Variant report

Variant	rs41347350
Chromosome Location	chr19:18389393-18389394
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:202)
CpG islands
(count:0)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:202 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr19:18388695-18394026	HepG2	liver:	n/a	chr19:18390515-18390530 chr19:18392424-18392439 chr19:18393317-18393332
2	CTCF	chr19:18389380-18389530	HepG2	liver:	n/a	n/a
3	POLR2A	chr19:18382150-18392613	HepG2	liver:	n/a	n/a
4	POLR2A	chr19:18389318-18391619	U87	brain:	n/a	n/a
5	POLR2A	chr19:18388084-18394020	GM12891	blood:	n/a	n/a
6	CTCF	chr19:18389380-18389530	AG09319	gingival:	n/a	n/a
7	POLR2A	chr19:18388712-18391582	PFSK-1	brain:	n/a	n/a
8	POLR2A	chr19:18388704-18391047	GM12891	blood:	n/a	n/a
9	CTCF	chr19:18389380-18389530	BJ	skin:	n/a	n/a
10	CHD2	chr19:18388743-18390759	K562	blood:	n/a	n/a
11	CTCF	chr19:18389300-18389450	HRE	kidney:	n/a	n/a
12	CTCF	chr19:18389345-18389555	K562	blood:	n/a	n/a
13	POLR2A	chr19:18388625-18393808	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr19:18389349-18389570	GM19240	blood:	n/a	n/a
15	POLR2A	chr19:18388631-18392724	GM12878	blood:	n/a	n/a
16	CTCF	chr19:18389380-18389530	GM12864	blood:	n/a	n/a
17	CTCF	chr19:18389380-18389530	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr19:18389310-18389568	GM10266	blood:	n/a	n/a
19	CTCF	chr19:18389380-18389530	AG04449	skin:	n/a	n/a
20	POLR2A	chr19:18388705-18392782	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr19:18388652-18391631	U87	brain:	n/a	n/a
22	POLR2A	chr19:18385002-18394564	K562	blood:	n/a	n/a
23	CTCF	chr19:18389359-18389610	IMR90	lung:	n/a	n/a
24	POLR2A	chr19:18388996-18393928	HCT-116	colon:	n/a	n/a
25	FOXM1	chr19:18389165-18389838	GM12878	blood:	n/a	n/a
26	RAD21	chr19:18389217-18393748	SK-N-SH	brain:	n/a	chr19:18392832-18392845
27	CTCF	chr19:18389380-18389544	Fibrobl	skin:	n/a	n/a
28	POLR2A	chr19:18382160-18394577	MCF10A-Er-Src	breast:	n/a	n/a
29	CTCF	chr19:18389360-18389551	GM12892	blood:	n/a	n/a
30	SIN3AK20	chr19:18389361-18391722	MCF-7	breast:	n/a	n/a
31	POU2F2	chr19:18388713-18389994	GM12891	blood:	n/a	n/a
32	POLR2A	chr19:18388726-18394103	HL-60	blood:	n/a	n/a
33	POLR2A	chr19:18388084-18392768	GM12891	blood:	n/a	n/a
34	CTCF	chr19:18389382-18389494	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr19:18389320-18389470	HFF	foreskin:	n/a	n/a
36	POLR2A	chr19:18388733-18393961	HL-60	blood:	n/a	n/a
37	CTCF	chr19:18389340-18389490	GM12864	blood:	n/a	n/a
38	POLR2A	chr19:18389346-18393675	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr19:18382204-18393752	HUVEC	blood vessel:	n/a	n/a
40	POLR2A	chr19:18388778-18391640	HepG2	liver:	n/a	n/a
41	POLR2A	chr19:18384125-18394577	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr19:18389380-18389530	HPF	lung:	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	CTCF	chr19:18389383-18389538	GM13976	blood:	n/a	n/a
46	CTCF	chr19:18389355-18389547	HepG2	liver:	n/a	n/a
47	CTCF	chr19:18389342-18389577	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:18389332-18389574	GM12891	blood:	n/a	n/a
49	POLR2A	chr19:18388711-18390169	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr19:18389357-18389549	Spleen_OC	spleen:	n/a	n/a

No data

(count:41 , 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	chr19:18343280..18346156-chr19:18388321..18390224,2	K562	blood:
16	chr19:18337559..18339091-chr19:18388443..18390350,2	MCF-7	breast:
17	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
18	chr19:18382564..18395263-chr19:18409643..18446343,165	MCF-7	breast:
19	chr19:18302787..18307396-chr19:18383842..18390051,8	K562	blood:
20	chr19:18389024..18389840-chr19:18433961..18434770,2	MCF-7	breast:
21	chr19:18388917..18393354-chr19:18447866..18453758,9	MCF-7	breast:
22	chr19:18388963..18390088-chr19:18434096..18435108,4	MCF-7	breast:
23	chr19:18375824..18378589-chr19:18388804..18391228,3	MCF-7	breast:
24	chr19:18223413..18225267-chr19:18389021..18391701,2	MCF-7	breast:
25	chr19:18276990..18278607-chr19:18389377..18392205,2	K562	blood:
26	chr19:18334725..18337698-chr19:18389039..18394023,6	K562	blood:
27	chr19:18389320..18390897-chr19:18488070..18489594,2	MCF-7	breast:
28	chr19:18232174..18234032-chr19:18387928..18389889,2	K562	blood:
29	chr19:18389073..18391254-chr19:18491178..18493280,2	K562	blood:
30	chr19:18332417..18336925-chr19:18388887..18394072,11	K562	blood:
31	chr19:18388413..18390013-chr19:18483305..18484834,2	MCF-7	breast:
32	chr19:18387676..18394344-chr19:18495021..18501696,25	K562	blood:
33	chr19:18383365..18408325-chr19:18518460..18533256,66	K562	blood:
34	chr19:18321259..18323821-chr19:18388878..18390408,2	K562	blood:
35	chr19:18389237..18391890-chr19:18553028..18555362,2	K562	blood:
36	chr19:18387663..18390272-chr19:18513098..18515988,2	K562	blood:
37	chr19:18388462..18393408-chr19:18545945..18551144,14	K562	blood:
38	chr19:18388807..18393519-chr19:18545945..18551144,10	K562	blood:
39	chr19:18388723..18391469-chr19:18447700..18450655,3	MCF-7	breast:
40	chr19:18342752..18344966-chr19:18388974..18391959,2	K562	blood:
41	chr19:18311642..18316628-chr19:18388957..18392513,10	K562	blood:

No data

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

Extended variants
information (count: 42 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1079165	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1079166	0.97[ASN][1000 genomes]
rs10854164	1.00[ASN][1000 genomes]
rs12459276	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12460547	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12461261	0.97[ASN][1000 genomes]
rs12461701	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12461751	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1421720	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1549143	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17711565	0.81[ASN][1000 genomes]
rs41481544	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4808125	0.94[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];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57090641	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58555271	0.89[EUR][1000 genomes]
rs59961449	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs60086589	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60170051	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62120437	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7247237	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7247767	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7248070	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8103549	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]

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:2)

SNP	Gene	Cis/trans	Tissue	Source
rs41347350	KIAA1683	cis	Thyroid	GTEx
rs41347350	KIAA1683	cis	Skin Sun Exposed Lower leg	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18366400-18389400	Weak transcription	Fetal Brain Male	brain
2	chr19:18366600-18390000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr19:18384600-18389800	Genic enhancers	Primary B cells from peripheral blood	blood
4	chr19:18385400-18390200	Genic enhancers	Spleen	Spleen
5	chr19:18385600-18389600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr19:18386000-18390000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr19:18386800-18389600	Weak transcription	HSMMtube	muscle
8	chr19:18387200-18389600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr19:18388200-18389600	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr19:18388200-18389600	Genic enhancers	Brain Anterior Caudate	brain
11	chr19:18388200-18390400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
12	chr19:18388400-18389600	Genic enhancers	Lung	lung
13	chr19:18388600-18390200	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr19:18388800-18389400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr19:18388800-18389400	Genic enhancers	HUES48 Cell Line	embryonic stem cell
16	chr19:18388800-18389400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
17	chr19:18388800-18389400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr19:18388800-18389600	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr19:18388800-18389600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr19:18388800-18389600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr19:18388800-18389600	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr19:18388800-18389600	Genic enhancers	Brain Substantia Nigra	brain
23	chr19:18388800-18389600	Genic enhancers	Esophagus	oesophagus
24	chr19:18388800-18389600	Genic enhancers	Left Ventricle	heart
25	chr19:18388800-18389600	Genic enhancers	Stomach Mucosa	stomach
26	chr19:18388800-18389600	Genic enhancers	GM12878-XiMat	blood
27	chr19:18388800-18389600	Strong transcription	NHEK	skin
28	chr19:18388800-18389800	Enhancers	Fetal Heart	heart
29	chr19:18388800-18389800	Transcr. at gene 5' and 3'	Ovary	ovary
30	chr19:18388800-18389800	Enhancers	Psoas Muscle	Psoas
31	chr19:18388800-18389800	Flanking Active TSS	Right Atrium	heart
32	chr19:18388800-18390000	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr19:18388800-18390000	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Liver	Liver
37	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Colonic Mucosa	Colon
38	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
39	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Rectal Mucosa Donor 29	rectum
40	chr19:18388800-18390000	Transcr. at gene 5' and 3'	Hela-S3	cervix
41	chr19:18388800-18390200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr19:18388800-18390200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Cortex derived primary cultured neurospheres	brain
45	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Adipose Nuclei	Adipose
47	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Brain Inferior Temporal Lobe	brain
48	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Fetal Lung	lung
49	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Pancreas	Pancrea
50	chr19:18388800-18390200	Transcr. at gene 5' and 3'	Thymus	Thymus

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