Variant report

Variant	rs7739385
Chromosome Location	chr6:34867478-34867479
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34867094..34869111-chr6:34869478..34871062,2	K562	blood:
2	chr6:34866548..34869381-chr6:34871968..34873734,2	K562	blood:
3	chr6:34832033..34834649-chr6:34867129..34869415,2	K562	blood:

Extended variants
information (count: 150 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:134)

rs_ID	r²[population]
rs1018622	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1051115	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10947536	0.86[YRI][hapmap]
rs11552398	1.00[JPT][hapmap]
rs11961041	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11963234	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11966100	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11967912	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11968954	1.00[CEU][hapmap];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11968972	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12111129	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12212217	0.86[YRI][hapmap]
rs13193526	0.91[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs13195029	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13195361	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13195490	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13196367	0.81[ASN][1000 genomes]
rs13196785	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13196983	0.82[EUR][1000 genomes]
rs13200792	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13205210	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13206245	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13207848	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs13208149	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13210470	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13212699	0.83[EUR][1000 genomes]
rs13213239	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13213288	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13213604	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13214596	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13215208	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs13216424	1.00[JPT][hapmap]
rs13219307	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13219624	0.82[YRI][hapmap]
rs16895659	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16896559	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs1737727	0.82[YRI][hapmap]
rs1747517	1.00[JPT][hapmap]
rs1880090	0.85[CHB][hapmap]
rs2140418	0.86[YRI][hapmap]
rs2177380	0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2177381	0.86[YRI][hapmap]
rs2273006	0.86[YRI][hapmap]
rs2293242	0.86[YRI][hapmap]
rs2296361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2296362	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2395603	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2395605	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2473613	0.83[YRI][hapmap]
rs2504162	0.86[YRI][hapmap]
rs2762336	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs28360525	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2985	0.86[YRI][hapmap]
rs34261333	0.87[EUR][1000 genomes]
rs34355573	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34377413	0.88[EUR][1000 genomes]
rs34463942	0.88[EUR][1000 genomes]
rs34480956	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34681295	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34840245	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35081279	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35103554	0.83[EUR][1000 genomes]
rs35143960	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35186650	0.88[EUR][1000 genomes]
rs35195182	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35203657	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35285054	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs35369977	0.88[EUR][1000 genomes]
rs35444671	0.84[EUR][1000 genomes]
rs35576171	0.82[ASN][1000 genomes]
rs35744142	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35940001	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs36026951	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3734261	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs3734266	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3800451	0.83[YRI][hapmap]
rs4438945	0.87[EUR][1000 genomes]
rs4646933	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57844307	0.81[ASN][1000 genomes]
rs6457792	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6457796	0.85[CHB][hapmap];0.80[ASN][1000 genomes]
rs6457797	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6457798	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66672772	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs66926909	0.87[EUR][1000 genomes]
rs67622212	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs67895864	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6904996	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6908462	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs6909393	0.83[EUR][1000 genomes]
rs6910824	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6914031	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6914351	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6918872	0.83[YRI][hapmap]
rs6925175	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6926373	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6932857	0.83[YRI][hapmap]
rs6934741	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6941453	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs71567467	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72892238	0.82[ASN][1000 genomes]
rs72892286	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72910111	0.83[EUR][1000 genomes]
rs72910167	0.86[EUR][1000 genomes]
rs7743724	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7743949	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7749750	0.83[EUR][1000 genomes]
rs7755354	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7758743	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7759412	0.82[EUR][1000 genomes]
rs7759985	0.83[EUR][1000 genomes]
rs7761391	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7763989	0.82[EUR][1000 genomes]
rs7764126	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7775947	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7776439	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs820062	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs820065	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs820066	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs820069	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs820095	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs820099	1.00[JPT][hapmap]
rs820101	1.00[JPT][hapmap]
rs820103	0.81[JPT][hapmap]
rs847848	0.89[YRI][hapmap]
rs912717	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9296133	0.90[ASN][1000 genomes]
rs9296139	0.82[YRI][hapmap]
rs9357188	0.83[YRI][hapmap]
rs9462003	0.81[EUR][1000 genomes]
rs9462027	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9469852	0.83[EUR][1000 genomes]
rs9469904	0.92[ASN][1000 genomes]
rs9968782	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv885785	chr6:34404636-34874002	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv885793	chr6:34520267-34886436	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	esv2763967	chr6:34566255-34925463	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv1020710	chr6:34607214-34890143	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	nsv870010	chr6:34713359-34880048	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv1025374	chr6:34723723-34887316	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv462905	chr6:34728253-34886436	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv602906	chr6:34728253-34886436	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv1015792	chr6:34741917-34887316	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv1021733	chr6:34751052-34887316	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
13	nsv1026121	chr6:34786887-34961360	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	19 gene(s)	inside rSNPs	diseases
14	nsv885797	chr6:34791027-34980601	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
15	nsv1033135	chr6:34802652-34957093	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
16	nsv508402	chr6:34840961-34951288	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7739385	UHRF1BP1	cis	Muscle Skeletal	GTEx
rs7739385	C6orf107	cis	uninvolved skin	skin_eQTL

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34857800-34869200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:34858000-34877600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:34858200-34870800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:34858200-34873400	Weak transcription	Esophagus	oesophagus
5	chr6:34858400-34877400	Weak transcription	Aorta	Aorta
6	chr6:34858600-34869400	Weak transcription	NHDF-Ad	bronchial
7	chr6:34858600-34879200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr6:34858800-34880200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr6:34859000-34868600	Weak transcription	Osteobl	bone
10	chr6:34859000-34869000	Weak transcription	Fetal Lung	lung
11	chr6:34859000-34869400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:34859000-34869400	Weak transcription	Lung	lung
13	chr6:34859000-34871600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr6:34859000-34874000	Weak transcription	Brain Anterior Caudate	brain
15	chr6:34859000-34875200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:34859000-34879600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr6:34859200-34868400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr6:34859200-34874800	Weak transcription	K562	blood
19	chr6:34859200-34876800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr6:34859200-34879000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:34859200-34882400	Weak transcription	Fetal Stomach	stomach
22	chr6:34859200-34884600	Weak transcription	Fetal Muscle Leg	muscle
23	chr6:34859200-34884800	Weak transcription	Right Ventricle	heart
24	chr6:34859200-34890800	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr6:34859400-34873400	Weak transcription	Stomach Mucosa	stomach
26	chr6:34859400-34879400	Weak transcription	Primary T cells from cord blood	blood
27	chr6:34859400-34880200	Weak transcription	Primary B cells from cord blood	blood
28	chr6:34859600-34872800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr6:34859600-34873800	Weak transcription	Ovary	ovary
30	chr6:34860000-34868200	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr6:34860000-34868600	Weak transcription	Liver	Liver
32	chr6:34860000-34869200	Weak transcription	NHEK	skin
33	chr6:34860000-34876000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr6:34860200-34873000	Weak transcription	Gastric	stomach
35	chr6:34860200-34879600	Weak transcription	Psoas Muscle	Psoas
36	chr6:34861000-34880000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:34861200-34880000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:34861600-34886000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr6:34863200-34879200	Weak transcription	Primary hematopoietic stem cells	blood
40	chr6:34863400-34872600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:34863400-34877600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr6:34865200-34868200	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr6:34865200-34869000	Enhancers	Fetal Intestine Large	intestine
44	chr6:34865400-34870000	Enhancers	Fetal Intestine Small	intestine
45	chr6:34865400-34870800	Weak transcription	HSMMtube	muscle
46	chr6:34866000-34868400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:34866000-34869400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:34866000-34873600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr6:34866000-34873800	Weak transcription	Left Ventricle	heart
50	chr6:34866200-34873600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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