Variant report

Variant	rs12461701
Chromosome Location	chr19:18389620-18389621
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:163)
CpG islands
(count:0)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:163 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:18389480-18389770	ECC-1	luminal epithelium:	n/a	n/a
2	HEY1	chr19:18388695-18394026	HepG2	liver:	n/a	chr19:18390515-18390530 chr19:18392424-18392439 chr19:18393317-18393332
3	CTCF	chr19:18389560-18389710	BE2_C	brain:	n/a	n/a
4	RCOR1	chr19:18389492-18390615	K562	blood:	n/a	n/a
5	POLR2A	chr19:18382150-18392613	HepG2	liver:	n/a	n/a
6	CTCF	chr19:18389520-18389670	RPTEC	kidney:	n/a	n/a
7	HCFC1	chr19:18389403-18391720	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr19:18389487-18390835	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr19:18389318-18391619	U87	brain:	n/a	n/a
10	POLR2A	chr19:18388084-18394020	GM12891	blood:	n/a	n/a
11	POLR2A	chr19:18388712-18391582	PFSK-1	brain:	n/a	n/a
12	POLR2A	chr19:18388704-18391047	GM12891	blood:	n/a	n/a
13	CHD2	chr19:18388743-18390759	K562	blood:	n/a	n/a
14	POLR2A	chr19:18388625-18393808	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr19:18388631-18392724	GM12878	blood:	n/a	n/a
16	MAZ	chr19:18389512-18391564	HepG2	liver:	n/a	n/a
17	CTCF	chr19:18389540-18389690	GM12866	blood:	n/a	n/a
18	USF2	chr19:18389524-18390003	K562	blood:	n/a	n/a
19	POLR2A	chr19:18388705-18392782	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr19:18388652-18391631	U87	brain:	n/a	n/a
21	POLR2A	chr19:18385002-18394564	K562	blood:	n/a	n/a
22	POLR2A	chr19:18388996-18393928	HCT-116	colon:	n/a	n/a
23	FOXM1	chr19:18389165-18389838	GM12878	blood:	n/a	n/a
24	RAD21	chr19:18389217-18393748	SK-N-SH	brain:	n/a	chr19:18392832-18392845
25	POLR2A	chr19:18382160-18394577	MCF10A-Er-Src	breast:	n/a	n/a
26	SIN3AK20	chr19:18389361-18391722	MCF-7	breast:	n/a	n/a
27	POU2F2	chr19:18388713-18389994	GM12891	blood:	n/a	n/a
28	CTCF	chr19:18389520-18389670	HFF-Myc	foreskin:	n/a	n/a
29	POLR2A	chr19:18388726-18394103	HL-60	blood:	n/a	n/a
30	POLR2A	chr19:18388084-18392768	GM12891	blood:	n/a	n/a
31	CTCF	chr19:18389600-18389750	A549	lung:	n/a	n/a
32	CTCF	chr19:18389560-18389710	WI-38	lung:	n/a	n/a
33	POLR2A	chr19:18388733-18393961	HL-60	blood:	n/a	n/a
34	POLR2A	chr19:18389346-18393675	HUVEC	blood vessel:	n/a	n/a
35	TBL1XR1	chr19:18389501-18391643	K562	blood:	n/a	n/a
36	CTCF	chr19:18389600-18389750	HVMF	connective:	n/a	n/a
37	POLR2A	chr19:18382204-18393752	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr19:18388778-18391640	HepG2	liver:	n/a	n/a
39	PML	chr19:18389450-18391721	GM12878	blood:	n/a	n/a
40	POLR2A	chr19:18384125-18394577	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr19:18389480-18389630	HFF-Myc	foreskin:	n/a	n/a
42	MAX	chr19:18389415-18389895	K562	blood:	n/a	n/a
43	POLR2A	chr19:18388801-18393779	HepG2	liver:	n/a	n/a
44	POLR2A	chr19:18388773-18391623	GM12891	blood:	n/a	n/a
45	CEBPB	chr19:18389589-18390992	GM12878	blood:	n/a	n/a
46	JUN	chr19:18389539-18393965	K562	blood:	n/a	n/a
47	POLR2A	chr19:18388711-18390169	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr19:18388766-18394040	GM12878	blood:	n/a	n/a
49	NR2F2	chr19:18389481-18391033	K562	blood:	n/a	n/a
50	POU2F2	chr19:18388725-18389738	GM12891	blood:	n/a	n/a

No data

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18311216..18316508-chr19:18389022..18394678,9	MCF-7	breast:
2	chr19:18388991..18389671-chr5:42992257..42993081,2	Hela-S3	cervix:
3	chr19:18385043..18394940-chr19:18518893..18533267,53	K562	blood:
4	chr19:18388809..18393836-chr19:18524501..18532718,14	MCF-7	breast:
5	chr19:18388423..18395098-chr19:18483334..18487110,13	K562	blood:
6	chr19:18389169..18391132-chr19:18534059..18535898,2	K562	blood:
7	chr19:18388472..18395098-chr19:18481027..18487774,21	K562	blood:
8	chr19:18303093..18307365-chr19:18386584..18393500,10	K562	blood:
9	chr19:18387502..18390021-chr9:123629758..123632738,2	K562	blood:
10	chr19:18313659..18316582-chr19:18386529..18393683,9	K562	blood:
11	chr19:18260692..18269532-chr19:18383927..18395911,19	K562	blood:
12	chr19:18387676..18394124-chr19:18495437..18503905,30	K562	blood:
13	chr19:18262621..18264588-chr19:18388729..18391542,2	MCF-7	breast:
14	chr19:18283857..18287210-chr19:18388230..18390509,3	K562	blood:
15	chr19:18389586..18390376-chr19:18439009..18439886,2	MCF-7	breast:
16	chr19:18343280..18346156-chr19:18388321..18390224,2	K562	blood:
17	chr19:18337559..18339091-chr19:18388443..18390350,2	MCF-7	breast:
18	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
19	chr19:18382564..18395263-chr19:18409643..18446343,165	MCF-7	breast:
20	chr19:18302787..18307396-chr19:18383842..18390051,8	K562	blood:
21	chr19:18389024..18389840-chr19:18433961..18434770,2	MCF-7	breast:
22	chr19:18388917..18393354-chr19:18447866..18453758,9	MCF-7	breast:
23	chr19:18388963..18390088-chr19:18434096..18435108,4	MCF-7	breast:
24	chr19:18375824..18378589-chr19:18388804..18391228,3	MCF-7	breast:
25	chr19:18223413..18225267-chr19:18389021..18391701,2	MCF-7	breast:
26	chr19:18276990..18278607-chr19:18389377..18392205,2	K562	blood:
27	chr19:18334725..18337698-chr19:18389039..18394023,6	K562	blood:
28	chr19:18389320..18390897-chr19:18488070..18489594,2	MCF-7	breast:
29	chr19:18232174..18234032-chr19:18387928..18389889,2	K562	blood:
30	chr19:18389073..18391254-chr19:18491178..18493280,2	K562	blood:
31	chr19:18332417..18336925-chr19:18388887..18394072,11	K562	blood:
32	chr19:18388413..18390013-chr19:18483305..18484834,2	MCF-7	breast:
33	chr19:18387676..18394344-chr19:18495021..18501696,25	K562	blood:
34	chr19:18383365..18408325-chr19:18518460..18533256,66	K562	blood:
35	chr19:18321259..18323821-chr19:18388878..18390408,2	K562	blood:
36	chr19:18389237..18391890-chr19:18553028..18555362,2	K562	blood:
37	chr19:18301148..18305001-chr19:18389528..18394862,10	MCF-7	breast:
38	chr19:18387663..18390272-chr19:18513098..18515988,2	K562	blood:
39	chr19:18328659..18330867-chr19:18389570..18391557,2	K562	blood:
40	chr19:18388462..18393408-chr19:18545945..18551144,14	K562	blood:
41	chr19:18388807..18393519-chr19:18545945..18551144,10	K562	blood:
42	chr19:18388723..18391469-chr19:18447700..18450655,3	MCF-7	breast:
43	chr19:18342752..18344966-chr19:18388974..18391959,2	K562	blood:
44	chr19:18300044..18302631-chr19:18389476..18391618,2	K562	blood:
45	chr19:18311642..18316628-chr19:18388957..18392513,10	K562	blood:

No data

Variant related genes	Relation type
KIAA1683	TF binding region
MIR3188	TF binding region
ENSG00000221167	Chromatin interaction
ENSG00000264175	Chromatin interaction
ENSG00000105647	Chromatin interaction
ENSG00000269145	Chromatin interaction
ENSG00000216490	Chromatin interaction
ENSG00000105649	Chromatin interaction
ENSG00000268650	Chromatin interaction
ENSG00000256989	Chromatin interaction
ENSG00000130513	Chromatin interaction
ENSG00000130520	Chromatin interaction
ENSG00000105650	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000254858	Chromatin interaction
ENSG00000119403	Chromatin interaction
ENSG00000130517	Chromatin interaction
ENSG00000239821	Chromatin interaction
ENSG00000268173	Chromatin interaction
ENSG00000130511	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 7 )

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

rs_ID	r²[population]
rs1035363	0.90[CEU][hapmap];0.87[GIH][hapmap];0.90[MEX][hapmap]
rs1079165	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1079166	1.00[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs10854164	1.00[ASN][1000 genomes]
rs12459276	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12460547	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12461261	0.97[ASN][1000 genomes]
rs12461751	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12608843	0.90[CEU][hapmap];0.87[GIH][hapmap];0.95[MEX][hapmap]
rs1421720	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1477269	0.95[CEU][hapmap]
rs1549143	0.95[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17711565	0.86[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs2287656	0.90[CEU][hapmap];0.87[GIH][hapmap]
rs2287657	0.90[CEU][hapmap];0.87[GIH][hapmap]
rs3810432	0.90[CEU][hapmap]
rs3810433	0.90[CEU][hapmap];0.87[GIH][hapmap];0.95[MEX][hapmap]
rs3810434	0.90[CEU][hapmap];0.87[GIH][hapmap];0.90[MEX][hapmap]
rs41347350	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41481544	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808125	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4808777	0.82[ASN][1000 genomes]
rs4808778	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57090641	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58555271	0.88[EUR][1000 genomes]
rs59961449	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60086589	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60170051	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62120437	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7247237	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7247767	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7248070	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8103549	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8105176	0.90[CEU][hapmap];0.87[GIH][hapmap];0.90[MEX][hapmap]
rs8105503	0.90[CEU][hapmap];0.87[GIH][hapmap];0.90[MEX][hapmap]
rs8108675	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs8109771	0.90[CEU][hapmap]
rs8113654	0.89[CEU][hapmap]
rs888666	0.84[ASW][hapmap]
rs999814	0.90[CEU][hapmap];0.87[GIH][hapmap];0.90[MEX][hapmap]
rs999815	0.90[CEU][hapmap];0.87[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:17 , 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	esv1837595	chr19:18085428-18393682	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
3	nsv833775	chr19:18213761-18390074	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv911251	chr19:18224729-18422364	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer 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	136 gene(s)	inside rSNPs	diseases
5	nsv911253	chr19:18240127-18418044	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
6	nsv916325	chr19:18244780-18534927	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
7	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
8	nsv911268	chr19:18351674-18395537	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	103 gene(s)	inside rSNPs	diseases
9	nsv911269	chr19:18351674-18418044	Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
10	nsv911270	chr19:18351674-18422364	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
11	nsv911271	chr19:18362940-18453124	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	135 gene(s)	inside rSNPs	diseases
12	nsv828472	chr19:18377725-18404131	Flanking Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	117 gene(s)	inside rSNPs	diseases
13	esv1833305	chr19:18378219-18408222	Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	117 gene(s)	inside rSNPs	diseases
14	nsv911272	chr19:18378219-18439383	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	135 gene(s)	inside rSNPs	diseases
15	nsv578744	chr19:18380072-18392873	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
16	esv1793726	chr19:18381600-18400786	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	104 gene(s)	inside rSNPs	diseases
17	nsv911273	chr19:18386798-18454825	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	134 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs12461701	KIAA1683	cis	Skin Sun Exposed Lower leg	GTEx
rs12461701	ISYNA1	cis	cerebellum	SCAN
rs12461701	FAM129C	cis	parietal	SCAN
rs12461701	KIAA1683	cis	cerebellum	SCAN
rs12461701	UBA52	cis	parietal	SCAN
rs12461701	PLVAP	cis	parietal	SCAN
rs12461701	KIAA1683	cis	Thyroid	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18366600-18390000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:18384600-18389800	Genic enhancers	Primary B cells from peripheral blood	blood
3	chr19:18385400-18390200	Genic enhancers	Spleen	Spleen
4	chr19:18386000-18390000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr19:18388200-18390400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
6	chr19:18388600-18390200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr19:18388800-18389800	Enhancers	Fetal Heart	heart
8	chr19:18388800-18389800	Transcr. at gene 5' and 3'	Ovary	ovary
9	chr19:18388800-18389800	Enhancers	Psoas Muscle	Psoas
10	chr19:18388800-18389800	Flanking Active TSS	Right Atrium	heart
11	chr19:18388800-18390000	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr19:18388800-18390000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Liver	Liver
16	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Colonic Mucosa	Colon
17	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
18	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 29	rectum
19	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Hela-S3	cervix
20	chr19:18388800-18390200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr19:18388800-18390200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Cortex derived primary cultured neurospheres	brain
24	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Adipose Nuclei	Adipose
26	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Brain Inferior Temporal Lobe	brain
27	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Fetal Lung	lung
28	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Pancreas	Pancrea
29	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Thymus	Thymus
30	chr19:18388800-18390200	Transcr. at gene 5' and 3'	HSMM	muscle
31	chr19:18388800-18390200	Transcr. at gene 5' and 3'	K562	blood
32	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
33	chr19:18388800-18390200	Transcr. at gene 5' and 3'	NHLF	lung
34	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Osteobl	bone
35	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Primary monocytes fromperipheralblood	blood
37	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Primary T cells from cord blood	blood
38	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
39	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
40	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Primary T helper cells fromperipheralblood	blood
41	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
44	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
45	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Placenta	Placenta
46	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
47	chr19:18388800-18390400	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 31	rectum
48	chr19:18388800-18390400	Transcr. at gene 5' and 3'	A549	lung
49	chr19:18388800-18390400	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
50	chr19:18388800-18390600	Transcr. at gene 5' and 3'	Fetal Stomach	stomach

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