Variant report

Variant	rs10875745
Chromosome Location	chr12:48515405-48515406
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48515382-48515432	NHDF-neo	bronchial:	n/a
2	chr12:48515382-48515432	HCM	heart:	n/a
3	chr12:48515382-48515432	MCF-7	breast:	n/a
4	chr12:48515382-48515432	SK-N-SH_RA	brain:	n/a
5	chr12:48515382-48515432	ProgFib	skin:	n/a
6	chr12:48515382-48515432	GM12892	blood:	n/a
7	chr12:48515382-48515432	AoSMC	blood vessel:	n/a
8	chr12:48515382-48515432	Hepatocyte	liver:	n/a
9	chr12:48515382-48515432	NT2-D1	testis:	n/a
10	chr12:48515382-48515432	A549	lung:	n/a
11	chr12:48515382-48515432	NB4	blood:	n/a
12	chr12:48515382-48515432	MCF10A-Er-Src	breast:	n/a
13	chr12:48515382-48515432	HEEpiC	esophagus:	n/a
14	chr12:48515382-48515432	HL-60	blood:	n/a
15	chr12:48515382-48515432	LNCaP	prostate:	n/a
16	chr12:48515382-48515432	BE2_C	brain:	n/a
17	chr12:48515382-48515432	AG04450	lung:	fetal
18	chr12:48515382-48515432	AG09319	gingival:	n/a
19	chr12:48515382-48515432	SK-N-MC	brain:	n/a
20	chr12:48515382-48515432	H1-hESC	embryonic stem cell:	embryo
21	chr12:48515382-48515432	HCT-116	colon:	n/a
22	chr12:48515382-48515432	AG10803	skin:	n/a
23	chr12:48515382-48515432	AG09309	skin:	n/a
24	chr12:48515382-48515432	HRCEpiC	kidney:	n/a
25	chr12:48515382-48515432	SK-N-SH	brain:	n/a
26	chr12:48515382-48515432	PFSK-1	brain:	n/a
27	chr12:48515382-48515432	NH-A	brain:	n/a
28	chr12:48515382-48515432	HIPEpiC	eye:	n/a
29	chr12:48515382-48515432	HAEpiC	amniotic membrane:	n/a
30	chr12:48515382-48515432	HNPCEpiC	eye:	n/a
31	chr12:48515382-48515432	CMK	blood:	n/a
32	chr12:48515382-48515432	HCPEpiC	choroid plexus:	n/a
33	chr12:48515382-48515432	GM19239	blood:	n/a
34	chr12:48515382-48515432	HepG2	liver:	n/a
35	chr12:48515382-48515432	HEK293	kidney:	embryo
36	chr12:48515382-48515432	NHBE	bronchial:	n/a
37	chr12:48515382-48515432	K562	blood:	n/a
38	chr12:48515382-48515432	BJ	skin:	n/a
39	chr12:48515382-48515432	AG04449	skin:	fetal
40	chr12:48515382-48515432	HUVEC	blood vessel:	n/a
41	chr12:48515382-48515432	Jurkat	blood:	n/a
42	chr12:48515382-48515432	ECC-1	luminal epithelium:	n/a
43	chr12:48515382-48515432	HMEC	breast:	n/a
44	chr12:48515382-48515432	GM12891	blood:	n/a
45	chr12:48515382-48515432	GM06990	blood:	n/a
46	chr12:48515382-48515432	PrEC	prostate:	n/a
47	chr12:48515382-48515432	U87	brain:	n/a
48	chr12:48515382-48515432	RPTEC	kidney:	n/a
49	chr12:48515382-48515432	T-47D	breast:	n/a
50	chr12:48515382-48515432	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:48498567..48501846-chr12:48512929..48518601,8	MCF-7	breast:

No data

Variant related genes	Relation type
PFKM	CpG island
ENSG00000079387	Chromatin interaction
ENSG00000152556	Chromatin interaction

Extended variants
information (count: 113 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs10082861	0.86[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10219623	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10219645	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10467101	0.88[CHB][hapmap];0.84[JPT][hapmap]
rs10875724	0.93[JPT][hapmap]
rs10875725	0.96[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.91[TSI][hapmap]
rs10875732	1.00[JPT][hapmap]
rs10875735	0.85[AMR][1000 genomes]
rs10875736	0.82[AMR][1000 genomes]
rs10875737	0.85[AMR][1000 genomes]
rs10875738	0.85[AMR][1000 genomes]
rs10875740	0.85[AMR][1000 genomes]
rs10875746	0.94[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10875747	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10875748	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10875750	1.00[CHB][hapmap];0.97[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10875756	0.90[ASN][1000 genomes]
rs10875762	0.81[ASN][1000 genomes]
rs10875767	0.88[CHB][hapmap];0.93[JPT][hapmap]
rs10875770	0.89[CHB][hapmap];0.88[CHD][hapmap];0.93[JPT][hapmap]
rs10875772	0.89[CHB][hapmap];0.88[CHD][hapmap];0.93[JPT][hapmap]
rs10875792	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs10875793	0.82[CHB][hapmap];0.92[JPT][hapmap]
rs11168355	0.88[GIH][hapmap]
rs11168357	0.85[GIH][hapmap];0.93[JPT][hapmap];0.84[MKK][hapmap]
rs11168369	1.00[JPT][hapmap]
rs11168371	0.88[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];1.00[MKK][hapmap]
rs11168383	0.85[AMR][1000 genomes]
rs11168386	0.83[AMR][1000 genomes]
rs11168401	0.85[AMR][1000 genomes]
rs11168403	1.00[JPT][hapmap];0.85[AMR][1000 genomes]
rs11168413	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11168414	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.89[MKK][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11168415	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11168416	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11168418	0.80[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.89[MKK][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11168420	0.94[CHB][hapmap];0.97[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.89[MKK][hapmap];0.93[ASN][1000 genomes]
rs11168421	0.87[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.97[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11168422	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11168425	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.94[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11168427	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.89[MKK][hapmap];0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11168433	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11168450	0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs11168459	0.89[CHB][hapmap];0.88[CHD][hapmap];0.93[JPT][hapmap]
rs11168516	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs11558768	0.82[ASN][1000 genomes]
rs12297004	0.85[AMR][1000 genomes]
rs12297470	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12301339	0.85[AMR][1000 genomes]
rs12304476	0.82[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.98[MKK][hapmap];0.85[AMR][1000 genomes]
rs12305182	0.93[JPT][hapmap]
rs12305511	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs12306290	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12306451	0.85[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.85[AMR][1000 genomes]
rs12310813	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12311774	0.85[AMR][1000 genomes]
rs12311953	0.85[AMR][1000 genomes]
rs12312134	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12313300	0.85[AMR][1000 genomes]
rs12313404	0.83[AMR][1000 genomes]
rs12315625	0.85[AMR][1000 genomes]
rs17122620	0.85[AMR][1000 genomes]
rs17122666	0.94[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.86[MKK][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs17122812	0.89[CHB][hapmap];0.93[JPT][hapmap]
rs1859445	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2012773	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs2079295	0.93[JPT][hapmap]
rs2107638	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2158516	0.85[AMR][1000 genomes]
rs2228500	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.89[MKK][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2269933	0.83[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2269935	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2269936	1.00[JPT][hapmap]
rs2279464	0.82[CHB][hapmap];0.87[JPT][hapmap]
rs2286021	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3782910	1.00[JPT][hapmap];0.85[AMR][1000 genomes]
rs3782911	0.85[AMR][1000 genomes]
rs4760609	0.88[GIH][hapmap];0.93[JPT][hapmap]
rs4760619	0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4760622	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs4760680	0.85[AMR][1000 genomes]
rs4760681	0.80[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.89[MKK][hapmap];0.92[YRI][hapmap];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4760684	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4760687	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4760689	0.90[ASN][1000 genomes]
rs4760690	0.90[ASN][1000 genomes]
rs4760695	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs4760696	0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs4760697	0.94[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs58952582	0.85[AMR][1000 genomes]
rs60106007	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60761335	0.85[AMR][1000 genomes]
rs61343568	0.91[ASN][1000 genomes]
rs61918806	0.85[AMR][1000 genomes]
rs61918809	0.80[AMR][1000 genomes]
rs61918810	0.85[AMR][1000 genomes]
rs6580659	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs7135779	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs719008	0.93[JPT][hapmap]
rs725454	0.80[ASW][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.89[MKK][hapmap];0.93[YRI][hapmap];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7299135	0.93[JPT][hapmap]
rs7299271	0.93[JPT][hapmap]
rs73102065	0.85[AMR][1000 genomes]
rs73102067	0.82[AMR][1000 genomes]
rs7485355	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7486424	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8804	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.89[MKK][hapmap];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs886588	0.85[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];0.85[AMR][1000 genomes]
rs9634261	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs989144	1.00[JPT][hapmap];0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh 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 miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv508673	chr12:48489786-48567138	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs10875745	FAM186B	cis	parietal	SCAN
rs10875745	RPAP3	cis	cerebellum	SCAN
rs10875745	LMBR1L	cis	cerebellum	SCAN
rs10875745	RP1-228P16.1	cis	Skin Sun Exposed Lower leg	GTEx
rs10875745	RP1-228P16.1	cis	Thyroid	GTEx
rs10875745	ASB8	cis	cerebellum	SCAN
rs10875745	SENP1	cis	parietal	SCAN
rs10875745	RP1-228P16.1	cis	Artery Tibial	GTEx
rs10875745	C12orf41	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48512600-48516400	Active TSS	Right Atrium	heart
2	chr12:48512800-48515800	Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr12:48513400-48524800	Weak transcription	Liver	Liver
4	chr12:48513400-48526600	Weak transcription	Spleen	Spleen
5	chr12:48513600-48516000	Weak transcription	Small Intestine	intestine
6	chr12:48513600-48516400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:48513600-48526400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr12:48513600-48527000	Weak transcription	Pancreas	Pancrea
9	chr12:48513800-48516200	Weak transcription	Stomach Mucosa	stomach
10	chr12:48513800-48516600	Weak transcription	Fetal Thymus	thymus
11	chr12:48513800-48519400	Weak transcription	Primary T cells from cord blood	blood
12	chr12:48513800-48524400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr12:48513800-48525000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr12:48513800-48525000	Weak transcription	Lung	lung
15	chr12:48513800-48525800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr12:48513800-48526000	Weak transcription	Colonic Mucosa	Colon
17	chr12:48513800-48526400	Weak transcription	Gastric	stomach
18	chr12:48513800-48526600	Weak transcription	Thymus	Thymus
19	chr12:48513800-48526800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:48514000-48516000	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr12:48514000-48516200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr12:48514000-48516200	Weak transcription	Fetal Intestine Large	intestine
23	chr12:48514000-48516400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:48514000-48516400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:48514000-48516400	Weak transcription	Fetal Muscle Trunk	muscle
26	chr12:48514000-48516400	Weak transcription	Fetal Stomach	stomach
27	chr12:48514000-48516800	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr12:48514000-48516800	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr12:48514000-48518600	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr12:48514000-48520200	Weak transcription	Fetal Lung	lung
31	chr12:48514000-48520600	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr12:48514000-48521200	Weak transcription	Primary B cells from cord blood	blood
33	chr12:48514000-48522000	Weak transcription	Primary hematopoietic stem cells	blood
34	chr12:48514000-48522200	Weak transcription	Adipose Nuclei	Adipose
35	chr12:48514000-48523200	Weak transcription	Fetal Kidney	kidney
36	chr12:48514000-48524200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr12:48514000-48524200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr12:48514000-48524600	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr12:48514000-48525000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr12:48514000-48525000	Weak transcription	Brain Substantia Nigra	brain
41	chr12:48514000-48525000	Weak transcription	Esophagus	oesophagus
42	chr12:48514000-48525600	Weak transcription	Placenta	Placenta
43	chr12:48514000-48526400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr12:48514000-48526600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:48514000-48526600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr12:48514000-48536600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr12:48514000-48537200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr12:48514200-48515800	Weak transcription	NHDF-Ad	bronchial
49	chr12:48514200-48516200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr12:48514200-48516200	Enhancers	Brain Anterior Caudate	brain

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