Variant report

Variant	nsv482478
Chromosome Location	chr6:167071366-167265821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2243)
CpG islands
(count:4033)
Chromatin interactive
region (count:97)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2243 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167200218-167200546	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167264235-167264605	K562	blood:	n/a	n/a
3	ARID3A	chr6:167188768-167188974	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167089914-167090051	K562	blood:	n/a	n/a
5	ATF1	chr6:167240077-167240150	K562	blood:	n/a	n/a
6	ATF1	chr6:167264121-167264564	K562	blood:	n/a	n/a
7	ATF1	chr6:167238143-167238339	K562	blood:	n/a	n/a
8	ATF1	chr6:167190190-167190394	K562	blood:	n/a	n/a
9	ATF1	chr6:167091973-167092242	K562	blood:	n/a	n/a
10	ATF1	chr6:167106355-167106363	K562	blood:	n/a	n/a
11	ATF1	chr6:167260351-167260433	K562	blood:	n/a	n/a
12	ATF1	chr6:167255068-167255231	K562	blood:	n/a	n/a
13	ATF1	chr6:167213787-167214099	K562	blood:	n/a	n/a
14	ATF2	chr6:167200233-167200574	GM12878	blood:	n/a	n/a
15	ATF2	chr6:167263194-167263607	GM12878	blood:	n/a	n/a
16	ATF2	chr6:167243498-167244485	GM12878	blood:	n/a	n/a
17	ATF2	chr6:167243583-167244420	GM12878	blood:	n/a	n/a
18	ATF2	chr6:167247521-167247974	GM12878	blood:	n/a	n/a
19	ATF2	chr6:167247492-167247983	GM12878	blood:	n/a	n/a
20	BACH1	chr6:167080570-167080599	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:167183960-167184643	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:167198886-167198899	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:167196277-167196415	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:167108688-167108908	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:167085611-167085744	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:167216081-167216348	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:167174931-167175059	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:167164829-167164988	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:167180403-167180549	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167101913-167101935	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr6:167243631-167244353	GM12878	blood:	n/a	n/a
32	BATF	chr6:167197282-167197733	GM12878	blood:	n/a	n/a
33	BATF	chr6:167243652-167243968	GM12878	blood:	n/a	n/a
34	BATF	chr6:167263100-167263391	GM12878	blood:	n/a	n/a
35	BATF	chr6:167197269-167197664	GM12878	blood:	n/a	n/a
36	BATF	chr6:167247594-167247848	GM12878	blood:	n/a	n/a
37	BATF	chr6:167247528-167247858	GM12878	blood:	n/a	n/a
38	BATF	chr6:167263166-167263351	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:167244064-167244380	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:167197263-167197805	GM12878	blood:	n/a	n/a
41	BCL11A	chr6:167197224-167197721	GM12878	blood:	n/a	n/a
42	BCL11A	chr6:167243593-167243973	GM12878	blood:	n/a	n/a
43	BCL11A	chr6:167244040-167244445	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:167243668-167243958	GM12878	blood:	n/a	n/a
45	BCL3	chr6:167073691-167073910	GM12878	blood:	n/a	n/a
46	BCL3	chr6:167073673-167073994	GM12878	blood:	n/a	n/a
47	BCL3	chr6:167210070-167210405	GM12878	blood:	n/a	n/a
48	BCL3	chr6:167210133-167210520	GM12878	blood:	n/a	n/a
49	BCL3	chr6:167136250-167136646	GM12878	blood:	n/a	chr6:167136381-167136389
50	BCLAF1	chr6:167247514-167247888	GM12878	blood:	n/a	n/a

(count:4033 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167192488-167192538	SKMC	muscle:	n/a
2	chr6:167189543-167189593	NHDF-neo	bronchial:	n/a
3	chr6:167171394-167171444	Jurkat	blood:	n/a
4	chr6:167195910-167195960	H1-hESC	embryonic stem cell:	embryo
5	chr6:167167603-167167653	MCF-7	breast:	n/a
6	chr6:167101267-167101317	HMEC	breast:	n/a
7	chr6:167197893-167197943	ProgFib	skin:	n/a
8	chr6:167192488-167192538	SKMC	muscle:	n/a
9	chr6:167189543-167189593	NHDF-neo	bronchial:	n/a
10	chr6:167171394-167171444	Jurkat	blood:	n/a
11	chr6:167195910-167195960	H1-hESC	embryonic stem cell:	embryo
12	chr6:167167603-167167653	MCF-7	breast:	n/a
13	chr6:167101267-167101317	HMEC	breast:	n/a
14	chr6:167197893-167197943	ProgFib	skin:	n/a
15	chr6:167178233-167178283	MCF10A-Er-Src	breast:	n/a
16	chr6:167250429-167250479	BJ	skin:	n/a
17	chr6:167178260-167178310	PrEC	prostate:	n/a
18	chr6:167263025-167263075	AoSMC	blood vessel:	n/a
19	chr6:167171727-167171777	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:167189543-167189593	AG10803	skin:	n/a
21	chr6:167136206-167136256	NHDF-neo	bronchial:	n/a
22	chr6:167263225-167263275	AG10803	skin:	n/a
23	chr6:167104677-167104727	BE2_C	brain:	n/a
24	chr6:167195910-167195960	HL-60	blood:	n/a
25	chr6:167188753-167188803	Hepatocyte	liver:	n/a
26	chr6:167136367-167136417	HRCEpiC	kidney:	n/a
27	chr6:167136367-167136417	HEEpiC	esophagus:	n/a
28	chr6:167194813-167194863	HAEpiC	amniotic membrane:	n/a
29	chr6:167171394-167171444	Hepatocyte	liver:	n/a
30	chr6:167263025-167263075	GM12891	blood:	n/a
31	chr6:167190034-167190084	GM12878	blood:	n/a
32	chr6:167136432-167136482	HEEpiC	esophagus:	n/a
33	chr6:167167603-167167653	AG10803	skin:	n/a
34	chr6:167135251-167135301	SKMC	muscle:	n/a
35	chr6:167189213-167189263	HAEpiC	amniotic membrane:	n/a
36	chr6:167135251-167135301	GM12878	blood:	n/a
37	chr6:167104677-167104727	SK-N-MC	brain:	n/a
38	chr6:167136432-167136482	HUVEC	blood vessel:	n/a
39	chr6:167263025-167263075	LNCaP	prostate:	n/a
40	chr6:167178280-167178330	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:167136367-167136417	HEK293	kidney:	embryo
42	chr6:167129857-167129907	ovcar-3	ovarian:	n/a
43	chr6:167104926-167104976	K562	blood:	n/a
44	chr6:167175937-167175987	HEEpiC	esophagus:	n/a
45	chr6:167263225-167263275	HUVEC	blood vessel:	n/a
46	chr6:167135152-167135202	NT2-D1	testis:	n/a
47	chr6:167189543-167189593	RPTEC	kidney:	n/a
48	chr6:167136367-167136417	HRPEpiC	eye:	n/a
49	chr6:167250541-167250591	AG09319	gingival:	n/a
50	chr6:167263193-167263243	GM19239	blood:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:167179347..167182239-chr6:167183994..167186208,2	K562	blood:
2	chr6:167105343..167108325-chr6:167108497..167110048,2	MCF-7	breast:
3	chr6:167187969..167188996-chr6:167555512..167556325,4	MCF-7	breast:
4	chr6:167039986..167042610-chr6:167119069..167121517,2	MCF-7	breast:
5	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
6	chr6:167094171..167096219-chr6:167102346..167104221,2	K562	blood:
7	chr6:167209245..167212049-chr6:167411313..167412932,2	K562	blood:
8	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
9	chr6:167137568..167139620-chr6:167143450..167146444,3	K562	blood:
10	chr6:167212524..167215294-chr6:167216154..167217898,2	K562	blood:
11	chr6:167097647..167100107-chr6:167101291..167103727,2	K562	blood:
12	chr6:167198453..167200233-chr6:167409946..167412844,2	K562	blood:
13	chr6:167039628..167041364-chr6:167163244..167165367,2	MCF-7	breast:
14	chr6:167200158..167200693-chr6:167401004..167401948,2	K562	blood:
15	chr6:167199917..167200852-chr6:167555354..167555927,2	MCF-7	breast:
16	chr6:167118192..167119844-chr6:167123770..167126237,2	MCF-7	breast:
17	chr6:167187491..167189760-chr6:167193508..167196442,3	K562	blood:
18	chr6:167172216..167176506-chr6:167180840..167185522,4	K562	blood:
19	chr6:167050618..167053160-chr6:167077513..167080245,2	K562	blood:
20	chr6:167146144..167148491-chr6:167149549..167153230,4	K562	blood:
21	chr6:167095053..167097754-chr6:167110301..167112969,2	K562	blood:
22	chr6:167129723..167131439-chr6:167133367..167136362,2	K562	blood:
23	chr6:167074591..167076523-chr6:167109521..167111565,2	K562	blood:
24	chr6:167234151..167235885-chr6:167241479..167243381,2	K562	blood:
25	chr6:166870182..166872414-chr6:167234943..167236564,2	K562	blood:
26	chr6:167172089..167173654-chr6:167192090..167194256,2	K562	blood:
27	chr6:167188018..167188945-chr6:167458801..167459761,3	MCF-7	breast:
28	chr6:167187491..167189760-chr6:167193508..167196442,3	K562	blood:
29	chr6:167097647..167100107-chr6:167101291..167103727,2	K562	blood:
30	chr6:167200059..167200966-chr6:167402403..167403438,4	K562	blood:
31	chr6:167172089..167173654-chr6:167192090..167194256,2	K562	blood:
32	chr6:167200031..167200812-chr6:167555407..167555996,2	K562	blood:
33	chr6:167137568..167139620-chr6:167143450..167146444,3	K562	blood:
34	chr6:167075814..167078811-chr6:167080757..167083595,2	MCF-7	breast:
35	chr6:167187491..167191588-chr6:167191761..167196442,4	K562	blood:
36	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
37	chr6:167099352..167102037-chr6:167146508..167149347,2	MCF-7	breast:
38	chr6:167075814..167078811-chr6:167080757..167083595,2	MCF-7	breast:
39	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
40	chr6:167185783..167186302-chr6:167555369..167556350,2	K562	blood:
41	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
42	chr6:167160489..167162374-chr6:167163032..167165986,2	K562	blood:
43	chr6:167244459..167246952-chr6:167353805..167356355,2	K562	blood:
44	chr6:167105343..167108325-chr6:167108497..167110048,2	MCF-7	breast:
45	chr6:167120732..167121236-chr6:167185691..167186290,2	MCF-7	breast:
46	chr6:167095053..167097754-chr6:167110301..167112969,2	K562	blood:
47	chr6:167188755..167189454-chr6:167555413..167556221,2	MCF-7	breast:
48	chr6:167182263..167184637-chr6:167557115..167559460,2	K562	blood:
49	chr6:167097647..167099488-chr6:167100247..167103727,3	K562	blood:
50	chr6:167094171..167096219-chr6:167102346..167104221,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-11	chr6:167237176-167237266	NONHSAT116055
2	lnc-FGFR1OP-10	chr6:167242352-167242576	l_3320_chr6:167242351-167255400_testes
3	lnc-FGFR1OP-10	chr6:167254947-167255400	l_3320_chr6:167242351-167255400_testes
4	lnc-FGFR1OP-11	chr6:167237778-167238313	NONHSAT116055

No data

Variant related genes	Relation type
ENSG00000235008	TF binding region
RPS6KA2	TF binding region
ENSG00000235008	CpG island
RPS6KA2	CpG island
ENSG00000265828	chromatin interactions
ENSG00000071242	chromatin interactions
ENSG00000272980	chromatin interactions
ENSG00000026297	chromatin interactions
ENSG00000197146	chromatin interactions
ENSG00000227598	chromatin interactions
ENSG00000213066	chromatin interactions

Extended variants
information (count: 8686 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:8686 , 50 per page) page: 1 2 3 4 5 6 7 ... 174

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140352422	chr6:167071387-167071388	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs559603375	chr6:167071394-167071395	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs184304745	chr6:167071428-167071429	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs371023175	chr6:167071449-167071450	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs533040242	chr6:167071474-167071475	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs536767737	chr6:167071513-167071514	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs145402917	chr6:167071524-167071525	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs148009883	chr6:167071558-167071559	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs541323264	chr6:167071581-167071582	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs569747786	chr6:167071582-167071583	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs559836762	chr6:167071583-167071584	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs575088594	chr6:167071588-167071589	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs541809816	chr6:167071595-167071596	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs111925966	chr6:167071608-167071609	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377751750	chr6:167071612-167071613	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530991382	chr6:167071613-167071614	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376062198	chr6:167071625-167071626	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112621078	chr6:167071629-167071630	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369866174	chr6:167071654-167071655	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565048115	chr6:167071669-167071670	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532391685	chr6:167071685-167071686	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374342087	chr6:167071690-167071691	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547702920	chr6:167071709-167071710	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565793935	chr6:167071791-167071792	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116164722	chr6:167071803-167071804	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189113195	chr6:167071831-167071832	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs16899289	chr6:167071835-167071836	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs181973021	chr6:167071851-167071852	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138408310	chr6:167071856-167071857	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570702992	chr6:167071886-167071887	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375049651	chr6:167071897-167071898	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184702199	chr6:167071899-167071900	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78411296	chr6:167071900-167071901	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs60647082	chr6:167071910-167071911	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs557821668	chr6:167071916-167071917	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9348164	chr6:167071948-167071949	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs557061680	chr6:167071960-167071961	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114640543	chr6:167072003-167072004	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs35537854	chr6:167072030-167072031	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs149604169	chr6:167072055-167072056	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs4710075	chr6:167072059-167072060	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs142679363	chr6:167072063-167072064	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs147542566	chr6:167072068-167072069	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs540841960	chr6:167072072-167072073	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs559516535	chr6:167072128-167072129	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs529941824	chr6:167072142-167072143	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs138513511	chr6:167072163-167072164	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs189101146	chr6:167072174-167072175	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs375648762	chr6:167072185-167072186	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs530465322	chr6:167072187-167072188	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22549408	CNVD

Chromatin state (count:1851 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167061800-167071800	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:167064200-167079000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:167068200-167073600	Weak transcription	Fetal Heart	heart
4	chr6:167069000-167077200	Weak transcription	Right Atrium	heart
5	chr6:167069200-167073200	Enhancers	Spleen	Spleen
6	chr6:167070400-167071400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr6:167070400-167071600	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr6:167070600-167071600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:167070600-167071600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:167070800-167071400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
11	chr6:167070800-167071400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
12	chr6:167070800-167071400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:167070800-167071400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
14	chr6:167070800-167071800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr6:167070800-167071800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr6:167070800-167072000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:167071000-167071600	Enhancers	Primary B cells from peripheral blood	blood
18	chr6:167071000-167071600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:167071000-167072400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr6:167071000-167073400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr6:167071000-167074000	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr6:167071200-167071400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
23	chr6:167071200-167071400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
24	chr6:167071200-167071600	Enhancers	Primary B cells from cord blood	blood
25	chr6:167071200-167072400	Enhancers	Duodenum Mucosa	Duodenum
26	chr6:167071200-167076800	Weak transcription	Pancreas	Pancrea
27	chr6:167071400-167071800	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr6:167071600-167072000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr6:167071600-167072400	Enhancers	Primary hematopoietic stem cells	blood
30	chr6:167071600-167072600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr6:167071600-167072600	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr6:167071600-167072800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:167071800-167074200	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr6:167071800-167076400	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr6:167072000-167072200	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
36	chr6:167072000-167072200	Enhancers	Fetal Brain Female	brain
37	chr6:167072000-167072600	Bivalent Enhancer	HepG2	liver
38	chr6:167072000-167073800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:167072200-167073000	Enhancers	Brain Germinal Matrix	brain
40	chr6:167072600-167072800	Weak transcription	Fetal Brain Female	brain
41	chr6:167073000-167073200	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr6:167073200-167076400	Weak transcription	Spleen	Spleen
43	chr6:167073600-167074200	Enhancers	Fetal Heart	heart
44	chr6:167073600-167074800	Enhancers	Fetal Brain Male	brain
45	chr6:167073800-167074000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:167074000-167081400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:167074000-167084600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr6:167074200-167077400	Weak transcription	Fetal Heart	heart
49	chr6:167074200-167084800	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:167074600-167074800	Enhancers	Brain Germinal Matrix	brain

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