Variant report

Variant	rs4633785
Chromosome Location	chr18:12698606-12698607
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	MYC	chr18:12698382-12698751	MCF10A-Er-Src	breast:	n/a	n/a
2	MYC	chr18:12698359-12698720	MCF10A-Er-Src	breast:	n/a	n/a
3	FOS	chr18:12698343-12698854	MCF10A-Er-Src	breast:	n/a	n/a
4	STAT3	chr18:12698347-12698717	MCF10A-Er-Src	breast:	n/a	n/a
5	FOS	chr18:12698399-12698742	MCF10A-Er-Src	breast:	n/a	n/a
6	JUND	chr18:12698485-12698645	HepG2	liver:	n/a	chr18:12698577-12698588
7	STAT3	chr18:12698361-12698717	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr18:12698395-12698772	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr18:12698352-12698765	MCF10A-Er-Src	breast:	n/a	n/a
10	STAT3	chr18:12698479-12698630	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:12696763..12699239-chr18:12701108..12704411,4	MCF-7	breast:
2	chr18:12685127..12688617-chr18:12697968..12702228,5	MCF-7	breast:

Variant related genes	Relation type
PSMG2	TF binding region
CEP76	TF binding region
ENSG00000101624	Chromatin interaction
ENSG00000128789	Chromatin interaction

Extended variants
information (count: 142 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:131)

rs_ID	r²[population]
rs1062235	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11080585	0.92[YRI][hapmap]
rs11080590	0.92[YRI][hapmap]
rs11080592	0.82[ASN][1000 genomes]
rs1129214	0.89[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11663958	1.00[YRI][hapmap]
rs12373207	0.94[CHB][hapmap];0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs12373259	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12455268	0.92[ASN][1000 genomes]
rs12455295	0.92[ASN][1000 genomes]
rs12457026	0.94[CHB][hapmap];0.93[JPT][hapmap]
rs12457771	0.94[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs12458097	0.92[ASN][1000 genomes]
rs12458895	0.91[ASN][1000 genomes]
rs12604184	1.00[YRI][hapmap]
rs12954079	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12957555	0.92[ASN][1000 genomes]
rs12957603	0.92[ASN][1000 genomes]
rs12957810	0.92[ASN][1000 genomes]
rs12960623	1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12960997	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12962598	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12963505	0.92[ASN][1000 genomes]
rs12964507	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12965733	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12965990	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12966246	0.88[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12966367	0.92[ASN][1000 genomes]
rs12966424	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12968771	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12969300	0.92[ASN][1000 genomes]
rs12969446	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12969567	1.00[YRI][hapmap]
rs12969938	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12971256	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1362709	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1549011	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1592642	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs1592643	0.94[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17616402	1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs1940975	0.92[YRI][hapmap]
rs1971702	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2011575	0.92[ASN][1000 genomes]
rs2011579	0.92[ASN][1000 genomes]
rs2051262	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2186907	0.92[YRI][hapmap]
rs2302768	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28820339	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28832066	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34040888	0.89[ASN][1000 genomes]
rs34120824	0.92[ASN][1000 genomes]
rs34277169	0.92[ASN][1000 genomes]
rs34537593	0.89[ASN][1000 genomes]
rs34632667	0.91[ASN][1000 genomes]
rs34847769	0.91[ASN][1000 genomes]
rs35322088	0.91[ASN][1000 genomes]
rs35506854	0.92[ASN][1000 genomes]
rs35634465	0.85[ASN][1000 genomes]
rs35699948	0.92[ASN][1000 genomes]
rs35898717	0.89[ASN][1000 genomes]
rs3809919	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3902981	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4073592	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4296322	0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs45589535	0.92[ASN][1000 genomes]
rs45596833	0.92[ASN][1000 genomes]
rs55870255	0.92[ASN][1000 genomes]
rs62095975	0.92[ASN][1000 genomes]
rs62096023	0.92[ASN][1000 genomes]
rs62096046	0.89[ASN][1000 genomes]
rs62096048	0.86[ASN][1000 genomes]
rs6505760	0.94[CHB][hapmap];0.93[JPT][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs66808227	0.92[ASN][1000 genomes]
rs7229168	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs7233175	1.00[CHB][hapmap];0.93[JPT][hapmap];0.91[ASN][1000 genomes]
rs7233694	0.92[ASN][1000 genomes]
rs7237732	0.92[YRI][hapmap]
rs723836	0.83[YRI][hapmap]
rs7507018	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs755021	0.92[YRI][hapmap]
rs8083182	0.92[ASN][1000 genomes]
rs8083217	0.88[ASN][1000 genomes]
rs8086094	0.92[YRI][hapmap]
rs8086099	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs8086265	0.92[ASN][1000 genomes]
rs8093532	0.96[YRI][hapmap]
rs8095160	1.00[YRI][hapmap]
rs8097134	0.94[ASN][1000 genomes]
rs9303772	0.92[YRI][hapmap]
rs9303773	0.92[YRI][hapmap]
rs9303774	1.00[CHB][hapmap];0.93[JPT][hapmap];0.99[ASN][1000 genomes]
rs9303775	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9303776	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs933600	0.92[ASN][1000 genomes]
rs948301	1.00[YRI][hapmap]
rs948302	0.92[YRI][hapmap]
rs948319	0.88[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs963920	0.91[ASN][1000 genomes]
rs9675543	0.92[YRI][hapmap]
rs9945140	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9945644	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9945801	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9948844	0.90[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs9949293	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9949582	0.92[YRI][hapmap]
rs9950365	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9951576	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9952000	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9954054	0.91[YRI][hapmap]
rs9954112	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9955985	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9957880	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9958100	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9958412	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9958666	0.92[YRI][hapmap]
rs9959039	0.92[ASN][1000 genomes]
rs9959458	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9959536	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9959611	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9960555	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9960824	0.92[YRI][hapmap]
rs9961799	0.94[CHB][hapmap];0.93[JPT][hapmap];0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs9962006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9963809	0.94[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs9964868	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9966464	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9966490	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9966672	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9967437	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9967553	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9989506	0.92[YRI][hapmap]

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	nsv1063125	chr18:12046892-12918251	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
2	nsv491873	chr18:12159445-12739784	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
3	esv3528039	chr18:12396582-12851293	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	esv3528041	chr18:12396641-12851245	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
5	nsv523743	chr18:12474505-12742809	Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	esv1820040	chr18:12635601-12725236	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	esv1817845	chr18:12635601-12733705	Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
8	esv1821625	chr18:12635601-12733705	Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	nsv1062014	chr18:12687210-13183383	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
10	nsv543655	chr18:12687210-13183383	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
11	nsv1064273	chr18:12697601-12828251	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4633785	SPIRE1	cis	Muscle Skeletal	GTEx
rs4633785	CEP76	cis	Stomach	GTEx

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:12658800-12701800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr18:12659000-12700200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr18:12660400-12700800	Weak transcription	Fetal Brain Male	brain
4	chr18:12662800-12701600	Weak transcription	Aorta	Aorta
5	chr18:12667000-12701600	Weak transcription	Gastric	stomach
6	chr18:12672200-12701400	Weak transcription	Colonic Mucosa	Colon
7	chr18:12673200-12701600	Weak transcription	Psoas Muscle	Psoas
8	chr18:12674600-12701600	Weak transcription	Right Ventricle	heart
9	chr18:12674600-12701600	Weak transcription	Small Intestine	intestine
10	chr18:12674800-12700600	Weak transcription	Brain Substantia Nigra	brain
11	chr18:12674800-12701400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr18:12678200-12701400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr18:12678400-12701200	Weak transcription	NH-A	brain
14	chr18:12678400-12701600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr18:12678400-12701600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr18:12678400-12701600	Weak transcription	HSMMtube	muscle
17	chr18:12679600-12700400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr18:12679600-12700400	Weak transcription	Colon Smooth Muscle	Colon
19	chr18:12679600-12700600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr18:12679600-12701000	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr18:12679600-12701000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr18:12679600-12701200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr18:12679600-12701600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr18:12679800-12698800	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr18:12679800-12701000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr18:12679800-12701000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr18:12679800-12701000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr18:12680000-12698800	Weak transcription	NHDF-Ad	bronchial
29	chr18:12680000-12701200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr18:12680000-12701600	Weak transcription	Esophagus	oesophagus
31	chr18:12680000-12701600	Weak transcription	Ovary	ovary
32	chr18:12680200-12700800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr18:12680800-12701400	Weak transcription	Primary B cells from peripheral blood	blood
34	chr18:12684800-12701600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr18:12685200-12701600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr18:12685400-12701400	Weak transcription	Fetal Intestine Small	intestine
37	chr18:12685600-12701400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr18:12686400-12701000	Weak transcription	Brain Hippocampus Middle	brain
39	chr18:12686800-12700800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr18:12686800-12701600	Weak transcription	Lung	lung
41	chr18:12687200-12701000	Weak transcription	Primary B cells from cord blood	blood
42	chr18:12687200-12701200	Weak transcription	Stomach Smooth Muscle	stomach
43	chr18:12687400-12701000	Weak transcription	Fetal Lung	lung
44	chr18:12688400-12701400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr18:12688800-12700000	Strong transcription	Fetal Thymus	thymus
46	chr18:12690600-12701000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr18:12691000-12700800	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr18:12692200-12700000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr18:12692400-12699400	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr18:12692400-12699800	Strong transcription	Osteobl	bone

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