Variant report

Variant	rs11673604
Chromosome Location	chr19:18540988-18540989
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	POLR2A	chr19:18538913-18542153	SK-N-MC	brain:	n/a	n/a
2	POLR2A	chr19:18538551-18551124	K562	blood:	n/a	n/a
3	POLR2A	chr19:18534926-18553479	K562	blood:	n/a	n/a
4	POLR2A	chr19:18540650-18541120	H1-hESC	embryonic stem cell:	n/a	n/a
5	STAT5A	chr19:18539508-18541125	GM12878	blood:	n/a	chr19:18540393-18540405 chr19:18540676-18540688 chr19:18540276-18540288 chr19:18540471-18540483 chr19:18540966-18540978 chr19:18540020-18540032 chr19:18540053-18540065 chr19:18540277-18540289 chr19:18540618-18540630
6	POLR2A	chr19:18540643-18541031	PFSK-1	brain:	n/a	n/a
7	POLR2A	chr19:18540881-18541024	MCF-7	breast:	n/a	n/a
8	NFATC1	chr19:18540174-18540991	GM12878	blood:	n/a	n/a
9	POLR2A	chr19:18539600-18541000	K562	blood:	n/a	n/a
10	MTA3	chr19:18539376-18541026	GM12878	blood:	n/a	n/a
11	RUNX3	chr19:18540424-18540994	GM12878	blood:	n/a	chr19:18540910-18540925
12	POLR2A	chr19:18539622-18542014	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18495232..18499014-chr19:18539147..18542857,5	K562	blood:
2	chr19:18540459..18542781-chr19:18632920..18634658,2	K562	blood:
3	chr19:18527431..18533703-chr19:18536573..18544512,11	MCF-7	breast:
4	chr19:18539549..18542308-chr19:18573841..18576282,3	K562	blood:
5	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
6	chr19:18388633..18392429-chr19:18537213..18541674,5	K562	blood:
7	chr19:18385704..18387487-chr19:18538825..18541635,2	K562	blood:

Variant related genes	Relation type
SSBP4	TF binding region
ENSG00000264175	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000105656	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000130513	Chromatin interaction

Extended variants
information (count: 86 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10164319	1.00[CEU][hapmap];0.88[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10164323	0.93[JPT][hapmap]
rs10403249	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10405479	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10405636	1.00[CEU][hapmap];0.88[JPT][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10408290	1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10409003	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10409483	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10409505	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10411009	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10413237	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10419404	0.81[EUR][1000 genomes]
rs10425982	1.00[CEU][hapmap];0.88[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10427083	1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1043327	0.83[ASW][hapmap];1.00[CEU][hapmap];0.82[CHD][hapmap];0.93[GIH][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];0.97[TSI][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10442	0.83[ASW][hapmap];1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1560118	1.00[CEU][hapmap];0.88[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1560119	1.00[CEU][hapmap];0.88[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1806980	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2007981	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2278238	0.83[ASW][hapmap];1.00[CEU][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap]
rs2288428	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2303695	0.96[CEU][hapmap];0.88[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2303696	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2303697	1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2385088	1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2385089	0.83[ASW][hapmap];1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs271621	1.00[CEU][hapmap];0.88[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs271622	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs271623	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs271624	1.00[CEU][hapmap];0.88[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs271626	1.00[CEU][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs271628	1.00[CEU][hapmap];0.88[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs271629	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28572537	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34010330	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34053595	1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34171762	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34256197	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34509804	0.85[EUR][1000 genomes]
rs34746918	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3810429	0.83[ASW][hapmap];1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4595905	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4808133	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4808134	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4808136	0.96[CEU][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4808801	1.00[CEU][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4808804	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7249020	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7251653	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7252707	0.96[CEU][hapmap];0.88[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7252848	0.96[CEU][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7253990	1.00[CEU][hapmap];0.88[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7254249	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7256534	1.00[CEU][hapmap];0.88[JPT][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7257932	0.96[CEU][hapmap];0.83[JPT][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7258465	1.00[CEU][hapmap];0.82[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs748609	1.00[CEU][hapmap];0.88[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs76194	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs76195	0.81[ASW][hapmap];1.00[CEU][hapmap];0.95[GIH][hapmap];0.88[JPT][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8100767	1.00[CEU][hapmap];0.88[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8103622	1.00[CEU][hapmap];0.88[JPT][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8103660	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8105994	1.00[CEU][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];0.88[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8106096	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8107347	0.89[CEU][hapmap];0.88[JPT][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8107351	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8107367	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8107743	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8109573	0.96[CEU][hapmap];0.88[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8111708	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs875396	1.00[CEU][hapmap];0.88[JPT][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking 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 miRNA	162 gene(s)	inside rSNPs	diseases
3	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
7	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
8	nsv911276	chr19:18497141-18554972	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
9	nsv911277	chr19:18520231-18552139	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
11	nsv911278	chr19:18526536-18550276	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
12	nsv911279	chr19:18533642-18550276	Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
13	nsv911280	chr19:18533642-18552139	Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs11673604	ZNF431	cis	parietal	SCAN
rs11673604	ISYNA1	cis	parietal	SCAN
rs11673604	SSBP4	cis	lymphoblastoid	seeQTL
rs11673604	SSBP4	cis	cerebellum	SCAN
rs11673604	ZNF100	cis	parietal	SCAN
rs11673604	SSBP4	cis	Skin Sun Exposed Lower leg	GTEx
rs11673604	GATAD2A	cis	parietal	SCAN
rs11673604	SSBP4	cis	Esophagus Mucosa	GTEx

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18531400-18543000	Enhancers	Fetal Brain Male	brain
2	chr19:18532800-18547600	Weak transcription	HepG2	liver
3	chr19:18533800-18541000	Enhancers	Placenta	Placenta
4	chr19:18536200-18541200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr19:18536600-18542200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr19:18537400-18541600	Genic enhancers	NHLF	lung
7	chr19:18537400-18543800	Weak transcription	NHEK	skin
8	chr19:18537400-18544000	Weak transcription	HMEC	breast
9	chr19:18538000-18547600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr19:18538000-18548400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr19:18539000-18541200	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr19:18539200-18541000	Enhancers	Fetal Lung	lung
13	chr19:18539200-18541000	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr19:18539200-18541000	Enhancers	NHDF-Ad	bronchial
15	chr19:18539200-18541600	Enhancers	Stomach Mucosa	stomach
16	chr19:18539200-18544000	Enhancers	Fetal Heart	heart
17	chr19:18539400-18541000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:18539600-18541000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr19:18539600-18541000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
20	chr19:18539600-18541000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr19:18539600-18541000	Enhancers	Lung	lung
22	chr19:18539600-18541000	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr19:18539600-18541000	Enhancers	HSMMtube	muscle
24	chr19:18539600-18541400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr19:18539800-18541000	Active TSS	H9 Cell Line	embryonic stem cell
26	chr19:18540000-18541000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
27	chr19:18540000-18541000	Enhancers	Pancreas	Pancrea
28	chr19:18540000-18541000	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr19:18540000-18541000	Active TSS	Rectal Smooth Muscle	rectum
30	chr19:18540000-18541000	Enhancers	Spleen	Spleen
31	chr19:18540200-18541000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr19:18540200-18541000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr19:18540200-18541000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr19:18540200-18541600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr19:18540200-18543600	Weak transcription	Brain Angular Gyrus	brain
36	chr19:18540400-18541000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr19:18540400-18541000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr19:18540400-18541000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr19:18540400-18541000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr19:18540400-18541000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr19:18540400-18541000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr19:18540400-18541000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr19:18540400-18541000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:18540400-18541000	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr19:18540400-18541000	Enhancers	Brain Substantia Nigra	brain
46	chr19:18540400-18541000	Enhancers	Colonic Mucosa	Colon
47	chr19:18540400-18541000	Genic enhancers	Fetal Intestine Large	intestine
48	chr19:18540400-18541000	Enhancers	Fetal Thymus	thymus
49	chr19:18540400-18541000	Enhancers	Placenta Amnion	Placenta Amnion
50	chr19:18540400-18541000	Enhancers	HSMM	muscle

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