Variant report

Variant	rs11227221
Chromosome Location	chr11:65319265-65319266
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	CTCF	chr11:65319160-65319310	GM12873	blood:	n/a	n/a
2	TEAD4	chr11:65318262-65319427	K562	blood:	n/a	n/a
3	RCOR1	chr11:65319057-65319383	K562	blood:	n/a	n/a
4	TEAD4	chr11:65318919-65319432	HepG2	liver:	n/a	n/a
5	ATF3	chr11:65319097-65319371	K562	blood:	n/a	chr11:65319204-65319213
6	HNF4G	chr11:65318942-65319953	HepG2	liver:	n/a	chr11:65319379-65319394 chr11:65319293-65319308 chr11:65319407-65319429 chr11:65319159-65319173 chr11:65319152-65319165 chr11:65319153-65319165 chr11:65319286-65319300 chr11:65319287-65319299 chr11:65319229-65319243 chr11:65319153-65319165 chr11:65319152-65319165 chr11:65319152-65319165 chr11:65319150-65319165 chr11:65319287-65319299 chr11:65319230-65319242 chr11:65319153-65319165 chr11:65319157-65319169 chr11:65319153-65319166 chr11:65319152-65319166 chr11:65319150-65319168 chr11:65319153-65319165 chr11:65319154-65319166 chr11:65319291-65319303
7	FOXA1	chr11:65318907-65319372	HepG2	liver:	n/a	n/a
8	RCOR1	chr11:65319067-65319831	K562	blood:	n/a	n/a
9	HDAC2	chr11:65318992-65319404	K562	blood:	n/a	n/a
10	USF2	chr11:65319038-65319374	Hela-S3	cervix:	n/a	chr11:65319202-65319213
11	NR2C2	chr11:65318963-65319847	HepG2	liver:	n/a	chr11:65319295-65319304 chr11:65319154-65319163 chr11:65319286-65319299 chr11:65319159-65319172 chr11:65319381-65319390 chr11:65319288-65319297 chr11:65319229-65319242 chr11:65319152-65319165 chr11:65319161-65319170
12	NR2C2	chr11:65318818-65319908	Hela-S3	cervix:	n/a	chr11:65319295-65319304 chr11:65319154-65319163 chr11:65319286-65319299 chr11:65319159-65319172 chr11:65319381-65319390 chr11:65319288-65319297 chr11:65319229-65319242 chr11:65319152-65319165 chr11:65319161-65319170
13	NR2F2	chr11:65318330-65320420	HepG2	liver:	n/a	n/a
14	RCOR1	chr11:65319190-65319379	Hela-S3	cervix:	n/a	n/a
15	NR2F2	chr11:65318315-65320282	K562	blood:	n/a	n/a
16	USF1	chr11:65319052-65319337	HepG2	liver:	n/a	chr11:65319202-65319213
17	USF1	chr11:65318943-65319396	K562	blood:	n/a	chr11:65319202-65319213
18	NR2C2	chr11:65319025-65319935	GM12878	blood:	n/a	chr11:65319295-65319304 chr11:65319154-65319163 chr11:65319286-65319299 chr11:65319159-65319172 chr11:65319381-65319390 chr11:65319288-65319297 chr11:65319229-65319242 chr11:65319152-65319165 chr11:65319161-65319170
19	USF1	chr11:65318976-65319409	K562	blood:	n/a	chr11:65319202-65319213
20	USF1	chr11:65319001-65319419	HepG2	liver:	n/a	chr11:65319202-65319213
21	HNF4G	chr11:65318963-65319423	HepG2	liver:	n/a	chr11:65319379-65319394 chr11:65319293-65319308 chr11:65319159-65319173 chr11:65319152-65319165 chr11:65319153-65319165 chr11:65319286-65319300 chr11:65319287-65319299 chr11:65319229-65319243 chr11:65319153-65319165 chr11:65319152-65319165 chr11:65319152-65319165 chr11:65319150-65319165 chr11:65319287-65319299 chr11:65319230-65319242 chr11:65319153-65319165 chr11:65319157-65319169 chr11:65319153-65319166 chr11:65319152-65319166 chr11:65319150-65319168 chr11:65319153-65319165 chr11:65319154-65319166 chr11:65319291-65319303
22	FOXA1	chr11:65319006-65319409	HepG2	liver:	n/a	n/a
23	USF2	chr11:65318944-65319329	HepG2	liver:	n/a	chr11:65319202-65319213
24	NFIC	chr11:65319045-65319438	HepG2	liver:	n/a	n/a
25	HNF4A	chr11:65318913-65319413	HepG2	liver:	n/a	chr11:65319379-65319394 chr11:65319293-65319308 chr11:65319159-65319173 chr11:65319152-65319165 chr11:65319153-65319165 chr11:65319286-65319300 chr11:65319287-65319299 chr11:65319229-65319243 chr11:65319153-65319165 chr11:65319152-65319165 chr11:65319152-65319165 chr11:65319287-65319299 chr11:65319230-65319242 chr11:65319153-65319165 chr11:65319157-65319169 chr11:65319153-65319166 chr11:65319152-65319166 chr11:65319150-65319168 chr11:65319153-65319165 chr11:65319154-65319166 chr11:65319291-65319303
26	CBX3	chr11:65318395-65319375	K562	blood:	n/a	n/a
27	NR2F2	chr11:65318476-65320139	HepG2	liver:	n/a	n/a
28	RCOR1	chr11:65319234-65319371	HepG2	liver:	n/a	n/a
29	RXRA	chr11:65318973-65319844	HepG2	liver:	n/a	chr11:65319229-65319242 chr11:65319156-65319176 chr11:65319149-65319169 chr11:65319152-65319165 chr11:65319159-65319172 chr11:65319151-65319165 chr11:65319286-65319299 chr11:65319152-65319165 chr11:65319131-65319138 chr11:65319152-65319165 chr11:65319159-65319172 chr11:65319151-65319167 chr11:65319159-65319172 chr11:65319286-65319299 chr11:65319680-65319693 chr11:65319229-65319242 chr11:65319285-65319299 chr11:65319286-65319299 chr11:65319382-65319398
30	ZNF263	chr11:65318427-65319349	HEK293-T-REx	kidney:	n/a	n/a
31	FOXA1	chr11:65319042-65319451	HepG2	liver:	n/a	n/a
32	NR2F2	chr11:65318392-65320318	K562	blood:	n/a	n/a
33	HDAC2	chr11:65318420-65319485	HepG2	liver:	n/a	n/a
34	FOXA2	chr11:65318990-65319431	HepG2	liver:	n/a	n/a
35	CTCF	chr11:65319120-65319270	GM12864	blood:	n/a	n/a
36	NR2F2	chr11:65318416-65319986	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:65318875-65320420	A549	lung:	n/a	n/a
38	MYBL2	chr11:65318365-65319947	HepG2	liver:	n/a	n/a
39	USF1	chr11:65319046-65319306	H1-hESC	embryonic stem cell:	n/a	chr11:65319202-65319213
40	RXRA	chr11:65318854-65320247	HepG2	liver:	n/a	chr11:65319229-65319242 chr11:65319156-65319176 chr11:65319149-65319169 chr11:65319152-65319165 chr11:65319159-65319172 chr11:65319151-65319165 chr11:65319286-65319299 chr11:65319152-65319165 chr11:65319131-65319138 chr11:65319152-65319165 chr11:65319159-65319172 chr11:65319151-65319167 chr11:65319159-65319172 chr11:65319286-65319299 chr11:65319680-65319693 chr11:65319229-65319242 chr11:65319285-65319299 chr11:65319286-65319299 chr11:65319382-65319398 chr11:65320172-65320188
41	NFIC	chr11:65318917-65319475	HepG2	liver:	n/a	n/a
42	HNF4A	chr11:65318968-65319424	HepG2	liver:	n/a	chr11:65319379-65319394 chr11:65319293-65319308 chr11:65319159-65319173 chr11:65319152-65319165 chr11:65319153-65319165 chr11:65319286-65319300 chr11:65319287-65319299 chr11:65319229-65319243 chr11:65319153-65319165 chr11:65319152-65319165 chr11:65319152-65319165 chr11:65319287-65319299 chr11:65319230-65319242 chr11:65319153-65319165 chr11:65319157-65319169 chr11:65319153-65319166 chr11:65319152-65319166 chr11:65319150-65319168 chr11:65319153-65319165 chr11:65319154-65319166 chr11:65319291-65319303
43	NR2F2	chr11:65318294-65320454	MCF-7	breast:	n/a	n/a
44	EP300	chr11:65318706-65319878	HepG2	liver:	n/a	chr11:65319191-65319201
45	ESRRA	chr11:65319085-65320216	HepG2	liver:	n/a	chr11:65319236-65319246
46	FOXA1	chr11:65318910-65319371	HepG2	liver:	n/a	n/a
47	USF1	chr11:65319064-65319395	H1-hESC	embryonic stem cell:	n/a	chr11:65319202-65319213
48	HNF4A	chr11:65319119-65320437	HepG2	liver:	n/a	chr11:65319379-65319394 chr11:65319293-65319308 chr11:65319407-65319429 chr11:65319159-65319173 chr11:65319152-65319165 chr11:65319153-65319165 chr11:65319286-65319300 chr11:65319287-65319299 chr11:65319229-65319243 chr11:65319153-65319165 chr11:65319152-65319165 chr11:65319152-65319165 chr11:65319287-65319299 chr11:65319230-65319242 chr11:65319153-65319165 chr11:65319157-65319169 chr11:65320172-65320188 chr11:65319153-65319166 chr11:65319152-65319166 chr11:65319150-65319168 chr11:65319153-65319165 chr11:65319154-65319166 chr11:65319291-65319303
49	CTCF	chr11:65319251-65320171	SK-N-SH	brain:	n/a	n/a
50	MYBL2	chr11:65318906-65319970	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65317456..65320108-chr11:65409381..65411829,2	K562	blood:
2	chr11:65317657..65319340-chr11:65625571..65627845,2	K562	blood:
3	chr11:65264365..65266366-chr11:65317003..65319991,2	K562	blood:
4	chr11:65317777..65320540-chr11:65382585..65385188,2	K562	blood:
5	chr11:65264483..65267723-chr11:65317387..65320009,5	MCF-7	breast:
6	chr11:65264479..65268560-chr11:65318003..65330456,22	MCF-7	breast:
7	chr11:65308291..65309442-chr11:65319131..65320116,6	MCF-7	breast:
8	chr11:65307648..65308488-chr11:65318954..65319482,2	MCF-7	breast:
9	chr11:65190162..65194738-chr11:65316952..65321274,6	K562	blood:
10	chr11:65184371..65196984-chr11:65316952..65328208,29	K562	blood:
11	chr11:65318195..65320071-chr11:65547732..65549881,2	K562	blood:

Variant related genes	Relation type
LTBP3	TF binding region
ENSG00000270117	Chromatin interaction
ENSG00000213445	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000254470	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000168056	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10896015	0.80[JPT][hapmap]
rs10896016	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.95[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1111934	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1151517	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11601767	0.92[ASW][hapmap];0.82[CEU][hapmap];0.85[CHB][hapmap];0.97[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.89[YRI][hapmap];0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11604423	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11607147	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1194076	0.80[JPT][hapmap]
rs12270054	0.80[JPT][hapmap]
rs1787663	0.80[JPT][hapmap]
rs3782091	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.94[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4244811	1.00[ASW][hapmap];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[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs600231	0.90[MKK][hapmap];0.89[TSI][hapmap]

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	nsv897715	chr11:65083491-65427346	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
2	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS 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	999 gene(s)	inside rSNPs	diseases
3	esv1829999	chr11:65136686-65343124	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers 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 miRNA miRNA target site	963 gene(s)	inside rSNPs	diseases
4	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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	1003 gene(s)	inside rSNPs	diseases
5	nsv541068	chr11:65142779-65331136	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	953 gene(s)	inside rSNPs	diseases
6	nsv541069	chr11:65142779-65368787	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	965 gene(s)	inside rSNPs	diseases
7	nsv541070	chr11:65142779-65397058	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription 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 miRNA target site	972 gene(s)	inside rSNPs	diseases
8	nsv541071	chr11:65142779-65429352	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
9	nsv897719	chr11:65157094-65335705	Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
10	nsv541073	chr11:65171202-65331136	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
11	nsv541074	chr11:65171202-65368787	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	961 gene(s)	inside rSNPs	diseases
12	nsv541075	chr11:65210592-65331136	Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	620 gene(s)	inside rSNPs	diseases
13	nsv541076	chr11:65210592-65397058	Flanking Active TSS Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	645 gene(s)	inside rSNPs	diseases
14	nsv897720	chr11:65213434-65445950	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' 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	665 gene(s)	inside rSNPs	diseases
15	nsv897721	chr11:65278461-65422853	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
16	nsv897722	chr11:65278461-65436888	Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS 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 miRNA target site	102 gene(s)	inside rSNPs	diseases
17	nsv897723	chr11:65294830-65481166	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers 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	107 gene(s)	inside rSNPs	diseases
18	nsv897729	chr11:65302893-65322548	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	30 gene(s)	inside rSNPs	diseases
19	nsv897730	chr11:65302893-65376484	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs11227221	TPCN2	cis	parietal	SCAN
rs11227221	BBS1	cis	parietal	SCAN
rs11227221	NEAT1	cis	Nerve Tibial	GTEx
rs11227221	EIF1AD	cis	cerebellum	SCAN
rs11227221	INCENP	cis	cerebellum	SCAN
rs11227221	LTBP3	cis	cerebellum	SCAN
rs11227221	TncRNA	Cis_1M	lymphoblastoid	RTeQTL
rs11227221	TTC9C	cis	parietal	SCAN
rs11227221	CDK2AP2	cis	cerebellum	SCAN
rs11227221	NEAT1	cis	Esophagus Muscularis	GTEx

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65307200-65322600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:65309200-65320600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr11:65309200-65320600	Strong transcription	Osteobl	bone
4	chr11:65309200-65322200	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr11:65309200-65323000	Weak transcription	Psoas Muscle	Psoas
6	chr11:65309400-65319400	Weak transcription	HSMM	muscle
7	chr11:65309400-65323000	Weak transcription	Right Atrium	heart
8	chr11:65309800-65322200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:65310200-65320400	Strong transcription	Muscle Satellite Cultured Cells	--
10	chr11:65310200-65320800	Strong transcription	Brain Cingulate Gyrus	brain
11	chr11:65310400-65322000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:65310800-65324000	Weak transcription	Fetal Kidney	kidney
13	chr11:65313000-65320800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr11:65314600-65321000	Strong transcription	Fetal Stomach	stomach
15	chr11:65314800-65320600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr11:65314800-65321600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr11:65314800-65322800	Weak transcription	NHEK	skin
18	chr11:65315000-65319800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr11:65315000-65320200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr11:65315200-65320200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr11:65315200-65320400	Strong transcription	Colon Smooth Muscle	Colon
22	chr11:65315200-65321200	Weak transcription	Fetal Brain Male	brain
23	chr11:65315400-65321200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:65315600-65319600	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr11:65316200-65319400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr11:65316200-65319600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:65316600-65320800	Strong transcription	Brain Hippocampus Middle	brain
28	chr11:65316600-65321200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:65317000-65322400	Weak transcription	HSMMtube	muscle
30	chr11:65317200-65319600	Strong transcription	Ovary	ovary
31	chr11:65317600-65321400	Weak transcription	Fetal Brain Female	brain
32	chr11:65318000-65320400	Strong transcription	Aorta	Aorta
33	chr11:65318000-65320600	Strong transcription	Brain Germinal Matrix	brain
34	chr11:65318000-65321000	Genic enhancers	Placenta	Placenta
35	chr11:65318200-65319800	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr11:65318200-65320200	Strong transcription	NH-A	brain
37	chr11:65318400-65319400	Genic enhancers	Primary T cells fromperipheralblood	blood
38	chr11:65318400-65319400	Strong transcription	Brain Inferior Temporal Lobe	brain
39	chr11:65318400-65319600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:65318400-65319800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:65318400-65319800	Strong transcription	Left Ventricle	heart
42	chr11:65318400-65320000	Flanking Active TSS	Hela-S3	cervix
43	chr11:65318400-65320200	Genic enhancers	Pancreas	Pancrea
44	chr11:65318400-65320400	Genic enhancers	Esophagus	oesophagus
45	chr11:65318400-65320400	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr11:65318400-65320400	Strong transcription	HUVEC	blood vessel
47	chr11:65318400-65320600	Genic enhancers	A549	lung
48	chr11:65318400-65320800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr11:65318400-65320800	Genic enhancers	Spleen	Spleen
50	chr11:65318400-65321600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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