Variant report

Variant	nsv917077
Chromosome Location	chr19:23624807-23868394
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:782)
CpG islands
(count:428)
Chromatin interactive
region (count:17)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:782 , 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	ARID3A	chr19:23832807-23833062	HepG2	liver:	n/a	n/a
2	ATF1	chr19:23632171-23632277	K562	blood:	n/a	n/a
3	BACH1	chr19:23665785-23666020	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr19:23835428-23835588	K562	blood:	n/a	n/a
5	BHLHE40	chr19:23832694-23833139	HepG2	liver:	n/a	n/a
6	BHLHE40	chr19:23832727-23833119	K562	blood:	n/a	n/a
7	BRCA1	chr19:23737404-23737655	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr19:23842683-23842692	GM12878	blood:	n/a	n/a
9	CBX3	chr19:23836447-23836735	K562	blood:	n/a	n/a
10	CBX3	chr19:23836427-23836724	K562	blood:	n/a	n/a
11	CBX3	chr19:23832569-23832979	K562	blood:	n/a	n/a
12	CEBPB	chr19:23644084-23644837	A549	lung:	n/a	chr19:23644704-23644715
13	CEBPB	chr19:23744142-23744447	K562	blood:	n/a	n/a
14	CEBPB	chr19:23643455-23643717	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:23626884-23626929	HepG2	liver:	n/a	chr19:23626905-23626918 chr19:23626906-23626917
16	CEBPB	chr19:23778491-23778833	Hela-S3	cervix:	n/a	chr19:23778651-23778660 chr19:23778649-23778662 chr19:23778651-23778660 chr19:23778651-23778660 chr19:23778649-23778660
17	CEBPB	chr19:23742002-23742164	A549	lung:	n/a	n/a
18	CEBPB	chr19:23702897-23704641	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:23726629-23726742	HepG2	liver:	n/a	n/a
20	CEBPB	chr19:23707275-23707432	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:23728169-23728655	HepG2	liver:	n/a	n/a
22	CEBPB	chr19:23705291-23705718	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:23641566-23642084	A549	lung:	n/a	chr19:23641688-23641699
24	CEBPB	chr19:23778499-23778754	A549	lung:	n/a	chr19:23778651-23778660 chr19:23778649-23778662 chr19:23778651-23778660 chr19:23778651-23778660 chr19:23778649-23778660
25	CEBPB	chr19:23748134-23748691	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:23705300-23705591	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:23702877-23703664	A549	lung:	n/a	n/a
28	CEBPB	chr19:23643222-23643770	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:23714110-23714827	HepG2	liver:	n/a	chr19:23714556-23714567
30	CEBPB	chr19:23778546-23778776	HepG2	liver:	n/a	chr19:23778651-23778660 chr19:23778649-23778662 chr19:23778651-23778660 chr19:23778651-23778660 chr19:23778649-23778660
31	CEBPB	chr19:23726192-23726392	A549	lung:	n/a	n/a
32	CEBPB	chr19:23744045-23744862	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr19:23644241-23644836	IMR90	lung:	n/a	chr19:23644704-23644715
34	CEBPB	chr19:23728072-23728616	A549	lung:	n/a	n/a
35	CEBPB	chr19:23646302-23646762	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:23705280-23705623	IMR90	lung:	n/a	n/a
37	CEBPB	chr19:23641669-23642085	IMR90	lung:	n/a	chr19:23641688-23641699
38	CEBPB	chr19:23778468-23778821	ECC-1	luminal epithelium:	n/a	chr19:23778651-23778660 chr19:23778649-23778662 chr19:23778651-23778660 chr19:23778651-23778660 chr19:23778649-23778660
39	CEBPB	chr19:23714492-23714717	IMR90	lung:	n/a	chr19:23714556-23714567
40	CEBPB	chr19:23746267-23746490	HepG2	liver:	n/a	n/a
41	CEBPB	chr19:23744087-23744680	A549	lung:	n/a	n/a
42	CEBPB	chr19:23742030-23742215	IMR90	lung:	n/a	n/a
43	CEBPB	chr19:23728287-23728951	IMR90	lung:	n/a	n/a
44	CEBPB	chr19:23702925-23703368	IMR90	lung:	n/a	n/a
45	CEBPB	chr19:23705193-23705662	MCF-7	breast:	n/a	n/a
46	CEBPB	chr19:23746254-23746481	A549	lung:	n/a	n/a
47	CEBPB	chr19:23778495-23778758	H1-hESC	embryonic stem cell:	n/a	chr19:23778651-23778660 chr19:23778649-23778662 chr19:23778651-23778660 chr19:23778651-23778660 chr19:23778649-23778660
48	CEBPB	chr19:23703034-23704567	HepG2	liver:	n/a	n/a
49	CEBPB	chr19:23683137-23683277	A549	lung:	n/a	chr19:23683224-23683235
50	CEBPB	chr19:23683114-23683405	IMR90	lung:	n/a	chr19:23683224-23683235

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23657425-23657475	IMR90	lung:	fetal
2	chr19:23657425-23657475	IMR90	lung:	fetal
3	chr19:23657425-23657475	LNCaP	prostate:	n/a
4	chr19:23657425-23657475	GM12878	blood:	n/a
5	chr19:23654159-23654209	Hela-S3	cervix:	n/a
6	chr19:23653837-23653887	ProgFib	skin:	n/a
7	chr19:23654159-23654209	PrEC	prostate:	n/a
8	chr19:23654274-23654324	HMEC	breast:	n/a
9	chr19:23653996-23654046	HRE	kidney:	n/a
10	chr19:23657425-23657475	PANC-1	pancreas:	n/a
11	chr19:23654159-23654209	SK-N-SH	brain:	n/a
12	chr19:23654274-23654324	HEEpiC	esophagus:	n/a
13	chr19:23653200-23653250	PrEC	prostate:	n/a
14	chr19:23654274-23654324	HCM	heart:	n/a
15	chr19:23653200-23653250	BJ	skin:	n/a
16	chr19:23654274-23654324	RPTEC	kidney:	n/a
17	chr19:23653996-23654046	ovcar-3	ovarian:	n/a
18	chr19:23657425-23657475	GM19239	blood:	n/a
19	chr19:23653837-23653887	HUVEC	blood vessel:	n/a
20	chr19:23653837-23653887	HNPCEpiC	eye:	n/a
21	chr19:23653200-23653250	SK-N-SH_RA	brain:	n/a
22	chr19:23653200-23653250	GM12892	blood:	n/a
23	chr19:23653996-23654046	GM19239	blood:	n/a
24	chr19:23653996-23654046	NHBE	bronchial:	n/a
25	chr19:23654159-23654209	HNPCEpiC	eye:	n/a
26	chr19:23654274-23654324	K562	blood:	n/a
27	chr19:23653996-23654046	NB4	blood:	n/a
28	chr19:23653837-23653887	HRE	kidney:	n/a
29	chr19:23653200-23653250	U87	brain:	n/a
30	chr19:23654159-23654209	GM19239	blood:	n/a
31	chr19:23654227-23654277	Caco-2	colon:	n/a
32	chr19:23657425-23657475	HIPEpiC	eye:	n/a
33	chr19:23653996-23654046	Caco-2	colon:	n/a
34	chr19:23653996-23654046	HepG2	liver:	n/a
35	chr19:23654227-23654277	AG10803	skin:	n/a
36	chr19:23654227-23654277	HCF	heart:	n/a
37	chr19:23654274-23654324	PANC-1	pancreas:	n/a
38	chr19:23653996-23654046	MCF-7	breast:	n/a
39	chr19:23653837-23653887	CMK	blood:	n/a
40	chr19:23653200-23653250	LNCaP	prostate:	n/a
41	chr19:23657425-23657475	SK-N-MC	brain:	n/a
42	chr19:23654227-23654277	HMEC	breast:	n/a
43	chr19:23654159-23654209	HCF	heart:	n/a
44	chr19:23654274-23654324	T-47D	breast:	n/a
45	chr19:23654227-23654277	AG04449	skin:	fetal
46	chr19:23653837-23653887	T-47D	breast:	n/a
47	chr19:23657425-23657475	T-47D	breast:	n/a
48	chr19:23654227-23654277	SAEC	small airway:	n/a
49	chr19:23653996-23654046	AG09319	gingival:	n/a
50	chr19:23654159-23654209	GM12878	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:23716991..23718899-chr19:23719198..23721188,2	MCF-7	breast:
2	chr19:23859469..23861719-chr19:23863257..23865886,2	K562	blood:
3	chr19:23864035..23867567-chr19:23868052..23870516,3	K562	blood:
4	chr19:23865183..23867116-chr19:23868642..23870620,2	MCF-7	breast:
5	chr19:23716991..23718899-chr19:23719198..23721188,2	MCF-7	breast:
6	chr19:23861116..23863669-chr19:23863772..23867457,3	K562	blood:
7	chr19:23862169..23863759-chr19:23865204..23869096,3	K562	blood:
8	chr19:23846178..23848550-chr19:23856528..23858347,2	K562	blood:
9	chr19:23861116..23863669-chr19:23863772..23867457,3	K562	blood:
10	chr19:23858949..23860753-chr19:23868653..23870197,2	K562	blood:
11	chr19:23862120..23864692-chr19:23868183..23870195,2	MCF-7	breast:
12	chr19:23576348..23579660-chr19:23867719..23870587,3	MCF-7	breast:
13	chr19:23859469..23861719-chr19:23863257..23865886,2	K562	blood:
14	chr19:23846178..23848550-chr19:23856528..23858347,2	K562	blood:
15	chr19:23675218..23675970-chr2:239597148..239597648,2	NB4	blood:
16	chr19:23862169..23863759-chr19:23865204..23869096,3	K562	blood:
17	chr19:23829651..23831958-chr19:23839297..23841446,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF675-1	chr19:23710720-23710816	XLOC_013278
2	lnc-ZNF91-3	chr19:23680678-23680837	NONHSAT063921
3	lnc-ZNF730-16	chr19:23627064-23627991	NONHSAT063920
4	lnc-RPSAP58-5	chr19:23785369-23785908	NONHSAT063930
5	lnc-ZNF675-1	chr19:23708438-23709389	XLOC_013278
6	lnc-ZNF675-1	chr19:23710720-23710821	NONHSAT063926
7	lnc-RPSAP58-6	chr19:23780143-23780394	NONHSAT063929
8	lnc-RPSAP58-1	chr19:23740397-23740511	XLOC_013022
9	lnc-ZNF675-1	chr19:23748014-23748050	XLOC_013278
10	lnc-ZNF675-1	chr19:23708876-23709389	NONHSAT063926
11	lnc-RPSAP58-1	chr19:23741124-23741642	XLOC_013022
12	lnc-ZNF675-1	chr19:23714333-23714492	XLOC_013278
13	lnc-ZNF675-1	chr19:23710720-23710816	XLOC_013278
14	lnc-RPSAP58-1	chr19:23734519-23734611	XLOC_013022
15	lnc-ZNF675-1	chr19:23708550-23709389	XLOC_013278
16	lnc-RPSAP58-1	chr19:23741124-23741230	XLOC_013022
17	lnc-ZNF91-3	chr19:23688077-23688167	NONHSAT063921

No data

Variant related genes	Relation type
RPS27P29	TF binding region
ZNF725P	TF binding region
ZNF675	TF binding region
VN1R92P	TF binding region
ENSG00000268455	TF binding region
VN1R93P	TF binding region
RPS27P29	CpG island
ZNF725P	CpG island
ZNF675	CpG island
VN1R92P	CpG island
ENSG00000268455	CpG island
VN1R93P	CpG island
ENSG00000197372	chromatin interactions
ENSG00000167232	chromatin interactions
RAB34	miRNA target sites
CYR61	miRNA target sites
MASTL	miRNA target sites
TRAM1	miRNA target sites
USP6NL	miRNA target sites
NEO1	miRNA target sites
SKIV2L2	miRNA target sites

Extended variants
information (count: 6642 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:6642 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564654679	chr19:23625589-23625590	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs562804236	chr19:23625616-23625617	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs538861996	chr19:23625625-23625626	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs533102076	chr19:23625655-23625656	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs17491363	chr19:23625662-23625663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569488267	chr19:23625663-23625664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs532221425	chr19:23626127-23626128	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs550938602	chr19:23626133-23626134	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs549256616	chr19:23626135-23626136	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536809258	chr19:23626148-23626149	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs548923374	chr19:23626158-23626159	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567125688	chr19:23626177-23626178	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567273779	chr19:23626186-23626187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs190560963	chr19:23626189-23626190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs147123484	chr19:23626199-23626200	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs537811868	chr19:23626201-23626202	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs538315689	chr19:23626208-23626209	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs556912746	chr19:23626235-23626236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs187401464	chr19:23626247-23626248	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575410085	chr19:23626264-23626265	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs12971898	chr19:23626274-23626275	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs73551076	chr19:23626326-23626327	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141983763	chr19:23626905-23626906	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs554331174	chr19:23627077-23627078	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs553150452	chr19:23627121-23627122	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs369940340	chr19:23627167-23627168	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs572846572	chr19:23627235-23627236	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs373115718	chr19:23627237-23627238	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs149284590	chr19:23627271-23627272	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs573243434	chr19:23627296-23627297	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs186493108	chr19:23627305-23627306	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs539158489	chr19:23627306-23627307	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs534234871	chr19:23627426-23627427	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs543816433	chr19:23627477-23627478	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs34575232	chr19:23627492-23627493	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs191792078	chr19:23627623-23627624	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs529807444	chr19:23627662-23627663	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs183026077	chr19:23627699-23627700	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs144544867	chr19:23627720-23627721	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs138067850	chr19:23627840-23627841	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs376167529	chr19:23627875-23627876	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs187558784	chr19:23627876-23627877	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs17000147	chr19:23627882-23627883	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535452615	chr19:23627897-23627898	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs531733368	chr19:23627901-23627902	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs201699709	chr19:23632040-23632041	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs653425	chr19:23632051-23632052	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs687611	chr19:23632060-23632061	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs113895679	chr19:23632068-23632069	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs73553136	chr19:23632090-23632091	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:46)

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
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23632000-23632200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr19:23632600-23632800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr19:23643400-23644000	Enhancers	Placenta	Placenta
4	chr19:23643400-23644200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr19:23643400-23644200	Enhancers	HMEC	breast
6	chr19:23648000-23653000	Weak transcription	Lung	lung
7	chr19:23648200-23651400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:23648400-23652000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr19:23650800-23651200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr19:23652400-23653800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
11	chr19:23652400-23654000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr19:23652800-23654600	ZNF genes & repeats	Fetal Brain Female	brain
13	chr19:23653000-23654200	ZNF genes & repeats	Lung	lung
14	chr19:23653000-23654600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr19:23653200-23654200	ZNF genes & repeats	Placenta	Placenta
16	chr19:23653200-23654400	ZNF genes & repeats	Fetal Stomach	stomach
17	chr19:23653200-23654800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr19:23653400-23653600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:23653400-23654400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
20	chr19:23653400-23654400	Active TSS	Colonic Mucosa	Colon
21	chr19:23653400-23654400	ZNF genes & repeats	Esophagus	oesophagus
22	chr19:23653600-23653800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr19:23653600-23653800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr19:23653600-23654000	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr19:23653600-23654000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
26	chr19:23653600-23654000	Enhancers	Placenta Amnion	Placenta Amnion
27	chr19:23653600-23654200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
28	chr19:23653600-23654400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr19:23653600-23654400	ZNF genes & repeats	Pancreas	Pancrea
30	chr19:23653600-23654400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
31	chr19:23653600-23654600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
32	chr19:23653800-23654000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr19:23653800-23654000	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr19:23653800-23654000	Bivalent/Poised TSS	Left Ventricle	heart
35	chr19:23653800-23654200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr19:23653800-23654200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr19:23653800-23654200	Flanking Bivalent TSS/Enh	Right Ventricle	heart
38	chr19:23653800-23654200	Flanking Bivalent TSS/Enh	NHEK	skin
39	chr19:23653800-23654400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr19:23653800-23654400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr19:23653800-23654400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
42	chr19:23653800-23654400	Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr19:23653800-23654400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
44	chr19:23653800-23654400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
45	chr19:23653800-23654400	Active TSS	Fetal Kidney	kidney
46	chr19:23653800-23654400	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr19:23653800-23654400	Active TSS	Rectal Smooth Muscle	rectum
48	chr19:23653800-23654400	Active TSS	Right Atrium	heart
49	chr19:23653800-23654400	ZNF genes & repeats	HMEC	breast
50	chr19:23653800-23654600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell

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