Variant report

Variant	rs2286620
Chromosome Location	chr11:67166984-67166985
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:67166832-67167265	GM12892	blood:	n/a	n/a
2	POLR2A	chr11:67166090-67167256	GM12891	blood:	n/a	n/a
3	POLR2A	chr11:67163972-67167371	HL-60	blood:	n/a	n/a
4	POLR2A	chr11:67165819-67167288	GM12891	blood:	n/a	n/a
5	POLR2A	chr11:67166172-67167245	HL-60	blood:	n/a	n/a
6	POLR2A	chr11:67166941-67167157	MCF-7	breast:	n/a	n/a
7	POLR2A	chr11:67164821-67167639	HepG2	liver:	n/a	n/a
8	POLR2A	chr11:67165990-67167288	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr11:67166805-67167108	A549	lung:	n/a	n/a
10	POLR2A	chr11:67164715-67167476	PFSK-1	brain:	n/a	n/a
11	POLR2A	chr11:67164525-67167300	K562	blood:	n/a	n/a
12	POLR2A	chr11:67162849-67167326	GM12878	blood:	n/a	n/a
13	POLR2A	chr11:67164777-67167449	SK-N-MC	brain:	n/a	n/a
14	POLR2A	chr11:67162831-67167316	K562	blood:	n/a	n/a
15	POLR2A	chr11:67165842-67167307	GM12892	blood:	n/a	n/a
16	POLR2A	chr11:67164695-67167286	PANC-1	pancreas:	n/a	n/a
17	POLR2A	chr11:67164786-67167247	MCF-7	breast:	n/a	n/a
18	POLR2A	chr11:67163677-67167294	GM12892	blood:	n/a	n/a
19	POLR2A	chr11:67162599-67167265	PFSK-1	brain:	n/a	n/a
20	POLR2A	chr11:67166810-67167060	GM12891	blood:	n/a	n/a
21	POLR2A	chr11:67163149-67167243	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr11:67166874-67167153	MCF-7	breast:	n/a	n/a
23	POLR2A	chr11:67166957-67167336	ECC-1	luminal epithelium:	n/a	n/a
24	POLR2A	chr11:67164736-67167236	U87	brain:	n/a	n/a
25	POLR2A	chr11:67162873-67167363	GM12892	blood:	n/a	n/a
26	ELF1	chr11:67166428-67167157	GM12878	blood:	n/a	chr11:67166656-67166667
27	POLR2A	chr11:67166668-67167174	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr11:67162822-67167423	K562	blood:	n/a	n/a
29	POLR2A	chr11:67165405-67167061	U87	brain:	n/a	n/a
30	POLR2A	chr11:67166837-67167048	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr11:67163762-67167367	K562	blood:	n/a	n/a
32	POLR2A	chr11:67166048-67167288	GM12878	blood:	n/a	n/a
33	POLR2A	chr11:67165976-67167260	GM12878	blood:	n/a	n/a
34	POLR2A	chr11:67163626-67167320	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr11:67166456-67167107	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr11:67163577-67167470	PANC-1	pancreas:	n/a	n/a
37	POLR2A	chr11:67162931-67167248	GM12878	blood:	n/a	n/a
38	POLR2A	chr11:67166896-67167167	HUVEC	blood vessel:	n/a	n/a
39	HEY1	chr11:67166740-67167199	K562	blood:	n/a	n/a
40	POLR2A	chr11:67162854-67167503	K562	blood:	n/a	n/a
41	POLR2A	chr11:67166003-67167160	GM12891	blood:	n/a	n/a
42	ZNF263	chr11:67166688-67167184	HEK293-T-REx	kidney:	n/a	chr11:67167004-67167013 chr11:67167008-67167029
43	POLR2A	chr11:67166840-67167245	GM12878	blood:	n/a	n/a
44	POLR2A	chr11:67164874-67167097	K562	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67166766..67171737-chr11:67231413..67236466,7	K562	blood:
2	chr11:67165362..67170814-chr11:67205782..67211749,9	K562	blood:
3	chr11:67164456..67171429-chr11:67268926..67279263,19	K562	blood:
4	chr11:67164667..67170931-chr11:67232207..67238345,15	MCF-7	breast:
5	chr11:67166559..67171272-chr11:67271633..67274655,6	MCF-7	breast:
6	chr11:67164491..67170697-chr11:67268115..67277759,17	MCF-7	breast:

No data

Variant related genes	Relation type
TBC1D10C	TF binding region
RNU6-1238P	TF binding region
ENSG00000110697	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000172725	Chromatin interaction
ENSG00000167797	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10896167	0.88[CEU][hapmap];0.86[CHD][hapmap];0.83[GIH][hapmap];0.84[JPT][hapmap]
rs10896172	0.83[CHB][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap]
rs1115051	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11227756	0.84[CHD][hapmap]
rs11227788	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12276833	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12288107	0.80[CEU][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs12290164	0.80[CEU][hapmap];1.00[GIH][hapmap];0.84[TSI][hapmap];0.87[EUR][1000 genomes]
rs12788752	0.84[CHD][hapmap];0.83[GIH][hapmap];0.84[JPT][hapmap]
rs12805811	0.85[MEX][hapmap]
rs1558256	0.80[CEU][hapmap];0.85[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1558257	0.83[CHB][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap]
rs1638566	0.88[CEU][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap]
rs1638567	0.88[CEU][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap]
rs1638571	0.88[CEU][hapmap];0.85[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1638586	1.00[GIH][hapmap];0.84[TSI][hapmap];0.86[EUR][1000 genomes]
rs1790733	0.80[CEU][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs1790740	0.88[CEU][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap]
rs1790747	0.80[CEU][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs1790748	0.83[EUR][1000 genomes]
rs2066496	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2071007	0.84[CHD][hapmap]
rs2256154	0.82[CHD][hapmap]
rs2514256	1.00[CEU][hapmap];0.85[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.91[TSI][hapmap];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2514258	0.81[ASN][1000 genomes]
rs34087937	0.85[MEX][hapmap]
rs34596169	0.83[EUR][1000 genomes]
rs35821109	0.85[MEX][hapmap]
rs3758943	0.88[CEU][hapmap];0.83[CHB][hapmap];0.92[JPT][hapmap]
rs3781941	0.88[CEU][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs3781942	0.88[CEU][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs3781943	0.88[CEU][hapmap];0.84[CHD][hapmap];0.83[GIH][hapmap];0.84[JPT][hapmap]
rs3927807	0.88[CEU][hapmap]
rs4255546	0.88[CEU][hapmap];0.84[CHD][hapmap];0.83[GIH][hapmap]
rs4542419	0.84[CHD][hapmap]
rs4930192	0.88[CEU][hapmap];0.83[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.86[ASN][1000 genomes]
rs4930197	0.88[CEU][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs4930418	0.88[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap];0.86[ASN][1000 genomes]
rs7480390	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs872109	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs872110	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.91[TSI][hapmap];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
3	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers 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 miRNA target site	206 gene(s)	inside rSNPs	diseases
4	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
5	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
6	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
8	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
9	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription 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	122 gene(s)	inside rSNPs	diseases
10	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
11	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
12	nsv897805	chr11:67155210-67283891	ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
13	nsv897806	chr11:67155210-67294308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
14	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
15	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
16	nsv897809	chr11:67156875-67276235	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription 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	148 gene(s)	inside rSNPs	diseases
17	nsv516453	chr11:67164495-67186000	Genic enhancers Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
18	nsv555254	chr11:67164495-67288594	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription 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 miRNA target site	146 gene(s)	inside rSNPs	diseases
19	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
20	nsv897810	chr11:67166310-67196237	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
21	nsv897811	chr11:67166984-67218909	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2286620	RPS6KB2	cis	lymphoblastoid	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67160200-67167000	Weak transcription	Psoas Muscle	Psoas
2	chr11:67160400-67167800	Weak transcription	Right Atrium	heart
3	chr11:67160800-67167000	Strong transcription	Fetal Intestine Large	intestine
4	chr11:67160800-67167200	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr11:67160800-67167200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:67161000-67167400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:67161000-67167600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:67161200-67167000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:67161200-67168000	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr11:67161400-67167000	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr11:67161400-67167800	Strong transcription	NHEK	skin
12	chr11:67161400-67168000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:67161600-67167800	Strong transcription	Brain Substantia Nigra	brain
14	chr11:67162600-67167000	Strong transcription	Brain Anterior Caudate	brain
15	chr11:67162800-67167200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
16	chr11:67162800-67167400	Strong transcription	Osteobl	bone
17	chr11:67162800-67167800	Genic enhancers	Primary T cells fromperipheralblood	blood
18	chr11:67162800-67168000	Strong transcription	H9 Cell Line	embryonic stem cell
19	chr11:67163000-67167200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr11:67163000-67167800	Genic enhancers	Fetal Thymus	thymus
21	chr11:67163000-67168000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:67163000-67168800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr11:67163200-67167200	Strong transcription	Ovary	ovary
24	chr11:67163400-67167800	Genic enhancers	Primary T cells from cord blood	blood
25	chr11:67163400-67167800	Genic enhancers	Fetal Muscle Leg	muscle
26	chr11:67163400-67168000	Genic enhancers	Fetal Muscle Trunk	muscle
27	chr11:67163600-67167200	Strong transcription	Brain Angular Gyrus	brain
28	chr11:67163800-67167400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
29	chr11:67163800-67167600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:67163800-67167800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr11:67163800-67167800	Strong transcription	Brain Inferior Temporal Lobe	brain
32	chr11:67164000-67167200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:67164000-67167200	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr11:67164000-67167800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
35	chr11:67164000-67167800	Genic enhancers	Placenta	Placenta
36	chr11:67164000-67168000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr11:67164200-67167200	Genic enhancers	Adipose Nuclei	Adipose
38	chr11:67164200-67167800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
39	chr11:67164200-67167800	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr11:67164200-67168000	Genic enhancers	Primary B cells from peripheral blood	blood
41	chr11:67164400-67167600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:67164400-67167600	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr11:67164600-67167200	Strong transcription	H1 Cell Line	embryonic stem cell
44	chr11:67164600-67167600	Genic enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:67164600-67167800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:67164800-67167200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr11:67164800-67167200	Strong transcription	Left Ventricle	heart
48	chr11:67164800-67167600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr11:67164800-67167600	Genic enhancers	Primary B cells from cord blood	blood
50	chr11:67164800-67167800	Genic enhancers	Cortex derived primary cultured neurospheres	brain

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