Variant report

Variant	esv17267
Chromosome Location	chr19:19174047-19177125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:639)
CpG islands
(count:671)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:19173214-19174819	K562	blood:	n/a	n/a
2	ARID3A	chr19:19174131-19174515	HepG2	liver:	n/a	n/a
3	ATF2	chr19:19174248-19174743	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:19174038-19174741	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:19174162-19174784	GM12878	blood:	n/a	n/a
6	BACH1	chr19:19174961-19175138	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr19:19174009-19174838	A549	lung:	n/a	n/a
8	BCL3	chr19:19174063-19174921	GM12878	blood:	n/a	n/a
9	BCL3	chr19:19173920-19174853	A549	lung:	n/a	n/a
10	BHLHE40	chr19:19175893-19176494	GM12878	blood:	n/a	n/a
11	BHLHE40	chr19:19174157-19175585	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:19173291-19175133	K562	blood:	n/a	n/a
13	BHLHE40	chr19:19175860-19175976	K562	blood:	n/a	n/a
14	BRCA1	chr19:19175451-19175525	HepG2	liver:	n/a	n/a
15	BRCA1	chr19:19174972-19175003	GM12878	blood:	n/a	n/a
16	BRCA1	chr19:19174099-19174787	HepG2	liver:	n/a	n/a
17	BRCA1	chr19:19174256-19174557	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr19:19174975-19175071	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr19:19174217-19174767	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr19:19173110-19174697	K562	blood:	n/a	n/a
21	CCNT2	chr19:19173957-19175259	K562	blood:	n/a	chr19:19174511-19174520 chr19:19175021-19175030
22	CEBPB	chr19:19173751-19174267	K562	blood:	n/a	n/a
23	CEBPB	chr19:19174161-19174705	HepG2	liver:	n/a	chr19:19174673-19174681
24	CEBPD	chr19:19174011-19175068	HepG2	liver:	n/a	n/a
25	CEBPD	chr19:19174651-19174901	HepG2	liver:	n/a	n/a
26	CEBPZ	chr19:19174101-19174794	HepG2	liver:	n/a	n/a
27	CHD2	chr19:19174130-19175115	GM12878	blood:	n/a	chr19:19174953-19174963
28	CHD2	chr19:19174014-19175056	Hela-S3	cervix:	n/a	chr19:19174953-19174963
29	CHD2	chr19:19174158-19175073	HepG2	liver:	n/a	chr19:19174953-19174963
30	CHD2	chr19:19175453-19175653	K562	blood:	n/a	n/a
31	CHD2	chr19:19174019-19175094	H1-hESC	embryonic stem cell:	n/a	chr19:19174953-19174963
32	CHD2	chr19:19174068-19175184	K562	blood:	n/a	chr19:19174953-19174963
33	CREB1	chr19:19174522-19174795	A549	lung:	n/a	n/a
34	CREB1	chr19:19174043-19175300	GM12878	blood:	n/a	n/a
35	CREB1	chr19:19174210-19174965	ECC-1	luminal epithelium:	n/a	n/a
36	CREB1	chr19:19174126-19175188	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr19:19173990-19175386	HepG2	liver:	n/a	n/a
38	CREB1	chr19:19173885-19175215	HepG2	liver:	n/a	n/a
39	CREB1	chr19:19173886-19175255	K562	blood:	n/a	n/a
40	CREB1	chr19:19174135-19174932	A549	lung:	n/a	n/a
41	CTCF	chr19:19175000-19175150	GM12864	blood:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
42	CTCF	chr19:19175025-19175116	GM10248	blood:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
43	CTCF	chr19:19175000-19175150	AG09309	skin:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
44	CTCF	chr19:19174960-19175110	HMEC	breast:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
45	CTCF	chr19:19174704-19174806	Lung_OC	lung:	n/a	n/a
46	CTCF	chr19:19175026-19175138	MCF-7	breast:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
47	CTCF	chr19:19174960-19175110	HCPEpiC	choroid plexus:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
48	CTCF	chr19:19175009-19175143	MCF-7	breast:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
49	CTCF	chr19:19174977-19175155	K562	blood:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061
50	CTCF	chr19:19175000-19175150	NHEK	skin:	n/a	chr19:19175049-19175058 chr19:19175045-19175058 chr19:19175043-19175061

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:19174731-19174781	RPTEC	kidney:	n/a
2	chr19:19174295-19174345	A549	lung:	n/a
3	chr19:19175730-19175780	HAEpiC	amniotic membrane:	n/a
4	chr19:19175730-19175780	GM12878	blood:	n/a
5	chr19:19175730-19175780	PFSK-1	brain:	n/a
6	chr19:19174831-19174881	SK-N-SH	brain:	n/a
7	chr19:19175039-19175089	GM12891	blood:	n/a
8	chr19:19174709-19174759	HUVEC	blood vessel:	n/a
9	chr19:19174767-19174817	ProgFib	skin:	n/a
10	chr19:19174767-19174817	HEK293	kidney:	embryo
11	chr19:19175039-19175089	HUVEC	blood vessel:	n/a
12	chr19:19174709-19174759	ECC-1	luminal epithelium:	n/a
13	chr19:19174151-19174201	H1-hESC	embryonic stem cell:	embryo
14	chr19:19174831-19174881	BJ	skin:	n/a
15	chr19:19174709-19174759	HRPEpiC	eye:	n/a
16	chr19:19174767-19174817	CMK	blood:	n/a
17	chr19:19174604-19174654	PrEC	prostate:	n/a
18	chr19:19174709-19174759	CMK	blood:	n/a
19	chr19:19174831-19174881	AoSMC	blood vessel:	n/a
20	chr19:19174604-19174654	RPTEC	kidney:	n/a
21	chr19:19174295-19174345	ProgFib	skin:	n/a
22	chr19:19174767-19174817	ovcar-3	ovarian:	n/a
23	chr19:19174604-19174654	GM19239	blood:	n/a
24	chr19:19174767-19174817	MCF-7	breast:	n/a
25	chr19:19174295-19174345	HMEC	breast:	n/a
26	chr19:19175730-19175780	RPTEC	kidney:	n/a
27	chr19:19174762-19174812	MCF-7	breast:	n/a
28	chr19:19174731-19174781	BE2_C	brain:	n/a
29	chr19:19174957-19175007	HRCEpiC	kidney:	n/a
30	chr19:19175730-19175780	AoSMC	blood vessel:	n/a
31	chr19:19174767-19174817	HNPCEpiC	eye:	n/a
32	chr19:19174762-19174812	RPTEC	kidney:	n/a
33	chr19:19174709-19174759	RPTEC	kidney:	n/a
34	chr19:19174957-19175007	Hela-S3	cervix:	n/a
35	chr19:19174709-19174759	PFSK-1	brain:	n/a
36	chr19:19174604-19174654	IMR90	lung:	fetal
37	chr19:19174295-19174345	AG04450	lung:	fetal
38	chr19:19174151-19174201	HRCEpiC	kidney:	n/a
39	chr19:19175730-19175780	A549	lung:	n/a
40	chr19:19174957-19175007	Hepatocyte	liver:	n/a
41	chr19:19174731-19174781	GM06990	blood:	n/a
42	chr19:19174957-19175007	IMR90	lung:	fetal
43	chr19:19174762-19174812	ProgFib	skin:	n/a
44	chr19:19174604-19174654	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:19174151-19174201	HRPEpiC	eye:	n/a
46	chr19:19174731-19174781	SK-N-MC	brain:	n/a
47	chr19:19174831-19174881	HCT-116	colon:	n/a
48	chr19:19174731-19174781	MCF10A-Er-Src	breast:	n/a
49	chr19:19174831-19174881	Hepatocyte	liver:	n/a
50	chr19:19174295-19174345	HepG2	liver:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:19042101..19044216-chr19:19173856..19175729,2	K562	blood:
2	chr19:19171826..19174275-chr19:19223519..19227124,3	K562	blood:
3	chr19:19129913..19132824-chr19:19171752..19174736,2	K562	blood:
4	chr12:6716092..6716619-chr19:19173988..19174537,2	HCT-116	colon:
5	chr19:19110096..19111022-chr19:19173704..19174740,6	MCF-7	breast:
6	chr19:19141992..19145925-chr19:19172787..19177854,10	K562	blood:
7	chr19:19162360..19163114-chr19:19173888..19174551,2	MCF-7	breast:
8	chr19:19172859..19177096-chr19:19213191..19220004,7	K562	blood:
9	chr19:19141992..19145825-chr19:19171077..19177701,15	K562	blood:
10	chr19:19172595..19175925-chr19:19247411..19251399,4	MCF-7	breast:
11	chr19:19170465..19178046-chr19:19213939..19220242,15	K562	blood:
12	chr19:19109933..19111022-chr19:19173938..19174740,6	MCF-7	breast:
13	chr19:19161417..19167211-chr19:19171135..19175299,5	MCF-7	breast:
14	chr19:19169646..19176667-chr19:19241603..19249514,19	K562	blood:
15	chr19:19169646..19176603-chr19:19241603..19250623,23	K562	blood:
16	chr19:19143657..19146284-chr19:19174594..19176382,2	MCF-7	breast:
17	chr19:18943405..18943938-chr19:19173944..19174627,2	MCF-7	breast:
18	chr19:4182504..4183123-chr19:19174511..19175337,2	NB4	blood:
19	chr19:19176303..19177932-chr19:19191338..19193529,2	K562	blood:
20	chr19:19170341..19177029-chr19:19229928..19235464,11	K562	blood:
21	chr19:19169419..19177029-chr19:19229685..19233171,13	K562	blood:
22	chr1:76250892..76253394-chr19:19175061..19177790,2	K562	blood:
23	chr19:19176990..19179338-chr19:19181628..19184971,3	K562	blood:

No data

Variant related genes	Relation type
SLC25A42	TF binding region
SLC25A42	CpG island
ENSG00000105676	chromatin interactions
ENSG00000206620	chromatin interactions
ENSG00000181035	chromatin interactions
ENSG00000064607	chromatin interactions
ENSG00000077463	chromatin interactions
ENSG00000051128	chromatin interactions
ENSG00000064545	chromatin interactions
ENSG00000137955	chromatin interactions
ENSG00000111642	chromatin interactions

Extended variants
information (count: 113 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561331978	chr19:19174054-19174055	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs188495263	chr19:19174062-19174063	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs371642710	chr19:19174072-19174073	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs537300283	chr19:19174142-19174143	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs146554225	chr19:19174143-19174144	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs569446669	chr19:19174144-19174145	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs369431252	chr19:19174146-19174147	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs571097157	chr19:19174158-19174159	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs539044015	chr19:19174173-19174174	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs8111524	chr19:19174223-19174224	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs8110629	chr19:19174237-19174238	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs534620093	chr19:19174265-19174266	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs554887450	chr19:19174274-19174275	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs535187749	chr19:19174275-19174276	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs555241718	chr19:19174337-19174338	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs369428587	chr19:19174344-19174345	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs192711078	chr19:19174353-19174354	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs556681468	chr19:19174356-19174357	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs576627790	chr19:19174357-19174358	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs575397543	chr19:19174375-19174376	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs184776887	chr19:19174379-19174380	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs558996663	chr19:19174382-19174383	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs572660229	chr19:19174451-19174452	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs541352278	chr19:19174462-19174463	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs561673113	chr19:19174470-19174471	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs530215787	chr19:19174490-19174491	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs373215873	chr19:19174566-19174567	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs543623774	chr19:19174581-19174582	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs563015354	chr19:19174584-19174585	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs189234209	chr19:19174586-19174587	Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs551712916	chr19:19174634-19174635	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs180774346	chr19:19174651-19174652	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs528132434	chr19:19174671-19174672	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs548162644	chr19:19174673-19174674	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs568380321	chr19:19174681-19174682	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs143308984	chr19:19174712-19174713	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs557216533	chr19:19174742-19174743	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs570119881	chr19:19174807-19174808	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs539145936	chr19:19174831-19174832	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs559134784	chr19:19174960-19174961	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs148322727	chr19:19174969-19174970	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs541443777	chr19:19174971-19174972	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs554929341	chr19:19174973-19174974	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs12981861	chr19:19175006-19175007	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs544120135	chr19:19175025-19175026	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs575097838	chr19:19175100-19175101	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs10402411	chr19:19175245-19175246	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs373382773	chr19:19175251-19175252	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs10404077	chr19:19175297-19175298	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs545488355	chr19:19175329-19175330	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
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
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
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	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
Bladder cancer	21909424	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:19170600-19174200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr19:19170800-19174200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:19172200-19174400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
4	chr19:19173000-19174600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr19:19173400-19174200	Enhancers	Spleen	Spleen
6	chr19:19173400-19174200	Flanking Active TSS	K562	blood
7	chr19:19173600-19174200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
8	chr19:19173600-19174400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr19:19173800-19174200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr19:19173800-19174200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr19:19173800-19174200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr19:19173800-19174200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
13	chr19:19173800-19174200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr19:19173800-19174200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr19:19173800-19174200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
16	chr19:19173800-19174200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
17	chr19:19173800-19174200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
18	chr19:19173800-19174200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr19:19173800-19174200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr19:19173800-19174200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr19:19173800-19174200	Flanking Active TSS	Brain Angular Gyrus	brain
22	chr19:19173800-19174200	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr19:19173800-19174200	Flanking Active TSS	Brain Cingulate Gyrus	brain
24	chr19:19173800-19174200	Flanking Active TSS	Brain Germinal Matrix	brain
25	chr19:19173800-19174200	Flanking Active TSS	Brain Hippocampus Middle	brain
26	chr19:19173800-19174200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
27	chr19:19173800-19174200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr19:19173800-19174200	Flanking Active TSS	Brain Substantia Nigra	brain
29	chr19:19173800-19174200	Flanking Active TSS	Colon Smooth Muscle	Colon
30	chr19:19173800-19174200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr19:19173800-19174200	Enhancers	Fetal Brain Male	brain
32	chr19:19173800-19174200	Flanking Active TSS	Fetal Brain Female	brain
33	chr19:19173800-19174200	Flanking Active TSS	Fetal Heart	heart
34	chr19:19173800-19174200	Flanking Active TSS	Fetal Intestine Large	intestine
35	chr19:19173800-19174200	Flanking Active TSS	Fetal Muscle Leg	muscle
36	chr19:19173800-19174200	Flanking Active TSS	Stomach Smooth Muscle	stomach
37	chr19:19173800-19174200	Flanking Active TSS	GM12878-XiMat	blood
38	chr19:19173800-19174200	Flanking Active TSS	HepG2	liver
39	chr19:19173800-19174200	Flanking Active TSS	NHDF-Ad	bronchial
40	chr19:19173800-19174400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
41	chr19:19173800-19174400	Flanking Active TSS	Primary B cells from cord blood	blood
42	chr19:19173800-19174400	Flanking Active TSS	Primary T cells from cord blood	blood
43	chr19:19173800-19174400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
44	chr19:19173800-19174400	Flanking Active TSS	Primary hematopoietic stem cells	blood
45	chr19:19173800-19174400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
46	chr19:19173800-19174400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr19:19173800-19174400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr19:19173800-19174400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr19:19173800-19174400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr19:19173800-19174400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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