Variant report

Variant	esv7204
Chromosome Location	chr19:21274198-21336396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:794)
CpG islands
(count:671)
Chromatin interactive
region (count:17)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21320974-21321431	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:21324594-21324991	K562	blood:	n/a	n/a
3	ARID3A	chr19:21310732-21311042	K562	blood:	n/a	n/a
4	ARID3A	chr19:21317764-21318041	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:21311642-21311836	K562	blood:	n/a	n/a
6	ARID3A	chr19:21298266-21298592	K562	blood:	n/a	n/a
7	ARID3A	chr19:21324511-21325033	HepG2	liver:	n/a	n/a
8	ARID3A	chr19:21334536-21334657	HepG2	liver:	n/a	n/a
9	ARID3A	chr19:21309568-21309872	K562	blood:	n/a	n/a
10	ARID3A	chr19:21326481-21326923	K562	blood:	n/a	n/a
11	ATF1	chr19:21311655-21311901	K562	blood:	n/a	n/a
12	ATF1	chr19:21309871-21310055	K562	blood:	n/a	n/a
13	ATF1	chr19:21323783-21324152	K562	blood:	n/a	n/a
14	ATF1	chr19:21324532-21324958	K562	blood:	n/a	n/a
15	BACH1	chr19:21334389-21334437	K562	blood:	n/a	n/a
16	BATF	chr19:21284292-21284552	GM12878	blood:	n/a	chr19:21284437-21284448
17	BATF	chr19:21284333-21284518	GM12878	blood:	n/a	chr19:21284437-21284448
18	BHLHE40	chr19:21325755-21325765	K562	blood:	n/a	n/a
19	BHLHE40	chr19:21324647-21325001	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:21324578-21325040	K562	blood:	n/a	n/a
21	BHLHE40	chr19:21277600-21277808	GM12878	blood:	n/a	n/a
22	CBX3	chr19:21313141-21313522	K562	blood:	n/a	n/a
23	CBX3	chr19:21324429-21325106	K562	blood:	n/a	n/a
24	CBX3	chr19:21317713-21318138	K562	blood:	n/a	n/a
25	CBX3	chr19:21313134-21313546	K562	blood:	n/a	n/a
26	CBX3	chr19:21311545-21312525	K562	blood:	n/a	n/a
27	CCNT2	chr19:21298323-21298579	K562	blood:	n/a	n/a
28	CCNT2	chr19:21324680-21324880	K562	blood:	n/a	n/a
29	CCNT2	chr19:21311599-21311941	K562	blood:	n/a	n/a
30	CEBPB	chr19:21324595-21324879	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:21309862-21309933	K562	blood:	n/a	n/a
32	CEBPB	chr19:21279665-21279786	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr19:21324525-21324869	K562	blood:	n/a	n/a
34	CEBPB	chr19:21309819-21310094	K562	blood:	n/a	n/a
35	CEBPB	chr19:21317815-21318034	K562	blood:	n/a	n/a
36	CEBPB	chr19:21330138-21330368	IMR90	lung:	n/a	chr19:21330243-21330254
37	CEBPB	chr19:21324542-21325274	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr19:21324607-21324698	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr19:21330144-21330361	K562	blood:	n/a	chr19:21330243-21330254
40	CEBPB	chr19:21287270-21287272	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr19:21324616-21324713	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:21277976-21278043	K562	blood:	n/a	n/a
43	CEBPB	chr19:21287289-21287319	K562	blood:	n/a	n/a
44	CEBPB	chr19:21324597-21324775	A549	lung:	n/a	n/a
45	CEBPB	chr19:21311395-21312007	K562	blood:	n/a	n/a
46	CEBPB	chr19:21330247-21330280	HepG2	liver:	n/a	n/a
47	CEBPB	chr19:21326562-21327122	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr19:21311478-21311988	K562	blood:	n/a	n/a
49	CEBPD	chr19:21324601-21324988	K562	blood:	n/a	n/a
50	CEBPD	chr19:21311549-21312059	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21324833-21324883	HRPEpiC	eye:	n/a
2	chr19:21305635-21305685	AG09309	skin:	n/a
3	chr19:21324130-21324180	Hepatocyte	liver:	n/a
4	chr19:21324444-21324494	HRE	kidney:	n/a
5	chr19:21324444-21324494	HEK293	kidney:	embryo
6	chr19:21324782-21324832	AG09309	skin:	n/a
7	chr19:21323534-21323584	T-47D	breast:	n/a
8	chr19:21324130-21324180	NH-A	brain:	n/a
9	chr19:21324796-21324846	PANC-1	pancreas:	n/a
10	chr19:21324750-21324800	GM06990	blood:	n/a
11	chr19:21325005-21325055	U87	brain:	n/a
12	chr19:21324444-21324494	MCF10A-Er-Src	breast:	n/a
13	chr19:21323534-21323584	A549	lung:	n/a
14	chr19:21324807-21324857	LNCaP	prostate:	n/a
15	chr19:21324707-21324757	AG09309	skin:	n/a
16	chr19:21324796-21324846	Hepatocyte	liver:	n/a
17	chr19:21305635-21305685	HepG2	liver:	n/a
18	chr19:21324130-21324180	PrEC	prostate:	n/a
19	chr19:21324782-21324832	PFSK-1	brain:	n/a
20	chr19:21324833-21324883	ovcar-3	ovarian:	n/a
21	chr19:21324807-21324857	IMR90	lung:	fetal
22	chr19:21324833-21324883	AoSMC	blood vessel:	n/a
23	chr19:21324807-21324857	Caco-2	colon:	n/a
24	chr19:21324707-21324757	Jurkat	blood:	n/a
25	chr19:21325005-21325055	Caco-2	colon:	n/a
26	chr19:21305635-21305685	SKMC	muscle:	n/a
27	chr19:21324782-21324832	HMEC	breast:	n/a
28	chr19:21305635-21305685	HMEC	breast:	n/a
29	chr19:21324707-21324757	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:21324444-21324494	AG10803	skin:	n/a
31	chr19:21305635-21305685	U87	brain:	n/a
32	chr19:21324750-21324800	SKMC	muscle:	n/a
33	chr19:21325005-21325055	BJ	skin:	n/a
34	chr19:21324130-21324180	HEEpiC	esophagus:	n/a
35	chr19:21324444-21324494	AG04450	lung:	fetal
36	chr19:21324130-21324180	HL-60	blood:	n/a
37	chr19:21324833-21324883	HEEpiC	esophagus:	n/a
38	chr19:21324807-21324857	HPAEpiC	pulmonary alveolar:	n/a
39	chr19:21324707-21324757	U87	brain:	n/a
40	chr19:21324707-21324757	GM12892	blood:	n/a
41	chr19:21324750-21324800	MCF-7	breast:	n/a
42	chr19:21324796-21324846	HCM	heart:	n/a
43	chr19:21325005-21325055	HEEpiC	esophagus:	n/a
44	chr19:21324444-21324494	Hepatocyte	liver:	n/a
45	chr19:21324782-21324832	Hepatocyte	liver:	n/a
46	chr19:21324833-21324883	BJ	skin:	n/a
47	chr19:21324796-21324846	HCT-116	colon:	n/a
48	chr19:21324130-21324180	NT2-D1	testis:	n/a
49	chr19:21324782-21324832	HPAEpiC	pulmonary alveolar:	n/a
50	chr19:21324833-21324883	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:21268071..21270842-chr19:21283139..21285114,2	K562	blood:
2	chr19:21325138..21326653-chr19:21327405..21328910,2	K562	blood:
3	chr14:39639460..39640068-chr19:21325033..21325860,2	Hela-S3	cervix:
4	chr19:21329795..21332186-chr19:21344748..21346568,2	K562	blood:
5	chr19:21266339..21268600-chr19:21281169..21284066,2	MCF-7	breast:
6	chr19:21324747..21325334-chr19:21541551..21542092,2	Hela-S3	cervix:
7	chr19:21268213..21268800-chr19:21327512..21328424,2	MCF-7	breast:
8	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
9	chr19:21327774..21330342-chr19:21332349..21334379,2	MCF-7	breast:
10	chr19:21319136..21321232-chr19:21323817..21326389,2	K562	blood:
11	chr19:21325138..21326653-chr19:21327405..21328910,2	K562	blood:
12	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
13	chr19:21328122..21331831-chr19:21332882..21335579,3	K562	blood:
14	chr19:21267358..21270716-chr19:21272495..21275149,3	MCF-7	breast:
15	chr19:21264016..21266575-chr19:21326485..21328797,2	MCF-7	breast:
16	chr19:21312896..21314771-chr19:21323680..21326350,2	K562	blood:
17	chr19:21324608..21326238-chr19:21328530..21331210,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF431-3	chr19:21301321-21301529	NONHSAT063686
2	lnc-ZNF714-1	chr19:21307764-21307881	NONHSAT063683
3	lnc-ZNF714-2	chr19:21306620-21306991	NONHSAT063687
4	lnc-ZNF430-2	chr19:21273717-21274564	NONHSAT063684

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF714	hsa-miR-222-3p	chr19:21304966-21304986

Variant related genes	Relation type
VN1R81P	TF binding region
ZNF431	TF binding region
RNA5SP469	TF binding region
ENSG00000256240	TF binding region
RPL7AP10	TF binding region
VN1R81P	CpG island
ZNF431	CpG island
RNA5SP469	CpG island
ENSG00000256240	CpG island
RPL7AP10	CpG island
ENSG00000240522	chromatin interactions
ENSG00000196705	chromatin interactions
ENSG00000160352	chromatin interactions
ENSG00000182400	chromatin interactions
ENSG00000172687	chromatin interactions

Extended variants
information (count: 2459 )
Associated
traits (count: 40 )

Variant overlapped rSNPs/rCNVs (count:2459 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181964710	chr19:21274245-21274246	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs150290624	chr19:21274296-21274297	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs527990638	chr19:21274307-21274308	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs371677123	chr19:21274308-21274309	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs576714681	chr19:21274325-21274326	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs113725001	chr19:21274337-21274338	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs149640296	chr19:21274347-21274348	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs530217601	chr19:21274356-21274357	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs541674304	chr19:21274400-21274401	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs561451549	chr19:21274404-21274405	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs530255548	chr19:21274414-21274415	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs10405537	chr19:21274466-21274467	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs10403761	chr19:21274471-21274472	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs70950323	chr19:21274477-21274478	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs10403768	chr19:21274478-21274479	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs532813241	chr19:21274530-21274531	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs565613181	chr19:21274536-21274537	Weak transcription Strong transcription Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs73022630	chr19:21274676-21274677	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112170977	chr19:21274678-21274679	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113798090	chr19:21274691-21274692	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568158138	chr19:21274732-21274733	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186012508	chr19:21274789-21274790	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190679614	chr19:21274806-21274807	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375143779	chr19:21274865-21274866	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369923582	chr19:21274903-21274904	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10404877	chr19:21274909-21274910	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs386474523	chr19:21274953-21274954	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372798024	chr19:21274974-21274975	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539412564	chr19:21274988-21274989	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552982975	chr19:21275059-21275060	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572811518	chr19:21275085-21275086	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs377236537	chr19:21275106-21275107	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112812752	chr19:21275273-21275274	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146371227	chr19:21275283-21275284	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561577473	chr19:21275284-21275285	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574890144	chr19:21275347-21275348	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139599326	chr19:21275357-21275358	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs202001284	chr19:21275381-21275382	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142888749	chr19:21275403-21275404	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568110880	chr19:21275427-21275428	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532563659	chr19:21275429-21275430	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs77628784	chr19:21275434-21275435	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367747309	chr19:21275517-21275518	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367760763	chr19:21275532-21275533	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10411471	chr19:21275540-21275541	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs187832849	chr19:21275575-21275576	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151034200	chr19:21275664-21275665	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369353034	chr19:21275712-21275713	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs386388717	chr19:21275732-21275733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56845417	chr19:21275733-21275734	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:40)

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
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21247400-21289600	Weak transcription	Aorta	Aorta
2	chr19:21265400-21274800	Weak transcription	Lung	lung
3	chr19:21265600-21275000	Weak transcription	Pancreas	Pancrea
4	chr19:21265600-21286400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr19:21265600-21295800	Weak transcription	Small Intestine	intestine
6	chr19:21265600-21300000	Weak transcription	Brain Angular Gyrus	brain
7	chr19:21265600-21305200	Weak transcription	Psoas Muscle	Psoas
8	chr19:21265800-21275000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr19:21265800-21275000	Weak transcription	Primary B cells from cord blood	blood
10	chr19:21265800-21275000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr19:21265800-21275400	Weak transcription	Brain Hippocampus Middle	brain
12	chr19:21265800-21282600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr19:21265800-21289800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr19:21265800-21290600	Weak transcription	Adipose Nuclei	Adipose
15	chr19:21265800-21297200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr19:21265800-21297200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr19:21265800-21299600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr19:21265800-21299800	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr19:21265800-21302200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr19:21265800-21302800	Weak transcription	Fetal Muscle Trunk	muscle
21	chr19:21265800-21303000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr19:21266000-21275000	Weak transcription	Fetal Heart	heart
23	chr19:21266000-21276400	Weak transcription	Fetal Intestine Small	intestine
24	chr19:21266000-21278800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr19:21266000-21286000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr19:21266000-21287600	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr19:21266000-21287800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr19:21266000-21288400	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr19:21266000-21289400	Weak transcription	Primary hematopoietic stem cells	blood
30	chr19:21266000-21290800	Weak transcription	Brain Anterior Caudate	brain
31	chr19:21266000-21290800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr19:21266000-21290800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr19:21266000-21292600	Weak transcription	Fetal Kidney	kidney
34	chr19:21266000-21297400	Weak transcription	HUVEC	blood vessel
35	chr19:21266200-21274600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr19:21266200-21274600	Weak transcription	Rectal Smooth Muscle	rectum
37	chr19:21266200-21275000	Weak transcription	Fetal Stomach	stomach
38	chr19:21266200-21276400	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr19:21266200-21288600	Weak transcription	Thymus	Thymus
40	chr19:21266200-21288800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr19:21266200-21289800	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr19:21266200-21292400	Weak transcription	Primary T cells from cord blood	blood
43	chr19:21266200-21296600	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr19:21266200-21301600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr19:21266400-21275000	Weak transcription	Colon Smooth Muscle	Colon
46	chr19:21266400-21288200	Weak transcription	Brain Germinal Matrix	brain
47	chr19:21266600-21275000	Weak transcription	HepG2	liver
48	chr19:21266600-21279600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr19:21266800-21275000	Weak transcription	Fetal Lung	lung
50	chr19:21266800-21292600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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