Variant report

Variant	esv3446773
Chromosome Location	chr19:18652777-18655825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:560)
CpG islands
(count:428)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr19:18654720-18655068	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:18654677-18655190	GM12878	blood:	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	chr19:18654639-18655145	GM12878	blood:	n/a	n/a
8	BCLAF1	chr19:18654617-18655225	K562	blood:	n/a	n/a
9	BCLAF1	chr19:18654656-18655175	K562	blood:	n/a	n/a
10	BHLHE40	chr19:18653849-18653869	K562	blood:	n/a	n/a
11	BHLHE40	chr19:18655805-18655820	HepG2	liver:	n/a	n/a
12	BHLHE40	chr19:18654660-18655082	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:18653850-18654041	GM12878	blood:	n/a	chr19:18653936-18653952
14	BHLHE40	chr19:18654701-18655935	K562	blood:	n/a	n/a
15	BRCA1	chr19:18654814-18655014	GM12878	blood:	n/a	n/a
16	CBX3	chr19:18654619-18655458	K562	blood:	n/a	n/a
17	CBX3	chr19:18654720-18655204	K562	blood:	n/a	n/a
18	CCNT2	chr19:18654368-18655218	K562	blood:	n/a	chr19:18654390-18654399 chr19:18655020-18655040
19	CCNT2	chr19:18653932-18653960	K562	blood:	n/a	n/a
20	CEBPB	chr19:18655566-18655713	A549	lung:	n/a	chr19:18655618-18655629
21	CEBPB	chr19:18654663-18655942	K562	blood:	n/a	chr19:18655618-18655629
22	CEBPB	chr19:18654839-18655780	K562	blood:	n/a	chr19:18655618-18655629
23	CEBPB	chr19:18655566-18655732	HepG2	liver:	n/a	chr19:18655618-18655629
24	CEBPD	chr19:18654642-18655360	K562	blood:	n/a	n/a
25	CEBPD	chr19:18654164-18654632	HepG2	liver:	n/a	n/a
26	CEBPD	chr19:18654573-18655402	K562	blood:	n/a	n/a
27	CHD1	chr19:18654665-18655129	GM12878	blood:	n/a	n/a
28	CHD2	chr19:18654222-18655118	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr19:18653887-18653997	GM12878	blood:	n/a	n/a
30	CHD2	chr19:18653579-18653616	GM12878	blood:	n/a	n/a
31	CHD2	chr19:18654303-18654534	HepG2	liver:	n/a	n/a
32	CHD2	chr19:18654203-18655183	GM12878	blood:	n/a	n/a
33	CHD2	chr19:18654261-18655073	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:18654243-18655137	K562	blood:	n/a	n/a
35	CREB1	chr19:18653722-18655186	GM12878	blood:	n/a	n/a
36	CREB1	chr19:18654184-18654531	A549	lung:	n/a	n/a
37	CREB1	chr19:18654174-18655309	K562	blood:	n/a	n/a
38	CREB1	chr19:18654732-18655071	A549	lung:	n/a	n/a
39	CTCF	chr19:18654784-18655162	K562	blood:	n/a	n/a
40	CTCF	chr19:18655020-18655170	BE2_C	brain:	n/a	n/a
41	CTCF	chr19:18654840-18654990	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:18654956-18655018	GM20000	blood:	n/a	n/a
43	CTCF	chr19:18654702-18655154	K562	blood:	n/a	chr19:18654726-18654739
44	CTCF	chr19:18654880-18655030	GM12866	blood:	n/a	n/a
45	CTCF	chr19:18654797-18655119	K562	blood:	n/a	n/a
46	CTCF	chr19:18653920-18654070	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr19:18654900-18655050	GM12874	blood:	n/a	n/a
48	CTCF	chr19:18654580-18655367	A549	lung:	n/a	chr19:18654726-18654739
49	CTCF	chr19:18654860-18655010	GM12868	blood:	n/a	n/a
50	CTCF	chr19:18654840-18654990	HPAF	blood vessel:	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	chr19:18654548-18654598	HL-60	blood:	n/a
2	chr19:18654548-18654598	HL-60	blood:	n/a
3	chr19:18653918-18653968	MCF10A-Er-Src	breast:	n/a
4	chr19:18654361-18654411	NB4	blood:	n/a
5	chr19:18654361-18654411	Jurkat	blood:	n/a
6	chr19:18654949-18654999	HCM	heart:	n/a
7	chr19:18653918-18653968	HIPEpiC	eye:	n/a
8	chr19:18654548-18654598	GM06990	blood:	n/a
9	chr19:18654548-18654598	HCM	heart:	n/a
10	chr19:18654548-18654598	GM12892	blood:	n/a
11	chr19:18654548-18654598	PANC-1	pancreas:	n/a
12	chr19:18654267-18654317	HCT-116	colon:	n/a
13	chr19:18654361-18654411	HMEC	breast:	n/a
14	chr19:18654267-18654317	ovcar-3	ovarian:	n/a
15	chr19:18654361-18654411	PFSK-1	brain:	n/a
16	chr19:18654433-18654483	Caco-2	colon:	n/a
17	chr19:18654949-18654999	GM12891	blood:	n/a
18	chr19:18654267-18654317	AG04450	lung:	fetal
19	chr19:18654681-18654731	HCF	heart:	n/a
20	chr19:18654433-18654483	GM06990	blood:	n/a
21	chr19:18654267-18654317	NH-A	brain:	n/a
22	chr19:18654361-18654411	HL-60	blood:	n/a
23	chr19:18654433-18654483	CMK	blood:	n/a
24	chr19:18654361-18654411	GM06990	blood:	n/a
25	chr19:18654681-18654731	HIPEpiC	eye:	n/a
26	chr19:18654433-18654483	BE2_C	brain:	n/a
27	chr19:18653918-18653968	HUVEC	blood vessel:	n/a
28	chr19:18653918-18653968	HPAEpiC	pulmonary alveolar:	n/a
29	chr19:18654433-18654483	Jurkat	blood:	n/a
30	chr19:18654949-18654999	HNPCEpiC	eye:	n/a
31	chr19:18654548-18654598	HAEpiC	amniotic membrane:	n/a
32	chr19:18654361-18654411	SK-N-SH_RA	brain:	n/a
33	chr19:18653918-18653968	Jurkat	blood:	n/a
34	chr19:18653918-18653968	HNPCEpiC	eye:	n/a
35	chr19:18654433-18654483	GM12892	blood:	n/a
36	chr19:18654433-18654483	HEK293	kidney:	embryo
37	chr19:18654548-18654598	Hepatocyte	liver:	n/a
38	chr19:18654548-18654598	GM12878	blood:	n/a
39	chr19:18654361-18654411	HEK293	kidney:	embryo
40	chr19:18654361-18654411	SK-N-SH	brain:	n/a
41	chr19:18654267-18654317	CMK	blood:	n/a
42	chr19:18654267-18654317	Jurkat	blood:	n/a
43	chr19:18654681-18654731	SK-N-MC	brain:	n/a
44	chr19:18654267-18654317	K562	blood:	n/a
45	chr19:18654361-18654411	CMK	blood:	n/a
46	chr19:18654681-18654731	SK-N-SH_RA	brain:	n/a
47	chr19:18654949-18654999	GM06990	blood:	n/a
48	chr19:18654267-18654317	HEK293	kidney:	embryo
49	chr19:18654267-18654317	AG04449	skin:	fetal
50	chr19:18653918-18653968	HCPEpiC	choroid plexus:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18640357..18642464-chr19:18650908..18653787,2	MCF-7	breast:
2	chr19:18630875..18635401-chr19:18651200..18655863,9	MCF-7	breast:
3	chr19:18653590..18656982-chr19:18704077..18706738,3	K562	blood:
4	chr19:18629748..18634724-chr19:18652806..18658264,15	K562	blood:
5	chr19:18653470..18656783-chr19:18680897..18684291,6	K562	blood:
6	chr19:18653476..18656385-chr19:18700159..18703130,5	K562	blood:
7	chr19:18629917..18634196-chr19:18652150..18655589,5	MCF-7	breast:
8	chr19:18648889..18650815-chr19:18652717..18655388,4	K562	blood:
9	chr19:18642522..18644970-chr19:18651017..18653848,4	K562	blood:
10	chr19:18652388..18654838-chr19:18668474..18670630,2	K562	blood:
11	chr19:18653886..18656782-chr19:18668675..18670368,2	MCF-7	breast:
12	chr19:18651498..18655648-chr19:18680777..18683781,5	MCF-7	breast:
13	chr19:18653032..18656930-chr19:18667045..18670995,8	MCF-7	breast:
14	chr19:18652388..18655450-chr19:18667016..18670630,4	K562	blood:
15	chr19:18536175..18537815-chr19:18653605..18655763,2	MCF-7	breast:
16	chr19:18650801..18653024-chr19:18671456..18674102,2	K562	blood:
17	chr19:18649378..18653671-chr19:18667425..18670328,5	MCF-7	breast:
18	chr19:18653459..18656385-chr19:18699225..18703130,9	K562	blood:
19	chr19:18651038..18656783-chr19:18680897..18685521,14	K562	blood:
20	chr19:18629959..18634840-chr19:18652830..18656407,13	K562	blood:

No data

Variant related genes	Relation type
FKBP8	TF binding region
FKBP8	CpG island
ENSG00000269191	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000268030	chromatin interactions
ENSG00000006015	chromatin interactions
ENSG00000105656	chromatin interactions
ENSG00000105701	chromatin interactions
ENSG00000006016	chromatin interactions
ENSG00000105700	chromatin interactions
ENSG00000130511	chromatin interactions
ENSG00000268938	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563584235	chr19:18652809-18652810	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs368293221	chr19:18652815-18652816	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs532658624	chr19:18652819-18652820	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs10854166	chr19:18652844-18652845	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	mRNA abundance
5	rs190035707	chr19:18652885-18652886	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs528737936	chr19:18652920-18652921	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs532395591	chr19:18652951-18652952	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs548517905	chr19:18652962-18652963	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs567709302	chr19:18653014-18653015	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs536603059	chr19:18653054-18653055	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs36004044	chr19:18653056-18653057	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs182201637	chr19:18653097-18653098	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs570425062	chr19:18653122-18653123	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs544395564	chr19:18653137-18653138	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs552496839	chr19:18653223-18653224	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
16	rs539537648	chr19:18653241-18653242	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
17	rs186552068	chr19:18653273-18653274	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
18	rs10421611	chr19:18653293-18653294	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs141965305	chr19:18653309-18653310	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
20	rs192021720	chr19:18653315-18653316	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
21	rs575496595	chr19:18653329-18653330	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
22	rs11574804	chr19:18653344-18653345	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	rs139218213	chr19:18653621-18653622	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs550275672	chr19:18653750-18653751	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs373784248	chr19:18653765-18653766	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs570462724	chr19:18653766-18653767	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs539140908	chr19:18653791-18653792	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	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
37	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
38	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
39	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
40	rs555620558	chr19:18654232-18654233	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs575413299	chr19:18654269-18654270	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs538173892	chr19:18654373-18654374	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs557049782	chr19:18654429-18654430	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs183945390	chr19:18654505-18654506	Weak transcription Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs545883303	chr19:18654555-18654556	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs79235328	chr19:18654561-18654562	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs78334826	chr19:18654575-18654576	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs62135138	chr19:18654580-18654581	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs79392397	chr19:18654582-18654583	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs79802726	chr19:18654587-18654588	Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Breast cancer	22522925	CNVD

Chromatin state (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18632800-18652800	Weak transcription	Stomach Mucosa	stomach
2	chr19:18632800-18654600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr19:18633000-18653400	Weak transcription	Psoas Muscle	Psoas
4	chr19:18633200-18653200	Weak transcription	Right Atrium	heart
5	chr19:18633800-18652800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:18633800-18653400	Weak transcription	Fetal Kidney	kidney
7	chr19:18641800-18652800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr19:18641800-18653000	Strong transcription	Fetal Stomach	stomach
9	chr19:18642000-18652800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr19:18642000-18652800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr19:18642000-18652800	Strong transcription	Fetal Intestine Small	intestine
12	chr19:18642200-18652800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr19:18642200-18652800	Strong transcription	Fetal Thymus	thymus
14	chr19:18642200-18653000	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr19:18644200-18652800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr19:18645200-18652800	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr19:18646000-18652800	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr19:18646000-18652800	Strong transcription	Primary B cells from peripheral blood	blood
19	chr19:18646200-18652800	Strong transcription	Primary hematopoietic stem cells	blood
20	chr19:18646600-18652800	Strong transcription	Fetal Brain Female	brain
21	chr19:18646600-18653200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr19:18647000-18653200	Weak transcription	Small Intestine	intestine
23	chr19:18647800-18653200	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr19:18648400-18653000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr19:18649400-18653200	Weak transcription	HSMMtube	muscle
26	chr19:18649800-18652800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr19:18650000-18652800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr19:18650000-18652800	Strong transcription	Colon Smooth Muscle	Colon
29	chr19:18650200-18652800	Strong transcription	HSMM	muscle
30	chr19:18650600-18652800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr19:18651200-18652800	Weak transcription	Left Ventricle	heart
32	chr19:18651200-18652800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr19:18651800-18653000	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr19:18652000-18652800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
35	chr19:18652000-18652800	Genic enhancers	Placenta	Placenta
36	chr19:18652000-18653000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr19:18652000-18653000	Genic enhancers	Brain Inferior Temporal Lobe	brain
38	chr19:18652000-18653200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr19:18652000-18653600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr19:18652200-18652800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr19:18652200-18652800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr19:18652200-18652800	Genic enhancers	Primary T cells fromperipheralblood	blood
43	chr19:18652200-18652800	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr19:18652200-18652800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr19:18652200-18652800	Genic enhancers	Stomach Smooth Muscle	stomach
46	chr19:18652200-18652800	Transcr. at gene 5' and 3'	Dnd41	blood
47	chr19:18652200-18653000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr19:18652200-18653000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr19:18652200-18653000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr19:18652200-18653000	Strong transcription	Colonic Mucosa	Colon

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