Variant report

Variant	esv1005660
Chromosome Location	chr19:40784738-40790835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:516)
CpG islands
(count:366)
Chromatin interactive
region (count:12)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40790820-40790836	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40789369-40789589	HepG2	liver:	n/a	n/a
3	ATF2	chr19:40790193-40790807	GM12878	blood:	n/a	n/a
4	ATF2	chr19:40790198-40790631	GM12878	blood:	n/a	n/a
5	BACH1	chr19:40790582-40790682	K562	blood:	n/a	n/a
6	BACH1	chr19:40790565-40791170	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr19:40790365-40790896	GM12878	blood:	n/a	chr19:40790787-40790796
8	BHLHE40	chr19:40790557-40791836	K562	blood:	n/a	n/a
9	BHLHE40	chr19:40790243-40791812	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:40786194-40786488	GM12878	blood:	n/a	n/a
11	BHLHE40	chr19:40790617-40791643	HepG2	liver:	n/a	n/a
12	BRCA1	chr19:40790306-40791007	GM12878	blood:	n/a	n/a
13	BRCA1	chr19:40790704-40791922	H1-hESC	embryonic stem cell:	n/a	n/a
14	CCNT2	chr19:40790650-40791835	K562	blood:	n/a	chr19:40790666-40790675
15	CEBPB	chr19:40787778-40787948	A549	lung:	n/a	n/a
16	CEBPB	chr19:40787820-40787910	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:40789312-40789807	HepG2	liver:	n/a	n/a
18	CEBPD	chr19:40790642-40791383	HepG2	liver:	n/a	n/a
19	CHD1	chr19:40789834-40791914	GM12878	blood:	n/a	n/a
20	CHD1	chr19:40790433-40791809	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr19:40789452-40792116	IMR90	lung:	n/a	n/a
22	CHD2	chr19:40790654-40791846	K562	blood:	n/a	n/a
23	CHD2	chr19:40786311-40786381	GM12878	blood:	n/a	n/a
24	CHD2	chr19:40790135-40790690	GM12878	blood:	n/a	n/a
25	CHD2	chr19:40790659-40791368	HepG2	liver:	n/a	n/a
26	CHD2	chr19:40789629-40789952	HepG2	liver:	n/a	n/a
27	CREB1	chr19:40790774-40791823	HepG2	liver:	n/a	n/a
28	CREB1	chr19:40790709-40791255	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr19:40790492-40791995	HepG2	liver:	n/a	n/a
30	CREB1	chr19:40790027-40791952	GM12878	blood:	n/a	n/a
31	CREB1	chr19:40790705-40791913	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr19:40790451-40791818	A549	lung:	n/a	n/a
33	CREB1	chr19:40790623-40791799	K562	blood:	n/a	n/a
34	CTCF	chr19:40785120-40785270	HEK293	kidney:	n/a	n/a
35	CTCF	chr19:40790759-40790764	GM12891	blood:	n/a	n/a
36	CTCF	chr19:40785260-40785410	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr19:40785220-40785370	BJ	skin:	n/a	n/a
38	CTCF	chr19:40785160-40785310	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr19:40785240-40785390	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr19:40785280-40785430	AG10803	skin:	n/a	n/a
41	CTCF	chr19:40789080-40789230	HMF	breast:	n/a	n/a
42	CTCF	chr19:40790740-40791010	GM12864	blood:	n/a	n/a
43	CTCF	chr19:40789160-40789310	GM06990	blood:	n/a	n/a
44	CTCF	chr19:40790730-40790790	GM13976	blood:	n/a	n/a
45	CTCF	chr19:40785220-40785370	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr19:40785200-40785350	HCFaa	heart:	n/a	n/a
47	CTCF	chr19:40790670-40790785	GM19239	blood:	n/a	n/a
48	CTCF	chr19:40789200-40789350	HRPEpiC	eye:	n/a	chr19:40789304-40789313
49	CTCF	chr19:40785280-40785430	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr19:40790800-40790950	GM12869	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40788787-40788837	GM12892	blood:	n/a
2	chr19:40788926-40788976	HUVEC	blood vessel:	n/a
3	chr19:40790591-40790641	BE2_C	brain:	n/a
4	chr19:40790591-40790641	SAEC	small airway:	n/a
5	chr19:40789866-40789916	H1-hESC	embryonic stem cell:	embryo
6	chr19:40790165-40790215	HRCEpiC	kidney:	n/a
7	chr19:40790165-40790215	AG09319	gingival:	n/a
8	chr19:40790591-40790641	SK-N-SH	brain:	n/a
9	chr19:40790591-40790641	HRPEpiC	eye:	n/a
10	chr19:40788787-40788837	AG09319	gingival:	n/a
11	chr19:40789857-40789907	SK-N-SH_RA	brain:	n/a
12	chr19:40788926-40788976	GM19239	blood:	n/a
13	chr19:40788787-40788837	HEEpiC	esophagus:	n/a
14	chr19:40790165-40790215	GM12878	blood:	n/a
15	chr19:40790591-40790641	IMR90	lung:	fetal
16	chr19:40790591-40790641	Caco-2	colon:	n/a
17	chr19:40789857-40789907	GM12878	blood:	n/a
18	chr19:40788787-40788837	HEK293	kidney:	embryo
19	chr19:40788787-40788837	HIPEpiC	eye:	n/a
20	chr19:40788926-40788976	SK-N-MC	brain:	n/a
21	chr19:40788926-40788976	GM12891	blood:	n/a
22	chr19:40790165-40790215	H1-hESC	embryonic stem cell:	embryo
23	chr19:40789857-40789907	HPAEpiC	pulmonary alveolar:	n/a
24	chr19:40788926-40788976	HIPEpiC	eye:	n/a
25	chr19:40788926-40788976	AG09309	skin:	n/a
26	chr19:40789857-40789907	AG04450	lung:	fetal
27	chr19:40789857-40789907	HL-60	blood:	n/a
28	chr19:40790165-40790215	GM12891	blood:	n/a
29	chr19:40790165-40790215	NHBE	bronchial:	n/a
30	chr19:40788926-40788976	HCF	heart:	n/a
31	chr19:40789857-40789907	ovcar-3	ovarian:	n/a
32	chr19:40788787-40788837	HUVEC	blood vessel:	n/a
33	chr19:40788787-40788837	GM06990	blood:	n/a
34	chr19:40789857-40789907	T-47D	breast:	n/a
35	chr19:40788787-40788837	PFSK-1	brain:	n/a
36	chr19:40790165-40790215	HCM	heart:	n/a
37	chr19:40789857-40789907	HIPEpiC	eye:	n/a
38	chr19:40790591-40790641	HRCEpiC	kidney:	n/a
39	chr19:40788787-40788837	MCF10A-Er-Src	breast:	n/a
40	chr19:40790165-40790215	A549	lung:	n/a
41	chr19:40789857-40789907	HCF	heart:	n/a
42	chr19:40788926-40788976	ovcar-3	ovarian:	n/a
43	chr19:40790165-40790215	Hepatocyte	liver:	n/a
44	chr19:40788787-40788837	SK-N-SH	brain:	n/a
45	chr19:40789866-40789916	HRPEpiC	eye:	n/a
46	chr19:40789857-40789907	AoSMC	blood vessel:	n/a
47	chr19:40790591-40790641	Hela-S3	cervix:	n/a
48	chr19:40789857-40789907	HCM	heart:	n/a
49	chr19:40788787-40788837	HL-60	blood:	n/a
50	chr19:40790165-40790215	T-47D	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:40768260..40771807-chr19:40783478..40786593,4	K562	blood:
2	chr19:40788680..40791212-chr19:40852795..40854366,2	K562	blood:
3	chr19:40695407..40698481-chr19:40788292..40792778,5	K562	blood:
4	chr19:40790406..40791402-chr22:50968889..50969883,2	Hela-S3	cervix:
5	chr19:40787579..40789839-chr19:40846986..40849835,2	MCF-7	breast:
6	chr19:40789948..40791553-chr19:41119261..41121070,2	K562	blood:
7	chr19:40731324..40733318-chr19:40786434..40789035,2	MCF-7	breast:
8	chr19:40783887..40786272-chr19:41107076..41108731,2	K562	blood:
9	chr19:40789879..40793059-chr19:40870323..40872928,3	K562	blood:
10	chr19:40776468..40779839-chr19:40784717..40787633,5	MCF-7	breast:
11	chr19:40790365..40793125-chr19:40949596..40951580,2	K562	blood:
12	chr19:40746630..40748490-chr19:40790537..40793116,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC118344.1-3	chr19:40788155-40788351	NONHSAT066363
2	lnc-AC118344.1-3	chr19:40788615-40789072	NONHSAT066363
3	lnc-AC118344.1-2	chr19:40785014-40785131	NONHSAT066360

miRNA name	Chromosome Location	mirBase accession
hsa-miR-641	chr19:40788510-40788533	MIMAT0003311

No data

Variant related genes	Relation type
MIR641	TF binding region
ENSG00000205041	TF binding region
AKT2	TF binding region
MIR641	CpG island
ENSG00000205041	CpG island
AKT2	CpG island
ENSG00000105223	chromatin interactions
ENSG00000090006	chromatin interactions
ENSG00000167565	chromatin interactions
ENSG00000105219	chromatin interactions
ENSG00000160392	chromatin interactions
ENSG00000130758	chromatin interactions
ENSG00000206925	chromatin interactions
ENSG00000177989	chromatin interactions
ENSG00000105221	chromatin interactions
TOB1	Mature miRNA region

Extended variants
information (count: 227 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:227 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553590009	chr19:40784772-40784773	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs370393497	chr19:40784780-40784781	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575054603	chr19:40784792-40784793	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs8111619	chr19:40784838-40784839	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs556735119	chr19:40784839-40784840	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs11669006	chr19:40784859-40784860	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs139197799	chr19:40784903-40784904	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs563784734	chr19:40784931-40784932	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs149958099	chr19:40784932-40784933	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs540169715	chr19:40784933-40784934	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs551193002	chr19:40784978-40784979	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs73933239	chr19:40784985-40784986	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529048867	chr19:40785028-40785029	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs533515381	chr19:40785054-40785055	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs550751792	chr19:40785110-40785111	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs570009754	chr19:40785125-40785126	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs73933240	chr19:40785164-40785165	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552269408	chr19:40785217-40785218	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs570895633	chr19:40785222-40785223	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs376091107	chr19:40785244-40785245	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs535033494	chr19:40785344-40785345	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs553676545	chr19:40785347-40785348	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs568774587	chr19:40785417-40785418	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs367843854	chr19:40785423-40785424	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs557572527	chr19:40785487-40785488	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs4332845	chr19:40785505-40785506	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs113008495	chr19:40785522-40785523	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs373429346	chr19:40785556-40785557	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs576341810	chr19:40785559-40785560	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs34623198	chr19:40785560-40785561	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs5828063	chr19:40785575-40785576	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs200065640	chr19:40785576-40785577	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs202121115	chr19:40785583-40785584	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs545910550	chr19:40785609-40785610	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs557313942	chr19:40785656-40785657	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs374086939	chr19:40785667-40785668	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs75397302	chr19:40785668-40785669	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs75018496	chr19:40785683-40785684	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs561599310	chr19:40785704-40785705	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs529194185	chr19:40785723-40785724	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs544075661	chr19:40785735-40785736	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs562733238	chr19:40785753-40785754	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs7259541	chr19:40785779-40785780	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs556283922	chr19:40785783-40785784	Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs114184099	chr19:40785895-40785896	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs181265949	chr19:40785909-40785910	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs542506639	chr19:40785910-40785911	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs528448693	chr19:40785913-40785914	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs560575898	chr19:40785921-40785922	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs576251412	chr19:40785939-40785940	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 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:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40766200-40788600	Weak transcription	HSMMtube	muscle
2	chr19:40770000-40789600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:40770000-40789600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr19:40770200-40789600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr19:40770200-40790200	Weak transcription	Aorta	Aorta
6	chr19:40771400-40789400	Weak transcription	HUVEC	blood vessel
7	chr19:40771600-40786000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr19:40776000-40787400	Weak transcription	A549	lung
9	chr19:40776400-40785000	Weak transcription	NHLF	lung
10	chr19:40776600-40785800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:40778000-40786400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr19:40778800-40785200	Weak transcription	HMEC	breast
13	chr19:40778800-40786200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr19:40778800-40787600	Weak transcription	Hela-S3	cervix
15	chr19:40779000-40786800	Weak transcription	Dnd41	blood
16	chr19:40779400-40789600	Enhancers	Left Ventricle	heart
17	chr19:40779800-40789800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr19:40780600-40784800	Weak transcription	Fetal Brain Female	brain
19	chr19:40780600-40786200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:40781000-40785400	Weak transcription	Brain Germinal Matrix	brain
21	chr19:40781000-40785800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr19:40781000-40787800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr19:40781200-40786000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr19:40781400-40785400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr19:40781400-40785600	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr19:40781400-40788000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:40781400-40788000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr19:40781600-40784800	Weak transcription	Primary T cells from cord blood	blood
29	chr19:40781600-40785800	Enhancers	K562	blood
30	chr19:40781600-40787400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr19:40781800-40785000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr19:40782000-40785000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
33	chr19:40782200-40789400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr19:40782400-40785000	Enhancers	Right Ventricle	heart
35	chr19:40782800-40785800	Enhancers	Liver	Liver
36	chr19:40782800-40786800	Enhancers	Primary T cells fromperipheralblood	blood
37	chr19:40783000-40784800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr19:40783000-40785000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr19:40783000-40785000	Enhancers	Ovary	ovary
40	chr19:40783000-40788200	Enhancers	Pancreas	Pancrea
41	chr19:40783000-40789600	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr19:40783200-40784800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr19:40783200-40784800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr19:40783200-40786000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr19:40783200-40787000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr19:40783200-40787400	Enhancers	Fetal Intestine Large	intestine
47	chr19:40783200-40787600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr19:40783200-40788200	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr19:40783200-40789200	Enhancers	Brain Cingulate Gyrus	brain
50	chr19:40783400-40784800	Enhancers	Duodenum Smooth Muscle	Duodenum

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