Variant report

Variant	nsv602919
Chromosome Location	chr6:35464698-35465749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:459)
CpG islands
(count:122)
Chromatin interactive
region (count:40)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:35465448-35466198	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:35465018-35466097	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:35465385-35465467	K562	blood:	n/a	n/a
4	BHLHE40	chr6:35465035-35465358	GM12878	blood:	n/a	chr6:35465324-35465340
5	BHLHE40	chr6:35464925-35466949	K562	blood:	n/a	chr6:35465324-35465340 chr6:35466465-35466481
6	CBX3	chr6:35465319-35466849	K562	blood:	n/a	n/a
7	CBX3	chr6:35465435-35465782	K562	blood:	n/a	n/a
8	CCNT2	chr6:35464027-35466338	K562	blood:	n/a	chr6:35464480-35464489 chr6:35464739-35464748 chr6:35464464-35464473 chr6:35464364-35464373
9	CEBPD	chr6:35464886-35465232	HepG2	liver:	n/a	n/a
10	CEBPD	chr6:35465562-35465982	HepG2	liver:	n/a	n/a
11	CEBPD	chr6:35464085-35464869	HepG2	liver:	n/a	n/a
12	CHD1	chr6:35465591-35466082	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr6:35464674-35464717	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr6:35465634-35465895	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr6:35464391-35466037	Hela-S3	cervix:	n/a	chr6:35465063-35465073 chr6:35465017-35465027 chr6:35465585-35465595 chr6:35465520-35465530
16	CHD2	chr6:35465678-35465729	K562	blood:	n/a	n/a
17	CREB1	chr6:35464980-35465367	A549	lung:	n/a	n/a
18	CREB1	chr6:35463565-35466162	HepG2	liver:	n/a	n/a
19	CTBP2	chr6:35465183-35466438	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr6:35464640-35464790	Caco-2	colon:	n/a	n/a
21	CTCF	chr6:35465680-35465830	HRE	kidney:	n/a	n/a
22	CTCF	chr6:35464580-35464730	GM12866	blood:	n/a	n/a
23	CTCF	chr6:35464580-35464730	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr6:35464580-35464730	AG09319	gingival:	n/a	n/a
25	CTCF	chr6:35464480-35464770	GM12870	blood:	n/a	n/a
26	CTCF	chr6:35464580-35464730	GM12869	blood:	n/a	n/a
27	CTCF	chr6:35465580-35465730	GM06990	blood:	n/a	n/a
28	CTCF	chr6:35465600-35465750	HFF	foreskin:	n/a	n/a
29	CTCF	chr6:35465397-35465797	K562	blood:	n/a	n/a
30	CTCF	chr6:35465540-35465704	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:35464560-35464710	GM12864	blood:	n/a	n/a
32	CTCF	chr6:35464560-35464710	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr6:35464560-35464710	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr6:35464620-35464725	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:35464600-35464750	HFF	foreskin:	n/a	n/a
36	CTCF	chr6:35464532-35464890	K562	blood:	n/a	n/a
37	CTCF	chr6:35465404-35465660	K562	blood:	n/a	n/a
38	CTCF	chr6:35464600-35464750	GM12868	blood:	n/a	n/a
39	CTCF	chr6:35464560-35464710	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr6:35464560-35464710	HCFaa	heart:	n/a	n/a
41	CTCF	chr6:35465580-35465730	HVMF	connective:	n/a	n/a
42	CTCF	chr6:35464600-35464750	GM12867	blood:	n/a	n/a
43	CTCF	chr6:35464550-35464800	HepG2	liver:	n/a	n/a
44	CTCF	chr6:35465540-35465690	HepG2	liver:	n/a	n/a
45	CTCF	chr6:35465520-35465670	BJ	skin:	n/a	n/a
46	CTCF	chr6:35465460-35465610	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr6:35465553-35465680	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:35464580-35464730	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr6:35464580-35464730	HRE	kidney:	n/a	n/a
50	CTCF	chr6:35465613-35465656	HUVEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35465342-35465392	MCF-7	breast:	n/a
2	chr6:35464939-35464989	AG10803	skin:	n/a
3	chr6:35465342-35465392	SAEC	small airway:	n/a
4	chr6:35465342-35465392	U87	brain:	n/a
5	chr6:35464939-35464989	HIPEpiC	eye:	n/a
6	chr6:35464939-35464989	AG04450	lung:	fetal
7	chr6:35464939-35464989	LNCaP	prostate:	n/a
8	chr6:35464939-35464989	ovcar-3	ovarian:	n/a
9	chr6:35465342-35465392	AG04450	lung:	fetal
10	chr6:35465342-35465392	HL-60	blood:	n/a
11	chr6:35465342-35465392	K562	blood:	n/a
12	chr6:35465342-35465392	A549	lung:	n/a
13	chr6:35464939-35464989	PrEC	prostate:	n/a
14	chr6:35465342-35465392	ProgFib	skin:	n/a
15	chr6:35464939-35464989	Hela-S3	cervix:	n/a
16	chr6:35465342-35465392	HEEpiC	esophagus:	n/a
17	chr6:35465342-35465392	PANC-1	pancreas:	n/a
18	chr6:35464939-35464989	HNPCEpiC	eye:	n/a
19	chr6:35464939-35464989	RPTEC	kidney:	n/a
20	chr6:35465342-35465392	HCPEpiC	choroid plexus:	n/a
21	chr6:35464939-35464989	H1-hESC	embryonic stem cell:	embryo
22	chr6:35464939-35464989	HAEpiC	amniotic membrane:	n/a
23	chr6:35465342-35465392	Hepatocyte	liver:	n/a
24	chr6:35464939-35464989	HepG2	liver:	n/a
25	chr6:35464939-35464989	PFSK-1	brain:	n/a
26	chr6:35464939-35464989	GM06990	blood:	n/a
27	chr6:35465342-35465392	HepG2	liver:	n/a
28	chr6:35464939-35464989	HRE	kidney:	n/a
29	chr6:35464939-35464989	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:35464939-35464989	SK-N-MC	brain:	n/a
31	chr6:35465342-35465392	SKMC	muscle:	n/a
32	chr6:35465342-35465392	GM12878	blood:	n/a
33	chr6:35465342-35465392	SK-N-SH	brain:	n/a
34	chr6:35465342-35465392	HIPEpiC	eye:	n/a
35	chr6:35465342-35465392	NB4	blood:	n/a
36	chr6:35465342-35465392	AoSMC	blood vessel:	n/a
37	chr6:35464939-35464989	ProgFib	skin:	n/a
38	chr6:35465342-35465392	HUVEC	blood vessel:	n/a
39	chr6:35465342-35465392	CMK	blood:	n/a
40	chr6:35465342-35465392	HRPEpiC	eye:	n/a
41	chr6:35464939-35464989	NT2-D1	testis:	n/a
42	chr6:35464939-35464989	PANC-1	pancreas:	n/a
43	chr6:35464939-35464989	CMK	blood:	n/a
44	chr6:35464939-35464989	Jurkat	blood:	n/a
45	chr6:35464939-35464989	HUVEC	blood vessel:	n/a
46	chr6:35465342-35465392	LNCaP	prostate:	n/a
47	chr6:35464939-35464989	Hepatocyte	liver:	n/a
48	chr6:35465342-35465392	SK-N-MC	brain:	n/a
49	chr6:35465342-35465392	GM06990	blood:	n/a
50	chr6:35464939-35464989	HCF	heart:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:11198114..11200950-chr6:35464173..35466447,2	K562	blood:
2	chr2:176033099..176033744-chr6:35465562..35466338,2	Hela-S3	cervix:
3	chr6:35465082..35466862-chr6:35699908..35701462,2	MCF-7	breast:
4	chr6:35465223..35467694-chr6:35696445..35698937,2	K562	blood:
5	chr6:35463384..35465009-chr6:35703029..35705389,2	K562	blood:
6	chr6:35463571..35465690-chr6:35654249..35656915,2	K562	blood:
7	chr6:35465054..35467000-chr6:36192851..36194879,2	MCF-7	breast:
8	chr20:47894747..47895275-chr6:35464852..35465455,2	Hela-S3	cervix:
9	chr6:35270724..35273111-chr6:35465041..35467348,2	K562	blood:
10	chr6:35227208..35228940-chr6:35464081..35465836,2	K562	blood:
11	chr11:33757381..33758237-chr6:35465059..35466295,3	Hela-S3	cervix:
12	chr6:35260813..35263112-chr6:35464822..35466518,2	K562	blood:
13	chr6:35464935..35465692-chr7:44835784..44836776,2	Hela-S3	cervix:
14	chr6:35423795..35426623-chr6:35465037..35468781,3	K562	blood:
15	chr6:35310112..35312932-chr6:35464368..35466518,2	K562	blood:
16	chr6:35376688..35379327-chr6:35465068..35467470,3	K562	blood:
17	chr17:36905700..36906366-chr6:35464667..35465593,2	Hela-S3	cervix:
18	chr6:35225785..35227535-chr6:35464894..35467017,2	K562	blood:
19	chr6:35462682..35465009-chr6:35702407..35705389,2	K562	blood:
20	chr6:35289938..35291662-chr6:35465459..35467668,2	K562	blood:
21	chr6:35310114..35311915-chr6:35462651..35465491,3	MCF-7	breast:
22	chr6:35465083..35467815-chr6:35613967..35615894,2	MCF-7	breast:
23	chr6:35464312..35466499-chr6:35694204..35696742,2	MCF-7	breast:
24	chr5:130531404..130532060-chr6:35465194..35466059,2	Hela-S3	cervix:
25	chr6:35465446..35468035-chr6:35607430..35610345,2	K562	blood:
26	chr6:35464601..35467910-chr6:35655207..35659461,3	K562	blood:
27	chr1:210547375..210547960-chr6:35465386..35466203,2	Hela-S3	cervix:
28	chr20:15349649..15350459-chr6:35465170..35465747,2	MCF-7	breast:
29	chr6:35418643..35423313-chr6:35462563..35468017,10	K562	blood:
30	chr5:43514826..43515720-chr6:35464905..35465668,2	Hela-S3	cervix:
31	chr6:35310058..35310620-chr6:35464293..35465068,2	K562	blood:
32	chr1:153699734..153700587-chr6:35465219..35465916,2	Hela-S3	cervix:
33	chr21:46237169..46238057-chr6:35464670..35465479,2	Hela-S3	cervix:
34	chr6:35264944..35267460-chr6:35465302..35468823,3	MCF-7	breast:
35	chr6:35265003..35267090-chr6:35463346..35464932,2	K562	blood:
36	chr6:35419956..35422517-chr6:35464991..35466898,2	MCF-7	breast:
37	chr17:7387197..7388120-chr6:35464620..35465289,2	Hela-S3	cervix:
38	chr6:35263661..35265616-chr6:35463054..35466039,2	MCF-7	breast:
39	chr6:35464241..35466956-chr6:35695881..35700309,4	MCF-7	breast:
40	chr6:35310116..35312027-chr6:35462385..35465150,2	MCF-7	breast:

No data

Variant related genes	Relation type
TEAD3	TF binding region
TEAD3	CpG island
ENSG00000112039	chromatin interactions
ENSG00000248240	chromatin interactions
ENSG00000196262	chromatin interactions
ENSG00000112033	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000115966	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000056661	chromatin interactions
ENSG00000181222	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000130164	chromatin interactions
ENSG00000232909	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000143624	chromatin interactions
ENSG00000184900	chromatin interactions
ENSG00000157343	chromatin interactions
ENSG00000023892	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000177410	chromatin interactions

Extended variants
information (count: 28 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185265331	chr6:35464871-35464872	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
2	rs112559313	chr6:35464972-35464973	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
3	rs537135476	chr6:35465017-35465018	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
4	rs9470041	chr6:35465023-35465024	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
5	rs144922138	chr6:35465039-35465040	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
6	rs540791143	chr6:35465052-35465053	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
7	rs188779831	chr6:35465115-35465116	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
8	rs574345053	chr6:35465135-35465136	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
9	rs192869384	chr6:35465233-35465234	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
10	rs563127112	chr6:35465291-35465292	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
11	rs202127806	chr6:35465293-35465294	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
12	rs530560913	chr6:35465298-35465299	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
13	rs564174661	chr6:35465342-35465343	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
14	rs528205602	chr6:35465376-35465377	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
15	rs529373409	chr6:35465458-35465459	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
16	rs370641312	chr6:35465468-35465469	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs547964257	chr6:35465504-35465505	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
18	rs45493300	chr6:35465580-35465581	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs185839943	chr6:35465593-35465594	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
20	rs548935646	chr6:35465594-35465595	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs569930903	chr6:35465612-35465613	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs537421924	chr6:35465656-35465657	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs554643340	chr6:35465659-35465660	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
24	rs558694509	chr6:35465689-35465690	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs577224839	chr6:35465702-35465703	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs534796159	chr6:35465720-35465721	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs552746401	chr6:35465721-35465722	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs559343621	chr6:35465722-35465723	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Esophageal adenocarcinoma	18820669	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
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35461000-35465000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:35461000-35465000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr6:35463200-35466000	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr6:35463200-35466200	Active TSS	Fetal Kidney	kidney
5	chr6:35463400-35465600	Active TSS	Sigmoid Colon	Sigmoid Colon
6	chr6:35463400-35465800	Active TSS	Small Intestine	intestine
7	chr6:35463400-35466000	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr6:35463600-35465400	Active TSS	Pancreas	Pancrea
9	chr6:35463600-35465400	Bivalent/Poised TSS	HepG2	liver
10	chr6:35463600-35465600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:35463600-35465600	Active TSS	Fetal Intestine Large	intestine
12	chr6:35463600-35465600	Active TSS	Placenta	Placenta
13	chr6:35463600-35465600	Active TSS	Rectal Mucosa Donor 29	rectum
14	chr6:35463600-35465600	Active TSS	Right Ventricle	heart
15	chr6:35463600-35465600	Bivalent/Poised TSS	Thymus	Thymus
16	chr6:35463600-35465800	Active TSS	Gastric	stomach
17	chr6:35463600-35466000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:35463600-35466000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:35463600-35466000	Active TSS	Colon Smooth Muscle	Colon
20	chr6:35463600-35466000	Active TSS	Esophagus	oesophagus
21	chr6:35463600-35466000	Active TSS	Ovary	ovary
22	chr6:35463600-35466000	Active TSS	A549	lung
23	chr6:35463600-35466000	Active TSS	NHLF	lung
24	chr6:35463600-35466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr6:35463600-35466200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:35463600-35466200	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr6:35463600-35466200	Active TSS	Aorta	Aorta
28	chr6:35463600-35466200	Active TSS	Placenta Amnion	Placenta Amnion
29	chr6:35463600-35466200	Active TSS	Rectal Smooth Muscle	rectum
30	chr6:35463600-35466200	Active TSS	HSMMtube	muscle
31	chr6:35463600-35466800	Active TSS	H9 Cell Line	embryonic stem cell
32	chr6:35463800-35465200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr6:35463800-35465400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr6:35463800-35465400	Active TSS	Liver	Liver
35	chr6:35463800-35465400	Active TSS	Brain Angular Gyrus	brain
36	chr6:35463800-35465400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:35463800-35465400	Active TSS	Duodenum Mucosa	Duodenum
38	chr6:35463800-35465400	Bivalent/Poised TSS	Fetal Thymus	thymus
39	chr6:35463800-35465400	Active TSS	Lung	lung
40	chr6:35463800-35465400	Active TSS	NH-A	brain
41	chr6:35463800-35465400	Active TSS	NHEK	skin
42	chr6:35463800-35465600	Active TSS	Brain Anterior Caudate	brain
43	chr6:35463800-35465600	Active TSS	Brain Hippocampus Middle	brain
44	chr6:35463800-35465600	Active TSS	Left Ventricle	heart
45	chr6:35463800-35465600	Active TSS	Stomach Smooth Muscle	stomach
46	chr6:35463800-35465800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:35463800-35465800	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr6:35463800-35466000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:35463800-35466000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:35463800-35466000	Active TSS	HUES48 Cell Line	embryonic stem cell

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