Variant report

Variant	nsv911411
Chromosome Location	chr19:21184533-21263518
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:972)
CpG islands
(count:550)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21203103-21203905	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:21203172-21203518	K562	blood:	n/a	n/a
3	ATF1	chr19:21203206-21203570	K562	blood:	n/a	n/a
4	ATF2	chr19:21211069-21211600	GM12878	blood:	n/a	n/a
5	ATF2	chr19:21203137-21203776	GM12878	blood:	n/a	n/a
6	ATF2	chr19:21211128-21211612	GM12878	blood:	n/a	n/a
7	ATF2	chr19:21205758-21206247	GM12878	blood:	n/a	n/a
8	ATF3	chr19:21205907-21206172	K562	blood:	n/a	n/a
9	BACH1	chr19:21203736-21203976	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr19:21203338-21203360	K562	blood:	n/a	n/a
11	BATF	chr19:21211304-21211567	GM12878	blood:	n/a	chr19:21211457-21211467
12	BATF	chr19:21205859-21206209	GM12878	blood:	n/a	n/a
13	BATF	chr19:21210999-21211662	GM12878	blood:	n/a	chr19:21211457-21211467
14	BATF	chr19:21211727-21212086	GM12878	blood:	n/a	n/a
15	BATF	chr19:21205876-21206186	GM12878	blood:	n/a	n/a
16	BCL11A	chr19:21210944-21211891	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
17	BCL11A	chr19:21211293-21211575	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
18	BCL11A	chr19:21205878-21206151	GM12878	blood:	n/a	n/a
19	BCL11A	chr19:21205905-21206089	GM12878	blood:	n/a	n/a
20	BCL3	chr19:21205826-21206186	GM12878	blood:	n/a	n/a
21	BCL3	chr19:21211314-21211625	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
22	BCLAF1	chr19:21203409-21203891	GM12878	blood:	n/a	n/a
23	BCLAF1	chr19:21203607-21204001	GM12878	blood:	n/a	n/a
24	BCLAF1	chr19:21211186-21211620	GM12878	blood:	n/a	chr19:21211460-21211469 chr19:21211459-21211468
25	BHLHE40	chr19:21203109-21203898	GM12878	blood:	n/a	n/a
26	BHLHE40	chr19:21211136-21211643	GM12878	blood:	n/a	n/a
27	BHLHE40	chr19:21203279-21203977	K562	blood:	n/a	n/a
28	BHLHE40	chr19:21221243-21221545	GM12878	blood:	n/a	n/a
29	BHLHE40	chr19:21205891-21206180	GM12878	blood:	n/a	n/a
30	BRCA1	chr19:21203325-21203834	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr19:21203108-21204025	K562	blood:	n/a	n/a
32	CCNT2	chr19:21203366-21203820	K562	blood:	n/a	chr19:21203640-21203649
33	CEBPB	chr19:21253959-21254016	H1-hESC	embryonic stem cell:	n/a	chr19:21253998-21254009
34	CEBPB	chr19:21204509-21204628	K562	blood:	n/a	n/a
35	CEBPB	chr19:21203180-21203905	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:21205930-21206254	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr19:21205808-21206145	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr19:21253004-21253205	K562	blood:	n/a	n/a
39	CEBPB	chr19:21230758-21230958	Hela-S3	cervix:	n/a	chr19:21230909-21230920
40	CEBPB	chr19:21220413-21220667	IMR90	lung:	n/a	n/a
41	CEBPB	chr19:21220419-21220619	K562	blood:	n/a	n/a
42	CEBPB	chr19:21253892-21254156	HepG2	liver:	n/a	chr19:21253998-21254009
43	CEBPB	chr19:21220067-21220100	HepG2	liver:	n/a	n/a
44	CEBPB	chr19:21219798-21220139	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr19:21205788-21206177	IMR90	lung:	n/a	n/a
46	CEBPB	chr19:21219937-21220069	K562	blood:	n/a	n/a
47	CEBPB	chr19:21220535-21220616	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr19:21198941-21199206	HepG2	liver:	n/a	chr19:21199102-21199113
49	CEBPB	chr19:21235748-21236054	K562	blood:	n/a	n/a
50	CEBPB	chr19:21205930-21205950	K562	blood:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21203493-21203543	RPTEC	kidney:	n/a
2	chr19:21203493-21203543	RPTEC	kidney:	n/a
3	chr19:21203359-21203409	NB4	blood:	n/a
4	chr19:21203469-21203519	HRE	kidney:	n/a
5	chr19:21203723-21203773	HIPEpiC	eye:	n/a
6	chr19:21240978-21241028	BJ	skin:	n/a
7	chr19:21203417-21203467	ovcar-3	ovarian:	n/a
8	chr19:21203417-21203467	HRPEpiC	eye:	n/a
9	chr19:21262035-21262085	HIPEpiC	eye:	n/a
10	chr19:21203444-21203494	HIPEpiC	eye:	n/a
11	chr19:21203469-21203519	PANC-1	pancreas:	n/a
12	chr19:21262035-21262085	HL-60	blood:	n/a
13	chr19:21203723-21203773	HRE	kidney:	n/a
14	chr19:21203493-21203543	NHDF-neo	bronchial:	n/a
15	chr19:21203417-21203467	RPTEC	kidney:	n/a
16	chr19:21203723-21203773	HCF	heart:	n/a
17	chr19:21203403-21203453	HEEpiC	esophagus:	n/a
18	chr19:21203403-21203453	SAEC	small airway:	n/a
19	chr19:21262035-21262085	GM12878	blood:	n/a
20	chr19:21203444-21203494	HepG2	liver:	n/a
21	chr19:21203723-21203773	HCPEpiC	choroid plexus:	n/a
22	chr19:21203493-21203543	GM06990	blood:	n/a
23	chr19:21203469-21203519	HCM	heart:	n/a
24	chr19:21203444-21203494	HRCEpiC	kidney:	n/a
25	chr19:21262035-21262085	PANC-1	pancreas:	n/a
26	chr19:21203469-21203519	HEEpiC	esophagus:	n/a
27	chr19:21240978-21241028	H1-hESC	embryonic stem cell:	embryo
28	chr19:21203493-21203543	HNPCEpiC	eye:	n/a
29	chr19:21240978-21241028	Jurkat	blood:	n/a
30	chr19:21203493-21203543	HMEC	breast:	n/a
31	chr19:21262035-21262085	ECC-1	luminal epithelium:	n/a
32	chr19:21203469-21203519	NT2-D1	testis:	n/a
33	chr19:21203469-21203519	LNCaP	prostate:	n/a
34	chr19:21203723-21203773	AG09319	gingival:	n/a
35	chr19:21203359-21203409	ProgFib	skin:	n/a
36	chr19:21203444-21203494	A549	lung:	n/a
37	chr19:21203444-21203494	GM19239	blood:	n/a
38	chr19:21203444-21203494	GM12892	blood:	n/a
39	chr19:21203403-21203453	AG04449	skin:	fetal
40	chr19:21203359-21203409	HNPCEpiC	eye:	n/a
41	chr19:21240978-21241028	NH-A	brain:	n/a
42	chr19:21203359-21203409	GM06990	blood:	n/a
43	chr19:21203359-21203409	NHDF-neo	bronchial:	n/a
44	chr19:21203403-21203453	AG09309	skin:	n/a
45	chr19:21203493-21203543	HEK293	kidney:	embryo
46	chr19:21262035-21262085	AG09319	gingival:	n/a
47	chr19:21203417-21203467	HEEpiC	esophagus:	n/a
48	chr19:21262035-21262085	Jurkat	blood:	n/a
49	chr19:21262035-21262085	PFSK-1	brain:	n/a
50	chr19:21203417-21203467	GM12892	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:21230722..21233642-chr19:21264436..21267129,2	K562	blood:
2	chr19:21217901..21220893-chr19:21222403..21225000,3	K562	blood:
3	chr19:21246343..21248444-chr19:21263959..21266875,2	K562	blood:
4	chr19:21238270..21239771-chr19:21264302..21266943,2	K562	blood:
5	chr19:21203226..21204874-chr19:21207837..21209473,2	MCF-7	breast:
6	chr19:21204714..21207211-chr19:21209787..21213344,3	K562	blood:
7	chr19:21203269..21205162-chr19:21263863..21266449,2	MCF-7	breast:
8	chr17:41398648..41400647-chr19:21234769..21236289,5	MCF-7	breast:
9	chr19:21236568..21238876-chr19:21241377..21243478,2	K562	blood:
10	chr19:21214855..21215355-chr5:68664827..68665328,2	NB4	blood:
11	chr19:21257717..21259573-chr19:21372943..21374798,2	K562	blood:
12	chr19:21217901..21220893-chr19:21222403..21225000,3	K562	blood:
13	chr19:21215243..21217384-chr19:21265595..21267237,2	K562	blood:
14	chr19:21183047..21184669-chr19:21201811..21203556,2	MCF-7	breast:
15	chr19:21203226..21204874-chr19:21207837..21209473,2	MCF-7	breast:
16	chr17:41381905..41383742-chr19:21236269..21237789,3	K562	blood:
17	chr19:21086946..21088802-chr19:21210415..21213328,2	MCF-7	breast:
18	chr19:21260366..21262135-chr19:21263416..21265253,2	K562	blood:
19	chr19:21260635..21262427-chr19:21263416..21266258,2	K562	blood:
20	chr17:41381927..41383535-chr19:21236269..21237789,2	MCF-7	breast:
21	chr19:21204714..21207211-chr19:21209787..21213344,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF430-1	chr19:21246730-21247067	NONHSAT063682

No data

Variant related genes	Relation type
ZNF714	TF binding region
ENSG00000271598	TF binding region
ENSG00000265650	TF binding region
VN1R80P	TF binding region
ZNF430	TF binding region
ZNF714	CpG island
ENSG00000271598	CpG island
ENSG00000265650	CpG island
VN1R80P	CpG island
ZNF430	CpG island
ENSG00000118620	chromatin interactions
ENSG00000271598	chromatin interactions
ENSG00000265650	chromatin interactions
ENSG00000085231	chromatin interactions
ENSG00000160352	chromatin interactions
ENSG00000152942	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 3089 )
Associated
traits (count: 39 )

Variant overlapped rSNPs/rCNVs (count:3089 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17447963	chr19:21184533-21184534	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551933789	chr19:21184641-21184642	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181343610	chr19:21184642-21184643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537390850	chr19:21184643-21184644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs56860207	chr19:21184665-21184666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371485403	chr19:21184669-21184670	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs199639444	chr19:21184670-21184671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146490346	chr19:21184671-21184672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370069170	chr19:21184673-21184674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201707567	chr19:21184678-21184679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371925950	chr19:21184687-21184688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550822629	chr19:21184688-21184689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200237192	chr19:21184690-21184691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56712182	chr19:21184691-21184692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35750070	chr19:21184703-21184704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539620170	chr19:21184713-21184714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373194612	chr19:21184732-21184733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs71174780	chr19:21184734-21184735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs57981503	chr19:21184746-21184747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559485422	chr19:21184815-21184816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142020237	chr19:21184903-21184904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113746720	chr19:21184904-21184905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555842846	chr19:21184910-21184911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575698158	chr19:21184941-21184942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150657454	chr19:21184992-21184993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534094202	chr19:21185032-21185033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564175821	chr19:21185033-21185034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10416560	chr19:21185037-21185038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs540018678	chr19:21185047-21185048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560277824	chr19:21185053-21185054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530720935	chr19:21185054-21185055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185124400	chr19:21185060-21185061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112181270	chr19:21185062-21185063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562154310	chr19:21185093-21185094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563385538	chr19:21185158-21185159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190366127	chr19:21185161-21185162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532370772	chr19:21185166-21185167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552282297	chr19:21185169-21185170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10416447	chr19:21185178-21185179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs571025560	chr19:21185238-21185239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182004391	chr19:21185265-21185266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548519206	chr19:21185284-21185285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546908498	chr19:21185331-21185332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567053891	chr19:21185343-21185344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147495183	chr19:21185344-21185345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555855056	chr19:21185370-21185371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575731481	chr19:21185371-21185372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569275063	chr19:21185390-21185391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs75376324	chr19:21185399-21185400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538211699	chr19:21185446-21185447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:39)

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
Schizophrenia	20967226	CNVD

Chromatin state (count:2315 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21183200-21186400	Weak transcription	Colon Smooth Muscle	Colon
2	chr19:21183400-21193800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:21183400-21196000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:21183800-21188600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr19:21183800-21188800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr19:21183800-21189000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr19:21183800-21190800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr19:21183800-21191000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr19:21183800-21194200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr19:21184000-21184600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr19:21184000-21188600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr19:21184000-21191200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:21184000-21198000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr19:21184400-21184800	Enhancers	Dnd41	blood
15	chr19:21184400-21196800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr19:21184600-21186200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr19:21184800-21185600	Weak transcription	Dnd41	blood
18	chr19:21185600-21186400	Enhancers	Dnd41	blood
19	chr19:21186200-21186400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr19:21186400-21190200	Weak transcription	Dnd41	blood
21	chr19:21188600-21189000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:21188600-21192200	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr19:21188600-21192600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr19:21188800-21189000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr19:21189000-21190200	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr19:21189000-21192200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:21189000-21192400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:21190200-21190800	Strong transcription	Dnd41	blood
29	chr19:21190200-21192400	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr19:21190800-21195400	Weak transcription	Dnd41	blood
31	chr19:21192200-21194000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:21192200-21203000	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr19:21192400-21203000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr19:21192400-21203400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr19:21192600-21203000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr19:21202800-21203000	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr19:21202800-21203000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr19:21202800-21203000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr19:21202800-21203000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr19:21202800-21203000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr19:21202800-21203000	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr19:21202800-21203000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr19:21202800-21203000	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr19:21202800-21203000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr19:21202800-21203000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr19:21202800-21203000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr19:21202800-21203000	Enhancers	Fetal Thymus	thymus
48	chr19:21202800-21203000	Enhancers	Thymus	Thymus
49	chr19:21202800-21203000	Active TSS	Dnd41	blood
50	chr19:21202800-21203200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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