Variant report

Variant	nsv969359
Chromosome Location	chr6:26443661-26453241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:103 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:26446081-26446917	GM12878	blood:	n/a	n/a
2	ATF2	chr6:26446043-26446908	GM12878	blood:	n/a	n/a
3	BATF	chr6:26446083-26446930	GM12878	blood:	n/a	n/a
4	BATF	chr6:26446214-26446536	GM12878	blood:	n/a	n/a
5	BATF	chr6:26446580-26446863	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:26446136-26446582	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:26446237-26446481	GM12878	blood:	n/a	n/a
8	BCL3	chr6:26446139-26446570	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:26446005-26446607	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:26446145-26446565	GM12878	blood:	n/a	n/a
11	CEBPB	chr6:26446124-26446753	GM12878	blood:	n/a	n/a
12	CHD1	chr6:26446192-26446347	GM12878	blood:	n/a	n/a
13	CHD2	chr6:26446180-26446493	GM12878	blood:	n/a	n/a
14	CREB1	chr6:26446062-26446564	GM12878	blood:	n/a	n/a
15	CREB1	chr6:26446066-26446965	GM12878	blood:	n/a	n/a
16	CTCF	chr6:26450690-26450757	K562	blood:	n/a	n/a
17	CTCF	chr6:26450681-26450726	GM12892	blood:	n/a	n/a
18	CTCF	chr6:26450647-26450785	GM12878	blood:	n/a	n/a
19	CTCF	chr6:26450714-26450804	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr6:26450633-26450787	MCF-7	breast:	n/a	n/a
21	CTCF	chr6:26450629-26450806	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:26450599-26450855	K562	blood:	n/a	n/a
23	CTCF	chr6:26450686-26450770	MCF-7	breast:	n/a	n/a
24	CTCF	chr6:26446080-26446230	GM12873	blood:	n/a	n/a
25	CTCF	chr6:26450620-26450770	GM12871	blood:	n/a	n/a
26	CTCF	chr6:26450670-26450809	HepG2	liver:	n/a	n/a
27	CTCF	chr6:26450620-26450770	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr6:26450626-26450825	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:26450685-26450750	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:26450669-26450748	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr6:26450647-26450768	HepG2	liver:	n/a	n/a
32	CTCF	chr6:26444169-26444234	GM20000	blood:	n/a	n/a
33	CUX1	chr6:26446242-26446694	GM12878	blood:	n/a	n/a
34	EBF1	chr6:26446181-26446813	GM12878	blood:	n/a	n/a
35	EBF1	chr6:26446184-26446507	GM12878	blood:	n/a	n/a
36	ELK1	chr6:26446324-26446645	GM12878	blood:	n/a	n/a
37	EP300	chr6:26446168-26446871	GM12878	blood:	n/a	n/a
38	EP300	chr6:26446283-26446563	GM12878	blood:	n/a	n/a
39	FOXM1	chr6:26446080-26446846	GM12878	blood:	n/a	n/a
40	FOXM1	chr6:26446071-26446768	GM12878	blood:	n/a	n/a
41	GATA3	chr6:26453241-26453354	SH-SY5Y	brain:	n/a	n/a
42	IKZF1	chr6:26446135-26446857	GM12878	blood:	n/a	n/a
43	IRF4	chr6:26445935-26446818	GM12878	blood:	n/a	n/a
44	IRF4	chr6:26446083-26446545	GM12878	blood:	n/a	n/a
45	MAX	chr6:26446241-26446416	GM12878	blood:	n/a	n/a
46	MAZ	chr6:26446237-26446581	GM12878	blood:	n/a	n/a
47	MTA3	chr6:26446169-26446586	GM12878	blood:	n/a	n/a
48	MTA3	chr6:26446022-26446899	GM12878	blood:	n/a	n/a
49	MXI1	chr6:26446214-26446775	GM12878	blood:	n/a	n/a
50	NFATC1	chr6:26446124-26446656	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26446387-26446437	LNCaP	prostate:	n/a
2	chr6:26446387-26446437	HEK293	kidney:	embryo
3	chr6:26446387-26446437	Hela-S3	cervix:	n/a
4	chr6:26446387-26446437	NHBE	bronchial:	n/a
5	chr6:26452680-26452730	AG09309	skin:	n/a
6	chr6:26452680-26452730	MCF10A-Er-Src	breast:	n/a
7	chr6:26446387-26446437	GM12878	blood:	n/a
8	chr6:26452680-26452730	HUVEC	blood vessel:	n/a
9	chr6:26446387-26446437	HEEpiC	esophagus:	n/a
10	chr6:26446387-26446437	GM06990	blood:	n/a
11	chr6:26446387-26446437	SAEC	small airway:	n/a
12	chr6:26452680-26452730	NHDF-neo	bronchial:	n/a
13	chr6:26446387-26446437	GM12892	blood:	n/a
14	chr6:26452680-26452730	HIPEpiC	eye:	n/a
15	chr6:26452680-26452730	MCF-7	breast:	n/a
16	chr6:26446387-26446437	HIPEpiC	eye:	n/a
17	chr6:26452680-26452730	HCF	heart:	n/a
18	chr6:26452680-26452730	AG04450	lung:	fetal
19	chr6:26452680-26452730	HCT-116	colon:	n/a
20	chr6:26452680-26452730	T-47D	breast:	n/a
21	chr6:26452680-26452730	AG10803	skin:	n/a
22	chr6:26446387-26446437	PrEC	prostate:	n/a
23	chr6:26446387-26446437	AG09319	gingival:	n/a
24	chr6:26446387-26446437	HCT-116	colon:	n/a
25	chr6:26452680-26452730	Hela-S3	cervix:	n/a
26	chr6:26446387-26446437	HCF	heart:	n/a
27	chr6:26446387-26446437	SKMC	muscle:	n/a
28	chr6:26452680-26452730	Caco-2	colon:	n/a
29	chr6:26446387-26446437	HNPCEpiC	eye:	n/a
30	chr6:26452680-26452730	HL-60	blood:	n/a
31	chr6:26452680-26452730	SAEC	small airway:	n/a
32	chr6:26446387-26446437	Hepatocyte	liver:	n/a
33	chr6:26452680-26452730	HRE	kidney:	n/a
34	chr6:26446387-26446437	GM12891	blood:	n/a
35	chr6:26446387-26446437	AG09309	skin:	n/a
36	chr6:26446387-26446437	HAEpiC	amniotic membrane:	n/a
37	chr6:26446387-26446437	HMEC	breast:	n/a
38	chr6:26452680-26452730	AG04449	skin:	fetal
39	chr6:26446387-26446437	U87	brain:	n/a
40	chr6:26446387-26446437	NB4	blood:	n/a
41	chr6:26446387-26446437	SK-N-MC	brain:	n/a
42	chr6:26452680-26452730	A549	lung:	n/a
43	chr6:26452680-26452730	SK-N-MC	brain:	n/a
44	chr6:26446387-26446437	HRPEpiC	eye:	n/a
45	chr6:26452680-26452730	Jurkat	blood:	n/a
46	chr6:26446387-26446437	NT2-D1	testis:	n/a
47	chr6:26446387-26446437	HL-60	blood:	n/a
48	chr6:26446387-26446437	PANC-1	pancreas:	n/a
49	chr6:26452680-26452730	SKMC	muscle:	n/a
50	chr6:26452680-26452730	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr6:26449553..26453974-chr6:26454911..26459271,5	K562	blood:
2	chr6:26341644..26342483-chr6:26450003..26451206,4	MCF-7	breast:
3	chr6:26447799..26450389-chr6:26451131..26452755,2	K562	blood:
4	chr6:26382632..26385246-chr6:26444412..26446084,2	K562	blood:
5	chr6:26441674..26444658-chr6:26456493..26459926,5	K562	blood:
6	chr6:26170156..26172522-chr6:26452443..26454404,2	K562	blood:
7	chr6:26449858..26453821-chr6:26456459..26459528,5	K562	blood:
8	chr6:26202174..26206210-chr6:26451824..26455536,3	K562	blood:
9	chr6:26445132..26448422-chr6:26449156..26450907,3	MCF-7	breast:
10	chr6:26445132..26448422-chr6:26449156..26450907,3	MCF-7	breast:
11	chr6:26408794..26411203-chr6:26449353..26451664,2	K562	blood:
12	chr6:26440449..26443327-chr6:26444566..26448075,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTN2A1-2	chr6:26449465-26449916	NONHSAT108282
2	lnc-BTN3A3-1	chr6:26447901-26448486	l_3143_chr6:26439933-26448332_testes
3	lnc-BTN2A1-3	chr6:26443610-26444032	NONHSAT108281
4	lnc-BTN2A1-3	chr6:26443798-26444167	NONHSAT108280
5	lnc-BTN2A1-2	chr6:26450335-26450442	NONHSAT108282
6	lnc-BTN2A1-3	chr6:26443610-26443670	NONHSAT108280

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BTN3A3	hsa-miR-186-5p	chr6:26452722-26452745

Variant related genes	Relation type
BTN2A1	TF binding region
BTN3A3	TF binding region
BTN2A1	CpG island
BTN3A3	CpG island
ENSG00000217275	chromatin interactions
ENSG00000026950	chromatin interactions
ENSG00000112763	chromatin interactions
ENSG00000111801	chromatin interactions
ENSG00000198518	chromatin interactions
ENSG00000124508	chromatin interactions

Extended variants
information (count: 423 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569182514	chr6:26443684-26443685	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs184175487	chr6:26443724-26443725	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs149858554	chr6:26443731-26443732	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs528724646	chr6:26443735-26443736	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs542820908	chr6:26443736-26443737	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs376649355	chr6:26443754-26443755	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs371007758	chr6:26443760-26443761	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs553279861	chr6:26443780-26443781	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs573044866	chr6:26443816-26443817	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs375127466	chr6:26443835-26443836	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs17611438	chr6:26443853-26443854	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs377535721	chr6:26443854-26443855	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs564730444	chr6:26443892-26443893	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs574866467	chr6:26443895-26443896	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs543919676	chr6:26443897-26443898	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs370797996	chr6:26443899-26443900	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs373687558	chr6:26443919-26443920	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs367717503	chr6:26443933-26443934	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs530261009	chr6:26443987-26443988	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs1796523	chr6:26444033-26444034	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs370269040	chr6:26444057-26444058	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs546877795	chr6:26444089-26444090	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs560883960	chr6:26444120-26444121	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs188971098	chr6:26444128-26444129	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs552804559	chr6:26444129-26444130	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs372971212	chr6:26444133-26444134	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs569286880	chr6:26444157-26444158	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs145862652	chr6:26444159-26444160	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs143665311	chr6:26444168-26444169	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
30	rs375578358	chr6:26444209-26444210	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376102561	chr6:26444241-26444242	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368285328	chr6:26444266-26444267	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs77474489	chr6:26444267-26444268	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200536472	chr6:26444272-26444273	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs371864834	chr6:26444285-26444286	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201309184	chr6:26444303-26444304	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs572947274	chr6:26444312-26444313	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs137957846	chr6:26444331-26444332	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs375239049	chr6:26444358-26444359	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1057923	chr6:26444375-26444376	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs376234984	chr6:26444379-26444380	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs138755245	chr6:26444392-26444393	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574930219	chr6:26444397-26444398	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149312684	chr6:26444400-26444401	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372313829	chr6:26444433-26444434	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560699662	chr6:26444450-26444451	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs574188656	chr6:26444472-26444473	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540273194	chr6:26444500-26444501	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs138400675	chr6:26444571-26444572	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs558450511	chr6:26444579-26444580	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	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
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	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
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	21569311	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26441200-26444200	Weak transcription	Spleen	Spleen
2	chr6:26441200-26444600	Weak transcription	Gastric	stomach
3	chr6:26441200-26444600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:26441200-26444600	Weak transcription	K562	blood
5	chr6:26441200-26446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:26441200-26449600	Weak transcription	Esophagus	oesophagus
7	chr6:26441200-26457000	Weak transcription	Brain Substantia Nigra	brain
8	chr6:26441200-26457600	Weak transcription	Pancreas	Pancrea
9	chr6:26441400-26444400	Weak transcription	Fetal Muscle Trunk	muscle
10	chr6:26441400-26444600	Weak transcription	Small Intestine	intestine
11	chr6:26441400-26444800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:26441400-26445600	Weak transcription	Aorta	Aorta
13	chr6:26441400-26448200	Weak transcription	Right Ventricle	heart
14	chr6:26441400-26453000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:26441400-26455600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:26441400-26457000	Weak transcription	Brain Anterior Caudate	brain
17	chr6:26441400-26457400	Weak transcription	Psoas Muscle	Psoas
18	chr6:26441600-26445000	Weak transcription	Thymus	Thymus
19	chr6:26441600-26446000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:26441600-26448000	Weak transcription	Placenta	Placenta
21	chr6:26441600-26448800	Weak transcription	Fetal Intestine Large	intestine
22	chr6:26441600-26451200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr6:26441600-26452400	Weak transcription	HSMMtube	muscle
24	chr6:26441600-26452800	Weak transcription	HSMM	muscle
25	chr6:26442200-26444800	Weak transcription	Colon Smooth Muscle	Colon
26	chr6:26442200-26447000	Weak transcription	Fetal Intestine Small	intestine
27	chr6:26442200-26449200	Weak transcription	HUVEC	blood vessel
28	chr6:26442200-26455800	Weak transcription	HepG2	liver
29	chr6:26442200-26457400	Weak transcription	Fetal Kidney	kidney
30	chr6:26442400-26444400	Weak transcription	Liver	Liver
31	chr6:26442400-26444400	Weak transcription	Fetal Stomach	stomach
32	chr6:26442400-26444400	Weak transcription	Osteobl	bone
33	chr6:26442400-26444600	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr6:26442400-26444800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr6:26442400-26444800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:26442400-26445600	Weak transcription	Left Ventricle	heart
37	chr6:26442400-26446000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:26442400-26448000	Weak transcription	Primary hematopoietic stem cells	blood
39	chr6:26442400-26457400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:26442400-26457400	Weak transcription	Hela-S3	cervix
41	chr6:26442600-26444400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:26442600-26444600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr6:26442600-26444600	Weak transcription	Fetal Muscle Leg	muscle
44	chr6:26442600-26444600	Weak transcription	Ovary	ovary
45	chr6:26442600-26444800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr6:26442600-26444800	Weak transcription	Right Atrium	heart
47	chr6:26442600-26444800	Weak transcription	NHLF	lung
48	chr6:26442600-26445400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:26442600-26450000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:26442600-26457400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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