Variant report

Variant	nsv961286
Chromosome Location	chr19:36187862-36199437
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:628)
CpG islands
(count:612)
Chromatin interactive
region (count:15)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36195195-36195415	K562	blood:	n/a	n/a
2	ARID3A	chr19:36193208-36193573	K562	blood:	n/a	n/a
3	ATF1	chr19:36193198-36193542	K562	blood:	n/a	n/a
4	ATF2	chr19:36193068-36193786	GM12878	blood:	n/a	n/a
5	ATF2	chr19:36187617-36188240	GM12878	blood:	n/a	n/a
6	ATF3	chr19:36193036-36193862	A549	lung:	n/a	n/a
7	ATF3	chr19:36195213-36195434	K562	blood:	n/a	n/a
8	BACH1	chr19:36193707-36193906	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr19:36193110-36193332	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr19:36187728-36188127	GM12878	blood:	n/a	n/a
11	BATF	chr19:36187728-36188166	GM12878	blood:	n/a	n/a
12	BCL11A	chr19:36187745-36188143	GM12878	blood:	n/a	chr19:36187894-36187903
13	BCL3	chr19:36192937-36193932	A549	lung:	n/a	chr19:36193592-36193601 chr19:36193896-36193904 chr19:36193496-36193509
14	BCL3	chr19:36192934-36193904	A549	lung:	n/a	chr19:36193592-36193601 chr19:36193896-36193904 chr19:36193496-36193509
15	BCL3	chr19:36187700-36188134	GM12878	blood:	n/a	chr19:36187894-36187903
16	BCLAF1	chr19:36187798-36188206	GM12878	blood:	n/a	chr19:36187894-36187903
17	BCLAF1	chr19:36187665-36188189	GM12878	blood:	n/a	chr19:36187894-36187903
18	BHLHE40	chr19:36195198-36195530	K562	blood:	n/a	n/a
19	BHLHE40	chr19:36193138-36193492	K562	blood:	n/a	n/a
20	BHLHE40	chr19:36187734-36188180	GM12878	blood:	n/a	n/a
21	BHLHE40	chr19:36187759-36188130	HepG2	liver:	n/a	n/a
22	BHLHE40	chr19:36193001-36193898	GM12878	blood:	n/a	chr19:36193495-36193511
23	BRCA1	chr19:36193420-36193747	HepG2	liver:	n/a	n/a
24	BRCA1	chr19:36193271-36193519	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr19:36193093-36193855	GM12878	blood:	n/a	n/a
26	CBX3	chr19:36195014-36195570	K562	blood:	n/a	n/a
27	CBX3	chr19:36193037-36193490	K562	blood:	n/a	n/a
28	CBX3	chr19:36195213-36195564	K562	blood:	n/a	n/a
29	CEBPB	chr19:36190885-36191167	Hela-S3	cervix:	n/a	chr19:36191006-36191017
30	CEBPB	chr19:36190932-36191087	H1-hESC	embryonic stem cell:	n/a	chr19:36191006-36191017
31	CEBPB	chr19:36188564-36188724	K562	blood:	n/a	chr19:36188603-36188614
32	CEBPB	chr19:36190922-36191087	HepG2	liver:	n/a	chr19:36191006-36191017
33	CEBPB	chr19:36190854-36191191	A549	lung:	n/a	chr19:36191006-36191017
34	CEBPB	chr19:36193141-36193287	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr19:36187543-36188243	GM12878	blood:	n/a	n/a
36	CEBPB	chr19:36188500-36188801	HepG2	liver:	n/a	chr19:36188603-36188614
37	CEBPB	chr19:36190864-36191194	HepG2	liver:	n/a	chr19:36191006-36191017
38	CEBPB	chr19:36188592-36188905	A549	lung:	n/a	chr19:36188603-36188614
39	CEBPB	chr19:36190852-36191189	K562	blood:	n/a	chr19:36191006-36191017
40	CEBPB	chr19:36189516-36189733	K562	blood:	n/a	n/a
41	CEBPB	chr19:36188599-36188682	Hela-S3	cervix:	n/a	chr19:36188603-36188614
42	CEBPB	chr19:36193347-36193411	K562	blood:	n/a	n/a
43	CEBPB	chr19:36188569-36188877	IMR90	lung:	n/a	chr19:36188603-36188614
44	CEBPB	chr19:36189527-36189804	HepG2	liver:	n/a	n/a
45	CEBPB	chr19:36190863-36191183	IMR90	lung:	n/a	chr19:36191006-36191017
46	CEBPB	chr19:36193196-36193580	Hela-S3	cervix:	n/a	chr19:36193419-36193427 chr19:36193477-36193485
47	CEBPD	chr19:36193388-36193707	HepG2	liver:	n/a	n/a
48	CEBPZ	chr19:36193202-36193565	HepG2	liver:	n/a	n/a
49	CHD1	chr19:36187911-36187979	GM12878	blood:	n/a	n/a
50	CHD1	chr19:36192998-36193863	GM12878	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36195835-36195885	AG09319	gingival:	n/a
2	chr19:36193577-36193627	NT2-D1	testis:	n/a
3	chr19:36195835-36195885	AG09319	gingival:	n/a
4	chr19:36193577-36193627	NT2-D1	testis:	n/a
5	chr19:36195363-36195413	H1-hESC	embryonic stem cell:	embryo
6	chr19:36195835-36195885	HL-60	blood:	n/a
7	chr19:36195455-36195505	LNCaP	prostate:	n/a
8	chr19:36198177-36198227	BJ	skin:	n/a
9	chr19:36195268-36195318	HCF	heart:	n/a
10	chr19:36198177-36198227	SK-N-MC	brain:	n/a
11	chr19:36193407-36193457	HEK293	kidney:	embryo
12	chr19:36193165-36193215	U87	brain:	n/a
13	chr19:36189979-36190029	SK-N-SH	brain:	n/a
14	chr19:36195835-36195885	HEK293	kidney:	embryo
15	chr19:36195835-36195885	HMEC	breast:	n/a
16	chr19:36195363-36195413	Hela-S3	cervix:	n/a
17	chr19:36195455-36195505	HMEC	breast:	n/a
18	chr19:36193165-36193215	Caco-2	colon:	n/a
19	chr19:36195363-36195413	SAEC	small airway:	n/a
20	chr19:36195268-36195318	HIPEpiC	eye:	n/a
21	chr19:36193577-36193627	HCM	heart:	n/a
22	chr19:36193165-36193215	K562	blood:	n/a
23	chr19:36198177-36198227	SK-N-SH_RA	brain:	n/a
24	chr19:36195268-36195318	A549	lung:	n/a
25	chr19:36198177-36198227	Hepatocyte	liver:	n/a
26	chr19:36189979-36190029	NHDF-neo	bronchial:	n/a
27	chr19:36193165-36193215	SKMC	muscle:	n/a
28	chr19:36189979-36190029	AG04450	lung:	fetal
29	chr19:36189979-36190029	Hela-S3	cervix:	n/a
30	chr19:36198177-36198227	GM12891	blood:	n/a
31	chr19:36193577-36193627	HCPEpiC	choroid plexus:	n/a
32	chr19:36193407-36193457	HIPEpiC	eye:	n/a
33	chr19:36191758-36191808	HepG2	liver:	n/a
34	chr19:36195455-36195505	Hepatocyte	liver:	n/a
35	chr19:36195363-36195413	AG04450	lung:	fetal
36	chr19:36189979-36190029	SK-N-MC	brain:	n/a
37	chr19:36189979-36190029	NT2-D1	testis:	n/a
38	chr19:36193407-36193457	MCF10A-Er-Src	breast:	n/a
39	chr19:36189979-36190029	Hepatocyte	liver:	n/a
40	chr19:36195363-36195413	HepG2	liver:	n/a
41	chr19:36195455-36195505	AG04449	skin:	fetal
42	chr19:36195835-36195885	Jurkat	blood:	n/a
43	chr19:36195363-36195413	NT2-D1	testis:	n/a
44	chr19:36195363-36195413	NH-A	brain:	n/a
45	chr19:36195455-36195505	BJ	skin:	n/a
46	chr19:36193407-36193457	RPTEC	kidney:	n/a
47	chr19:36195455-36195505	SK-N-MC	brain:	n/a
48	chr19:36195455-36195505	GM12891	blood:	n/a
49	chr19:36195363-36195413	A549	lung:	n/a
50	chr19:36195835-36195885	MCF10A-Er-Src	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36192706..36195143-chr19:36207502..36210108,2	MCF-7	breast:
2	chr19:36195695..36198364-chr19:36200825..36204221,3	K562	blood:
3	chr19:36190946..36193857-chr19:36221816..36224169,2	K562	blood:
4	chr19:36193001..36195251-chr19:36206737..36211234,4	K562	blood:
5	chr19:36139132..36140724-chr19:36197337..36199740,2	MCF-7	breast:
6	chr19:36193425..36195138-chr19:36196726..36199415,4	K562	blood:
7	chr19:36193434..36194967-chr19:36206737..36208478,2	K562	blood:
8	chr19:36193425..36195138-chr19:36196726..36199415,4	K562	blood:
9	chr19:36134071..36136376-chr19:36193211..36195269,2	MCF-7	breast:
10	chr19:36184467..36185236-chr19:36193340..36194279,2	MCF-7	breast:
11	chr19:36198943..36200443-chr19:36207511..36209962,2	K562	blood:
12	chr19:36183210..36186350-chr19:36190384..36192650,3	K562	blood:
13	chr19:36195571..36197900-chr19:36202772..36204564,2	MCF-7	breast:
14	chr19:36193261..36195251-chr19:36208816..36211234,2	K562	blood:
15	chr19:36199124..36200965-chr19:36201478..36204089,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZBTB32-1	chr19:36198272-36198327	XLOC_013052
2	lnc-ZBTB32-1	chr19:36198868-36199158	XLOC_013052
3	lnc-ZBTB32-2	chr19:36195481-36195525	ENSG00000239352.1
4	lnc-ZBTB32-2	chr19:36195456-36195525	ENSG00000239352.1
5	lnc-ZBTB32-3	chr19:36192573-36192924	NONHSAT065887
6	lnc-ZBTB32-3	chr19:36188501-36188572	NONHSAT065887
7	lnc-ZBTB32-2	chr19:36195461-36195525	ENSG00000241762.1

No data

Variant related genes	Relation type
ZBTB32	TF binding region
ZBTB32	CpG island
ENSG00000105663	chromatin interactions
ENSG00000105672	chromatin interactions
ENSG00000126267	chromatin interactions
ENSG00000272333	chromatin interactions
ENSG00000011590	chromatin interactions
DNAJB9	miRNA target sites
ANKRD13D	miRNA target sites

Extended variants
information (count: 403 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538883680	chr19:36187902-36187903	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558708372	chr19:36187914-36187915	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184952255	chr19:36187975-36187976	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544300091	chr19:36188000-36188001	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370230902	chr19:36188009-36188010	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574112510	chr19:36188045-36188046	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539829644	chr19:36188059-36188060	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559664853	chr19:36188060-36188061	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs17776834	chr19:36188129-36188130	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs571818323	chr19:36188156-36188157	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553181972	chr19:36188172-36188173	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551616584	chr19:36188211-36188212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565476159	chr19:36188212-36188213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78029482	chr19:36188218-36188219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541881847	chr19:36188247-36188248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551068781	chr19:36188250-36188251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189801763	chr19:36188265-36188266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112218755	chr19:36188276-36188277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143140658	chr19:36188299-36188300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192918707	chr19:36188340-36188341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547014212	chr19:36188349-36188350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12977671	chr19:36188364-36188365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12977846	chr19:36188389-36188390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs12975122	chr19:36188425-36188426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12976939	chr19:36188433-36188434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148262896	chr19:36188435-36188436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs200440599	chr19:36188482-36188483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78278288	chr19:36188486-36188487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558525240	chr19:36188551-36188552	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs575420160	chr19:36188573-36188574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575913880	chr19:36188669-36188670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537611682	chr19:36188706-36188707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184352827	chr19:36188744-36188745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375440350	chr19:36188787-36188788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368408344	chr19:36188883-36188884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2335133	chr19:36188913-36188914	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs376915820	chr19:36188914-36188915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367986337	chr19:36188945-36188946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2428117	chr19:36188946-36188947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs576380807	chr19:36188962-36188963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371054213	chr19:36188967-36188968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545704082	chr19:36188993-36188994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573717139	chr19:36189098-36189099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565402804	chr19:36189104-36189105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs137948296	chr19:36189106-36189107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143509322	chr19:36189107-36189108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2619198	chr19:36189117-36189118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561413415	chr19:36189160-36189161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189547971	chr19:36189215-36189216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181819624	chr19:36189224-36189225	Weak transcription Enhancers	n/a	n/a	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:382 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr19:36187000-36188800	Enhancers	HepG2	liver
6	chr19:36187800-36188200	Flanking Active TSS	GM12878-XiMat	blood
7	chr19:36188200-36188800	Enhancers	GM12878-XiMat	blood
8	chr19:36188800-36189200	Weak transcription	GM12878-XiMat	blood
9	chr19:36188800-36190800	Weak transcription	HepG2	liver
10	chr19:36189200-36189800	Enhancers	GM12878-XiMat	blood
11	chr19:36189600-36193000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:36189800-36190800	Weak transcription	GM12878-XiMat	blood
13	chr19:36190800-36191400	Enhancers	GM12878-XiMat	blood
14	chr19:36190800-36191400	Enhancers	HepG2	liver
15	chr19:36191000-36191200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:36191000-36191200	Enhancers	Pancreas	Pancrea
17	chr19:36191200-36192800	Weak transcription	Pancreas	Pancrea
18	chr19:36191400-36192600	Weak transcription	GM12878-XiMat	blood
19	chr19:36191400-36192800	Weak transcription	HepG2	liver
20	chr19:36192400-36192600	Enhancers	Dnd41	blood
21	chr19:36192400-36192800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr19:36192600-36192800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr19:36192600-36192800	Enhancers	Primary B cells from peripheral blood	blood
24	chr19:36192600-36192800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr19:36192600-36192800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr19:36192600-36192800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr19:36192600-36192800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr19:36192600-36192800	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr19:36192600-36192800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
30	chr19:36192600-36192800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr19:36192600-36192800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr19:36192600-36192800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr19:36192600-36192800	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr19:36192600-36192800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr19:36192600-36192800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr19:36192600-36192800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr19:36192600-36192800	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr19:36192600-36192800	Enhancers	Colonic Mucosa	Colon
39	chr19:36192600-36192800	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr19:36192600-36192800	Flanking Active TSS	GM12878-XiMat	blood
41	chr19:36192600-36193000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
42	chr19:36192600-36193000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr19:36192600-36193000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:36192600-36193000	Enhancers	Placenta	Placenta
45	chr19:36192600-36193000	Enhancers	Fetal Thymus	thymus
46	chr19:36192600-36193600	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr19:36192600-36194000	Active TSS	H9 Cell Line	embryonic stem cell
48	chr19:36192600-36194200	Flanking Active TSS	Dnd41	blood
49	chr19:36192800-36193000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr19:36192800-36193000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood

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