Variant report

Variant	nsv917200
Chromosome Location	chr19:22020157-22101914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:767)
CpG islands
(count:549)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:767 , 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	ATF1	chr19:22022991-22023137	K562	blood:	n/a	n/a
2	BACH1	chr19:22034602-22034941	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr19:22023605-22023788	GM12878	blood:	n/a	chr19:22023726-22023737
4	BHLHE40	chr19:22034493-22035395	K562	blood:	n/a	chr19:22034546-22034562 chr19:22034554-22034570
5	BHLHE40	chr19:22034495-22034851	GM12878	blood:	n/a	chr19:22034546-22034562 chr19:22034554-22034570
6	BHLHE40	chr19:22022837-22023100	K562	blood:	n/a	n/a
7	BRCA1	chr19:22034663-22034857	HepG2	liver:	n/a	n/a
8	BRCA1	chr19:22034656-22034853	GM12878	blood:	n/a	n/a
9	CBX3	chr19:22034494-22035125	K562	blood:	n/a	n/a
10	CCNT2	chr19:22034488-22034857	K562	blood:	n/a	n/a
11	CEBPB	chr19:22061270-22061608	HepG2	liver:	n/a	n/a
12	CEBPB	chr19:22058895-22059134	HepG2	liver:	n/a	n/a
13	CEBPB	chr19:22064301-22064556	A549	lung:	n/a	n/a
14	CEBPB	chr19:22022903-22023063	K562	blood:	n/a	n/a
15	CEBPB	chr19:22022431-22022673	K562	blood:	n/a	n/a
16	CEBPB	chr19:22023936-22024736	A549	lung:	n/a	n/a
17	CEBPB	chr19:22090066-22090727	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr19:22088598-22089113	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:22094093-22094347	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:22060020-22060497	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:22088543-22089121	A549	lung:	n/a	n/a
22	CEBPB	chr19:22091700-22092444	A549	lung:	n/a	n/a
23	CEBPB	chr19:22061338-22061572	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:22022447-22023124	A549	lung:	n/a	n/a
25	CEBPB	chr19:22091335-22092461	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:22074282-22074665	A549	lung:	n/a	n/a
27	CEBPB	chr19:22061861-22062151	IMR90	lung:	n/a	n/a
28	CEBPB	chr19:22089618-22090768	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:22025888-22026221	HepG2	liver:	n/a	n/a
30	CEBPB	chr19:22061814-22062608	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:22100348-22100568	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:22023961-22024697	HepG2	liver:	n/a	n/a
33	CEBPB	chr19:22073980-22074675	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:22021783-22022082	HepG2	liver:	n/a	chr19:22021948-22021959
35	CEBPB	chr19:22032600-22032867	IMR90	lung:	n/a	chr19:22032699-22032710
36	CEBPB	chr19:22090207-22090581	K562	blood:	n/a	n/a
37	CEBPB	chr19:22029481-22029517	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr19:22060026-22060520	A549	lung:	n/a	n/a
39	CEBPB	chr19:22090103-22090793	A549	lung:	n/a	n/a
40	CEBPB	chr19:22032570-22032878	A549	lung:	n/a	chr19:22032699-22032710
41	CEBPB	chr19:22090118-22090712	IMR90	lung:	n/a	n/a
42	CEBPB	chr19:22022841-22023139	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:22021843-22022112	A549	lung:	n/a	chr19:22021948-22021959
44	CEBPB	chr19:22099724-22099976	HepG2	liver:	n/a	n/a
45	CEBPB	chr19:22032526-22032870	HepG2	liver:	n/a	chr19:22032699-22032710
46	CEBPB	chr19:22029204-22029763	HepG2	liver:	n/a	chr19:22029459-22029470
47	CEBPB	chr19:22094044-22094329	IMR90	lung:	n/a	n/a
48	CEBPB	chr19:22025927-22026228	IMR90	lung:	n/a	n/a
49	CEBPB	chr19:22084921-22085294	HepG2	liver:	n/a	n/a
50	CEBPB	chr19:22027759-22028408	A549	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:22034799-22034849	HRPEpiC	eye:	n/a
2	chr19:22034799-22034849	H1-hESC	embryonic stem cell:	embryo
3	chr19:22020888-22020938	HRPEpiC	eye:	n/a
4	chr19:22034747-22034797	HEEpiC	esophagus:	n/a
5	chr19:22020888-22020938	NH-A	brain:	n/a
6	chr19:22034523-22034573	Caco-2	colon:	n/a
7	chr19:22034799-22034849	HL-60	blood:	n/a
8	chr19:22034523-22034573	GM06990	blood:	n/a
9	chr19:22034418-22034468	AG04450	lung:	fetal
10	chr19:22034523-22034573	SAEC	small airway:	n/a
11	chr19:22034747-22034797	ovcar-3	ovarian:	n/a
12	chr19:22037616-22037666	NH-A	brain:	n/a
13	chr19:22037616-22037666	SK-N-SH_RA	brain:	n/a
14	chr19:22034799-22034849	AoSMC	blood vessel:	n/a
15	chr19:22020888-22020938	HCM	heart:	n/a
16	chr19:22030534-22030584	HRCEpiC	kidney:	n/a
17	chr19:22034747-22034797	GM12892	blood:	n/a
18	chr19:22034747-22034797	IMR90	lung:	fetal
19	chr19:22034747-22034797	GM06990	blood:	n/a
20	chr19:22037616-22037666	NT2-D1	testis:	n/a
21	chr19:22034523-22034573	ovcar-3	ovarian:	n/a
22	chr19:22033893-22033943	MCF10A-Er-Src	breast:	n/a
23	chr19:22034747-22034797	AG04450	lung:	fetal
24	chr19:22034747-22034797	HRE	kidney:	n/a
25	chr19:22034799-22034849	LNCaP	prostate:	n/a
26	chr19:22034418-22034468	HRCEpiC	kidney:	n/a
27	chr19:22020888-22020938	Hepatocyte	liver:	n/a
28	chr19:22034523-22034573	T-47D	breast:	n/a
29	chr19:22035024-22035074	K562	blood:	n/a
30	chr19:22035024-22035074	Hela-S3	cervix:	n/a
31	chr19:22034418-22034468	GM06990	blood:	n/a
32	chr19:22034799-22034849	U87	brain:	n/a
33	chr19:22033893-22033943	HAEpiC	amniotic membrane:	n/a
34	chr19:22034418-22034468	RPTEC	kidney:	n/a
35	chr19:22034799-22034849	HRE	kidney:	n/a
36	chr19:22034418-22034468	SK-N-SH	brain:	n/a
37	chr19:22020888-22020938	AG09319	gingival:	n/a
38	chr19:22034799-22034849	HNPCEpiC	eye:	n/a
39	chr19:22035024-22035074	H1-hESC	embryonic stem cell:	embryo
40	chr19:22034523-22034573	H1-hESC	embryonic stem cell:	embryo
41	chr19:22034799-22034849	HepG2	liver:	n/a
42	chr19:22034747-22034797	SK-N-MC	brain:	n/a
43	chr19:22037616-22037666	IMR90	lung:	fetal
44	chr19:22034747-22034797	AG10803	skin:	n/a
45	chr19:22035024-22035074	T-47D	breast:	n/a
46	chr19:22034747-22034797	HPAEpiC	pulmonary alveolar:	n/a
47	chr19:22034418-22034468	U87	brain:	n/a
48	chr19:22034418-22034468	K562	blood:	n/a
49	chr19:22034418-22034468	GM12878	blood:	n/a
50	chr19:22030534-22030584	LNCaP	prostate:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:22042019..22043696-chr19:22044247..22046757,2	MCF-7	breast:
2	chr19:22051797..22053500-chr19:22055067..22056734,2	K562	blood:
3	chr19:22018701..22020961-chr19:22029998..22031608,2	MCF-7	breast:
4	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
5	chr19:22042019..22043696-chr19:22044247..22046757,2	MCF-7	breast:
6	chr19:21686874..21688868-chr19:22034996..22036556,2	MCF-7	breast:
7	chr19:22051797..22053500-chr19:22055067..22056734,2	K562	blood:
8	chr19:21950144..21952867-chr19:22033592..22036117,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF257-1	chr19:22100052-22101719	XLOC_013010
2	lnc-ZNF257-4	chr19:22097817-22098563	NONHSAT063754
3	lnc-ZNF257-1	chr19:22085706-22085729	XLOC_013010
4	lnc-ZNF100-7	chr19:22022399-22024449	NONHSAT063748
5	lnc-ZNF257-5	chr19:22025860-22026637	NONHSAT063751
6	lnc-ZNF257-4	chr19:22099324-22099462	NONHSAT063754

No data

Variant related genes	Relation type
ZNF43	TF binding region
ZNF43	CpG island
ENSG00000198521	chromatin interactions
ENSG00000197020	chromatin interactions
ENSG00000197013	chromatin interactions

Extended variants
information (count: 1367 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:1367 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546185690	chr19:22020182-22020183	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539940868	chr19:22020234-22020235	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs28480566	chr19:22020251-22020252	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs559523747	chr19:22020265-22020266	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528762764	chr19:22020269-22020270	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576497244	chr19:22020292-22020293	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548647234	chr19:22020304-22020305	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543525145	chr19:22020313-22020314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561827338	chr19:22020330-22020331	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529477921	chr19:22020355-22020356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141434264	chr19:22020360-22020361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537255014	chr19:22020428-22020429	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115779019	chr19:22020429-22020430	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570508834	chr19:22020474-22020475	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189272677	chr19:22020476-22020477	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552157788	chr19:22020548-22020549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370976048	chr19:22020556-22020557	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570316173	chr19:22020650-22020651	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570235344	chr19:22020652-22020653	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113047551	chr19:22020677-22020678	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs537966247	chr19:22020713-22020714	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs11672034	chr19:22020770-22020771	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs75626984	chr19:22020888-22020889	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs182420949	chr19:22020967-22020968	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2457791	chr19:22021009-22021010	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs8108849	chr19:22021013-22021014	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs539320117	chr19:22021034-22021035	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558155366	chr19:22021060-22021061	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375370563	chr19:22021147-22021148	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67497021	chr19:22021202-22021203	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200442655	chr19:22021206-22021207	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35377796	chr19:22021207-22021208	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2435047	chr19:22021208-22021209	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs398034260	chr19:22021218-22021219	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185803471	chr19:22021233-22021234	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146990909	chr19:22021238-22021239	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543784926	chr19:22021344-22021345	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191128845	chr19:22021380-22021381	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573791752	chr19:22021390-22021391	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535731019	chr19:22021409-22021410	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541229447	chr19:22021415-22021416	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559480016	chr19:22021438-22021439	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533690924	chr19:22021543-22021544	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79135903	chr19:22021548-22021549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79631397	chr19:22021549-22021550	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs117088012	chr19:22021575-22021576	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563983683	chr19:22021620-22021621	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs575349373	chr19:22021694-22021695	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs531240667	chr19:22021710-22021711	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs549802000	chr19:22021714-22021715	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:43)

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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:945 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:22019000-22020400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr19:22019000-22020600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:22019000-22021600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr19:22019000-22021600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr19:22019000-22021800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr19:22019000-22022200	Weak transcription	Spleen	Spleen
7	chr19:22019000-22022400	Weak transcription	Lung	lung
8	chr19:22019000-22022600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr19:22019000-22022600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr19:22019000-22022800	Weak transcription	Gastric	stomach
11	chr19:22019000-22024800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr19:22019000-22027800	Weak transcription	Small Intestine	intestine
13	chr19:22019000-22034200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr19:22019200-22020600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:22019200-22021600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr19:22019200-22021600	Weak transcription	HSMM	muscle
17	chr19:22019200-22021800	Weak transcription	Ovary	ovary
18	chr19:22019200-22022000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr19:22019200-22022200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr19:22019200-22022600	Weak transcription	Aorta	Aorta
21	chr19:22019200-22022800	Weak transcription	Esophagus	oesophagus
22	chr19:22019200-22023000	Weak transcription	NHEK	skin
23	chr19:22019200-22023600	Weak transcription	HSMMtube	muscle
24	chr19:22019200-22025600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr19:22019200-22034000	Weak transcription	Colonic Mucosa	Colon
26	chr19:22019200-22034400	Weak transcription	Stomach Mucosa	stomach
27	chr19:22019400-22020400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr19:22019400-22020600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr19:22019400-22021400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr19:22019400-22021600	Weak transcription	Brain Germinal Matrix	brain
31	chr19:22019400-22021800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr19:22019400-22021800	Weak transcription	HUVEC	blood vessel
33	chr19:22019400-22021800	Weak transcription	K562	blood
34	chr19:22019400-22022400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr19:22019400-22022400	Weak transcription	NH-A	brain
36	chr19:22019400-22023800	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr19:22019400-22033600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr19:22019600-22020200	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr19:22019600-22020400	Enhancers	Dnd41	blood
40	chr19:22019600-22020600	Weak transcription	Fetal Heart	heart
41	chr19:22019600-22021200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr19:22019600-22021400	Weak transcription	Fetal Muscle Trunk	muscle
43	chr19:22019600-22021600	Weak transcription	Primary hematopoietic stem cells	blood
44	chr19:22019600-22021600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr19:22019600-22021600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:22019600-22021600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr19:22019600-22021600	Weak transcription	NHDF-Ad	bronchial
48	chr19:22019600-22021600	Weak transcription	Osteobl	bone
49	chr19:22019600-22021800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr19:22019600-22021800	Weak transcription	Fetal Lung	lung

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