Variant report

Variant	nsv602956
Chromosome Location	chr6:37909084-37986489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:595)
CpG islands
(count:124)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:595 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:37986366-37986833	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:37980412-37980698	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:37955840-37956504	HepG2	liver:	n/a	n/a
4	ATF1	chr6:37941107-37941385	K562	blood:	n/a	n/a
5	ATF2	chr6:37919745-37920149	GM12878	blood:	n/a	n/a
6	ATF3	chr6:37941105-37941373	K562	blood:	n/a	n/a
7	ATF3	chr6:37951538-37951908	K562	blood:	n/a	n/a
8	BATF	chr6:37919725-37920244	GM12878	blood:	n/a	n/a
9	BATF	chr6:37919813-37920222	GM12878	blood:	n/a	n/a
10	BATF	chr6:37928351-37928634	GM12878	blood:	n/a	chr6:37928490-37928501
11	BCLAF1	chr6:37919686-37920206	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:37950175-37950289	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:37953124-37953465	K562	blood:	n/a	n/a
14	BHLHE40	chr6:37951573-37951806	K562	blood:	n/a	n/a
15	BHLHE40	chr6:37953225-37953425	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:37911595-37911736	GM12878	blood:	n/a	n/a
17	CBX3	chr6:37942714-37943109	K562	blood:	n/a	n/a
18	CBX3	chr6:37942767-37943126	HCT-116	colon:	n/a	n/a
19	CBX3	chr6:37942643-37943172	HCT-116	colon:	n/a	n/a
20	CEBPB	chr6:37914665-37914890	MCF-7	breast:	n/a	chr6:37914761-37914772
21	CEBPB	chr6:37914667-37914876	K562	blood:	n/a	chr6:37914761-37914772
22	CEBPB	chr6:37955845-37956264	IMR90	lung:	n/a	n/a
23	CEBPB	chr6:37933369-37933655	IMR90	lung:	n/a	chr6:37933511-37933522
24	CEBPB	chr6:37951598-37951958	HepG2	liver:	n/a	chr6:37951765-37951776
25	CEBPB	chr6:37941046-37941429	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:37955987-37956313	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:37941097-37941388	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:37951615-37951897	ECC-1	luminal epithelium:	n/a	chr6:37951765-37951776
29	CEBPB	chr6:37951600-37951959	Hela-S3	cervix:	n/a	chr6:37951765-37951776
30	CEBPB	chr6:37980326-37980678	MCF-7	breast:	n/a	n/a
31	CEBPB	chr6:37950109-37950143	HepG2	liver:	n/a	chr6:37950120-37950129 chr6:37950119-37950130
32	CEBPB	chr6:37980529-37980674	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:37925010-37925295	IMR90	lung:	n/a	n/a
34	CEBPB	chr6:37941050-37941359	K562	blood:	n/a	n/a
35	CEBPB	chr6:37950045-37950303	IMR90	lung:	n/a	chr6:37950120-37950129 chr6:37950119-37950130
36	CEBPB	chr6:37951570-37951919	K562	blood:	n/a	chr6:37951765-37951776
37	CEBPB	chr6:37925003-37925244	A549	lung:	n/a	n/a
38	CEBPB	chr6:37941117-37941304	K562	blood:	n/a	n/a
39	CEBPB	chr6:37951531-37952038	MCF-7	breast:	n/a	chr6:37951765-37951776
40	CEBPB	chr6:37941059-37941507	HCT-116	colon:	n/a	n/a
41	CEBPB	chr6:37951591-37951960	K562	blood:	n/a	chr6:37951765-37951776
42	CEBPB	chr6:37951608-37951909	H1-hESC	embryonic stem cell:	n/a	chr6:37951765-37951776
43	CEBPB	chr6:37914648-37914918	HepG2	liver:	n/a	chr6:37914761-37914772
44	CEBPB	chr6:37924982-37925215	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:37941078-37941404	K562	blood:	n/a	n/a
46	CEBPB	chr6:37951610-37951952	A549	lung:	n/a	chr6:37951765-37951776
47	CEBPB	chr6:37934597-37934886	MCF-7	breast:	n/a	n/a
48	CEBPB	chr6:37933403-37933663	HepG2	liver:	n/a	chr6:37933511-37933522
49	CEBPB	chr6:37941048-37941538	HCT-116	colon:	n/a	n/a
50	CEBPB	chr6:37914630-37914897	IMR90	lung:	n/a	chr6:37914761-37914772

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:37913121-37913171	ovcar-3	ovarian:	n/a
2	chr6:37958953-37959003	T-47D	breast:	n/a
3	chr6:37913121-37913171	ovcar-3	ovarian:	n/a
4	chr6:37958953-37959003	T-47D	breast:	n/a
5	chr6:37958953-37959003	HNPCEpiC	eye:	n/a
6	chr6:37913121-37913171	A549	lung:	n/a
7	chr6:37913121-37913171	HCM	heart:	n/a
8	chr6:37958953-37959003	HCPEpiC	choroid plexus:	n/a
9	chr6:37913121-37913171	AG09319	gingival:	n/a
10	chr6:37958953-37959003	HCM	heart:	n/a
11	chr6:37913121-37913171	U87	brain:	n/a
12	chr6:37958953-37959003	SK-N-MC	brain:	n/a
13	chr6:37958953-37959003	AoSMC	blood vessel:	n/a
14	chr6:37913121-37913171	Hela-S3	cervix:	n/a
15	chr6:37913121-37913171	HRPEpiC	eye:	n/a
16	chr6:37958953-37959003	MCF-7	breast:	n/a
17	chr6:37958953-37959003	NH-A	brain:	n/a
18	chr6:37913121-37913171	HRE	kidney:	n/a
19	chr6:37958953-37959003	HepG2	liver:	n/a
20	chr6:37913121-37913171	Caco-2	colon:	n/a
21	chr6:37913121-37913171	BE2_C	brain:	n/a
22	chr6:37913121-37913171	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:37913121-37913171	HCPEpiC	choroid plexus:	n/a
24	chr6:37913121-37913171	ECC-1	luminal epithelium:	n/a
25	chr6:37913121-37913171	SK-N-MC	brain:	n/a
26	chr6:37913121-37913171	LNCaP	prostate:	n/a
27	chr6:37958953-37959003	PANC-1	pancreas:	n/a
28	chr6:37913121-37913171	T-47D	breast:	n/a
29	chr6:37913121-37913171	HepG2	liver:	n/a
30	chr6:37913121-37913171	H1-hESC	embryonic stem cell:	embryo
31	chr6:37913121-37913171	HIPEpiC	eye:	n/a
32	chr6:37913121-37913171	HRCEpiC	kidney:	n/a
33	chr6:37958953-37959003	SAEC	small airway:	n/a
34	chr6:37913121-37913171	IMR90	lung:	fetal
35	chr6:37913121-37913171	Hepatocyte	liver:	n/a
36	chr6:37913121-37913171	HL-60	blood:	n/a
37	chr6:37958953-37959003	AG09309	skin:	n/a
38	chr6:37913121-37913171	SKMC	muscle:	n/a
39	chr6:37913121-37913171	NT2-D1	testis:	n/a
40	chr6:37913121-37913171	PFSK-1	brain:	n/a
41	chr6:37958953-37959003	NT2-D1	testis:	n/a
42	chr6:37958953-37959003	AG09319	gingival:	n/a
43	chr6:37958953-37959003	HMEC	breast:	n/a
44	chr6:37913121-37913171	AG04449	skin:	fetal
45	chr6:37958953-37959003	PrEC	prostate:	n/a
46	chr6:37913121-37913171	GM06990	blood:	n/a
47	chr6:37958953-37959003	AG04450	lung:	fetal
48	chr6:37958953-37959003	GM06990	blood:	n/a
49	chr6:37958953-37959003	AG10803	skin:	n/a
50	chr6:37913121-37913171	AG10803	skin:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:37954058..37955830-chr6:37961204..37963273,2	K562	blood:
2	chr6:37924674..37926815-chr6:37929494..37931459,2	MCF-7	breast:
3	chr6:37956692..37960891-chr6:37962737..37966006,6	K562	blood:
4	chr6:37920868..37922667-chr6:37923260..37925049,2	K562	blood:
5	chr6:37924674..37926815-chr6:37929494..37931459,2	MCF-7	breast:
6	chr6:37927855..37929395-chr6:37932120..37934567,2	MCF-7	breast:
7	chr6:37786296..37788454-chr6:37912478..37914475,2	MCF-7	breast:
8	chr6:37920868..37922667-chr6:37923260..37925049,2	K562	blood:
9	chr6:37758900..37760044-chr6:37980106..37981056,5	MCF-7	breast:
10	chr6:37948324..37950868-chr6:37959290..37962178,2	MCF-7	breast:
11	chr6:37709829..37710411-chr6:37980026..37981018,4	MCF-7	breast:
12	chr6:37927855..37929395-chr6:37932120..37934567,2	MCF-7	breast:
13	chr6:37959253..37960891-chr6:37963216..37966169,3	K562	blood:
14	chr6:37961664..37964407-chr6:37965774..37967604,2	K562	blood:
15	chr6:37974723..37976308-chr6:37979935..37981504,2	MCF-7	breast:
16	chr6:37961664..37964407-chr6:37965774..37967604,2	K562	blood:
17	chr17:41392011..41394804-chr6:37916614..37918114,2	K562	blood:
18	chr6:37948324..37950868-chr6:37959290..37962178,2	MCF-7	breast:
19	chr6:37913945..37916886-chr6:37919030..37920758,2	K562	blood:
20	chr6:37959253..37960891-chr6:37963216..37966169,3	K562	blood:
21	chr6:37983748..37986719-chr6:38000048..38002009,3	K562	blood:
22	chr6:37786027..37788545-chr6:37979008..37980609,2	MCF-7	breast:
23	chr17:41400224..41402335-chr6:37916614..37918134,2	MCF-7	breast:
24	chr6:37923129..37926098-chr6:37932741..37935067,3	MCF-7	breast:
25	chr6:37919246..37922240-chr6:37953708..37956298,2	K562	blood:
26	chr6:37919246..37922240-chr6:37953708..37956298,2	K562	blood:
27	chr6:37974723..37976308-chr6:37979935..37981504,2	MCF-7	breast:
28	chr6:37786879..37788861-chr6:37985416..37988251,2	MCF-7	breast:
29	chr6:37913945..37916886-chr6:37919030..37920758,2	K562	blood:
30	chr6:37873063..37875947-chr6:37943285..37945175,2	K562	blood:
31	chr6:37954058..37955830-chr6:37961204..37963273,2	K562	blood:
32	chr6:37923129..37926098-chr6:37932741..37935067,3	MCF-7	breast:
33	chr6:37922083..37924500-chr6:37934489..37937047,2	K562	blood:
34	chr6:37961004..37963771-chr6:37970907..37973856,2	MCF-7	breast:
35	chr6:37922083..37924500-chr6:37934489..37937047,2	K562	blood:
36	chr6:37904858..37907835-chr6:37909386..37911345,2	K562	blood:
37	chr6:37956692..37960891-chr6:37962737..37966006,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD9-2	chr6:37970608-37971089	NONHSAT112289

No data

Variant related genes	Relation type
ENSG00000218521	TF binding region
ENSG00000218521	CpG island
ENSG00000225945	chromatin interactions
ENSG00000218521	chromatin interactions
ENSG00000156639	chromatin interactions

Extended variants
information (count: 2869 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2869 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2842510	chr6:37909084-37909085	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181440346	chr6:37909114-37909115	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs185805626	chr6:37909170-37909171	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs551853553	chr6:37909216-37909217	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs368199898	chr6:37909252-37909253	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs375924137	chr6:37909292-37909293	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs78987281	chr6:37909370-37909371	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs532804645	chr6:37909372-37909373	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs552087299	chr6:37909382-37909383	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs566123792	chr6:37909400-37909401	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs534823206	chr6:37909489-37909490	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs78512554	chr6:37909604-37909605	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs551451480	chr6:37909638-37909639	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs574468424	chr6:37909656-37909657	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs7770212	chr6:37909672-37909673	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs118091377	chr6:37909694-37909695	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs534135866	chr6:37909703-37909704	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs2842511	chr6:37909743-37909744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs2842512	chr6:37909855-37909856	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190611586	chr6:37909861-37909862	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs2842513	chr6:37909863-37909864	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs150248403	chr6:37909898-37909899	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs181270257	chr6:37909929-37909930	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs186731807	chr6:37909962-37909963	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs138927610	chr6:37909963-37909964	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369166768	chr6:37910018-37910019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201399942	chr6:37910037-37910038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs200029967	chr6:37910047-37910048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200835145	chr6:37910048-37910049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs3792706	chr6:37910049-37910050	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs190629195	chr6:37910051-37910052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72260071	chr6:37910064-37910065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs398065714	chr6:37910067-37910068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182873929	chr6:37910287-37910288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534844767	chr6:37910371-37910372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77862017	chr6:37910440-37910441	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs79523900	chr6:37910504-37910505	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs554041406	chr6:37910543-37910544	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs537046475	chr6:37910544-37910545	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs35749944	chr6:37910559-37910560	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs116631526	chr6:37910579-37910580	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs59103990	chr6:37910582-37910583	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs186356215	chr6:37910610-37910611	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs78697813	chr6:37910660-37910661	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs553505130	chr6:37910699-37910700	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs144855872	chr6:37910707-37910708	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs542447572	chr6:37910721-37910722	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs561092877	chr6:37910723-37910724	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs560960828	chr6:37910740-37910741	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs191108400	chr6:37910745-37910746	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	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
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1790 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37873400-37929200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:37880200-37930000	Weak transcription	Thymus	Thymus
3	chr6:37884800-37917000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr6:37887600-37933200	Weak transcription	NHDF-Ad	bronchial
5	chr6:37890800-37910400	Weak transcription	NHEK	skin
6	chr6:37892600-37910800	Weak transcription	Primary B cells from cord blood	blood
7	chr6:37892600-37928800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr6:37893200-37910400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:37896800-37929000	Weak transcription	Esophagus	oesophagus
10	chr6:37897200-37910600	Weak transcription	A549	lung
11	chr6:37898200-37913800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr6:37898600-37910400	Weak transcription	Fetal Kidney	kidney
13	chr6:37901000-37915400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr6:37902200-37909200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:37902200-37910600	Weak transcription	NHLF	lung
16	chr6:37902200-37913600	Weak transcription	HepG2	liver
17	chr6:37903400-37911400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:37904800-37920400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:37904800-37920400	Weak transcription	Small Intestine	intestine
20	chr6:37904800-37933400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:37905000-37910200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr6:37905000-37911000	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr6:37905000-37919600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr6:37905200-37909400	Enhancers	Primary hematopoietic stem cells	blood
25	chr6:37905200-37910400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr6:37905200-37910400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:37905200-37910800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr6:37905200-37910800	Weak transcription	HMEC	breast
29	chr6:37905600-37909600	Enhancers	Fetal Heart	heart
30	chr6:37905800-37911400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr6:37905800-37916200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:37905800-37916600	Weak transcription	Dnd41	blood
33	chr6:37905800-37924000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr6:37906600-37909600	Enhancers	Stomach Smooth Muscle	stomach
35	chr6:37906800-37909200	Weak transcription	Right Ventricle	heart
36	chr6:37906800-37909400	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr6:37906800-37909800	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr6:37906800-37910600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr6:37907000-37921200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr6:37907000-37926600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:37907200-37911200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr6:37907400-37909400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:37907400-37909400	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr6:37907600-37910000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr6:37907800-37909400	Weak transcription	Ovary	ovary
46	chr6:37907800-37909600	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr6:37907800-37910200	Enhancers	Fetal Brain Male	brain
48	chr6:37908000-37909200	Enhancers	Rectal Smooth Muscle	rectum
49	chr6:37908000-37909400	Enhancers	Brain Anterior Caudate	brain
50	chr6:37908000-37909800	Enhancers	Brain Substantia Nigra	brain

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