Variant report

Variant	nsv138418
Chromosome Location	chr19:36190656-36193931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:410)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36193208-36193573	K562	blood:	n/a	n/a
2	ATF1	chr19:36193198-36193542	K562	blood:	n/a	n/a
3	ATF2	chr19:36193068-36193786	GM12878	blood:	n/a	n/a
4	ATF3	chr19:36193036-36193862	A549	lung:	n/a	n/a
5	BACH1	chr19:36193110-36193332	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:36193707-36193906	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr19:36192934-36193904	A549	lung:	n/a	chr19:36193592-36193601 chr19:36193896-36193904 chr19:36193496-36193509
8	BCL3	chr19:36192937-36193932	A549	lung:	n/a	chr19:36193592-36193601 chr19:36193896-36193904 chr19:36193496-36193509
9	BHLHE40	chr19:36193001-36193898	GM12878	blood:	n/a	chr19:36193495-36193511
10	BHLHE40	chr19:36193138-36193492	K562	blood:	n/a	n/a
11	BRCA1	chr19:36193093-36193855	GM12878	blood:	n/a	n/a
12	BRCA1	chr19:36193271-36193519	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr19:36193420-36193747	HepG2	liver:	n/a	n/a
14	CBX3	chr19:36193037-36193490	K562	blood:	n/a	n/a
15	CEBPB	chr19:36190922-36191087	HepG2	liver:	n/a	chr19:36191006-36191017
16	CEBPB	chr19:36190863-36191183	IMR90	lung:	n/a	chr19:36191006-36191017
17	CEBPB	chr19:36190852-36191189	K562	blood:	n/a	chr19:36191006-36191017
18	CEBPB	chr19:36190885-36191167	Hela-S3	cervix:	n/a	chr19:36191006-36191017
19	CEBPB	chr19:36190854-36191191	A549	lung:	n/a	chr19:36191006-36191017
20	CEBPB	chr19:36193141-36193287	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:36193347-36193411	K562	blood:	n/a	n/a
22	CEBPB	chr19:36193196-36193580	Hela-S3	cervix:	n/a	chr19:36193419-36193427 chr19:36193477-36193485
23	CEBPB	chr19:36190932-36191087	H1-hESC	embryonic stem cell:	n/a	chr19:36191006-36191017
24	CEBPB	chr19:36190864-36191194	HepG2	liver:	n/a	chr19:36191006-36191017
25	CEBPD	chr19:36193388-36193707	HepG2	liver:	n/a	n/a
26	CEBPZ	chr19:36193202-36193565	HepG2	liver:	n/a	n/a
27	CHD1	chr19:36192998-36193863	GM12878	blood:	n/a	n/a
28	CHD2	chr19:36193222-36193703	HepG2	liver:	n/a	n/a
29	CHD2	chr19:36193123-36193778	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr19:36193178-36193646	K562	blood:	n/a	n/a
31	CHD2	chr19:36193026-36193916	GM12878	blood:	n/a	n/a
32	CHD2	chr19:36193073-36193797	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr19:36192952-36193932	A549	lung:	n/a	n/a
34	CREB1	chr19:36193035-36193726	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr19:36192979-36194032	HepG2	liver:	n/a	n/a
36	CREB1	chr19:36193153-36193688	A549	lung:	n/a	n/a
37	CREB1	chr19:36193024-36193955	GM12878	blood:	n/a	n/a
38	CTCF	chr19:36193040-36193190	GM12865	blood:	n/a	n/a
39	CTCF	chr19:36193760-36193910	GM12873	blood:	n/a	chr19:36193787-36193808
40	CTCF	chr19:36193176-36193490	K562	blood:	n/a	n/a
41	CTCF	chr19:36193680-36193830	SK-N-SH_RA	brain:	n/a	chr19:36193787-36193808
42	CTCF	chr19:36193293-36193295	GM12892	blood:	n/a	n/a
43	CTCF	chr19:36193193-36193511	GM12878	blood:	n/a	n/a
44	CTCF	chr19:36193200-36193350	GM12864	blood:	n/a	n/a
45	CTCF	chr19:36193220-36193370	BJ	skin:	n/a	n/a
46	CTCF	chr19:36193040-36193190	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr19:36193618-36193814	Spleen_OC	spleen:	n/a	chr19:36193787-36193808
48	CTCF	chr19:36193719-36193834	MCF-7	breast:	n/a	chr19:36193787-36193808
49	CTCF	chr19:36193680-36193830	MCF-7	breast:	n/a	chr19:36193787-36193808
50	CTCF	chr19:36193180-36193330	AG04449	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36193407-36193457	H1-hESC	embryonic stem cell:	embryo
2	chr19:36193407-36193457	HCT-116	colon:	n/a
3	chr19:36193165-36193215	GM06990	blood:	n/a
4	chr19:36191758-36191808	LNCaP	prostate:	n/a
5	chr19:36193165-36193215	AG04449	skin:	fetal
6	chr19:36191758-36191808	BE2_C	brain:	n/a
7	chr19:36193577-36193627	GM12892	blood:	n/a
8	chr19:36193407-36193457	T-47D	breast:	n/a
9	chr19:36193165-36193215	AG04450	lung:	fetal
10	chr19:36193407-36193457	ProgFib	skin:	n/a
11	chr19:36193407-36193457	NH-A	brain:	n/a
12	chr19:36193165-36193215	HCM	heart:	n/a
13	chr19:36193165-36193215	U87	brain:	n/a
14	chr19:36193577-36193627	HL-60	blood:	n/a
15	chr19:36193165-36193215	H1-hESC	embryonic stem cell:	embryo
16	chr19:36193577-36193627	BE2_C	brain:	n/a
17	chr19:36191758-36191808	A549	lung:	n/a
18	chr19:36191758-36191808	HCF	heart:	n/a
19	chr19:36193407-36193457	A549	lung:	n/a
20	chr19:36193407-36193457	U87	brain:	n/a
21	chr19:36193165-36193215	HNPCEpiC	eye:	n/a
22	chr19:36193407-36193457	PrEC	prostate:	n/a
23	chr19:36193577-36193627	HEK293	kidney:	embryo
24	chr19:36193407-36193457	HEEpiC	esophagus:	n/a
25	chr19:36193407-36193457	BE2_C	brain:	n/a
26	chr19:36193407-36193457	Hepatocyte	liver:	n/a
27	chr19:36193577-36193627	NT2-D1	testis:	n/a
28	chr19:36193165-36193215	SK-N-SH_RA	brain:	n/a
29	chr19:36193165-36193215	AoSMC	blood vessel:	n/a
30	chr19:36193165-36193215	HAEpiC	amniotic membrane:	n/a
31	chr19:36193165-36193215	SKMC	muscle:	n/a
32	chr19:36191758-36191808	HPAEpiC	pulmonary alveolar:	n/a
33	chr19:36193577-36193627	H1-hESC	embryonic stem cell:	embryo
34	chr19:36193577-36193627	PFSK-1	brain:	n/a
35	chr19:36193407-36193457	SK-N-MC	brain:	n/a
36	chr19:36193407-36193457	AG09319	gingival:	n/a
37	chr19:36191758-36191808	GM12891	blood:	n/a
38	chr19:36193407-36193457	RPTEC	kidney:	n/a
39	chr19:36193407-36193457	HEK293	kidney:	embryo
40	chr19:36193577-36193627	HCPEpiC	choroid plexus:	n/a
41	chr19:36193577-36193627	SK-N-SH	brain:	n/a
42	chr19:36193407-36193457	HIPEpiC	eye:	n/a
43	chr19:36193577-36193627	LNCaP	prostate:	n/a
44	chr19:36193407-36193457	HUVEC	blood vessel:	n/a
45	chr19:36193577-36193627	HCT-116	colon:	n/a
46	chr19:36193577-36193627	PrEC	prostate:	n/a
47	chr19:36191758-36191808	AG09319	gingival:	n/a
48	chr19:36191758-36191808	HepG2	liver:	n/a
49	chr19:36193577-36193627	HRPEpiC	eye:	n/a
50	chr19:36193407-36193457	NHBE	bronchial:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36183210..36186350-chr19:36190384..36192650,3	K562	blood:
2	chr19:36193425..36195138-chr19:36196726..36199415,4	K562	blood:
3	chr19:36192706..36195143-chr19:36207502..36210108,2	MCF-7	breast:
4	chr19:36193261..36195251-chr19:36208816..36211234,2	K562	blood:
5	chr19:36193434..36194967-chr19:36206737..36208478,2	K562	blood:
6	chr19:36184467..36185236-chr19:36193340..36194279,2	MCF-7	breast:
7	chr19:36134071..36136376-chr19:36193211..36195269,2	MCF-7	breast:
8	chr19:36193001..36195251-chr19:36206737..36211234,4	K562	blood:
9	chr19:36190946..36193857-chr19:36221816..36224169,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB32-3	chr19:36192573-36192924	NONHSAT065887

No data

Variant related genes	Relation type
ZBTB32	TF binding region
ZBTB32	CpG island
ENSG00000105672	chromatin interactions
ENSG00000105663	chromatin interactions
ENSG00000272333	chromatin interactions

Extended variants
information (count: 111 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:111 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577265959	chr19:36190669-36190670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs546222180	chr19:36190734-36190735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs3885794	chr19:36190775-36190776	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs554724697	chr19:36190802-36190803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs3885795	chr19:36190828-36190829	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs561631863	chr19:36190839-36190840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527510750	chr19:36190857-36190858	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs547185892	chr19:36190866-36190867	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs372348017	chr19:36190904-36190905	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs570568059	chr19:36190915-36190916	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs539169264	chr19:36190931-36190932	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs186387747	chr19:36190937-36190938	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141184321	chr19:36190940-36190941	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs3900972	chr19:36190942-36190943	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs569572891	chr19:36190979-36190980	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535397414	chr19:36190994-36190995	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs56849855	chr19:36191019-36191020	Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs575166286	chr19:36191037-36191038	Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553005077	chr19:36191074-36191075	Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs140997165	chr19:36191103-36191104	Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191246193	chr19:36191104-36191105	Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577317653	chr19:36191106-36191107	Weak transcription Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs368377729	chr19:36191216-36191217	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs77123726	chr19:36191257-36191258	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116882180	chr19:36191272-36191273	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs77680881	chr19:36191318-36191319	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541798064	chr19:36191390-36191391	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs561694059	chr19:36191407-36191408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs562582383	chr19:36191414-36191415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183534867	chr19:36191439-36191440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547249112	chr19:36191468-36191469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564130501	chr19:36191469-36191470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs8100488	chr19:36191517-36191518	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs3859576	chr19:36191518-36191519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs3927106	chr19:36191558-36191559	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549627081	chr19:36191575-36191576	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569718555	chr19:36191609-36191610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535472846	chr19:36191655-36191656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs368768835	chr19:36191656-36191657	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548998893	chr19:36191685-36191686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs568813590	chr19:36191687-36191688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534508901	chr19:36191771-36191772	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs73048504	chr19:36191817-36191818	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs75302209	chr19:36191875-36191876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540005532	chr19:36191926-36191927	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556409355	chr19:36191927-36191928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs574864672	chr19:36191945-36191946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541861214	chr19:36191988-36191989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185740703	chr19:36192099-36192100	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs75369290	chr19:36192101-36192102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36179200-36192800	Weak transcription	Right Atrium	heart
2	chr19:36183000-36193000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:36184800-36192600	Weak transcription	Placenta	Placenta
4	chr19:36185400-36192600	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr19:36188800-36190800	Weak transcription	HepG2	liver
6	chr19:36189600-36193000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr19:36189800-36190800	Weak transcription	GM12878-XiMat	blood
8	chr19:36190800-36191400	Enhancers	GM12878-XiMat	blood
9	chr19:36190800-36191400	Enhancers	HepG2	liver
10	chr19:36191000-36191200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:36191000-36191200	Enhancers	Pancreas	Pancrea
12	chr19:36191200-36192800	Weak transcription	Pancreas	Pancrea
13	chr19:36191400-36192600	Weak transcription	GM12878-XiMat	blood
14	chr19:36191400-36192800	Weak transcription	HepG2	liver
15	chr19:36192400-36192600	Enhancers	Dnd41	blood
16	chr19:36192400-36192800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr19:36192600-36192800	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr19:36192600-36192800	Enhancers	Primary B cells from peripheral blood	blood
19	chr19:36192600-36192800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr19:36192600-36192800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr19:36192600-36192800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr19:36192600-36192800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr19:36192600-36192800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr19:36192600-36192800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr19:36192600-36192800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr19:36192600-36192800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr19:36192600-36192800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr19:36192600-36192800	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr19:36192600-36192800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr19:36192600-36192800	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr19:36192600-36192800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr19:36192600-36192800	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr19:36192600-36192800	Enhancers	Colonic Mucosa	Colon
34	chr19:36192600-36192800	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr19:36192600-36192800	Flanking Active TSS	GM12878-XiMat	blood
36	chr19:36192600-36193000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
37	chr19:36192600-36193000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr19:36192600-36193000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr19:36192600-36193000	Enhancers	Placenta	Placenta
40	chr19:36192600-36193000	Enhancers	Fetal Thymus	thymus
41	chr19:36192600-36193600	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr19:36192600-36194000	Active TSS	H9 Cell Line	embryonic stem cell
43	chr19:36192600-36194200	Flanking Active TSS	Dnd41	blood
44	chr19:36192800-36193000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr19:36192800-36193000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
46	chr19:36192800-36193000	Enhancers	Primary B cells from cord blood	blood
47	chr19:36192800-36193000	Enhancers	Primary T cells from cord blood	blood
48	chr19:36192800-36193000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr19:36192800-36193000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr19:36192800-36193000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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