood:	n/a
19	chr6:109760831-109760881	LNCaP	prostate:	n/a
20	chr6:109757646-109757696	PrEC	prostate:	n/a
21	chr6:109760831-109760881	ovcar-3	ovarian:	n/a
22	chr6:109760831-109760881	GM12892	blood:	n/a
23	chr6:109760819-109760869	K562	blood:	n/a
24	chr6:109760819-109760869	AG04449	skin:	fetal
25	chr6:109760819-109760869	SK-N-MC	brain:	n/a
26	chr6:109760819-109760869	NB4	blood:	n/a
27	chr6:109760831-109760881	H1-hESC	embryonic stem cell:	embryo
28	chr6:109760819-109760869	T-47D	breast:	n/a
29	chr6:109757646-109757696	GM12878	blood:	n/a
30	chr6:109757646-109757696	HRCEpiC	kidney:	n/a
31	chr6:109757646-109757696	ECC-1	luminal epithelium:	n/a
32	chr6:109760831-109760881	HepG2	liver:	n/a
33	chr6:109760831-109760881	SAEC	small airway:	n/a
34	chr6:109760831-109760881	HPAEpiC	pulmonary alveolar:	n/a
35	chr6:109760819-109760869	HMEC	breast:	n/a
36	chr6:109760819-109760869	HCPEpiC	choroid plexus:	n/a
37	chr6:109757646-109757696	LNCaP	prostate:	n/a
38	chr6:109757646-109757696	HCPEpiC	choroid plexus:	n/a
39	chr6:109760819-109760869	SAEC	small airway:	n/a
40	chr6:109760819-109760869	HNPCEpiC	eye:	n/a
41	chr6:109760831-109760881	AG04449	skin:	fetal
42	chr6:109760819-109760869	GM06990	blood:	n/a
43	chr6:109757646-109757696	HEK293	kidney:	embryo
44	chr6:109760819-109760869	Caco-2	colon:	n/a
45	chr6:109757646-109757696	SK-N-MC	brain:	n/a
46	chr6:109757646-109757696	AG04449	skin:	fetal
47	chr6:109760831-109760881	Hepatocyte	liver:	n/a
48	chr6:109757646-109757696	K562	blood:	n/a
49	chr6:109760819-109760869	HEK293	kidney:	embryo
50	chr6:109757646-109757696	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:109414651..109418067-chr6:109760738..109763991,4	MCF-7	breast:
2	chr6:109751127..109754853-chr6:109756908..109760360,4	K562	blood:
3	chr6:109755900..109759113-chr6:109760239..109764541,6	MCF-7	breast:
4	chr6:108880181..108882285-chr6:109761167..109763162,2	MCF-7	breast:
5	chr6:109760182..109762059-chr6:109802883..109805670,2	MCF-7	breast:
6	chr6:109702022..109707287-chr6:109760251..109763953,8	MCF-7	breast:
7	chr6:109747606..109750215-chr6:109758639..109760987,2	K562	blood:
8	chr6:109759652..109764361-chr6:109800705..109806354,8	K562	blood:
9	chr6:109702383..109706611-chr6:109760202..109762116,4	K562	blood:
10	chr6:109747606..109757389-chr6:109757828..109761794,11	K562	blood:
11	chr6:109747606..109757389-chr6:109757828..109761794,11	K562	blood:
12	chr6:109756751..109759661-chr6:109767137..109769430,2	MCF-7	breast:
13	chr6:109760146..109763576-chr6:109804047..109805770,3	MCF-7	breast:
14	chr6:109759628..109764398-chr6:109803414..109806709,4	K562	blood:
15	chr6:109750853..109754544-chr6:109754754..109757262,3	MCF-7	breast:
16	chr6:109415348..109417479-chr6:109760287..109762549,2	K562	blood:
17	chr6:109752212..109757242-chr6:109759553..109764133,7	MCF-7	breast:
18	chr6:109702065..109705528-chr6:109760483..109765471,8	MCF-7	breast:
19	chr6:109752212..109757242-chr6:109759553..109764133,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000239160	TF binding region
SMPD2	TF binding region
PPIL6	TF binding region
ENSG00000239160	CpG island
SMPD2	CpG island
PPIL6	CpG island
ENSG00000239160	chromatin interactions
ENSG00000260273	chromatin interactions
ENSG00000135587	chromatin interactions
ENSG00000185250	chromatin interactions
ENSG00000118689	chromatin interactions
ENSG00000183137	chromatin interactions
ENSG00000112365	chromatin interactions
ENSG00000135535	chromatin interactions
ENSG00000080546	chromatin interactions

Extended variants
information (count: 143 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533196423	chr6:109757240-109757241	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs375005416	chr6:109757279-109757280	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs377735159	chr6:109757290-109757291	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs371158486	chr6:109757304-109757305	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs374677619	chr6:109757320-109757321	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs374937011	chr6:109757373-109757374	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs549991729	chr6:109757390-109757391	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs200986902	chr6:109757392-109757393	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs9487107	chr6:109757411-109757412	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs548621455	chr6:109757412-109757413	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs150129238	chr6:109757477-109757478	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs534166781	chr6:109757487-109757488	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs9487108	chr6:109757499-109757500	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs367730892	chr6:109757508-109757509	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs113551855	chr6:109757525-109757526	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs9487109	chr6:109757526-109757527	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs556344392	chr6:109757603-109757604	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs561406572	chr6:109757645-109757646	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs576191201	chr6:109757646-109757647	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs527306388	chr6:109757647-109757648	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs546960266	chr6:109757663-109757664	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs561795695	chr6:109757698-109757699	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs185431007	chr6:109757746-109757747	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs541006664	chr6:109757820-109757821	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs576158775	chr6:109757834-109757835	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs190680386	chr6:109757843-109757844	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs533261588	chr6:109757848-109757849	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs12213313	chr6:109757893-109757894	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs149309293	chr6:109757913-109757914	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs112593411	chr6:109757920-109757921	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs34320275	chr6:109757963-109757964	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs183573750	chr6:109757984-109757985	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs375274861	chr6:109757990-109757991	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs542435240	chr6:109758074-109758075	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs75893085	chr6:109758114-109758115	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs560387948	chr6:109758123-109758124	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs144588502	chr6:109758127-109758128	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs570468318	chr6:109758211-109758212	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs138225683	chr6:109758221-109758222	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs143800088	chr6:109758224-109758225	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs576252125	chr6:109758278-109758279	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs147250959	chr6:109758300-109758301	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs555205224	chr6:109758313-109758314	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs569353867	chr6:109758349-109758350	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs527995877	chr6:109758481-109758482	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs188244129	chr6:109758543-109758544	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs370991395	chr6:109758548-109758549	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs540716244	chr6:109758552-109758553	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs116304488	chr6:109758563-109758564	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs3757237	chr6:109758678-109758679	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:114)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109721200-109760600	Weak transcription	Fetal Brain Female	brain
2	chr6:109725800-109760800	Weak transcription	Brain Anterior Caudate	brain
3	chr6:109736600-109760800	Weak transcription	Brain Angular Gyrus	brain
4	chr6:109745600-109760800	Weak transcription	Gastric	stomach
5	chr6:109750800-109760200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:109750800-109760400	Weak transcription	Ovary	ovary
7	chr6:109750800-109760800	Weak transcription	Brain Substantia Nigra	brain
8	chr6:109751000-109760200	Weak transcription	Osteobl	bone
9	chr6:109751000-109760800	Weak transcription	Right Atrium	heart
10	chr6:109751200-109760400	Weak transcription	Fetal Muscle Leg	muscle
11	chr6:109751200-109761400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr6:109751400-109760800	Weak transcription	Fetal Stomach	stomach
13	chr6:109751600-109760400	Weak transcription	NHEK	skin
14	chr6:109753800-109760800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr6:109754000-109760800	Weak transcription	Pancreas	Pancrea
16	chr6:109754200-109758400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:109754800-109760400	Weak transcription	K562	blood
18	chr6:109754800-109760600	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:109755200-109758200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr6:109756000-109760800	Weak transcription	Spleen	Spleen
21	chr6:109756200-109757400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr6:109756200-109760200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:109756200-109760400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr6:109756400-109758400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:109756400-109760600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr6:109756800-109761400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:109757200-109757600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr6:109757200-109760400	Weak transcription	Fetal Intestine Small	intestine
29	chr6:109757200-109760600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:109757400-109757800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr6:109758200-109758600	Enhancers	Primary hematopoietic stem cells	blood
32	chr6:109758200-109758800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:109758400-109758600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:109758400-109758800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:109758400-109759200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:109758600-109760800	Weak transcription	Primary hematopoietic stem cells	blood
37	chr6:109758600-109760800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr6:109758800-109760600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:109758800-109760600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:109759200-109760800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr6:109760000-109760200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr6:109760000-109760600	Enhancers	Stomach Mucosa	stomach
43	chr6:109760200-109760400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:109760200-109760400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr6:109760200-109760600	Enhancers	HSMM	muscle
46	chr6:109760200-109760600	Enhancers	HSMMtube	muscle
47	chr6:109760200-109760600	Enhancers	Osteobl	bone
48	chr6:109760200-109760800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:109760200-109760800	Active TSS	Hela-S3	cervix
50	chr6:109760200-109761600	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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