Variant report

Variant	esv1825718
Chromosome Location	chr6:140476088-140584384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:424)
CpG islands
(count:61)
Chromatin interactive
region (count:61)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:140519795-140519962	K562	blood:	n/a	n/a
2	ATF1	chr6:140488573-140488780	K562	blood:	n/a	n/a
3	BACH1	chr6:140508327-140508411	K562	blood:	n/a	n/a
4	BCL11A	chr6:140501480-140501721	GM12878	blood:	n/a	n/a
5	BRCA1	chr6:140577325-140577716	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr6:140513220-140513479	K562	blood:	n/a	n/a
7	CBX3	chr6:140513098-140513521	K562	blood:	n/a	n/a
8	CBX3	chr6:140509683-140510073	K562	blood:	n/a	n/a
9	CBX3	chr6:140514433-140514788	K562	blood:	n/a	n/a
10	CBX3	chr6:140514504-140514838	K562	blood:	n/a	n/a
11	CCNT2	chr6:140531068-140531268	K562	blood:	n/a	n/a
12	CEBPB	chr6:140548597-140549071	HepG2	liver:	n/a	chr6:140548925-140548938 chr6:140549060-140549071 chr6:140548913-140548924 chr6:140548913-140548926
13	CEBPB	chr6:140499820-140500157	IMR90	lung:	n/a	chr6:140499978-140499991 chr6:140499980-140499991
14	CEBPB	chr6:140549789-140549981	Hela-S3	cervix:	n/a	chr6:140549845-140549856
15	CEBPB	chr6:140499950-140499975	K562	blood:	n/a	n/a
16	CEBPB	chr6:140495616-140496138	A549	lung:	n/a	n/a
17	CEBPB	chr6:140495647-140496069	IMR90	lung:	n/a	n/a
18	CEBPB	chr6:140549703-140550015	A549	lung:	n/a	chr6:140549845-140549856
19	CEBPB	chr6:140495627-140496083	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:140495677-140496046	A549	lung:	n/a	n/a
21	CEBPB	chr6:140519916-140520206	HepG2	liver:	n/a	chr6:140520026-140520037 chr6:140520094-140520105
22	CEBPB	chr6:140548745-140549040	IMR90	lung:	n/a	chr6:140548925-140548938 chr6:140548913-140548924 chr6:140548913-140548926
23	CEBPB	chr6:140495607-140496093	MCF-7	breast:	n/a	n/a
24	CEBPB	chr6:140573322-140573576	K562	blood:	n/a	chr6:140573438-140573449
25	CEBPB	chr6:140573277-140573617	HepG2	liver:	n/a	chr6:140573438-140573449
26	CEBPB	chr6:140495642-140496132	MCF-7	breast:	n/a	n/a
27	CEBPB	chr6:140573286-140573611	IMR90	lung:	n/a	chr6:140573438-140573449
28	CEBPB	chr6:140554159-140554212	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:140522218-140522432	HepG2	liver:	n/a	chr6:140522337-140522348
30	CEBPB	chr6:140519930-140520165	K562	blood:	n/a	chr6:140520026-140520037 chr6:140520094-140520105
31	CEBPB	chr6:140495556-140496093	HCT-116	colon:	n/a	n/a
32	CEBPB	chr6:140533216-140533242	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr6:140495678-140496054	A549	lung:	n/a	n/a
34	CEBPB	chr6:140549691-140550009	IMR90	lung:	n/a	chr6:140549845-140549856
35	CEBPB	chr6:140549693-140549919	K562	blood:	n/a	chr6:140549845-140549856
36	CEBPB	chr6:140499985-140500002	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr6:140531005-140531322	HepG2	liver:	n/a	chr6:140531173-140531184
38	CEBPB	chr6:140573302-140573566	A549	lung:	n/a	chr6:140573438-140573449
39	CEBPB	chr6:140519874-140520197	Hela-S3	cervix:	n/a	chr6:140520026-140520037 chr6:140520094-140520105
40	CEBPB	chr6:140577286-140577819	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr6:140531069-140531318	H1-hESC	embryonic stem cell:	n/a	chr6:140531173-140531184
42	CEBPB	chr6:140495701-140496059	HCT-116	colon:	n/a	n/a
43	CEBPB	chr6:140549688-140550018	HepG2	liver:	n/a	chr6:140549845-140549856
44	CREB1	chr6:140577318-140577763	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr6:140550282-140550305	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:140546046-140546068	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr6:140516506-140516561	LNCaP	prostate:	n/a	n/a
48	CTCF	chr6:140505820-140505970	BJ	skin:	n/a	n/a
49	CTCF	chr6:140561560-140561639	GM13977	blood:	n/a	n/a
50	CTCF	chr6:140480434-140480482	Kidney_OC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:140495807-140495857	HepG2	liver:	n/a
2	chr6:140495807-140495857	HCM	heart:	n/a
3	chr6:140495807-140495857	IMR90	lung:	fetal
4	chr6:140495807-140495857	NH-A	brain:	n/a
5	chr6:140495807-140495857	Jurkat	blood:	n/a
6	chr6:140495807-140495857	AG10803	skin:	n/a
7	chr6:140495807-140495857	HMEC	breast:	n/a
8	chr6:140495807-140495857	HEEpiC	esophagus:	n/a
9	chr6:140495807-140495857	HCT-116	colon:	n/a
10	chr6:140495807-140495857	HUVEC	blood vessel:	n/a
11	chr6:140495807-140495857	PANC-1	pancreas:	n/a
12	chr6:140495807-140495857	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:140495807-140495857	HCF	heart:	n/a
14	chr6:140495807-140495857	PrEC	prostate:	n/a
15	chr6:140495807-140495857	GM12892	blood:	n/a
16	chr6:140495807-140495857	HRPEpiC	eye:	n/a
17	chr6:140495807-140495857	HIPEpiC	eye:	n/a
18	chr6:140495807-140495857	ovcar-3	ovarian:	n/a
19	chr6:140495807-140495857	GM19239	blood:	n/a
20	chr6:140495807-140495857	ProgFib	skin:	n/a
21	chr6:140495807-140495857	SK-N-SH	brain:	n/a
22	chr6:140495807-140495857	PFSK-1	brain:	n/a
23	chr6:140495807-140495857	GM12891	blood:	n/a
24	chr6:140495807-140495857	ECC-1	luminal epithelium:	n/a
25	chr6:140495807-140495857	HEK293	kidney:	embryo
26	chr6:140495807-140495857	HRE	kidney:	n/a
27	chr6:140495807-140495857	AG09319	gingival:	n/a
28	chr6:140495807-140495857	AG04450	lung:	fetal
29	chr6:140495807-140495857	SK-N-SH_RA	brain:	n/a
30	chr6:140495807-140495857	SAEC	small airway:	n/a
31	chr6:140495807-140495857	BE2_C	brain:	n/a
32	chr6:140495807-140495857	SKMC	muscle:	n/a
33	chr6:140495807-140495857	AG04449	skin:	fetal
34	chr6:140495807-140495857	CMK	blood:	n/a
35	chr6:140495807-140495857	NB4	blood:	n/a
36	chr6:140495807-140495857	HNPCEpiC	eye:	n/a
37	chr6:140495807-140495857	K562	blood:	n/a
38	chr6:140495807-140495857	LNCaP	prostate:	n/a
39	chr6:140495807-140495857	A549	lung:	n/a
40	chr6:140495807-140495857	Caco-2	colon:	n/a
41	chr6:140495807-140495857	MCF-7	breast:	n/a
42	chr6:140495807-140495857	Hepatocyte	liver:	n/a
43	chr6:140495807-140495857	RPTEC	kidney:	n/a
44	chr6:140495807-140495857	NT2-D1	testis:	n/a
45	chr6:140495807-140495857	H1-hESC	embryonic stem cell:	embryo
46	chr6:140495807-140495857	T-47D	breast:	n/a
47	chr6:140495807-140495857	AoSMC	blood vessel:	n/a
48	chr6:140495807-140495857	HL-60	blood:	n/a
49	chr6:140495807-140495857	HCPEpiC	choroid plexus:	n/a
50	chr6:140495807-140495857	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:140469961..140471694-chr6:140504902..140507388,2	K562	blood:
2	chr6:140525279..140526991-chr6:140532137..140534862,2	MCF-7	breast:
3	chr6:140481943..140484484-chr6:140504896..140507347,2	K562	blood:
4	chr6:140538760..140541434-chr6:140543079..140545018,2	K562	blood:
5	chr6:140499649..140502750-chr6:140506344..140509801,3	K562	blood:
6	chr6:140494924..140496945-chr6:140505930..140507735,2	K562	blood:
7	chr6:140494924..140496945-chr6:140505930..140507735,2	K562	blood:
8	chr6:140525648..140527331-chr6:140535285..140538098,2	K562	blood:
9	chr6:140480820..140482701-chr6:140485695..140487316,2	K562	blood:
10	chr6:140467252..140471466-chr6:140472412..140477060,5	K562	blood:
11	chr6:140521774..140524611-chr6:140525360..140528267,2	MCF-7	breast:
12	chr1:166545251..166548120-chr6:140575352..140577699,2	MCF-7	breast:
13	chr6:140506210..140508246-chr6:140511712..140513687,2	K562	blood:
14	chr6:140475534..140478099-chr6:140479068..140483254,4	K562	blood:
15	chr13:105377776..105378623-chr6:140538409..140539126,2	MCF-7	breast:
16	chr6:140534052..140535840-chr6:140537958..140540728,3	K562	blood:
17	chr6:139694055..139695955-chr6:140478931..140481857,2	K562	blood:
18	chr6:140503911..140507978-chr6:140508654..140513269,4	K562	blood:
19	chr6:140470460..140473376-chr6:140484391..140487088,2	K562	blood:
20	chr6:140534009..140535840-chr6:140539228..140542033,2	K562	blood:
21	chr6:140566708..140568790-chr6:140577042..140579091,2	K562	blood:
22	chr6:139693727..139695746-chr6:140566409..140568106,2	MCF-7	breast:
23	chr6:140532063..140533672-chr6:140539512..140541736,2	K562	blood:
24	chr6:140520638..140522194-chr6:140526984..140528486,2	K562	blood:
25	chr6:140533963..140536569-chr6:140568826..140570409,2	K562	blood:
26	chr6:140481943..140484484-chr6:140504896..140507347,2	K562	blood:
27	chr6:140524041..140529376-chr6:140531337..140535137,6	K562	blood:
28	chr6:140520638..140522194-chr6:140526984..140528486,2	K562	blood:
29	chr6:140534009..140535840-chr6:140539228..140542033,2	K562	blood:
30	chr6:140558826..140560857-chr6:140562655..140564583,2	K562	blood:
31	chr6:140499649..140502750-chr6:140506344..140509801,3	K562	blood:
32	chr6:140506210..140508246-chr6:140511712..140513687,2	K562	blood:
33	chr2:242041141..242041804-chr6:140570392..140571031,2	MCF-7	breast:
34	chr6:140562032..140563790-chr6:140568097..140570245,2	K562	blood:
35	chr6:140503911..140507978-chr6:140508654..140513269,4	K562	blood:
36	chr6:139695739..139698033-chr6:140494036..140495935,2	MCF-7	breast:
37	chr20:48809431..48812147-chr6:140474358..140476603,2	MCF-7	breast:
38	chr6:140534052..140535840-chr6:140537958..140540728,3	K562	blood:
39	chr6:140558826..140560857-chr6:140562655..140564583,2	K562	blood:
40	chr6:140473947..140477365-chr6:140478769..140481102,4	K562	blood:
41	chr6:140468617..140471093-chr6:140487211..140489040,2	K562	blood:
42	chr6:140511544..140514524-chr6:140522660..140525197,2	K562	blood:
43	chr6:140511544..140514524-chr6:140522660..140525197,2	K562	blood:
44	chr6:140469028..140473078-chr6:140508512..140512504,3	K562	blood:
45	chr6:140480820..140482701-chr6:140485695..140487316,2	K562	blood:
46	chr6:139737465..139739803-chr6:140504147..140506921,2	K562	blood:
47	chr6:140469107..140471606-chr6:140489334..140493465,3	K562	blood:
48	chr6:140562032..140563790-chr6:140568097..140570245,2	K562	blood:
49	chr6:140520321..140522194-chr6:140526298..140528486,2	K562	blood:
50	chr6:140532063..140533672-chr6:140539512..140541736,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HECA-9	chr6:140515859-140520210	NONHSAT115283

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3668	chr6:140526397-140526417	MIMAT0018091

No data

Variant related genes	Relation type
RNA5SP220	TF binding region
MIR3668	TF binding region
RNA5SP220	CpG island
MIR3668	CpG island
ENSG00000263514	chromatin interactions
ENSG00000164442	chromatin interactions
ENSG00000122085	chromatin interactions
ENSG00000252107	chromatin interactions

Extended variants
information (count: 3286 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3286 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201285	chr6:140476088-140476089	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150942137	chr6:140476140-140476141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375436462	chr6:140476143-140476144	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552595663	chr6:140476145-140476146	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570230038	chr6:140476177-140476178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201498035	chr6:140476193-140476194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs9385901	chr6:140476201-140476202	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs140770376	chr6:140476344-140476345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574939880	chr6:140476499-140476500	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370521346	chr6:140476521-140476522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144704795	chr6:140476573-140476574	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554198505	chr6:140476704-140476705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138393974	chr6:140476711-140476712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577683430	chr6:140476740-140476741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543056729	chr6:140476741-140476742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564895038	chr6:140476784-140476785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs533508379	chr6:140476807-140476808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553360338	chr6:140476832-140476833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs368303222	chr6:140476910-140476911	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577092481	chr6:140476927-140476928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191897127	chr6:140476940-140476941	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145136327	chr6:140476942-140476943	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35194791	chr6:140476963-140476964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs73777462	chr6:140476998-140476999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs17069827	chr6:140477015-140477016	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184780663	chr6:140477067-140477068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189193905	chr6:140477276-140477277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149440951	chr6:140477291-140477292	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs570806044	chr6:140477326-140477327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs528796462	chr6:140477356-140477357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531972685	chr6:140477362-140477363	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547245831	chr6:140477378-140477379	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369069232	chr6:140477419-140477420	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535615728	chr6:140477438-140477439	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542508304	chr6:140477483-140477484	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557125869	chr6:140477538-140477539	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs182323219	chr6:140477539-140477540	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144668463	chr6:140477554-140477555	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs186064588	chr6:140477559-140477560	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576171785	chr6:140477594-140477595	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576739905	chr6:140477611-140477612	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373278699	chr6:140477670-140477671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs117282027	chr6:140477675-140477676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs189441942	chr6:140477686-140477687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs574774398	chr6:140477690-140477691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561005589	chr6:140477696-140477697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs542091389	chr6:140477735-140477736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs111752468	chr6:140477796-140477797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563448511	chr6:140477805-140477806	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148094187	chr6:140477810-140477811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Autism	21448237	CNVD
Autism	22495311	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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140471400-140479200	Weak transcription	Placenta	Placenta
2	chr6:140476400-140477400	Weak transcription	K562	blood
3	chr6:140477400-140477600	ZNF genes & repeats	K562	blood
4	chr6:140477600-140479800	Weak transcription	K562	blood
5	chr6:140479200-140479400	ZNF genes & repeats	Placenta	Placenta
6	chr6:140479400-140481600	Weak transcription	Placenta	Placenta
7	chr6:140479800-140480200	Strong transcription	K562	blood
8	chr6:140480200-140481200	Weak transcription	K562	blood
9	chr6:140481200-140481600	Strong transcription	K562	blood
10	chr6:140481600-140488600	Weak transcription	K562	blood
11	chr6:140488600-140489000	ZNF genes & repeats	K562	blood
12	chr6:140489000-140495800	Weak transcription	K562	blood
13	chr6:140491600-140492600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr6:140492200-140493400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:140492400-140493000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr6:140492600-140492800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:140492600-140495400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:140492800-140495000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:140493400-140495200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:140494800-140497000	Enhancers	NHDF-Ad	bronchial
21	chr6:140495000-140495600	Enhancers	Hela-S3	cervix
22	chr6:140495000-140495600	Enhancers	NHLF	lung
23	chr6:140495000-140495800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr6:140495000-140496200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr6:140495000-140496800	Enhancers	NHEK	skin
26	chr6:140495000-140496800	Enhancers	Osteobl	bone
27	chr6:140495000-140497000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:140495000-140497000	Enhancers	HMEC	breast
29	chr6:140495000-140497200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr6:140495000-140497400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:140495200-140495600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:140495200-140495800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:140495200-140496000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:140495200-140497000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr6:140495400-140496200	Enhancers	Placenta	Placenta
36	chr6:140495400-140497200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr6:140495600-140496600	Weak transcription	Hela-S3	cervix
38	chr6:140495600-140499200	Weak transcription	NHLF	lung
39	chr6:140495600-140499800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:140495800-140496200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:140495800-140498200	Strong transcription	K562	blood
42	chr6:140495800-140499400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr6:140496000-140499200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:140496200-140497000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:140496200-140501200	Weak transcription	Placenta	Placenta
46	chr6:140496600-140496800	Enhancers	Hela-S3	cervix
47	chr6:140496800-140499200	Weak transcription	Osteobl	bone
48	chr6:140497000-140498600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:140497000-140499000	Weak transcription	NHDF-Ad	bronchial
50	chr6:140497000-140500000	Weak transcription	HMEC	breast

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