Variant report

Variant	nsv828647
Chromosome Location	chr19:56701488-56758401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:56732773-56733067	K562	blood:	n/a	n/a
2	BATF	chr19:56745875-56746197	GM12878	blood:	n/a	n/a
3	BRCA1	chr19:56720561-56720808	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr19:56745473-56745601	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr19:56732796-56733078	A549	lung:	n/a	chr19:56732934-56732945
6	CEBPB	chr19:56736715-56737020	A549	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
7	CEBPB	chr19:56744051-56744221	K562	blood:	n/a	n/a
8	CEBPB	chr19:56741719-56741891	K562	blood:	n/a	chr19:56741810-56741821
9	CEBPB	chr19:56732764-56733076	HepG2	liver:	n/a	chr19:56732934-56732945
10	CEBPB	chr19:56716429-56716798	A549	lung:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
11	CEBPB	chr19:56723261-56723384	K562	blood:	n/a	n/a
12	CEBPB	chr19:56716360-56717024	Hela-S3	cervix:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
13	CEBPB	chr19:56741714-56741974	IMR90	lung:	n/a	chr19:56741810-56741821
14	CEBPB	chr19:56741646-56741970	HepG2	liver:	n/a	chr19:56741810-56741821
15	CEBPB	chr19:56716455-56716760	IMR90	lung:	n/a	chr19:56716533-56716544
16	CEBPB	chr19:56732773-56733100	IMR90	lung:	n/a	chr19:56732934-56732945
17	CEBPB	chr19:56705414-56705462	HepG2	liver:	n/a	chr19:56705438-56705449
18	CEBPB	chr19:56709309-56709335	K562	blood:	n/a	n/a
19	CEBPB	chr19:56705321-56705483	K562	blood:	n/a	chr19:56705438-56705449
20	CEBPB	chr19:56711159-56711500	A549	lung:	n/a	chr19:56711325-56711336
21	CEBPB	chr19:56716510-56716908	K562	blood:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
22	CEBPB	chr19:56732645-56733248	Hela-S3	cervix:	n/a	chr19:56732934-56732945
23	CEBPB	chr19:56732726-56733084	MCF-7	breast:	n/a	chr19:56732934-56732945
24	CEBPB	chr19:56720517-56720847	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr19:56741741-56741909	H1-hESC	embryonic stem cell:	n/a	chr19:56741810-56741821
26	CEBPB	chr19:56741649-56741971	A549	lung:	n/a	chr19:56741810-56741821
27	CEBPB	chr19:56732731-56733102	K562	blood:	n/a	chr19:56732934-56732945
28	CEBPB	chr19:56732791-56733124	H1-hESC	embryonic stem cell:	n/a	chr19:56732934-56732945
29	CEBPB	chr19:56732803-56733050	K562	blood:	n/a	chr19:56732934-56732945
30	CEBPB	chr19:56711237-56711378	HepG2	liver:	n/a	chr19:56711325-56711336
31	CEBPB	chr19:56736739-56736963	HepG2	liver:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
32	CEBPB	chr19:56711122-56711514	HepG2	liver:	n/a	chr19:56711325-56711336
33	CEBPB	chr19:56732730-56733098	A549	lung:	n/a	chr19:56732934-56732945
34	CEBPB	chr19:56736697-56737012	IMR90	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
35	CEBPB	chr19:56744025-56744198	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr19:56736713-56736976	K562	blood:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
37	CEBPB	chr19:56705349-56705533	A549	lung:	n/a	chr19:56705438-56705449
38	CEBPB	chr19:56711177-56711471	IMR90	lung:	n/a	chr19:56711325-56711336
39	CEBPB	chr19:56736709-56737013	Hela-S3	cervix:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
40	CEBPB	chr19:56711153-56711485	Hela-S3	cervix:	n/a	chr19:56711325-56711336
41	CEBPB	chr19:56711156-56711414	HepG2	liver:	n/a	chr19:56711325-56711336
42	CEBPB	chr19:56732747-56733109	K562	blood:	n/a	chr19:56732934-56732945
43	CEBPB	chr19:56716430-56716674	HepG2	liver:	n/a	chr19:56716533-56716544
44	CEBPB	chr19:56741673-56741957	K562	blood:	n/a	chr19:56741810-56741821
45	CEBPB	chr19:56711161-56711465	K562	blood:	n/a	chr19:56711325-56711336
46	CEBPB	chr19:56711141-56711460	HepG2	liver:	n/a	chr19:56711325-56711336
47	CEBPB	chr19:56707830-56708066	K562	blood:	n/a	n/a
48	CEBPB	chr19:56711145-56711495	H1-hESC	embryonic stem cell:	n/a	chr19:56711325-56711336
49	CEBPD	chr19:56732776-56733035	K562	blood:	n/a	n/a
50	CHD2	chr19:56720040-56720297	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56739741-56739791	HIPEpiC	eye:	n/a
2	chr19:56739741-56739791	HIPEpiC	eye:	n/a
3	chr19:56739782-56739832	AG10803	skin:	n/a
4	chr19:56742355-56742405	NH-A	brain:	n/a
5	chr19:56707808-56707858	BE2_C	brain:	n/a
6	chr19:56728589-56728639	NH-A	brain:	n/a
7	chr19:56704341-56704391	SKMC	muscle:	n/a
8	chr19:56739749-56739799	NHBE	bronchial:	n/a
9	chr19:56742355-56742405	NT2-D1	testis:	n/a
10	chr19:56738933-56738983	ECC-1	luminal epithelium:	n/a
11	chr19:56728422-56728472	HRPEpiC	eye:	n/a
12	chr19:56739749-56739799	H1-hESC	embryonic stem cell:	embryo
13	chr19:56732932-56732982	Hepatocyte	liver:	n/a
14	chr19:56739573-56739623	HUVEC	blood vessel:	n/a
15	chr19:56739749-56739799	ECC-1	luminal epithelium:	n/a
16	chr19:56739782-56739832	HRE	kidney:	n/a
17	chr19:56739868-56739918	AG04449	skin:	fetal
18	chr19:56705386-56705436	CMK	blood:	n/a
19	chr19:56709655-56709705	AoSMC	blood vessel:	n/a
20	chr19:56739788-56739838	BE2_C	brain:	n/a
21	chr19:56730494-56730544	BE2_C	brain:	n/a
22	chr19:56730494-56730544	GM12891	blood:	n/a
23	chr19:56726303-56726353	AG09309	skin:	n/a
24	chr19:56730494-56730544	AG04450	lung:	fetal
25	chr19:56732932-56732982	AG09309	skin:	n/a
26	chr19:56730494-56730544	NHBE	bronchial:	n/a
27	chr19:56732932-56732982	ECC-1	luminal epithelium:	n/a
28	chr19:56733045-56733095	GM12891	blood:	n/a
29	chr19:56730494-56730544	SK-N-SH	brain:	n/a
30	chr19:56728422-56728472	SK-N-SH_RA	brain:	n/a
31	chr19:56739788-56739838	HCF	heart:	n/a
32	chr19:56739782-56739832	HMEC	breast:	n/a
33	chr19:56739788-56739838	BJ	skin:	n/a
34	chr19:56740672-56740722	GM12891	blood:	n/a
35	chr19:56741019-56741069	HEEpiC	esophagus:	n/a
36	chr19:56709655-56709705	LNCaP	prostate:	n/a
37	chr19:56742355-56742405	HEEpiC	esophagus:	n/a
38	chr19:56739788-56739838	LNCaP	prostate:	n/a
39	chr19:56707808-56707858	H1-hESC	embryonic stem cell:	embryo
40	chr19:56739573-56739623	GM12878	blood:	n/a
41	chr19:56741019-56741069	PFSK-1	brain:	n/a
42	chr19:56730494-56730544	Hepatocyte	liver:	n/a
43	chr19:56728589-56728639	RPTEC	kidney:	n/a
44	chr19:56739868-56739918	AG09319	gingival:	n/a
45	chr19:56728422-56728472	PFSK-1	brain:	n/a
46	chr19:56709056-56709106	LNCaP	prostate:	n/a
47	chr19:56709228-56709278	BJ	skin:	n/a
48	chr19:56741019-56741069	SKMC	muscle:	n/a
49	chr19:56739868-56739918	T-47D	breast:	n/a
50	chr19:56738933-56738983	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56731454..56732253-chr19:56820726..56821606,2	MCF-7	breast:
2	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
3	chr19:56750344..56752392-chr19:56783866..56786080,2	K562	blood:
4	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
5	chr19:56587934..56588448-chr19:56732565..56733070,2	MCF-7	breast:
6	chr19:56706835..56708923-chr19:56717136..56719247,2	K562	blood:

Variant related genes	Relation type
ZSCAN5B	TF binding region
ZSCAN5D	TF binding region
ZSCAN5C	TF binding region
ENSG00000242411	TF binding region
ZSCAN5A	TF binding region
ZSCAN5B	CpG island
ZSCAN5D	CpG island
ZSCAN5C	CpG island
ENSG00000242411	CpG island
ZSCAN5A	CpG island
ENSG00000267710	chromatin interactions
ENSG00000204532	chromatin interactions

Extended variants
information (count: 2348 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2348 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202218504	chr19:56701488-56701489	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs377383565	chr19:56701489-56701490	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370425792	chr19:56701490-56701491	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376043891	chr19:56701497-56701498	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368461762	chr19:56701498-56701499	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534584381	chr19:56701513-56701514	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371555338	chr19:56701553-56701554	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189564920	chr19:56701571-56701572	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs61738499	chr19:56701578-56701579	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558592538	chr19:56701596-56701597	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373469763	chr19:56701609-56701610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537974249	chr19:56701610-56701611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377366357	chr19:56701616-56701617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370054206	chr19:56701620-56701621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373817287	chr19:56701625-56701626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200185124	chr19:56701626-56701627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150688455	chr19:56701631-56701632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370948217	chr19:56701637-56701638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201048831	chr19:56701647-56701648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192204188	chr19:56701649-56701650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184226738	chr19:56701652-56701653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200285996	chr19:56701660-56701661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367587385	chr19:56701664-56701665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201658700	chr19:56701665-56701666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577337778	chr19:56701671-56701672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200898843	chr19:56701679-56701680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201080393	chr19:56701686-56701687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372588974	chr19:56701712-56701713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs200312845	chr19:56701724-56701725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368088200	chr19:56701730-56701731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138952005	chr19:56701754-56701755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376623371	chr19:56701755-56701756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561737213	chr19:56701759-56701760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527687405	chr19:56701766-56701767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs892183	chr19:56701774-56701775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs892184	chr19:56701778-56701779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538794260	chr19:56701781-56701782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376632539	chr19:56701789-56701790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200350099	chr19:56701792-56701793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61742626	chr19:56701801-56701802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537939197	chr19:56701802-56701803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61742631	chr19:56701817-56701818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373709117	chr19:56701818-56701819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs61742633	chr19:56701824-56701825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370488746	chr19:56701825-56701826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs61742634	chr19:56701827-56701828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375696908	chr19:56701830-56701831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370255759	chr19:56701832-56701833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs111915100	chr19:56701842-56701843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368972539	chr19:56701861-56701862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56688600-56702400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:56701000-56701600	Enhancers	K562	blood
3	chr19:56701200-56701600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr19:56702400-56702800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:56705400-56705800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr19:56710800-56712400	Enhancers	Liver	Liver
7	chr19:56711000-56711200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr19:56711000-56711800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr19:56711600-56711800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr19:56716600-56717200	Bivalent Enhancer	Hela-S3	cervix
11	chr19:56723600-56727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:56724400-56728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr19:56725000-56725200	Active TSS	A549	lung
14	chr19:56725200-56727400	Weak transcription	A549	lung
15	chr19:56727400-56727600	ZNF genes & repeats	A549	lung
16	chr19:56727400-56727800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:56727400-56728200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr19:56727600-56735800	Weak transcription	A549	lung
19	chr19:56727800-56728000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:56727800-56729000	Enhancers	Dnd41	blood
21	chr19:56728000-56728400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr19:56728000-56728400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr19:56728000-56728400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr19:56728000-56728400	Enhancers	Esophagus	oesophagus
27	chr19:56728000-56728800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr19:56728000-56729400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr19:56728200-56728400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr19:56728200-56728400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr19:56728200-56728400	Enhancers	Primary hematopoietic stem cells	blood
32	chr19:56728200-56728400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr19:56728200-56728400	Enhancers	HMEC	breast
36	chr19:56728200-56728400	Enhancers	HUVEC	blood vessel
37	chr19:56728200-56728600	Bivalent Enhancer	Thymus	Thymus
38	chr19:56728200-56728800	Bivalent Enhancer	Placenta	Placenta
39	chr19:56728200-56728800	Bivalent Enhancer	Fetal Thymus	thymus
40	chr19:56728200-56729200	Active TSS	Rectal Mucosa Donor 31	rectum
41	chr19:56728200-56729400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr19:56728200-56729400	Enhancers	Fetal Heart	heart
43	chr19:56728400-56728600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
44	chr19:56728400-56728600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr19:56728400-56728600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr19:56728400-56728600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
47	chr19:56728400-56728600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr19:56728400-56728600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr19:56728400-56728600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr19:56728400-56728600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin

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