Variant report

Variant	rs1615350
Chromosome Location	chr12:123650335-123650336
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 174 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:165)

rs_ID	r²[population]
rs1047158	0.83[EUR][1000 genomes]
rs1051431	0.84[ASW][hapmap];0.89[CEU][hapmap];0.92[GIH][hapmap];0.84[TSI][hapmap];0.84[EUR][1000 genomes]
rs1051434	0.81[CHB][hapmap];0.94[CHD][hapmap];0.84[JPT][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1060105	0.82[TSI][hapmap]
rs10732573	0.90[CEU][hapmap];1.00[YRI][hapmap]
rs10744150	1.00[YRI][hapmap];0.83[AMR][1000 genomes]
rs10744151	1.00[YRI][hapmap];0.81[AMR][1000 genomes]
rs10772993	0.84[EUR][1000 genomes]
rs10772997	0.86[AMR][1000 genomes]
rs10772998	0.89[CEU][hapmap]
rs10772999	0.80[EUR][1000 genomes]
rs10773002	0.83[ASW][hapmap];0.85[CEU][hapmap];0.86[MEX][hapmap];0.86[TSI][hapmap]
rs10773003	0.84[JPT][hapmap]
rs10773005	0.84[JPT][hapmap]
rs10773921	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[TSI][hapmap]
rs10846486	0.89[CEU][hapmap]
rs10846489	0.83[ASW][hapmap]
rs10848428	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs11057189	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11057192	0.84[CEU][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs11057202	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11057205	0.80[EUR][1000 genomes]
rs11057207	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11057209	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11057251	0.84[JPT][hapmap]
rs11057276	0.83[ASW][hapmap];0.84[JPT][hapmap]
rs1106240	0.89[CEU][hapmap];0.89[GIH][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes]
rs1106241	0.89[CEU][hapmap];0.89[GIH][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs1109559	0.83[ASW][hapmap]
rs11608305	0.84[JPT][hapmap]
rs11608811	0.83[CHB][hapmap];0.82[TSI][hapmap]
rs12298826	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs12316131	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs12317452	0.84[JPT][hapmap]
rs12322888	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs12366872	0.84[JPT][hapmap]
rs12425009	0.83[CHB][hapmap];0.82[TSI][hapmap]
rs1260294	0.84[CEU][hapmap]
rs12817892	0.84[CEU][hapmap]
rs1402274	0.89[CEU][hapmap];0.84[TSI][hapmap];0.81[EUR][1000 genomes]
rs1463877	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs1533703	0.82[CEU][hapmap]
rs1568427	0.83[ASW][hapmap];0.81[CEU][hapmap];0.82[MEX][hapmap];0.86[TSI][hapmap];1.00[YRI][hapmap]
rs1568428	0.83[ASW][hapmap]
rs1569068	0.89[CEU][hapmap];0.92[GIH][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs1609520	0.90[CEU][hapmap];0.89[TSI][hapmap]
rs1611973	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1616131	0.82[EUR][1000 genomes]
rs1616181	0.82[EUR][1000 genomes]
rs1617156	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs1617434	0.83[EUR][1000 genomes]
rs1618679	0.81[EUR][1000 genomes]
rs1621194	0.84[EUR][1000 genomes]
rs1627724	0.83[EUR][1000 genomes]
rs1716157	0.89[CEU][hapmap];0.84[TSI][hapmap]
rs1716160	0.89[CEU][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs1716164	0.89[CEU][hapmap];0.84[TSI][hapmap]
rs1716165	0.84[ASW][hapmap];0.89[CEU][hapmap];0.92[GIH][hapmap];0.84[TSI][hapmap];0.84[EUR][1000 genomes]
rs1716167	0.84[ASW][hapmap];0.89[CEU][hapmap];0.89[GIH][hapmap];0.80[LWK][hapmap];0.84[TSI][hapmap];0.84[EUR][1000 genomes]
rs1716168	0.84[ASW][hapmap];0.89[CEU][hapmap];0.89[GIH][hapmap];0.84[TSI][hapmap];0.84[EUR][1000 genomes]
rs1716170	0.89[CEU][hapmap];0.82[TSI][hapmap]
rs1716171	0.89[CEU][hapmap];0.82[TSI][hapmap]
rs1716175	0.89[CEU][hapmap]
rs1716176	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs1716177	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs1716184	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1716185	0.81[EUR][1000 genomes]
rs1727286	0.80[AMR][1000 genomes]
rs1727290	0.81[EUR][1000 genomes]
rs1727293	0.83[ASW][hapmap];0.91[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.85[TSI][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1727294	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs1727295	0.90[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs1727296	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs1727301	0.84[CHD][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs1727302	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1727305	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1727306	0.89[CEU][hapmap]
rs1727307	0.83[CHB][hapmap];0.81[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs1727309	0.89[CEU][hapmap]
rs1727312	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1727313	0.89[CEU][hapmap];0.89[GIH][hapmap];0.82[TSI][hapmap];0.83[EUR][1000 genomes]
rs1727314	0.82[EUR][1000 genomes]
rs1727315	0.84[ASW][hapmap];0.89[CEU][hapmap];0.92[GIH][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs1727316	0.82[EUR][1000 genomes]
rs1727319	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1727320	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs1727323	0.89[CEU][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs1727324	0.89[CEU][hapmap]
rs1727325	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs1727331	0.90[CEU][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap];0.87[AMR][1000 genomes]
rs1727332	0.87[AMR][1000 genomes]
rs1727334	0.81[CEU][hapmap]
rs1790089	0.81[EUR][1000 genomes]
rs1790090	0.83[EUR][1000 genomes]
rs1790094	0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs1790095	0.89[CEU][hapmap];0.84[TSI][hapmap];0.81[EUR][1000 genomes]
rs1790098	0.89[CEU][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs1790100	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs1790104	0.90[JPT][hapmap]
rs1790106	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs1790108	0.89[CEU][hapmap];0.89[GIH][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs1790109	0.83[EUR][1000 genomes]
rs1790116	0.84[CEU][hapmap];0.89[GIH][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes]
rs1790121	0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs1790123	0.89[CEU][hapmap];0.82[TSI][hapmap]
rs1790129	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1790130	0.81[EUR][1000 genomes]
rs1790131	0.89[CEU][hapmap];0.84[TSI][hapmap]
rs1879379	0.83[ASW][hapmap]
rs1879380	0.89[CEU][hapmap]
rs1969354	0.84[CEU][hapmap]
rs1980252	0.84[CEU][hapmap]
rs2049114	0.89[CEU][hapmap]
rs2102949	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2337934	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs2682427	0.84[CHD][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs2682429	0.83[EUR][1000 genomes]
rs2682431	0.80[EUR][1000 genomes]
rs2682434	0.89[CEU][hapmap];0.84[TSI][hapmap];0.80[EUR][1000 genomes]
rs2695478	0.89[CEU][hapmap];0.82[TSI][hapmap]
rs2695481	0.83[EUR][1000 genomes]
rs2695482	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs2851438	0.83[EUR][1000 genomes]
rs2851443	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2851447	1.00[CEU][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2851450	0.80[EUR][1000 genomes]
rs3018098	0.82[EUR][1000 genomes]
rs3088303	0.84[JPT][hapmap]
rs3759111	0.81[CHD][hapmap];0.84[JPT][hapmap]
rs3759113	0.81[CHD][hapmap];0.84[JPT][hapmap]
rs3759115	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[TSI][hapmap]
rs3897102	0.83[CHB][hapmap]
rs4148863	0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs4372492	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs4460848	0.92[ASW][hapmap];1.00[CEU][hapmap];0.81[CHD][hapmap];0.81[GIH][hapmap];0.84[JPT][hapmap];0.95[MEX][hapmap];0.92[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4759367	0.82[JPT][hapmap]
rs4759371	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs4759377	0.84[JPT][hapmap]
rs4759407	0.81[CHD][hapmap];0.84[JPT][hapmap]
rs4759409	0.84[CEU][hapmap]
rs4759415	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs520088	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs58991895	0.87[ASN][1000 genomes]
rs61041384	0.89[ASN][1000 genomes]
rs61187102	0.87[ASN][1000 genomes]
rs641760	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs655293	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs7135296	0.83[ASW][hapmap];0.83[CHB][hapmap];0.83[MEX][hapmap];0.82[TSI][hapmap]
rs7137286	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7296418	0.81[TSI][hapmap]
rs7304782	0.83[ASW][hapmap];0.90[CEU][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs7305511	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[TSI][hapmap]
rs7313483	0.89[CEU][hapmap]
rs7315453	0.84[JPT][hapmap]
rs7953929	0.89[CEU][hapmap]
rs7959415	0.84[JPT][hapmap]
rs7972811	0.84[JPT][hapmap]
rs883263	0.81[GIH][hapmap];0.81[TSI][hapmap]
rs884548	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs884956	0.83[ASW][hapmap]
rs937564	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs941305	0.89[CEU][hapmap]
rs941306	0.89[CEU][hapmap]
rs949142	0.83[EUR][1000 genomes]
rs949143	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3388790	chr12:123275902-123655103	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv517200	chr12:123312051-123654498	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv427924	chr12:123412172-123722059	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
4	nsv1042550	chr12:123532028-123659500	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer 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 target site	18 gene(s)	inside rSNPs	diseases
5	esv1825473	chr12:123582855-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS 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 target site	73 gene(s)	inside rSNPs	diseases
6	nsv870326	chr12:123585990-123719323	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
7	esv2761773	chr12:123616003-123723460	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	esv1803368	chr12:123640853-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
9	esv1830566	chr12:123640853-123822503	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs1615350	PITPNM2	cis	cerebellum	SCAN
rs1615350	CDK2AP1	cis	Esophagus Mucosa	GTEx
rs1615350	ARL6IP4	Cis_1M	lymphoblastoid	RTeQTL
rs1615350	MPHOSPH9	Cis_1M	lymphoblastoid	RTeQTL
rs1615350	CCDC92	cis	cerebellum	SCAN
rs1615350	ANAPC5	cis	parietal	SCAN
rs1615350	SBNO1	Cis_1M	lymphoblastoid	RTeQTL
rs1615350	RP11-282O18.3	cis	Esophagus Mucosa	GTEx
rs1615350	ABCB9	cis	Heart Left Ventricle	GTEx
rs1615350	CDK2AP1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123636600-123660800	Weak transcription	Colon Smooth Muscle	Colon
2	chr12:123636600-123676200	Weak transcription	Gastric	stomach
3	chr12:123636600-123716600	Weak transcription	Esophagus	oesophagus
4	chr12:123636800-123675200	Weak transcription	Fetal Heart	heart
5	chr12:123636800-123679600	Weak transcription	Colonic Mucosa	Colon
6	chr12:123636800-123687400	Weak transcription	Psoas Muscle	Psoas
7	chr12:123637000-123673400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr12:123637000-123713000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:123637200-123716400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr12:123638000-123652400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:123638000-123652800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr12:123638200-123652400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr12:123638200-123652800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:123638600-123650400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr12:123638600-123687200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr12:123638800-123685000	Strong transcription	Fetal Thymus	thymus
17	chr12:123640200-123652800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr12:123640400-123676000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr12:123640600-123657800	Weak transcription	NHLF	lung
20	chr12:123643000-123651800	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr12:123643000-123652800	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr12:123643000-123652800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr12:123643000-123652800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:123643200-123651800	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr12:123643200-123652000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:123643200-123652600	Strong transcription	Fetal Muscle Leg	muscle
27	chr12:123643400-123651800	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr12:123643400-123652400	Strong transcription	Fetal Muscle Trunk	muscle
29	chr12:123643600-123651600	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr12:123643600-123652600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr12:123643800-123652400	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr12:123643800-123652600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr12:123644000-123650800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr12:123644000-123651600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr12:123644000-123652400	Strong transcription	Primary hematopoietic stem cells	blood
36	chr12:123644000-123652800	Strong transcription	Dnd41	blood
37	chr12:123644200-123650600	Strong transcription	HSMM	muscle
38	chr12:123644600-123653000	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr12:123644800-123651800	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr12:123645000-123650800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:123645000-123651400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
42	chr12:123645000-123652800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr12:123645200-123651200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr12:123645200-123651600	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr12:123645200-123652200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr12:123645400-123660000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:123645600-123660800	Weak transcription	Fetal Brain Male	brain
48	chr12:123646000-123651000	Weak transcription	NHDF-Ad	bronchial
49	chr12:123646200-123650600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:123646600-123651200	Strong transcription	NH-A	brain

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