Variant report

Variant	nsv458391
Chromosome Location	chr19:20576399-20819154
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1045)
CpG islands
(count:855)
Chromatin interactive
region (count:6)
LncRNA
region (count:32)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:20748414-20748945	HepG2	liver:	n/a	n/a
2	ATF1	chr19:20642156-20642192	K562	blood:	n/a	n/a
3	ATF2	chr19:20607498-20607907	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr19:20607365-20608019	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr19:20606309-20606691	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr19:20627245-20627563	GM12878	blood:	n/a	n/a
7	BATF	chr19:20627328-20627551	GM12878	blood:	n/a	n/a
8	BATF	chr19:20596997-20597185	GM12878	blood:	n/a	chr19:20597085-20597096
9	BATF	chr19:20750653-20750854	GM12878	blood:	n/a	n/a
10	BATF	chr19:20614379-20614702	GM12878	blood:	n/a	n/a
11	BATF	chr19:20741371-20741591	GM12878	blood:	n/a	chr19:20741474-20741484 chr19:20741473-20741484
12	BATF	chr19:20614381-20614704	GM12878	blood:	n/a	n/a
13	BCL3	chr19:20627365-20627560	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:20747755-20747953	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:20748462-20748819	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:20606499-20606703	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:20615639-20615680	GM12878	blood:	n/a	n/a
18	CEBPB	chr19:20611669-20611732	HepG2	liver:	n/a	chr19:20611703-20611714
19	CEBPB	chr19:20795986-20796186	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr19:20606353-20606525	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:20818042-20818117	K562	blood:	n/a	n/a
22	CEBPB	chr19:20805003-20805118	K562	blood:	n/a	n/a
23	CEBPB	chr19:20795985-20796246	HepG2	liver:	n/a	n/a
24	CEBPB	chr19:20647209-20647401	A549	lung:	n/a	n/a
25	CEBPB	chr19:20642156-20642190	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr19:20618506-20618602	A549	lung:	n/a	n/a
27	CEBPB	chr19:20607373-20607485	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr19:20641992-20642192	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr19:20748293-20748471	GM12878	blood:	n/a	n/a
30	CHD1	chr19:20605888-20607933	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr19:20607426-20607584	GM12878	blood:	n/a	n/a
32	CHD2	chr19:20606924-20607261	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr19:20606264-20606714	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:20607545-20607990	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr19:20748430-20748833	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr19:20748146-20748843	GM12878	blood:	n/a	n/a
37	CHD2	chr19:20615460-20615657	GM12878	blood:	n/a	n/a
38	CHD2	chr19:20748454-20748777	HepG2	liver:	n/a	n/a
39	CHD2	chr19:20607746-20607930	GM12878	blood:	n/a	n/a
40	CREB1	chr19:20606098-20606620	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr19:20740989-20741055	A549	lung:	n/a	n/a
42	CTCF	chr19:20695543-20695578	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr19:20661834-20662092	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr19:20661860-20662010	HEK293	kidney:	n/a	n/a
45	CTCF	chr19:20748116-20748409	IMR90	lung:	n/a	chr19:20748144-20748153
46	CTCF	chr19:20763654-20763675	Lung_OC	lung:	n/a	n/a
47	CTCF	chr19:20661780-20662050	A549	lung:	n/a	n/a
48	CTCF	chr19:20740900-20741050	BE2_C	brain:	n/a	n/a
49	CTCF	chr19:20748200-20748350	GM12866	blood:	n/a	n/a
50	CTCF	chr19:20748200-20748350	Caco-2	colon:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:20748646-20748696	SK-N-MC	brain:	n/a
2	chr19:20748646-20748696	SK-N-MC	brain:	n/a
3	chr19:20748646-20748696	GM06990	blood:	n/a
4	chr19:20607461-20607511	Hepatocyte	liver:	n/a
5	chr19:20585206-20585256	HepG2	liver:	n/a
6	chr19:20748468-20748518	ovcar-3	ovarian:	n/a
7	chr19:20608968-20609018	HL-60	blood:	n/a
8	chr19:20749738-20749788	GM12878	blood:	n/a
9	chr19:20748661-20748711	NT2-D1	testis:	n/a
10	chr19:20585212-20585262	PANC-1	pancreas:	n/a
11	chr19:20748646-20748696	GM12878	blood:	n/a
12	chr19:20748468-20748518	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:20748661-20748711	AG04450	lung:	fetal
14	chr19:20607461-20607511	Caco-2	colon:	n/a
15	chr19:20585206-20585256	SAEC	small airway:	n/a
16	chr19:20748468-20748518	NHBE	bronchial:	n/a
17	chr19:20608968-20609018	ECC-1	luminal epithelium:	n/a
18	chr19:20608968-20609018	HPAEpiC	pulmonary alveolar:	n/a
19	chr19:20748661-20748711	HRE	kidney:	n/a
20	chr19:20748616-20748666	GM12878	blood:	n/a
21	chr19:20608532-20608582	SKMC	muscle:	n/a
22	chr19:20585212-20585262	NH-A	brain:	n/a
23	chr19:20608968-20609018	GM12878	blood:	n/a
24	chr19:20607771-20607821	ovcar-3	ovarian:	n/a
25	chr19:20607461-20607511	AG09309	skin:	n/a
26	chr19:20749810-20749860	Jurkat	blood:	n/a
27	chr19:20607461-20607511	BJ	skin:	n/a
28	chr19:20607771-20607821	HCT-116	colon:	n/a
29	chr19:20748661-20748711	AG04449	skin:	fetal
30	chr19:20749810-20749860	NB4	blood:	n/a
31	chr19:20748468-20748518	HEK293	kidney:	embryo
32	chr19:20608532-20608582	Caco-2	colon:	n/a
33	chr19:20608968-20609018	NHBE	bronchial:	n/a
34	chr19:20607771-20607821	SKMC	muscle:	n/a
35	chr19:20585206-20585256	PANC-1	pancreas:	n/a
36	chr19:20585206-20585256	NHDF-neo	bronchial:	n/a
37	chr19:20748646-20748696	A549	lung:	n/a
38	chr19:20607771-20607821	ProgFib	skin:	n/a
39	chr19:20749738-20749788	HCF	heart:	n/a
40	chr19:20749738-20749788	GM19239	blood:	n/a
41	chr19:20608968-20609018	HIPEpiC	eye:	n/a
42	chr19:20576478-20576528	HCF	heart:	n/a
43	chr19:20576478-20576528	GM12891	blood:	n/a
44	chr19:20585206-20585256	NH-A	brain:	n/a
45	chr19:20576478-20576528	NB4	blood:	n/a
46	chr19:20748176-20748226	HEK293	kidney:	embryo
47	chr19:20749810-20749860	GM12892	blood:	n/a
48	chr19:20748468-20748518	PrEC	prostate:	n/a
49	chr19:20748661-20748711	HIPEpiC	eye:	n/a
50	chr19:20607771-20607821	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:20745828..20748309-chr19:20749076..20751697,2	MCF-7	breast:
2	chr19:20731694..20733934-chr19:20746401..20748786,2	MCF-7	breast:
3	chr19:20791082..20791689-chr19:20802219..20802843,2	MCF-7	breast:
4	chr19:20745828..20748309-chr19:20749076..20751697,2	MCF-7	breast:
5	chr19:20791082..20791689-chr19:20802219..20802843,2	MCF-7	breast:
6	chr19:20722765..20724479-chr19:20726583..20728878,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF626-1	chr19:20763013-20763127	ENSG00000269110.1
2	lnc-ZNF486-10	chr19:20599320-20599875	NONHSAT063660
3	lnc-ZNF737-3	chr19:20575923-20579006	NONHSAT063654
4	lnc-ZNF737-3	chr19:20607592-20607765	NONHSAT063649
5	lnc-ZNF486-11	chr19:20711000-20711421	ENSG00000269043.1
6	lnc-ZNF737-3	chr19:20607592-20607775	NONHSAT063648
7	lnc-ZNF737-2	chr19:20626021-20626531	NONHSAT063662
8	lnc-ZNF486-2	chr19:20657011-20657239	XLOC_013000
9	lnc-ZNF737-3	chr19:20607592-20607727	NONHSAT063652
10	lnc-ZNF486-9	chr19:20588238-20588951	NONHSAT063655
11	lnc-ZNF737-3	chr19:20591750-20591845	NONHSAT063657
12	lnc-ZNF737-3	chr19:20600472-20600589	NONHSAT063658
13	lnc-ZNF737-3	chr19:20607592-20607762	NONHSAT063654
14	lnc-ZNF486-9	chr19:20578693-20579002	NONHSAT063655
15	lnc-ZNF486-2	chr19:20655812-20655992	XLOC_013000
16	lnc-ZNF737-3	chr19:20588513-20588955	NONHSAT063657
17	lnc-ZNF737-3	chr19:20591750-20591824	NONHSAT063654
18	lnc-ZNF626-1	chr19:20736598-20736641	ENSG00000269110.1
19	lnc-ZNF486-11	chr19:20679888-20680020	ENSG00000269043.1
20	lnc-ZNF737-3	chr19:20591750-20591824	NR_036455
21	lnc-ZNF737-1	chr19:20765890-20766453	NONHSAT063668
22	lnc-ZNF737-3	chr19:20607592-20607762	NONHSAT063658
23	lnc-ZNF737-3	chr19:20607592-20607775	NONHSAT063653
24	lnc-ZNF737-3	chr19:20607592-20607771	NR_036455
25	lnc-ZNF486-9	chr19:20591746-20591845	NONHSAT063655
26	lnc-ZNF737-3	chr19:20607592-20607679	NONHSAT063657
27	lnc-ZNF737-3	chr19:20607592-20607810	NONHSAT063659
28	lnc-ZNF737-3	chr19:20598111-20598457	NONHSAT063658
29	lnc-ZNF486-11	chr19:20615358-20615517	ENSG00000269043.1
30	lnc-ZNF737-3	chr19:20578626-20579006	NR_036455
31	lnc-ZNF486-11	chr19:20634999-20635094	ENSG00000269043.1
32	lnc-ZNF737-3	chr19:20598219-20598457	NONHSAT063659

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1270	chr19:20579288-20579310	MIMAT0005924_1

No data

Variant related genes	Relation type
ENSG00000268560	TF binding region
ENSG00000268335	TF binding region
ENSG00000269043	TF binding region
MIR1270-2	TF binding region
ENSG00000269372	TF binding region
ZNF826P	TF binding region
VN1R78P	TF binding region
ZNF737	TF binding region
ENSG00000268174	TF binding region
ENSG00000268560	CpG island
ENSG00000268335	CpG island
ENSG00000269043	CpG island
MIR1270-2	CpG island
ENSG00000269372	CpG island
ZNF826P	CpG island
VN1R78P	CpG island
ZNF737	CpG island
ENSG00000268174	CpG island
ENSG00000237440	chromatin interactions
TLE4	miRNA target sites

Extended variants
information (count: 7330 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:7330 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62109031	chr19:20576491-20576492	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114131799	chr19:20576522-20576523	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs2545969	chr19:20576525-20576526	Inactive region	lncRNA	n/a	Overlapped CNVs	mRNA abundance
4	rs186566809	chr19:20576527-20576528	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs201899021	chr19:20576552-20576553	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs368799232	chr19:20576794-20576795	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs373507372	chr19:20576797-20576798	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs149645971	chr19:20577197-20577198	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs147010391	chr19:20577240-20577241	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs62109032	chr19:20577257-20577258	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs200104441	chr19:20577268-20577269	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs201856178	chr19:20577269-20577270	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs201498941	chr19:20577336-20577337	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs139385611	chr19:20577384-20577385	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs116135031	chr19:20577521-20577522	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs45515503	chr19:20577581-20577582	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs199590665	chr19:20577603-20577604	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs200214241	chr19:20577822-20577823	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs202047926	chr19:20577832-20577833	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs199857800	chr19:20577857-20577858	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs62109033	chr19:20577989-20577990	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs56274924	chr19:20578110-20578111	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs28420526	chr19:20578168-20578169	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs201086933	chr19:20578236-20578237	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs116707145	chr19:20578276-20578277	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs56743591	chr19:20578328-20578329	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs11879305	chr19:20578444-20578445	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs114045614	chr19:20578599-20578600	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs201195045	chr19:20578848-20578849	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs114475690	chr19:20578850-20578851	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs76538538	chr19:20585207-20585208	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs79543753	chr19:20585249-20585250	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs28441322	chr19:20587429-20587430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56065323	chr19:20587566-20587567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs28532776	chr19:20587655-20587656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28565387	chr19:20587729-20587730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs58713218	chr19:20587904-20587905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28787345	chr19:20587962-20587963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587714240	chr19:20588001-20588002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28417609	chr19:20588009-20588010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587612612	chr19:20588028-20588029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2545945	chr19:20588206-20588207	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs200656463	chr19:20588289-20588290	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs59168000	chr19:20588481-20588482	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs113980919	chr19:20588528-20588529	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs374506164	chr19:20588672-20588673	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs2545946	chr19:20588912-20588913	Weak transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
48	rs2545947	chr19:20588927-20588928	Weak transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
49	rs7258093	chr19:20588973-20588974	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs62109034	chr19:20588979-20588980	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20841430	CNVD
small cell lung cancer	20016488	CNVD
Autism	19492091	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Ductal carcinoma	22052326	CNVD

Chromatin state (count:2095 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20587200-20595200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:20587200-20595400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr19:20588200-20595200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr19:20589000-20595800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr19:20593800-20595400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr19:20593800-20595400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr19:20593800-20596200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr19:20593800-20605200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr19:20594000-20596200	Weak transcription	Dnd41	blood
10	chr19:20594200-20602600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr19:20594400-20596600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr19:20594600-20596200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr19:20594800-20596200	Weak transcription	Ovary	ovary
14	chr19:20594800-20605600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr19:20594800-20605600	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr19:20595000-20595400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:20595200-20597000	Weak transcription	Primary B cells from peripheral blood	blood
18	chr19:20595200-20597400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr19:20595200-20598200	Weak transcription	Adipose Nuclei	Adipose
20	chr19:20595200-20599200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr19:20595200-20600200	Weak transcription	Thymus	Thymus
22	chr19:20595200-20602400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr19:20595200-20602800	Weak transcription	Fetal Brain Female	brain
24	chr19:20595200-20605000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr19:20595200-20605600	Weak transcription	Fetal Stomach	stomach
26	chr19:20595400-20595800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr19:20595400-20595800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr19:20595400-20595800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
29	chr19:20595400-20596800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr19:20595400-20596800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr19:20595400-20597400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr19:20595400-20602400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr19:20595400-20603800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr19:20595400-20605400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:20595600-20595800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr19:20595600-20596600	Weak transcription	Primary B cells from cord blood	blood
37	chr19:20595600-20596800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr19:20595600-20598800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr19:20595600-20600400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
40	chr19:20595600-20603400	Weak transcription	Fetal Muscle Leg	muscle
41	chr19:20595600-20605800	Weak transcription	Fetal Intestine Large	intestine
42	chr19:20595800-20596800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr19:20595800-20597000	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr19:20595800-20599200	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr19:20595800-20599800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr19:20595800-20600400	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr19:20595800-20605400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr19:20595800-20605600	Weak transcription	Brain Germinal Matrix	brain
49	chr19:20596000-20603600	Weak transcription	Gastric	stomach
50	chr19:20596200-20596400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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