Variant report

Variant	nsv538542
Chromosome Location	chr6:167194653-167355961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1714)
CpG islands
(count:3175)
Chromatin interactive
region (count:66)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1714 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167264235-167264605	K562	blood:	n/a	n/a
2	ARID3A	chr6:167353960-167354308	K562	blood:	n/a	n/a
3	ARID3A	chr6:167324658-167325218	K562	blood:	n/a	n/a
4	ARID3A	chr6:167200218-167200546	HepG2	liver:	n/a	n/a
5	ATF1	chr6:167240077-167240150	K562	blood:	n/a	n/a
6	ATF1	chr6:167320881-167321225	K562	blood:	n/a	n/a
7	ATF1	chr6:167345566-167345627	K562	blood:	n/a	n/a
8	ATF1	chr6:167238143-167238339	K562	blood:	n/a	n/a
9	ATF1	chr6:167328715-167329352	K562	blood:	n/a	n/a
10	ATF1	chr6:167287376-167287880	K562	blood:	n/a	n/a
11	ATF1	chr6:167213787-167214099	K562	blood:	n/a	n/a
12	ATF1	chr6:167260351-167260433	K562	blood:	n/a	n/a
13	ATF1	chr6:167255068-167255231	K562	blood:	n/a	n/a
14	ATF1	chr6:167264121-167264564	K562	blood:	n/a	n/a
15	ATF1	chr6:167324192-167325358	K562	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	chr6:167200233-167200574	GM12878	blood:	n/a	n/a
19	ATF2	chr6:167247521-167247974	GM12878	blood:	n/a	n/a
20	ATF2	chr6:167320633-167321310	GM12878	blood:	n/a	n/a
21	ATF2	chr6:167247492-167247983	GM12878	blood:	n/a	n/a
22	ATF2	chr6:167263194-167263607	GM12878	blood:	n/a	n/a
23	BACH1	chr6:167354162-167354365	K562	blood:	n/a	n/a
24	BACH1	chr6:167216081-167216348	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:167317880-167318113	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:167276270-167276880	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:167198886-167198899	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:167354196-167354394	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:167196277-167196415	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167290924-167291004	K562	blood:	n/a	n/a
31	BATF	chr6:167263100-167263391	GM12878	blood:	n/a	n/a
32	BATF	chr6:167243652-167243968	GM12878	blood:	n/a	n/a
33	BATF	chr6:167247528-167247858	GM12878	blood:	n/a	n/a
34	BATF	chr6:167263166-167263351	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	chr6:167197282-167197733	GM12878	blood:	n/a	n/a
38	BATF	chr6:167320864-167321175	GM12878	blood:	n/a	n/a
39	BATF	chr6:167243631-167244353	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:167197263-167197805	GM12878	blood:	n/a	n/a
41	BCL11A	chr6:167244064-167244380	GM12878	blood:	n/a	n/a
42	BCL11A	chr6:167243593-167243973	GM12878	blood:	n/a	n/a
43	BCL11A	chr6:167197224-167197721	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:167244040-167244445	GM12878	blood:	n/a	n/a
45	BCL11A	chr6:167243668-167243958	GM12878	blood:	n/a	n/a
46	BCL3	chr6:167313871-167314706	GM12878	blood:	n/a	n/a
47	BCL3	chr6:167314979-167315950	GM12878	blood:	n/a	n/a
48	BCL3	chr6:167312133-167313195	GM12878	blood:	n/a	chr6:167312871-167312884 chr6:167312873-167312882 chr6:167312876-167312885
49	BCL3	chr6:167210070-167210405	GM12878	blood:	n/a	n/a
50	BCL3	chr6:167315018-167316313	GM12878	blood:	n/a	n/a

(count:3175 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167314233-167314283	HMEC	breast:	n/a
2	chr6:167313144-167313194	GM19239	blood:	n/a
3	chr6:167283835-167283885	SK-N-MC	brain:	n/a
4	chr6:167314233-167314283	HMEC	breast:	n/a
5	chr6:167313144-167313194	GM19239	blood:	n/a
6	chr6:167283835-167283885	SK-N-MC	brain:	n/a
7	chr6:167250429-167250479	AoSMC	blood vessel:	n/a
8	chr6:167275395-167275445	BJ	skin:	n/a
9	chr6:167283835-167283885	PrEC	prostate:	n/a
10	chr6:167276419-167276469	HMEC	breast:	n/a
11	chr6:167312423-167312473	AG09309	skin:	n/a
12	chr6:167276650-167276700	HepG2	liver:	n/a
13	chr6:167276359-167276409	HAEpiC	amniotic membrane:	n/a
14	chr6:167275832-167275882	HL-60	blood:	n/a
15	chr6:167284353-167284403	NH-A	brain:	n/a
16	chr6:167313144-167313194	AG10803	skin:	n/a
17	chr6:167318108-167318158	MCF-7	breast:	n/a
18	chr6:167263454-167263504	NHBE	bronchial:	n/a
19	chr6:167197893-167197943	MCF-7	breast:	n/a
20	chr6:167198539-167198589	HNPCEpiC	eye:	n/a
21	chr6:167200499-167200549	AG10803	skin:	n/a
22	chr6:167200499-167200549	HRPEpiC	eye:	n/a
23	chr6:167271883-167271933	CMK	blood:	n/a
24	chr6:167250541-167250591	HNPCEpiC	eye:	n/a
25	chr6:167263066-167263116	NH-A	brain:	n/a
26	chr6:167283835-167283885	GM12891	blood:	n/a
27	chr6:167271883-167271933	Hepatocyte	liver:	n/a
28	chr6:167284353-167284403	HCT-116	colon:	n/a
29	chr6:167275684-167275734	NB4	blood:	n/a
30	chr6:167263193-167263243	HRPEpiC	eye:	n/a
31	chr6:167315975-167316025	PANC-1	pancreas:	n/a
32	chr6:167195910-167195960	NHBE	bronchial:	n/a
33	chr6:167276650-167276700	HEEpiC	esophagus:	n/a
34	chr6:167312934-167312984	SK-N-SH	brain:	n/a
35	chr6:167313267-167313317	AG04450	lung:	fetal
36	chr6:167314745-167314795	CMK	blood:	n/a
37	chr6:167314745-167314795	RPTEC	kidney:	n/a
38	chr6:167284983-167285033	SK-N-SH_RA	brain:	n/a
39	chr6:167275781-167275831	SK-N-MC	brain:	n/a
40	chr6:167313144-167313194	HRCEpiC	kidney:	n/a
41	chr6:167263025-167263075	ECC-1	luminal epithelium:	n/a
42	chr6:167263193-167263243	HEEpiC	esophagus:	n/a
43	chr6:167284462-167284512	SAEC	small airway:	n/a
44	chr6:167318108-167318158	HNPCEpiC	eye:	n/a
45	chr6:167314745-167314795	PANC-1	pancreas:	n/a
46	chr6:167263225-167263275	HIPEpiC	eye:	n/a
47	chr6:167317799-167317849	LNCaP	prostate:	n/a
48	chr6:167195910-167195960	SAEC	small airway:	n/a
49	chr6:167271883-167271933	Jurkat	blood:	n/a
50	chr6:167200499-167200549	GM06990	blood:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:167327598..167330047-chr6:167367070..167369538,2	K562	blood:
2	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
3	chr6:167285809..167288027-chr6:167289441..167291420,2	K562	blood:
4	chr6:167274608..167276505-chr6:167368344..167370567,2	MCF-7	breast:
5	chr6:167353995..167356024-chr6:167413983..167416895,2	K562	blood:
6	chr6:167327579..167329886-chr6:167332499..167334100,2	K562	blood:
7	chr6:167334630..167336985-chr6:167348242..167350494,2	K562	blood:
8	chr6:167200031..167200812-chr6:167555407..167555996,2	K562	blood:
9	chr6:167339433..167341286-chr6:167346948..167348863,2	K562	blood:
10	chr6:167324257..167326145-chr6:167328411..167330868,2	K562	blood:
11	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
12	chr6:167244459..167246952-chr6:167353805..167356355,2	K562	blood:
13	chr6:167344148..167347113-chr6:167348259..167349932,2	K562	blood:
14	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
15	chr6:167345950..167348546-chr6:167353895..167356364,2	K562	blood:
16	chr6:167187491..167189760-chr6:167193508..167196442,3	K562	blood:
17	chr6:167200327..167200836-chr6:167459295..167459843,2	K562	blood:
18	chr6:167344148..167347081-chr6:167347085..167349759,2	K562	blood:
19	chr6:167280811..167283547-chr6:167284862..167287593,2	K562	blood:
20	chr6:167327579..167329886-chr6:167332499..167334100,2	K562	blood:
21	chr6:167285809..167288027-chr6:167289441..167291420,2	K562	blood:
22	chr6:167232177..167234702-chr6:167235338..167237852,2	K562	blood:
23	chr6:167355022..167357881-chr6:167358676..167361500,2	K562	blood:
24	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
25	chr6:167198453..167200233-chr6:167409946..167412844,2	K562	blood:
26	chr6:167287783..167290388-chr6:167293843..167295742,3	K562	blood:
27	chr6:167221917..167225316-chr6:167226153..167228902,3	K562	blood:
28	chr6:167307243..167309166-chr6:167369086..167371594,2	MCF-7	breast:
29	chr6:167280811..167283547-chr6:167284862..167287593,2	K562	blood:
30	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
31	chr6:167316933..167319053-chr6:167320800..167322909,2	K562	blood:
32	chr6:167199917..167200852-chr6:167555354..167555927,2	MCF-7	breast:
33	chr6:167234151..167235885-chr6:167241479..167243381,2	K562	blood:
34	chr6:167324856..167326395-chr6:167326764..167328274,2	K562	blood:
35	chr6:167334630..167336985-chr6:167348242..167350494,2	K562	blood:
36	chr6:167324476..167326634-chr6:167338829..167341348,2	K562	blood:
37	chr6:167263153..167265718-chr6:167272365..167274771,2	K562	blood:
38	chr6:167324257..167326145-chr6:167328411..167330868,2	K562	blood:
39	chr6:167212524..167215294-chr6:167216154..167217898,2	K562	blood:
40	chr6:167268417..167269941-chr6:167289089..167292061,2	K562	blood:
41	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
42	chr6:167200158..167200693-chr6:167401004..167401948,2	K562	blood:
43	chr6:167320098..167322424-chr6:167348297..167350309,2	K562	blood:
44	chr6:166870182..166872414-chr6:167234943..167236564,2	K562	blood:
45	chr6:167287783..167289646-chr6:167293843..167295409,2	K562	blood:
46	chr6:167200059..167200966-chr6:167402403..167403438,4	K562	blood:
47	chr6:167266120..167268418-chr6:167368019..167370456,2	K562	blood:
48	chr6:167287783..167289646-chr6:167293843..167295409,2	K562	blood:
49	chr6:167232177..167234702-chr6:167235338..167237852,2	K562	blood:
50	chr6:167339433..167341286-chr6:167346948..167348863,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-1	chr6:167317186-167317276	NR_046644
2	lnc-FGFR1OP-1	chr6:167317788-167318557	NR_046644
3	lnc-FGFR1OP-1	chr6:167319514-167321259	l_3322_chr6:167314133-167321259_testes
4	lnc-RNASET2-3	chr6:167317848-167318299	NONHSAT116059
5	lnc-FGFR1OP-1	chr6:167321422-167321647	l_3322_chr6:167314133-167321259_testes
6	lnc-FGFR1OP-11	chr6:167237176-167237266	NONHSAT116055
7	lnc-FGFR1OP-11	chr6:167237778-167238313	NONHSAT116055
8	lnc-RNASET2-3	chr6:167315613-167316152	NONHSAT116059
9	lnc-FGFR1OP-1	chr6:167317788-167318323	XLOC_005539
10	lnc-FGFR1OP-10	chr6:167254947-167255400	l_3320_chr6:167242351-167255400_testes
11	lnc-FGFR1OP-1	chr6:167317186-167317276	XLOC_005539
12	lnc-RNASET2-2	chr6:167346863-167347624	NONHSAT116063
13	lnc-FGFR1OP-10	chr6:167242352-167242576	l_3320_chr6:167242351-167255400_testes
14	lnc-FGFR1OP-1	chr6:167314134-167317318	l_3322_chr6:167314133-167321259_testes

No data

Variant related genes	Relation type
RPS6KA2	TF binding region
RPS6KA2-AS1	TF binding region
RNASET2	TF binding region
RPS6KA2	CpG island
RPS6KA2-AS1	CpG island
RNASET2	CpG island
ENSG00000213066	chromatin interactions
ENSG00000265828	chromatin interactions
ENSG00000272980	chromatin interactions
ENSG00000197146	chromatin interactions
ENSG00000249141	chromatin interactions
ENSG00000026297	chromatin interactions
ENSG00000231654	chromatin interactions
ENSG00000227598	chromatin interactions

Extended variants
information (count: 6947 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6947 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375209508	chr6:167194663-167194664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570575035	chr6:167194677-167194678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534766054	chr6:167194694-167194695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546583691	chr6:167194700-167194701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187575361	chr6:167194745-167194746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535743113	chr6:167194779-167194780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146718976	chr6:167194798-167194799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575279665	chr6:167194802-167194803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs193301453	chr6:167194813-167194814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551873348	chr6:167194817-167194818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114691687	chr6:167194855-167194856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76368569	chr6:167194871-167194872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs78668569	chr6:167194872-167194873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs75124356	chr6:167194888-167194889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561943593	chr6:167194908-167194909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112644117	chr6:167194937-167194938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142543814	chr6:167194946-167194947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537750749	chr6:167194947-167194948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7749522	chr6:167195006-167195007	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs545174268	chr6:167195044-167195045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150937062	chr6:167195046-167195047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs7753589	chr6:167195051-167195052	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs73266823	chr6:167195071-167195072	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7753731	chr6:167195088-167195089	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs7768138	chr6:167195096-167195097	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550868144	chr6:167195097-167195098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146906741	chr6:167195112-167195113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539381730	chr6:167195140-167195141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139393276	chr6:167195192-167195193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375870214	chr6:167195211-167195212	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533631457	chr6:167195218-167195219	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555573987	chr6:167195233-167195234	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573861028	chr6:167195238-167195239	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544524852	chr6:167195248-167195249	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556392277	chr6:167195308-167195309	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577965098	chr6:167195317-167195318	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545423421	chr6:167195318-167195319	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7768490	chr6:167195320-167195321	Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs112068878	chr6:167195382-167195383	Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542722424	chr6:167195414-167195415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184535742	chr6:167195473-167195474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371532473	chr6:167195499-167195500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529054322	chr6:167195500-167195501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs550906864	chr6:167195576-167195577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569214767	chr6:167195666-167195667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533074572	chr6:167195667-167195668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35637883	chr6:167195716-167195717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187399344	chr6:167195731-167195732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77852948	chr6:167195770-167195771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71721078	chr6:167195771-167195772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Autism	22549408	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1663 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167182200-167218600	Weak transcription	Right Atrium	heart
2	chr6:167190400-167195200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:167190800-167195200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:167192400-167195200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr6:167193800-167194800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:167194800-167195200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:167195200-167195400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:167195200-167195400	Enhancers	Brain Inferior Temporal Lobe	brain
9	chr6:167195200-167196200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr6:167195400-167196200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr6:167196200-167196400	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr6:167196400-167198600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr6:167196800-167197000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:167198400-167198800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr6:167198600-167198800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:167198600-167198800	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr6:167207200-167212000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:167208000-167212000	Weak transcription	Brain Anterior Caudate	brain
19	chr6:167208400-167213400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:167208600-167211600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr6:167208800-167211000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr6:167209800-167218600	Weak transcription	Gastric	stomach
23	chr6:167210000-167214800	Weak transcription	Esophagus	oesophagus
24	chr6:167211600-167212600	Enhancers	Brain Cingulate Gyrus	brain
25	chr6:167211800-167212200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr6:167212000-167212200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr6:167212000-167212400	Enhancers	Brain Germinal Matrix	brain
28	chr6:167212000-167212600	Enhancers	Brain Anterior Caudate	brain
29	chr6:167212200-167212400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr6:167212200-167212600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:167212200-167215200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr6:167212400-167212800	Active TSS	Brain Germinal Matrix	brain
33	chr6:167212400-167213600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr6:167212600-167212800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:167212600-167213400	Weak transcription	Brain Anterior Caudate	brain
36	chr6:167212600-167217000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr6:167212800-167213000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:167213000-167213200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:167213200-167214800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:167213400-167213600	Enhancers	Lung	lung
41	chr6:167213400-167214000	Enhancers	Brain Anterior Caudate	brain
42	chr6:167213400-167214200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:167213400-167214400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr6:167213600-167214000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr6:167213800-167214000	Bivalent Enhancer	Brain Hippocampus Middle	brain
46	chr6:167213800-167214200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr6:167214000-167216800	Weak transcription	Brain Anterior Caudate	brain
48	chr6:167214200-167216600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:167214400-167216800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:167215200-167216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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