Variant report

Variant	rs483962
Chromosome Location	chr11:64527751-64527752
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:64526823-64532053	H1-hESC	embryonic stem cell:	n/a	n/a
2	POLR2A	chr11:64527055-64528857	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr11:64527522-64527875	GM12892	blood:	n/a	n/a
4	POLR2A	chr11:64526696-64538505	K562	blood:	n/a	n/a
5	POLR2A	chr11:64525013-64542071	HepG2	liver:	n/a	n/a
6	PBX3	chr11:64527224-64528765	A549	lung:	n/a	chr11:64527729-64527749 chr11:64527396-64527407 chr11:64528003-64528012
7	NFATC1	chr11:64527442-64527814	GM12878	blood:	n/a	n/a
8	ELF1	chr11:64527447-64527889	A549	lung:	n/a	n/a
9	POLR2A	chr11:64527020-64528218	A549	lung:	n/a	n/a
10	POLR2A	chr11:64527708-64528150	A549	lung:	n/a	n/a
11	POLR2A	chr11:64527656-64528817	HUVEC	blood vessel:	n/a	n/a
12	MTA3	chr11:64527728-64528887	GM12878	blood:	n/a	n/a
13	POLR2A	chr11:64527251-64528108	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr11:64526524-64528786	MCF-7	breast:	n/a	n/a
15	POLR2A	chr11:64526438-64528797	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr11:64527103-64528795	PANC-1	pancreas:	n/a	n/a
17	CTCF	chr11:64527680-64527830	SK-N-SH_RA	brain:	n/a	n/a
18	POLR2A	chr11:64527305-64538579	K562	blood:	n/a	n/a
19	POLR2A	chr11:64527090-64528534	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr11:64527577-64529483	GM12878	blood:	n/a	n/a
21	BCL3	chr11:64526711-64528847	A549	lung:	n/a	chr11:64527737-64527745 chr11:64528231-64528240 chr11:64527081-64527094
22	POLR2A	chr11:64527719-64528746	HCT-116	colon:	n/a	n/a
23	STAT5A	chr11:64527711-64528731	GM12878	blood:	n/a	n/a
24	SIN3AK20	chr11:64527650-64528007	A549	lung:	n/a	n/a
25	POLR2A	chr11:64527332-64528797	GM12878	blood:	n/a	n/a
26	POLR2A	chr11:64527428-64528701	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr11:64525521-64533450	A549	lung:	n/a	n/a
28	POLR2A	chr11:64527155-64528762	ECC-1	luminal epithelium:	n/a	n/a
29	POLR2A	chr11:64526677-64528825	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr11:64527599-64527788	ProgFib	skin:	n/a	n/a
31	MAX	chr11:64527515-64527824	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr11:64526700-64528765	Hela-S3	cervix:	n/a	n/a
33	CTBP2	chr11:64527292-64528061	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr11:64527706-64528711	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:64527378-64527963	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr11:64527511-64528817	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr11:64527640-64527790	WERI-Rb-1	eye:	n/a	n/a
38	POLR2A	chr11:64527082-64533748	GM12878	blood:	n/a	n/a
39	POLR2A	chr11:64527223-64528819	PFSK-1	brain:	n/a	n/a
40	GTF2F1	chr11:64527746-64527925	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chr11:64527020-64529295	A549	lung:	n/a	chr11:64528703-64528717 chr11:64527497-64527506
42	POLR2A	chr11:64527460-64534329	GM12892	blood:	n/a	n/a
43	MAX	chr11:64527502-64528063	NB4	blood:	n/a	n/a
44	POLR2A	chr11:64526410-64533727	GM12891	blood:	n/a	n/a
45	POLR2A	chr11:64526670-64528853	HL-60	blood:	n/a	n/a
46	POLR2A	chr11:64526681-64528796	K562	blood:	n/a	n/a
47	MAX	chr11:64527285-64528174	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr11:64527210-64528692	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:64526727-64528774	U87	brain:	n/a	n/a
50	POLR2A	chr11:64526682-64529488	GM12891	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:64509047..64511433-chr11:64527648..64529214,2	MCF-7	breast:
2	chr11:64507790..64516181-chr11:64524582..64537783,30	K562	blood:

Variant related genes	Relation type
PYGM	TF binding region
ENSG00000068831	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10400348	0.84[EUR][1000 genomes]
rs10792444	0.85[EUR][1000 genomes]
rs10897524	0.94[TSI][hapmap];0.98[EUR][1000 genomes]
rs10897525	0.89[MEX][hapmap]
rs11231853	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs11231859	1.00[CEU][hapmap];0.83[MEX][hapmap];0.87[TSI][hapmap];0.97[EUR][1000 genomes]
rs11231869	0.91[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];0.89[MEX][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1143937	1.00[CEU][hapmap];0.86[GIH][hapmap];0.89[MEX][hapmap]
rs1207181	0.87[EUR][1000 genomes]
rs12223914	0.85[EUR][1000 genomes]
rs12417551	0.87[EUR][1000 genomes]
rs12575704	0.85[EUR][1000 genomes]
rs1633462	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17146121	0.89[CEU][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.82[EUR][1000 genomes]
rs2003293	0.97[EUR][1000 genomes]
rs2073797	0.88[EUR][1000 genomes]
rs2073798	0.86[CHB][hapmap];0.86[GIH][hapmap];0.89[MEX][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes]
rs2230414	0.97[EUR][1000 genomes]
rs2267918	1.00[CEU][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.98[EUR][1000 genomes]
rs2284301	1.00[CEU][hapmap];0.81[CHB][hapmap];0.83[MEX][hapmap];0.94[TSI][hapmap];0.98[EUR][1000 genomes]
rs2375335	0.95[EUR][1000 genomes]
rs2959652	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[GIH][hapmap];0.89[MEX][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes]
rs3741398	1.00[CEU][hapmap];0.86[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3809076	0.89[CEU][hapmap];0.89[MEX][hapmap];0.87[TSI][hapmap];0.92[EUR][1000 genomes]
rs474707	0.82[ASW][hapmap];0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs476037	0.89[CEU][hapmap];0.89[MEX][hapmap];0.82[EUR][1000 genomes]
rs477549	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs487105	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs489192	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[GIH][hapmap];0.85[JPT][hapmap];0.87[TSI][hapmap];0.86[EUR][1000 genomes]
rs490980	0.89[CEU][hapmap];0.92[EUR][1000 genomes]
rs494128	0.93[EUR][1000 genomes]
rs496914	1.00[CEU][hapmap];0.89[MEX][hapmap];0.94[TSI][hapmap];0.98[EUR][1000 genomes]
rs523200	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs523752	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs532747	0.89[MEX][hapmap];0.81[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs547066	0.85[GIH][hapmap];0.88[MEX][hapmap];0.81[TSI][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs555974	0.88[EUR][1000 genomes]
rs569602	0.86[CHB][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.86[EUR][1000 genomes]
rs580374	0.98[EUR][1000 genomes]
rs58483071	0.97[EUR][1000 genomes]
rs589691	1.00[CEU][hapmap];0.85[CHB][hapmap];0.86[GIH][hapmap];0.89[MEX][hapmap];0.94[TSI][hapmap];0.97[EUR][1000 genomes]
rs593394	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs606458	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs607389	1.00[CEU][hapmap];0.81[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs620006	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs624975	0.90[CEU][hapmap];0.82[GIH][hapmap];0.89[MEX][hapmap]
rs625172	0.86[CHB][hapmap];0.86[GIH][hapmap];0.89[MEX][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes]
rs630966	0.88[EUR][1000 genomes]
rs633923	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs637332	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs667237	0.97[EUR][1000 genomes]
rs669976	0.90[CEU][hapmap];0.86[GIH][hapmap];0.89[MEX][hapmap]
rs674297	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs677298	1.00[CEU][hapmap];0.83[MEX][hapmap]
rs680273	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs683841	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs684720	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs686171	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs693235	0.90[CEU][hapmap];0.89[MEX][hapmap];0.94[TSI][hapmap]
rs72643567	0.90[EUR][1000 genomes]
rs72643568	0.90[EUR][1000 genomes]
rs7938455	0.86[EUR][1000 genomes]
rs7939965	0.89[CEU][hapmap];0.89[MEX][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
2	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS 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	75 gene(s)	inside rSNPs	diseases
3	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
4	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
5	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
6	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
8	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv897697	chr11:64447420-64584959	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
10	nsv897698	chr11:64447420-64621573	Active TSS Bivalent Enhancer Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription 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	82 gene(s)	inside rSNPs	diseases
11	nsv897699	chr11:64447420-64638041	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
12	nsv897700	chr11:64447420-64701030	Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Weak transcription 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	1071 gene(s)	inside rSNPs	diseases
13	nsv555202	chr11:64477050-64573589	Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
14	nsv468597	chr11:64477050-64584959	Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
15	nsv468598	chr11:64477050-64584959	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
16	nsv555203	chr11:64477050-64584959	Strong transcription Genic enhancers Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
17	nsv1049744	chr11:64486615-64630149	Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
18	nsv832189	chr11:64487183-64620199	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
19	nsv469962	chr11:64527080-64621573	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs483962	LRRN4CL	cis	cerebellum	SCAN
rs483962	SF1	cis	multi-tissue	Pritchard
rs483962	TMEM138	cis	cerebellum	SCAN
rs483962	MALAT1	cis	parietal	SCAN
rs483962	SF1	cis	lymphoblastoid	seeQTL
rs483962	TMEM138	cis	parietal	SCAN
rs483962	B3GNT1	cis	cerebellum	SCAN
rs483962	SF1	Cis_1M	lymphoblastoid	RTeQTL
rs483962	POLA2	cis	cerebellum	SCAN
rs483962	CABP2	cis	parietal	SCAN
rs483962	PYGM	cis	cerebellum	SCAN
rs483962	EHD1	cis	cerebellum	SCAN
rs483962	ANKRD13D	cis	parietal	SCAN
rs483962	PYGM	cis	parietal	SCAN

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64513400-64529800	Weak transcription	Liver	Liver
2	chr11:64513400-64530000	Weak transcription	Aorta	Aorta
3	chr11:64514000-64529800	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr11:64514600-64529800	Weak transcription	Dnd41	blood
5	chr11:64516000-64529800	Weak transcription	Fetal Brain Female	brain
6	chr11:64520600-64529600	Weak transcription	NHEK	skin
7	chr11:64524600-64529600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:64524800-64530000	Strong transcription	Thymus	Thymus
9	chr11:64525000-64529800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr11:64525000-64530000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr11:64525000-64530400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr11:64525200-64530000	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr11:64525400-64533400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:64525800-64528400	Enhancers	Placenta	Placenta
15	chr11:64525800-64528800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:64525800-64528800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr11:64526000-64528000	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr11:64526000-64528200	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr11:64526000-64528200	Genic enhancers	Spleen	Spleen
20	chr11:64526000-64528400	Enhancers	Primary T cells fromperipheralblood	blood
21	chr11:64526000-64530400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr11:64526000-64530600	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr11:64526200-64527800	Flanking Active TSS	Fetal Muscle Trunk	muscle
24	chr11:64526200-64528000	Flanking Active TSS	Fetal Muscle Leg	muscle
25	chr11:64526200-64528600	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr11:64526200-64528600	Enhancers	Hela-S3	cervix
27	chr11:64526200-64531200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:64526400-64528400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:64526400-64528600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:64526400-64528600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr11:64526400-64528800	Enhancers	Ovary	ovary
32	chr11:64526400-64529600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr11:64526400-64529800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr11:64526400-64529800	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr11:64526400-64529800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr11:64526600-64528000	Enhancers	Placenta Amnion	Placenta Amnion
37	chr11:64526600-64529000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr11:64526600-64529800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:64526600-64530000	Enhancers	Primary T cells from cord blood	blood
40	chr11:64526600-64530200	Enhancers	Primary B cells from cord blood	blood
41	chr11:64526600-64530600	Enhancers	K562	blood
42	chr11:64526800-64527800	Enhancers	NHDF-Ad	bronchial
43	chr11:64526800-64528000	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr11:64526800-64528000	Enhancers	Lung	lung
45	chr11:64526800-64528200	Enhancers	Duodenum Mucosa	Duodenum
46	chr11:64526800-64528400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr11:64526800-64528400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:64526800-64528400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr11:64526800-64528400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:64526800-64528400	Enhancers	HSMMtube	muscle

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