Variant report

Variant	rs17303902
Chromosome Location	chr19:38042814-38042815
allele	C/T
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	CTCF	chr19:38042707-38042941	K562	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
2	CTCF	chr19:38042717-38042923	GM10266	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
3	CTCF	chr19:38042760-38042910	HUVEC	blood vessel:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
4	E2F6	chr19:38042652-38042858	K562	blood:	n/a	n/a
5	CTCF	chr19:38042740-38042890	AG09309	skin:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
6	CTCF	chr19:38042760-38042910	GM12878	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
7	CTCF	chr19:38042760-38042910	GM12867	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
8	MAX	chr19:38042445-38042910	K562	blood:	n/a	n/a
9	CTCF	chr19:38042760-38042910	GM12870	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
10	CTCF	chr19:38042740-38042890	HUVEC	blood vessel:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
11	CTCF	chr19:38042760-38042910	SAEC	small airway:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
12	CTCF	chr19:38042780-38042930	HVMF	connective:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
13	CTCF	chr19:38041976-38043042	SK-N-SH	brain:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
14	CTCF	chr19:38042760-38042910	HPAF	blood vessel:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
15	CTCF	chr19:38042557-38042928	K562	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
16	CTCF	chr19:38042720-38042870	GM12868	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
17	CTCF	chr19:38042780-38042930	HBMEC	blood vessel:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
18	CTCF	chr19:38042733-38042926	SK-N-SH_RA	brain:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
19	CTCF	chr19:38042780-38042930	A549	lung:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
20	MAZ	chr19:38042666-38042880	K562	blood:	n/a	n/a
21	CTCF	chr19:38042780-38042930	NHLF	lung:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
22	CTCF	chr19:38042760-38042910	HRPEpiC	eye:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
23	CTCF	chr19:38042740-38042890	HepG2	liver:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
24	CTCF	chr19:38042740-38042890	GM12864	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
25	CTCF	chr19:38042752-38042846	H1-hESC	embryonic stem cell:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
26	CTCF	chr19:38042760-38042910	WERI-Rb-1	eye:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
27	CTCF	chr19:38042740-38042890	HMEC	breast:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
28	CTCF	chr19:38042740-38042890	HFF-Myc	foreskin:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
29	CTCF	chr19:38042780-38042930	HCM	heart:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
30	CTCF	chr19:38042720-38042870	HRE	kidney:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
31	CTCF	chr19:38042753-38042844	LNCaP	prostate:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
32	CTCF	chr19:38042707-38042946	Spleen_OC	spleen:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
33	CTCF	chr19:38042731-38042860	Fibrobl	skin:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
34	CTCF	chr19:38042740-38042890	HEEpiC	esophagus:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
35	CTCF	chr19:38042760-38042910	AG04449	skin:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
36	MAX	chr19:38042646-38042855	K562	blood:	n/a	n/a
37	CTCF	chr19:38042720-38042870	AG04450	lung:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
38	RAD21	chr19:38042580-38042931	SK-N-SH_RA	brain:	n/a	chr19:38042817-38042826 chr19:38042811-38042830
39	CTCF	chr19:38042746-38042917	GM10248	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
40	CTCF	chr19:38042780-38042930	GM06990	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
41	SMC3	chr19:38042684-38042986	K562	blood:	n/a	chr19:38042815-38042829
42	CTCF	chr19:38042740-38042890	NHDF-neo	bronchial:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
43	CTCF	chr19:38042720-38042870	GM12869	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
44	CTCF	chr19:38042680-38042830	NHEK	skin:	n/a	chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
45	CTCF	chr19:38042800-38042950	GM12864	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
46	CTCF	chr19:38042740-38042890	SK-N-SH_RA	brain:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
47	CTCF	chr19:38042760-38042910	GM12875	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
48	CTCF	chr19:38042740-38042890	MCF-7	breast:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
49	CTCF	chr19:38042716-38042921	GM13976	blood:	n/a	chr19:38042813-38042831 chr19:38042815-38042828 chr19:38042815-38042828 chr19:38042808-38042829 chr19:38042814-38042830
50	RAD21	chr19:38042637-38043012	H1-hESC	embryonic stem cell:	n/a	chr19:38042817-38042826 chr19:38042811-38042830

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:37860446..37862285-chr19:38041060..38043682,2	K562	blood:

Variant related genes	Relation type
ENSG00000180458	TF binding region
ENSG00000189164	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10445548	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1048505	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1061753	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1061756	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12151156	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17244713	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17244769	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17304703	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17305193	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17305228	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17305823	0.95[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17306900	0.86[ASN][1000 genomes]
rs1871196	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2291001	1.00[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2306201	1.00[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2385005	0.96[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35153242	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs502546	0.81[CEU][hapmap]
rs55681348	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55718806	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55743020	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55754546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55865869	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55909413	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56277404	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56351266	0.86[ASN][1000 genomes]
rs57654288	0.97[EUR][1000 genomes]
rs57943942	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62108291	0.82[EUR][1000 genomes]
rs62108306	0.80[EUR][1000 genomes]
rs7245855	0.86[ASN][1000 genomes]
rs7259272	0.92[CEU][hapmap];0.82[TSI][hapmap];0.80[EUR][1000 genomes]
rs73031330	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73033122	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73033134	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73033142	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73035159	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73035160	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73039029	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73041006	0.86[ASN][1000 genomes]
rs8101610	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8104282	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8104994	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8108268	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8111790	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757695	chr19:37794850-38051606	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	esv2758759	chr19:37794850-38051606	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv833819	chr19:37899501-38051599	ZNF genes & repeats Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv579468	chr19:37977609-38293487	ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv2478	chr19:38025340-38043818	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv949296	chr19:38034722-38763140	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:21)

SNP	Gene	Cis/trans	Tissue	Source
rs17303902	AC012309.5	cis	Artery Tibial	GTEx
rs17303902	PAK4	cis	cerebellum	SCAN
rs17303902	POU2F2	cis	parietal	SCAN
rs17303902	AC012309.5	cis	lung	GTEx
rs17303902	AC012309.5	cis	Esophagus Mucosa	GTEx
rs17303902	ZNF781	cis	Thyroid	GTEx
rs17303902	ZNF781	trans	cerebellum	SCAN
rs17303902	PLEKHG2	cis	cerebellum	SCAN
rs17303902	AC012309.5	cis	Skin Sun Exposed Lower leg	GTEx
rs17303902	CCDC97	cis	cerebellum	SCAN
rs17303902	AC012309.5	cis	Esophagus Muscularis	GTEx
rs17303902	AC012309.5	cis	Muscle Skeletal	GTEx
rs17303902	ZNF585A	Cis_1M	lymphoblastoid	RTeQTL
rs17303902	AC012309.5	cis	Heart Left Ventricle	GTEx
rs17303902	DMPK	cis	parietal	SCAN
rs17303902	CEACAM3	cis	parietal	SCAN
rs17303902	PHLDB3	cis	cerebellum	SCAN
rs17303902	RASGRP4	cis	parietal	SCAN
rs17303902	PVR	cis	parietal	SCAN
rs17303902	C19orf61	cis	cerebellum	SCAN
rs17303902	AC012309.5	cis	Thyroid	GTEx

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38032400-38080800	ZNF genes & repeats	Liver	Liver
2	chr19:38032600-38075200	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr19:38037800-38043000	ZNF genes & repeats	Fetal Brain Female	brain
4	chr19:38037800-38043200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr19:38037800-38043800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
6	chr19:38037800-38045400	ZNF genes & repeats	Brain Anterior Caudate	brain
7	chr19:38038000-38043000	ZNF genes & repeats	Brain Germinal Matrix	brain
8	chr19:38038000-38078400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr19:38038600-38079600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
10	chr19:38038800-38045600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
11	chr19:38039000-38043000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr19:38039200-38043000	ZNF genes & repeats	Thymus	Thymus
13	chr19:38039800-38043000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr19:38040200-38043200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
15	chr19:38040600-38043000	ZNF genes & repeats	Fetal Stomach	stomach
16	chr19:38040600-38043200	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr19:38040800-38043000	ZNF genes & repeats	Fetal Muscle Leg	muscle
18	chr19:38041000-38043000	ZNF genes & repeats	NH-A	brain
19	chr19:38041200-38043000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
20	chr19:38041200-38079600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr19:38041400-38043000	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr19:38041400-38043000	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
23	chr19:38041400-38043000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
24	chr19:38041400-38043000	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
25	chr19:38041400-38043000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr19:38041400-38043000	ZNF genes & repeats	NHEK	skin
27	chr19:38041400-38043200	Active TSS	Primary T cells from cord blood	blood
28	chr19:38041400-38045200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr19:38041600-38043000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
30	chr19:38041600-38043000	ZNF genes & repeats	Fetal Intestine Large	intestine
31	chr19:38041600-38043000	Active TSS	Fetal Kidney	kidney
32	chr19:38041600-38043000	ZNF genes & repeats	HSMM	muscle
33	chr19:38041600-38043000	ZNF genes & repeats	HSMMtube	muscle
34	chr19:38041600-38043200	Active TSS	Fetal Heart	heart
35	chr19:38041800-38043000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
36	chr19:38041800-38043000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
37	chr19:38041800-38043000	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr19:38041800-38043000	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr19:38041800-38043000	Active TSS	K562	blood
40	chr19:38041800-38043000	Active TSS	NHLF	lung
41	chr19:38041800-38043200	Active TSS	HUVEC	blood vessel
42	chr19:38041800-38059600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr19:38042000-38043000	Active TSS	Osteobl	bone
44	chr19:38042200-38043000	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr19:38042200-38043000	Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr19:38042200-38043000	Active TSS	Muscle Satellite Cultured Cells	--
47	chr19:38042200-38043000	Active TSS	Fetal Muscle Trunk	muscle
48	chr19:38042200-38043000	Active TSS	Fetal Thymus	thymus
49	chr19:38042200-38043000	Active TSS	Right Ventricle	heart
50	chr19:38042400-38043000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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