Variant report

Variant	esv3343415
Chromosome Location	chr19:28315698-28581894
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1104)
CpG islands
(count:366)
Chromatin interactive
region (count:21)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1104 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:28508411-28508510	K562	blood:	n/a	n/a
2	ATF1	chr19:28339161-28339543	K562	blood:	n/a	n/a
3	ATF2	chr19:28558788-28559212	GM12878	blood:	n/a	n/a
4	ATF2	chr19:28558630-28559212	GM12878	blood:	n/a	n/a
5	ATF2	chr19:28565484-28566197	GM12878	blood:	n/a	n/a
6	BACH1	chr19:28466591-28466642	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr19:28558746-28559077	GM12878	blood:	n/a	n/a
8	BATF	chr19:28453293-28453547	GM12878	blood:	n/a	chr19:28453431-28453442 chr19:28453416-28453425
9	BATF	chr19:28561672-28561976	GM12878	blood:	n/a	n/a
10	BATF	chr19:28558735-28559113	GM12878	blood:	n/a	n/a
11	BCL11A	chr19:28558773-28559078	GM12878	blood:	n/a	n/a
12	BCL11A	chr19:28565709-28565961	GM12878	blood:	n/a	n/a
13	BCL11A	chr19:28565658-28565991	GM12878	blood:	n/a	n/a
14	BCL3	chr19:28558727-28558985	GM12878	blood:	n/a	n/a
15	BCL3	chr19:28565554-28566090	GM12878	blood:	n/a	n/a
16	BCL3	chr19:28525929-28526130	GM12878	blood:	n/a	n/a
17	BCL3	chr19:28565660-28566051	GM12878	blood:	n/a	n/a
18	BCL3	chr19:28558679-28559115	GM12878	blood:	n/a	chr19:28559075-28559084
19	BCLAF1	chr19:28565603-28566016	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:28558729-28559196	GM12878	blood:	n/a	n/a
21	BHLHE40	chr19:28563493-28563605	GM12878	blood:	n/a	n/a
22	BHLHE40	chr19:28484544-28484743	GM12878	blood:	n/a	n/a
23	BHLHE40	chr19:28464926-28465289	GM12878	blood:	n/a	n/a
24	BHLHE40	chr19:28331210-28331428	GM12878	blood:	n/a	n/a
25	BHLHE40	chr19:28501657-28501858	K562	blood:	n/a	n/a
26	BHLHE40	chr19:28565642-28566013	GM12878	blood:	n/a	n/a
27	BHLHE40	chr19:28331408-28331601	K562	blood:	n/a	n/a
28	BRCA1	chr19:28330124-28330322	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr19:28321368-28321405	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr19:28540734-28541094	K562	blood:	n/a	chr19:28540900-28540911
31	CEBPB	chr19:28566976-28567198	IMR90	lung:	n/a	n/a
32	CEBPB	chr19:28512130-28512202	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr19:28490646-28490735	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:28375451-28375743	A549	lung:	n/a	n/a
35	CEBPB	chr19:28337973-28338214	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:28409910-28410170	HepG2	liver:	n/a	chr19:28410026-28410037 chr19:28410025-28410038
37	CEBPB	chr19:28566944-28567138	HepG2	liver:	n/a	n/a
38	CEBPB	chr19:28512031-28512307	A549	lung:	n/a	n/a
39	CEBPB	chr19:28321784-28322155	K562	blood:	n/a	n/a
40	CEBPB	chr19:28512136-28512257	HepG2	liver:	n/a	n/a
41	CEBPB	chr19:28321916-28322067	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr19:28461957-28462469	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr19:28329508-28329962	HepG2	liver:	n/a	chr19:28329780-28329791
44	CEBPB	chr19:28530474-28530807	MCF-7	breast:	n/a	n/a
45	CEBPB	chr19:28490679-28490748	A549	lung:	n/a	n/a
46	CEBPB	chr19:28531517-28531724	A549	lung:	n/a	chr19:28531625-28531636 chr19:28531625-28531636
47	CEBPB	chr19:28378818-28378941	HepG2	liver:	n/a	n/a
48	CEBPB	chr19:28421407-28421661	A549	lung:	n/a	n/a
49	CEBPB	chr19:28510387-28510609	A549	lung:	n/a	n/a
50	CEBPB	chr19:28323919-28324162	A549	lung:	n/a	chr19:28324037-28324054

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:28403514-28403564	SK-N-MC	brain:	n/a
2	chr19:28400822-28400872	HEK293	kidney:	embryo
3	chr19:28397061-28397111	A549	lung:	n/a
4	chr19:28397061-28397111	HAEpiC	amniotic membrane:	n/a
5	chr19:28400822-28400872	HNPCEpiC	eye:	n/a
6	chr19:28400822-28400872	HepG2	liver:	n/a
7	chr19:28397061-28397111	NB4	blood:	n/a
8	chr19:28401100-28401150	HRCEpiC	kidney:	n/a
9	chr19:28400822-28400872	GM12878	blood:	n/a
10	chr19:28399736-28399786	SK-N-MC	brain:	n/a
11	chr19:28400281-28400331	U87	brain:	n/a
12	chr19:28397061-28397111	AG10803	skin:	n/a
13	chr19:28397061-28397111	HRPEpiC	eye:	n/a
14	chr19:28400281-28400331	SK-N-MC	brain:	n/a
15	chr19:28399736-28399786	CMK	blood:	n/a
16	chr19:28403514-28403564	HCF	heart:	n/a
17	chr19:28400822-28400872	BE2_C	brain:	n/a
18	chr19:28399736-28399786	HRCEpiC	kidney:	n/a
19	chr19:28397061-28397111	HL-60	blood:	n/a
20	chr19:28400822-28400872	SK-N-MC	brain:	n/a
21	chr19:28397061-28397111	GM12891	blood:	n/a
22	chr19:28403514-28403564	U87	brain:	n/a
23	chr19:28400281-28400331	GM12878	blood:	n/a
24	chr19:28401100-28401150	NT2-D1	testis:	n/a
25	chr19:28403514-28403564	HAEpiC	amniotic membrane:	n/a
26	chr19:28400822-28400872	U87	brain:	n/a
27	chr19:28400281-28400331	Jurkat	blood:	n/a
28	chr19:28399736-28399786	SAEC	small airway:	n/a
29	chr19:28397061-28397111	GM12892	blood:	n/a
30	chr19:28400281-28400331	HepG2	liver:	n/a
31	chr19:28400822-28400872	ProgFib	skin:	n/a
32	chr19:28403514-28403564	Hela-S3	cervix:	n/a
33	chr19:28400281-28400331	HIPEpiC	eye:	n/a
34	chr19:28400281-28400331	AG09319	gingival:	n/a
35	chr19:28403514-28403564	Jurkat	blood:	n/a
36	chr19:28400822-28400872	PrEC	prostate:	n/a
37	chr19:28400281-28400331	NHBE	bronchial:	n/a
38	chr19:28400281-28400331	NB4	blood:	n/a
39	chr19:28400281-28400331	GM06990	blood:	n/a
40	chr19:28400281-28400331	HCF	heart:	n/a
41	chr19:28400281-28400331	PrEC	prostate:	n/a
42	chr19:28400822-28400872	HEEpiC	esophagus:	n/a
43	chr19:28400822-28400872	ovcar-3	ovarian:	n/a
44	chr19:28403514-28403564	CMK	blood:	n/a
45	chr19:28399736-28399786	NT2-D1	testis:	n/a
46	chr19:28400822-28400872	HIPEpiC	eye:	n/a
47	chr19:28403514-28403564	MCF10A-Er-Src	breast:	n/a
48	chr19:28400822-28400872	AG10803	skin:	n/a
49	chr19:28403514-28403564	LNCaP	prostate:	n/a
50	chr19:28397061-28397111	SKMC	muscle:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:28539840..28540682-chr5:3520532..3521075,2	MCF-7	breast:
2	chr19:28331441..28333608-chr19:28335036..28336613,2	K562	blood:
3	chr19:28331279..28332941-chr19:28335036..28337118,2	K562	blood:
4	chr19:28456998..28457870-chr2:21351809..21352309,2	MCF-7	breast:
5	chr19:28398796..28401321-chr19:28401925..28404487,2	K562	blood:
6	chr19:28464838..28465364-chr19:28707556..28708271,2	MCF-7	breast:
7	chr14:105940702..105944648-chr19:28339771..28342771,5	MCF-7	breast:
8	chr14:105940951..105942780-chr19:28339771..28341271,2	MCF-7	breast:
9	chr19:28557128..28559611-chr19:28575041..28577843,2	K562	blood:
10	chr19:28395608..28398274-chr19:28399828..28402146,2	K562	blood:
11	chr19:28502331..28503989-chr19:28509235..28511001,2	MCF-7	breast:
12	chr19:28360092..28362208-chr19:28365123..28367340,2	K562	blood:
13	chr19:28464703..28465634-chr19:28707512..28708625,5	MCF-7	breast:
14	chr19:28502331..28503989-chr19:28509235..28511001,2	MCF-7	breast:
15	chr19:28331441..28333608-chr19:28335036..28336613,2	K562	blood:
16	chr19:28395608..28398274-chr19:28399828..28402146,2	K562	blood:
17	chr19:28503418..28504150-chr19:28707502..28708498,2	MCF-7	breast:
18	chr19:28557128..28559611-chr19:28575041..28577843,2	K562	blood:
19	chr19:28464493..28465594-chr19:28815026..28816551,6	MCF-7	breast:
20	chr19:28331279..28332941-chr19:28335036..28337118,2	K562	blood:
21	chr19:28360092..28362208-chr19:28365123..28367340,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UQCRFS1-6	chr19:28380013-28380130	ENSG00000266977.1
2	lnc-UQCRFS1-6	chr19:28340562-28340977	XLOC_013284
3	lnc-UQCRFS1-5	chr19:28477699-28477915	XLOC_013285
4	lnc-VSTM2B-17	chr19:28556174-28556272	ENSG00000267509.1
5	lnc-UQCRFS1-5	chr19:28491139-28491243	XLOC_013285
6	lnc-UQCRFS1-18	chr19:28473940-28474240	NONHSAT064026
7	lnc-VSTM2B-17	chr19:28556174-28556272	ENSG00000267509.1
8	lnc-UQCRFS1-6	chr19:28340638-28340977	ENSG00000266977.1
9	lnc-UQCRFS1-5	chr19:28480019-28480183	XLOC_013285
10	lnc-VSTM2B-9	chr19:28447110-28447494	NONHSAT064022
11	lnc-VSTM2B-9	chr19:28393503-28393602	NONHSAT064022
12	lnc-UQCRFS1-5	chr19:28479862-28480740	XLOC_013285
13	lnc-UQCRFS1-6	chr19:28380013-28380105	XLOC_013284
14	lnc-UQCRFS1-5	chr19:28491139-28491271	XLOC_013285

No data

Variant related genes	Relation type
ENSG00000267623	TF binding region
ENSG00000267768	TF binding region
ENSG00000267509	TF binding region
ENSG00000267630	TF binding region
ENSG00000266977	TF binding region
ENSG00000267389	TF binding region
ENSG00000266906	TF binding region
ENSG00000267623	CpG island
ENSG00000267768	CpG island
ENSG00000267509	CpG island
ENSG00000267630	CpG island
ENSG00000266977	CpG island
ENSG00000267389	CpG island
ENSG00000266906	CpG island
ENSG00000267768	chromatin interactions
ENSG00000182809	chromatin interactions
SRP72	miRNA target sites
SRPK1	miRNA target sites

Extended variants
information (count: 6502 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:6502 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73033885	chr19:28315701-28315702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376369474	chr19:28315713-28315714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs563019841	chr19:28315748-28315749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191918089	chr19:28315806-28315807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548605278	chr19:28315837-28315838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148402680	chr19:28315845-28315846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113783960	chr19:28315860-28315861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527991452	chr19:28315867-28315868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112991920	chr19:28315897-28315898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551964616	chr19:28315899-28315900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184347554	chr19:28315943-28315944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62116566	chr19:28315951-28315952	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs77915659	chr19:28315975-28315976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74665241	chr19:28315976-28315977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368795446	chr19:28316025-28316026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538093269	chr19:28316026-28316027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556328024	chr19:28316028-28316029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567821811	chr19:28316046-28316047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528188564	chr19:28316053-28316054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535134234	chr19:28316091-28316092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73033890	chr19:28316108-28316109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10420486	chr19:28316116-28316117	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs73033893	chr19:28316119-28316120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs71169712	chr19:28316132-28316133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73033895	chr19:28316142-28316143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78702812	chr19:28316147-28316148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs78826471	chr19:28316149-28316150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78460030	chr19:28316155-28316156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77102238	chr19:28316158-28316159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142128249	chr19:28316161-28316162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377415300	chr19:28316162-28316163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75359233	chr19:28316168-28316169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545468175	chr19:28316175-28316176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80311143	chr19:28316178-28316179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10411325	chr19:28316179-28316180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs79504474	chr19:28316187-28316188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77762634	chr19:28316188-28316189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74487303	chr19:28316197-28316198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76358492	chr19:28316199-28316200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77005842	chr19:28316200-28316201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77794671	chr19:28316202-28316203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79460809	chr19:28316208-28316209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546874393	chr19:28316221-28316222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78877998	chr19:28316223-28316224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188409817	chr19:28316233-28316234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74539892	chr19:28316237-28316238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568442736	chr19:28316238-28316239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74402474	chr19:28316243-28316244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74497000	chr19:28316248-28316249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181222618	chr19:28316250-28316251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

Disease	PMID	Source
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
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	19287141	CNVD
Lung cancer	18438408	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Astrocytoma	17387387	CNVD
renal disease	20603712	CNVD

Chromatin state (count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:28314200-28319200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr19:28318400-28319600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr19:28318600-28319200	ZNF genes & repeats	Aorta	Aorta
4	chr19:28319200-28320000	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr19:28320000-28320200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:28321800-28322200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
7	chr19:28323800-28324000	Enhancers	Right Atrium	heart
8	chr19:28323800-28324400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr19:28323800-28324600	Enhancers	NHEK	skin
10	chr19:28329000-28329600	Enhancers	Dnd41	blood
11	chr19:28329400-28332200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
12	chr19:28329600-28330400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr19:28329600-28331200	Weak transcription	Dnd41	blood
14	chr19:28331200-28331600	Enhancers	Dnd41	blood
15	chr19:28339000-28344000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr19:28339200-28340200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr19:28339400-28340000	ZNF genes & repeats	HepG2	liver
18	chr19:28341400-28342800	ZNF genes & repeats	Colonic Mucosa	Colon
19	chr19:28341400-28342800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
20	chr19:28341800-28342800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:28342000-28343000	ZNF genes & repeats	Gastric	stomach
22	chr19:28342000-28343000	ZNF genes & repeats	Dnd41	blood
23	chr19:28342200-28342800	ZNF genes & repeats	Spleen	Spleen
24	chr19:28342200-28343000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
25	chr19:28342400-28343000	ZNF genes & repeats	Adipose Nuclei	Adipose
26	chr19:28344000-28344400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr19:28349400-28352600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr19:28350000-28353200	ZNF genes & repeats	Adipose Nuclei	Adipose
29	chr19:28350200-28353200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
30	chr19:28356800-28357800	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr19:28358600-28359600	Enhancers	HSMMtube	muscle
32	chr19:28363200-28363800	ZNF genes & repeats	Pancreas	Pancrea
33	chr19:28367600-28368600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr19:28368000-28373800	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr19:28374600-28376200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr19:28375600-28377000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr19:28376200-28376400	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr19:28376400-28376800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr19:28377600-28378000	Enhancers	HSMMtube	muscle
40	chr19:28378600-28378800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
41	chr19:28378600-28379400	Active TSS	Fetal Heart	heart
42	chr19:28378800-28379200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr19:28379400-28379800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr19:28379400-28381000	Weak transcription	Fetal Heart	heart
45	chr19:28380200-28389200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr19:28381000-28381400	Active TSS	Fetal Heart	heart
47	chr19:28384800-28385600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr19:28385200-28385400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr19:28385600-28386600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr19:28387200-28387400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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