Variant report

Variant	rs34746918
Chromosome Location	chr19:18539744-18539745
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	EBF1	chr19:18539743-18540114	GM12878	blood:	n/a	n/a
3	ZBTB7A	chr19:18539505-18540853	ECC-1	luminal epithelium:	n/a	chr19:18540747-18540755
4	FOXP2	chr19:18539589-18540288	SK-N-MC	brain:	n/a	n/a
5	MAX	chr19:18539741-18540202	ECC-1	luminal epithelium:	n/a	chr19:18540138-18540147 chr19:18539850-18539859
6	POLR2A	chr19:18539573-18540248	U87	brain:	n/a	n/a
7	YY1	chr19:18539630-18540878	K562	blood:	n/a	chr19:18540470-18540479 chr19:18540151-18540165 chr19:18540055-18540064 chr19:18540275-18540284 chr19:18540052-18540061 chr19:18540276-18540287 chr19:18540278-18540287 chr19:18540214-18540228 chr19:18539889-18539903 chr19:18540045-18540056 chr19:18540272-18540286 chr19:18540053-18540064 chr19:18539780-18539794 chr19:18540148-18540162
8	TAF1	chr19:18539561-18539859	H1-neurons	neurons:	n/a	n/a
9	POLR2A	chr19:18538551-18551124	K562	blood:	n/a	n/a
10	CTCF	chr19:18539710-18539877	GM19238	blood:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
11	CTCF	chr19:18539660-18539810	GM12873	blood:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
12	MAX	chr19:18539721-18540142	NB4	blood:	n/a	chr19:18539850-18539859
13	CTCF	chr19:18539620-18539770	BJ	skin:	n/a	n/a
14	CTCF	chr19:18539620-18539770	GM12867	blood:	n/a	n/a
15	CTCF	chr19:18539680-18539830	AG09319	gingival:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
16	POLR2A	chr19:18539713-18540364	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr19:18539720-18539870	K562	blood:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
18	MXI1	chr19:18539544-18540284	IMR90	lung:	n/a	chr19:18540134-18540149 chr19:18540132-18540147 chr19:18539850-18539865 chr19:18539848-18539863
19	POLR2A	chr19:18539740-18540324	PANC-1	pancreas:	n/a	n/a
20	POLR2A	chr19:18534926-18553479	K562	blood:	n/a	n/a
21	YY1	chr19:18539719-18540057	K562	blood:	n/a	chr19:18539889-18539903 chr19:18540045-18540056 chr19:18539780-18539794
22	SIN3AK20	chr19:18539710-18540240	H1-hESC	embryonic stem cell:	n/a	n/a
23	EBF1	chr19:18539740-18540110	GM12878	blood:	n/a	n/a
24	POLR2A	chr19:18539579-18540941	PANC-1	pancreas:	n/a	n/a
25	SIN3A	chr19:18539735-18540217	GM12878	blood:	n/a	n/a
26	HDAC2	chr19:18539658-18540005	K562	blood:	n/a	n/a
27	CTCF	chr19:18539680-18539830	AG10803	skin:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
28	ELF1	chr19:18539683-18540520	K562	blood:	n/a	chr19:18539896-18539908
29	POLR2A	chr19:18539642-18540463	HUVEC	blood vessel:	n/a	n/a
30	PML	chr19:18539681-18540057	K562	blood:	n/a	n/a
31	CTCF	chr19:18539660-18539810	GM12870	blood:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
32	POLR2A	chr19:18539684-18540037	GM12891	blood:	n/a	n/a
33	TAF1	chr19:18539522-18540224	H1-neurons	neurons:	n/a	n/a
34	POLR2A	chr19:18539738-18540174	SK-N-SH	brain:	n/a	n/a
35	CTCF	chr19:18539680-18539830	AG04449	skin:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
36	CTCF	chr19:18539676-18539899	Spleen_OC	spleen:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
37	ZNF143	chr19:18539681-18540123	GM12878	blood:	n/a	chr19:18539859-18539869
38	CCNT2	chr19:18539679-18540283	K562	blood:	n/a	chr19:18540045-18540054 chr19:18540052-18540061
39	MAX	chr19:18539696-18540204	K562	blood:	n/a	chr19:18540138-18540147 chr19:18539850-18539859
40	POLR2A	chr19:18539728-18540212	U87	brain:	n/a	n/a
41	SIN3A	chr19:18539647-18540460	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr19:18539720-18539870	HUVEC	blood vessel:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
43	ETS1	chr19:18539686-18540173	K562	blood:	n/a	chr19:18540043-18540054 chr19:18540049-18540060 chr19:18540040-18540051 chr19:18539782-18539793
44	PML	chr19:18539423-18540193	GM12878	blood:	n/a	n/a
45	POLR2A	chr19:18539581-18540000	GM12892	blood:	n/a	n/a
46	RCOR1	chr19:18539609-18540252	K562	blood:	n/a	n/a
47	CTCF	chr19:18539740-18539890	GM12864	blood:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
48	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
49	CTCF	chr19:18539687-18539933	GM12892	blood:	n/a	chr19:18539781-18539794 chr19:18539781-18539794
50	SP1	chr19:18539640-18540232	A549	lung:	n/a	chr19:18540075-18540084 chr19:18540053-18540062 chr19:18540045-18540054 chr19:18540048-18540062 chr19:18540073-18540085 chr19:18539799-18539811 chr19:18540052-18540061 chr19:18540073-18540085 chr19:18540044-18540056 chr19:18540051-18540063 chr19:18540074-18540083 chr19:18540052-18540062 chr19:18540051-18540063 chr19:18539799-18539811 chr19:18540044-18540056 chr19:18539737-18539751

No.	Distal block	Cell Line	Cell type
1	chr19:18495232..18499014-chr19:18539147..18542857,5	K562	blood:
2	chr19:18538215..18540689-chr19:18541318..18544057,3	MCF-7	breast:
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	chr19:18401175..18404023-chr19:18537863..18539807,2	K562	blood:
7	chr19:18537918..18539910-chr19:18546510..18549015,3	MCF-7	breast:
8	chr19:18483975..18485616-chr19:18538435..18540189,2	K562	blood:
9	chr19:18388633..18392429-chr19:18537213..18541674,5	K562	blood:
10	chr19:18385704..18387487-chr19:18538825..18541635,2	K562	blood:

Variant related genes	Relation type
SSBP4	TF binding region
ENSG00000130511	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000267959	Chromatin interaction

Extended variants
information (count: 90 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10164319	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10403249	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10405479	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10405636	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10408290	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10409003	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10409483	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10409505	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10411009	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10413237	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10419404	0.87[ASN][1000 genomes]
rs10425982	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10427083	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1043327	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10442	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11673604	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12162221	0.83[ASN][1000 genomes]
rs12162223	0.81[ASN][1000 genomes]
rs12981981	0.83[ASN][1000 genomes]
rs1560118	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1560119	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs172032	0.83[ASN][1000 genomes]
rs1806980	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2007981	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2288428	0.95[ASN][1000 genomes]
rs2303695	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2303696	0.92[ASN][1000 genomes]
rs2303697	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2385088	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2385089	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs271621	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs271622	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs271623	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs271624	0.86[ASN][1000 genomes]
rs271626	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs271628	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs271629	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28375303	0.84[ASN][1000 genomes]
rs28572537	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34010330	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34053595	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34171762	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34256197	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34509804	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3810429	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4595905	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4808133	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4808134	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4808136	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4808801	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808804	0.92[ASN][1000 genomes]
rs62121135	0.83[ASN][1000 genomes]
rs7249020	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7251653	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7252707	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7252848	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7253990	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7254249	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7256534	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7257932	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7258465	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs748609	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs76194	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs76195	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8100767	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8103622	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8103660	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8105994	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8106096	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8107347	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8107351	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8107367	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8107743	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8109573	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8111708	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs875396	0.84[EUR][1000 genomes];0.91[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:1)

SNP	Gene	Cis/trans	Tissue	Source
rs34746918	SSBP4	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18531200-18540000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr19:18531400-18539800	Weak transcription	Brain Substantia Nigra	brain
3	chr19:18531400-18543000	Enhancers	Fetal Brain Male	brain
4	chr19:18532800-18547600	Weak transcription	HepG2	liver
5	chr19:18533800-18541000	Enhancers	Placenta	Placenta
6	chr19:18534200-18540200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr19:18534600-18539800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr19:18535800-18539800	Weak transcription	Small Intestine	intestine
9	chr19:18536200-18541200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr19:18536600-18542200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:18537000-18540000	Weak transcription	Pancreas	Pancrea
12	chr19:18537400-18541600	Genic enhancers	NHLF	lung
13	chr19:18537400-18543800	Weak transcription	NHEK	skin
14	chr19:18537400-18544000	Weak transcription	HMEC	breast
15	chr19:18537600-18539800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr19:18537800-18539800	Weak transcription	Left Ventricle	heart
17	chr19:18538000-18547600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:18538000-18548400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr19:18538400-18540600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr19:18539000-18539800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr19:18539000-18539800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:18539000-18539800	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr19:18539000-18539800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr19:18539000-18541200	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr19:18539200-18539800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr19:18539200-18539800	Enhancers	Esophagus	oesophagus
27	chr19:18539200-18539800	Genic enhancers	Fetal Intestine Large	intestine
28	chr19:18539200-18539800	Genic enhancers	Fetal Intestine Small	intestine
29	chr19:18539200-18539800	Enhancers	Right Ventricle	heart
30	chr19:18539200-18539800	Enhancers	GM12878-XiMat	blood
31	chr19:18539200-18540000	Enhancers	Fetal Muscle Trunk	muscle
32	chr19:18539200-18540000	Enhancers	Placenta Amnion	Placenta Amnion
33	chr19:18539200-18540800	Flanking Active TSS	Fetal Brain Female	brain
34	chr19:18539200-18541000	Enhancers	Fetal Lung	lung
35	chr19:18539200-18541000	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr19:18539200-18541000	Enhancers	NHDF-Ad	bronchial
37	chr19:18539200-18541600	Enhancers	Stomach Mucosa	stomach
38	chr19:18539200-18544000	Enhancers	Fetal Heart	heart
39	chr19:18539400-18539800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr19:18539400-18539800	Weak transcription	Primary T cells from cord blood	blood
41	chr19:18539400-18539800	Enhancers	Primary hematopoietic stem cells	blood
42	chr19:18539400-18539800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr19:18539400-18539800	Flanking Active TSS	Brain Anterior Caudate	brain
44	chr19:18539400-18539800	Flanking Active TSS	Brain Germinal Matrix	brain
45	chr19:18539400-18539800	Genic enhancers	Right Atrium	heart
46	chr19:18539400-18539800	Enhancers	Spleen	Spleen
47	chr19:18539400-18540000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr19:18539400-18540600	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr19:18539400-18540600	Flanking Active TSS	Stomach Smooth Muscle	stomach
50	chr19:18539400-18540600	Flanking Active TSS	Thymus	Thymus

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