Variant report

Variant	rs7792762
Chromosome Location	chr7:66004138-66004139
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 150 )
Associated
traits (count: 24 )

rSNPs within LD-proxies of this variant (count:139)

rs_ID	r²[population]
rs10107	0.89[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes]
rs1016265	0.83[EUR][1000 genomes]
rs10233806	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10244498	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10278014	0.88[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.92[LWK][hapmap];0.83[MEX][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap]
rs10281499	0.83[CHB][hapmap];0.94[YRI][hapmap]
rs10755833	0.81[EUR][1000 genomes]
rs10950041	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10950043	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs11765965	0.95[CEU][hapmap]
rs11769079	0.86[YRI][hapmap]
rs12532998	1.00[CEU][hapmap];0.91[GIH][hapmap];0.87[MEX][hapmap];0.89[MKK][hapmap];0.95[TSI][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12533997	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12535036	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12668936	0.81[EUR][1000 genomes]
rs12673450	0.89[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes]
rs12673810	0.82[EUR][1000 genomes]
rs12698520	1.00[CEU][hapmap];0.91[MEX][hapmap];0.88[MKK][hapmap];0.82[EUR][1000 genomes]
rs12698522	0.82[AMR][1000 genomes]
rs12698523	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12698526	0.82[AMR][1000 genomes]
rs12698532	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13226170	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13227219	0.87[CEU][hapmap]
rs13232191	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13240501	0.83[AFR][1000 genomes]
rs13308803	0.87[CEU][hapmap];0.86[CHB][hapmap];0.94[YRI][hapmap]
rs13309022	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13536	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.92[LWK][hapmap];0.82[MEX][hapmap];0.81[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap];0.85[AFR][1000 genomes]
rs1363055	0.84[EUR][1000 genomes]
rs1544549	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1695820	0.92[CEU][hapmap];0.88[YRI][hapmap]
rs17747530	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1807064	0.81[EUR][1000 genomes]
rs1833495	0.82[EUR][1000 genomes]
rs1860469	0.92[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap]
rs1968225	1.00[CEU][hapmap]
rs1974769	0.83[EUR][1000 genomes]
rs1981798	0.80[EUR][1000 genomes]
rs1981799	0.80[EUR][1000 genomes]
rs2003300	0.83[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2013908	0.89[CEU][hapmap];0.93[YRI][hapmap]
rs2024192	0.81[AFR][1000 genomes]
rs2042133	0.83[EUR][1000 genomes]
rs2077593	1.00[CEU][hapmap]
rs2088653	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.88[LWK][hapmap];0.83[MEX][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap]
rs2109295	0.80[AMR][1000 genomes]
rs2109297	0.89[CEU][hapmap];0.83[CHB][hapmap];0.85[GIH][hapmap];0.92[LWK][hapmap];0.81[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap]
rs2161065	0.83[EUR][1000 genomes]
rs2277911	0.83[EUR][1000 genomes]
rs2420591	0.81[EUR][1000 genomes]
rs2420599	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2420610	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2420611	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs2420820	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2659892	0.83[CEU][hapmap]
rs2659893	0.88[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap]
rs2659894	0.86[EUR][1000 genomes]
rs2659895	0.87[EUR][1000 genomes]
rs2659897	0.87[EUR][1000 genomes]
rs2659900	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2659904	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2659914	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2707824	0.89[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap]
rs2707839	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28714531	0.83[AMR][1000 genomes]
rs28731376	0.83[AFR][1000 genomes]
rs34406470	0.82[EUR][1000 genomes]
rs35149210	0.83[EUR][1000 genomes]
rs35378740	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs3735148	1.00[CEU][hapmap];0.91[GIH][hapmap];0.87[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3764903	0.80[MKK][hapmap]
rs3846973	0.89[CEU][hapmap];0.83[CHB][hapmap];0.85[GIH][hapmap];0.92[LWK][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap]
rs3857687	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3981131	0.83[EUR][1000 genomes]
rs4717299	0.84[EUR][1000 genomes]
rs4717300	0.82[EUR][1000 genomes]
rs4718349	0.80[EUR][1000 genomes]
rs4718357	0.85[EUR][1000 genomes]
rs4718358	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4718383	0.89[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap]
rs60193905	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6460292	1.00[CEU][hapmap];0.89[GIH][hapmap];0.84[MEX][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap]
rs6460293	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.85[LWK][hapmap];0.83[MEX][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap]
rs6460296	1.00[CEU][hapmap]
rs6460300	0.84[EUR][1000 genomes]
rs6460302	0.89[CEU][hapmap];0.88[YRI][hapmap]
rs6460303	0.83[AMR][1000 genomes]
rs6460304	0.89[CEU][hapmap];0.88[YRI][hapmap]
rs6460307	0.89[CEU][hapmap];0.87[GIH][hapmap];0.92[LWK][hapmap];0.83[MEX][hapmap];0.82[MKK][hapmap];0.91[TSI][hapmap];0.94[YRI][hapmap]
rs6945019	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs6945032	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs6947339	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.92[LWK][hapmap];0.83[MEX][hapmap];0.82[MKK][hapmap];0.89[TSI][hapmap];0.88[YRI][hapmap]
rs6950137	0.89[CEU][hapmap];0.94[YRI][hapmap]
rs6951302	0.86[CEU][hapmap];0.80[CHB][hapmap];0.93[YRI][hapmap]
rs6955837	0.89[CEU][hapmap];0.83[CHB][hapmap];0.94[YRI][hapmap];0.81[AFR][1000 genomes]
rs6956179	1.00[CEU][hapmap];0.89[GIH][hapmap];0.80[MEX][hapmap];0.95[TSI][hapmap]
rs6957199	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6958200	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6958271	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6958277	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6959268	0.89[CEU][hapmap];0.85[GIH][hapmap];0.85[LWK][hapmap];0.89[TSI][hapmap];0.89[YRI][hapmap]
rs6961155	0.84[EUR][1000 genomes]
rs6961990	0.81[AFR][1000 genomes]
rs6962717	0.89[CEU][hapmap];0.88[YRI][hapmap]
rs6969679	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6970030	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6970357	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6970860	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6976714	0.88[LWK][hapmap];0.82[YRI][hapmap]
rs6978429	0.83[EUR][1000 genomes]
rs709595	1.00[CEU][hapmap]
rs7781061	0.82[EUR][1000 genomes]
rs7782704	0.88[CEU][hapmap];0.89[YRI][hapmap]
rs7783613	0.92[ASW][hapmap];1.00[CEU][hapmap];0.95[GIH][hapmap];0.86[LWK][hapmap];0.84[MEX][hapmap];0.89[MKK][hapmap];0.98[TSI][hapmap];0.89[YRI][hapmap]
rs778697	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.92[LWK][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap];0.88[YRI][hapmap]
rs778702	0.88[CEU][hapmap]
rs778706	1.00[CEU][hapmap]
rs778711	0.89[CEU][hapmap];0.88[YRI][hapmap]
rs778720	0.87[CEU][hapmap];0.92[YRI][hapmap]
rs778722	1.00[CEU][hapmap]
rs778734	0.92[CEU][hapmap];0.89[YRI][hapmap]
rs778736	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.85[LWK][hapmap];0.83[MEX][hapmap];0.80[MKK][hapmap];0.91[TSI][hapmap];0.88[YRI][hapmap]
rs7788984	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7789554	0.83[EUR][1000 genomes]
rs7789768	1.00[CEU][hapmap];0.89[GIH][hapmap];0.87[MEX][hapmap];0.89[MKK][hapmap];0.95[TSI][hapmap];0.84[EUR][1000 genomes]
rs7803416	0.83[EUR][1000 genomes]
rs801194	0.82[AFR][1000 genomes]
rs801195	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.89[LWK][hapmap];0.83[MEX][hapmap];0.81[MKK][hapmap];0.91[TSI][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes]
rs801202	0.85[AFR][1000 genomes]
rs801203	0.85[AFR][1000 genomes]
rs801204	0.92[CEU][hapmap];0.83[CHB][hapmap];0.93[YRI][hapmap]
rs801206	0.85[AFR][1000 genomes]
rs801208	0.84[AFR][1000 genomes]
rs801209	0.85[AFR][1000 genomes]
rs9691480	0.84[EUR][1000 genomes]
rs974239	0.85[EUR][1000 genomes]
rs9791713	0.89[CEU][hapmap];0.83[CHB][hapmap];0.85[GIH][hapmap];0.92[LWK][hapmap];0.82[MEX][hapmap];0.83[MKK][hapmap];0.88[TSI][hapmap];0.94[YRI][hapmap]
rs9791895	0.82[EUR][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	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
2	nsv1026559	chr7:65617368-66370805	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
3	nsv1035107	chr7:65814901-66114919	Genic enhancers Strong transcription ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
4	nsv538909	chr7:65814901-66114919	Strong transcription Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
5	nsv888326	chr7:65825257-66066999	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS 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	41 gene(s)	inside rSNPs	diseases
6	nsv482441	chr7:65885824-66061788	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
7	esv3447484	chr7:65909457-66033145	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	esv3377926	chr7:65934493-66051484	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
9	nsv888327	chr7:65938980-66029429	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
10	esv3423847	chr7:65941210-66054107	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
11	nsv967444	chr7:65992587-66013934	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:24)

SNP	Gene	Cis/trans	Tissue	Source
rs7792762	RP4-756H11.3	cis	Heart Left Ventricle	GTEx
rs7792762	RP4-756H11.3	cis	Esophagus Mucosa	GTEx
rs7792762	GS1-124K5.4	cis	Whole Blood	GTEx
rs7792762	RNU6-96P	cis	Thyroid	GTEx
rs7792762	TPST1	cis	lymphoblastoid	seeQTL
rs7792762	RP4-756H11.3	cis	Skin Sun Exposed Lower leg	GTEx
rs7792762	RP4-756H11.3	cis	Artery Tibial	GTEx
rs7792762	RP4-756H11.3	cis	Esophagus Muscularis	GTEx
rs7792762	RP4-756H11.3	cis	Muscle Skeletal	GTEx
rs7792762	ASL	cis	cerebellum	SCAN
rs7792762	GTF2IRD1P1	cis	Thyroid	GTEx
rs7792762	RP4-756H11.3	cis	lung	GTEx
rs7792762	GS1-124K5.11	cis	Thyroid	GTEx
rs7792762	RP4-756H11.3	cis	Artery Aorta	GTEx
rs7792762	ASL	Cis_1M	lymphoblastoid	RTeQTL
rs7792762	RABGEF1	cis	parietal	SCAN
rs7792762	GUSB	cis	parietal	SCAN
rs7792762	RP4-756H11.3	cis	Nerve Tibial	GTEx
rs7792762	RP4-756H11.3	cis	Adipose Subcutaneous	GTEx
rs7792762	RP4-756H11.3	cis	Thyroid	GTEx
rs7792762	KCTD7	cis	parietal	SCAN
rs7792762	GS1-124K5.4	cis	Stomach	GTEx
rs7792762	GS1-124K5.4	cis	Artery Aorta	GTEx
rs7792762	CRCP	cis	cerebellum	SCAN

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65983400-66006000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:65985800-66006200	Weak transcription	Pancreas	Pancrea
3	chr7:65987800-66006200	Weak transcription	Gastric	stomach
4	chr7:65988400-66006200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:65988600-66006200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr7:65988600-66009000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:65988600-66009000	Weak transcription	HSMMtube	muscle
8	chr7:65988800-66008200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr7:65989000-66006200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:65989000-66007600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:65989800-66004200	Weak transcription	Dnd41	blood
12	chr7:65990000-66009000	Weak transcription	Rectal Smooth Muscle	rectum
13	chr7:65990600-66005600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:65991200-66009800	Weak transcription	Small Intestine	intestine
15	chr7:65991400-66006200	Weak transcription	Primary B cells from cord blood	blood
16	chr7:65991400-66006200	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr7:65991600-66006200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:65991800-66007600	Weak transcription	NH-A	brain
19	chr7:65992000-66005000	Weak transcription	Left Ventricle	heart
20	chr7:65992400-66006200	Weak transcription	Osteobl	bone
21	chr7:65993000-66006200	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr7:65993400-66006200	Weak transcription	Colonic Mucosa	Colon
23	chr7:65993600-66006200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr7:65993600-66009000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr7:65993600-66009400	Weak transcription	HSMM	muscle
26	chr7:65993800-66006200	Weak transcription	NHEK	skin
27	chr7:65994000-66006200	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr7:65994000-66008400	Weak transcription	Primary B cells from peripheral blood	blood
29	chr7:65994000-66014400	Weak transcription	Colon Smooth Muscle	Colon
30	chr7:65995000-66006200	Weak transcription	Right Ventricle	heart
31	chr7:65995000-66010000	Weak transcription	Fetal Lung	lung
32	chr7:65995000-66017200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr7:65995200-66009000	Weak transcription	Fetal Thymus	thymus
34	chr7:65995400-66006200	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr7:65995400-66006400	Weak transcription	Brain Germinal Matrix	brain
36	chr7:65995400-66009000	Weak transcription	Brain Angular Gyrus	brain
37	chr7:65995600-66004800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:65995600-66006200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:65995600-66006200	Weak transcription	Primary T cells from cord blood	blood
40	chr7:65995600-66006200	Weak transcription	Brain Anterior Caudate	brain
41	chr7:65995600-66006200	Weak transcription	Brain Hippocampus Middle	brain
42	chr7:65995600-66006200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr7:65995600-66006200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr7:65995600-66006200	Weak transcription	Esophagus	oesophagus
45	chr7:65995600-66006200	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr7:65995600-66006200	Weak transcription	NHLF	lung
47	chr7:65995600-66007800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr7:65995800-66006200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:65996600-66006200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr7:65996800-66006200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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