Variant report

Variant	esv3424104
Chromosome Location	chr19:22223429-22436512
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:409)
CpG islands
(count:1222)
Chromatin interactive
region (count:3)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:409 , 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	chr19:22235032-22235378	K562	blood:	n/a	n/a
2	ATF1	chr19:22317299-22317405	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	chr19:22234952-22235406	K562	blood:	n/a	n/a
7	CBX3	chr19:22327284-22327512	HCT-116	colon:	n/a	n/a
8	CBX3	chr19:22327182-22327501	K562	blood:	n/a	n/a
9	CEBPB	chr19:22318107-22318751	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr19:22428273-22428410	A549	lung:	n/a	n/a
11	CEBPB	chr19:22268516-22268793	IMR90	lung:	n/a	n/a
12	CEBPB	chr19:22235002-22235306	K562	blood:	n/a	n/a
13	CEBPB	chr19:22258511-22258573	HepG2	liver:	n/a	n/a
14	CEBPB	chr19:22320441-22320600	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:22228160-22228895	HepG2	liver:	n/a	n/a
16	CEBPB	chr19:22232727-22233148	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:22416547-22416648	A549	lung:	n/a	n/a
18	CEBPB	chr19:22268494-22268820	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:22435325-22435617	A549	lung:	n/a	n/a
20	CEBPB	chr19:22435333-22435533	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:22318406-22318779	HepG2	liver:	n/a	n/a
22	CEBPB	chr19:22232756-22233017	A549	lung:	n/a	n/a
23	CEBPB	chr19:22268460-22268665	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr19:22226449-22227119	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:22229982-22231755	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:22316363-22316659	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:22228314-22228872	IMR90	lung:	n/a	n/a
28	CEBPB	chr19:22320453-22320571	A549	lung:	n/a	n/a
29	CEBPB	chr19:22229978-22231113	A549	lung:	n/a	n/a
30	CEBPB	chr19:22268451-22268763	K562	blood:	n/a	n/a
31	CEBPB	chr19:22228175-22228904	A549	lung:	n/a	n/a
32	CEBPB	chr19:22316342-22316684	A549	lung:	n/a	n/a
33	CEBPB	chr19:22372087-22372275	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:22268542-22268703	A549	lung:	n/a	n/a
35	CEBPB	chr19:22231099-22231711	K562	blood:	n/a	n/a
36	CEBPB	chr19:22228739-22228939	K562	blood:	n/a	n/a
37	CEBPB	chr19:22423125-22423259	IMR90	lung:	n/a	n/a
38	CEBPB	chr19:22353367-22353394	HepG2	liver:	n/a	chr19:22353370-22353381
39	CEBPB	chr19:22423082-22423250	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:22377473-22377491	A549	lung:	n/a	n/a
41	CEBPB	chr19:22427533-22427881	A549	lung:	n/a	n/a
42	CEBPB	chr19:22226274-22227084	A549	lung:	n/a	n/a
43	CEBPB	chr19:22226283-22227250	HepG2	liver:	n/a	n/a
44	CEBPB	chr19:22223974-22224098	A549	lung:	n/a	n/a
45	CEBPB	chr19:22231337-22231754	A549	lung:	n/a	n/a
46	CEBPB	chr19:22435325-22435556	HepG2	liver:	n/a	n/a
47	CEBPB	chr19:22317520-22317702	HepG2	liver:	n/a	n/a
48	CEBPB	chr19:22427609-22427849	HepG2	liver:	n/a	n/a
49	CEBPZ	chr19:22327227-22327553	HepG2	liver:	n/a	n/a
50	CHD2	chr19:22235124-22235488	K562	blood:	n/a	chr19:22235183-22235193

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:22233809-22233859	GM19239	blood:	n/a
2	chr19:22235551-22235601	HEK293	kidney:	embryo
3	chr19:22233809-22233859	GM19239	blood:	n/a
4	chr19:22235551-22235601	HEK293	kidney:	embryo
5	chr19:22233809-22233859	SKMC	muscle:	n/a
6	chr19:22235409-22235459	AG04450	lung:	fetal
7	chr19:22233809-22233859	HCM	heart:	n/a
8	chr19:22235281-22235331	AG04450	lung:	fetal
9	chr19:22233809-22233859	HEK293	kidney:	embryo
10	chr19:22235281-22235331	PrEC	prostate:	n/a
11	chr19:22320869-22320919	SAEC	small airway:	n/a
12	chr19:22379264-22379314	NHBE	bronchial:	n/a
13	chr19:22379264-22379314	GM19239	blood:	n/a
14	chr19:22235022-22235072	GM19239	blood:	n/a
15	chr19:22320869-22320919	AG09319	gingival:	n/a
16	chr19:22235850-22235900	SKMC	muscle:	n/a
17	chr19:22235022-22235072	HRCEpiC	kidney:	n/a
18	chr19:22321700-22321750	Jurkat	blood:	n/a
19	chr19:22321700-22321750	AG04449	skin:	fetal
20	chr19:22235144-22235194	HEK293	kidney:	embryo
21	chr19:22235454-22235504	AG04450	lung:	fetal
22	chr19:22235850-22235900	HUVEC	blood vessel:	n/a
23	chr19:22320744-22320794	MCF-7	breast:	n/a
24	chr19:22235454-22235504	GM12878	blood:	n/a
25	chr19:22321700-22321750	ECC-1	luminal epithelium:	n/a
26	chr19:22235256-22235306	GM19239	blood:	n/a
27	chr19:22320975-22321025	T-47D	breast:	n/a
28	chr19:22323107-22323157	HAEpiC	amniotic membrane:	n/a
29	chr19:22235551-22235601	T-47D	breast:	n/a
30	chr19:22233809-22233859	HIPEpiC	eye:	n/a
31	chr19:22234992-22235042	HL-60	blood:	n/a
32	chr19:22235551-22235601	MCF10A-Er-Src	breast:	n/a
33	chr19:22235199-22235249	CMK	blood:	n/a
34	chr19:22235199-22235249	A549	lung:	n/a
35	chr19:22320744-22320794	HEEpiC	esophagus:	n/a
36	chr19:22235850-22235900	HEEpiC	esophagus:	n/a
37	chr19:22235551-22235601	CMK	blood:	n/a
38	chr19:22234992-22235042	NB4	blood:	n/a
39	chr19:22235409-22235459	HNPCEpiC	eye:	n/a
40	chr19:22235144-22235194	AG04450	lung:	fetal
41	chr19:22235272-22235322	HRCEpiC	kidney:	n/a
42	chr19:22235022-22235072	GM12892	blood:	n/a
43	chr19:22235850-22235900	HepG2	liver:	n/a
44	chr19:22235144-22235194	ovcar-3	ovarian:	n/a
45	chr19:22235850-22235900	LNCaP	prostate:	n/a
46	chr19:22233809-22233859	HRE	kidney:	n/a
47	chr19:22235454-22235504	ProgFib	skin:	n/a
48	chr19:22320744-22320794	GM12878	blood:	n/a
49	chr19:22320869-22320919	HEEpiC	esophagus:	n/a
50	chr19:22319196-22319246	GM06990	blood:	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:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF676-1	chr19:22429547-22429561	NONHSAT063770
2	lnc-ZNF208-2	chr19:22226302-22226327	ENSG00000269199.1
3	lnc-ZNF676-3	chr19:22312574-22313120	NONHSAT063766
4	lnc-ZNF729-7	chr19:22246881-22247134	NONHSAT063763
5	lnc-ZNF676-1	chr19:22427704-22428234	XLOC_013266
6	lnc-ZNF729-5	chr19:22386687-22386805	NONHSAT063769
7	lnc-ZNF676-1	chr19:22427704-22428003	XLOC_013266
8	lnc-ZNF676-1	chr19:22427343-22428234	NONHSAT063770
9	lnc-ZNF676-1	chr19:22428580-22428688	NONHSAT063770
10	lnc-ZNF676-3	chr19:22314709-22314736	NONHSAT063766
11	lnc-ZNF676-2	chr19:22357568-22357993	NONHSAT063768
12	lnc-ZNF208-2	chr19:22228681-22228787	ENSG00000269199.1
13	lnc-ZNF676-1	chr19:22426056-22428149	ENSG00000267872.1
14	lnc-ZNF676-1	chr19:22427128-22427457	XLOC_013266
15	lnc-ZNF729-7	chr19:22243310-22243430	NONHSAT063763
16	lnc-ZNF676-1	chr19:22427128-22427457	XLOC_013266
17	lnc-ZNF676-1	chr19:22429191-22429226	NONHSAT063770
18	lnc-ZNF208-2	chr19:22228893-22229114	ENSG00000269199.1
19	lnc-ZNF676-3	chr19:22312079-22312249	NONHSAT063766
20	lnc-ZNF676-1	chr19:22427150-22428234	XLOC_013266
21	lnc-ZNF676-1	chr19:22422350-22422570	NONHSAT063770
22	lnc-ZNF676-1	chr19:22428580-22428995	XLOC_013266
23	lnc-ZNF208-3	chr19:22248630-22249200	NONHSAT063765
24	lnc-ZNF729-7	chr19:22235326-22235437	NONHSAT063763
25	lnc-ZNF676-1	chr19:22426867-22427457	XLOC_013266
26	lnc-ZNF729-5	chr19:22385930-22386384	NONHSAT063769
27	lnc-ZNF676-1	chr19:22428580-22428995	XLOC_013266
28	lnc-ZNF208-2	chr19:22232617-22232807	ENSG00000269199.1
29	lnc-ZNF676-3	chr19:22311429-22311769	NONHSAT063766

No data

Variant related genes	Relation type
VN1R85P	TF binding region
ENSG00000269504	TF binding region
ENSG00000269575	TF binding region
ZNF257	TF binding region
ENSG00000267872	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
ENSG00000267872	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
CEBPB	miRNA target sites
PHF19	miRNA target sites
PSME1	miRNA target sites

Extended variants
information (count: 4902 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:4902 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150903215	chr19:22223989-22223990	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs185728945	chr19:22223990-22223991	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs417947	chr19:22224030-22224031	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs189419358	chr19:22224031-22224032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs565852684	chr19:22224054-22224055	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs541227227	chr19:22224077-22224078	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs533030786	chr19:22224087-22224088	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs544710151	chr19:22226414-22226415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562793877	chr19:22226418-22226419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530325750	chr19:22226425-22226426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548458516	chr19:22226440-22226441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541219875	chr19:22226445-22226446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553639274	chr19:22226547-22226548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79833848	chr19:22226550-22226551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76817931	chr19:22226555-22226556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546222751	chr19:22226566-22226567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147289699	chr19:22226574-22226575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs62112917	chr19:22226580-22226581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs545076920	chr19:22226633-22226634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114951439	chr19:22226661-22226662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140903977	chr19:22226668-22226669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141483909	chr19:22226713-22226714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187357646	chr19:22226739-22226740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190809307	chr19:22226742-22226743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182275865	chr19:22226754-22226755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534067347	chr19:22226859-22226860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150850724	chr19:22226907-22226908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34797845	chr19:22226924-22226925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71180511	chr19:22226925-22226926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200333610	chr19:22226926-22226927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547711552	chr19:22226949-22226950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186531512	chr19:22226959-22226960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544575124	chr19:22226972-22226973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567504078	chr19:22227054-22227055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79984252	chr19:22227058-22227059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62112918	chr19:22227079-22227080	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs62112919	chr19:22227145-22227146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112830356	chr19:22227146-22227147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs62112920	chr19:22227149-22227150	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs368879640	chr19:22227162-22227163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560504559	chr19:22227163-22227164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538586081	chr19:22227180-22227181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528017677	chr19:22227204-22227205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568246022	chr19:22227205-22227206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139275587	chr19:22227227-22227228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190136770	chr19:22227228-22227229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531991201	chr19:22227234-22227235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550273751	chr19:22227252-22227253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568955991	chr19:22227334-22227335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78226360	chr19:22227343-22227344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

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
Melanoma	20877625	CNVD

Chromatin state (count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:22226400-22228800	Weak transcription	Aorta	Aorta
2	chr19:22231200-22231400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
3	chr19:22234200-22234800	Enhancers	Primary hematopoietic stem cells	blood
4	chr19:22234200-22236600	Active TSS	K562	blood
5	chr19:22234400-22235000	Enhancers	Primary B cells from peripheral blood	blood
6	chr19:22234400-22235200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
7	chr19:22234600-22234800	Enhancers	Primary T cells fromperipheralblood	blood
8	chr19:22234600-22234800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr19:22234600-22234800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr19:22234600-22234800	Enhancers	Fetal Muscle Trunk	muscle
11	chr19:22234600-22235000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr19:22234600-22235000	Enhancers	Colon Smooth Muscle	Colon
13	chr19:22234600-22235200	Active TSS	Monocytes-CD14+_RO01746	blood
14	chr19:22234600-22235600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr19:22234600-22235800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
16	chr19:22234600-22236000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr19:22234600-22236200	Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr19:22234600-22236200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
19	chr19:22234800-22235000	Enhancers	Primary B cells from cord blood	blood
20	chr19:22234800-22235000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
21	chr19:22234800-22235000	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr19:22234800-22235000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:22234800-22235000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
24	chr19:22234800-22235200	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr19:22234800-22235200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
26	chr19:22234800-22235200	Flanking Active TSS	Fetal Muscle Trunk	muscle
27	chr19:22234800-22235400	Active TSS	Adipose Nuclei	Adipose
28	chr19:22234800-22235400	ZNF genes & repeats	Fetal Brain Female	brain
29	chr19:22234800-22235400	Active TSS	Placenta	Placenta
30	chr19:22234800-22235800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
31	chr19:22234800-22235800	Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr19:22234800-22235800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr19:22234800-22235800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr19:22234800-22235800	Active TSS	Brain Substantia Nigra	brain
35	chr19:22234800-22235800	Active TSS	Psoas Muscle	Psoas
36	chr19:22234800-22235800	Active TSS	Rectal Smooth Muscle	rectum
37	chr19:22234800-22235800	Active TSS	HUVEC	blood vessel
38	chr19:22234800-22235800	Active TSS	Osteobl	bone
39	chr19:22234800-22236000	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr19:22234800-22236000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr19:22234800-22236000	Active TSS	Brain Inferior Temporal Lobe	brain
42	chr19:22234800-22236000	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr19:22234800-22236000	Active TSS	Fetal Intestine Large	intestine
44	chr19:22234800-22236000	Active TSS	Fetal Intestine Small	intestine
45	chr19:22234800-22236000	Active TSS	Fetal Kidney	kidney
46	chr19:22234800-22236000	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr19:22234800-22236000	ZNF genes & repeats	Fetal Stomach	stomach
48	chr19:22234800-22236000	Active TSS	Left Ventricle	heart
49	chr19:22234800-22236000	Active TSS	Pancreas	Pancrea
50	chr19:22234800-22236000	Active TSS	Stomach Smooth Muscle	stomach

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