Variant report

Variant	rs10407726
Chromosome Location	chr19:20011018-20011019
allele	G/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	POLR2A	chr19:20010944-20012842	SK-N-SH	brain:	n/a	n/a
2	TRIM28	chr19:20010941-20011878	K562	blood:	n/a	n/a
3	POLR2A	chr19:20010955-20011254	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr19:20010916-20013396	GM12878	blood:	n/a	n/a
5	POLR2A	chr19:20010993-20013006	K562	blood:	n/a	n/a
6	ATF1	chr19:20010975-20011943	K562	blood:	n/a	n/a
7	TEAD4	chr19:20010949-20011291	K562	blood:	n/a	n/a
8	POLR2A	chr19:20010967-20011169	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr19:20010914-20012037	K562	blood:	n/a	n/a
10	POLR2A	chr19:20010941-20012869	K562	blood:	n/a	n/a
11	TBP	chr19:20011000-20013016	K562	blood:	n/a	n/a
12	POLR2A	chr19:20010990-20013139	GM12891	blood:	n/a	n/a
13	MAX	chr19:20010944-20012634	NB4	blood:	n/a	chr19:20011612-20011622 chr19:20011646-20011656
14	JUN	chr19:20010926-20012772	K562	blood:	n/a	chr19:20011502-20011514 chr19:20011488-20011500
15	POLR2A	chr19:20010919-20012868	IMR90	lung:	n/a	n/a
16	MAZ	chr19:20010971-20012785	K562	blood:	n/a	chr19:20011646-20011656
17	POLR2A	chr19:20010849-20013285	H1-hESC	embryonic stem cell:	n/a	n/a
18	CUX1	chr19:20010922-20011933	K562	blood:	n/a	n/a
19	CUX1	chr19:20010973-20011442	GM12878	blood:	n/a	n/a
20	MAX	chr19:20010957-20011275	K562	blood:	n/a	n/a
21	NR2F2	chr19:20010854-20011949	K562	blood:	n/a	n/a
22	ZMIZ1	chr19:20011006-20012806	K562	blood:	n/a	n/a
23	MYC	chr19:20010935-20012287	NB4	blood:	n/a	chr19:20011612-20011622 chr19:20011646-20011656
24	FOSL1	chr19:20010965-20011321	K562	blood:	n/a	n/a
25	POLR2A	chr19:20010999-20012749	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr19:20010968-20013535	H1-hESC	embryonic stem cell:	n/a	n/a
27	GATA2	chr19:20010938-20011274	K562	blood:	n/a	n/a
28	POLR2A	chr19:20006661-20013292	K562	blood:	n/a	n/a
29	ATF3	chr19:20010946-20011204	K562	blood:	n/a	n/a
30	RUNX3	chr19:20010994-20011290	GM12878	blood:	n/a	n/a
31	MAZ	chr19:20010970-20012908	IMR90	lung:	n/a	chr19:20011646-20011656
32	POLR2A	chr19:20010999-20012771	MCF10A-Er-Src	breast:	n/a	n/a
33	MYC	chr19:20011016-20011782	H1-hESC	embryonic stem cell:	n/a	chr19:20011612-20011622 chr19:20011646-20011656
34	MAX	chr19:20010997-20011234	K562	blood:	n/a	n/a
35	POLR2A	chr19:20010974-20012848	PFSK-1	brain:	n/a	n/a
36	EP300	chr19:20010923-20012108	K562	blood:	n/a	n/a
37	PML	chr19:20010899-20012749	K562	blood:	n/a	n/a
38	GATA3	chr19:20010828-20011440	SK-N-SH	brain:	n/a	n/a
39	GATA3	chr19:20010790-20011893	SK-N-SH	brain:	n/a	n/a
40	PBX3	chr19:20010894-20012065	SK-N-SH	brain:	n/a	chr19:20011630-20011639
41	SRF	chr19:20010966-20011368	K562	blood:	n/a	n/a
42	SRF	chr19:20010995-20011308	H1-hESC	embryonic stem cell:	n/a	n/a
43	MXI1	chr19:20010907-20012860	IMR90	lung:	n/a	n/a
44	RCOR1	chr19:20010972-20012810	K562	blood:	n/a	n/a
45	JUND	chr19:20010926-20012869	K562	blood:	n/a	chr19:20011502-20011514 chr19:20011488-20011500
46	NR2F2	chr19:20010935-20011324	K562	blood:	n/a	n/a
47	CHD1	chr19:20011011-20013111	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr19:20010988-20012775	K562	blood:	n/a	n/a
49	TEAD4	chr19:20010808-20012797	K562	blood:	n/a	n/a
50	EP300	chr19:20010922-20011561	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:19650831..19653075-chr19:20010995..20012617,3	K562	blood:

Variant related genes	Relation type
ENSG00000267565	TF binding region
ENSG00000267268	TF binding region
ZNF93	TF binding region
ENSG00000160161	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1019279	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10403255	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.87[TSI][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10408752	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10412710	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.94[TSI][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10414919	1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs10415179	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10421280	0.86[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs10426937	0.83[EUR][1000 genomes]
rs1048421	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12151060	0.81[CEU][hapmap]
rs13344370	0.86[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.87[CHD][hapmap];0.84[GIH][hapmap];0.88[JPT][hapmap];0.88[MEX][hapmap];0.94[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1469700	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1469701	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs2060239	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2160156	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2335365	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2335366	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2335368	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28590063	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.94[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3943792	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4808221	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs4809006	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4809015	0.95[CHB][hapmap];0.90[CHD][hapmap];0.94[JPT][hapmap]
rs4809016	0.83[ASN][1000 genomes]
rs55739609	0.83[EUR][1000 genomes]
rs60765256	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6511058	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6511059	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs66970424	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7246569	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.84[GIH][hapmap];0.94[JPT][hapmap];0.92[MEX][hapmap];0.94[TSI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7252079	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7253407	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7254355	0.85[EUR][1000 genomes]
rs7256224	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7258260	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8105329	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8105482	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8108528	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8109743	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8113576	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8113694	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1063273	chr19:19591146-20061367	ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv911314	chr19:19866371-20021046	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv519535	chr19:19871250-20595412	Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
4	nsv911315	chr19:19872093-20021046	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv911316	chr19:19890450-20021046	Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv961192	chr19:19906394-20083740	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	esv3319016	chr19:19917475-20819154	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
8	esv3319017	chr19:19917475-20819154	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	56 gene(s)	inside rSNPs	diseases
9	esv3413756	chr19:19936066-20072059	ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	esv3380276	chr19:19936583-20073601	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	esv3429980	chr19:19943721-20102072	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic 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	15 gene(s)	inside rSNPs	diseases
12	nsv1061846	chr19:19946927-20595412	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
13	esv3390957	chr19:19965887-20819154	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
14	nsv869122	chr19:19969851-20595412	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
15	nsv1057569	chr19:19973268-20193556	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
16	nsv1059158	chr19:19973489-20576161	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Enhancers 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	43 gene(s)	inside rSNPs	diseases
17	esv3407363	chr19:20000919-20059307	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
18	esv1845482	chr19:20006144-20014389	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs10407726	ZNF93	cis	Thyroid	GTEx
rs10407726	ZNF253	cis	Nerve Tibial	GTEx
rs10407726	SUGP2	cis	parietal	SCAN
rs10407726	ZNF93	cis	cerebellum	SCAN
rs10407726	ZNF682	cis	Muscle Skeletal	GTEx
rs10407726	HOMER3	cis	cerebellum	SCAN
rs10407726	C19orf44	cis	cerebellum	SCAN
rs10407726	ZNF506	Cis_1M	lymphoblastoid	RTeQTL
rs10407726	SLC5A5	cis	parietal	SCAN
rs10407726	ATP13A1	cis	parietal	SCAN
rs10407726	ZNF506	cis	cerebellum	SCAN
rs10407726	ZNF253	cis	parietal	SCAN

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20003200-20011200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:20004800-20011200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr19:20009400-20011800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:20010200-20011200	Flanking Active TSS	Dnd41	blood
5	chr19:20010600-20011200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr19:20010600-20011400	Flanking Active TSS	Primary hematopoietic stem cells	blood
7	chr19:20010600-20011600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr19:20010600-20013000	Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr19:20010800-20011200	Flanking Active TSS	K562	blood
10	chr19:20010800-20011400	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr19:20010800-20012600	Active TSS	Primary hematopoietic stem cells short term culture	blood
12	chr19:20010800-20012800	ZNF genes & repeats	Liver	Liver
13	chr19:20010800-20013200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:20010800-20013400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr19:20011000-20011200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr19:20011000-20011200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr19:20011000-20011200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr19:20011000-20011200	Flanking Active TSS	Primary B cells from peripheral blood	blood
19	chr19:20011000-20011200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
20	chr19:20011000-20011200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
21	chr19:20011000-20011200	Enhancers	Fetal Brain Male	brain
22	chr19:20011000-20011200	Flanking Active TSS	Fetal Heart	heart
23	chr19:20011000-20011200	Flanking Active TSS	Fetal Intestine Small	intestine
24	chr19:20011000-20011200	Flanking Active TSS	Fetal Lung	lung
25	chr19:20011000-20011200	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr19:20011000-20011200	Flanking Active TSS	HSMMtube	muscle
27	chr19:20011000-20011200	Active TSS	HUVEC	blood vessel
28	chr19:20011000-20011200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr19:20011000-20011400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr19:20011000-20011400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr19:20011000-20011400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr19:20011000-20011400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr19:20011000-20011400	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr19:20011000-20011400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
35	chr19:20011000-20011400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr19:20011000-20011400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr19:20011000-20011400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr19:20011000-20011400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
39	chr19:20011000-20011400	Flanking Active TSS	Adipose Nuclei	Adipose
40	chr19:20011000-20011400	Flanking Active TSS	Brain Germinal Matrix	brain
41	chr19:20011000-20011400	Enhancers	Esophagus	oesophagus
42	chr19:20011000-20011400	Flanking Active TSS	Fetal Brain Female	brain
43	chr19:20011000-20011400	Flanking Active TSS	Fetal Muscle Leg	muscle
44	chr19:20011000-20011400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr19:20011000-20011400	Enhancers	Small Intestine	intestine
46	chr19:20011000-20011600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr19:20011000-20011600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
48	chr19:20011000-20011600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr19:20011000-20011600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr19:20011000-20011600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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