Variant report

Variant	rs1784859
Chromosome Location	chr11:65220749-65220750
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	CEBPB	chr11:65220587-65221168	A549	lung:	n/a	n/a
2	RAD21	chr11:65220583-65220919	Hela-S3	cervix:	n/a	n/a
3	JUN	chr11:65220616-65221024	Hela-S3	cervix:	n/a	n/a
4	STAT3	chr11:65220591-65221089	MCF10A-Er-Src	breast:	n/a	chr11:65220714-65220722 chr11:65220863-65220874
5	MYC	chr11:65220394-65220944	MCF10A-Er-Src	breast:	n/a	n/a
6	CHD2	chr11:65220624-65220830	Hela-S3	cervix:	n/a	n/a
7	MYC	chr11:65220373-65221076	MCF10A-Er-Src	breast:	n/a	n/a
8	STAT3	chr11:65220608-65221021	Hela-S3	cervix:	n/a	chr11:65220714-65220722 chr11:65220863-65220874
9	ELK4	chr11:65220471-65220918	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr11:65220567-65220843	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:65220654-65221095	IMR90	lung:	n/a	n/a
12	CEBPB	chr11:65220702-65221060	A549	lung:	n/a	n/a
13	STAT3	chr11:65220620-65221045	MCF10A-Er-Src	breast:	n/a	chr11:65220714-65220722 chr11:65220863-65220874
14	TBP	chr11:65220595-65220992	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr11:65219749-65221240	U87	brain:	n/a	n/a
16	USF2	chr11:65220655-65220854	Hela-S3	cervix:	n/a	n/a
17	GTF2F1	chr11:65220597-65220896	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr11:65220609-65220800	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr11:65220010-65221032	SK-N-SH	brain:	n/a	n/a
20	FOSL2	chr11:65220204-65221121	SK-N-SH	brain:	n/a	n/a
21	TCF12	chr11:65219871-65221149	SK-N-SH	brain:	n/a	chr11:65220699-65220709
22	NFIC	chr11:65220066-65221003	SK-N-SH	brain:	n/a	n/a
23	ELK1	chr11:65220571-65220860	Hela-S3	cervix:	n/a	n/a
24	PBX3	chr11:65220036-65221065	SK-N-SH	brain:	n/a	n/a
25	TCF12	chr11:65219915-65221094	SK-N-SH	brain:	n/a	chr11:65220699-65220709
26	GTF3C2	chr11:65220621-65221216	Hela-S3	cervix:	n/a	n/a
27	SMC3	chr11:65220604-65220945	Hela-S3	cervix:	n/a	n/a
28	MAZ	chr11:65220601-65220817	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr11:65219867-65221167	U87	brain:	n/a	n/a
30	E2F4	chr11:65220641-65221077	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr11:65220581-65221085	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr11:65220616-65221054	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr11:65219846-65221167	U87	brain:	n/a	n/a
34	TAF1	chr11:65220203-65220774	PFSK-1	brain:	n/a	n/a
35	RFX5	chr11:65220649-65221030	Hela-S3	cervix:	n/a	n/a
36	RFX5	chr11:65220717-65220886	K562	blood:	n/a	n/a
37	FOS	chr11:65220510-65221073	MCF10A-Er-Src	breast:	n/a	n/a
38	STAT3	chr11:65220562-65221092	MCF10A-Er-Src	breast:	n/a	chr11:65220714-65220722 chr11:65220863-65220874
39	POLR2A	chr11:65219993-65220851	PFSK-1	brain:	n/a	n/a
40	PBX3	chr11:65220124-65220947	SK-N-SH	brain:	n/a	n/a
41	POLR2A	chr11:65220101-65220783	PFSK-1	brain:	n/a	n/a
42	FOS	chr11:65220525-65221079	MCF10A-Er-Src	breast:	n/a	n/a
43	JUND	chr11:65220583-65220972	Hela-S3	cervix:	n/a	n/a
44	TCF7L2	chr11:65220612-65220793	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:65220716-65221040	A549	lung:	n/a	n/a
46	POLR2A	chr11:65220214-65220881	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr11:65219800-65221139	U87	brain:	n/a	n/a
48	EP300	chr11:65220588-65221052	Hela-S3	cervix:	n/a	n/a
49	RCOR1	chr11:65220574-65220990	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr11:65220554-65221095	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65122004..65123879-chr11:65220475..65223059,2	K562	blood:
2	chr11:62608095..62609669-chr11:65220631..65223111,2	MCF-7	breast:
3	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000769.1-1	chr11:65219924-65221119	NONHSAT022120

Variant related genes	Relation type
ENSG00000173727	TF binding region
ENSG00000133316	Chromatin interaction
ENSG00000173825	Chromatin interaction
ENSG00000245532	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10896001	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11227204	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1152619	0.86[JPT][hapmap]
rs11822111	0.84[AMR][1000 genomes]
rs1616810	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1621277	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1626021	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1784100	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1784101	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1784858	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1784860	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2105608	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2508711	0.86[ASN][1000 genomes]
rs2508712	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2846861	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2957268	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2957269	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3015965	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3015966	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3016343	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3132743	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3132767	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs512715	0.83[MEX][hapmap]
rs587080	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs587390	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs588298	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs600231	0.82[JPT][hapmap];0.82[MEX][hapmap]
rs602838	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs604676	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs605035	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs660588	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs661403	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs674485	0.83[MEX][hapmap]
rs682845	0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs694243	0.83[MEX][hapmap]
rs7114809	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7934628	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic 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	1539 gene(s)	inside rSNPs	diseases
2	esv2422285	chr11:65013294-65254540	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong 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	474 gene(s)	inside rSNPs	diseases
3	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
4	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
5	nsv541065	chr11:65117387-65271894	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	835 gene(s)	inside rSNPs	diseases
6	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
7	nsv897717	chr11:65140209-65278461	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	942 gene(s)	inside rSNPs	diseases
8	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
9	nsv541066	chr11:65142779-65271894	Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers 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	833 gene(s)	inside rSNPs	diseases
10	nsv541067	chr11:65142779-65313799	Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	950 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	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
15	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
16	nsv541072	chr11:65171202-65313799	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	946 gene(s)	inside rSNPs	diseases
17	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
18	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
19	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
20	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
21	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
22	esv32703	chr11:65213860-65222026	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs1784859	NEAT1	cis	Adipose Subcutaneous	GTEx
rs1784859	C11orf83	cis	parietal	SCAN
rs1784859	NEAT1	cis	Muscle Skeletal	GTEx
rs1784859	BBS1	cis	parietal	SCAN
rs1784859	SCGB2A2	cis	parietal	SCAN
rs1784859	VWCE	cis	parietal	SCAN
rs1784859	NEAT1	cis	Nerve Tibial	GTEx
rs1784859	NEAT1	cis	Esophagus Mucosa	GTEx

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65206600-65222000	Weak transcription	Fetal Kidney	kidney
2	chr11:65210000-65222000	Weak transcription	Brain Angular Gyrus	brain
3	chr11:65210000-65222200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr11:65210800-65222000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr11:65211400-65222000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr11:65211600-65221800	Weak transcription	HUVEC	blood vessel
7	chr11:65212200-65221800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:65212200-65222000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr11:65212200-65222200	Weak transcription	Liver	Liver
10	chr11:65212400-65222000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr11:65212400-65222000	Weak transcription	Aorta	Aorta
12	chr11:65212400-65222000	Weak transcription	Fetal Lung	lung
13	chr11:65212600-65222000	Weak transcription	Brain Anterior Caudate	brain
14	chr11:65212800-65221800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:65212800-65222000	Weak transcription	Primary T cells from cord blood	blood
16	chr11:65212800-65222000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr11:65212800-65222200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr11:65212800-65222400	Weak transcription	Stomach Mucosa	stomach
19	chr11:65213000-65221800	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr11:65213000-65222000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr11:65213200-65221800	Weak transcription	Duodenum Mucosa	Duodenum
22	chr11:65213400-65222000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr11:65213400-65222000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr11:65213800-65222000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr11:65213800-65222200	Weak transcription	Gastric	stomach
26	chr11:65213800-65222200	Weak transcription	Pancreas	Pancrea
27	chr11:65214000-65221800	Weak transcription	Right Atrium	heart
28	chr11:65214200-65222000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr11:65214200-65222000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:65214200-65222200	Weak transcription	Colon Smooth Muscle	Colon
31	chr11:65214400-65221800	Weak transcription	Thymus	Thymus
32	chr11:65214400-65221800	Weak transcription	Spleen	Spleen
33	chr11:65214400-65222000	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr11:65214400-65222200	Weak transcription	Brain Cingulate Gyrus	brain
35	chr11:65214400-65222200	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr11:65214600-65221400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:65214600-65221400	Weak transcription	Colonic Mucosa	Colon
38	chr11:65214600-65221400	Weak transcription	Right Ventricle	heart
39	chr11:65214600-65221800	Weak transcription	Ovary	ovary
40	chr11:65214600-65222000	Weak transcription	Brain Substantia Nigra	brain
41	chr11:65214600-65222000	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr11:65214600-65222000	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr11:65214800-65221800	Weak transcription	Stomach Smooth Muscle	stomach
44	chr11:65214800-65222000	Weak transcription	Brain Hippocampus Middle	brain
45	chr11:65216400-65221600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:65216600-65221800	Weak transcription	Primary B cells from peripheral blood	blood
47	chr11:65216800-65221800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr11:65217000-65221400	Weak transcription	GM12878-XiMat	blood
49	chr11:65217200-65221800	Weak transcription	K562	blood
50	chr11:65217200-65222000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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