Variant report

Variant	rs12283777
Chromosome Location	chr11:67380516-67380517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:67380317..67383233-chr11:67433739..67435714,2	MCF-7	breast:
2	chr11:67349088..67352896-chr11:67377453..67387652,15	K562	blood:
3	chr11:67377022..67387637-chr11:67394926..67400114,17	MCF-7	breast:
4	chr11:67378665..67384491-chr11:67395408..67398335,5	MCF-7	breast:
5	chr11:67348020..67353194-chr11:67379787..67385803,14	K562	blood:
6	chr11:67372725..67386378-chr11:67392399..67400639,29	K562	blood:

Variant related genes	Relation type
ENSG00000132746	Chromatin interaction
ENSG00000255318	Chromatin interaction
ENSG00000167799	Chromatin interaction
ENSG00000084207	Chromatin interaction

Extended variants
information (count: 84 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10082595	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10896187	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227829	0.85[AFR][1000 genomes]
rs11227843	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227847	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227853	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227856	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227858	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227859	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227863	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227864	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227867	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227870	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227872	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11501414	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12270939	0.87[AFR][1000 genomes]
rs12271238	0.93[AFR][1000 genomes]
rs12271246	1.00[AMR][1000 genomes]
rs12273818	0.91[AFR][1000 genomes]
rs12275583	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12277603	0.84[AFR][1000 genomes]
rs12279654	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12279771	1.00[AMR][1000 genomes]
rs12281959	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12283583	1.00[AMR][1000 genomes]
rs12284337	0.82[YRI][hapmap]
rs12285190	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12285294	0.94[YRI][hapmap];0.82[AFR][1000 genomes]
rs12285568	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12286629	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12287042	0.88[AFR][1000 genomes]
rs12288767	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12288862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12288915	0.93[AFR][1000 genomes]
rs12291861	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12293788	0.90[YRI][hapmap]
rs12295232	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28856416	0.93[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28894705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6591248	0.90[AFR][1000 genomes]
rs7112719	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7129806	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7940179	1.00[AMR][1000 genomes]
rs7945411	1.00[AMR][1000 genomes]
rs7952329	1.00[AMR][1000 genomes]
rs8191431	0.93[YRI][hapmap];0.93[AFR][1000 genomes]
rs8191448	0.89[YRI][hapmap];0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:37 , 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	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
3	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
4	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
5	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
6	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription 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 miRNA target site	146 gene(s)	inside rSNPs	diseases
7	nsv1041988	chr11:67319916-67749246	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
8	nsv897814	chr11:67339949-67460529	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
9	nsv1050463	chr11:67343421-67717338	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
10	nsv1038189	chr11:67345320-67749246	Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
11	nsv1047236	chr11:67345320-67764068	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
12	nsv555268	chr11:67346743-67752972	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription 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	81 gene(s)	inside rSNPs	diseases
13	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
14	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription 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 miRNA target site	139 gene(s)	inside rSNPs	diseases
15	nsv897815	chr11:67347595-67408791	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS 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	47 gene(s)	inside rSNPs	diseases
16	nsv1053811	chr11:67349444-67749246	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
17	esv1817852	chr11:67349899-67626567	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
18	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
19	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS 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	136 gene(s)	inside rSNPs	diseases
20	nsv897816	chr11:67353579-67460529	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer 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	49 gene(s)	inside rSNPs	diseases
21	nsv1041887	chr11:67357365-67464893	Flanking Active TSS Genic enhancers Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
22	nsv541080	chr11:67357365-67464893	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
23	nsv529452	chr11:67358204-67465721	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
24	nsv492253	chr11:67358204-67574402	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
25	nsv1043487	chr11:67360899-67662476	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
26	nsv897817	chr11:67372477-67414492	Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
27	nsv897818	chr11:67372477-67419855	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
28	nsv468607	chr11:67372477-67423892	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
29	nsv555270	chr11:67372477-67423892	Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
30	nsv897819	chr11:67372477-67426797	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
31	nsv468608	chr11:67372477-67433869	Genic enhancers Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription 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	48 gene(s)	inside rSNPs	diseases
32	nsv555271	chr11:67372477-67433869	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
33	nsv897820	chr11:67372477-67460529	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
34	nsv897821	chr11:67378594-67430762	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
35	nsv897822	chr11:67378594-67441553	Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
36	nsv897823	chr11:67378594-67460529	Enhancers Bivalent Enhancer Active TSS Genic enhancers Weak transcription Flanking Active TSS Strong transcription 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	44 gene(s)	inside rSNPs	diseases
37	nsv897824	chr11:67379575-67418202	Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	40 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12283777	NUDT8	cis	multi-tissue	Pritchard

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67375200-67383200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:67375400-67381000	Weak transcription	NHDF-Ad	bronchial
3	chr11:67375400-67381200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:67375400-67381400	Weak transcription	NH-A	brain
5	chr11:67375400-67381600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:67375400-67383000	Weak transcription	HUVEC	blood vessel
7	chr11:67375600-67380800	Strong transcription	Cortex derived primary cultured neurospheres	brain
8	chr11:67375600-67380800	Weak transcription	Stomach Mucosa	stomach
9	chr11:67375600-67381000	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr11:67375800-67380600	Strong transcription	Placenta	Placenta
11	chr11:67375800-67380800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:67375800-67380800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr11:67375800-67381000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:67375800-67381000	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:67375800-67381000	Strong transcription	NHEK	skin
16	chr11:67375800-67381200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:67375800-67381200	Strong transcription	Fetal Stomach	stomach
18	chr11:67375800-67381200	Strong transcription	NHLF	lung
19	chr11:67375800-67381400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:67375800-67381600	Strong transcription	Fetal Brain Female	brain
21	chr11:67376000-67380600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr11:67376000-67380600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr11:67376000-67380600	Strong transcription	Lung	lung
24	chr11:67376000-67380600	Strong transcription	Spleen	Spleen
25	chr11:67376000-67380800	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr11:67376000-67380800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:67376000-67380800	Strong transcription	Liver	Liver
28	chr11:67376000-67380800	Strong transcription	Brain Substantia Nigra	brain
29	chr11:67376000-67380800	Strong transcription	Duodenum Mucosa	Duodenum
30	chr11:67376000-67380800	Strong transcription	Fetal Intestine Large	intestine
31	chr11:67376000-67380800	Strong transcription	Fetal Muscle Trunk	muscle
32	chr11:67376000-67380800	Strong transcription	Gastric	stomach
33	chr11:67376000-67380800	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr11:67376000-67381000	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr11:67376000-67381000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr11:67376000-67381000	Strong transcription	Brain Hippocampus Middle	brain
37	chr11:67376000-67381000	Strong transcription	Colonic Mucosa	Colon
38	chr11:67376000-67381000	Strong transcription	Right Ventricle	heart
39	chr11:67376000-67381000	Strong transcription	Stomach Smooth Muscle	stomach
40	chr11:67376000-67381200	Strong transcription	H9 Cell Line	embryonic stem cell
41	chr11:67376000-67381200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:67376000-67381200	Strong transcription	Fetal Intestine Small	intestine
43	chr11:67376000-67381200	Strong transcription	Fetal Muscle Leg	muscle
44	chr11:67376000-67381400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:67376000-67381400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:67376000-67381400	Strong transcription	Brain Angular Gyrus	brain
47	chr11:67376000-67381400	Strong transcription	Brain Germinal Matrix	brain
48	chr11:67376000-67381600	Strong transcription	Brain Inferior Temporal Lobe	brain
49	chr11:67376200-67380600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:67376200-67380600	Strong transcription	Placenta Amnion	Placenta Amnion

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