Variant report

Variant	nsv603090
Chromosome Location	chr6:49431569-49447295
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:96)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:96 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr6:49430703-49431594	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr6:49430824-49431570	K562	blood:	n/a	chr6:49431417-49431428 chr6:49431417-49431428 chr6:49431415-49431428
3	CHD1	chr6:49431112-49431905	H1-hESC	embryonic stem cell:	n/a	n/a
4	CREB1	chr6:49430395-49431675	HepG2	liver:	n/a	n/a
5	CREB1	chr6:49430334-49431675	K562	blood:	n/a	n/a
6	CREB1	chr6:49430545-49431633	K562	blood:	n/a	n/a
7	CTCF	chr6:49438213-49438303	Fibrobl	skin:	n/a	n/a
8	CTCF	chr6:49432980-49433130	NHDF-neo	bronchial:	n/a	n/a
9	CUX1	chr6:49430955-49431847	K562	blood:	n/a	n/a
10	E2F4	chr6:49430648-49431624	Hela-S3	cervix:	n/a	chr6:49431113-49431124 chr6:49431112-49431123 chr6:49431109-49431126 chr6:49430905-49430917 chr6:49431109-49431126
11	E2F4	chr6:49439994-49440400	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr6:49430698-49431584	K562	blood:	n/a	chr6:49431113-49431124 chr6:49431112-49431123 chr6:49431109-49431126 chr6:49430905-49430917 chr6:49431109-49431126
13	E2F4	chr6:49430391-49432209	MCF10A-Er-Src	breast:	n/a	chr6:49431113-49431124 chr6:49431112-49431123 chr6:49431109-49431126 chr6:49430905-49430917 chr6:49431109-49431126
14	E2F6	chr6:49430625-49431640	K562	blood:	n/a	chr6:49431112-49431123 chr6:49431109-49431126 chr6:49430905-49430917 chr6:49431109-49431126
15	ELF1	chr6:49430673-49431586	HepG2	liver:	n/a	chr6:49431377-49431388 chr6:49431082-49431093 chr6:49431082-49431093 chr6:49431083-49431092
16	ELF1	chr6:49430747-49431587	K562	blood:	n/a	chr6:49431377-49431388 chr6:49431082-49431093 chr6:49431082-49431093 chr6:49431083-49431092
17	ELK1	chr6:49430313-49431590	Hela-S3	cervix:	n/a	n/a
18	ELK4	chr6:49430837-49431582	Hela-S3	cervix:	n/a	chr6:49431080-49431091 chr6:49431059-49431070
19	EP300	chr6:49430717-49431644	GM12878	blood:	n/a	chr6:49431083-49431090
20	GABPA	chr6:49430615-49431630	A549	lung:	n/a	chr6:49431064-49431071
21	GABPA	chr6:49430316-49431849	MCF-7	breast:	n/a	chr6:49431064-49431071
22	GTF2F1	chr6:49432418-49432427	K562	blood:	n/a	n/a
23	HEY1	chr6:49430505-49431732	K562	blood:	n/a	n/a
24	IRF1	chr6:49431748-49431797	K562	blood:	n/a	n/a
25	JUN	chr6:49430865-49431785	K562	blood:	n/a	chr6:49431701-49431715 chr6:49431164-49431172
26	KAP1	chr6:49437805-49437991	K562	blood:	n/a	n/a
27	MAFK	chr6:49434719-49435175	HepG2	liver:	n/a	n/a
28	MAX	chr6:49430637-49431638	NB4	blood:	n/a	n/a
29	MAZ	chr6:49430336-49431604	K562	blood:	n/a	n/a
30	MXI1	chr6:49429642-49431594	GM12878	blood:	n/a	n/a
31	MXI1	chr6:49429538-49431842	SK-N-SH	brain:	n/a	n/a
32	MXI1	chr6:49430712-49431669	K562	blood:	n/a	n/a
33	MXI1	chr6:49437826-49437863	GM12878	blood:	n/a	n/a
34	MXI1	chr6:49430526-49431686	IMR90	lung:	n/a	n/a
35	MYC	chr6:49430378-49431732	K562	blood:	n/a	n/a
36	MYC	chr6:49430372-49431596	K562	blood:	n/a	n/a
37	NFYA	chr6:49430704-49431651	K562	blood:	n/a	n/a
38	NR2F2	chr6:49430496-49431647	K562	blood:	n/a	n/a
39	POLR2A	chr6:49430132-49431947	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr6:49435767-49436045	K562	blood:	n/a	n/a
41	POLR2A	chr6:49430500-49431715	SK-N-MC	brain:	n/a	n/a
42	POLR2A	chr6:49432000-49433254	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr6:49430551-49431634	HepG2	liver:	n/a	n/a
44	POLR2A	chr6:49430597-49431630	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr6:49430550-49431578	K562	blood:	n/a	n/a
46	POLR2A	chr6:49430399-49431827	GM12878	blood:	n/a	n/a
47	POLR2A	chr6:49430218-49431629	GM12878	blood:	n/a	n/a
48	POLR2A	chr6:49432162-49432172	ProgFib	skin:	n/a	n/a
49	POLR2A	chr6:49430241-49431637	PFSK-1	brain:	n/a	n/a
50	POLR2A	chr6:49430699-49431734	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:49434230-49434280	AG09309	skin:	n/a
2	chr6:49434230-49434280	BJ	skin:	n/a
3	chr6:49434230-49434280	BE2_C	brain:	n/a
4	chr6:49434230-49434280	T-47D	breast:	n/a
5	chr6:49434230-49434280	SK-N-SH	brain:	n/a
6	chr6:49434230-49434280	AG04449	skin:	fetal
7	chr6:49434230-49434280	GM12892	blood:	n/a
8	chr6:49434230-49434280	LNCaP	prostate:	n/a
9	chr6:49434230-49434280	MCF-7	breast:	n/a
10	chr6:49434230-49434280	HepG2	liver:	n/a
11	chr6:49434230-49434280	Jurkat	blood:	n/a
12	chr6:49434230-49434280	MCF10A-Er-Src	breast:	n/a
13	chr6:49434230-49434280	HIPEpiC	eye:	n/a
14	chr6:49434230-49434280	PANC-1	pancreas:	n/a
15	chr6:49434230-49434280	HMEC	breast:	n/a
16	chr6:49434230-49434280	Caco-2	colon:	n/a
17	chr6:49434230-49434280	ProgFib	skin:	n/a
18	chr6:49434230-49434280	SAEC	small airway:	n/a
19	chr6:49434230-49434280	HAEpiC	amniotic membrane:	n/a
20	chr6:49434230-49434280	AoSMC	blood vessel:	n/a
21	chr6:49434230-49434280	Hepatocyte	liver:	n/a
22	chr6:49434230-49434280	HEEpiC	esophagus:	n/a
23	chr6:49434230-49434280	HUVEC	blood vessel:	n/a
24	chr6:49434230-49434280	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:49434230-49434280	HCM	heart:	n/a
26	chr6:49434230-49434280	SK-N-MC	brain:	n/a
27	chr6:49434230-49434280	GM19239	blood:	n/a
28	chr6:49434230-49434280	HCF	heart:	n/a
29	chr6:49434230-49434280	GM06990	blood:	n/a
30	chr6:49434230-49434280	IMR90	lung:	fetal
31	chr6:49434230-49434280	NHDF-neo	bronchial:	n/a
32	chr6:49434230-49434280	GM12891	blood:	n/a
33	chr6:49434230-49434280	HCPEpiC	choroid plexus:	n/a
34	chr6:49434230-49434280	NH-A	brain:	n/a
35	chr6:49434230-49434280	HNPCEpiC	eye:	n/a
36	chr6:49434230-49434280	HL-60	blood:	n/a
37	chr6:49434230-49434280	AG04450	lung:	fetal
38	chr6:49434230-49434280	NT2-D1	testis:	n/a
39	chr6:49434230-49434280	ovcar-3	ovarian:	n/a
40	chr6:49434230-49434280	HRPEpiC	eye:	n/a
41	chr6:49434230-49434280	HRCEpiC	kidney:	n/a
42	chr6:49434230-49434280	SKMC	muscle:	n/a
43	chr6:49434230-49434280	SK-N-SH_RA	brain:	n/a
44	chr6:49434230-49434280	NHBE	bronchial:	n/a
45	chr6:49434230-49434280	ECC-1	luminal epithelium:	n/a
46	chr6:49434230-49434280	H1-hESC	embryonic stem cell:	embryo
47	chr6:49434230-49434280	K562	blood:	n/a
48	chr6:49434230-49434280	A549	lung:	n/a
49	chr6:49434230-49434280	PFSK-1	brain:	n/a
50	chr6:49434230-49434280	HEK293	kidney:	embryo

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:49429949..49432434-chr6:49603239..49605832,3	K562	blood:
2	chr6:49431208..49433199-chr6:49629940..49632995,3	K562	blood:
3	chr6:49438767..49441151-chr6:49557071..49559499,2	K562	blood:
4	chr6:49435298..49437139-chr6:49437563..49440093,3	K562	blood:
5	chr6:49435298..49437139-chr6:49437563..49440093,3	K562	blood:
6	chr1:173836868..173837651-chr6:49432317..49433018,2	Hela-S3	cervix:
7	chr6:49401244..49402947-chr6:49432509..49434814,2	K562	blood:
8	chr6:49445932..49448619-chr6:49451327..49454522,3	K562	blood:
9	chr12:53845489..53846145-chr6:49430663..49431569,2	Hela-S3	cervix:
10	chr6:49438004..49440787-chr6:49447034..49448674,2	K562	blood:
11	chr6:49434330..49436569-chr6:49445501..49447295,2	K562	blood:
12	chr6:49434330..49436569-chr6:49445501..49447295,2	K562	blood:
13	chr6:49431721..49433516-chr6:49458650..49460317,2	K562	blood:
14	chr6:49444826..49447432-chr6:49451327..49454178,2	K562	blood:
15	chr6:49429390..49432411-chr6:49516710..49519961,3	MCF-7	breast:
16	chr6:49431483..49432991-chr6:49522409..49524636,2	MCF-7	breast:
17	chr6:49429898..49432613-chr6:49432665..49435098,5	K562	blood:
18	chr6:49428636..49430625-chr6:49435581..49438306,2	MCF-7	breast:
19	chr6:49430814..49434554-chr6:49435303..49440470,7	K562	blood:
20	chr6:49423687..49425386-chr6:49433841..49436360,2	K562	blood:
21	chr6:20401677..20404627-chr6:49430582..49432502,2	K562	blood:
22	chr6:49431034..49433183-chr6:49434842..49436900,4	MCF-7	breast:
23	chr6:49429532..49432172-chr6:49444762..49446300,2	K562	blood:
24	chr6:49427543..49430477-chr6:49436132..49438156,2	K562	blood:
25	chr6:49438004..49440787-chr6:49447034..49448674,2	K562	blood:

No data

Variant related genes	Relation type
MUT	TF binding region
MUT	CpG island
ENSG00000112242	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000112077	chromatin interactions
ENSG00000031691	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000146085	chromatin interactions
ENSG00000197111	chromatin interactions
ENSG00000197261	chromatin interactions

Extended variants
information (count: 573 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3806988	chr6:49431569-49431570	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114400046	chr6:49431613-49431614	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs531112116	chr6:49431624-49431625	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs3823114	chr6:49431720-49431721	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs558735266	chr6:49431758-49431759	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs572247750	chr6:49431791-49431792	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs561342186	chr6:49431804-49431805	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs185548886	chr6:49431809-49431810	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs546936310	chr6:49431824-49431825	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs571544494	chr6:49431843-49431844	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs146543457	chr6:49431844-49431845	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs189258695	chr6:49431877-49431878	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs536009060	chr6:49431886-49431887	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs554259522	chr6:49431916-49431917	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs180894632	chr6:49432075-49432076	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs141014463	chr6:49432136-49432137	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs149978803	chr6:49432152-49432153	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs554547713	chr6:49432211-49432212	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs150215820	chr6:49432245-49432246	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs558569683	chr6:49432286-49432287	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs576754814	chr6:49432316-49432317	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs545720174	chr6:49432407-49432408	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs557666964	chr6:49432483-49432484	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs138902543	chr6:49432499-49432500	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs187346057	chr6:49432545-49432546	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs543018245	chr6:49432569-49432570	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs561379140	chr6:49432643-49432644	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs574566972	chr6:49432658-49432659	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs192119577	chr6:49432668-49432669	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs182951846	chr6:49432692-49432693	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs186233618	chr6:49432827-49432828	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs148974272	chr6:49432854-49432855	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs79125444	chr6:49432894-49432895	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs568776126	chr6:49432912-49432913	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs529846863	chr6:49432940-49432941	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs547934478	chr6:49432941-49432942	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs566327320	chr6:49432979-49432980	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs563637550	chr6:49432994-49432995	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs34303307	chr6:49433004-49433005	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs78172334	chr6:49433005-49433006	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs113785666	chr6:49433016-49433017	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs190702675	chr6:49433080-49433081	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs546175192	chr6:49433086-49433087	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs529376487	chr6:49433123-49433124	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs537416702	chr6:49433125-49433126	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs557705618	chr6:49433139-49433140	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs377536532	chr6:49433146-49433147	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs7759071	chr6:49433198-49433199	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs182575819	chr6:49433221-49433222	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs187994027	chr6:49433279-49433280	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Olfactory neuroblastoma	18408657	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49429000-49434200	Active TSS	GM12878-XiMat	blood
2	chr6:49429200-49432000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:49429400-49432000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:49429400-49432000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:49429400-49432200	Active TSS	Ovary	ovary
6	chr6:49429400-49432200	Active TSS	Right Atrium	heart
7	chr6:49429600-49431600	Active TSS	Brain Cingulate Gyrus	brain
8	chr6:49429600-49431600	Active TSS	Brain Substantia Nigra	brain
9	chr6:49429600-49431600	Active TSS	Stomach Smooth Muscle	stomach
10	chr6:49429600-49431800	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr6:49429600-49431800	Active TSS	Psoas Muscle	Psoas
12	chr6:49429600-49431800	Active TSS	Right Ventricle	heart
13	chr6:49429600-49432000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:49429600-49432000	Active TSS	Colonic Mucosa	Colon
15	chr6:49429600-49432000	Active TSS	NHDF-Ad	bronchial
16	chr6:49429600-49432200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr6:49429600-49432200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:49429600-49432200	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr6:49429600-49432200	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr6:49429600-49432200	Active TSS	Fetal Kidney	kidney
21	chr6:49429600-49432200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
22	chr6:49429600-49432200	Active TSS	NHLF	lung
23	chr6:49429800-49431600	Active TSS	Aorta	Aorta
24	chr6:49429800-49431800	Active TSS	Left Ventricle	heart
25	chr6:49429800-49432000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:49429800-49432000	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr6:49429800-49432000	Active TSS	HSMMtube	muscle
28	chr6:49429800-49432400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:49430000-49431600	Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr6:49430000-49431600	Active TSS	Fetal Intestine Small	intestine
31	chr6:49430000-49431600	Active TSS	Rectal Smooth Muscle	rectum
32	chr6:49430000-49431800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:49430000-49431800	Active TSS	Fetal Intestine Large	intestine
34	chr6:49430000-49432000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:49430000-49432000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr6:49430000-49432000	Active TSS	Fetal Muscle Trunk	muscle
37	chr6:49430000-49432000	Active TSS	Fetal Thymus	thymus
38	chr6:49430000-49432200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:49430000-49432200	Active TSS	Fetal Lung	lung
40	chr6:49430000-49432200	Active TSS	A549	lung
41	chr6:49430000-49432400	Active TSS	K562	blood
42	chr6:49430000-49432600	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr6:49430000-49432600	Active TSS	Muscle Satellite Cultured Cells	--
44	chr6:49430200-49431600	ZNF genes & repeats	Fetal Brain Male	brain
45	chr6:49430200-49431600	Active TSS	Fetal Brain Female	brain
46	chr6:49430200-49431600	Active TSS	Placenta	Placenta
47	chr6:49430200-49431800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:49430200-49431800	Active TSS	Fetal Heart	heart
49	chr6:49430200-49431800	Bivalent/Poised TSS	HepG2	liver
50	chr6:49430200-49432000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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