Variant report

Variant	nsv1067364
Chromosome Location	chr19:36921204-36985874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:972)
CpG islands
(count:1343)
Chromatin interactive
region (count:49)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:36980095-36981066	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:36980366-36980986	K562	blood:	n/a	n/a
3	ATF1	chr19:36979820-36981054	K562	blood:	n/a	n/a
4	ATF1	chr19:36927570-36927771	K562	blood:	n/a	n/a
5	ATF2	chr19:36980143-36980828	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr19:36980410-36980762	K562	blood:	n/a	n/a
7	BACH1	chr19:36980096-36980202	K562	blood:	n/a	n/a
8	BACH1	chr19:36979896-36980517	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr19:36980976-36981310	GM12878	blood:	n/a	n/a
10	BATF	chr19:36981007-36981331	GM12878	blood:	n/a	n/a
11	BCL3	chr19:36979628-36981249	A549	lung:	n/a	chr19:36981235-36981244 chr19:36980891-36980904
12	BCLAF1	chr19:36979675-36980848	GM12878	blood:	n/a	n/a
13	BCLAF1	chr19:36979639-36981344	GM12878	blood:	n/a	chr19:36981235-36981244 chr19:36980891-36980904
14	BHLHE40	chr19:36979860-36980623	HepG2	liver:	n/a	n/a
15	BHLHE40	chr19:36983648-36984011	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:36979753-36980523	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:36979782-36981117	K562	blood:	n/a	n/a
18	BRCA1	chr19:36980124-36981181	GM12878	blood:	n/a	n/a
19	BRCA1	chr19:36980110-36980967	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr19:36979929-36980952	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr19:36979827-36980823	HepG2	liver:	n/a	n/a
22	CBX3	chr19:36979776-36980650	K562	blood:	n/a	n/a
23	CBX3	chr19:36983957-36984274	K562	blood:	n/a	n/a
24	CCNT2	chr19:36980106-36980795	K562	blood:	n/a	chr19:36980345-36980354
25	CEBPB	chr19:36980082-36980373	A549	lung:	n/a	n/a
26	CEBPB	chr19:36980069-36980845	K562	blood:	n/a	n/a
27	CEBPB	chr19:36979331-36979852	IMR90	lung:	n/a	n/a
28	CEBPB	chr19:36980090-36980785	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:36980171-36980887	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr19:36980451-36980653	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:36979985-36980783	MCF-7	breast:	n/a	n/a
32	CEBPB	chr19:36980395-36980856	K562	blood:	n/a	n/a
33	CEBPB	chr19:36980083-36980759	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:36979733-36980899	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr19:36980248-36981044	HepG2	liver:	n/a	n/a
36	CEBPD	chr19:36980298-36981086	K562	blood:	n/a	n/a
37	CEBPZ	chr19:36957239-36957402	HepG2	liver:	n/a	n/a
38	CHD1	chr19:36967497-36967636	GM12878	blood:	n/a	n/a
39	CHD1	chr19:36980108-36981204	GM12878	blood:	n/a	n/a
40	CHD2	chr19:36979733-36981206	GM12878	blood:	n/a	n/a
41	CHD2	chr19:36979768-36981002	HepG2	liver:	n/a	n/a
42	CHD2	chr19:36979798-36981053	K562	blood:	n/a	n/a
43	CHD2	chr19:36984172-36984227	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr19:36979947-36981032	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr19:36979779-36980988	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr19:36980032-36980978	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr19:36927503-36927869	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr19:36927539-36927776	HepG2	liver:	n/a	n/a
49	CREB1	chr19:36980342-36980925	A549	lung:	n/a	n/a
50	CREB1	chr19:36979831-36981205	A549	lung:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:36980750-36980800	H1-hESC	embryonic stem cell:	embryo
2	chr19:36980750-36980800	H1-hESC	embryonic stem cell:	embryo
3	chr19:36980602-36980652	AG10803	skin:	n/a
4	chr19:36976461-36976511	MCF-7	breast:	n/a
5	chr19:36980699-36980749	T-47D	breast:	n/a
6	chr19:36980461-36980511	GM12878	blood:	n/a
7	chr19:36980659-36980709	CMK	blood:	n/a
8	chr19:36980750-36980800	HMEC	breast:	n/a
9	chr19:36980545-36980595	ProgFib	skin:	n/a
10	chr19:36980659-36980709	ProgFib	skin:	n/a
11	chr19:36980257-36980307	SK-N-SH_RA	brain:	n/a
12	chr19:36980257-36980307	AG09309	skin:	n/a
13	chr19:36980483-36980533	SK-N-SH	brain:	n/a
14	chr19:36980485-36980535	HPAEpiC	pulmonary alveolar:	n/a
15	chr19:36980459-36980509	GM12891	blood:	n/a
16	chr19:36980257-36980307	Hela-S3	cervix:	n/a
17	chr19:36980459-36980509	T-47D	breast:	n/a
18	chr19:36980565-36980615	Caco-2	colon:	n/a
19	chr19:36980257-36980307	SK-N-SH	brain:	n/a
20	chr19:36980699-36980749	HIPEpiC	eye:	n/a
21	chr19:36980461-36980511	SK-N-SH	brain:	n/a
22	chr19:36979833-36979883	A549	lung:	n/a
23	chr19:36980702-36980752	MCF-7	breast:	n/a
24	chr19:36980545-36980595	HCM	heart:	n/a
25	chr19:36980545-36980595	HIPEpiC	eye:	n/a
26	chr19:36980565-36980615	BJ	skin:	n/a
27	chr19:36980917-36980967	GM06990	blood:	n/a
28	chr19:36937832-36937882	BE2_C	brain:	n/a
29	chr19:36980545-36980595	GM12892	blood:	n/a
30	chr19:36980917-36980967	PFSK-1	brain:	n/a
31	chr19:36980732-36980782	A549	lung:	n/a
32	chr19:36980545-36980595	Jurkat	blood:	n/a
33	chr19:36980545-36980595	SK-N-MC	brain:	n/a
34	chr19:36980364-36980414	AG04450	lung:	fetal
35	chr19:36980565-36980615	GM06990	blood:	n/a
36	chr19:36980503-36980553	K562	blood:	n/a
37	chr19:36980732-36980782	HL-60	blood:	n/a
38	chr19:36980750-36980800	SAEC	small airway:	n/a
39	chr19:36980659-36980709	HIPEpiC	eye:	n/a
40	chr19:36976461-36976511	HAEpiC	amniotic membrane:	n/a
41	chr19:36980545-36980595	HRPEpiC	eye:	n/a
42	chr19:36980702-36980752	SK-N-SH_RA	brain:	n/a
43	chr19:36961371-36961421	SK-N-MC	brain:	n/a
44	chr19:36980503-36980553	HMEC	breast:	n/a
45	chr19:36980364-36980414	HMEC	breast:	n/a
46	chr19:36980483-36980533	H1-hESC	embryonic stem cell:	embryo
47	chr19:36979833-36979883	NHDF-neo	bronchial:	n/a
48	chr19:36961371-36961421	GM12891	blood:	n/a
49	chr19:36980732-36980782	PFSK-1	brain:	n/a
50	chr19:36980461-36980511	PANC-1	pancreas:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:36979193..36981748-chr19:37061672..37065426,4	K562	blood:
2	chr19:36940091..36943076-chr19:37061156..37065481,3	K562	blood:
3	chr19:36909374..36910931-chr19:36934594..36936776,2	K562	blood:
4	chr19:36921260..36923762-chr19:37063794..37066625,2	K562	blood:
5	chr19:36944101..36946636-chr19:36951837..36953729,2	K562	blood:
6	chr19:36963358..36966840-chr19:36977934..36981487,4	K562	blood:
7	chr19:36962098..36963692-chr19:36979457..36982115,2	MCF-7	breast:
8	chr19:36979124..36982554-chr19:37017679..37020247,4	MCF-7	breast:
9	chr19:36969479..36972173-chr19:36979052..36981581,2	MCF-7	breast:
10	chr19:36704170..36706461-chr19:36978975..36980989,3	K562	blood:
11	chr19:36867662..36870599-chr19:36976598..36980024,4	K562	blood:
12	chr19:36966764..36969281-chr19:36976956..36980463,3	K562	blood:
13	chr19:36973873..36977110-chr19:36978222..36981283,6	MCF-7	breast:
14	chr19:36963358..36964984-chr19:36977934..36980406,2	K562	blood:
15	chr19:36971191..36972829-chr19:36978934..36980961,2	K562	blood:
16	chr19:36962037..36966050-chr19:36978792..36981702,4	MCF-7	breast:
17	chr19:36979208..36981780-chr19:37261367..37264210,2	K562	blood:
18	chr19:36977221..36979834-chr19:36983552..36985787,2	K562	blood:
19	chr19:36966894..36968985-chr19:36971010..36973941,3	MCF-7	breast:
20	chr19:36979933..36980756-chr6:30711805..30712354,2	HCT-116	colon:
21	chr19:36924487..36927399-chr19:37259800..37262103,2	K562	blood:
22	chr19:36965657..36967855-chr19:36968852..36972035,4	K562	blood:
23	chr19:36944101..36946636-chr19:36951837..36953729,2	K562	blood:
24	chr19:36978237..36981071-chr19:36988174..36990152,2	K562	blood:
25	chr19:36978237..36981428-chr19:36988174..36990245,3	K562	blood:
26	chr19:36969427..36971707-chr19:36977964..36979970,2	MCF-7	breast:
27	chr19:36978148..36981795-chr19:37018105..37021194,8	K562	blood:
28	chr19:36952422..36955146-chr19:36978594..36981025,2	K562	blood:
29	chr19:36963141..36965549-chr19:36969405..36971789,2	MCF-7	breast:
30	chr19:36979323..36981752-chr19:37018816..37021173,2	MCF-7	breast:
31	chr19:36965657..36967339-chr19:36969186..36972035,2	K562	blood:
32	chr19:36704032..36706423-chr19:36978429..36980490,2	MCF-7	breast:
33	chr19:36965657..36967339-chr19:36969186..36972035,2	K562	blood:
34	chr19:36963141..36965549-chr19:36969405..36971789,2	MCF-7	breast:
35	chr19:36979379..36982047-chr19:37063909..37066157,2	K562	blood:
36	chr19:36982470..36984222-chr19:37017696..37019546,2	K562	blood:
37	chr19:36972928..36975852-chr19:36978689..36981265,4	K562	blood:
38	chr19:36868112..36870123-chr19:36976598..36979565,2	K562	blood:
39	chr19:36979900..36980804-chr9:127624247..127624899,2	Hela-S3	cervix:
40	chr19:36706883..36709067-chr19:36978381..36980309,2	K562	blood:
41	chr19:36977340..36979938-chr19:37058785..37061352,2	K562	blood:
42	chr19:36966894..36968985-chr19:36971010..36973941,3	MCF-7	breast:
43	chr19:36958063..36960933-chr19:36978148..36980352,2	K562	blood:
44	chr19:36978821..36980790-chr19:37017858..37020685,3	K562	blood:
45	chr19:36974608..36976540-chr19:36978966..36980563,2	MCF-7	breast:
46	chr19:36980411..36980990-chr19:37019063..37019816,2	Hela-S3	cervix:
47	chr19:36965657..36967855-chr19:36968852..36972035,4	K562	blood:
48	chr19:36977221..36979834-chr19:36983552..36985787,2	K562	blood:
49	chr19:36969427..36971707-chr19:36977964..36979970,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC092295.7.1-5	chr19:36980765-36981410	NONHSAT066005

No data

Variant related genes	Relation type
ZNF566	TF binding region
ENSG00000267309	TF binding region
ZNF566	CpG island
ENSG00000267309	CpG island
ENSG00000233527	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000186017	chromatin interactions
ENSG00000254004	chromatin interactions
ENSG00000266973	chromatin interactions
ENSG00000267041	chromatin interactions
ENSG00000267091	chromatin interactions
ENSG00000267260	chromatin interactions
ENSG00000196357	chromatin interactions
ENSG00000136942	chromatin interactions
ENSG00000228629	chromatin interactions
ENSG00000167635	chromatin interactions
ENSG00000142065	chromatin interactions
ENSG00000186020	chromatin interactions
ENSG00000181007	chromatin interactions
ENSG00000267309	chromatin interactions
ENSG00000136950	chromatin interactions

Extended variants
information (count: 2010 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2010 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11881655	chr19:36921272-36921273	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs372745967	chr19:36921286-36921287	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs116502430	chr19:36921324-36921325	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs539373115	chr19:36921395-36921396	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs577672895	chr19:36921444-36921445	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs143454633	chr19:36921473-36921474	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs143946303	chr19:36921483-36921484	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76491696	chr19:36921484-36921485	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142115277	chr19:36921500-36921501	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs151078478	chr19:36921595-36921596	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs577698862	chr19:36921661-36921662	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs537544441	chr19:36921739-36921740	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555981028	chr19:36921744-36921745	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs113716513	chr19:36921837-36921838	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs577400743	chr19:36921845-36921846	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs111255823	chr19:36921943-36921944	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs59201255	chr19:36921964-36921965	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs191677931	chr19:36922018-36922019	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544791117	chr19:36922057-36922058	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs143870970	chr19:36922093-36922094	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs146886080	chr19:36922099-36922100	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs62113873	chr19:36922125-36922126	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531891938	chr19:36922128-36922129	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs35142772	chr19:36922182-36922183	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs35103455	chr19:36922198-36922199	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs568573458	chr19:36922230-36922231	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546743267	chr19:36922251-36922252	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565503885	chr19:36922253-36922254	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs140504504	chr19:36922285-36922286	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571722315	chr19:36922311-36922312	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs181894211	chr19:36922320-36922321	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs114757462	chr19:36922326-36922327	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374014921	chr19:36922333-36922334	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549010107	chr19:36922344-36922345	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs186256453	chr19:36922354-36922355	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189885506	chr19:36922368-36922369	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs182141319	chr19:36922370-36922371	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577291641	chr19:36922381-36922382	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs538463505	chr19:36922388-36922389	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs553648273	chr19:36922449-36922450	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs35359396	chr19:36922452-36922453	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs542556919	chr19:36922533-36922534	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561377292	chr19:36922553-36922554	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs576481846	chr19:36922601-36922602	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145197497	chr19:36922618-36922619	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs115641077	chr19:36922682-36922683	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532609903	chr19:36922741-36922742	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs547972250	chr19:36922758-36922759	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs569195760	chr19:36922763-36922764	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs71354197	chr19:36922809-36922810	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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
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
Breast cancer	21509527	CNVD

Chromatin state (count:1683 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36930400-36930800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
2	chr19:36931800-36946800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
3	chr19:36934000-36937800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr19:36934200-36950000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr19:36934400-36934600	ZNF genes & repeats	Brain Germinal Matrix	brain
6	chr19:36934400-36935200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
7	chr19:36934400-36935200	ZNF genes & repeats	Rectal Smooth Muscle	rectum
8	chr19:36934400-36944000	ZNF genes & repeats	Adipose Nuclei	Adipose
9	chr19:36934400-36946600	ZNF genes & repeats	Liver	Liver
10	chr19:36934600-36936800	Weak transcription	Brain Germinal Matrix	brain
11	chr19:36934800-36939800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr19:36935400-36938600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr19:36936000-36950000	ZNF genes & repeats	Fetal Brain Female	brain
14	chr19:36936200-36937000	ZNF genes & repeats	Fetal Lung	lung
15	chr19:36936200-36942600	ZNF genes & repeats	Fetal Brain Male	brain
16	chr19:36936200-36943600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr19:36936200-36949600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:36936400-36936800	ZNF genes & repeats	Ovary	ovary
19	chr19:36936400-36937200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr19:36936400-36938600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr19:36936400-36943600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
22	chr19:36936400-36943600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
23	chr19:36936400-36946600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
24	chr19:36936400-36978400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr19:36936600-36937000	ZNF genes & repeats	Brain Cingulate Gyrus	brain
26	chr19:36936800-36937200	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
27	chr19:36936800-36938200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
28	chr19:36936800-36940000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr19:36936800-36943800	ZNF genes & repeats	A549	lung
30	chr19:36936800-36944200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr19:36937200-36937600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr19:36937200-36939600	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr19:36937200-36943600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
34	chr19:36937600-36938200	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr19:36937600-36940000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr19:36937600-36942600	ZNF genes & repeats	Colon Smooth Muscle	Colon
37	chr19:36937600-36943000	ZNF genes & repeats	Psoas Muscle	Psoas
38	chr19:36937800-36938200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr19:36937800-36938200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr19:36937800-36938200	ZNF genes & repeats	Fetal Stomach	stomach
41	chr19:36937800-36938200	ZNF genes & repeats	Pancreas	Pancrea
42	chr19:36937800-36943400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr19:36937800-36943600	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
44	chr19:36937800-36944200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr19:36938000-36938200	ZNF genes & repeats	Left Ventricle	heart
46	chr19:36938000-36943600	ZNF genes & repeats	Stomach Smooth Muscle	stomach
47	chr19:36938000-36943800	ZNF genes & repeats	Primary B cells from cord blood	blood
48	chr19:36938000-36946600	ZNF genes & repeats	Brain Germinal Matrix	brain
49	chr19:36938200-36938600	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr19:36938200-36939000	Weak transcription	Primary hematopoietic stem cells	blood

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