Variant report

Variant	rs172032
Chromosome Location	chr19:18633755-18633756
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	MAZ	chr19:18630650-18633965	IMR90	lung:	n/a	chr19:18633375-18633390 chr19:18633377-18633384 chr19:18633376-18633385 chr19:18631508-18631518
2	SP1	chr19:18632700-18633859	GM12878	blood:	n/a	chr19:18633262-18633272 chr19:18632976-18632986 chr19:18633205-18633217 chr19:18633205-18633216 chr19:18633354-18633368 chr19:18633261-18633273 chr19:18633262-18633276 chr19:18633357-18633369 chr19:18633059-18633069 chr19:18633133-18633147 chr19:18633262-18633271 chr19:18633205-18633217 chr19:18633206-18633220 chr19:18633415-18633425 chr19:18633206-18633215 chr19:18633261-18633273 chr19:18632975-18632987 chr19:18633207-18633216 chr19:18633263-18633272 chr19:18633415-18633425 chr19:18633133-18633142 chr19:18633059-18633069 chr19:18633132-18633144 chr19:18633359-18633368 chr19:18632975-18632987 chr19:18633262-18633272 chr19:18633261-18633272 chr19:18633132-18633144 chr19:18633357-18633369 chr19:18633262-18633271 chr19:18632976-18632986
3	HA-E2F1	chr19:18632497-18633808	MCF-7	breast:	n/a	chr19:18633434-18633448 chr19:18632884-18632893 chr19:18632596-18632605 chr19:18633207-18633216 chr19:18633202-18633212
4	YY1	chr19:18633350-18633903	ECC-1	luminal epithelium:	n/a	chr19:18633393-18633407
5	NRF1	chr19:18632677-18634073	SK-N-SH	brain:	n/a	chr19:18632884-18632893 chr19:18633402-18633411 chr19:18632882-18632891
6	POLR2A	chr19:18633347-18633795	GM12878	blood:	n/a	n/a
7	MYC	chr19:18632643-18633908	A549	lung:	n/a	chr19:18633375-18633390 chr19:18633377-18633384 chr19:18633375-18633385 chr19:18633376-18633385
8	POLR2A	chr19:18632386-18633783	Hela-S3	cervix:	n/a	n/a
9	MTA3	chr19:18633273-18633801	GM12878	blood:	n/a	n/a
10	KAP1	chr19:18633110-18633807	HEK293	kidney:	n/a	n/a
11	RFX5	chr19:18632285-18633931	IMR90	lung:	n/a	n/a
12	CTCF	chr19:18633659-18633761	GM19238	blood:	n/a	n/a
13	MYBL2	chr19:18632644-18633786	HepG2	liver:	n/a	n/a
14	TEAD4	chr19:18633251-18633775	HepG2	liver:	n/a	n/a
15	YY1	chr19:18633496-18633853	HepG2	liver:	n/a	n/a
16	POLR2A	chr19:18633125-18633898	U87	brain:	n/a	n/a
17	CREB1	chr19:18632330-18633944	HepG2	liver:	n/a	n/a
18	CBX3	chr19:18633522-18633826	K562	blood:	n/a	n/a
19	RCOR1	chr19:18632956-18633812	K562	blood:	n/a	n/a
20	RAD21	chr19:18630574-18633896	SK-N-SH	brain:	n/a	chr19:18633520-18633539 chr19:18632170-18632183 chr19:18631191-18631205 chr19:18631851-18631861
21	YY1	chr19:18633528-18633871	K562	blood:	n/a	n/a
22	YY1	chr19:18633418-18633862	GM12892	blood:	n/a	n/a
23	POLR2A	chr19:18632190-18633903	K562	blood:	n/a	n/a
24	POLR2A	chr19:18633304-18633787	GM12878	blood:	n/a	n/a
25	TEAD4	chr19:18632637-18633942	K562	blood:	n/a	n/a
26	CTCF	chr19:18633671-18633767	MCF-7	breast:	n/a	n/a
27	PAX5	chr19:18633452-18633864	GM12878	blood:	n/a	n/a
28	YY1	chr19:18633434-18633873	SK-N-SH_RA	brain:	n/a	n/a
29	JUN	chr19:18632634-18633992	K562	blood:	n/a	chr19:18633234-18633245
30	YY1	chr19:18632196-18633924	GM12878	blood:	n/a	chr19:18632437-18632451 chr19:18632382-18632391 chr19:18633393-18633407 chr19:18632855-18632875 chr19:18632299-18632310
31	YY1	chr19:18633433-18633825	H1-hESC	embryonic stem cell:	n/a	n/a
32	YY1	chr19:18633422-18633793	SK-N-SH_RA	brain:	n/a	n/a
33	RCOR1	chr19:18633435-18633782	K562	blood:	n/a	n/a
34	POLR2A	chr19:18633156-18633827	SK-N-MC	brain:	n/a	n/a
35	MXI1	chr19:18630632-18633816	IMR90	lung:	n/a	chr19:18633378-18633387
36	MAX	chr19:18632483-18633828	A549	lung:	n/a	chr19:18633375-18633390 chr19:18633377-18633384 chr19:18633375-18633385 chr19:18633376-18633385
37	PAX5	chr19:18632938-18633761	GM12878	blood:	n/a	chr19:18633436-18633445
38	NR2F2	chr19:18632324-18633896	K562	blood:	n/a	n/a
39	SRF	chr19:18632663-18633775	MCF-7	breast:	n/a	n/a
40	YY1	chr19:18633358-18633911	GM12878	blood:	n/a	chr19:18633393-18633407
41	CTCF	chr19:18633665-18633786	GM12891	blood:	n/a	n/a
42	SP1	chr19:18632711-18633757	H1-hESC	embryonic stem cell:	n/a	chr19:18633262-18633272 chr19:18632976-18632986 chr19:18633205-18633217 chr19:18633205-18633216 chr19:18633354-18633368 chr19:18633261-18633273 chr19:18633262-18633276 chr19:18633357-18633369 chr19:18633059-18633069 chr19:18633133-18633147 chr19:18633262-18633271 chr19:18633205-18633217 chr19:18633206-18633220 chr19:18633415-18633425 chr19:18633206-18633215 chr19:18633261-18633273 chr19:18632975-18632987 chr19:18633207-18633216 chr19:18633263-18633272 chr19:18633415-18633425 chr19:18633133-18633142 chr19:18633059-18633069 chr19:18633132-18633144 chr19:18633359-18633368 chr19:18632975-18632987 chr19:18633262-18633272 chr19:18633261-18633272 chr19:18633132-18633144 chr19:18633357-18633369 chr19:18633262-18633271 chr19:18632976-18632986
43	POLR2A	chr19:18633125-18633869	U87	brain:	n/a	n/a
44	ELF1	chr19:18632502-18633826	GM12878	blood:	n/a	chr19:18633161-18633174
45	CBX3	chr19:18632622-18633903	K562	blood:	n/a	n/a
46	ZNF384	chr19:18633466-18633897	K562	blood:	n/a	n/a
47	WRNIP1	chr19:18633451-18633768	GM12878	blood:	n/a	n/a
48	ZNF143	chr19:18632955-18633783	K562	blood:	n/a	n/a
49	TBL1XR1	chr19:18632781-18633765	K562	blood:	n/a	n/a
50	YY1	chr19:18633273-18633841	SK-N-SH	brain:	n/a	chr19:18633393-18633407

No.	Distal block	Cell Line	Cell type
1	chr19:18629832..18635572-chr19:18680910..18686315,11	K562	blood:
2	chr12:120729232..120730736-chr19:18631698..18634072,2	MCF-7	breast:
3	chr19:18540459..18542781-chr19:18632920..18634658,2	K562	blood:
4	chr19:18632726..18634686-chr19:18649463..18652079,3	MCF-7	breast:
5	chr19:18631688..18633803-chr19:18698894..18701519,3	MCF-7	breast:
6	chr19:18630875..18635401-chr19:18651200..18655863,9	MCF-7	breast:
7	chr19:18629748..18634724-chr19:18652806..18658264,15	K562	blood:
8	chr19:18630919..18637145-chr19:18698949..18704438,10	K562	blood:
9	chr19:18629832..18634516-chr19:18680910..18685097,11	K562	blood:
10	chr19:18633212..18634980-chr19:18648549..18650137,2	K562	blood:
11	chr19:18629917..18634196-chr19:18652150..18655589,5	MCF-7	breast:
12	chr19:18392155..18393766-chr19:18633090..18634763,2	K562	blood:
13	chr19:18629959..18634840-chr19:18652830..18656407,13	K562	blood:
14	chr19:18628801..18634367-chr19:18680492..18684131,12	MCF-7	breast:
15	chr19:18546603..18548898-chr19:18631485..18634393,2	MCF-7	breast:
16	chr19:18530114..18532262-chr19:18631255..18634040,2	MCF-7	breast:
17	chr19:18633341..18635579-chr19:18650519..18652255,2	K562	blood:
18	chr19:18630485..18634839-chr19:18666846..18671916,7	MCF-7	breast:
19	chr19:18629422..18634718-chr19:18699285..18702887,8	K562	blood:
20	chr19:18632022..18634941-chr19:18640789..18642587,3	K562	blood:
21	chr19:18631257..18635225-chr19:18680941..18684038,5	MCF-7	breast:
22	chr19:18392266..18394628-chr19:18631659..18634590,3	K562	blood:

Variant related genes	Relation type
ELL	TF binding region
ENSG00000130511	Chromatin interaction
ENSG00000221983	Chromatin interaction
ENSG00000105701	Chromatin interaction
ENSG00000105700	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000105655	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000006015	Chromatin interaction
ENSG00000268938	Chromatin interaction
ENSG00000202538	Chromatin interaction

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10164319	0.86[ASN][1000 genomes]
rs10403249	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10405479	0.86[ASN][1000 genomes]
rs10405636	0.84[ASN][1000 genomes]
rs10408290	0.85[ASN][1000 genomes]
rs10409003	0.85[ASN][1000 genomes]
rs10409483	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10409505	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10411009	0.92[ASN][1000 genomes]
rs10419404	0.81[ASN][1000 genomes]
rs10425982	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs10427083	0.83[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1043327	0.84[ASN][1000 genomes]
rs10442	0.85[ASN][1000 genomes]
rs12162221	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12162223	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12981981	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1560118	0.86[ASN][1000 genomes]
rs1560119	0.88[ASN][1000 genomes]
rs1806980	0.85[ASN][1000 genomes]
rs2007981	0.86[ASN][1000 genomes]
rs2288428	0.82[ASN][1000 genomes]
rs2303695	0.85[ASN][1000 genomes]
rs2303697	0.85[ASN][1000 genomes]
rs2385088	0.85[ASN][1000 genomes]
rs271621	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs271622	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs271623	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs271624	0.91[ASN][1000 genomes]
rs271626	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs271628	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs271629	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs28572537	0.86[ASN][1000 genomes]
rs34010330	0.86[ASN][1000 genomes]
rs34053595	0.86[ASN][1000 genomes]
rs34171762	0.86[ASN][1000 genomes]
rs34256197	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs34746918	0.83[ASN][1000 genomes]
rs3810429	0.85[ASN][1000 genomes]
rs4595905	0.85[ASN][1000 genomes]
rs4808133	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4808134	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4808136	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4808801	0.86[ASN][1000 genomes]
rs4808804	0.89[ASN][1000 genomes]
rs62121135	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7249020	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7251653	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7252707	0.92[ASN][1000 genomes]
rs7252848	0.92[ASN][1000 genomes]
rs7253990	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7254249	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7256534	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7258465	0.85[ASN][1000 genomes]
rs748609	0.86[ASN][1000 genomes]
rs76194	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs76195	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8100767	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs8103622	0.86[ASN][1000 genomes]
rs8103660	0.86[ASN][1000 genomes]
rs8105994	0.90[ASN][1000 genomes]
rs8106096	0.85[ASN][1000 genomes]
rs8107347	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs8107351	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs8107367	0.86[ASN][1000 genomes]
rs8107743	0.86[ASN][1000 genomes]
rs8109573	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs8111708	0.86[ASN][1000 genomes]
rs875396	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	nsv1061733	chr19:18574940-18679155	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
8	nsv1055794	chr19:18611545-18676933	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	nsv911281	chr19:18613917-18758255	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
10	nsv911282	chr19:18624964-18928480	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
11	nsv911283	chr19:18626732-18689830	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18630800-18633800	Active TSS	HUES64 Cell Line	embryonic stem cell
2	chr19:18630800-18633800	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr19:18631000-18633800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr19:18631000-18634000	Active TSS	GM12878-XiMat	blood
5	chr19:18631200-18633800	Active TSS	H1 Cell Line	embryonic stem cell
6	chr19:18631200-18633800	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr19:18631200-18633800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr19:18631200-18633800	Active TSS	Brain Angular Gyrus	brain
9	chr19:18631200-18633800	Active TSS	A549	lung
10	chr19:18631200-18633800	Active TSS	NHDF-Ad	bronchial
11	chr19:18631200-18634000	Active TSS	Duodenum Mucosa	Duodenum
12	chr19:18631400-18633800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr19:18631400-18633800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr19:18631400-18633800	Active TSS	Fetal Intestine Large	intestine
15	chr19:18631400-18633800	Active TSS	HMEC	breast
16	chr19:18631400-18633800	Active TSS	HUVEC	blood vessel
17	chr19:18631400-18633800	Active TSS	Osteobl	bone
18	chr19:18631400-18634000	Active TSS	Fetal Lung	lung
19	chr19:18631800-18633800	Active TSS	NH-A	brain
20	chr19:18632000-18633800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:18632000-18633800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
22	chr19:18632000-18633800	Active TSS	Brain Hippocampus Middle	brain
23	chr19:18632000-18633800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr19:18632000-18633800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
25	chr19:18632200-18633800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr19:18632200-18633800	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr19:18632200-18633800	Active TSS	Fetal Brain Female	brain
28	chr19:18632200-18634000	Active TSS	Brain Substantia Nigra	brain
29	chr19:18632800-18633800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
30	chr19:18632800-18633800	Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr19:18632800-18633800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr19:18632800-18633800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr19:18632800-18633800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr19:18632800-18633800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr19:18632800-18633800	Active TSS	Brain Germinal Matrix	brain
36	chr19:18632800-18641000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr19:18632800-18642200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr19:18632800-18642200	Weak transcription	Aorta	Aorta
39	chr19:18632800-18652200	Weak transcription	Fetal Heart	heart
40	chr19:18632800-18652800	Weak transcription	Stomach Mucosa	stomach
41	chr19:18632800-18654600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr19:18633000-18633800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr19:18633000-18637000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr19:18633000-18637200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr19:18633000-18638600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr19:18633000-18640400	Weak transcription	Right Ventricle	heart
47	chr19:18633000-18640400	Weak transcription	Spleen	Spleen
48	chr19:18633000-18642000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr19:18633000-18642000	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr19:18633000-18642000	Weak transcription	Lung	lung

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