Variant report

Variant	nsv458376
Chromosome Location	chr19:20021046-20151257
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1082)
CpG islands
(count:732)
Chromatin interactive
region (count:17)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:20103566-20103765	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:20150099-20150414	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:20022098-20022278	K562	blood:	n/a	n/a
4	ATF1	chr19:20054705-20055077	K562	blood:	n/a	n/a
5	ATF1	chr19:20022066-20022334	K562	blood:	n/a	n/a
6	ATF2	chr19:20067472-20067936	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:20111633-20111647	K562	blood:	n/a	n/a
8	BACH1	chr19:20045497-20045918	K562	blood:	n/a	n/a
9	BACH1	chr19:20046041-20046383	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr19:20149962-20150229	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr19:20021998-20022308	GM12878	blood:	n/a	chr19:20022190-20022201 chr19:20022191-20022201
12	BATF	chr19:20022034-20022268	GM12878	blood:	n/a	chr19:20022190-20022201 chr19:20022191-20022201
13	BATF	chr19:20071227-20071388	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:20070163-20070165	K562	blood:	n/a	n/a
15	BRCA1	chr19:20149987-20150214	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr19:20077721-20077986	K562	blood:	n/a	n/a
17	CBX3	chr19:20069962-20070297	K562	blood:	n/a	n/a
18	CBX3	chr19:20041129-20041481	K562	blood:	n/a	n/a
19	CBX3	chr19:20044616-20045003	K562	blood:	n/a	n/a
20	CBX3	chr19:20077683-20078014	K562	blood:	n/a	n/a
21	CBX3	chr19:20044625-20045016	K562	blood:	n/a	n/a
22	CCNT2	chr19:20054515-20055058	K562	blood:	n/a	n/a
23	CEBPB	chr19:20103565-20103780	HepG2	liver:	n/a	n/a
24	CEBPB	chr19:20054769-20054955	K562	blood:	n/a	n/a
25	CEBPB	chr19:20150124-20150847	HepG2	liver:	n/a	chr19:20150648-20150661 chr19:20150648-20150659
26	CEBPB	chr19:20150469-20150835	H1-hESC	embryonic stem cell:	n/a	chr19:20150648-20150661 chr19:20150648-20150659
27	CEBPB	chr19:20054683-20055081	K562	blood:	n/a	n/a
28	CEBPB	chr19:20150231-20150800	IMR90	lung:	n/a	chr19:20150648-20150661 chr19:20150648-20150659
29	CEBPB	chr19:20067607-20067926	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr19:20054667-20055058	K562	blood:	n/a	n/a
31	CEBPD	chr19:20150089-20150326	HepG2	liver:	n/a	n/a
32	CEBPD	chr19:20054680-20055111	K562	blood:	n/a	n/a
33	CEBPD	chr19:20054674-20055126	K562	blood:	n/a	n/a
34	CEBPZ	chr19:20110840-20110868	HepG2	liver:	n/a	n/a
35	CEBPZ	chr19:20148416-20148688	HepG2	liver:	n/a	n/a
36	CHD1	chr19:20149458-20150283	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr19:20044710-20045023	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr19:20150079-20150485	GM12878	blood:	n/a	n/a
39	CHD2	chr19:20149961-20150586	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr19:20149949-20150491	HepG2	liver:	n/a	n/a
41	CHD2	chr19:20067439-20067838	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr19:20050875-20050901	K562	blood:	n/a	n/a
43	CHD2	chr19:20045329-20047088	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr19:20045481-20045981	K562	blood:	n/a	n/a
45	CREB1	chr19:20149793-20150493	GM12878	blood:	n/a	n/a
46	CREB1	chr19:20149804-20150666	HepG2	liver:	n/a	n/a
47	CREB1	chr19:20149860-20150645	HepG2	liver:	n/a	n/a
48	CREB1	chr19:20149878-20150565	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr19:20069992-20070377	GM12878	blood:	n/a	n/a
50	CTCF	chr19:20070066-20070335	GM12878	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:20150441-20150491	ECC-1	luminal epithelium:	n/a
2	chr19:20150159-20150209	AG10803	skin:	n/a
3	chr19:20149684-20149734	HCM	heart:	n/a
4	chr19:20150232-20150282	IMR90	lung:	fetal
5	chr19:20150505-20150555	PFSK-1	brain:	n/a
6	chr19:20150441-20150491	GM12892	blood:	n/a
7	chr19:20149684-20149734	H1-hESC	embryonic stem cell:	embryo
8	chr19:20150334-20150384	PANC-1	pancreas:	n/a
9	chr19:20150441-20150491	NT2-D1	testis:	n/a
10	chr19:20150159-20150209	HRCEpiC	kidney:	n/a
11	chr19:20149886-20149936	SK-N-MC	brain:	n/a
12	chr19:20150505-20150555	MCF-7	breast:	n/a
13	chr19:20150334-20150384	ovcar-3	ovarian:	n/a
14	chr19:20150943-20150993	MCF-7	breast:	n/a
15	chr19:20150441-20150491	AoSMC	blood vessel:	n/a
16	chr19:20147046-20147096	A549	lung:	n/a
17	chr19:20150232-20150282	SKMC	muscle:	n/a
18	chr19:20150441-20150491	GM19239	blood:	n/a
19	chr19:20149886-20149936	NHDF-neo	bronchial:	n/a
20	chr19:20150441-20150491	Hepatocyte	liver:	n/a
21	chr19:20150232-20150282	PrEC	prostate:	n/a
22	chr19:20150317-20150367	LNCaP	prostate:	n/a
23	chr19:20150159-20150209	Hela-S3	cervix:	n/a
24	chr19:20150159-20150209	PFSK-1	brain:	n/a
25	chr19:20149831-20149881	HRPEpiC	eye:	n/a
26	chr19:20150159-20150209	HCM	heart:	n/a
27	chr19:20150943-20150993	CMK	blood:	n/a
28	chr19:20150317-20150367	IMR90	lung:	fetal
29	chr19:20150242-20150292	GM19239	blood:	n/a
30	chr19:20150943-20150993	HepG2	liver:	n/a
31	chr19:20149886-20149936	ovcar-3	ovarian:	n/a
32	chr19:20149886-20149936	CMK	blood:	n/a
33	chr19:20150943-20150993	NHDF-neo	bronchial:	n/a
34	chr19:20147046-20147096	HCPEpiC	choroid plexus:	n/a
35	chr19:20150943-20150993	HRPEpiC	eye:	n/a
36	chr19:20150317-20150367	ECC-1	luminal epithelium:	n/a
37	chr19:20150242-20150292	GM06990	blood:	n/a
38	chr19:20150159-20150209	SK-N-SH	brain:	n/a
39	chr19:20150159-20150209	GM12878	blood:	n/a
40	chr19:20150242-20150292	SKMC	muscle:	n/a
41	chr19:20150334-20150384	HRCEpiC	kidney:	n/a
42	chr19:20150505-20150555	AoSMC	blood vessel:	n/a
43	chr19:20149886-20149936	MCF10A-Er-Src	breast:	n/a
44	chr19:20150242-20150292	HL-60	blood:	n/a
45	chr19:20149831-20149881	ProgFib	skin:	n/a
46	chr19:20147046-20147096	NB4	blood:	n/a
47	chr19:20147046-20147096	HUVEC	blood vessel:	n/a
48	chr19:20150232-20150282	LNCaP	prostate:	n/a
49	chr19:20150317-20150367	SKMC	muscle:	n/a
50	chr19:20150317-20150367	HPAEpiC	pulmonary alveolar:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:20142180..20144378-chr19:20148043..20150229,2	MCF-7	breast:
2	chr19:20124182..20126498-chr19:20128063..20130239,2	MCF-7	breast:
3	chr19:20125599..20128590-chr19:20148799..20150667,2	MCF-7	breast:
4	chr19:20142180..20144378-chr19:20148043..20150229,2	MCF-7	breast:
5	chr19:20124182..20126498-chr19:20128063..20130239,2	MCF-7	breast:
6	chr19:19976572..19978622-chr19:20025763..20027868,3	K562	blood:
7	chr19:20048978..20051171-chr19:20052679..20055327,2	K562	blood:
8	chr19:19743070..19745753-chr19:20069128..20070689,2	MCF-7	breast:
9	chr19:20010657..20013465-chr19:20046032..20047914,3	K562	blood:
10	chr19:20107929..20110799-chr19:21687232..21688823,2	MCF-7	breast:
11	chr19:20015522..20017242-chr19:20021366..20023292,2	MCF-7	breast:
12	chr19:20048978..20051171-chr19:20052679..20055327,2	K562	blood:
13	chr19:20011096..20014012-chr19:20021090..20024486,4	K562	blood:
14	chr19:19976102..19978027-chr19:20081868..20083854,2	K562	blood:
15	chr19:19772761..19775083-chr19:20066186..20068546,2	MCF-7	breast:
16	chr19:20012861..20014472-chr19:20018867..20021328,2	K562	blood:
17	chr19:20048311..20052863-chr19:20053827..20056431,4	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF90-3	chr19:20144674-20145141	NONHSAT063622
2	lnc-ZNF90-3	chr19:20144253-20144356	NONHSAT063622
3	lnc-ZNF506-8	chr19:20141526-20141691	NONHSAT063621
4	lnc-ZNF93-1	chr19:20073928-20074273	ENSG00000267268.1
5	lnc-ZNF93-1	chr19:20042817-20043805	NONHSAT063615
6	lnc-ZNF93-1	chr19:20069298-20069363	ENSG00000267268.1
7	lnc-ZNF506-8	chr19:20150152-20150259	NONHSAT063621
8	lnc-ZNF506-8	chr19:20141802-20141922	NONHSAT063621
9	lnc-ZNF93-1	chr19:20067547-20067825	ENSG00000267268.1

No data

Variant related genes	Relation type
ENSG00000268461	TF binding region
ENSG00000264441	TF binding region
ENSG00000268070	TF binding region
ZNF682	TF binding region
ENSG00000268461	CpG island
ENSG00000264441	CpG island
ENSG00000268070	CpG island
ZNF682	CpG island
ENSG00000105726	chromatin interactions
ENSG00000197013	chromatin interactions
ENSG00000268461	chromatin interactions
ENSG00000256771	chromatin interactions
ENSG00000268070	chromatin interactions
ENSG00000267268	chromatin interactions
ENSG00000184635	chromatin interactions
ENSG00000197124	chromatin interactions

Extended variants
information (count: 3920 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:3920 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13344370	chr19:20021046-20021047	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544093906	chr19:20021056-20021057	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564086399	chr19:20021107-20021108	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560233250	chr19:20021192-20021193	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs568820404	chr19:20021248-20021249	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532919837	chr19:20021317-20021318	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs34576592	chr19:20021353-20021354	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs546313825	chr19:20021356-20021357	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs78064675	chr19:20021358-20021359	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs142102833	chr19:20021398-20021399	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548757839	chr19:20021424-20021425	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35098061	chr19:20021460-20021461	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs75833362	chr19:20021461-20021462	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs79606859	chr19:20021462-20021463	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs111740622	chr19:20021473-20021474	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs78525614	chr19:20021474-20021475	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs142385411	chr19:20021482-20021483	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs151175506	chr19:20021495-20021496	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12460823	chr19:20021505-20021506	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139081605	chr19:20021571-20021572	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568660723	chr19:20021573-20021574	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs537688509	chr19:20021590-20021591	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs551271301	chr19:20021620-20021621	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571089667	chr19:20021659-20021660	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs548570483	chr19:20021692-20021693	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs11673233	chr19:20021695-20021696	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs540190213	chr19:20021700-20021701	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs539783672	chr19:20021754-20021755	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74425267	chr19:20021783-20021784	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs566912468	chr19:20021797-20021798	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190710568	chr19:20021807-20021808	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs180727050	chr19:20021841-20021842	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs575096229	chr19:20021860-20021861	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs10423312	chr19:20021861-20021862	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142050067	chr19:20021874-20021875	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577876504	chr19:20021922-20021923	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs186055928	chr19:20021960-20021961	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs190042080	chr19:20021991-20021992	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs73530957	chr19:20022056-20022057	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs571018018	chr19:20022070-20022071	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs542741038	chr19:20022119-20022120	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562598429	chr19:20022122-20022123	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181189731	chr19:20022142-20022143	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs10423992	chr19:20022152-20022153	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs151155843	chr19:20022176-20022177	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547252027	chr19:20022365-20022366	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530933081	chr19:20022383-20022384	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs533458917	chr19:20022391-20022392	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs546934518	chr19:20022396-20022397	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs566745187	chr19:20022412-20022413	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Nasopharyngeal cancer	20548289	CNVD
Schizophrenia	20967226	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20012600-20030000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:20012800-20034200	Weak transcription	Pancreas	Pancrea
3	chr19:20012800-20034200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr19:20012800-20034600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr19:20012800-20043400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr19:20013000-20022600	Weak transcription	Aorta	Aorta
7	chr19:20013000-20024200	Weak transcription	Ovary	ovary
8	chr19:20013000-20034000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:20013000-20034600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr19:20013000-20034600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr19:20013000-20035200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr19:20013000-20039600	Weak transcription	Colon Smooth Muscle	Colon
13	chr19:20013200-20021800	Weak transcription	Fetal Heart	heart
14	chr19:20013200-20026000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr19:20013200-20026200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr19:20013200-20027400	Weak transcription	HSMMtube	muscle
17	chr19:20013200-20027600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr19:20013200-20028600	Weak transcription	Adipose Nuclei	Adipose
19	chr19:20013200-20028800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
20	chr19:20013200-20034600	Weak transcription	Primary T cells from cord blood	blood
21	chr19:20013200-20043600	Weak transcription	Fetal Brain Male	brain
22	chr19:20013400-20027400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr19:20013400-20033600	Weak transcription	Primary B cells from peripheral blood	blood
24	chr19:20013400-20034000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr19:20013400-20034000	Weak transcription	Placenta	Placenta
26	chr19:20013400-20034200	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr19:20013400-20035800	Weak transcription	Osteobl	bone
28	chr19:20014000-20028800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr19:20014000-20032600	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr19:20014400-20027600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr19:20014800-20027000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr19:20014800-20034000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr19:20015400-20021600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr19:20015800-20024400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr19:20015800-20033400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr19:20016000-20034200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr19:20016000-20034800	Weak transcription	K562	blood
38	chr19:20016400-20034000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr19:20016600-20033400	Weak transcription	Thymus	Thymus
40	chr19:20016800-20028800	ZNF genes & repeats	Dnd41	blood
41	chr19:20016800-20034000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr19:20017000-20022400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr19:20017400-20024800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr19:20018200-20022000	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr19:20018200-20025000	Weak transcription	Fetal Lung	lung
46	chr19:20018200-20025400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
47	chr19:20018400-20021400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr19:20018400-20022200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr19:20018400-20027400	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr19:20018400-20027400	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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