Variant report

Variant	nsv436253
Chromosome Location	chr19:22188479-22385212
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:419)
CpG islands
(count:1771)
Chromatin interactive
region (count:5)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	ATF1	chr19:22235032-22235378	K562	blood:	n/a	n/a
3	BACH1	chr19:22276070-22276088	K562	blood:	n/a	n/a
4	BCLAF1	chr19:22327265-22327471	GM12878	blood:	n/a	n/a
5	CBX3	chr19:22327195-22327536	K562	blood:	n/a	n/a
6	CBX3	chr19:22327182-22327501	K562	blood:	n/a	n/a
7	CBX3	chr19:22327284-22327512	HCT-116	colon:	n/a	n/a
8	CBX3	chr19:22234952-22235406	K562	blood:	n/a	n/a
9	CEBPB	chr19:22217116-22217618	IMR90	lung:	n/a	n/a
10	CEBPB	chr19:22258511-22258573	HepG2	liver:	n/a	n/a
11	CEBPB	chr19:22232756-22233017	A549	lung:	n/a	n/a
12	CEBPB	chr19:22211407-22211566	IMR90	lung:	n/a	chr19:22211437-22211448
13	CEBPB	chr19:22232727-22233148	HepG2	liver:	n/a	n/a
14	CEBPB	chr19:22209162-22209823	A549	lung:	n/a	chr19:22209630-22209641
15	CEBPB	chr19:22219004-22219042	A549	lung:	n/a	n/a
16	CEBPB	chr19:22228739-22228939	K562	blood:	n/a	n/a
17	CEBPB	chr19:22317520-22317702	HepG2	liver:	n/a	n/a
18	CEBPB	chr19:22194238-22194449	K562	blood:	n/a	n/a
19	CEBPB	chr19:22217046-22217652	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:22268516-22268793	IMR90	lung:	n/a	n/a
21	CEBPB	chr19:22194279-22194483	MCF-7	breast:	n/a	n/a
22	CEBPB	chr19:22231337-22231754	A549	lung:	n/a	n/a
23	CEBPB	chr19:22229978-22231113	A549	lung:	n/a	n/a
24	CEBPB	chr19:22218058-22218252	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:22226449-22227119	IMR90	lung:	n/a	n/a
26	CEBPB	chr19:22194337-22194423	A549	lung:	n/a	n/a
27	CEBPB	chr19:22268451-22268763	K562	blood:	n/a	n/a
28	CEBPB	chr19:22268494-22268820	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:22217019-22217672	A549	lung:	n/a	n/a
30	CEBPB	chr19:22209221-22209818	IMR90	lung:	n/a	chr19:22209630-22209641
31	CEBPB	chr19:22320453-22320571	A549	lung:	n/a	n/a
32	CEBPB	chr19:22231099-22231711	K562	blood:	n/a	n/a
33	CEBPB	chr19:22316363-22316659	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:22209167-22209821	HepG2	liver:	n/a	chr19:22209630-22209641
35	CEBPB	chr19:22217968-22218168	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:22215569-22215843	A549	lung:	n/a	n/a
37	CEBPB	chr19:22318406-22318779	HepG2	liver:	n/a	n/a
38	CEBPB	chr19:22316342-22316684	A549	lung:	n/a	n/a
39	CEBPB	chr19:22268460-22268665	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr19:22228175-22228904	A549	lung:	n/a	n/a
41	CEBPB	chr19:22235002-22235306	K562	blood:	n/a	n/a
42	CEBPB	chr19:22229982-22231755	HepG2	liver:	n/a	n/a
43	CEBPB	chr19:22318107-22318751	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr19:22222624-22222824	HepG2	liver:	n/a	n/a
45	CEBPB	chr19:22211370-22212109	A549	lung:	n/a	chr19:22211437-22211448
46	CEBPB	chr19:22211380-22212031	HepG2	liver:	n/a	chr19:22211437-22211448
47	CEBPB	chr19:22226274-22227084	A549	lung:	n/a	n/a
48	CEBPB	chr19:22217961-22218207	A549	lung:	n/a	n/a
49	CEBPB	chr19:22212805-22213005	HepG2	liver:	n/a	chr19:22212827-22212838
50	CEBPB	chr19:22377473-22377491	A549	lung:	n/a	n/a

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:22320869-22320919	CMK	blood:	n/a
2	chr19:22235454-22235504	ECC-1	luminal epithelium:	n/a
3	chr19:22320869-22320919	CMK	blood:	n/a
4	chr19:22235454-22235504	ECC-1	luminal epithelium:	n/a
5	chr19:22234992-22235042	ECC-1	luminal epithelium:	n/a
6	chr19:22197547-22197597	SK-N-SH_RA	brain:	n/a
7	chr19:22235144-22235194	IMR90	lung:	fetal
8	chr19:22235281-22235331	HCF	heart:	n/a
9	chr19:22193911-22193961	Jurkat	blood:	n/a
10	chr19:22235199-22235249	ovcar-3	ovarian:	n/a
11	chr19:22320744-22320794	HIPEpiC	eye:	n/a
12	chr19:22235281-22235331	BE2_C	brain:	n/a
13	chr19:22235144-22235194	GM12891	blood:	n/a
14	chr19:22235256-22235306	K562	blood:	n/a
15	chr19:22193479-22193529	RPTEC	kidney:	n/a
16	chr19:22235022-22235072	PANC-1	pancreas:	n/a
17	chr19:22235454-22235504	HCF	heart:	n/a
18	chr19:22193293-22193343	SK-N-SH	brain:	n/a
19	chr19:22379264-22379314	Jurkat	blood:	n/a
20	chr19:22193911-22193961	PANC-1	pancreas:	n/a
21	chr19:22193724-22193774	T-47D	breast:	n/a
22	chr19:22235409-22235459	SKMC	muscle:	n/a
23	chr19:22235256-22235306	HEEpiC	esophagus:	n/a
24	chr19:22193293-22193343	K562	blood:	n/a
25	chr19:22234992-22235042	HEK293	kidney:	embryo
26	chr19:22235256-22235306	HUVEC	blood vessel:	n/a
27	chr19:22193349-22193399	MCF-7	breast:	n/a
28	chr19:22235272-22235322	Hela-S3	cervix:	n/a
29	chr19:22318466-22318516	HCPEpiC	choroid plexus:	n/a
30	chr19:22193911-22193961	HAEpiC	amniotic membrane:	n/a
31	chr19:22320975-22321025	GM19239	blood:	n/a
32	chr19:22320869-22320919	SK-N-SH	brain:	n/a
33	chr19:22235551-22235601	GM12892	blood:	n/a
34	chr19:22235199-22235249	SK-N-MC	brain:	n/a
35	chr19:22235272-22235322	CMK	blood:	n/a
36	chr19:22235256-22235306	SK-N-SH_RA	brain:	n/a
37	chr19:22318466-22318516	RPTEC	kidney:	n/a
38	chr19:22193759-22193809	AG04450	lung:	fetal
39	chr19:22234992-22235042	LNCaP	prostate:	n/a
40	chr19:22323107-22323157	HUVEC	blood vessel:	n/a
41	chr19:22193293-22193343	ProgFib	skin:	n/a
42	chr19:22193540-22193590	NB4	blood:	n/a
43	chr19:22193479-22193529	Caco-2	colon:	n/a
44	chr19:22320744-22320794	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:22235199-22235249	HRE	kidney:	n/a
46	chr19:22193479-22193529	HRPEpiC	eye:	n/a
47	chr19:22235199-22235249	A549	lung:	n/a
48	chr19:22235850-22235900	K562	blood:	n/a
49	chr19:22321700-22321750	K562	blood:	n/a
50	chr19:22320744-22320794	ProgFib	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:22203510..22205947-chr19:22215522..22217797,2	K562	blood:
2	chr19:22236195..22238676-chr19:22281763..22284450,2	K562	blood:
3	chr19:22203510..22205947-chr19:22215522..22217797,2	K562	blood:
4	chr19:22234996..22236729-chr19:22244257..22246826,2	MCF-7	breast:
5	chr19:22236195..22238676-chr19:22281763..22284450,2	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF208-2	chr19:22232617-22232807	ENSG00000269199.1
2	lnc-ZNF208-1	chr19:22218967-22219117	ENSG00000269504.1
3	lnc-ZNF208-2	chr19:22228893-22229114	ENSG00000269199.1
4	lnc-ZNF208-1	chr19:22217683-22217800	ENSG00000269504.1
5	lnc-ZNF208-1	chr19:22217475-22217599	ENSG00000269504.1
6	lnc-ZNF676-2	chr19:22357568-22357993	NONHSAT063768
7	lnc-ZNF676-3	chr19:22311429-22311769	NONHSAT063766
8	lnc-ZNF676-3	chr19:22312079-22312249	NONHSAT063766
9	lnc-ZNF676-3	chr19:22312574-22313120	NONHSAT063766
10	lnc-ZNF208-1	chr19:22209038-22209147	ENSG00000269504.1
11	lnc-ZNF208-2	chr19:22228681-22228787	ENSG00000269199.1
12	lnc-ZNF208-1	chr19:22208108-22209147	XLOC_013265
13	lnc-ZNF208-1	chr19:22210001-22210213	XLOC_013265
14	lnc-ZNF208-1	chr19:22210001-22210146	ENSG00000269504.1
15	lnc-ZNF729-7	chr19:22243310-22243430	NONHSAT063763
16	lnc-ZNF729-7	chr19:22235326-22235437	NONHSAT063763
17	lnc-ZNF208-2	chr19:22226302-22226327	ENSG00000269199.1
18	lnc-ZNF208-1	chr19:22217900-22217980	XLOC_013265
19	lnc-ZNF208-1	chr19:22200761-22201063	ENSG00000269504.1
20	lnc-ZNF676-3	chr19:22314709-22314736	NONHSAT063766
21	lnc-ZNF208-1	chr19:22205274-22205401	ENSG00000269504.1
22	lnc-ZNF208-1	chr19:22204886-22205086	ENSG00000269504.1
23	lnc-ZNF729-7	chr19:22246881-22247134	NONHSAT063763
24	lnc-ZNF208-1	chr19:22217900-22218011	ENSG00000269504.1
25	lnc-ZNF208-3	chr19:22248630-22249200	NONHSAT063765

No data

Variant related genes	Relation type
VN1R85P	TF binding region
ENSG00000269504	TF binding region
ENSG00000269575	TF binding region
ZNF257	TF binding region
ZNF208	TF binding region
ENSG00000268116	TF binding region
ZNF92P2	TF binding region
ENSG00000268079	TF binding region
PCGF7P	TF binding region
ZNF676	TF binding region
ENSG00000269199	TF binding region
ENSG00000269742	TF binding region
VN1R85P	CpG island
ENSG00000269504	CpG island
ENSG00000269575	CpG island
ZNF257	CpG island
ZNF208	CpG island
ENSG00000268116	CpG island
ZNF92P2	CpG island
ENSG00000268079	CpG island
PCGF7P	CpG island
ZNF676	CpG island
ENSG00000269199	CpG island
ENSG00000269742	CpG island
ENSG00000197134	chromatin interactions

Extended variants
information (count: 4537 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:4537 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577916369	chr19:22188483-22188484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181001733	chr19:22188497-22188498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs151134503	chr19:22188501-22188502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575917534	chr19:22188569-22188570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543518287	chr19:22188571-22188572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11878668	chr19:22188606-22188607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs372788664	chr19:22188652-22188653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573908950	chr19:22188670-22188671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541224887	chr19:22188686-22188687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116394195	chr19:22188702-22188703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533267141	chr19:22188705-22188706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7248488	chr19:22188709-22188710	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs550568068	chr19:22188724-22188725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188769962	chr19:22188756-22188757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530778418	chr19:22188796-22188797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201287807	chr19:22188798-22188799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549101728	chr19:22188807-22188808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181154682	chr19:22188813-22188814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570442610	chr19:22188815-22188816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187010544	chr19:22188819-22188820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571459202	chr19:22188848-22188849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369368502	chr19:22188849-22188850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529678095	chr19:22188855-22188856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539339003	chr19:22188907-22188908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368386902	chr19:22188921-22188922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557335715	chr19:22188994-22188995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569666024	chr19:22188997-22188998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536620333	chr19:22189042-22189043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539098447	chr19:22189143-22189144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191391791	chr19:22189172-22189173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139022412	chr19:22189187-22189188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1057136	chr19:22189192-22189193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541087986	chr19:22189215-22189216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1057135	chr19:22189218-22189219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553208060	chr19:22189222-22189223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73017852	chr19:22189239-22189240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs1057134	chr19:22189245-22189246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs1064265	chr19:22189248-22189249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545305418	chr19:22189289-22189290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs8103464	chr19:22189294-22189295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375607688	chr19:22189295-22189296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1135213	chr19:22189304-22189305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1057133	chr19:22189313-22189314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542611064	chr19:22189320-22189321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561090115	chr19:22189352-22189353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1057132	chr19:22189457-22189458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1064264	chr19:22189515-22189516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181864262	chr19:22189540-22189541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186420791	chr19:22189626-22189627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190825640	chr19:22189634-22189635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:47)

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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:22183000-22192600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr19:22188200-22192600	Weak transcription	Aorta	Aorta
3	chr19:22191000-22192600	Weak transcription	Right Ventricle	heart
4	chr19:22191400-22194000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr19:22191600-22194000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr19:22192200-22193800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr19:22192200-22193800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:22192200-22194000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
9	chr19:22192400-22193800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr19:22192400-22194000	ZNF genes & repeats	Pancreas	Pancrea
11	chr19:22192600-22193200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr19:22192600-22193200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:22192600-22193800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:22192600-22193800	Active TSS	Aorta	Aorta
15	chr19:22192600-22193800	Active TSS	Esophagus	oesophagus
16	chr19:22192600-22193800	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr19:22192600-22193800	Active TSS	Right Ventricle	heart
18	chr19:22192600-22194000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
19	chr19:22192600-22194000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
20	chr19:22192600-22194000	Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr19:22192600-22194000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr19:22192600-22194000	Active TSS	Adipose Nuclei	Adipose
23	chr19:22192600-22194000	Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr19:22192600-22194000	Active TSS	Left Ventricle	heart
25	chr19:22192600-22194000	Active TSS	Ovary	ovary
26	chr19:22192600-22194000	Active TSS	Placenta Amnion	Placenta Amnion
27	chr19:22192600-22194000	Active TSS	Right Atrium	heart
28	chr19:22192600-22194000	Active TSS	Stomach Smooth Muscle	stomach
29	chr19:22192600-22194200	Active TSS	Brain Hippocampus Middle	brain
30	chr19:22192600-22194200	Active TSS	Colon Smooth Muscle	Colon
31	chr19:22192800-22193400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr19:22192800-22193800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr19:22192800-22193800	Active TSS	Duodenum Mucosa	Duodenum
34	chr19:22192800-22193800	Active TSS	Fetal Kidney	kidney
35	chr19:22192800-22193800	Active TSS	Psoas Muscle	Psoas
36	chr19:22192800-22194000	Active TSS	Brain Cingulate Gyrus	brain
37	chr19:22192800-22194000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
38	chr19:22192800-22194000	Active TSS	Rectal Mucosa Donor 29	rectum
39	chr19:22192800-22194000	Active TSS	Rectal Mucosa Donor 31	rectum
40	chr19:22193000-22193400	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
41	chr19:22193000-22193800	Active TSS	Brain Anterior Caudate	brain
42	chr19:22193000-22194000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr19:22193200-22193400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr19:22193200-22193600	Active TSS	Colonic Mucosa	Colon
45	chr19:22193200-22193800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
46	chr19:22193200-22193800	Active TSS	Osteobl	bone
47	chr19:22193200-22194000	Active TSS	Primary B cells from peripheral blood	blood
48	chr19:22193200-22194000	Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr19:22193200-22194000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr19:22193200-22194000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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