Variant report

Variant	rs949250
Chromosome Location	chr11:67234278-67234279
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:20)
CpG islands
(count:0)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:20 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:67233890-67234459	HepG2	liver:	n/a	n/a
2	POLR2A	chr11:67233847-67235390	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:67233735-67235254	PANC-1	pancreas:	n/a	n/a
4	POLR2A	chr11:67233859-67234751	GM12891	blood:	n/a	n/a
5	POLR2A	chr11:67234229-67234523	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr11:67233795-67237091	K562	blood:	n/a	n/a
7	POLR2A	chr11:67233915-67234455	MCF-7	breast:	n/a	n/a
8	POLR2A	chr11:67233833-67234520	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:67233789-67234476	ECC-1	luminal epithelium:	n/a	n/a
10	POLR2A	chr11:67233700-67234489	K562	blood:	n/a	n/a
11	POLR2A	chr11:67233884-67237113	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr11:67233884-67237151	Raji	blood:	n/a	n/a
13	POLR2A	chr11:67233777-67234400	GM12892	blood:	n/a	n/a
14	POLR2A	chr11:67233981-67234412	K562	blood:	n/a	n/a
15	POLR2A	chr11:67234099-67234278	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr11:67233590-67234912	SK-N-MC	brain:	n/a	n/a
17	POLR2A	chr11:67233698-67237165	HCT-116	colon:	n/a	n/a
18	POLR2A	chr11:67230966-67237458	HepG2	liver:	n/a	n/a
19	POLR2A	chr11:67233718-67235007	HCT-116	colon:	n/a	n/a
20	POLR2A	chr11:67233783-67234425	HepG2	liver:	n/a	n/a

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67232230..67238185-chr11:67272105..67277120,9	K562	blood:
2	chr11:67175949..67181191-chr11:67230601..67234346,6	K562	blood:
3	chr11:67119569..67122629-chr11:67231645..67234377,4	MCF-7	breast:
4	chr11:67156700..67160978-chr11:67234255..67237148,8	MCF-7	breast:
5	chr11:67231244..67235869-chr11:67255079..67259378,6	MCF-7	breast:
6	chr11:67215208..67219901-chr11:67230573..67236211,5	K562	blood:
7	chr11:67171798..67174416-chr11:67233067..67235225,2	K562	blood:
8	chr11:67201248..67204152-chr11:67232413..67236121,3	K562	blood:
9	chr11:67164667..67170931-chr11:67232207..67238345,15	MCF-7	breast:
10	chr11:67230107..67238941-chr11:67268499..67277838,23	MCF-7	breast:
11	chr11:67232230..67234303-chr11:67273494..67275304,2	K562	blood:
12	chr11:67175789..67179239-chr11:67234277..67236634,3	MCF-7	breast:
13	chr11:67166766..67171737-chr11:67231413..67236466,7	K562	blood:
14	chr11:67229962..67234772-chr11:67234827..67242516,28	K562	blood:
15	chr11:66383175..66385697-chr11:67233661..67236166,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000270169	TF binding region
TMEM134	TF binding region
ENSG00000167797	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000248643	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000110711	Chromatin interaction
ENSG00000175544	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000255949	Chromatin interaction
ENSG00000239306	Chromatin interaction
ENSG00000172613	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10896175	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227796	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227804	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11821703	1.00[EUR][1000 genomes]
rs12288316	1.00[EUR][1000 genomes]
rs12293606	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1382089	1.00[EUR][1000 genomes]
rs1618605	0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1620333	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1624189	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625032	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625892	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1630068	0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1632616	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638558	0.85[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638559	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638560	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638561	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638562	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638563	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638570	1.00[EUR][1000 genomes]
rs1638572	1.00[EUR][1000 genomes]
rs1638575	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638576	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638577	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638581	0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638584	0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638585	0.90[AMR][1000 genomes]
rs1638587	1.00[EUR][1000 genomes]
rs1790729	1.00[EUR][1000 genomes]
rs1790730	1.00[EUR][1000 genomes]
rs1790734	1.00[EUR][1000 genomes]
rs1790736	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790741	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790743	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790744	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790745	1.00[EUR][1000 genomes]
rs1790749	1.00[EUR][1000 genomes]
rs1790750	1.00[EUR][1000 genomes]
rs1790754	1.00[EUR][1000 genomes]
rs1790756	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790763	0.93[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790764	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790765	1.00[EUR][1000 genomes]
rs1824712	1.00[EUR][1000 genomes]
rs2054409	1.00[EUR][1000 genomes]
rs2447590	1.00[EUR][1000 genomes]
rs2447591	1.00[EUR][1000 genomes]
rs2447597	1.00[EUR][1000 genomes]
rs2511058	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2511059	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514013	1.00[EUR][1000 genomes]
rs2514014	1.00[EUR][1000 genomes]
rs2514015	1.00[EUR][1000 genomes]
rs2514024	1.00[EUR][1000 genomes]
rs2514045	1.00[EUR][1000 genomes]
rs2514064	1.00[EUR][1000 genomes]
rs2514259	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2514262	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514263	1.00[EUR][1000 genomes]
rs2885171	1.00[EUR][1000 genomes]
rs3016861	1.00[EUR][1000 genomes]
rs35363135	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36052107	1.00[EUR][1000 genomes]
rs56050553	1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56405884	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57047868	1.00[EUR][1000 genomes]
rs57134963	1.00[EUR][1000 genomes]
rs57748654	1.00[EUR][1000 genomes]
rs57749415	1.00[EUR][1000 genomes]
rs57757103	1.00[EUR][1000 genomes]
rs57955602	1.00[EUR][1000 genomes]
rs58999825	1.00[EUR][1000 genomes]
rs59500232	1.00[EUR][1000 genomes]
rs596431	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs596944	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs601363	0.89[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60136955	1.00[EUR][1000 genomes]
rs602220	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs604540	0.90[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs611697	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61282424	1.00[EUR][1000 genomes]
rs61429992	1.00[EUR][1000 genomes]
rs61610719	1.00[EUR][1000 genomes]
rs618633	1.00[EUR][1000 genomes]
rs641081	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6591267	1.00[EUR][1000 genomes]
rs7104627	1.00[EUR][1000 genomes]
rs7121803	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7124630	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73490545	1.00[EUR][1000 genomes]
rs73490554	1.00[EUR][1000 genomes]
rs73501797	1.00[EUR][1000 genomes]
rs73501800	1.00[EUR][1000 genomes]
rs73506004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506015	1.00[EUR][1000 genomes]
rs73506054	1.00[EUR][1000 genomes]
rs73506056	1.00[EUR][1000 genomes]
rs73506069	1.00[EUR][1000 genomes]
rs73506074	1.00[EUR][1000 genomes]
rs743679	1.00[EUR][1000 genomes]
rs7934566	1.00[EUR][1000 genomes]
rs7941752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7947114	1.00[EUR][1000 genomes]
rs8191436	1.00[EUR][1000 genomes]
rs8191446	1.00[EUR][1000 genomes]
rs8191449	1.00[EUR][1000 genomes]
rs949251	0.92[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949252	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949253	0.83[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949254	0.89[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949255	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	nsv897813	chr11:67175692-67283891	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
17	nsv521723	chr11:67175692-67311258	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
18	nsv468604	chr11:67186000-67283891	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
19	nsv555256	chr11:67186000-67283891	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
20	nsv527056	chr11:67207426-67294308	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer 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 miRNA target site	115 gene(s)	inside rSNPs	diseases
21	esv1813337	chr11:67217703-67235815	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
22	nsv983155	chr11:67220251-67251432	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67232000-67235200	Weak transcription	HSMMtube	muscle
2	chr11:67232600-67235600	Weak transcription	Ovary	ovary
3	chr11:67232800-67234600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:67232800-67234600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr11:67232800-67234600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr11:67232800-67234800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr11:67232800-67234800	Genic enhancers	Fetal Muscle Trunk	muscle
8	chr11:67232800-67235000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:67232800-67235200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:67232800-67235800	Weak transcription	Aorta	Aorta
11	chr11:67233000-67234400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr11:67233000-67234600	Genic enhancers	Primary B cells from peripheral blood	blood
13	chr11:67233000-67234600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr11:67233000-67234600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr11:67233000-67234600	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr11:67233000-67234800	Weak transcription	Lung	lung
17	chr11:67233000-67235000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:67233000-67235000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr11:67233000-67235000	Weak transcription	Adipose Nuclei	Adipose
20	chr11:67233000-67235000	Weak transcription	Brain Angular Gyrus	brain
21	chr11:67233000-67235000	Weak transcription	Brain Substantia Nigra	brain
22	chr11:67233000-67235000	Weak transcription	Fetal Heart	heart
23	chr11:67233000-67235000	Weak transcription	Right Atrium	heart
24	chr11:67233000-67235200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:67233000-67235200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:67233000-67235200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:67233000-67235200	Weak transcription	Brain Germinal Matrix	brain
28	chr11:67233000-67235200	Weak transcription	Right Ventricle	heart
29	chr11:67233000-67235400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr11:67233000-67235400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr11:67233000-67235400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:67233000-67235400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr11:67233000-67235400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr11:67233000-67235400	Weak transcription	Psoas Muscle	Psoas
35	chr11:67233000-67235400	Weak transcription	Small Intestine	intestine
36	chr11:67233000-67235400	Weak transcription	HSMM	muscle
37	chr11:67233000-67235400	Weak transcription	NHDF-Ad	bronchial
38	chr11:67233000-67235600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:67233000-67235600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr11:67233000-67235600	Weak transcription	Left Ventricle	heart
41	chr11:67233000-67235600	Weak transcription	HUVEC	blood vessel
42	chr11:67233000-67235800	Weak transcription	Fetal Kidney	kidney
43	chr11:67233200-67234400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr11:67233200-67234400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr11:67233200-67234400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr11:67233200-67234600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr11:67233200-67234600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr11:67233200-67234600	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr11:67233200-67234600	Weak transcription	NHLF	lung
50	chr11:67233200-67234800	Weak transcription	Colon Smooth Muscle	Colon

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