Variant report

Variant	rs11968954
Chromosome Location	chr6:34741174-34741175
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34622560..34624840-chr6:34739559..34741975,2	K562	blood:
2	chr6:34736115..34738612-chr6:34739380..34741719,2	MCF-7	breast:
3	chr6:34739182..34741863-chr6:34755673..34758068,2	K562	blood:
4	chr6:34723826..34725518-chr6:34739318..34741861,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000124562	Chromatin interaction

Extended variants
information (count: 136 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:119)

rs_ID	r²[population]
rs1018622	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];0.96[TSI][hapmap];0.84[YRI][hapmap];0.83[AFR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1051115	1.00[CEU][hapmap];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11961041	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11963234	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11966100	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11967912	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11968972	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1201872	1.00[GIH][hapmap]
rs12111129	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13193526	0.80[ASN][1000 genomes]
rs13195029	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13195361	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13195490	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13196785	1.00[CEU][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13196983	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13200792	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13205210	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];0.96[TSI][hapmap];0.84[YRI][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13206245	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13208149	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13209544	0.82[CEU][hapmap]
rs13210470	0.81[AFR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13212699	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13213239	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13213288	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13213604	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13214596	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16892386	1.00[CEU][hapmap]
rs16895659	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs205261	1.00[CEU][hapmap]
rs205263	1.00[CEU][hapmap]
rs205265	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap]
rs205266	0.92[CEU][hapmap]
rs205267	0.92[CEU][hapmap]
rs205284	1.00[GIH][hapmap]
rs2296361	1.00[CEU][hapmap];1.00[GIH][hapmap];0.84[LWK][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2296362	1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2395603	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2395605	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28360525	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34261333	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34355573	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34377413	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34463942	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34480956	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34681295	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34840245	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35081279	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35103554	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35143960	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35186650	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35195182	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35203657	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35285054	0.80[ASN][1000 genomes]
rs35369977	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35444671	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35684630	0.83[ASN][1000 genomes]
rs35744142	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35940001	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs36026951	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3734261	1.00[GIH][hapmap];0.80[ASN][1000 genomes]
rs3734266	1.00[GIH][hapmap];0.81[LWK][hapmap];0.96[TSI][hapmap];0.85[ASN][1000 genomes]
rs4438945	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs451603	1.00[CEU][hapmap];0.96[TSI][hapmap]
rs4646933	1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];0.96[TSI][hapmap];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6457792	0.95[ASN][1000 genomes]
rs6457797	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.85[EUR][1000 genomes]
rs6457798	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs66672772	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs66926909	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67622212	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67895864	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6900426	1.00[CEU][hapmap];1.00[GIH][hapmap];0.93[TSI][hapmap]
rs6904996	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6908462	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6909393	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6909637	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap]
rs6910824	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6914031	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6914351	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6925175	1.00[CEU][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6926373	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6934741	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6941453	1.00[CEU][hapmap];1.00[GIH][hapmap];0.86[MKK][hapmap];0.96[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71567467	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72892238	0.94[ASN][1000 genomes]
rs72892286	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72910111	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72910167	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7739385	1.00[CEU][hapmap];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7743724	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7743949	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.94[LWK][hapmap];0.96[TSI][hapmap];0.84[YRI][hapmap];0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7749750	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7755354	0.92[CEU][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];0.96[MKK][hapmap];0.96[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7758743	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7759412	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7759985	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7761391	0.92[CEU][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];0.93[TSI][hapmap];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7763989	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7764126	1.00[CEU][hapmap];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7764921	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap]
rs7775947	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7776439	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs912717	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9296133	0.84[ASN][1000 genomes]
rs9461992	1.00[CEU][hapmap]
rs9462001	0.88[ASN][1000 genomes]
rs9462002	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9462003	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9462027	0.81[ASN][1000 genomes]
rs9469812	0.84[CEU][hapmap]
rs9469814	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap]
rs9469820	1.00[CEU][hapmap]
rs9469836	1.00[CEU][hapmap];1.00[GIH][hapmap];0.96[TSI][hapmap]
rs9469838	1.00[CEU][hapmap]
rs9469847	0.86[ASN][1000 genomes]
rs9469852	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9469904	0.81[ASN][1000 genomes]
rs9689160	0.82[ASN][1000 genomes]
rs9968782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 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	nsv1033583	chr6:34471572-34828372	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	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
6	nsv1032557	chr6:34565802-34802008	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv538196	chr6:34565802-34802008	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	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
9	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
10	nsv885795	chr6:34704613-34823187	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	24 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	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
15	nsv1028363	chr6:34733071-34859045	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv885796	chr6:34739726-34823187	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	20 gene(s)	inside rSNPs	diseases
17	nsv965714	chr6:34740808-34741703	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11968954	C6orf107	cis	uninvolved skin	skin_eQTL
rs11968954	UHRF1BP1	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34726000-34747800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:34726000-34750000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:34726800-34747800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:34727000-34743400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr6:34727000-34743800	Strong transcription	Rectal Mucosa Donor 29	rectum
6	chr6:34727000-34744000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:34727000-34744200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr6:34727000-34745200	Strong transcription	Fetal Thymus	thymus
9	chr6:34727200-34743800	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr6:34727200-34743800	Strong transcription	Skeletal Muscle Female	skeletal muscle
11	chr6:34727200-34746600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr6:34727400-34745200	Strong transcription	Fetal Intestine Large	intestine
13	chr6:34727800-34744800	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr6:34727800-34745200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr6:34728400-34743200	Strong transcription	Brain Germinal Matrix	brain
16	chr6:34728400-34744400	Strong transcription	Dnd41	blood
17	chr6:34728600-34743800	Strong transcription	Liver	Liver
18	chr6:34728600-34748400	Weak transcription	Fetal Heart	heart
19	chr6:34728800-34745400	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr6:34729200-34741400	Strong transcription	Ovary	ovary
21	chr6:34729400-34743600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
22	chr6:34729400-34744600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:34729600-34743200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:34729600-34743200	Strong transcription	Placenta	Placenta
25	chr6:34729600-34743200	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr6:34729600-34743600	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr6:34729600-34743800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:34729600-34743800	Strong transcription	Fetal Muscle Trunk	muscle
29	chr6:34729600-34743800	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr6:34729600-34744400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:34729600-34745000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:34729800-34743400	Strong transcription	Thymus	Thymus
33	chr6:34729800-34743800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr6:34729800-34743800	Strong transcription	Adipose Nuclei	Adipose
35	chr6:34730200-34741800	Strong transcription	H9 Cell Line	embryonic stem cell
36	chr6:34730200-34743800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:34730400-34743600	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr6:34731200-34741200	Weak transcription	Fetal Brain Male	brain
39	chr6:34731200-34744000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:34731800-34743400	Strong transcription	Spleen	Spleen
41	chr6:34732400-34743000	Strong transcription	H1 Cell Line	embryonic stem cell
42	chr6:34732400-34743200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chr6:34732400-34743800	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr6:34732600-34743600	Strong transcription	HepG2	liver
45	chr6:34732600-34744200	Strong transcription	Primary B cells from peripheral blood	blood
46	chr6:34732800-34741600	Strong transcription	HUVEC	blood vessel
47	chr6:34732800-34741800	Strong transcription	GM12878-XiMat	blood
48	chr6:34732800-34743800	Strong transcription	HUES48 Cell Line	embryonic stem cell
49	chr6:34732800-34743800	Strong transcription	Duodenum Mucosa	Duodenum
50	chr6:34732800-34745000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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