Variant report

Variant	esv3330851
Chromosome Location	chr19:19755507-19852881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2365)
CpG islands
(count:3234)
Chromatin interactive
region (count:104)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2365 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:19779132-19779853	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:19774939-19775152	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:19774570-19775126	K562	blood:	n/a	n/a
4	ARID3A	chr19:19779417-19779631	K562	blood:	n/a	n/a
5	ARID3A	chr19:19843833-19844345	HepG2	liver:	n/a	n/a
6	ARID3A	chr19:19774393-19774684	HepG2	liver:	n/a	n/a
7	ATF2	chr19:19779453-19779906	GM12878	blood:	n/a	n/a
8	ATF2	chr19:19774403-19774888	GM12878	blood:	n/a	n/a
9	ATF2	chr19:19772464-19772970	GM12878	blood:	n/a	chr19:19772686-19772697
10	ATF2	chr19:19773648-19774134	GM12878	blood:	n/a	n/a
11	ATF2	chr19:19774452-19774850	GM12878	blood:	n/a	n/a
12	ATF2	chr19:19780710-19781019	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr19:19774461-19774897	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr19:19778911-19779446	GM12878	blood:	n/a	n/a
15	ATF2	chr19:19772281-19773158	GM12878	blood:	n/a	chr19:19772686-19772697
16	ATF3	chr19:19852066-19852400	K562	blood:	n/a	chr19:19852091-19852105
17	BACH1	chr19:19773895-19773967	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCLAF1	chr19:19778811-19780035	GM12878	blood:	n/a	chr19:19779998-19780011 chr19:19779557-19779565 chr19:19779994-19780007 chr19:19779626-19779635
19	BCLAF1	chr19:19779447-19779937	GM12878	blood:	n/a	chr19:19779557-19779565 chr19:19779626-19779635
20	BCLAF1	chr19:19772371-19773166	GM12878	blood:	n/a	n/a
21	BCLAF1	chr19:19773791-19774868	GM12878	blood:	n/a	chr19:19774531-19774540 chr19:19774494-19774503 chr19:19774707-19774716
22	BCLAF1	chr19:19774092-19774891	GM12878	blood:	n/a	chr19:19774531-19774540 chr19:19774494-19774503 chr19:19774707-19774716
23	BHLHE40	chr19:19849881-19850182	K562	blood:	n/a	n/a
24	BHLHE40	chr19:19772514-19773180	GM12878	blood:	n/a	n/a
25	BHLHE40	chr19:19773790-19775110	K562	blood:	n/a	n/a
26	BHLHE40	chr19:19779281-19779835	K562	blood:	n/a	n/a
27	BHLHE40	chr19:19778942-19779864	GM12878	blood:	n/a	n/a
28	BHLHE40	chr19:19779048-19779848	HepG2	liver:	n/a	n/a
29	BHLHE40	chr19:19844032-19844325	HepG2	liver:	n/a	n/a
30	BHLHE40	chr19:19773994-19774808	GM12878	blood:	n/a	n/a
31	BHLHE40	chr19:19773604-19773616	GM12878	blood:	n/a	n/a
32	BRCA1	chr19:19779159-19779710	HepG2	liver:	n/a	n/a
33	BRCA1	chr19:19843820-19844003	HepG2	liver:	n/a	n/a
34	BRCA1	chr19:19779363-19779848	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr19:19774554-19774808	HepG2	liver:	n/a	chr19:19774587-19774594
36	BRCA1	chr19:19772509-19772806	GM12878	blood:	n/a	n/a
37	BRCA1	chr19:19780074-19780129	GM12878	blood:	n/a	n/a
38	BRCA1	chr19:19843919-19843953	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr19:19774243-19774859	Hela-S3	cervix:	n/a	chr19:19774587-19774594
40	BRCA1	chr19:19844290-19844296	GM12878	blood:	n/a	n/a
41	BRCA1	chr19:19773268-19773418	GM12878	blood:	n/a	n/a
42	CBX3	chr19:19774390-19775224	K562	blood:	n/a	n/a
43	CBX3	chr19:19822096-19823012	K562	blood:	n/a	n/a
44	CBX3	chr19:19823445-19823679	K562	blood:	n/a	n/a
45	CBX3	chr19:19822080-19822914	K562	blood:	n/a	n/a
46	CBX3	chr19:19779599-19779849	K562	blood:	n/a	n/a
47	CBX3	chr19:19843634-19844502	K562	blood:	n/a	n/a
48	CBX3	chr19:19830634-19830946	K562	blood:	n/a	n/a
49	CBX3	chr19:19823175-19823828	K562	blood:	n/a	n/a
50	CBX3	chr19:19843830-19844294	K562	blood:	n/a	n/a

(count:3234 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19764685-19764735	HPAEpiC	pulmonary alveolar:	n/a
2	chr19:19764685-19764735	HPAEpiC	pulmonary alveolar:	n/a
3	chr19:19843912-19843962	BJ	skin:	n/a
4	chr19:19773992-19774042	HepG2	liver:	n/a
5	chr19:19774554-19774604	GM12891	blood:	n/a
6	chr19:19844278-19844328	AG09319	gingival:	n/a
7	chr19:19774667-19774717	GM12891	blood:	n/a
8	chr19:19764685-19764735	CMK	blood:	n/a
9	chr19:19822024-19822074	BE2_C	brain:	n/a
10	chr19:19843560-19843610	HPAEpiC	pulmonary alveolar:	n/a
11	chr19:19841125-19841175	NHBE	bronchial:	n/a
12	chr19:19772686-19772736	Caco-2	colon:	n/a
13	chr19:19774104-19774154	HCT-116	colon:	n/a
14	chr19:19843912-19843962	GM06990	blood:	n/a
15	chr19:19774664-19774714	MCF10A-Er-Src	breast:	n/a
16	chr19:19774945-19774995	HCPEpiC	choroid plexus:	n/a
17	chr19:19767731-19767781	T-47D	breast:	n/a
18	chr19:19774512-19774562	GM19239	blood:	n/a
19	chr19:19844224-19844274	HIPEpiC	eye:	n/a
20	chr19:19780767-19780817	AG09309	skin:	n/a
21	chr19:19779231-19779281	HCM	heart:	n/a
22	chr19:19770860-19770910	MCF-7	breast:	n/a
23	chr19:19844057-19844107	HL-60	blood:	n/a
24	chr19:19844224-19844274	IMR90	lung:	fetal
25	chr19:19774878-19774928	NHBE	bronchial:	n/a
26	chr19:19773992-19774042	AG10803	skin:	n/a
27	chr19:19779231-19779281	GM12878	blood:	n/a
28	chr19:19764795-19764845	T-47D	breast:	n/a
29	chr19:19774664-19774714	NHBE	bronchial:	n/a
30	chr19:19843934-19843984	GM12891	blood:	n/a
31	chr19:19774878-19774928	HCPEpiC	choroid plexus:	n/a
32	chr19:19770860-19770910	Jurkat	blood:	n/a
33	chr19:19778986-19779036	GM12878	blood:	n/a
34	chr19:19774664-19774714	GM12892	blood:	n/a
35	chr19:19843456-19843506	GM12878	blood:	n/a
36	chr19:19843991-19844041	HCF	heart:	n/a
37	chr19:19763973-19764023	HIPEpiC	eye:	n/a
38	chr19:19763973-19764023	AG04450	lung:	fetal
39	chr19:19779880-19779930	ProgFib	skin:	n/a
40	chr19:19844278-19844328	HCM	heart:	n/a
41	chr19:19774554-19774604	NH-A	brain:	n/a
42	chr19:19774523-19774573	K562	blood:	n/a
43	chr19:19843707-19843757	Hela-S3	cervix:	n/a
44	chr19:19783341-19783391	GM12891	blood:	n/a
45	chr19:19770860-19770910	HNPCEpiC	eye:	n/a
46	chr19:19779476-19779526	HCPEpiC	choroid plexus:	n/a
47	chr19:19844076-19844126	Hela-S3	cervix:	n/a
48	chr19:19763973-19764023	AG10803	skin:	n/a
49	chr19:19774664-19774714	AG04449	skin:	fetal
50	chr19:19760711-19760761	GM06990	blood:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr19:19757212..19759308-chr19:19762231..19764306,2	K562	blood:
2	chr19:19625550..19627956-chr19:19752305..19756076,5	MCF-7	breast:
3	chr19:19647870..19650487-chr19:19773815..19776020,2	MCF-7	breast:
4	chr19:19837998..19841957-chr19:19842344..19844108,3	MCF-7	breast:
5	chr19:19758273..19759976-chr19:19769882..19772025,2	K562	blood:
6	chr19:19763223..19765065-chr19:19765114..19767818,2	MCF-7	breast:
7	chr19:19763223..19765065-chr19:19765114..19767818,2	MCF-7	breast:
8	chr19:19843963..19845573-chr19:19852096..19854779,2	MCF-7	breast:
9	chr19:19757747..19759331-chr19:19762568..19765721,3	K562	blood:
10	chr19:19773987..19774730-chr6:26199521..26200292,2	Hela-S3	cervix:
11	chr19:19814568..19817544-chr19:19975321..19978730,3	MCF-7	breast:
12	chr19:19496290..19497914-chr19:19774313..19776411,2	MCF-7	breast:
13	chr19:19751259..19758144-chr19:19770384..19776332,14	K562	blood:
14	chr19:19751259..19757786-chr19:19771999..19776232,8	K562	blood:
15	chr19:19758424..19760184-chr19:19766453..19768345,2	MCF-7	breast:
16	chr19:19651192..19652936-chr19:19774066..19776214,2	MCF-7	breast:
17	chr19:19755727..19757407-chr19:19763663..19765667,2	MCF-7	breast:
18	chr19:19784664..19786349-chr19:19788589..19791062,2	K562	blood:
19	chr19:19623259..19625867-chr19:19772617..19774685,2	MCF-7	breast:
20	chr19:19772412..19775307-chr19:19800186..19802110,2	K562	blood:
21	chr19:19727841..19730107-chr19:19763060..19764845,2	MCF-7	breast:
22	chr19:19779981..19782160-chr19:19842451..19845691,3	MCF-7	breast:
23	chr19:19754977..19756747-chr19:19789710..19792104,2	K562	blood:
24	chr19:19728090..19730297-chr19:19774010..19775598,2	K562	blood:
25	chr19:19780471..19782017-chr19:19786498..19789488,2	K562	blood:
26	chr19:19753162..19754752-chr19:19769276..19770855,2	MCF-7	breast:
27	chr19:19758607..19760316-chr19:19772581..19775332,2	K562	blood:
28	chr19:19763068..19765978-chr19:19768250..19769834,2	MCF-7	breast:
29	chr19:19757747..19759331-chr19:19762568..19765721,3	K562	blood:
30	chr19:19639119..19641341-chr19:19760899..19763693,2	K562	blood:
31	chr19:19751259..19758144-chr19:19770384..19776332,14	K562	blood:
32	chr19:19767560..19771032-chr19:19771876..19774701,8	MCF-7	breast:
33	chr19:19755704..19761642-chr19:19771468..19774473,6	MCF-7	breast:
34	chr19:19842192..19843794-chr19:19857515..19860071,2	K562	blood:
35	chr19:19755704..19761642-chr19:19771468..19774473,6	MCF-7	breast:
36	chr19:19825299..19827793-chr19:19827916..19829892,2	K562	blood:
37	chr19:19784981..19786975-chr19:19793453..19795583,2	K562	blood:
38	chr19:19729417..19731495-chr19:19772370..19774542,2	MCF-7	breast:
39	chr19:19758424..19760184-chr19:19766453..19768345,2	MCF-7	breast:
40	chr19:19779580..19781549-chr19:19783005..19784899,2	K562	blood:
41	chr19:19779650..19782100-chr19:19976513..19978467,2	MCF-7	breast:
42	chr19:19649331..19652417-chr19:19771491..19776120,6	K562	blood:
43	chr19:19787138..19789132-chr19:19790779..19792628,2	K562	blood:
44	chr19:19649879..19653588-chr19:19753029..19755939,4	K562	blood:
45	chr19:19754487..19757148-chr19:19764604..19766993,2	K562	blood:
46	chr19:19843963..19845573-chr19:19852096..19854779,2	MCF-7	breast:
47	chr19:19773005..19774535-chr19:19843985..19845654,2	K562	blood:
48	chr19:19772164..19776257-chr19:19777737..19781997,10	MCF-7	breast:
49	chr19:19828998..19830532-chr19:20011609..20013262,2	MCF-7	breast:
50	chr19:19772600..19774395-chr19:19886060..19888388,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF101-4	chr19:19821997-19822576	NONHSAT063083
2	lnc-ZNF101-3	chr19:19792103-19792278	NONHSAT063080
3	lnc-ZNF101-3	chr19:19793892-19794318	NONHSAT063080
4	lnc-ZNF101-4	chr19:19822661-19822691	NONHSAT063083

No data

Variant related genes	Relation type
ENSG00000270402	TF binding region
GMIP	TF binding region
ATP13A1	TF binding region
ZNF14	TF binding region
ENSG00000271283	TF binding region
ZNF101	TF binding region
ENSG00000270402	CpG island
GMIP	CpG island
ATP13A1	CpG island
ZNF14	CpG island
ENSG00000271283	CpG island
ZNF101	CpG island
ENSG00000258674	chromatin interactions
ENSG00000089639	chromatin interactions
ENSG00000181896	chromatin interactions
ENSG00000065548	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000167491	chromatin interactions
ENSG00000267268	chromatin interactions
ENSG00000105717	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000186010	chromatin interactions
ENSG00000064547	chromatin interactions
ENSG00000184635	chromatin interactions
ENSG00000271283	chromatin interactions
ENSG00000256771	chromatin interactions
ENSG00000105708	chromatin interactions
ENSG00000160161	chromatin interactions
ENSG00000178093	chromatin interactions
ENSG00000270402	chromatin interactions
ENSG00000105726	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000250067	chromatin interactions
ENSG00000267419	chromatin interactions
ENSG00000266904	chromatin interactions

Extended variants
information (count: 3962 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3962 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563308359	chr19:19755509-19755510	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs532099869	chr19:19755510-19755511	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs552554777	chr19:19755514-19755515	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs565972376	chr19:19755540-19755541	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs576852072	chr19:19755543-19755544	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs374323712	chr19:19755558-19755559	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs548385543	chr19:19755574-19755575	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs572263873	chr19:19755575-19755576	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs536757856	chr19:19755589-19755590	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs556335871	chr19:19755600-19755601	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs569761025	chr19:19755603-19755604	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs190518185	chr19:19755633-19755634	Weak transcription Strong transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs148886798	chr19:19755642-19755643	Weak transcription Strong transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs572384694	chr19:19755661-19755662	Weak transcription Strong transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs534959553	chr19:19755694-19755695	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs555160622	chr19:19755702-19755703	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs183045543	chr19:19755714-19755715	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs574894551	chr19:19755729-19755730	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs543510333	chr19:19755758-19755759	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs577428127	chr19:19755792-19755793	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs563236912	chr19:19755837-19755838	Weak transcription Strong transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs189013418	chr19:19755895-19755896	Weak transcription Strong transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs542103278	chr19:19755912-19755913	Weak transcription Strong transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs143496568	chr19:19755914-19755915	Weak transcription Strong transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs80135136	chr19:19755933-19755934	Weak transcription Strong transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs10423449	chr19:19755946-19755947	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs193134505	chr19:19755959-19755960	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs201453294	chr19:19755960-19755961	Weak transcription Strong transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs561920919	chr19:19755990-19755991	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs184367152	chr19:19756040-19756041	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs73537247	chr19:19756051-19756052	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs3841260	chr19:19756074-19756075	Weak transcription Strong transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs113554060	chr19:19756079-19756080	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs148015026	chr19:19756117-19756118	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs552175944	chr19:19756118-19756119	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs565703079	chr19:19756151-19756152	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs535335446	chr19:19756165-19756166	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs112268372	chr19:19756166-19756167	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs566217835	chr19:19756178-19756179	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs373283716	chr19:19756186-19756187	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs199852689	chr19:19756193-19756194	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs61739682	chr19:19756268-19756269	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs141473818	chr19:19756270-19756271	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs374647506	chr19:19756279-19756280	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs369690860	chr19:19756281-19756282	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs145136517	chr19:19756285-19756286	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs545878556	chr19:19756314-19756315	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs201101592	chr19:19756318-19756319	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs200525190	chr19:19756346-19756347	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs370911404	chr19:19756347-19756348	Weak transcription Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Nasopharyngeal cancer	20548289	CNVD

Chromatin state (count:3132 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19754400-19755800	Weak transcription	Small Intestine	intestine
2	chr19:19754600-19756000	Weak transcription	Gastric	stomach
3	chr19:19754800-19755600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr19:19754800-19755600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr19:19754800-19755600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr19:19754800-19755600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr19:19754800-19755600	Weak transcription	A549	lung
8	chr19:19754800-19755600	Weak transcription	NHLF	lung
9	chr19:19754800-19755800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr19:19754800-19755800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr19:19754800-19755800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr19:19754800-19755800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr19:19754800-19755800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr19:19754800-19755800	Weak transcription	Esophagus	oesophagus
15	chr19:19754800-19755800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr19:19754800-19755800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr19:19754800-19755800	Weak transcription	HUVEC	blood vessel
18	chr19:19754800-19756000	Weak transcription	Left Ventricle	heart
19	chr19:19754800-19756000	Weak transcription	Lung	lung
20	chr19:19754800-19756000	Weak transcription	Ovary	ovary
21	chr19:19754800-19756000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr19:19754800-19756200	Weak transcription	Aorta	Aorta
23	chr19:19754800-19756200	Weak transcription	Rectal Smooth Muscle	rectum
24	chr19:19754800-19756400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:19754800-19756400	Weak transcription	Psoas Muscle	Psoas
26	chr19:19754800-19756400	Weak transcription	HMEC	breast
27	chr19:19754800-19756400	Weak transcription	HSMMtube	muscle
28	chr19:19754800-19756600	Weak transcription	Brain Substantia Nigra	brain
29	chr19:19754800-19757600	Weak transcription	NH-A	brain
30	chr19:19754800-19757800	Weak transcription	NHDF-Ad	bronchial
31	chr19:19754800-19761400	Weak transcription	HSMM	muscle
32	chr19:19754800-19763600	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr19:19754800-19764200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr19:19754800-19767200	Weak transcription	Fetal Brain Male	brain
35	chr19:19754800-19769000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr19:19754800-19772400	Weak transcription	Right Atrium	heart
37	chr19:19755000-19755600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr19:19755000-19755600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr19:19755000-19755600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr19:19755000-19755600	Weak transcription	Stomach Smooth Muscle	stomach
41	chr19:19755000-19755800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr19:19755000-19756000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr19:19755000-19756000	Weak transcription	Colonic Mucosa	Colon
44	chr19:19755000-19756000	Weak transcription	Pancreas	Pancrea
45	chr19:19755000-19756000	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr19:19755000-19756800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr19:19755000-19757000	Weak transcription	Stomach Mucosa	stomach
48	chr19:19755000-19759000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr19:19755000-19759000	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr19:19755000-19759000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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