Variant report

Variant	esv2760532
Chromosome Location	chr19:22236219-22355753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:190)
CpG islands
(count:428)
Chromatin interactive
region (count:3)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:190 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:22317299-22317405	K562	blood:	n/a	n/a
2	BACH1	chr19:22276070-22276088	K562	blood:	n/a	n/a
3	BCLAF1	chr19:22327265-22327471	GM12878	blood:	n/a	n/a
4	CBX3	chr19:22327195-22327536	K562	blood:	n/a	n/a
5	CBX3	chr19:22327284-22327512	HCT-116	colon:	n/a	n/a
6	CBX3	chr19:22327182-22327501	K562	blood:	n/a	n/a
7	CEBPB	chr19:22316363-22316659	HepG2	liver:	n/a	n/a
8	CEBPB	chr19:22320441-22320600	HepG2	liver:	n/a	n/a
9	CEBPB	chr19:22320453-22320571	A549	lung:	n/a	n/a
10	CEBPB	chr19:22318406-22318779	HepG2	liver:	n/a	n/a
11	CEBPB	chr19:22268451-22268763	K562	blood:	n/a	n/a
12	CEBPB	chr19:22317520-22317702	HepG2	liver:	n/a	n/a
13	CEBPB	chr19:22268460-22268665	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr19:22258511-22258573	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:22268542-22268703	A549	lung:	n/a	n/a
16	CEBPB	chr19:22268494-22268820	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:22316342-22316684	A549	lung:	n/a	n/a
18	CEBPB	chr19:22318107-22318751	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:22353367-22353394	HepG2	liver:	n/a	chr19:22353370-22353381
20	CEBPB	chr19:22268516-22268793	IMR90	lung:	n/a	n/a
21	CEBPZ	chr19:22327227-22327553	HepG2	liver:	n/a	n/a
22	CTCF	chr19:22347623-22347657	GM10248	blood:	n/a	n/a
23	CTCF	chr19:22323327-22323369	Fibrobl	skin:	n/a	n/a
24	CTCF	chr19:22350251-22350267	GM13976	blood:	n/a	n/a
25	CTCF	chr19:22326760-22326910	MCF-7	breast:	n/a	n/a
26	CTCF	chr19:22326880-22327030	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr19:22344343-22344384	GM20000	blood:	n/a	n/a
28	CTCF	chr19:22353464-22353507	Lung_OC	lung:	n/a	n/a
29	CTCF	chr19:22323766-22323791	MCF-7	breast:	n/a	n/a
30	CTCF	chr19:22323184-22323240	ProgFib	skin:	n/a	n/a
31	CTCF	chr19:22354495-22354502	Medullo	brain:	n/a	n/a
32	CTCF	chr19:22342028-22342100	LNCaP	prostate:	n/a	n/a
33	CTCF	chr19:22295793-22295878	GM20000	blood:	n/a	n/a
34	CTCF	chr19:22294750-22294821	GM13976	blood:	n/a	n/a
35	CTCF	chr19:22322395-22322424	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr19:22306400-22306550	HEK293	kidney:	n/a	n/a
37	CTCF	chr19:22278949-22278977	GM20000	blood:	n/a	n/a
38	CTCF	chr19:22288010-22288081	GM13977	blood:	n/a	n/a
39	CTCF	chr19:22306343-22306483	K562	blood:	n/a	n/a
40	CUX1	chr19:22259318-22259340	K562	blood:	n/a	n/a
41	E2F4	chr19:22299519-22299743	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr19:22253719-22253919	MCF10A-Er-Src	breast:	n/a	n/a
43	EGR1	chr19:22296773-22296918	GM12878	blood:	n/a	n/a
44	ELF1	chr19:22235966-22236234	K562	blood:	n/a	chr19:22236088-22236101
45	EP300	chr19:22271257-22271259	GM12878	blood:	n/a	n/a
46	EP300	chr19:22327314-22327434	GM12878	blood:	n/a	n/a
47	EP300	chr19:22327307-22327434	GM12878	blood:	n/a	n/a
48	GATA3	chr19:22248546-22248714	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr19:22245677-22245864	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr19:22254271-22254410	SH-SY5Y	brain:	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	chr19:22318466-22318516	AG09319	gingival:	n/a
2	chr19:22318466-22318516	AG09319	gingival:	n/a
3	chr19:22318466-22318516	NHBE	bronchial:	n/a
4	chr19:22321700-22321750	U87	brain:	n/a
5	chr19:22323107-22323157	K562	blood:	n/a
6	chr19:22320869-22320919	HEK293	kidney:	embryo
7	chr19:22320869-22320919	K562	blood:	n/a
8	chr19:22323107-22323157	HMEC	breast:	n/a
9	chr19:22318466-22318516	BE2_C	brain:	n/a
10	chr19:22320869-22320919	HCM	heart:	n/a
11	chr19:22320975-22321025	HCM	heart:	n/a
12	chr19:22321700-22321750	NT2-D1	testis:	n/a
13	chr19:22319196-22319246	SK-N-SH_RA	brain:	n/a
14	chr19:22318466-22318516	AoSMC	blood vessel:	n/a
15	chr19:22320975-22321025	HRE	kidney:	n/a
16	chr19:22323107-22323157	Hela-S3	cervix:	n/a
17	chr19:22320869-22320919	GM06990	blood:	n/a
18	chr19:22319196-22319246	RPTEC	kidney:	n/a
19	chr19:22319196-22319246	SAEC	small airway:	n/a
20	chr19:22319196-22319246	GM06990	blood:	n/a
21	chr19:22321700-22321750	HepG2	liver:	n/a
22	chr19:22318466-22318516	CMK	blood:	n/a
23	chr19:22320975-22321025	MCF-7	breast:	n/a
24	chr19:22319196-22319246	AG10803	skin:	n/a
25	chr19:22318466-22318516	HNPCEpiC	eye:	n/a
26	chr19:22319196-22319246	GM12878	blood:	n/a
27	chr19:22320975-22321025	AoSMC	blood vessel:	n/a
28	chr19:22320869-22320919	Hepatocyte	liver:	n/a
29	chr19:22320869-22320919	A549	lung:	n/a
30	chr19:22323107-22323157	HCT-116	colon:	n/a
31	chr19:22318466-22318516	HepG2	liver:	n/a
32	chr19:22318466-22318516	Hepatocyte	liver:	n/a
33	chr19:22321700-22321750	AG04450	lung:	fetal
34	chr19:22320869-22320919	HRCEpiC	kidney:	n/a
35	chr19:22323107-22323157	MCF10A-Er-Src	breast:	n/a
36	chr19:22320869-22320919	HepG2	liver:	n/a
37	chr19:22320975-22321025	NHDF-neo	bronchial:	n/a
38	chr19:22320744-22320794	HUVEC	blood vessel:	n/a
39	chr19:22321700-22321750	CMK	blood:	n/a
40	chr19:22319196-22319246	HAEpiC	amniotic membrane:	n/a
41	chr19:22321700-22321750	BJ	skin:	n/a
42	chr19:22321700-22321750	T-47D	breast:	n/a
43	chr19:22318466-22318516	H1-hESC	embryonic stem cell:	embryo
44	chr19:22320869-22320919	NH-A	brain:	n/a
45	chr19:22319196-22319246	NHBE	bronchial:	n/a
46	chr19:22320744-22320794	HNPCEpiC	eye:	n/a
47	chr19:22320975-22321025	Caco-2	colon:	n/a
48	chr19:22320744-22320794	HCT-116	colon:	n/a
49	chr19:22323107-22323157	AoSMC	blood vessel:	n/a
50	chr19:22319196-22319246	HRE	kidney:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:22236195..22238676-chr19:22281763..22284450,2	K562	blood:
2	chr19:22234996..22236729-chr19:22244257..22246826,2	MCF-7	breast:
3	chr19:22236195..22238676-chr19:22281763..22284450,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF729-7	chr19:22246881-22247134	NONHSAT063763
2	lnc-ZNF676-3	chr19:22314709-22314736	NONHSAT063766
3	lnc-ZNF208-3	chr19:22248630-22249200	NONHSAT063765
4	lnc-ZNF676-3	chr19:22312574-22313120	NONHSAT063766
5	lnc-ZNF676-3	chr19:22312079-22312249	NONHSAT063766
6	lnc-ZNF676-3	chr19:22311429-22311769	NONHSAT063766
7	lnc-ZNF729-7	chr19:22243310-22243430	NONHSAT063763

No data

Variant related genes	Relation type
ENSG00000268116	TF binding region
PCGF7P	TF binding region
ENSG00000269575	TF binding region
ZNF92P2	TF binding region
ENSG00000269199	TF binding region
ENSG00000269742	TF binding region
ENSG00000268116	CpG island
PCGF7P	CpG island
ENSG00000269575	CpG island
ZNF92P2	CpG island
ENSG00000269199	CpG island
ENSG00000269742	CpG island
ENSG00000197134	chromatin interactions

Extended variants
information (count: 2562 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:2562 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563522941	chr19:22236314-22236315	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs575854426	chr19:22236316-22236317	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs147167588	chr19:22236328-22236329	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs186972917	chr19:22236347-22236348	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs539847863	chr19:22236355-22236356	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs140373029	chr19:22236373-22236374	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs371200666	chr19:22236374-22236375	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs6511314	chr19:22236395-22236396	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs115855689	chr19:22236449-22236450	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs144220574	chr19:22236453-22236454	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs569309527	chr19:22236476-22236477	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs6511315	chr19:22236503-22236504	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548681398	chr19:22236533-22236534	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs566992160	chr19:22236620-22236621	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139015281	chr19:22236622-22236623	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375183078	chr19:22236624-22236625	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552874386	chr19:22236731-22236732	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577907713	chr19:22236751-22236752	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538552591	chr19:22236820-22236821	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs192226046	chr19:22236862-22236863	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs147379303	chr19:22236876-22236877	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs79029126	chr19:22236878-22236879	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs369639117	chr19:22236998-22236999	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs78367666	chr19:22237028-22237029	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs116220423	chr19:22237041-22237042	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs573353726	chr19:22237075-22237076	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs540857635	chr19:22237079-22237080	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs145383649	chr19:22237089-22237090	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs532888758	chr19:22237114-22237115	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs141350636	chr19:22237156-22237157	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs562804536	chr19:22237165-22237166	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs77231673	chr19:22237172-22237173	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs78845399	chr19:22237174-22237175	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs372264265	chr19:22237175-22237176	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs536138261	chr19:22237196-22237197	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs548546066	chr19:22237201-22237202	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs374861617	chr19:22237315-22237316	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs184251378	chr19:22237318-22237319	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs7259971	chr19:22237319-22237320	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs145093503	chr19:22237372-22237373	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs547030446	chr19:22237487-22237488	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs117779622	chr19:22237522-22237523	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200417995	chr19:22237553-22237554	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs538785469	chr19:22237584-22237585	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557308273	chr19:22237609-22237610	Weak transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6511316	chr19:22237629-22237630	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs536674006	chr19:22237633-22237634	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs190466491	chr19:22237645-22237646	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs573417379	chr19:22237684-22237685	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs182242646	chr19:22237705-22237706	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:44)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:22234200-22236600	Active TSS	K562	blood
2	chr19:22234800-22236400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr19:22234800-22236400	Active TSS	Brain Anterior Caudate	brain
4	chr19:22234800-22236400	Active TSS	Rectal Mucosa Donor 29	rectum
5	chr19:22234800-22236400	Active TSS	NHEK	skin
6	chr19:22234800-22236600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr19:22235000-22236400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr19:22235000-22236400	Active TSS	Primary T killer memory cells from peripheral blood	blood
9	chr19:22235000-22236400	ZNF genes & repeats	Fetal Thymus	thymus
10	chr19:22235200-22236400	Active TSS	Primary B cells from cord blood	blood
11	chr19:22235600-22236400	Active TSS	Monocytes-CD14+_RO01746	blood
12	chr19:22235800-22236400	Active TSS	Placenta	Placenta
13	chr19:22235800-22236600	Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr19:22235800-22237800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr19:22235800-22258000	Weak transcription	Aorta	Aorta
16	chr19:22235800-22258200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr19:22235800-22262200	Weak transcription	Gastric	stomach
18	chr19:22235800-22270400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr19:22236000-22236400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr19:22236000-22236400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr19:22236000-22236400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr19:22236000-22236600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:22236000-22236600	Enhancers	Fetal Muscle Trunk	muscle
24	chr19:22236000-22238800	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr19:22236000-22242600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr19:22236000-22244200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr19:22236000-22245800	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr19:22236000-22247000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr19:22236000-22257200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr19:22236000-22258000	Weak transcription	Pancreas	Pancrea
31	chr19:22236200-22236400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr19:22236200-22236600	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr19:22236200-22241200	Weak transcription	Primary T cells from cord blood	blood
34	chr19:22236200-22262400	Weak transcription	Ovary	ovary
35	chr19:22236400-22236600	Flanking Active TSS	Placenta	Placenta
36	chr19:22236400-22236800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr19:22236400-22238000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr19:22236400-22239200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr19:22236400-22246600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr19:22236600-22236800	Enhancers	Placenta	Placenta
41	chr19:22236600-22237400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr19:22236600-22239200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
43	chr19:22236600-22247000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr19:22236800-22249800	Weak transcription	Thymus	Thymus
45	chr19:22236800-22252000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:22237400-22237800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr19:22238600-22241600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr19:22239200-22240000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr19:22239400-22241600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:22240000-22250200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin

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