Variant report

Variant	esv3350085
Chromosome Location	chr19:53213910-53275524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1181)
CpG islands
(count:1404)
Chromatin interactive
region (count:16)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:53228340-53228382	K562	blood:	n/a	n/a
2	ARID3A	chr19:53228598-53228749	K562	blood:	n/a	n/a
3	ARID3A	chr19:53227189-53227366	K562	blood:	n/a	n/a
4	ARID3A	chr19:53238204-53238593	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:53227580-53227746	HepG2	liver:	n/a	n/a
6	ATF1	chr19:53219224-53219418	K562	blood:	n/a	n/a
7	ATF1	chr19:53233027-53233245	K562	blood:	n/a	n/a
8	ATF1	chr19:53227069-53227523	K562	blood:	n/a	n/a
9	ATF1	chr19:53238100-53238672	K562	blood:	n/a	n/a
10	ATF1	chr19:53260119-53260246	K562	blood:	n/a	n/a
11	ATF2	chr19:53239019-53239370	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr19:53238937-53239428	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr19:53238046-53238465	K562	blood:	n/a	n/a
14	ATF3	chr19:53228814-53229132	K562	blood:	n/a	n/a
15	BACH1	chr19:53238107-53238408	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr19:53218901-53219394	GM12878	blood:	n/a	chr19:53219199-53219209 chr19:53219203-53219213
17	BATF	chr19:53243525-53243726	GM12878	blood:	n/a	n/a
18	BATF	chr19:53245884-53246161	GM12878	blood:	n/a	chr19:53245986-53245996 chr19:53245985-53245996 chr19:53245990-53246000
19	BATF	chr19:53218901-53219396	GM12878	blood:	n/a	chr19:53219199-53219209 chr19:53219203-53219213
20	BATF	chr19:53245915-53246089	GM12878	blood:	n/a	chr19:53245986-53245996 chr19:53245985-53245996 chr19:53245990-53246000
21	BCL11A	chr19:53238080-53238304	GM12878	blood:	n/a	n/a
22	BCL11A	chr19:53219085-53219334	GM12878	blood:	n/a	chr19:53219201-53219210
23	BCL11A	chr19:53240555-53240723	GM12878	blood:	n/a	n/a
24	BCL11A	chr19:53219022-53219347	GM12878	blood:	n/a	chr19:53219201-53219210
25	BCL3	chr19:53235753-53236010	GM12878	blood:	n/a	n/a
26	BCLAF1	chr19:53237957-53238447	GM12878	blood:	n/a	chr19:53238422-53238435
27	BHLHE40	chr19:53229503-53229523	K562	blood:	n/a	n/a
28	BHLHE40	chr19:53227179-53227448	K562	blood:	n/a	n/a
29	BHLHE40	chr19:53238239-53238453	GM12878	blood:	n/a	n/a
30	BHLHE40	chr19:53228364-53229160	K562	blood:	n/a	n/a
31	BHLHE40	chr19:53238124-53238500	K562	blood:	n/a	n/a
32	BRCA1	chr19:53238025-53238612	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr19:53219929-53220101	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr19:53238114-53238309	GM12878	blood:	n/a	n/a
35	CBX3	chr19:53238334-53238591	K562	blood:	n/a	n/a
36	CBX3	chr19:53269789-53270224	K562	blood:	n/a	n/a
37	CBX3	chr19:53228183-53229250	K562	blood:	n/a	n/a
38	CBX3	chr19:53238062-53238800	K562	blood:	n/a	n/a
39	CBX3	chr19:53269115-53269526	K562	blood:	n/a	n/a
40	CBX3	chr19:53226892-53227577	K562	blood:	n/a	n/a
41	CCNT2	chr19:53228300-53228706	K562	blood:	n/a	n/a
42	CCNT2	chr19:53237915-53238524	K562	blood:	n/a	chr19:53238372-53238381
43	CCNT2	chr19:53228944-53229189	K562	blood:	n/a	n/a
44	CEBPB	chr19:53238697-53238841	HepG2	liver:	n/a	chr19:53238809-53238820
45	CEBPB	chr19:53232571-53232835	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr19:53225607-53225921	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr19:53251811-53252145	K562	blood:	n/a	chr19:53251983-53251994
48	CEBPB	chr19:53251834-53252142	H1-hESC	embryonic stem cell:	n/a	chr19:53251983-53251994
49	CEBPB	chr19:53238233-53238408	K562	blood:	n/a	n/a
50	CEBPB	chr19:53219942-53220105	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53237645-53237695	BE2_C	brain:	n/a
2	chr19:53237645-53237695	BE2_C	brain:	n/a
3	chr19:53238445-53238495	HCPEpiC	choroid plexus:	n/a
4	chr19:53237871-53237921	RPTEC	kidney:	n/a
5	chr19:53233245-53233295	SKMC	muscle:	n/a
6	chr19:53238498-53238548	ProgFib	skin:	n/a
7	chr19:53233164-53233214	AG04450	lung:	fetal
8	chr19:53239200-53239250	SKMC	muscle:	n/a
9	chr19:53238492-53238542	AG10803	skin:	n/a
10	chr19:53228974-53229024	HCT-116	colon:	n/a
11	chr19:53269486-53269536	IMR90	lung:	fetal
12	chr19:53238434-53238484	AG09309	skin:	n/a
13	chr19:53233083-53233133	AG04449	skin:	fetal
14	chr19:53242420-53242470	BE2_C	brain:	n/a
15	chr19:53233083-53233133	PrEC	prostate:	n/a
16	chr19:53238498-53238548	IMR90	lung:	fetal
17	chr19:53229096-53229146	GM12878	blood:	n/a
18	chr19:53237645-53237695	CMK	blood:	n/a
19	chr19:53269486-53269536	HEK293	kidney:	embryo
20	chr19:53234126-53234176	HUVEC	blood vessel:	n/a
21	chr19:53238492-53238542	SAEC	small airway:	n/a
22	chr19:53239200-53239250	Hepatocyte	liver:	n/a
23	chr19:53239200-53239250	HCF	heart:	n/a
24	chr19:53237862-53237912	HCT-116	colon:	n/a
25	chr19:53233245-53233295	Hepatocyte	liver:	n/a
26	chr19:53228974-53229024	BJ	skin:	n/a
27	chr19:53228974-53229024	HCPEpiC	choroid plexus:	n/a
28	chr19:53238445-53238495	MCF-7	breast:	n/a
29	chr19:53233164-53233214	SK-N-SH_RA	brain:	n/a
30	chr19:53229766-53229816	HL-60	blood:	n/a
31	chr19:53233368-53233418	CMK	blood:	n/a
32	chr19:53237645-53237695	U87	brain:	n/a
33	chr19:53233245-53233295	Hela-S3	cervix:	n/a
34	chr19:53238498-53238548	CMK	blood:	n/a
35	chr19:53239146-53239196	GM12891	blood:	n/a
36	chr19:53233083-53233133	HEK293	kidney:	embryo
37	chr19:53229096-53229146	HepG2	liver:	n/a
38	chr19:53237862-53237912	Hela-S3	cervix:	n/a
39	chr19:53229766-53229816	ECC-1	luminal epithelium:	n/a
40	chr19:53238434-53238484	AG04450	lung:	fetal
41	chr19:53238434-53238484	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:53237862-53237912	MCF10A-Er-Src	breast:	n/a
43	chr19:53237645-53237695	HUVEC	blood vessel:	n/a
44	chr19:53239200-53239250	AoSMC	blood vessel:	n/a
45	chr19:53237645-53237695	HCF	heart:	n/a
46	chr19:53233164-53233214	HRPEpiC	eye:	n/a
47	chr19:53269486-53269536	AG09309	skin:	n/a
48	chr19:53239200-53239250	HEK293	kidney:	embryo
49	chr19:53237645-53237695	SK-N-MC	brain:	n/a
50	chr19:53238492-53238542	Hepatocyte	liver:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53227642..53230112-chr19:53236849..53239461,2	K562	blood:
2	chr19:53233250..53234773-chr19:53236233..53238057,2	K562	blood:
3	chr19:53236244..53237950-chr19:53242142..53244901,2	K562	blood:
4	chr19:53115970..53118193-chr19:53236786..53238588,2	K562	blood:
5	chr19:53226674..53228672-chr19:53232730..53234940,2	K562	blood:
6	chr19:53215678..53217452-chr19:53219568..53222029,2	K562	blood:
7	chr19:53236450..53239197-chr19:53240698..53243642,2	K562	blood:
8	chr19:53226674..53228672-chr19:53232730..53234940,2	K562	blood:
9	chr19:53215678..53217452-chr19:53219568..53222029,2	K562	blood:
10	chr19:53227707..53230460-chr19:53236213..53239636,6	K562	blood:
11	chr14:93214475..93215046-chr19:53237894..53238692,2	Hela-S3	cervix:
12	chr19:53227642..53230112-chr19:53236849..53239461,2	K562	blood:
13	chr19:53233250..53234773-chr19:53236233..53238057,2	K562	blood:
14	chr19:53227707..53230460-chr19:53236213..53239636,6	K562	blood:
15	chr19:53236244..53237950-chr19:53242142..53244901,2	K562	blood:
16	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF83-5	chr19:53231983-53232084	NONHSAT067580
2	lnc-ZNF83-5	chr19:53238254-53238326	NONHSAT067579
3	lnc-ZNF83-5	chr19:53224406-53224520	NONHSAT067579
4	lnc-ZNF83-5	chr19:53227124-53227242	NONHSAT067579
5	lnc-ZNF83-5	chr19:53224436-53224520	NONHSAT067580
6	lnc-ZNF83-5	chr19:53238254-53238268	NONHSAT067580
7	lnc-ZNF83-5	chr19:53233159-53233258	NONHSAT067580
8	lnc-ZNF83-5	chr19:53226674-53227917	NONHSAT067581
9	lnc-ZNF83-5	chr19:53233159-53233258	NONHSAT067579
10	lnc-ZNF83-5	chr19:53231983-53232084	NONHSAT067579

No data

Variant related genes	Relation type
ZNF611	TF binding region
ZNF611	CpG island
ENSG00000100600	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000213020	chromatin interactions
ENSG00000242779	chromatin interactions

Extended variants
information (count: 3515 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3515 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11084184	chr19:53213939-53213940	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143524831	chr19:53213958-53213959	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs112881642	chr19:53213959-53213960	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs529658538	chr19:53214005-53214006	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs534327422	chr19:53214048-53214049	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs558803451	chr19:53214062-53214063	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs193093444	chr19:53214114-53214115	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs548140101	chr19:53214147-53214148	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs71794173	chr19:53214172-53214173	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs199681737	chr19:53214175-53214176	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs149700522	chr19:53214177-53214178	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs200222563	chr19:53214178-53214179	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs201261040	chr19:53214182-53214183	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs199593963	chr19:53214183-53214184	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs374023456	chr19:53214194-53214195	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs556549062	chr19:53214257-53214258	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs575256378	chr19:53214274-53214275	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs144440171	chr19:53214344-53214345	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs148409529	chr19:53214372-53214373	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs368163683	chr19:53214383-53214384	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs572525996	chr19:53214396-53214397	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs142553370	chr19:53214404-53214405	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs371620532	chr19:53214439-53214440	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs531267593	chr19:53214478-53214479	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs549371409	chr19:53214525-53214526	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs113879305	chr19:53214526-53214527	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs529193646	chr19:53214539-53214540	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs547361872	chr19:53214541-53214542	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs551833364	chr19:53214547-53214548	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs184964034	chr19:53214555-53214556	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs368952950	chr19:53214587-53214588	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs11084185	chr19:53214600-53214601	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs201523533	chr19:53214604-53214605	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs199826993	chr19:53214611-53214612	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200451610	chr19:53214612-53214613	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs570858063	chr19:53214618-53214619	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs398041069	chr19:53214622-53214623	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538338297	chr19:53214636-53214637	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs542359576	chr19:53214643-53214644	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs150961159	chr19:53214667-53214668	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs532524997	chr19:53214681-53214682	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs189759045	chr19:53214686-53214687	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs536183920	chr19:53214706-53214707	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs180967619	chr19:53214707-53214708	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs572666281	chr19:53214709-53214710	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs142506851	chr19:53214731-53214732	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs11084186	chr19:53214754-53214755	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs575780626	chr19:53214781-53214782	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs11878847	chr19:53214782-53214783	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs561383898	chr19:53214792-53214793	Weak transcription Strong transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	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
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1939 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53194800-53218800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:53202800-53217400	ZNF genes & repeats	Liver	Liver
3	chr19:53205600-53217400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
4	chr19:53206600-53217800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr19:53206600-53227200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr19:53206800-53214000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr19:53207200-53215400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr19:53207200-53217600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
9	chr19:53207200-53218800	Strong transcription	Placenta	Placenta
10	chr19:53207400-53214600	Weak transcription	Stomach Mucosa	stomach
11	chr19:53207400-53216400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:53207400-53219400	Strong transcription	Dnd41	blood
13	chr19:53207600-53216000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:53208000-53216400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
15	chr19:53208200-53219400	Strong transcription	Fetal Muscle Trunk	muscle
16	chr19:53208400-53216000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
17	chr19:53208400-53217400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr19:53208400-53218800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr19:53208600-53214000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
20	chr19:53209400-53214600	Weak transcription	Fetal Brain Female	brain
21	chr19:53209400-53225800	Weak transcription	Hela-S3	cervix
22	chr19:53209600-53218200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr19:53209600-53219200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr19:53209600-53219400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:53209600-53223800	Weak transcription	NHLF	lung
26	chr19:53209600-53224000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr19:53209600-53224000	Weak transcription	Right Ventricle	heart
28	chr19:53209800-53215200	Weak transcription	NH-A	brain
29	chr19:53210200-53214000	Weak transcription	Brain Hippocampus Middle	brain
30	chr19:53210200-53214000	Strong transcription	Fetal Lung	lung
31	chr19:53210200-53218800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr19:53210200-53219000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr19:53210200-53223400	Weak transcription	Colonic Mucosa	Colon
34	chr19:53210200-53227000	Weak transcription	Fetal Heart	heart
35	chr19:53210400-53214600	Weak transcription	NHEK	skin
36	chr19:53210400-53215000	Weak transcription	Fetal Kidney	kidney
37	chr19:53210400-53215200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr19:53210400-53215200	Weak transcription	Colon Smooth Muscle	Colon
39	chr19:53210400-53215400	Weak transcription	Fetal Brain Male	brain
40	chr19:53210400-53218200	Weak transcription	HUVEC	blood vessel
41	chr19:53210400-53219000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr19:53210400-53225200	Weak transcription	HMEC	breast
43	chr19:53210400-53236600	Weak transcription	Psoas Muscle	Psoas
44	chr19:53210600-53215400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr19:53210600-53216200	Weak transcription	Brain Cingulate Gyrus	brain
46	chr19:53210600-53218600	ZNF genes & repeats	Fetal Intestine Small	intestine
47	chr19:53210600-53219000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
48	chr19:53210600-53237200	Weak transcription	NHDF-Ad	bronchial
49	chr19:53210800-53214000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr19:53210800-53214400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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