Variant report

Variant	rs1011219
Chromosome Location	chr11:63973396-63973397
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	RCOR1	chr11:63973282-63973415	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:63972847-63976061	GM12891	blood:	n/a	n/a
3	POLR2A	chr11:63973087-63975757	GM12878	blood:	n/a	n/a
4	NFIC	chr11:63972901-63973446	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:63972904-63976551	GM12878	blood:	n/a	n/a
6	POLR2A	chr11:63973231-63976656	GM12878	blood:	n/a	n/a
7	POLR2A	chr11:63972968-63979020	GM12878	blood:	n/a	n/a
8	BCLAF1	chr11:63972886-63973574	GM12878	blood:	n/a	n/a
9	POLR2A	chr11:63973082-63976238	K562	blood:	n/a	n/a
10	POLR2A	chr11:63972926-63975688	HL-60	blood:	n/a	n/a
11	ELF1	chr11:63972952-63975775	GM12878	blood:	n/a	chr11:63973154-63973165 chr11:63975062-63975071 chr11:63975061-63975072 chr11:63973114-63973127
12	ATF2	chr11:63973260-63974846	GM12878	blood:	n/a	n/a
13	ELK1	chr11:63973255-63973520	GM12878	blood:	n/a	n/a
14	POLR2A	chr11:63973327-63973623	HepG2	liver:	n/a	n/a
15	EBF1	chr11:63972994-63973542	GM12878	blood:	n/a	chr11:63973254-63973263 chr11:63973253-63973263 chr11:63973252-63973265
16	POLR2A	chr11:63972869-63978649	K562	blood:	n/a	n/a
17	POLR2A	chr11:63973238-63973603	H1-neurons	neurons:	n/a	n/a
18	RELA	chr11:63973037-63974516	GM18951	blood:	n/a	n/a
19	POLR2A	chr11:63972859-63975682	PFSK-1	brain:	n/a	n/a
20	STAT5A	chr11:63972958-63975971	GM12878	blood:	n/a	chr11:63974138-63974150 chr11:63973245-63973256 chr11:63973221-63973228
21	POLR2A	chr11:63973192-63976000	HUVEC	blood vessel:	n/a	n/a
22	HMGN3	chr11:63973235-63973468	K562	blood:	n/a	n/a
23	POLR2A	chr11:63972913-63974731	PANC-1	pancreas:	n/a	n/a
24	POLR2A	chr11:63973220-63973720	U87	brain:	n/a	n/a
25	POLR2A	chr11:63972929-63976250	GM12892	blood:	n/a	n/a
26	HEY1	chr11:63973201-63977331	K562	blood:	n/a	chr11:63975289-63975298
27	BHLHE40	chr11:63973217-63973414	GM12878	blood:	n/a	n/a
28	SP1	chr11:63973071-63973506	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:63972963-63975964	SK-N-MC	brain:	n/a	n/a
30	CHD2	chr11:63973077-63975776	K562	blood:	n/a	n/a
31	IKZF1	chr11:63973019-63973433	GM12878	blood:	n/a	n/a
32	POLR2A	chr11:63973058-63976444	GM12892	blood:	n/a	n/a
33	POLR2A	chr11:63972937-63980346	K562	blood:	n/a	n/a
34	POLR2A	chr11:63971678-63979009	K562	blood:	n/a	n/a
35	POLR2A	chr11:63973268-63973555	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:63973003-63978509	GM18505	blood:	n/a	n/a
37	ZBTB7A	chr11:63973217-63973556	K562	blood:	n/a	n/a
38	POLR2A	chr11:63972908-63975998	GM12891	blood:	n/a	n/a
39	PML	chr11:63972855-63975913	GM12878	blood:	n/a	chr11:63975049-63975057 chr11:63975106-63975115
40	POLR2A	chr11:63972821-63976117	GM12892	blood:	n/a	n/a
41	POLR2A	chr11:63972884-63976921	PANC-1	pancreas:	n/a	n/a
42	RELA	chr11:63973018-63973475	GM19099	blood:	n/a	n/a
43	POLR2A	chr11:63973025-63977106	GM19193	blood:	n/a	n/a
44	POLR2A	chr11:63973075-63978498	K562	blood:	n/a	n/a
45	STAT5A	chr11:63973386-63973850	GM12878	blood:	n/a	n/a
46	MAZ	chr11:63973082-63973458	GM12878	blood:	n/a	chr11:63973237-63973246
47	POLR2A	chr11:63973218-63976169	K562	blood:	n/a	n/a
48	POLR2A	chr11:63973354-63973597	HCT-116	colon:	n/a	n/a
49	POLR2A	chr11:63972923-63976196	HL-60	blood:	n/a	n/a
50	NR2F2	chr11:63972999-63973751	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63967209..63969346-chr11:63971616..63974000,2	MCF-7	breast:
2	chr11:63972047..63977847-chr11:64122012..64128099,8	K562	blood:
3	chr11:63969363..63977705-chr11:64080619..64088284,16	K562	blood:
4	chr11:63972230..63976425-chr11:64106710..64112651,7	K562	blood:
5	chr11:63970860..63973755-chr11:64067299..64070043,2	MCF-7	breast:
6	chr11:63951359..63955952-chr11:63973161..63976481,4	MCF-7	breast:
7	chr11:62607620..62609636-chr11:63971953..63974699,2	MCF-7	breast:
8	chr11:63972287..63973832-chr11:64054154..64056547,2	MCF-7	breast:
9	chr11:63740485..63742258-chr11:63973387..63975999,2	K562	blood:
10	chr11:63971468..63973863-chr11:63975515..63979834,6	MCF-7	breast:
11	chr11:63930981..63933673-chr11:63971506..63975446,4	K562	blood:
12	chr11:63972384..63977847-chr11:64121311..64126015,8	K562	blood:
13	chr11:63972188..63973716-chr11:64116908..64119607,2	K562	blood:

Variant related genes	Relation type
FERMT3	TF binding region
ENSG00000168439	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000133316	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11231710	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11231713	0.81[CEU][hapmap];0.82[CHD][hapmap];0.91[GIH][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes]
rs11231726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11600628	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11600667	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11604083	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11605193	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11605856	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11607903	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12417635	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12419038	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17773078	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2005272	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2096706	0.82[CHD][hapmap];0.91[GIH][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2186572	0.81[CEU][hapmap];0.81[JPT][hapmap];0.88[EUR][1000 genomes]
rs3862371	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55942618	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55970968	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56207008	0.91[EUR][1000 genomes]
rs56311067	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57021319	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57831436	0.81[AMR][1000 genomes]
rs58779949	0.81[AMR][1000 genomes]
rs60394481	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs632603	0.82[CEU][hapmap]
rs641811	0.83[CEU][hapmap]
rs646384	0.83[GIH][hapmap];0.80[TSI][hapmap]
rs683996	0.83[CEU][hapmap]
rs7103915	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7109921	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7122408	0.81[EUR][1000 genomes]
rs7123026	0.81[JPT][hapmap];0.89[EUR][1000 genomes]
rs734762	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7941773	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs947939	0.81[CEU][hapmap];0.82[CHD][hapmap];0.91[GIH][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS 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	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription 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	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers 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 miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
11	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription 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	166 gene(s)	inside rSNPs	diseases
12	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
13	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
14	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS 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 miRNA target site	227 gene(s)	inside rSNPs	diseases
15	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
16	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription 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	212 gene(s)	inside rSNPs	diseases
17	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
18	nsv468595	chr11:63953121-64027888	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
19	nsv555187	chr11:63953121-64027888	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
20	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
21	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
22	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
23	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
24	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription 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 miRNA target site	179 gene(s)	inside rSNPs	diseases
25	nsv541061	chr11:63970174-64010995	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
26	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' 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	180 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63955200-63974400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:63955200-63975000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
3	chr11:63955200-63975200	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:63955800-63975400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:63956000-63973600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr11:63956200-63974200	Weak transcription	Right Atrium	heart
7	chr11:63957400-63974800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:63957400-63975800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:63959600-63975000	Strong transcription	NHEK	skin
10	chr11:63959600-63976000	Strong transcription	Fetal Brain Female	brain
11	chr11:63959600-63977000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
12	chr11:63959800-63973400	Strong transcription	Right Ventricle	heart
13	chr11:63959800-63976000	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr11:63960000-63973400	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr11:63960000-63974400	Strong transcription	Brain Substantia Nigra	brain
16	chr11:63960000-63975400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:63960000-63975600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:63960000-63976200	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr11:63960200-63973400	Strong transcription	Gastric	stomach
20	chr11:63964000-63975200	Strong transcription	Brain Angular Gyrus	brain
21	chr11:63964400-63974400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:63967200-63973800	Strong transcription	Pancreas	Pancrea
23	chr11:63967200-63974000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:63967200-63975600	Strong transcription	Placenta Amnion	Placenta Amnion
25	chr11:63967400-63976200	Strong transcription	Brain Germinal Matrix	brain
26	chr11:63968000-63974400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr11:63969400-63973400	Strong transcription	Liver	Liver
28	chr11:63969400-63974200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
29	chr11:63970200-63979000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:63970400-63973800	Genic enhancers	Fetal Thymus	thymus
31	chr11:63970600-63975200	Weak transcription	Fetal Brain Male	brain
32	chr11:63971000-63973400	Genic enhancers	Dnd41	blood
33	chr11:63971000-63974200	Weak transcription	Small Intestine	intestine
34	chr11:63971200-63973600	Genic enhancers	K562	blood
35	chr11:63971200-63974200	Genic enhancers	Fetal Muscle Leg	muscle
36	chr11:63971400-63974200	Genic enhancers	Fetal Muscle Trunk	muscle
37	chr11:63971600-63973800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:63971600-63973800	Genic enhancers	Fetal Intestine Small	intestine
39	chr11:63971600-63973800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
40	chr11:63971600-63974000	Genic enhancers	Placenta	Placenta
41	chr11:63971600-63992800	Weak transcription	Fetal Kidney	kidney
42	chr11:63971800-63973400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:63971800-63973400	Genic enhancers	Adipose Nuclei	Adipose
44	chr11:63971800-63973400	Enhancers	Duodenum Mucosa	Duodenum
45	chr11:63971800-63973400	Genic enhancers	Spleen	Spleen
46	chr11:63971800-63973600	Enhancers	Primary hematopoietic stem cells	blood
47	chr11:63971800-63973600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:63971800-63973600	Genic enhancers	HSMMtube	muscle
49	chr11:63971800-63973800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr11:63971800-63973800	Genic enhancers	Stomach Smooth Muscle	stomach

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