Variant report

Variant	esv3339801
Chromosome Location	chr19:18653352-18655350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:542)
CpG islands
(count:428)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:542 , 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	chr19:18654723-18655389	K562	blood:	n/a	n/a
2	ATF1	chr19:18654709-18655209	K562	blood:	n/a	n/a
3	ATF2	chr19:18654677-18655190	GM12878	blood:	n/a	n/a
4	ATF2	chr19:18654720-18655068	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr19:18654747-18655106	K562	blood:	n/a	n/a
6	BCL3	chr19:18654653-18655249	K562	blood:	n/a	n/a
7	BCLAF1	chr19:18654617-18655225	K562	blood:	n/a	n/a
8	BCLAF1	chr19:18654656-18655175	K562	blood:	n/a	n/a
9	BCLAF1	chr19:18654639-18655145	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:18654701-18655935	K562	blood:	n/a	n/a
11	BHLHE40	chr19:18653850-18654041	GM12878	blood:	n/a	chr19:18653936-18653952
12	BHLHE40	chr19:18654660-18655082	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:18653849-18653869	K562	blood:	n/a	n/a
14	BRCA1	chr19:18654814-18655014	GM12878	blood:	n/a	n/a
15	CBX3	chr19:18654619-18655458	K562	blood:	n/a	n/a
16	CBX3	chr19:18654720-18655204	K562	blood:	n/a	n/a
17	CCNT2	chr19:18653932-18653960	K562	blood:	n/a	n/a
18	CCNT2	chr19:18654368-18655218	K562	blood:	n/a	chr19:18654390-18654399 chr19:18655020-18655040
19	CEBPB	chr19:18654839-18655780	K562	blood:	n/a	chr19:18655618-18655629
20	CEBPB	chr19:18654663-18655942	K562	blood:	n/a	chr19:18655618-18655629
21	CEBPD	chr19:18654573-18655402	K562	blood:	n/a	n/a
22	CEBPD	chr19:18654164-18654632	HepG2	liver:	n/a	n/a
23	CEBPD	chr19:18654642-18655360	K562	blood:	n/a	n/a
24	CHD1	chr19:18654665-18655129	GM12878	blood:	n/a	n/a
25	CHD2	chr19:18654243-18655137	K562	blood:	n/a	n/a
26	CHD2	chr19:18653579-18653616	GM12878	blood:	n/a	n/a
27	CHD2	chr19:18654303-18654534	HepG2	liver:	n/a	n/a
28	CHD2	chr19:18654222-18655118	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr19:18654261-18655073	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr19:18653887-18653997	GM12878	blood:	n/a	n/a
31	CHD2	chr19:18654203-18655183	GM12878	blood:	n/a	n/a
32	CREB1	chr19:18654732-18655071	A549	lung:	n/a	n/a
33	CREB1	chr19:18653722-18655186	GM12878	blood:	n/a	n/a
34	CREB1	chr19:18654174-18655309	K562	blood:	n/a	n/a
35	CREB1	chr19:18654184-18654531	A549	lung:	n/a	n/a
36	CTCF	chr19:18654860-18655010	GM06990	blood:	n/a	n/a
37	CTCF	chr19:18654800-18654950	GM12872	blood:	n/a	n/a
38	CTCF	chr19:18654884-18655071	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr19:18654863-18655095	GM10266	blood:	n/a	n/a
40	CTCF	chr19:18654952-18655025	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr19:18654860-18655010	AG09319	gingival:	n/a	n/a
42	CTCF	chr19:18654797-18655119	K562	blood:	n/a	n/a
43	CTCF	chr19:18654880-18655030	GM12865	blood:	n/a	n/a
44	CTCF	chr19:18654922-18655032	LNCaP	prostate:	n/a	n/a
45	CTCF	chr19:18654900-18655050	GM12873	blood:	n/a	n/a
46	CTCF	chr19:18654940-18655090	GM12864	blood:	n/a	n/a
47	CTCF	chr19:18654860-18655010	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr19:18654920-18655070	GM12871	blood:	n/a	n/a
49	CTCF	chr19:18654860-18655010	NHEK	skin:	n/a	n/a
50	CTCF	chr19:18654940-18655090	HFF	foreskin:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18654267-18654317	U87	brain:	n/a
2	chr19:18654267-18654317	U87	brain:	n/a
3	chr19:18654548-18654598	GM06990	blood:	n/a
4	chr19:18654361-18654411	SK-N-MC	brain:	n/a
5	chr19:18654949-18654999	SK-N-MC	brain:	n/a
6	chr19:18654433-18654483	AG04450	lung:	fetal
7	chr19:18654361-18654411	ProgFib	skin:	n/a
8	chr19:18654949-18654999	U87	brain:	n/a
9	chr19:18653918-18653968	AG04449	skin:	fetal
10	chr19:18654433-18654483	Jurkat	blood:	n/a
11	chr19:18654949-18654999	RPTEC	kidney:	n/a
12	chr19:18654267-18654317	HRPEpiC	eye:	n/a
13	chr19:18654433-18654483	HPAEpiC	pulmonary alveolar:	n/a
14	chr19:18654681-18654731	HUVEC	blood vessel:	n/a
15	chr19:18654548-18654598	AG10803	skin:	n/a
16	chr19:18654681-18654731	Hela-S3	cervix:	n/a
17	chr19:18654361-18654411	BJ	skin:	n/a
18	chr19:18654681-18654731	AG09319	gingival:	n/a
19	chr19:18654548-18654598	RPTEC	kidney:	n/a
20	chr19:18654681-18654731	MCF-7	breast:	n/a
21	chr19:18653918-18653968	AG09309	skin:	n/a
22	chr19:18654361-18654411	MCF10A-Er-Src	breast:	n/a
23	chr19:18654548-18654598	AG04450	lung:	fetal
24	chr19:18654949-18654999	IMR90	lung:	fetal
25	chr19:18654681-18654731	H1-hESC	embryonic stem cell:	embryo
26	chr19:18653918-18653968	ProgFib	skin:	n/a
27	chr19:18654433-18654483	HCF	heart:	n/a
28	chr19:18654548-18654598	HepG2	liver:	n/a
29	chr19:18654433-18654483	RPTEC	kidney:	n/a
30	chr19:18654433-18654483	NB4	blood:	n/a
31	chr19:18654681-18654731	HL-60	blood:	n/a
32	chr19:18654949-18654999	PrEC	prostate:	n/a
33	chr19:18654361-18654411	HCT-116	colon:	n/a
34	chr19:18654681-18654731	PANC-1	pancreas:	n/a
35	chr19:18654433-18654483	H1-hESC	embryonic stem cell:	embryo
36	chr19:18653918-18653968	NH-A	brain:	n/a
37	chr19:18653918-18653968	HRE	kidney:	n/a
38	chr19:18654681-18654731	NH-A	brain:	n/a
39	chr19:18654267-18654317	AG04449	skin:	fetal
40	chr19:18654361-18654411	HL-60	blood:	n/a
41	chr19:18654548-18654598	AG09319	gingival:	n/a
42	chr19:18654681-18654731	SK-N-SH	brain:	n/a
43	chr19:18653918-18653968	U87	brain:	n/a
44	chr19:18654681-18654731	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:18654681-18654731	Caco-2	colon:	n/a
46	chr19:18654433-18654483	HL-60	blood:	n/a
47	chr19:18654433-18654483	NHBE	bronchial:	n/a
48	chr19:18654267-18654317	AoSMC	blood vessel:	n/a
49	chr19:18654949-18654999	GM06990	blood:	n/a
50	chr19:18654681-18654731	U87	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18630875..18635401-chr19:18651200..18655863,9	MCF-7	breast:
2	chr19:18653459..18656385-chr19:18699225..18703130,9	K562	blood:
3	chr19:18651038..18656783-chr19:18680897..18685521,14	K562	blood:
4	chr19:18653476..18656385-chr19:18700159..18703130,5	K562	blood:
5	chr19:18629748..18634724-chr19:18652806..18658264,15	K562	blood:
6	chr19:18640357..18642464-chr19:18650908..18653787,2	MCF-7	breast:
7	chr19:18629959..18634840-chr19:18652830..18656407,13	K562	blood:
8	chr19:18629917..18634196-chr19:18652150..18655589,5	MCF-7	breast:
9	chr19:18652388..18654838-chr19:18668474..18670630,2	K562	blood:
10	chr19:18648889..18650815-chr19:18652717..18655388,4	K562	blood:
11	chr19:18651498..18655648-chr19:18680777..18683781,5	MCF-7	breast:
12	chr19:18652388..18655450-chr19:18667016..18670630,4	K562	blood:
13	chr19:18653470..18656783-chr19:18680897..18684291,6	K562	blood:
14	chr19:18653886..18656782-chr19:18668675..18670368,2	MCF-7	breast:
15	chr19:18653032..18656930-chr19:18667045..18670995,8	MCF-7	breast:
16	chr19:18649378..18653671-chr19:18667425..18670328,5	MCF-7	breast:
17	chr19:18642522..18644970-chr19:18651017..18653848,4	K562	blood:
18	chr19:18536175..18537815-chr19:18653605..18655763,2	MCF-7	breast:
19	chr19:18653590..18656982-chr19:18704077..18706738,3	K562	blood:

No data

Variant related genes	Relation type
FKBP8	TF binding region
FKBP8	CpG island
ENSG00000105701	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000268938	chromatin interactions
ENSG00000269191	chromatin interactions
ENSG00000105656	chromatin interactions
ENSG00000130511	chromatin interactions
ENSG00000006016	chromatin interactions
ENSG00000006015	chromatin interactions
ENSG00000105700	chromatin interactions

Extended variants
information (count: 53 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:53 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543421546	chr19:18653387-18653388	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs563716211	chr19:18653412-18653413	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs577249623	chr19:18653428-18653429	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs546306090	chr19:18653453-18653454	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs559516921	chr19:18653516-18653517	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs528701205	chr19:18653554-18653555	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs548384463	chr19:18653567-18653568	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs561998478	chr19:18653593-18653594	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs139218213	chr19:18653621-18653622	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs550275672	chr19:18653750-18653751	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs373784248	chr19:18653765-18653766	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs570462724	chr19:18653766-18653767	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs539140908	chr19:18653791-18653792	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs113569692	chr19:18653804-18653805	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs10402554	chr19:18653921-18653922	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs147533062	chr19:18653985-18653986	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs535596265	chr19:18654122-18654123	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs555620558	chr19:18654232-18654233	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs575413299	chr19:18654269-18654270	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs538173892	chr19:18654373-18654374	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs557049782	chr19:18654429-18654430	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs183945390	chr19:18654505-18654506	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs545883303	chr19:18654555-18654556	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs79235328	chr19:18654561-18654562	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs78334826	chr19:18654575-18654576	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs62135138	chr19:18654580-18654581	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs79392397	chr19:18654582-18654583	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs79802726	chr19:18654587-18654588	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs76615278	chr19:18654588-18654589	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs116706017	chr19:18654608-18654609	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs367564924	chr19:18654743-18654744	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs116927317	chr19:18654783-18654784	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs549310063	chr19:18654839-18654840	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs377286022	chr19:18654878-18654879	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs73923126	chr19:18654884-18654885	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs563925667	chr19:18654924-18654925	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs532896947	chr19:18654939-18654940	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs182665435	chr19:18654941-18654942	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs566542715	chr19:18654992-18654993	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs535558018	chr19:18654994-18654995	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs549182816	chr19:18655040-18655041	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs566123490	chr19:18655050-18655051	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs537746610	chr19:18655060-18655061	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs558073647	chr19:18655080-18655081	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs577868638	chr19:18655203-18655204	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs11670950	chr19:18655215-18655216	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs562852304	chr19:18655293-18655294	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs539401982	chr19:18655300-18655301	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs552972113	chr19:18655307-18655308	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs368525516	chr19:18655308-18655309	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18632800-18654600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:18633000-18653400	Weak transcription	Psoas Muscle	Psoas
3	chr19:18633800-18653400	Weak transcription	Fetal Kidney	kidney
4	chr19:18652000-18653600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr19:18652400-18653400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:18652400-18653600	Enhancers	Fetal Brain Male	brain
7	chr19:18652600-18653600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr19:18652600-18653800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
9	chr19:18652600-18654600	Active TSS	Brain Angular Gyrus	brain
10	chr19:18652800-18653400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr19:18652800-18653400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr19:18652800-18653400	Enhancers	Placenta	Placenta
13	chr19:18652800-18653400	Weak transcription	Gastric	stomach
14	chr19:18652800-18653400	Enhancers	Spleen	Spleen
15	chr19:18652800-18653600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
16	chr19:18652800-18653600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr19:18652800-18653600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr19:18652800-18653600	Enhancers	Fetal Heart	heart
19	chr19:18652800-18653600	Enhancers	Stomach Mucosa	stomach
20	chr19:18652800-18653600	Flanking Active TSS	Dnd41	blood
21	chr19:18652800-18653600	Flanking Active TSS	NHEK	skin
22	chr19:18652800-18653800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr19:18652800-18653800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr19:18652800-18654800	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr19:18652800-18654800	Active TSS	HSMM	muscle
26	chr19:18653000-18653400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr19:18653000-18653400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr19:18653000-18653400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:18653000-18653400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr19:18653000-18653400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr19:18653000-18653400	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr19:18653000-18653400	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr19:18653000-18653400	Flanking Active TSS	Fetal Brain Female	brain
34	chr19:18653000-18653400	Flanking Active TSS	K562	blood
35	chr19:18653000-18653400	Flanking Active TSS	NHLF	lung
36	chr19:18653000-18653600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr19:18653000-18653600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr19:18653000-18653600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr19:18653000-18653600	Flanking Active TSS	Primary T cells from cord blood	blood
40	chr19:18653000-18653600	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr19:18653000-18653600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr19:18653000-18653600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr19:18653000-18653600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
44	chr19:18653000-18653600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr19:18653000-18653600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:18653000-18653600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
47	chr19:18653000-18653600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr19:18653000-18653600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr19:18653000-18653600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:18653000-18653600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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