Variant report

Variant	esv3475033
Chromosome Location	chr6:31210396-31321602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1415)
CpG islands
(count:4829)
Chromatin interactive
region (count:46)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31213940-31214200	HepG2	liver:	n/a	n/a
2	ATF1	chr6:31272445-31272772	K562	blood:	n/a	n/a
3	ATF1	chr6:31239808-31240131	K562	blood:	n/a	n/a
4	ATF2	chr6:31234577-31234827	GM12878	blood:	n/a	n/a
5	ATF2	chr6:31300411-31301086	GM12878	blood:	n/a	n/a
6	ATF2	chr6:31239651-31240115	GM12878	blood:	n/a	n/a
7	ATF2	chr6:31300449-31301004	GM12878	blood:	n/a	n/a
8	ATF2	chr6:31272379-31272838	GM12878	blood:	n/a	n/a
9	ATF2	chr6:31318444-31319386	GM12878	blood:	n/a	n/a
10	ATF2	chr6:31319512-31321668	GM12878	blood:	n/a	n/a
11	ATF2	chr6:31235265-31236206	GM12878	blood:	n/a	n/a
12	ATF2	chr6:31235142-31236449	GM12878	blood:	n/a	n/a
13	ATF2	chr6:31319422-31321748	GM12878	blood:	n/a	n/a
14	ATF2	chr6:31272219-31272895	GM12878	blood:	n/a	n/a
15	ATF2	chr6:31318632-31319385	GM12878	blood:	n/a	n/a
16	BACH1	chr6:31239252-31239443	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:31276089-31276266	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:31239693-31240306	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr6:31241012-31241391	GM12878	blood:	n/a	n/a
20	BATF	chr6:31300476-31300903	GM12878	blood:	n/a	n/a
21	BATF	chr6:31300427-31300985	GM12878	blood:	n/a	n/a
22	BATF	chr6:31241031-31241428	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:31234485-31235770	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:31300656-31300925	GM12878	blood:	n/a	n/a
25	BCL11A	chr6:31318775-31319206	GM12878	blood:	n/a	n/a
26	BCL11A	chr6:31241052-31241373	GM12878	blood:	n/a	n/a
27	BCL11A	chr6:31320393-31320678	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:31241100-31241317	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:31319413-31321023	GM12878	blood:	n/a	n/a
30	BCL3	chr6:31319812-31321116	GM12878	blood:	n/a	n/a
31	BCL3	chr6:31319415-31320898	GM12878	blood:	n/a	n/a
32	BCL3	chr6:31235297-31235807	GM12878	blood:	n/a	n/a
33	BCL3	chr6:31235264-31235791	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:31318925-31319357	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:31319416-31321907	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
36	BCLAF1	chr6:31319409-31321119	GM12878	blood:	n/a	n/a
37	BCLAF1	chr6:31300404-31300834	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:31321125-31321669	GM12878	blood:	n/a	chr6:31321139-31321152 chr6:31321455-31321463
39	BCLAF1	chr6:31239585-31240141	GM12878	blood:	n/a	chr6:31240011-31240020
40	BCLAF1	chr6:31235268-31236420	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:31235169-31236336	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:31318701-31319362	GM12878	blood:	n/a	n/a
43	BCLAF1	chr6:31234491-31234960	GM12878	blood:	n/a	n/a
44	BCLAF1	chr6:31239341-31240264	GM12878	blood:	n/a	chr6:31240011-31240020
45	BHLHE40	chr6:31239743-31240181	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:31320567-31320928	GM12878	blood:	n/a	n/a
47	BHLHE40	chr6:31238745-31238982	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:31239841-31240041	K562	blood:	n/a	n/a
49	BHLHE40	chr6:31318412-31318711	GM12878	blood:	n/a	n/a
50	BHLHE40	chr6:31319623-31320237	GM12878	blood:	n/a	n/a

(count:4829 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31239243-31239293	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:31275666-31275716	HIPEpiC	eye:	n/a
3	chr6:31276667-31276717	Caco-2	colon:	n/a
4	chr6:31275718-31275768	PFSK-1	brain:	n/a
5	chr6:31237034-31237084	HCF	heart:	n/a
6	chr6:31276187-31276237	GM12892	blood:	n/a
7	chr6:31241000-31241050	HIPEpiC	eye:	n/a
8	chr6:31275551-31275601	HL-60	blood:	n/a
9	chr6:31238267-31238317	SAEC	small airway:	n/a
10	chr6:31239074-31239124	HRCEpiC	kidney:	n/a
11	chr6:31239243-31239293	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:31275666-31275716	HIPEpiC	eye:	n/a
13	chr6:31276667-31276717	Caco-2	colon:	n/a
14	chr6:31275718-31275768	PFSK-1	brain:	n/a
15	chr6:31237034-31237084	HCF	heart:	n/a
16	chr6:31276187-31276237	GM12892	blood:	n/a
17	chr6:31241000-31241050	HIPEpiC	eye:	n/a
18	chr6:31275551-31275601	HL-60	blood:	n/a
19	chr6:31238267-31238317	SAEC	small airway:	n/a
20	chr6:31239074-31239124	HRCEpiC	kidney:	n/a
21	chr6:31239259-31239309	AG09309	skin:	n/a
22	chr6:31276653-31276703	PrEC	prostate:	n/a
23	chr6:31276105-31276155	K562	blood:	n/a
24	chr6:31275807-31275857	ProgFib	skin:	n/a
25	chr6:31239910-31239960	GM12891	blood:	n/a
26	chr6:31239133-31239183	HCM	heart:	n/a
27	chr6:31251137-31251187	HepG2	liver:	n/a
28	chr6:31238803-31238853	NH-A	brain:	n/a
29	chr6:31275741-31275791	LNCaP	prostate:	n/a
30	chr6:31276434-31276484	NT2-D1	testis:	n/a
31	chr6:31239243-31239293	HRE	kidney:	n/a
32	chr6:31321433-31321483	GM12878	blood:	n/a
33	chr6:31275767-31275817	GM19239	blood:	n/a
34	chr6:31275807-31275857	GM12891	blood:	n/a
35	chr6:31275267-31275317	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:31237405-31237455	K562	blood:	n/a
37	chr6:31239767-31239817	GM12891	blood:	n/a
38	chr6:31275881-31275931	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:31240050-31240100	ProgFib	skin:	n/a
40	chr6:31239324-31239374	H1-hESC	embryonic stem cell:	embryo
41	chr6:31240050-31240100	Hela-S3	cervix:	n/a
42	chr6:31276667-31276717	HRPEpiC	eye:	n/a
43	chr6:31237034-31237084	HPAEpiC	pulmonary alveolar:	n/a
44	chr6:31275791-31275841	SAEC	small airway:	n/a
45	chr6:31239411-31239461	GM19239	blood:	n/a
46	chr6:31239074-31239124	AG09319	gingival:	n/a
47	chr6:31275791-31275841	HAEpiC	amniotic membrane:	n/a
48	chr6:31240045-31240095	LNCaP	prostate:	n/a
49	chr6:31239295-31239345	Caco-2	colon:	n/a
50	chr6:31276664-31276714	PrEC	prostate:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:
2	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
3	chr6:31262379..31263887-chr6:31264452..31266692,2	MCF-7	breast:
4	chr6:31272998..31275186-chr6:31333057..31335314,2	K562	blood:
5	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
6	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
7	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
8	chr6:29855138..29856405-chr6:31238835..31239948,4	HCT-116	colon:
9	chr6:31260315..31262066-chr6:31270612..31272546,2	MCF-7	breast:
10	chr6:31260319..31263250-chr6:31266330..31267976,2	K562	blood:
11	chr6:31235298..31236799-chr6:31321704..31323597,2	K562	blood:
12	chr6:31209841..31212396-chr6:31219604..31221505,2	K562	blood:
13	chr6:31234807..31237311-chr6:31237898..31240961,3	K562	blood:
14	chr6:31208671..31211485-chr6:31212417..31214896,3	MCF-7	breast:
15	chr6:31251033..31253649-chr6:31335443..31337577,2	MCF-7	breast:
16	chr6:31312332..31314314-chr6:31315849..31318317,2	K562	blood:
17	chr6:31273049..31275255-chr6:31283813..31285352,2	MCF-7	breast:
18	chr6:31208671..31211485-chr6:31212417..31214896,3	MCF-7	breast:
19	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
20	chr6:31274576..31277552-chr6:31281409..31285159,3	MCF-7	breast:
21	chr6:31164078..31167331-chr6:31260118..31263696,3	K562	blood:
22	chr6:31283440..31285991-chr6:31367270..31369843,2	K562	blood:
23	chr6:31272067..31274682-chr6:31275532..31277366,2	MCF-7	breast:
24	chr6:31238404..31240559-chr6:31321762..31324439,3	MCF-7	breast:
25	chr6:31296846..31298783-chr6:31302678..31304651,2	K562	blood:
26	chr6:31256122..31258941-chr6:31260246..31262615,2	MCF-7	breast:
27	chr6:31279746..31282778-chr6:31284004..31286802,3	K562	blood:
28	chr6:31164078..31166363-chr6:31260745..31263696,2	K562	blood:
29	chr6:31260315..31262066-chr6:31270612..31272546,2	MCF-7	breast:
30	chr6:29910138..29911769-chr6:31239456..31240978,2	MCF-7	breast:
31	chr6:31129596..31132185-chr6:31285768..31288675,2	MCF-7	breast:
32	chr6:31176797..31178729-chr6:31234671..31236847,2	K562	blood:
33	chr6:31209841..31212396-chr6:31219604..31221505,2	K562	blood:
34	chr6:31260319..31263250-chr6:31266330..31267976,2	K562	blood:
35	chr6:31233619..31236964-chr6:31319655..31321766,4	MCF-7	breast:
36	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
37	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
38	chr6:31232397..31234509-chr6:31319658..31321454,2	MCF-7	breast:
39	chr6:31187490..31190169-chr6:31217260..31219687,2	K562	blood:
40	chr6:31282655..31287685-chr6:31288202..31290762,5	K562	blood:
41	chr6:31274551..31276643-chr6:31277971..31279738,2	MCF-7	breast:
42	chr6:31238976..31240351-chr6:31324393..31325523,6	HCT-116	colon:
43	chr6:31251382..31252914-chr6:31343854..31345706,2	MCF-7	breast:
44	chr6:31260192..31262611-chr6:31284045..31286889,2	K562	blood:
45	chr6:31274011..31276374-chr6:31277383..31280033,2	K562	blood:
46	chr6:31262379..31263887-chr6:31264452..31266692,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-C-2	chr6:31237115-31237443	NONHSAT108746
2	lnc-HLA-C-2	chr6:31236526-31236950	NONHSAT108746
3	lnc-HLA-C-3	chr6:31253395-31253655	NONHSAT108749
4	lnc-HLA-C-1	chr6:31269249-31269419	ENSG00000256166
5	lnc-HLA-C-3	chr6:31249994-31250026	NONHSAT108749
6	lnc-HLA-C-1	chr6:31261992-31262072	ENSG00000256166
7	lnc-HLA-C-1	chr6:31261685-31261898	ENSG00000256166
8	lnc-HLA-C-1	chr6:31262721-31262790	ENSG00000256166
9	lnc-HLA-C-3	chr6:31249491-31249789	NONHSAT108749
10	lnc-HLA-C-4	chr6:31275592-31275824	NONHSAT108751
11	lnc-HLA-C-4	chr6:31276254-31276326	NONHSAT108751
12	lnc-HLA-C-2	chr6:31236531-31236950	NONHSAT108747

No data

Variant related genes	Relation type
USP8P1	TF binding region
ENSG00000271581	TF binding region
ENSG00000229836	TF binding region
WASF5P	TF binding region
RPL3P2	TF binding region
ENSG00000256166	TF binding region
HLA-C	TF binding region
USP8P1	CpG island
ENSG00000271581	CpG island
ENSG00000229836	CpG island
WASF5P	CpG island
RPL3P2	CpG island
ENSG00000256166	CpG island
HLA-C	CpG island
ENSG00000228432	chromatin interactions
ENSG00000206503	chromatin interactions
ENSG00000229836	chromatin interactions
ENSG00000271581	chromatin interactions
ENSG00000230521	chromatin interactions
ENSG00000227766	chromatin interactions
ENSG00000272501	chromatin interactions
ENSG00000206344	chromatin interactions
ENSG00000231402	chromatin interactions
ENSG00000206341	chromatin interactions
ENSG00000234745	chromatin interactions
ENSG00000206337	chromatin interactions
ENSG00000230994	chromatin interactions
ENSG00000204525	chromatin interactions

Extended variants
information (count: 4903 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:4903 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558566226	chr6:31210400-31210401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112196537	chr6:31210410-31210411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72502551	chr6:31210429-31210430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs386698910	chr6:31210462-31210463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115686299	chr6:31210463-31210464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116967475	chr6:31210470-31210471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113217647	chr6:31210488-31210489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182723937	chr6:31210490-31210491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28480108	chr6:31210532-31210533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs3134765	chr6:31210577-31210578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs79860141	chr6:31210599-31210600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs3130689	chr6:31210601-31210602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564831299	chr6:31210618-31210619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114210995	chr6:31210638-31210639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs187101606	chr6:31210647-31210648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191532305	chr6:31210664-31210665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs117976067	chr6:31210675-31210676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183768670	chr6:31210682-31210683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs3132494	chr6:31210691-31210692	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs117876434	chr6:31210703-31210704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112331580	chr6:31210709-31210710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs3134764	chr6:31210731-31210732	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs150454938	chr6:31210735-31210736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534711511	chr6:31210769-31210770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs3134763	chr6:31210774-31210775	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs539528653	chr6:31210779-31210780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3130537	chr6:31210796-31210797	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs536045559	chr6:31210838-31210839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs3134762	chr6:31210866-31210867	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs77582287	chr6:31210876-31210877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116849356	chr6:31210927-31210928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113196314	chr6:31210946-31210947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138587208	chr6:31210948-31210949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541053422	chr6:31210950-31210951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28361026	chr6:31210967-31210968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575873274	chr6:31210969-31210970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368743388	chr6:31210971-31210972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144055209	chr6:31211029-31211030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117922333	chr6:31211045-31211046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3130695	chr6:31211050-31211051	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs76977405	chr6:31211064-31211065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188050700	chr6:31211088-31211089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546688614	chr6:31211094-31211095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560472780	chr6:31211101-31211102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs80227257	chr6:31211106-31211107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193257224	chr6:31211111-31211112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369856310	chr6:31211119-31211120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs79433188	chr6:31211200-31211201	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs114475699	chr6:31211201-31211202	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs191407008	chr6:31211223-31211224	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Lung cancer	18438408	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
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	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
Renal cell carcinoma	18765545	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
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1299 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31202600-31213600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr6:31210600-31211400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
3	chr6:31210800-31211400	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr6:31210800-31211600	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr6:31210800-31211600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:31211000-31211600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:31211000-31211600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:31211000-31211600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:31211000-31211600	Enhancers	NHEK	skin
10	chr6:31211200-31211400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:31211200-31211400	Enhancers	Hela-S3	cervix
12	chr6:31211200-31211400	Enhancers	HMEC	breast
13	chr6:31211200-31211400	Bivalent Enhancer	NHDF-Ad	bronchial
14	chr6:31211200-31211600	Enhancers	Primary hematopoietic stem cells	blood
15	chr6:31211200-31211600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:31211200-31211600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:31211400-31213200	Weak transcription	HMEC	breast
18	chr6:31211400-31213600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr6:31211600-31212400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr6:31211600-31213000	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr6:31211600-31213000	Weak transcription	NHEK	skin
22	chr6:31211600-31213200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:31211600-31213200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr6:31211600-31213200	Weak transcription	Hela-S3	cervix
25	chr6:31211600-31213400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:31211600-31213400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:31211600-31213600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:31211600-31213600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr6:31212000-31213400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:31213000-31214400	Enhancers	NHEK	skin
31	chr6:31213200-31213400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr6:31213200-31213400	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr6:31213200-31213400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr6:31213200-31213800	Enhancers	Hela-S3	cervix
35	chr6:31213200-31214000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:31213200-31214600	Enhancers	HMEC	breast
37	chr6:31213400-31213600	Enhancers	Primary hematopoietic stem cells	blood
38	chr6:31213400-31213600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr6:31213400-31214400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:31213400-31214400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr6:31213400-31214400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:31213400-31214400	Enhancers	NHDF-Ad	bronchial
43	chr6:31213600-31214000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:31213600-31214000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr6:31213600-31214000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:31213600-31214000	Enhancers	Pancreas	Pancrea
47	chr6:31213600-31214200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr6:31213600-31214400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr6:31213600-31214400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:31213600-31214400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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