Variant report

Variant	rs12981980
Chromosome Location	chr19:57050648-57050649
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:29)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:29 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:57050540-57050690	SK-N-SH_RA	brain:	n/a	n/a
2	POLR2A	chr19:57050479-57050648	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr19:57050212-57050657	ECC-1	luminal epithelium:	n/a	n/a
4	RAD21	chr19:57050378-57050722	IMR90	lung:	n/a	n/a
5	YY1	chr19:57050212-57050661	SK-N-SH_RA	brain:	n/a	n/a
6	MAX	chr19:57050211-57050694	ECC-1	luminal epithelium:	n/a	n/a
7	MAZ	chr19:57049495-57051243	IMR90	lung:	n/a	n/a
8	MAX	chr19:57050233-57050791	A549	lung:	n/a	n/a
9	YY1	chr19:57050340-57050650	SK-N-SH_RA	brain:	n/a	n/a
10	TCF12	chr19:57050229-57050992	A549	lung:	n/a	n/a
11	JUN	chr19:57050593-57050745	H1-hESC	embryonic stem cell:	n/a	n/a
12	RAD21	chr19:57050361-57050653	SK-N-SH_RA	brain:	n/a	n/a
13	RAD21	chr19:57050299-57050679	H1-hESC	embryonic stem cell:	n/a	n/a
14	SIN3A	chr19:57050336-57050920	H1-hESC	embryonic stem cell:	n/a	n/a
15	E2F6	chr19:57050235-57050785	A549	lung:	n/a	n/a
16	YY1	chr19:57050333-57050713	H1-hESC	embryonic stem cell:	n/a	n/a
17	MAX	chr19:57050203-57050976	A549	lung:	n/a	n/a
18	RAD21	chr19:57050367-57050659	H1-hESC	embryonic stem cell:	n/a	n/a
19	TAF1	chr19:57050243-57050763	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr19:57050629-57050805	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr19:57050604-57050791	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr19:57050217-57050712	H1-neurons	neurons:	n/a	n/a
23	REST	chr19:57049096-57051000	H1-neurons	neurons:	n/a	chr19:57049698-57049706 chr19:57049912-57049925
24	BACH1	chr19:57050354-57050813	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr19:57050194-57050828	H1-hESC	embryonic stem cell:	n/a	n/a
26	JUND	chr19:57050264-57050674	H1-hESC	embryonic stem cell:	n/a	chr19:57050315-57050324
27	NRF1	chr19:57049135-57050750	SK-N-SH	brain:	n/a	chr19:57049806-57049817 chr19:57049808-57049817 chr19:57049803-57049817 chr19:57049806-57049820 chr19:57050290-57050299 chr19:57050288-57050297
28	SIN3AK20	chr19:57050400-57050717	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr19:57050200-57050648	SK-N-SH	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:57050620-57050670	PFSK-1	brain:	n/a
2	chr19:57050620-57050670	GM12878	blood:	n/a
3	chr19:57050620-57050670	GM12891	blood:	n/a
4	chr19:57050620-57050670	HCM	heart:	n/a
5	chr19:57050620-57050670	ProgFib	skin:	n/a
6	chr19:57050620-57050670	H1-hESC	embryonic stem cell:	embryo
7	chr19:57050620-57050670	SK-N-SH_RA	brain:	n/a
8	chr19:57050620-57050670	AG04449	skin:	fetal
9	chr19:57050620-57050670	SK-N-SH	brain:	n/a
10	chr19:57050620-57050670	HRE	kidney:	n/a
11	chr19:57050620-57050670	HCF	heart:	n/a
12	chr19:57050620-57050670	HAEpiC	amniotic membrane:	n/a
13	chr19:57050620-57050670	HEK293	kidney:	embryo
14	chr19:57050620-57050670	ovcar-3	ovarian:	n/a
15	chr19:57050620-57050670	NHBE	bronchial:	n/a
16	chr19:57050620-57050670	HCPEpiC	choroid plexus:	n/a
17	chr19:57050620-57050670	SAEC	small airway:	n/a
18	chr19:57050620-57050670	NH-A	brain:	n/a
19	chr19:57050620-57050670	SKMC	muscle:	n/a
20	chr19:57050620-57050670	HepG2	liver:	n/a
21	chr19:57050620-57050670	K562	blood:	n/a
22	chr19:57050620-57050670	HRCEpiC	kidney:	n/a
23	chr19:57050620-57050670	IMR90	lung:	fetal
24	chr19:57050620-57050670	U87	brain:	n/a
25	chr19:57050620-57050670	HRPEpiC	eye:	n/a
26	chr19:57050620-57050670	Hepatocyte	liver:	n/a
27	chr19:57050620-57050670	ECC-1	luminal epithelium:	n/a
28	chr19:57050620-57050670	AG04450	lung:	fetal
29	chr19:57050620-57050670	HIPEpiC	eye:	n/a
30	chr19:57050620-57050670	HCT-116	colon:	n/a
31	chr19:57050620-57050670	AoSMC	blood vessel:	n/a
32	chr19:57050620-57050670	Hela-S3	cervix:	n/a
33	chr19:57050620-57050670	HMEC	breast:	n/a
34	chr19:57050620-57050670	HPAEpiC	pulmonary alveolar:	n/a
35	chr19:57050620-57050670	Caco-2	colon:	n/a
36	chr19:57050620-57050670	PrEC	prostate:	n/a
37	chr19:57050620-57050670	HUVEC	blood vessel:	n/a
38	chr19:57050620-57050670	RPTEC	kidney:	n/a
39	chr19:57050620-57050670	MCF-7	breast:	n/a
40	chr19:57050620-57050670	NB4	blood:	n/a
41	chr19:57050620-57050670	NT2-D1	testis:	n/a
42	chr19:57050620-57050670	T-47D	breast:	n/a
43	chr19:57050620-57050670	GM12892	blood:	n/a
44	chr19:57050620-57050670	LNCaP	prostate:	n/a
45	chr19:57050620-57050670	BJ	skin:	n/a
46	chr19:57050620-57050670	HL-60	blood:	n/a
47	chr19:57050620-57050670	AG09309	skin:	n/a
48	chr19:57050620-57050670	GM19239	blood:	n/a
49	chr19:57050620-57050670	AG09319	gingival:	n/a
50	chr19:57050620-57050670	BE2_C	brain:	n/a

No data

Variant related genes	Relation type
ENSG00000267421	TF binding region
ENSG00000267421	CpG island

Extended variants
information (count: 68 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10417966	0.82[LWK][hapmap];0.80[YRI][hapmap]
rs10419553	0.82[LWK][hapmap];0.80[YRI][hapmap]
rs11084452	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11667052	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.83[TSI][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11671776	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11672822	0.87[AMR][1000 genomes]
rs12151151	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12151254	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12975138	0.89[AMR][1000 genomes]
rs12978999	0.94[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12980452	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes]
rs12981652	0.86[AMR][1000 genomes]
rs12981892	0.89[AMR][1000 genomes]
rs12982632	0.87[AMR][1000 genomes]
rs12986047	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs15507	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16987295	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16987303	0.84[CEU][hapmap]
rs16987310	0.94[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1939	0.89[AMR][1000 genomes]
rs2074941	0.87[LWK][hapmap];0.83[YRI][hapmap]
rs2074942	0.87[LWK][hapmap];0.83[YRI][hapmap]
rs2215151	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2215929	0.87[AMR][1000 genomes]
rs2286422	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2869891	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3088221	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34225229	0.89[AMR][1000 genomes]
rs34269477	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34760888	0.87[AMR][1000 genomes]
rs35347939	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35664312	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35908973	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36020383	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36062917	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36075900	0.89[AMR][1000 genomes]
rs3813141	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3813142	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3813143	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4267437	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4570977	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes]
rs4801334	0.94[YRI][hapmap]
rs56069810	0.87[AMR][1000 genomes]
rs61144294	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62123030	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62124070	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62124114	0.87[AMR][1000 genomes]
rs66522479	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7245557	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7246507	1.00[CHB][hapmap];0.89[AMR][1000 genomes]
rs7250075	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs741253	0.87[AMR][1000 genomes]
rs8110306	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8110403	0.87[AMR][1000 genomes]
rs917407	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs960997	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949121	chr19:56754719-57591038	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1062341	chr19:56794070-57273332	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	nsv544094	chr19:56794070-57273332	Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
4	nsv1056713	chr19:56799151-57265682	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
5	nsv544095	chr19:56799151-57265682	Strong transcription ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
6	nsv580385	chr19:56918598-57072433	ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv1057240	chr19:56919831-57153659	Flanking Active TSS Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv544097	chr19:56919831-57153659	Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv580386	chr19:56924761-57072433	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
10	nsv1055357	chr19:56933632-57190007	ZNF genes & repeats Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	nsv912518	chr19:56995737-57109821	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
12	nsv912519	chr19:57020754-57065189	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs12981980	ZFP28	cis	lymphoblastoid	seeQTL
rs12981980	ZNF837	cis	parietal	SCAN
rs12981980	ZFP28	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:57047400-57077800	ZNF genes & repeats	Liver	Liver
2	chr19:57048800-57051200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
3	chr19:57048800-57051400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr19:57048800-57051600	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
5	chr19:57048800-57053000	ZNF genes & repeats	Placenta	Placenta
6	chr19:57048800-57053000	ZNF genes & repeats	HSMM	muscle
7	chr19:57048800-57053800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr19:57049000-57050800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr19:57049000-57050800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr19:57049000-57050800	Active TSS	NHLF	lung
11	chr19:57049000-57051400	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr19:57049200-57050800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr19:57049200-57050800	Active TSS	H9 Cell Line	embryonic stem cell
14	chr19:57049200-57050800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr19:57049200-57050800	Active TSS	Psoas Muscle	Psoas
16	chr19:57049200-57050800	Active TSS	Right Atrium	heart
17	chr19:57049200-57051000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:57049200-57051000	Active TSS	Fetal Kidney	kidney
19	chr19:57049200-57051200	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr19:57049200-57051200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr19:57049200-57051400	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr19:57049400-57050800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr19:57049400-57050800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr19:57049400-57050800	Active TSS	Aorta	Aorta
25	chr19:57049400-57050800	Active TSS	Brain Angular Gyrus	brain
26	chr19:57049400-57050800	Active TSS	Gastric	stomach
27	chr19:57049400-57050800	Active TSS	Left Ventricle	heart
28	chr19:57049400-57050800	Active TSS	Ovary	ovary
29	chr19:57049400-57050800	Active TSS	NHDF-Ad	bronchial
30	chr19:57049400-57051000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr19:57049400-57051000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr19:57049400-57051000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr19:57049400-57051000	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
34	chr19:57049400-57051200	Active TSS	H1 Cell Line	embryonic stem cell
35	chr19:57049400-57051200	Active TSS	Small Intestine	intestine
36	chr19:57049400-57051400	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr19:57049600-57050800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr19:57049600-57050800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr19:57049600-57050800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr19:57049600-57050800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:57049600-57050800	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr19:57049600-57050800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr19:57049600-57050800	Active TSS	Brain Anterior Caudate	brain
44	chr19:57049600-57050800	Active TSS	Brain Cingulate Gyrus	brain
45	chr19:57049600-57050800	Active TSS	Brain Germinal Matrix	brain
46	chr19:57049600-57050800	Active TSS	Colon Smooth Muscle	Colon
47	chr19:57049600-57050800	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr19:57049600-57050800	Active TSS	Fetal Heart	heart
49	chr19:57049600-57050800	Active TSS	Fetal Intestine Large	intestine
50	chr19:57049600-57050800	Active TSS	Fetal Intestine Small	intestine

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