Variant report

Variant	esv13500
Chromosome Location	chr19:41283063-41285263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:601)
CpG islands
(count:734)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:601 , 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	chr19:41284214-41285201	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41283523-41284177	K562	blood:	n/a	n/a
3	ARID3A	chr19:41282972-41283984	HepG2	liver:	n/a	n/a
4	ATF1	chr19:41283029-41284572	K562	blood:	n/a	n/a
5	ATF2	chr19:41282934-41283894	GM12878	blood:	n/a	n/a
6	ATF2	chr19:41282825-41283855	GM12878	blood:	n/a	n/a
7	ATF2	chr19:41284796-41285246	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:41283955-41284260	K562	blood:	n/a	chr19:41284028-41284048
9	ATF3	chr19:41282795-41284237	A549	lung:	n/a	chr19:41284028-41284048 chr19:41283501-41283514
10	BACH1	chr19:41284242-41284811	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr19:41283096-41283473	GM12878	blood:	n/a	n/a
12	BCL11A	chr19:41282969-41283518	GM12878	blood:	n/a	chr19:41283403-41283412
13	BCL11A	chr19:41283081-41283349	GM12878	blood:	n/a	n/a
14	BCL3	chr19:41282605-41284860	A549	lung:	n/a	chr19:41284233-41284246 chr19:41284824-41284833 chr19:41284149-41284158 chr19:41284141-41284150 chr19:41283403-41283412 chr19:41284234-41284247
15	BCL3	chr19:41282648-41285310	A549	lung:	n/a	chr19:41284233-41284246 chr19:41284824-41284833 chr19:41284149-41284158 chr19:41284141-41284150 chr19:41283403-41283412 chr19:41284234-41284247
16	BCL3	chr19:41283007-41283418	GM12878	blood:	n/a	chr19:41283403-41283412
17	BCLAF1	chr19:41282905-41283981	GM12878	blood:	n/a	chr19:41283403-41283412
18	BCLAF1	chr19:41282831-41284441	GM12878	blood:	n/a	chr19:41284233-41284246 chr19:41284149-41284158 chr19:41284141-41284150 chr19:41283403-41283412 chr19:41284234-41284247
19	BHLHE40	chr19:41282878-41284707	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:41283062-41284796	K562	blood:	n/a	n/a
21	BHLHE40	chr19:41283159-41285010	HepG2	liver:	n/a	n/a
22	BRCA1	chr19:41283240-41284687	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr19:41283592-41284380	GM12878	blood:	n/a	n/a
24	BRCA1	chr19:41283277-41283808	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr19:41283061-41283848	HepG2	liver:	n/a	n/a
26	BRCA1	chr19:41284677-41284817	GM12878	blood:	n/a	n/a
27	CBX3	chr19:41282878-41283977	K562	blood:	n/a	n/a
28	CBX3	chr19:41284089-41284592	K562	blood:	n/a	n/a
29	CBX3	chr19:41284637-41285216	K562	blood:	n/a	n/a
30	CCNT2	chr19:41283756-41284386	K562	blood:	n/a	chr19:41283866-41283875 chr19:41284003-41284012
31	CEBPB	chr19:41283189-41283675	A549	lung:	n/a	chr19:41283651-41283659
32	CEBPB	chr19:41283087-41283449	GM12878	blood:	n/a	n/a
33	CEBPB	chr19:41283254-41283744	H1-hESC	embryonic stem cell:	n/a	chr19:41283651-41283659
34	CEBPB	chr19:41283370-41284447	Hela-S3	cervix:	n/a	chr19:41283651-41283659 chr19:41283984-41283992
35	CEBPB	chr19:41283204-41283744	K562	blood:	n/a	chr19:41283651-41283659
36	CEBPB	chr19:41283246-41283635	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:41282770-41283918	GM12878	blood:	n/a	chr19:41283651-41283659
38	CEBPD	chr19:41283608-41284316	HepG2	liver:	n/a	n/a
39	CEBPZ	chr19:41283487-41284162	HepG2	liver:	n/a	n/a
40	CHD1	chr19:41282866-41283968	GM12878	blood:	n/a	n/a
41	CHD1	chr19:41284206-41284295	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr19:41284791-41285083	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr19:41283490-41283869	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr19:41284178-41284976	GM12878	blood:	n/a	n/a
45	CHD2	chr19:41283640-41284328	HepG2	liver:	n/a	n/a
46	CHD2	chr19:41283453-41284339	K562	blood:	n/a	n/a
47	CHD2	chr19:41282745-41284890	GM12878	blood:	n/a	n/a
48	CHD2	chr19:41283335-41284831	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr19:41283227-41284920	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr19:41283162-41284451	K562	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41283578-41283628	HEEpiC	esophagus:	n/a
2	chr19:41283667-41283717	HepG2	liver:	n/a
3	chr19:41283578-41283628	HEEpiC	esophagus:	n/a
4	chr19:41283667-41283717	HepG2	liver:	n/a
5	chr19:41284057-41284107	H1-hESC	embryonic stem cell:	embryo
6	chr19:41284348-41284398	U87	brain:	n/a
7	chr19:41283090-41283140	BJ	skin:	n/a
8	chr19:41284032-41284082	HMEC	breast:	n/a
9	chr19:41284348-41284398	HAEpiC	amniotic membrane:	n/a
10	chr19:41283506-41283556	GM12891	blood:	n/a
11	chr19:41283667-41283717	BJ	skin:	n/a
12	chr19:41284348-41284398	PFSK-1	brain:	n/a
13	chr19:41284057-41284107	Hepatocyte	liver:	n/a
14	chr19:41284057-41284107	BE2_C	brain:	n/a
15	chr19:41283407-41283457	HEEpiC	esophagus:	n/a
16	chr19:41284057-41284107	ovcar-3	ovarian:	n/a
17	chr19:41284070-41284120	AG04449	skin:	fetal
18	chr19:41283407-41283457	SKMC	muscle:	n/a
19	chr19:41283578-41283628	HAEpiC	amniotic membrane:	n/a
20	chr19:41284348-41284398	NH-A	brain:	n/a
21	chr19:41283667-41283717	BE2_C	brain:	n/a
22	chr19:41284234-41284284	SK-N-SH_RA	brain:	n/a
23	chr19:41284032-41284082	NB4	blood:	n/a
24	chr19:41284006-41284056	MCF-7	breast:	n/a
25	chr19:41284006-41284056	IMR90	lung:	fetal
26	chr19:41284057-41284107	HPAEpiC	pulmonary alveolar:	n/a
27	chr19:41284006-41284056	HIPEpiC	eye:	n/a
28	chr19:41284057-41284107	AG04450	lung:	fetal
29	chr19:41283506-41283556	HL-60	blood:	n/a
30	chr19:41284070-41284120	IMR90	lung:	fetal
31	chr19:41284234-41284284	Hepatocyte	liver:	n/a
32	chr19:41284057-41284107	SAEC	small airway:	n/a
33	chr19:41284006-41284056	K562	blood:	n/a
34	chr19:41284348-41284398	Hepatocyte	liver:	n/a
35	chr19:41284348-41284398	RPTEC	kidney:	n/a
36	chr19:41284057-41284107	AG09309	skin:	n/a
37	chr19:41283407-41283457	PANC-1	pancreas:	n/a
38	chr19:41284057-41284107	NHDF-neo	bronchial:	n/a
39	chr19:41284070-41284120	K562	blood:	n/a
40	chr19:41284032-41284082	AG10803	skin:	n/a
41	chr19:41283667-41283717	AoSMC	blood vessel:	n/a
42	chr19:41284348-41284398	AoSMC	blood vessel:	n/a
43	chr19:41283090-41283140	LNCaP	prostate:	n/a
44	chr19:41283407-41283457	LNCaP	prostate:	n/a
45	chr19:41284234-41284284	MCF-7	breast:	n/a
46	chr19:41283578-41283628	GM12892	blood:	n/a
47	chr19:41284348-41284398	HRE	kidney:	n/a
48	chr19:41283407-41283457	NHDF-neo	bronchial:	n/a
49	chr19:41283578-41283628	NHBE	bronchial:	n/a
50	chr19:41284348-41284398	AG09319	gingival:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41274845..41278396-chr19:41279079..41284996,6	K562	blood:
2	chr19:41220672..41223321-chr19:41282772..41284711,3	K562	blood:
3	chr19:41281718..41286533-chr19:41301356..41311124,20	K562	blood:
4	chr19:41195631..41198231-chr19:41282908..41284681,3	K562	blood:
5	chr19:41283422..41285801-chr19:41305183..41308009,2	MCF-7	breast:
6	chr19:41254259..41260312-chr19:41280225..41287427,15	K562	blood:
7	chr19:41281732..41286442-chr19:41302482..41306628,13	K562	blood:
8	chr19:41221538..41223321-chr19:41282786..41284711,2	K562	blood:
9	chr19:41276921..41279823-chr19:41282678..41284570,2	MCF-7	breast:
10	chr19:41246510..41248162-chr19:41281990..41283890,2	K562	blood:
11	chr19:41280553..41283413-chr19:41284684..41288209,4	MCF-7	breast:
12	chr19:41254354..41258983-chr19:41282435..41286100,11	MCF-7	breast:
13	chr19:41220807..41223667-chr19:41282098..41285361,4	MCF-7	breast:
14	chr19:41282306..41285368-chr19:41311943..41315414,5	MCF-7	breast:
15	chr19:41280805..41286068-chr19:41308324..41316733,13	K562	blood:
16	chr19:41280553..41283413-chr19:41284684..41288209,4	MCF-7	breast:
17	chr19:41280731..41296556-chr19:41299561..41307605,30	MCF-7	breast:
18	chr19:41260895..41264688-chr19:41281653..41284501,3	MCF-7	breast:
19	chr14:102505039..102506720-chr19:41282932..41285736,2	MCF-7	breast:
20	chr19:41260700..41263624-chr19:41281746..41284711,4	K562	blood:
21	chr19:41254259..41259402-chr19:41281476..41286314,17	K562	blood:
22	chr19:41219466..41223288-chr19:41281896..41285456,5	MCF-7	breast:
23	chr19:41253800..41258892-chr19:41281807..41286457,14	MCF-7	breast:
24	chr19:41283851..41288555-chr19:41290136..41292963,4	MCF-7	breast:
25	chr19:41282692..41284743-chr19:41312820..41314498,2	MCF-7	breast:
26	chr19:41195540..41197710-chr19:41283825..41285603,2	MCF-7	breast:
27	chr19:41282175..41285758-chr19:41311471..41315456,8	K562	blood:
28	chr19:41282962..41284842-chr19:41308232..41310693,2	MCF-7	breast:

No data

Variant related genes	Relation type
RAB4B	TF binding region
RAB4B-EGLN2	TF binding region
RAB4B	CpG island
RAB4B-EGLN2	CpG island
ENSG00000261857	chromatin interactions
ENSG00000197102	chromatin interactions
ENSG00000123815	chromatin interactions
ENSG00000268797	chromatin interactions
ENSG00000105245	chromatin interactions
ENSG00000086544	chromatin interactions
ENSG00000167578	chromatin interactions
ENSG00000171570	chromatin interactions
ENSG00000077312	chromatin interactions
ENSG00000269858	chromatin interactions
ENSG00000188493	chromatin interactions

Extended variants
information (count: 98 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:98 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12981474	chr19:41283126-41283127	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
2	rs544505939	chr19:41283132-41283133	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs12982136	chr19:41283151-41283152	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
4	rs562761094	chr19:41283152-41283153	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
5	rs12983519	chr19:41283153-41283154	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
6	rs12983521	chr19:41283161-41283162	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
7	rs577764423	chr19:41283181-41283182	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
8	rs532160460	chr19:41283211-41283212	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
9	rs552116087	chr19:41283212-41283213	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
10	rs368147663	chr19:41283254-41283255	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
11	rs116382476	chr19:41283277-41283278	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
12	rs535992946	chr19:41283278-41283279	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs564437506	chr19:41283301-41283302	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs201734270	chr19:41283347-41283348	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
15	rs528544493	chr19:41283357-41283358	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
16	rs199922899	chr19:41283359-41283360	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
17	rs2233159	chr19:41283365-41283366	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs2233160	chr19:41283394-41283395	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
19	rs111679146	chr19:41283422-41283423	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs186319350	chr19:41283437-41283438	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs529211232	chr19:41283449-41283450	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs79016062	chr19:41283467-41283468	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs569508861	chr19:41283497-41283498	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs539663511	chr19:41283545-41283546	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs190656459	chr19:41283551-41283552	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs566597227	chr19:41283583-41283584	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs533868506	chr19:41283588-41283589	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
28	rs75967736	chr19:41283607-41283608	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs148240500	chr19:41283630-41283631	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
30	rs537800726	chr19:41283656-41283657	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs2604869	chr19:41283693-41283694	Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs577834439	chr19:41283738-41283739	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs553828373	chr19:41283822-41283823	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs558829956	chr19:41283882-41283883	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
35	rs554825429	chr19:41283911-41283912	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
36	rs560292000	chr19:41283912-41283913	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
37	rs79452631	chr19:41283917-41283918	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
38	rs183204460	chr19:41283930-41283931	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
39	rs561800744	chr19:41283973-41283974	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
40	rs529273619	chr19:41283981-41283982	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs558608886	chr19:41284002-41284003	Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs559043303	chr19:41284004-41284005	Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs537450371	chr19:41284010-41284011	Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs533651818	chr19:41284053-41284054	Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs541097807	chr19:41284070-41284071	Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
46	rs560961950	chr19:41284114-41284115	Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
47	rs567058858	chr19:41284121-41284122	Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
48	rs76240498	chr19:41284140-41284141	Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
49	rs370798991	chr19:41284163-41284164	Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs369735666	chr19:41284164-41284165	Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41260800-41283200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr19:41273400-41283200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:41273400-41283600	Weak transcription	Lung	lung
4	chr19:41281400-41283200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr19:41282400-41283200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr19:41282400-41283200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr19:41282600-41283200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr19:41282600-41283200	Flanking Active TSS	GM12878-XiMat	blood
9	chr19:41282600-41283400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr19:41282600-41283400	Enhancers	Spleen	Spleen
11	chr19:41282600-41283400	Flanking Active TSS	Dnd41	blood
12	chr19:41282600-41283400	Flanking Active TSS	HMEC	breast
13	chr19:41282800-41283200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
14	chr19:41282800-41283200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr19:41282800-41283200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:41282800-41283200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr19:41282800-41283200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr19:41282800-41283200	Flanking Active TSS	Primary B cells from cord blood	blood
19	chr19:41282800-41283200	Flanking Active TSS	Primary B cells from peripheral blood	blood
20	chr19:41282800-41283200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
21	chr19:41282800-41283200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:41282800-41283200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr19:41282800-41283200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr19:41282800-41283200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr19:41282800-41283200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr19:41282800-41283200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr19:41282800-41283200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:41282800-41283200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr19:41282800-41283200	Enhancers	Aorta	Aorta
30	chr19:41282800-41283200	Flanking Active TSS	Brain Angular Gyrus	brain
31	chr19:41282800-41283200	Flanking Active TSS	Brain Germinal Matrix	brain
32	chr19:41282800-41283200	Flanking Active TSS	Brain Hippocampus Middle	brain
33	chr19:41282800-41283200	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr19:41282800-41283200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
35	chr19:41282800-41283200	Enhancers	Esophagus	oesophagus
36	chr19:41282800-41283200	Flanking Active TSS	Fetal Lung	lung
37	chr19:41282800-41283200	Enhancers	Gastric	stomach
38	chr19:41282800-41283200	Enhancers	Pancreas	Pancrea
39	chr19:41282800-41283200	Enhancers	Psoas Muscle	Psoas
40	chr19:41282800-41283200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
41	chr19:41282800-41283200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr19:41282800-41283200	Flanking Active TSS	Rectal Smooth Muscle	rectum
43	chr19:41282800-41283200	Enhancers	Stomach Mucosa	stomach
44	chr19:41282800-41283200	Flanking Active TSS	HSMM	muscle
45	chr19:41282800-41283200	Flanking Active TSS	HSMMtube	muscle
46	chr19:41282800-41283200	Flanking Active TSS	NHDF-Ad	bronchial
47	chr19:41282800-41283400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr19:41282800-41283400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr19:41282800-41283400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
50	chr19:41282800-41283400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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