Variant report

Variant	nsv912828
Chromosome Location	chr20:25433015-25595175
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2637)
CpG islands
(count:1343)
Chromatin interactive
region (count:108)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2637 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25589872-25589910	K562	blood:	n/a	n/a
2	ARID3A	chr20:25519655-25520011	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:25506350-25507074	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:25530308-25530796	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:25488240-25489133	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:25566452-25566585	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:25565236-25565725	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:25555145-25555336	HepG2	liver:	n/a	n/a
9	ARID3A	chr20:25565954-25566222	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:25583644-25583908	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:25559627-25559973	HepG2	liver:	n/a	n/a
12	ARID3A	chr20:25557897-25557902	HepG2	liver:	n/a	n/a
13	ATF1	chr20:25520966-25521214	K562	blood:	n/a	n/a
14	ATF1	chr20:25524173-25524617	K562	blood:	n/a	n/a
15	ATF1	chr20:25450740-25450940	K562	blood:	n/a	n/a
16	ATF1	chr20:25587145-25587281	K562	blood:	n/a	n/a
17	ATF2	chr20:25520859-25521226	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr20:25523783-25524037	K562	blood:	n/a	n/a
19	ATF3	chr20:25488628-25489026	A549	lung:	n/a	n/a
20	BACH1	chr20:25470160-25470452	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr20:25565874-25566218	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr20:25520911-25521321	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr20:25583645-25583879	GM12878	blood:	n/a	n/a
24	BATF	chr20:25499248-25499445	GM12878	blood:	n/a	n/a
25	BCL3	chr20:25590098-25590301	GM12878	blood:	n/a	n/a
26	BCL3	chr20:25565131-25566237	A549	lung:	n/a	chr20:25565815-25565824 chr20:25565704-25565717 chr20:25565700-25565713 chr20:25565668-25565681 chr20:25565884-25565893 chr20:25565855-25565868 chr20:25565861-25565869
27	BCL3	chr20:25590100-25590330	GM12878	blood:	n/a	n/a
28	BHLHE40	chr20:25506414-25507116	HepG2	liver:	n/a	n/a
29	BHLHE40	chr20:25450555-25450968	K562	blood:	n/a	n/a
30	BHLHE40	chr20:25565204-25565583	HepG2	liver:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
31	BHLHE40	chr20:25488151-25489495	HepG2	liver:	n/a	n/a
32	BHLHE40	chr20:25567805-25567835	HepG2	liver:	n/a	n/a
33	BHLHE40	chr20:25565120-25566722	HepG2	liver:	n/a	chr20:25565810-25565826 chr20:25565361-25565382 chr20:25566118-25566134 chr20:25565368-25565377 chr20:25565365-25565378
34	BHLHE40	chr20:25583502-25583877	HepG2	liver:	n/a	n/a
35	BHLHE40	chr20:25565181-25565563	A549	lung:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
36	BHLHE40	chr20:25521004-25521027	GM12878	blood:	n/a	n/a
37	BHLHE40	chr20:25559687-25559971	HepG2	liver:	n/a	n/a
38	BHLHE40	chr20:25525020-25525162	K562	blood:	n/a	chr20:25525092-25525101
39	BHLHE40	chr20:25472243-25472376	K562	blood:	n/a	n/a
40	BHLHE40	chr20:25521000-25521317	K562	blood:	n/a	n/a
41	BHLHE40	chr20:25583008-25583802	HepG2	liver:	n/a	n/a
42	BHLHE40	chr20:25519611-25520246	HepG2	liver:	n/a	n/a
43	BRCA1	chr20:25582265-25582269	HepG2	liver:	n/a	n/a
44	BRCA1	chr20:25565272-25565601	HepG2	liver:	n/a	n/a
45	BRCA1	chr20:25554727-25554782	HepG2	liver:	n/a	n/a
46	BRCA1	chr20:25546120-25546182	GM12878	blood:	n/a	n/a
47	BRCA1	chr20:25565815-25566240	HepG2	liver:	n/a	n/a
48	BRCA1	chr20:25481050-25481069	HepG2	liver:	n/a	n/a
49	BRCA1	chr20:25488727-25489094	HepG2	liver:	n/a	n/a
50	BRCA1	chr20:25581339-25581343	HepG2	liver:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25566563-25566613	HIPEpiC	eye:	n/a
2	chr20:25566563-25566613	HIPEpiC	eye:	n/a
3	chr20:25566470-25566520	AG09319	gingival:	n/a
4	chr20:25566470-25566520	HMEC	breast:	n/a
5	chr20:25570529-25570579	HAEpiC	amniotic membrane:	n/a
6	chr20:25566563-25566613	HepG2	liver:	n/a
7	chr20:25583082-25583132	HUVEC	blood vessel:	n/a
8	chr20:25433878-25433928	PrEC	prostate:	n/a
9	chr20:25433878-25433928	Hepatocyte	liver:	n/a
10	chr20:25583324-25583374	AG09319	gingival:	n/a
11	chr20:25583652-25583702	T-47D	breast:	n/a
12	chr20:25570529-25570579	K562	blood:	n/a
13	chr20:25584456-25584506	Caco-2	colon:	n/a
14	chr20:25565879-25565929	BJ	skin:	n/a
15	chr20:25433878-25433928	NH-A	brain:	n/a
16	chr20:25570529-25570579	Caco-2	colon:	n/a
17	chr20:25566336-25566386	Hepatocyte	liver:	n/a
18	chr20:25584456-25584506	CMK	blood:	n/a
19	chr20:25450839-25450889	ovcar-3	ovarian:	n/a
20	chr20:25581368-25581418	HCT-116	colon:	n/a
21	chr20:25566178-25566228	AG04449	skin:	fetal
22	chr20:25566382-25566432	NHBE	bronchial:	n/a
23	chr20:25566336-25566386	IMR90	lung:	fetal
24	chr20:25583082-25583132	SK-N-SH	brain:	n/a
25	chr20:25479848-25479898	HEEpiC	esophagus:	n/a
26	chr20:25566513-25566563	HCF	heart:	n/a
27	chr20:25565667-25565717	PANC-1	pancreas:	n/a
28	chr20:25433878-25433928	HCF	heart:	n/a
29	chr20:25583652-25583702	AG09309	skin:	n/a
30	chr20:25566563-25566613	HRCEpiC	kidney:	n/a
31	chr20:25566513-25566563	HEK293	kidney:	embryo
32	chr20:25566563-25566613	HEEpiC	esophagus:	n/a
33	chr20:25450839-25450889	SAEC	small airway:	n/a
34	chr20:25566513-25566563	AoSMC	blood vessel:	n/a
35	chr20:25583652-25583702	MCF-7	breast:	n/a
36	chr20:25565460-25565510	HAEpiC	amniotic membrane:	n/a
37	chr20:25581368-25581418	H1-hESC	embryonic stem cell:	embryo
38	chr20:25450839-25450889	GM12891	blood:	n/a
39	chr20:25566180-25566230	GM12892	blood:	n/a
40	chr20:25565879-25565929	NB4	blood:	n/a
41	chr20:25565460-25565510	HMEC	breast:	n/a
42	chr20:25448861-25448911	RPTEC	kidney:	n/a
43	chr20:25583082-25583132	HMEC	breast:	n/a
44	chr20:25448861-25448911	GM19239	blood:	n/a
45	chr20:25565879-25565929	IMR90	lung:	fetal
46	chr20:25448861-25448911	HMEC	breast:	n/a
47	chr20:25570529-25570579	Hepatocyte	liver:	n/a
48	chr20:25566382-25566432	HEK293	kidney:	embryo
49	chr20:25566382-25566432	Caco-2	colon:	n/a
50	chr20:25566180-25566230	GM12878	blood:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:
2	chr20:25445981..25448619-chr20:25473407..25476003,2	K562	blood:
3	chr20:25560873..25562976-chr20:25579297..25581436,2	MCF-7	breast:
4	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
5	chr20:25464881..25466399-chr20:25468189..25469773,2	MCF-7	breast:
6	chr20:25593129..25595979-chr20:25604532..25607057,2	MCF-7	breast:
7	chr20:25521309..25522938-chr20:25526944..25528978,2	MCF-7	breast:
8	chr20:25589103..25590623-chr3:128879792..128881796,2	K562	blood:
9	chr20:25535541..25538221-chr20:25603940..25606059,2	MCF-7	breast:
10	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:
11	chr20:25499922..25502486-chr20:25510143..25513350,3	MCF-7	breast:
12	chr20:25388243..25389775-chr20:25480689..25482219,2	MCF-7	breast:
13	chr20:25371156..25372734-chr20:25509417..25511739,2	MCF-7	breast:
14	chr20:25591410..25597359-chr20:25600309..25606040,12	K562	blood:
15	chr20:25551184..25554457-chr20:25563697..25566263,4	MCF-7	breast:
16	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
17	chr20:25581473..25584276-chr20:25603857..25605738,2	K562	blood:
18	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
19	chr20:25471295..25474295-chr20:25476336..25479406,5	MCF-7	breast:
20	chr20:25499922..25502486-chr20:25510143..25513350,3	MCF-7	breast:
21	chr20:25588843..25590699-chr20:25604414..25605941,2	MCF-7	breast:
22	chr20:25585705..25588241-chr20:25603917..25606437,2	K562	blood:
23	chr20:25560873..25562976-chr20:25579297..25581436,2	MCF-7	breast:
24	chr20:25464605..25465563-chr20:25554811..25555726,5	MCF-7	breast:
25	chr20:25491958..25494931-chr20:25496004..25498993,2	MCF-7	breast:
26	chr20:25477099..25478848-chr20:25676437..25678716,2	MCF-7	breast:
27	chr20:25552816..25556954-chr20:25564456..25567707,4	MCF-7	breast:
28	chr20:25578107..25581222-chr20:25601982..25605095,3	MCF-7	breast:
29	chr20:25527993..25531935-chr20:25532103..25536605,5	MCF-7	breast:
30	chr20:25316897..25317523-chr20:25554784..25555668,2	MCF-7	breast:
31	chr20:25445981..25448619-chr20:25473407..25476003,2	K562	blood:
32	chr20:25573368..25577137-chr20:25602924..25606486,3	MCF-7	breast:
33	chr20:25274847..25275686-chr20:25555235..25555796,2	K562	blood:
34	chr20:25426609..25429585-chr20:25546782..25548440,2	MCF-7	breast:
35	chr20:25521309..25522938-chr20:25526944..25528978,2	MCF-7	breast:
36	chr20:25498962..25501422-chr20:25501455..25503650,2	MCF-7	breast:
37	chr20:25565180..25567156-chr20:25676091..25678288,2	MCF-7	breast:
38	chr20:25431598..25433481-chr20:25439717..25442541,2	MCF-7	breast:
39	chr20:25480268..25483016-chr20:25564719..25567825,3	MCF-7	breast:
40	chr20:25519449..25520233-chr20:25534260..25534819,2	MCF-7	breast:
41	chr20:25228557..25231308-chr20:25476839..25479017,2	MCF-7	breast:
42	chr20:25518724..25523016-chr20:25601749..25604904,3	MCF-7	breast:
43	chr20:25560435..25563283-chr20:25564652..25566367,3	MCF-7	breast:
44	chr20:25471295..25474295-chr20:25476336..25479406,5	MCF-7	breast:
45	chr20:25559789..25563161-chr20:25564263..25567245,3	MCF-7	breast:
46	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
47	chr20:25512408..25515336-chr20:25515482..25519858,3	MCF-7	breast:
48	chr20:25527993..25531935-chr20:25532103..25536605,5	MCF-7	breast:
49	chr20:25477682..25478236-chr20:25488620..25489236,2	MCF-7	breast:
50	chr20:25476255..25479902-chr20:25487059..25491596,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GINS1-4	chr20:25513663-25514148	NONHSAT079162

No data

Variant related genes	Relation type
RNU6ATAC17P	TF binding region
NINL	TF binding region
RNU6ATAC17P	CpG island
NINL	CpG island
ENSG00000236542	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000240682	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000261796	chromatin interactions
ENSG00000130684	chromatin interactions
ENSG00000101004	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000251883	chromatin interactions

Extended variants
information (count: 6736 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:6736 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112828245	chr20:25433015-25433016	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532354286	chr20:25433031-25433032	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552161603	chr20:25433051-25433052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568951255	chr20:25433108-25433109	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562374087	chr20:25433149-25433150	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537946798	chr20:25433167-25433168	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554668524	chr20:25433175-25433176	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376692920	chr20:25433184-25433185	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187599151	chr20:25433249-25433250	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192221421	chr20:25433306-25433307	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553752907	chr20:25433309-25433310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111332246	chr20:25433321-25433322	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577078079	chr20:25433443-25433444	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs5841058	chr20:25433447-25433448	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76291754	chr20:25433460-25433461	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs397802755	chr20:25433461-25433462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545822849	chr20:25433490-25433491	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556194509	chr20:25433497-25433498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367820322	chr20:25433514-25433515	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576134283	chr20:25433525-25433526	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2856	chr20:25433536-25433537	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs144439828	chr20:25433560-25433561	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139242901	chr20:25433561-25433562	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551291575	chr20:25433589-25433590	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560582611	chr20:25433590-25433591	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532830876	chr20:25433636-25433637	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184329227	chr20:25433647-25433648	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568886572	chr20:25433668-25433669	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531627509	chr20:25433672-25433673	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12428	chr20:25433821-25433822	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs568560169	chr20:25433822-25433823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533709511	chr20:25433850-25433851	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553925104	chr20:25433881-25433882	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187172673	chr20:25433911-25433912	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370852755	chr20:25433936-25433937	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539700473	chr20:25433937-25433938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556532563	chr20:25433959-25433960	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192731879	chr20:25433986-25433987	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs7360349	chr20:25434000-25434001	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs16987764	chr20:25434014-25434015	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs16987767	chr20:25434059-25434060	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs371309830	chr20:25434060-25434061	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142680711	chr20:25434093-25434094	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141181350	chr20:25434104-25434105	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572115385	chr20:25434123-25434124	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369509557	chr20:25434138-25434139	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs17857107	chr20:25434139-25434140	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs146439964	chr20:25434148-25434149	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532624786	chr20:25434161-25434162	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34802534	chr20:25434163-25434164	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4312 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25389000-25433600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr20:25390000-25434800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr20:25390600-25433400	Weak transcription	Brain Germinal Matrix	brain
4	chr20:25399800-25433600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr20:25399800-25434800	Weak transcription	NHLF	lung
6	chr20:25402800-25445200	Weak transcription	NHDF-Ad	bronchial
7	chr20:25412200-25433600	Weak transcription	Spleen	Spleen
8	chr20:25412600-25440200	Weak transcription	Placenta	Placenta
9	chr20:25414200-25436000	Weak transcription	Primary T cells from cord blood	blood
10	chr20:25415400-25433600	Weak transcription	Pancreas	Pancrea
11	chr20:25418200-25434800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr20:25418200-25436600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr20:25418200-25445200	Weak transcription	HSMM	muscle
14	chr20:25418400-25433600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr20:25418800-25439400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr20:25423400-25433200	Strong transcription	A549	lung
17	chr20:25424000-25435600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr20:25425600-25434800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr20:25425600-25453200	Weak transcription	Small Intestine	intestine
20	chr20:25426400-25450200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:25427200-25435400	Weak transcription	NH-A	brain
22	chr20:25427200-25488200	Weak transcription	Stomach Mucosa	stomach
23	chr20:25427400-25433600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr20:25427400-25433600	Weak transcription	HUVEC	blood vessel
25	chr20:25427400-25435400	Weak transcription	Fetal Kidney	kidney
26	chr20:25427400-25442400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr20:25427600-25442200	Weak transcription	GM12878-XiMat	blood
28	chr20:25427600-25446200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr20:25428000-25434800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr20:25428000-25434800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr20:25428400-25434000	Weak transcription	Osteobl	bone
32	chr20:25428400-25434800	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr20:25428600-25438600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr20:25428800-25433600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr20:25429400-25433800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr20:25429400-25463200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr20:25429600-25441000	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr20:25429800-25435200	Weak transcription	Primary hematopoietic stem cells	blood
39	chr20:25429800-25458800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr20:25430200-25436400	Strong transcription	Fetal Brain Female	brain
41	chr20:25430200-25484400	Strong transcription	Fetal Stomach	stomach
42	chr20:25430400-25433600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr20:25430400-25434200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr20:25430400-25434800	Weak transcription	HSMMtube	muscle
45	chr20:25430400-25442000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr20:25430800-25435000	Weak transcription	Brain Anterior Caudate	brain
47	chr20:25431200-25433600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr20:25431200-25436400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr20:25431200-25447400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr20:25431400-25436400	Strong transcription	Placenta Amnion	Placenta Amnion

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