Variant report

Variant	rs688741
Chromosome Location	chr11:85462141-85462142
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:85434439..85436977-chr11:85459317..85462236,2	MCF-7	breast:
2	chr11:85462033..85463782-chr11:85520601..85522192,2	MCF-7	breast:
3	chr11:85459647..85464805-chr11:85466382..85469125,4	K562	blood:
4	chr11:85459647..85463395-chr11:85466382..85468116,3	K562	blood:
5	chr11:85460961..85463869-chr11:85465217..85468287,3	MCF-7	breast:
6	chr11:85456348..85458453-chr11:85459854..85462602,2	K562	blood:
7	chr11:85456923..85462918-chr11:85517727..85523482,9	MCF-7	breast:
8	chr11:85459682..85462503-chr11:85466829..85468700,3	MCF-7	breast:
9	chr11:85461055..85463214-chr11:85468718..85471214,2	MCF-7	breast:
10	chr11:85456354..85459698-chr11:85460209..85463531,4	MCF-7	breast:
11	chr11:85461323..85463573-chr11:85539177..85540857,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000137501	Chromatin interaction

Extended variants
information (count: 115 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10501595	0.94[JPT][hapmap]
rs11234410	0.80[ASN][1000 genomes]
rs1151152	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11604141	0.88[CHD][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs11604178	0.82[ASN][1000 genomes]
rs1192	0.81[CHD][hapmap];0.88[JPT][hapmap]
rs1214001	0.81[CHD][hapmap];0.88[JPT][hapmap]
rs12419172	0.94[JPT][hapmap]
rs12792050	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1445513	0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs17208492	0.94[JPT][hapmap]
rs17208519	0.94[JPT][hapmap]
rs17810659	0.94[JPT][hapmap]
rs17817179	0.84[CHD][hapmap]
rs188311	0.88[ASW][hapmap];0.87[CEU][hapmap];0.90[CHB][hapmap];0.97[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.81[TSI][hapmap]
rs1892872	0.94[JPT][hapmap]
rs1991923	0.94[JPT][hapmap]
rs2290823	0.94[JPT][hapmap]
rs2467059	1.00[JPT][hapmap]
rs290175	0.87[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs290177	1.00[JPT][hapmap]
rs290182	0.94[JPT][hapmap]
rs290186	0.81[CHD][hapmap];1.00[JPT][hapmap]
rs290190	0.83[CEU][hapmap]
rs290194	0.91[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs290195	0.91[CEU][hapmap]
rs290196	0.87[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs290199	0.91[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs290200	0.83[CEU][hapmap]
rs290202	0.84[CEU][hapmap]
rs487964	0.84[ASN][1000 genomes]
rs489896	0.85[ASN][1000 genomes]
rs491867	0.87[CEU][hapmap]
rs493673	0.90[ASN][1000 genomes]
rs4943925	1.00[JPT][hapmap]
rs4944529	0.94[JPT][hapmap]
rs4944531	0.81[CHD][hapmap];0.94[JPT][hapmap]
rs4944539	0.82[CHD][hapmap]
rs496187	0.87[CEU][hapmap]
rs510948	0.87[CEU][hapmap];0.84[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.94[JPT][hapmap];0.81[TSI][hapmap];0.90[ASN][1000 genomes]
rs520629	0.91[CEU][hapmap];0.88[CHD][hapmap];0.82[GIH][hapmap];0.81[JPT][hapmap];0.86[TSI][hapmap];0.83[ASN][1000 genomes]
rs521764	0.82[ASN][1000 genomes]
rs537266	0.91[CEU][hapmap];0.95[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.86[ASN][1000 genomes]
rs537604	0.87[CEU][hapmap];0.84[CHB][hapmap];0.91[CHD][hapmap];0.82[GIH][hapmap];0.94[JPT][hapmap];0.81[TSI][hapmap];0.90[ASN][1000 genomes]
rs540063	0.91[CEU][hapmap]
rs543995	0.81[ASN][1000 genomes]
rs550404	0.83[CEU][hapmap];0.80[YRI][hapmap]
rs556669	0.83[CEU][hapmap]
rs558377	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs565494	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs56579	1.00[JPT][hapmap]
rs573766	0.87[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs578324	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs580459	0.83[CEU][hapmap]
rs583122	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs589327	0.91[CEU][hapmap]
rs592380	0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs592712	0.96[CEU][hapmap];0.84[CHB][hapmap];0.91[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.88[MEX][hapmap];0.92[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs597480	0.88[CEU][hapmap]
rs609012	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs613973	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs631104	0.90[ASN][1000 genomes]
rs631410	0.96[CEU][hapmap]
rs639688	0.95[CEU][hapmap];0.88[CHD][hapmap];0.88[JPT][hapmap];0.84[TSI][hapmap];0.84[ASN][1000 genomes]
rs640620	0.83[ASN][1000 genomes]
rs641393	0.88[CEU][hapmap]
rs644558	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs644972	0.96[CEU][hapmap]
rs647912	0.96[CEU][hapmap];0.81[MKK][hapmap]
rs650036	1.00[CEU][hapmap];0.90[CHB][hapmap];0.86[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.92[TSI][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs650970	0.89[ASN][1000 genomes]
rs653559	0.96[CEU][hapmap];0.90[CHB][hapmap];0.94[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs666176	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs679204	0.91[CEU][hapmap]
rs680498	0.87[CEU][hapmap]
rs681044	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs683903	0.81[ASN][1000 genomes]
rs7119617	0.88[JPT][hapmap]
rs7943586	0.94[JPT][hapmap]
rs881121	0.94[JPT][hapmap]
rs947861	0.94[JPT][hapmap]
rs947863	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv832222	chr11:85405712-85603981	Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv898050	chr11:85406915-85499290	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1052123	chr11:85425856-85471132	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv555633	chr11:85426330-85473883	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1036110	chr11:85429074-85471132	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1054027	chr11:85429074-85477283	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	esv3471508	chr11:85429687-85472395	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	esv3471519	chr11:85429687-85472395	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv555634	chr11:85430397-85464922	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv555635	chr11:85430397-85470893	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv555636	chr11:85431886-85465179	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv1042192	chr11:85433687-85464922	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv1039118	chr11:85433687-85468605	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	nsv1039830	chr11:85433687-85470589	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv1047001	chr11:85433687-85470941	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv1042942	chr11:85433687-85471132	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	nsv1052732	chr11:85434057-85468605	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
22	nsv1048844	chr11:85434057-85470941	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
23	nsv1051644	chr11:85434057-85471132	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	nsv555637	chr11:85435730-85470893	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
25	nsv555639	chr11:85436352-85495269	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
26	nsv1048750	chr11:85436840-85471132	Enhancers Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
27	esv2754674	chr11:85436852-85470852	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
28	esv2757459	chr11:85436868-85473347	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
29	nsv541112	chr11:85436956-85468985	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
30	nsv541113	chr11:85437155-85468845	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
31	nsv555640	chr11:85456703-85464922	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
32	nsv1047147	chr11:85459235-85594800	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
33	nsv541114	chr11:85459235-85594800	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs688741	ME3	cis	cerebellum	SCAN
rs688741	SYTL2	cis	lymphoblastoid	seeQTL
rs688741	SYTL2	cis	Muscle Skeletal	GTEx
rs688741	SYTL2	cis	cerebellum	SCAN
rs688741	CCT4	trans	parietal	SCAN

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85430400-85480400	Weak transcription	Aorta	Aorta
2	chr11:85431800-85466600	Weak transcription	Brain Substantia Nigra	brain
3	chr11:85448000-85463600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr11:85448000-85480600	Weak transcription	Fetal Stomach	stomach
5	chr11:85449200-85478400	Weak transcription	Right Ventricle	heart
6	chr11:85452000-85462600	Weak transcription	HSMMtube	muscle
7	chr11:85452800-85463000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:85453000-85471000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:85454200-85462600	Weak transcription	Left Ventricle	heart
10	chr11:85455000-85470800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:85456800-85468600	Weak transcription	Psoas Muscle	Psoas
12	chr11:85457000-85462600	Weak transcription	Pancreas	Pancrea
13	chr11:85457000-85469000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr11:85457000-85469000	Weak transcription	Gastric	stomach
15	chr11:85457400-85466400	Weak transcription	Colonic Mucosa	Colon
16	chr11:85457600-85466400	Weak transcription	Fetal Intestine Small	intestine
17	chr11:85457800-85466400	Weak transcription	Fetal Intestine Large	intestine
18	chr11:85459200-85462200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:85459200-85463400	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr11:85459400-85470600	Weak transcription	HSMM	muscle
21	chr11:85459800-85470600	Weak transcription	NHEK	skin
22	chr11:85460000-85465200	Enhancers	Primary hematopoietic stem cells	blood
23	chr11:85460200-85463000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr11:85460200-85463000	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr11:85460200-85463400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr11:85460400-85463000	Enhancers	NHLF	lung
27	chr11:85460400-85463400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr11:85460400-85463400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr11:85460400-85463600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:85460400-85463800	Bivalent Enhancer	Fetal Thymus	thymus
31	chr11:85460400-85463800	Enhancers	NHDF-Ad	bronchial
32	chr11:85460400-85464200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr11:85460400-85465200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr11:85460600-85463800	Enhancers	Duodenum Mucosa	Duodenum
35	chr11:85460600-85464200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr11:85460600-85483800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr11:85460800-85463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:85460800-85463800	Enhancers	Fetal Heart	heart
39	chr11:85460800-85464000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr11:85461000-85463200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:85461000-85463800	Enhancers	Fetal Lung	lung
42	chr11:85461200-85462400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:85461200-85463000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:85461200-85464200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr11:85461400-85463400	Enhancers	Small Intestine	intestine
46	chr11:85461400-85464600	Enhancers	Spleen	Spleen
47	chr11:85461600-85462600	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr11:85461600-85463000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr11:85461600-85464000	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr11:85461600-85464400	Enhancers	Lung	lung

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