Variant report

Variant	rs474901
Chromosome Location	chr11:64125387-64125388
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	HCFC1	chr11:64124546-64127782	Hela-S3	cervix:	n/a	n/a
2	HDAC2	chr11:64125304-64125547	K562	blood:	n/a	n/a
3	SMARCB1	chr11:64125210-64127144	Hela-S3	cervix:	n/a	n/a
4	MAX	chr11:64125386-64125569	K562	blood:	n/a	n/a
5	POLR2A	chr11:64125316-64127393	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr11:64125314-64126017	K562	blood:	n/a	n/a
7	POLR2A	chr11:64125303-64127100	Hela-S3	cervix:	n/a	n/a
8	YY1	chr11:64125377-64125889	K562	blood:	n/a	chr11:64125871-64125885
9	POLR2A	chr11:64125026-64127534	K562	blood:	n/a	n/a
10	FOSL1	chr11:64125363-64125613	K562	blood:	n/a	chr11:64125503-64125511 chr11:64125501-64125512
11	MAX	chr11:64125298-64127158	K562	blood:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125725-64125735
12	SMARCC2	chr11:64124862-64126548	Hela-S3	cervix:	n/a	n/a
13	MTA3	chr11:64125269-64125617	GM12878	blood:	n/a	n/a
14	NR2F2	chr11:64125226-64126455	K562	blood:	n/a	n/a
15	ZBTB7A	chr11:64125127-64127287	K562	blood:	n/a	n/a
16	POLR2A	chr11:64125206-64126100	K562	blood:	n/a	n/a
17	POLR2A	chr11:64125340-64125736	K562	blood:	n/a	n/a
18	POLR2A	chr11:64125379-64125946	Hela-S3	cervix:	n/a	n/a
19	JUND	chr11:64125332-64125742	K562	blood:	n/a	chr11:64125503-64125511
20	POLR2A	chr11:64125374-64125818	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:64125281-64125859	HCT-116	colon:	n/a	n/a
22	POLR2A	chr11:64125202-64125810	HCT-116	colon:	n/a	n/a
23	CBX3	chr11:64125256-64126131	K562	blood:	n/a	n/a
24	ZBTB7A	chr11:64125386-64127369	ECC-1	luminal epithelium:	n/a	n/a
25	MAX	chr11:64125381-64125903	K562	blood:	n/a	chr11:64125725-64125735
26	MAZ	chr11:64124649-64125918	IMR90	lung:	n/a	chr11:64125278-64125288 chr11:64125274-64125284 chr11:64125725-64125735
27	CTCF	chr11:64125300-64125450	HMEC	breast:	n/a	n/a
28	MAZ	chr11:64125259-64127214	Hela-S3	cervix:	n/a	chr11:64125961-64125977 chr11:64125278-64125288 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64125274-64125284 chr11:64125725-64125735
29	MAX	chr11:64125327-64127627	A549	lung:	n/a	chr11:64125961-64125977 chr11:64125970-64125977 chr11:64125969-64125978 chr11:64125972-64125988 chr11:64127233-64127243 chr11:64125725-64125735
30	SMARCC1	chr11:64125052-64126564	Hela-S3	cervix:	n/a	n/a
31	EP300	chr11:64125384-64125645	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr11:64125387-64125513	GM12878	blood:	n/a	n/a
33	RFX5	chr11:64125348-64125694	Hela-S3	cervix:	n/a	n/a
34	RCOR1	chr11:64125330-64126033	Hela-S3	cervix:	n/a	n/a
35	FOS	chr11:64125386-64125664	MCF10A-Er-Src	breast:	n/a	chr11:64125501-64125512 chr11:64125503-64125511
36	FOS	chr11:64125358-64125656	MCF10A-Er-Src	breast:	n/a	chr11:64125501-64125512 chr11:64125503-64125511
37	CHD2	chr11:64125266-64125793	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr11:64125342-64126037	K562	blood:	n/a	n/a
39	TFAP2C	chr11:64125325-64126858	Hela-S3	cervix:	n/a	chr11:64126461-64126476
40	SMC3	chr11:64125324-64125824	Hela-S3	cervix:	n/a	n/a
41	MXI1	chr11:64125319-64125989	Hela-S3	cervix:	n/a	n/a
42	FOS	chr11:64125360-64125689	HUVEC	blood vessel:	n/a	chr11:64125501-64125512 chr11:64125503-64125511
43	POLR2A	chr11:64125369-64128440	HL-60	blood:	n/a	n/a
44	FOSL2	chr11:64125268-64125688	HepG2	liver:	n/a	chr11:64125503-64125511
45	ZBTB7A	chr11:64125314-64127395	ECC-1	luminal epithelium:	n/a	n/a
46	RCOR1	chr11:64125357-64125723	K562	blood:	n/a	n/a
47	TEAD4	chr11:64125294-64125752	K562	blood:	n/a	n/a
48	FOS	chr11:64125360-64125664	MCF10A-Er-Src	breast:	n/a	chr11:64125501-64125512 chr11:64125503-64125511
49	JUN	chr11:64124797-64127116	K562	blood:	n/a	chr11:64125503-64125511
50	POLR2A	chr11:64125362-64125883	Gliobla	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64110456..64113002-chr11:64125236..64127679,2	MCF-7	breast:
2	chr11:63972047..63977847-chr11:64122012..64128099,8	K562	blood:
3	chr11:64041009..64043331-chr11:64125161..64128159,2	MCF-7	breast:
4	chr11:64082853..64088243-chr11:64119014..64129028,17	MCF-7	breast:
5	chr11:64070250..64072559-chr11:64125217..64126731,2	MCF-7	breast:
6	chr11:64125330..64128537-chr11:64215213..64218115,3	MCF-7	breast:
7	chr11:64073021..64075424-chr11:64122972..64125774,2	MCF-7	breast:
8	chr11:64123441..64125427-chr11:64411243..64414199,2	K562	blood:
9	chr11:64083884..64087111-chr11:64122613..64125426,3	K562	blood:
10	chr11:64017685..64020898-chr11:64124130..64127721,3	MCF-7	breast:
11	chr11:64000008..64002901-chr11:64125113..64127418,2	MCF-7	breast:
12	chr11:64070986..64076286-chr11:64124810..64128616,7	K562	blood:
13	chr11:64119430..64124364-chr11:64124831..64128743,7	MCF-7	breast:
14	chr11:64004012..64005762-chr11:64124323..64126720,2	MCF-7	breast:
15	chr11:64062668..64065011-chr11:64124225..64126837,3	MCF-7	breast:
16	chr11:64124497..64126994-chr11:64509396..64512374,2	K562	blood:
17	chr11:64008386..64010951-chr11:64125361..64127756,4	MCF-7	breast:
18	chr11:64053151..64055063-chr11:64124109..64127002,2	K562	blood:
19	chr11:64083913..64086967-chr11:64122125..64127376,8	MCF-7	breast:
20	chr11:64125259..64126829-chr11:64127521..64129918,2	MCF-7	breast:
21	chr11:64080620..64083894-chr11:64124180..64128334,3	MCF-7	breast:
22	chr11:64124989..64126699-chr11:64216058..64218143,2	K562	blood:
23	chr11:64124540..64126165-chr11:64416805..64418709,2	MCF-7	breast:
24	chr11:63972384..63977847-chr11:64121311..64126015,8	K562	blood:
25	chr11:64007008..64012234-chr11:64122125..64125548,6	K562	blood:

Variant related genes	Relation type
RPS6KA4	TF binding region
ENSG00000173264	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000256116	Chromatin interaction
ENSG00000149782	Chromatin interaction
ENSG00000110011	Chromatin interaction
ENSG00000207024	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000068831	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000181908	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000173511	Chromatin interaction
ENSG00000237410	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10897487	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10897488	0.87[ASW][hapmap];0.82[CHD][hapmap];0.95[GIH][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11231770	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11231771	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11231772	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11542299	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11601651	0.81[ASN][1000 genomes]
rs11606015	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11606081	0.87[ASW][hapmap];0.82[CHD][hapmap];0.95[GIH][hapmap];0.87[MEX][hapmap];0.84[TSI][hapmap];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1199045	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs1199046	1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17857342	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2510066	0.83[MEX][hapmap]
rs475032	0.81[ASN][1000 genomes]
rs479777	0.83[MEX][hapmap]
rs4930155	0.92[CEU][hapmap];0.86[GIH][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs499425	0.86[JPT][hapmap];0.86[MEX][hapmap]
rs508168	0.87[ASW][hapmap];0.82[CHD][hapmap];0.95[GIH][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs510372	0.93[GIH][hapmap];0.95[MEX][hapmap];0.81[AMR][1000 genomes]
rs516124	0.87[ASW][hapmap];0.81[CEU][hapmap];0.84[CHD][hapmap];0.95[GIH][hapmap];0.83[LWK][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs519763	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs521950	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs527465	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs538147	0.87[ASW][hapmap];0.84[CHD][hapmap];0.95[GIH][hapmap];0.95[MEX][hapmap];0.84[TSI][hapmap];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs541207	0.92[CEU][hapmap];0.88[GIH][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs542907	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs566128	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs574087	0.86[JPT][hapmap];0.87[MEX][hapmap];1.00[YRI][hapmap]
rs600377	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs612448	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs615540	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61886926	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs645078	0.87[ASW][hapmap];0.97[GIH][hapmap];0.91[MEX][hapmap];0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs646153	0.80[AFR][1000 genomes]
rs663743	0.85[JPT][hapmap];1.00[YRI][hapmap]
rs694739	0.87[ASW][hapmap];0.86[JPT][hapmap];0.83[MEX][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs72926005	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs72926006	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs915987	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:20 , 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	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
6	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
7	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
8	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
9	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
10	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
11	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
12	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
13	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
14	nsv897685	chr11:64048912-64150370	Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
15	nsv818841	chr11:64097233-64129722	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	37 gene(s)	inside rSNPs	diseases
16	nsv897688	chr11:64107735-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers 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	38 gene(s)	inside rSNPs	diseases
17	nsv897689	chr11:64109118-64148420	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
18	nsv897690	chr11:64118422-64135298	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
19	nsv897691	chr11:64118422-64137875	Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	31 gene(s)	inside rSNPs	diseases
20	nsv832187	chr11:64121969-64312300	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' 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	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs474901	CCDC88B	Cis_1M	lymphoblastoid	RTeQTL
rs474901	CCDC88B	cis	multi-tissue	Pritchard
rs474901	AP003774.1	cis	Whole Blood	GTEx

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64115400-64125600	Weak transcription	GM12878-XiMat	blood
2	chr11:64121800-64126000	Enhancers	Placenta	Placenta
3	chr11:64122000-64126000	Enhancers	Fetal Muscle Trunk	muscle
4	chr11:64123000-64125400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:64123000-64125400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr11:64123000-64125800	Weak transcription	Fetal Brain Male	brain
7	chr11:64123000-64126000	Weak transcription	Psoas Muscle	Psoas
8	chr11:64123200-64125400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:64123200-64125400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr11:64123200-64125400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:64123200-64125400	Weak transcription	Liver	Liver
12	chr11:64123200-64125400	Weak transcription	Brain Anterior Caudate	brain
13	chr11:64123200-64125400	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:64123200-64125400	Weak transcription	Ovary	ovary
15	chr11:64123200-64125400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:64123200-64125400	Weak transcription	Right Atrium	heart
17	chr11:64123200-64125400	Weak transcription	Right Ventricle	heart
18	chr11:64123200-64125400	Weak transcription	HSMM	muscle
19	chr11:64123200-64125400	Weak transcription	NHDF-Ad	bronchial
20	chr11:64123200-64125600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr11:64123200-64125600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:64123200-64125600	Weak transcription	Brain Germinal Matrix	brain
23	chr11:64123200-64125600	Weak transcription	Left Ventricle	heart
24	chr11:64123200-64125600	Weak transcription	Thymus	Thymus
25	chr11:64123200-64125600	Weak transcription	HSMMtube	muscle
26	chr11:64123200-64125800	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr11:64123200-64125800	Weak transcription	Brain Angular Gyrus	brain
28	chr11:64123200-64126000	Weak transcription	Aorta	Aorta
29	chr11:64123200-64126000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr11:64123200-64126000	Enhancers	HMEC	breast
31	chr11:64123200-64126200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr11:64123400-64125400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr11:64123400-64125400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:64123400-64125400	Weak transcription	Brain Hippocampus Middle	brain
35	chr11:64123400-64125400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr11:64123400-64125400	Weak transcription	Brain Substantia Nigra	brain
37	chr11:64123400-64125400	Weak transcription	Fetal Lung	lung
38	chr11:64123400-64125400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr11:64123400-64125400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr11:64123400-64125400	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr11:64123400-64125600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr11:64123400-64125600	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr11:64123400-64125800	Enhancers	Stomach Mucosa	stomach
44	chr11:64123400-64126000	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr11:64123800-64125800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr11:64123800-64126200	Enhancers	Pancreas	Pancrea
47	chr11:64124000-64125600	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr11:64124000-64125600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:64124000-64125600	Enhancers	NHEK	skin
50	chr11:64124000-64125800	Enhancers	Fetal Intestine Small	intestine

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