Variant report

Variant	nsv883533
Chromosome Location	chr6:29704237-29715997
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:316)
CpG islands
(count:2441)
Chromatin interactive
region (count:17)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:29706998-29707182	HepG2	liver:	n/a	chr6:29707124-29707135
2	CEBPB	chr6:29706945-29707271	IMR90	lung:	n/a	chr6:29707124-29707135
3	CEBPB	chr6:29705744-29706120	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr6:29714641-29715006	HepG2	liver:	n/a	n/a
5	CEBPB	chr6:29705772-29706113	A549	lung:	n/a	n/a
6	CEBPB	chr6:29706938-29707292	HepG2	liver:	n/a	chr6:29707124-29707135
7	CEBPB	chr6:29714568-29715006	MCF-7	breast:	n/a	n/a
8	CEBPB	chr6:29714652-29714992	A549	lung:	n/a	n/a
9	CEBPB	chr6:29714643-29714983	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr6:29705745-29706098	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:29714663-29714945	K562	blood:	n/a	n/a
12	CTCF	chr6:29705653-29705742	GM19238	blood:	n/a	n/a
13	CTCF	chr6:29705880-29706030	MCF-7	breast:	n/a	n/a
14	CTCF	chr6:29705920-29706070	HUVEC	blood vessel:	n/a	n/a
15	CTCF	chr6:29705920-29706070	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr6:29705785-29706178	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr6:29705940-29706090	SAEC	small airway:	n/a	n/a
18	CTCF	chr6:29705872-29706137	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr6:29705940-29706090	GM12871	blood:	n/a	n/a
20	CTCF	chr6:29705880-29706030	GM12873	blood:	n/a	n/a
21	CTCF	chr6:29705708-29706191	A549	lung:	n/a	n/a
22	CTCF	chr6:29705880-29706030	NHEK	skin:	n/a	n/a
23	CTCF	chr6:29705940-29706090	GM12873	blood:	n/a	n/a
24	CTCF	chr6:29705940-29706090	HCT-116	colon:	n/a	n/a
25	CTCF	chr6:29705620-29705770	AG04449	skin:	n/a	n/a
26	CTCF	chr6:29705480-29705630	HFF	foreskin:	n/a	n/a
27	CTCF	chr6:29705900-29706050	HMEC	breast:	n/a	n/a
28	CTCF	chr6:29705852-29706175	K562	blood:	n/a	n/a
29	CTCF	chr6:29705810-29706225	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:29705920-29706070	HMF	breast:	n/a	n/a
31	CTCF	chr6:29705900-29706050	BE2_C	brain:	n/a	n/a
32	CTCF	chr6:29705940-29706090	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr6:29705863-29706188	A549	lung:	n/a	n/a
34	CTCF	chr6:29709840-29709990	GM12867	blood:	n/a	n/a
35	CTCF	chr6:29705960-29706110	BJ	skin:	n/a	n/a
36	CTCF	chr6:29705827-29706158	GM19239	blood:	n/a	n/a
37	CTCF	chr6:29705920-29706070	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr6:29705920-29706070	AG09319	gingival:	n/a	n/a
39	CTCF	chr6:29705532-29706201	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr6:29705860-29706150	Lung_OC	lung:	n/a	n/a
41	CTCF	chr6:29705902-29706146	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:29705900-29706050	WI-38	lung:	n/a	n/a
43	CTCF	chr6:29705940-29706090	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr6:29705827-29706172	Gliobla	brain:	n/a	n/a
45	CTCF	chr6:29705920-29706070	AG04450	lung:	n/a	n/a
46	CTCF	chr6:29715181-29715244	K562	blood:	n/a	n/a
47	CTCF	chr6:29715090-29715399	K562	blood:	n/a	n/a
48	CTCF	chr6:29705920-29706070	HPF	lung:	n/a	n/a
49	CTCF	chr6:29705860-29706084	ECC-1	luminal epithelium:	n/a	n/a
50	CTCF	chr6:29705960-29706110	GM12874	blood:	n/a	n/a

(count:2441 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29711438-29711488	CMK	blood:	n/a
2	chr6:29711438-29711488	CMK	blood:	n/a
3	chr6:29711588-29711638	AG09319	gingival:	n/a
4	chr6:29710221-29710271	MCF-7	breast:	n/a
5	chr6:29713615-29713665	HNPCEpiC	eye:	n/a
6	chr6:29712115-29712165	NHDF-neo	bronchial:	n/a
7	chr6:29708164-29708214	SKMC	muscle:	n/a
8	chr6:29712541-29712591	Caco-2	colon:	n/a
9	chr6:29709610-29709660	AoSMC	blood vessel:	n/a
10	chr6:29711588-29711638	AG04449	skin:	fetal
11	chr6:29706377-29706427	HNPCEpiC	eye:	n/a
12	chr6:29714824-29714874	AoSMC	blood vessel:	n/a
13	chr6:29711975-29712025	Hela-S3	cervix:	n/a
14	chr6:29714043-29714093	AG04450	lung:	fetal
15	chr6:29714824-29714874	HepG2	liver:	n/a
16	chr6:29711249-29711299	HCT-116	colon:	n/a
17	chr6:29710109-29710159	HEEpiC	esophagus:	n/a
18	chr6:29711249-29711299	Hepatocyte	liver:	n/a
19	chr6:29708958-29709008	NHDF-neo	bronchial:	n/a
20	chr6:29711249-29711299	IMR90	lung:	fetal
21	chr6:29707887-29707937	HEK293	kidney:	embryo
22	chr6:29711465-29711515	HIPEpiC	eye:	n/a
23	chr6:29712877-29712927	NHBE	bronchial:	n/a
24	chr6:29712877-29712927	ProgFib	skin:	n/a
25	chr6:29711438-29711488	SAEC	small airway:	n/a
26	chr6:29712425-29712475	RPTEC	kidney:	n/a
27	chr6:29704545-29704595	MCF-7	breast:	n/a
28	chr6:29705939-29705989	HEEpiC	esophagus:	n/a
29	chr6:29708958-29709008	T-47D	breast:	n/a
30	chr6:29705878-29705928	NHBE	bronchial:	n/a
31	chr6:29706048-29706098	HCT-116	colon:	n/a
32	chr6:29712425-29712475	NH-A	brain:	n/a
33	chr6:29708311-29708361	T-47D	breast:	n/a
34	chr6:29714945-29714995	K562	blood:	n/a
35	chr6:29713615-29713665	MCF10A-Er-Src	breast:	n/a
36	chr6:29714059-29714109	AG09309	skin:	n/a
37	chr6:29710830-29710880	HCF	heart:	n/a
38	chr6:29714043-29714093	HCPEpiC	choroid plexus:	n/a
39	chr6:29715160-29715210	HUVEC	blood vessel:	n/a
40	chr6:29714945-29714995	PFSK-1	brain:	n/a
41	chr6:29706377-29706427	SK-N-SH_RA	brain:	n/a
42	chr6:29705878-29705928	NB4	blood:	n/a
43	chr6:29706048-29706098	Hela-S3	cervix:	n/a
44	chr6:29711588-29711638	H1-hESC	embryonic stem cell:	embryo
45	chr6:29715846-29715896	ProgFib	skin:	n/a
46	chr6:29711249-29711299	NH-A	brain:	n/a
47	chr6:29714824-29714874	A549	lung:	n/a
48	chr6:29708958-29709008	BE2_C	brain:	n/a
49	chr6:29705815-29705865	AG04449	skin:	fetal
50	chr6:29710109-29710159	ECC-1	luminal epithelium:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29710755..29712500-chr6:29714254..29717094,2	K562	blood:
2	chr6:29709817..29712750-chr6:29714477..29716450,2	MCF-7	breast:
3	chr6:29707158..29708968-chr6:29712786..29714883,2	K562	blood:
4	chr6:29673586..29674252-chr6:29706679..29707289,2	MCF-7	breast:
5	chr6:29712707..29714647-chr6:29717488..29720857,3	K562	blood:
6	chr6:29707158..29708968-chr6:29712786..29714883,2	K562	blood:
7	chr6:29710008..29711886-chr6:29712365..29714063,2	K562	blood:
8	chr6:29710008..29711886-chr6:29712365..29714063,2	K562	blood:
9	chr6:29692276..29694420-chr6:29705513..29707651,2	MCF-7	breast:
10	chr6:29713370..29715869-chr6:29729277..29731286,2	MCF-7	breast:
11	chr6:29709930..29711722-chr6:29720449..29722464,2	K562	blood:
12	chr6:29708611..29711552-chr6:29714400..29717446,4	MCF-7	breast:
13	chr6:29706366..29709213-chr6:29717872..29720570,2	MCF-7	breast:
14	chr6:29692092..29694262-chr6:29708323..29710900,2	K562	blood:
15	chr6:29712194..29714049-chr6:29781280..29783856,2	K562	blood:
16	chr6:29710119..29712623-chr6:29721345..29723379,2	MCF-7	breast:
17	chr6:29704423..29706634-chr6:29713030..29715317,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP57-7	chr6:29705536-29705978	ENSG00000214922.3
2	lnc-HLA-F-2	chr6:29704793-29705231	NONHSAT108546
3	lnc-ZFP57-7	chr6:29702805-29704597	ENSG00000214922.3
4	lnc-ZFP57-7	chr6:29711786-29711929	NONHSAT108548
5	lnc-ZFP57-7	chr6:29712044-29712321	NONHSAT108548
6	lnc-ZFP57-7	chr6:29706112-29706232	ENSG00000214922.3
7	lnc-ZFP57-7	chr6:29713250-29713504	ENSG00000214922.3
8	lnc-ZFP57-7	chr6:29706328-29706663	ENSG00000214922.3
9	lnc-ZFP57-7	chr6:29709508-29709632	NONHSAT108548
10	lnc-ZFP57-7	chr6:29705743-29705978	ENSG00000214922.3
11	lnc-HLA-F-2	chr6:29708090-29708504	NONHSAT108546
12	lnc-HLA-F-2	chr6:29709099-29709632	NONHSAT108546
13	lnc-ZFP57-7	chr6:29706112-29706221	ENSG00000214922.3
14	lnc-ZFP57-7	chr6:29706564-29706831	expReg_chr6_2271_-
15	lnc-ZFP57-7	chr6:29713250-29713504	NONHSAT108548
16	lnc-ZFP57-7	chr6:29712727-29713011	NONHSAT108548

No data

Variant related genes	Relation type
ENSG00000199290	TF binding region
HCG9P5	TF binding region
HLA-F-AS1	TF binding region
ENSG00000199290	CpG island
HCG9P5	CpG island
HLA-F-AS1	CpG island
ENSG00000235821	chromatin interactions
ENSG00000272236	chromatin interactions
ENSG00000273340	chromatin interactions
ENSG00000227758	chromatin interactions
ENSG00000204642	chromatin interactions
ENSG00000199290	chromatin interactions
ENSG00000214922	chromatin interactions
ENSG00000270896	chromatin interactions

Extended variants
information (count: 460 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9258206	chr6:29704237-29704238	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2743919	chr6:29704259-29704260	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs1736915	chr6:29704316-29704317	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs1736914	chr6:29704379-29704380	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs539397067	chr6:29704380-29704381	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs182116036	chr6:29704397-29704398	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs1736913	chr6:29704400-29704401	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs9258207	chr6:29704443-29704444	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs549814990	chr6:29704537-29704538	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs9258208	chr6:29704545-29704546	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
11	rs555127945	chr6:29704546-29704547	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs2517944	chr6:29704547-29704548	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
13	rs116878102	chr6:29704556-29704557	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs186086337	chr6:29704559-29704560	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs9500967	chr6:29704560-29704561	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs532675656	chr6:29704562-29704563	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs1633099	chr6:29704633-29704634	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs9368609	chr6:29704638-29704639	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs2523394	chr6:29704673-29704674	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs548429368	chr6:29704675-29704676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568559830	chr6:29704709-29704710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552189983	chr6:29704726-29704727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9500968	chr6:29704772-29704773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2517943	chr6:29704833-29704834	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs115479327	chr6:29704834-29704835	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs149129401	chr6:29704895-29704896	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs115042142	chr6:29704897-29704898	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs2743918	chr6:29704921-29704922	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs190406637	chr6:29704949-29704950	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs148371416	chr6:29704978-29704979	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs114549249	chr6:29704988-29704989	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs376989934	chr6:29704996-29704997	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs113724594	chr6:29705009-29705010	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs563042573	chr6:29705015-29705016	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs535446619	chr6:29705025-29705026	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs1633098	chr6:29705028-29705029	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs572109389	chr6:29705030-29705031	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs540432808	chr6:29705031-29705032	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs552920167	chr6:29705072-29705073	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs7751815	chr6:29705084-29705085	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs577118356	chr6:29705108-29705109	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs182531190	chr6:29705128-29705129	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs115130761	chr6:29705169-29705170	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs144026054	chr6:29705199-29705200	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs2844832	chr6:29705219-29705220	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs186813240	chr6:29705294-29705295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527823225	chr6:29705299-29705300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547608967	chr6:29705350-29705351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9258209	chr6:29705402-29705403	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs2743917	chr6:29705405-29705406	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:106)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	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
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29692200-29715800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:29692400-29715800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:29692800-29712000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:29693200-29711400	Weak transcription	Pancreas	Pancrea
5	chr6:29693400-29715600	Weak transcription	Esophagus	oesophagus
6	chr6:29693600-29715600	Weak transcription	NHLF	lung
7	chr6:29693800-29705400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr6:29693800-29715400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:29693800-29716000	Weak transcription	Small Intestine	intestine
10	chr6:29694000-29707000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr6:29694000-29711200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr6:29694000-29711400	Weak transcription	Gastric	stomach
13	chr6:29694000-29712200	Weak transcription	Aorta	Aorta
14	chr6:29694000-29715600	Weak transcription	Colon Smooth Muscle	Colon
15	chr6:29694200-29705600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:29696000-29705600	Weak transcription	Right Ventricle	heart
17	chr6:29696000-29715600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr6:29696000-29715600	Weak transcription	Ovary	ovary
19	chr6:29696200-29705600	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr6:29696200-29705800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr6:29696200-29711800	Weak transcription	Adipose Nuclei	Adipose
22	chr6:29696200-29715200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:29696200-29715600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr6:29696200-29715600	Weak transcription	Liver	Liver
25	chr6:29696400-29710800	Weak transcription	Lung	lung
26	chr6:29696400-29711400	Weak transcription	Spleen	Spleen
27	chr6:29696400-29711800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:29696400-29712000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr6:29696400-29715400	Weak transcription	Stomach Smooth Muscle	stomach
30	chr6:29696600-29715600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr6:29696800-29714600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr6:29696800-29715800	Weak transcription	Colonic Mucosa	Colon
33	chr6:29699200-29712400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr6:29700000-29715200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr6:29700600-29711600	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr6:29702000-29711200	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr6:29702000-29711600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:29702200-29705400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr6:29702400-29705600	Weak transcription	NHDF-Ad	bronchial
40	chr6:29702400-29709800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:29702400-29715400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:29702600-29707200	Weak transcription	NHEK	skin
43	chr6:29702600-29715400	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr6:29702800-29705600	Weak transcription	HMEC	breast
45	chr6:29702800-29712000	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr6:29702800-29712800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr6:29702800-29713800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr6:29702800-29715400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr6:29702800-29715600	Weak transcription	Primary B cells from peripheral blood	blood
50	chr6:29703200-29705600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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