Variant report

Variant	esv3373348
Chromosome Location	chr19:40789637-40792485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:685)
CpG islands
(count:856)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40791392-40791966	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40790820-40790836	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40791037-40791795	K562	blood:	n/a	n/a
4	ATF1	chr19:40791052-40791713	K562	blood:	n/a	n/a
5	ATF2	chr19:40790193-40790807	GM12878	blood:	n/a	n/a
6	ATF2	chr19:40791560-40791994	GM12878	blood:	n/a	n/a
7	ATF2	chr19:40791249-40791917	GM12878	blood:	n/a	n/a
8	ATF2	chr19:40790198-40790631	GM12878	blood:	n/a	n/a
9	ATF3	chr19:40790939-40792065	A549	lung:	n/a	n/a
10	BACH1	chr19:40790565-40791170	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr19:40790582-40790682	K562	blood:	n/a	n/a
12	BACH1	chr19:40791375-40791597	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr19:40791230-40792049	A549	lung:	n/a	chr19:40791339-40791348
14	BCL3	chr19:40790863-40792100	A549	lung:	n/a	chr19:40791339-40791348 chr19:40790928-40790941
15	BCLAF1	chr19:40791276-40791969	GM12878	blood:	n/a	chr19:40791339-40791348
16	BCLAF1	chr19:40790365-40790896	GM12878	blood:	n/a	chr19:40790787-40790796
17	BHLHE40	chr19:40790243-40791812	GM12878	blood:	n/a	n/a
18	BHLHE40	chr19:40790922-40791230	A549	lung:	n/a	n/a
19	BHLHE40	chr19:40790557-40791836	K562	blood:	n/a	n/a
20	BHLHE40	chr19:40790617-40791643	HepG2	liver:	n/a	n/a
21	BRCA1	chr19:40790704-40791922	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr19:40791028-40791834	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr19:40790306-40791007	GM12878	blood:	n/a	n/a
24	CBX3	chr19:40791287-40791973	K562	blood:	n/a	n/a
25	CCNT2	chr19:40790650-40791835	K562	blood:	n/a	chr19:40790666-40790675
26	CEBPB	chr19:40791353-40791487	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:40789312-40789807	HepG2	liver:	n/a	n/a
28	CEBPB	chr19:40791371-40791511	K562	blood:	n/a	n/a
29	CEBPD	chr19:40790642-40791383	HepG2	liver:	n/a	n/a
30	CEBPD	chr19:40790916-40791561	K562	blood:	n/a	n/a
31	CHD1	chr19:40789452-40792116	IMR90	lung:	n/a	n/a
32	CHD1	chr19:40789834-40791914	GM12878	blood:	n/a	n/a
33	CHD1	chr19:40790433-40791809	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:40789629-40789952	HepG2	liver:	n/a	n/a
35	CHD2	chr19:40790966-40791829	GM12878	blood:	n/a	n/a
36	CHD2	chr19:40790989-40791821	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr19:40790654-40791846	K562	blood:	n/a	n/a
38	CHD2	chr19:40790659-40791368	HepG2	liver:	n/a	n/a
39	CHD2	chr19:40790836-40791833	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr19:40790135-40790690	GM12878	blood:	n/a	n/a
41	CREB1	chr19:40791276-40791778	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr19:40790623-40791799	K562	blood:	n/a	n/a
43	CREB1	chr19:40790027-40791952	GM12878	blood:	n/a	n/a
44	CREB1	chr19:40791081-40791670	ECC-1	luminal epithelium:	n/a	n/a
45	CREB1	chr19:40790705-40791913	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr19:40791216-40791969	ECC-1	luminal epithelium:	n/a	n/a
47	CREB1	chr19:40790492-40791995	HepG2	liver:	n/a	n/a
48	CREB1	chr19:40790709-40791255	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr19:40790908-40791710	A549	lung:	n/a	n/a
50	CREB1	chr19:40790451-40791818	A549	lung:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40791102-40791152	SAEC	small airway:	n/a
2	chr19:40790165-40790215	GM06990	blood:	n/a
3	chr19:40791102-40791152	SAEC	small airway:	n/a
4	chr19:40790165-40790215	GM06990	blood:	n/a
5	chr19:40791701-40791751	SK-N-SH	brain:	n/a
6	chr19:40789857-40789907	IMR90	lung:	fetal
7	chr19:40791102-40791152	MCF10A-Er-Src	breast:	n/a
8	chr19:40791331-40791381	HAEpiC	amniotic membrane:	n/a
9	chr19:40790165-40790215	Hela-S3	cervix:	n/a
10	chr19:40791321-40791371	SAEC	small airway:	n/a
11	chr19:40789866-40789916	HCPEpiC	choroid plexus:	n/a
12	chr19:40791658-40791708	T-47D	breast:	n/a
13	chr19:40792011-40792061	HRE	kidney:	n/a
14	chr19:40790591-40790641	HCT-116	colon:	n/a
15	chr19:40789857-40789907	AG04450	lung:	fetal
16	chr19:40791701-40791751	PrEC	prostate:	n/a
17	chr19:40790165-40790215	A549	lung:	n/a
18	chr19:40791312-40791362	HPAEpiC	pulmonary alveolar:	n/a
19	chr19:40791658-40791708	SAEC	small airway:	n/a
20	chr19:40791701-40791751	Hepatocyte	liver:	n/a
21	chr19:40791481-40791531	ovcar-3	ovarian:	n/a
22	chr19:40791701-40791751	SAEC	small airway:	n/a
23	chr19:40791321-40791371	NB4	blood:	n/a
24	chr19:40791481-40791531	MCF10A-Er-Src	breast:	n/a
25	chr19:40792011-40792061	AG09309	skin:	n/a
26	chr19:40790591-40790641	IMR90	lung:	fetal
27	chr19:40792011-40792061	PrEC	prostate:	n/a
28	chr19:40791658-40791708	AG10803	skin:	n/a
29	chr19:40789866-40789916	T-47D	breast:	n/a
30	chr19:40790165-40790215	AG10803	skin:	n/a
31	chr19:40791701-40791751	HEK293	kidney:	embryo
32	chr19:40790591-40790641	SK-N-SH_RA	brain:	n/a
33	chr19:40791658-40791708	NH-A	brain:	n/a
34	chr19:40792011-40792061	HCF	heart:	n/a
35	chr19:40792011-40792061	HCT-116	colon:	n/a
36	chr19:40791331-40791381	SK-N-SH	brain:	n/a
37	chr19:40790165-40790215	SK-N-SH_RA	brain:	n/a
38	chr19:40789866-40789916	HCM	heart:	n/a
39	chr19:40789857-40789907	Hela-S3	cervix:	n/a
40	chr19:40791383-40791433	SK-N-MC	brain:	n/a
41	chr19:40791321-40791371	CMK	blood:	n/a
42	chr19:40790591-40790641	HEK293	kidney:	embryo
43	chr19:40791436-40791486	NHDF-neo	bronchial:	n/a
44	chr19:40791481-40791531	HAEpiC	amniotic membrane:	n/a
45	chr19:40791321-40791371	MCF-7	breast:	n/a
46	chr19:40791102-40791152	GM19239	blood:	n/a
47	chr19:40791331-40791381	HEK293	kidney:	embryo
48	chr19:40791481-40791531	HCF	heart:	n/a
49	chr19:40791383-40791433	GM06990	blood:	n/a
50	chr19:40790165-40790215	HRE	kidney:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40791053..40791604-chr6:74230235..74230760,2	Hela-S3	cervix:
2	chr19:40790365..40793125-chr19:40949596..40951580,2	K562	blood:
3	chr19:40791054..40792631-chr19:40929438..40932083,2	K562	blood:
4	chr19:40790880..40792731-chr19:40929438..40932853,4	K562	blood:
5	chr12:112856411..112856934-chr19:40791459..40792121,2	NB4	blood:
6	chr19:40789879..40793059-chr19:40870323..40872928,3	K562	blood:
7	chr19:40790406..40791402-chr22:50968889..50969883,2	Hela-S3	cervix:
8	chr19:40788680..40791212-chr19:40852795..40854366,2	K562	blood:
9	chr19:40791790..40793403-chr19:40794499..40796006,2	K562	blood:
10	chr19:40695407..40698481-chr19:40788292..40792778,5	K562	blood:
11	chr19:40746630..40748490-chr19:40790537..40793116,2	MCF-7	breast:
12	chr19:40791701..40793246-chr19:40980177..40982269,2	K562	blood:
13	chr19:40789948..40791553-chr19:41119261..41121070,2	K562	blood:
14	chr19:40787579..40789839-chr19:40846986..40849835,2	MCF-7	breast:
15	chr19:40791169..40791672-chr5:141303112..141303640,2	Hela-S3	cervix:
16	chr11:47736264..47737264-chr19:40791442..40792121,2	NB4	blood:

No data

Variant related genes	Relation type
AKT2	TF binding region
MIR641	TF binding region
AKT2	CpG island
MIR641	CpG island
ENSG00000206925	chromatin interactions
ENSG00000090006	chromatin interactions
ENSG00000197019	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000089009	chromatin interactions
ENSG00000167565	chromatin interactions
ENSG00000105221	chromatin interactions
ENSG00000177989	chromatin interactions
ENSG00000105223	chromatin interactions
ENSG00000179295	chromatin interactions
ENSG00000130758	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000160392	chromatin interactions
ENSG00000165923	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536806662	chr19:40789662-40789663	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs551996372	chr19:40789733-40789734	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs571406097	chr19:40789770-40789771	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs370893475	chr19:40789776-40789777	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs28550902	chr19:40789797-40789798	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs143194929	chr19:40789807-40789808	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs146630415	chr19:40789831-40789832	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs34013820	chr19:40789847-40789848	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs565902600	chr19:40789859-40789860	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs12459567	chr19:40789926-40789927	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs541632997	chr19:40789964-40789965	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs554916649	chr19:40790044-40790045	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs118098588	chr19:40790059-40790060	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs544018461	chr19:40790115-40790116	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs111252247	chr19:40790118-40790119	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs559239277	chr19:40790122-40790123	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs7249476	chr19:40790152-40790153	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs576989077	chr19:40790210-40790211	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs541159740	chr19:40790311-40790312	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs527577619	chr19:40790315-40790316	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs559422501	chr19:40790348-40790349	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs7250121	chr19:40790433-40790434	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs541822733	chr19:40790459-40790460	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs117431069	chr19:40790502-40790503	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs145105754	chr19:40790532-40790533	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs375453437	chr19:40790569-40790570	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs551931264	chr19:40790672-40790673	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs570349072	chr19:40790711-40790712	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs528287502	chr19:40790715-40790716	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs552485461	chr19:40790770-40790771	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs547456458	chr19:40790812-40790813	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs369728131	chr19:40790848-40790849	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs536211405	chr19:40790870-40790871	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs148351604	chr19:40790875-40790876	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs570246992	chr19:40790961-40790962	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs537766584	chr19:40790987-40790988	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs559178105	chr19:40790996-40790997	Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs577477016	chr19:40791019-40791020	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs541648886	chr19:40791032-40791033	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs552753966	chr19:40791033-40791034	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs539329378	chr19:40791050-40791051	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs371604268	chr19:40791051-40791052	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs7253731	chr19:40791071-40791072	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs541460496	chr19:40791190-40791191	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs563324770	chr19:40791359-40791360	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs574914973	chr19:40791363-40791364	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs150433094	chr19:40791381-40791382	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs545660060	chr19:40791382-40791383	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs570111225	chr19:40791402-40791403	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs564061931	chr19:40791407-40791408	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Pleomorphic liposarcoma	18784837	CNVD

Chromatin state (count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40770200-40790200	Weak transcription	Aorta	Aorta
2	chr19:40779800-40789800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr19:40783400-40790000	Enhancers	Right Atrium	heart
4	chr19:40783800-40790600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr19:40786000-40790000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:40786400-40790200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr19:40786800-40789800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr19:40787000-40790000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr19:40787000-40790000	Genic enhancers	Spleen	Spleen
10	chr19:40787200-40789800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr19:40787200-40790000	Weak transcription	Small Intestine	intestine
12	chr19:40787600-40789800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr19:40787800-40789800	Enhancers	Fetal Heart	heart
14	chr19:40787800-40790400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
15	chr19:40788000-40789800	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr19:40788000-40789800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr19:40788400-40790000	Enhancers	Gastric	stomach
18	chr19:40788400-40790200	Enhancers	Esophagus	oesophagus
19	chr19:40788600-40789800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:40788600-40789800	Enhancers	Primary B cells from peripheral blood	blood
21	chr19:40788600-40789800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:40788600-40789800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:40788600-40790200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr19:40788800-40789800	Enhancers	Fetal Kidney	kidney
25	chr19:40788800-40790000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr19:40788800-40790200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr19:40788800-40790400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr19:40788800-40790600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr19:40789000-40789800	Enhancers	Primary B cells from cord blood	blood
30	chr19:40789000-40789800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr19:40789000-40789800	Enhancers	Brain Substantia Nigra	brain
32	chr19:40789000-40789800	Enhancers	Lung	lung
33	chr19:40789000-40789800	Enhancers	Stomach Mucosa	stomach
34	chr19:40789000-40790000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr19:40789000-40790000	Transcr. at gene 5' and 3'	K562	blood
36	chr19:40789000-40790200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr19:40789000-40790600	Flanking Active TSS	Liver	Liver
38	chr19:40789000-40790600	Flanking Active TSS	Duodenum Mucosa	Duodenum
39	chr19:40789200-40789800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr19:40789200-40789800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr19:40789200-40789800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr19:40789200-40789800	Enhancers	Fetal Brain Male	brain
43	chr19:40789200-40789800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr19:40789200-40789800	Genic enhancers	Thymus	Thymus
45	chr19:40789200-40790000	Enhancers	Ovary	ovary
46	chr19:40789200-40790200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr19:40789200-40790200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr19:40789200-40790200	Flanking Active TSS	GM12878-XiMat	blood
49	chr19:40789200-40790400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr19:40789200-40790400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood

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