Variant report

Variant	rs2075660
Chromosome Location	chr11:65414709-65414710
allele	A/C
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	MAX	chr11:65414273-65415316	A549	lung:	n/a	chr11:65414824-65414834
2	POLR2A	chr11:65414532-65415338	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr11:65414275-65415194	H1-hESC	embryonic stem cell:	n/a	n/a
4	RAD21	chr11:65414183-65414771	H1-hESC	embryonic stem cell:	n/a	chr11:65414644-65414656
5	TAF1	chr11:65414575-65415022	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr11:65414334-65415302	HCT-116	colon:	n/a	n/a
7	POLR2A	chr11:65414371-65415029	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr11:65414580-65415203	HUVEC	blood vessel:	n/a	n/a
9	SP4	chr11:65414279-65415106	H1-hESC	embryonic stem cell:	n/a	chr11:65414823-65414839 chr11:65414784-65414800 chr11:65414821-65414837
10	POLR2A	chr11:65410580-65415232	GM12878	blood:	n/a	n/a
11	ZNF143	chr11:65414593-65414792	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr11:65414507-65415204	ECC-1	luminal epithelium:	n/a	chr11:65414824-65414834
13	CREB1	chr11:65414543-65415274	A549	lung:	n/a	n/a
14	TCF7L2	chr11:65414374-65415014	HCT-116	colon:	n/a	n/a
15	GABPA	chr11:65413985-65414851	H1-hESC	embryonic stem cell:	n/a	chr11:65414825-65414834 chr11:65414566-65414575
16	POLR2A	chr11:65414344-65415203	A549	lung:	n/a	n/a
17	CHD2	chr11:65414391-65414766	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr11:65414596-65415152	A549	lung:	n/a	n/a
19	POLR2A	chr11:65414632-65415111	A549	lung:	n/a	n/a
20	TBP	chr11:65414461-65414746	H1-hESC	embryonic stem cell:	n/a	n/a
21	MYC	chr11:65414401-65414737	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAX	chr11:65414202-65415168	H1-hESC	embryonic stem cell:	n/a	chr11:65414824-65414834
23	SP4	chr11:65414549-65415103	H1-hESC	embryonic stem cell:	n/a	chr11:65414823-65414839 chr11:65414784-65414800 chr11:65414821-65414837
24	SP1	chr11:65414325-65415163	H1-hESC	embryonic stem cell:	n/a	chr11:65414824-65414833 chr11:65414594-65414608 chr11:65414788-65414800 chr11:65414824-65414834 chr11:65414573-65414585 chr11:65414788-65414800 chr11:65415147-65415161 chr11:65414836-65414848 chr11:65414573-65414585 chr11:65414824-65414834 chr11:65414825-65414834 chr11:65414593-65414605 chr11:65414837-65414846 chr11:65414575-65414584 chr11:65414836-65414848 chr11:65414789-65414798 chr11:65414808-65414822 chr11:65414823-65414835 chr11:65414823-65414835
25	POLR2A	chr11:65414349-65415175	PANC-1	pancreas:	n/a	n/a
26	BCL3	chr11:65414561-65414868	A549	lung:	n/a	chr11:65414575-65414584 chr11:65414817-65414830
27	JUND	chr11:65414537-65415201	A549	lung:	n/a	n/a
28	BACH1	chr11:65414311-65415087	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:65413726-65418689	K562	blood:	n/a	n/a
30	POLR2A	chr11:65414198-65415354	H1-hESC	embryonic stem cell:	n/a	n/a
31	E2F6	chr11:65414353-65415232	A549	lung:	n/a	chr11:65414789-65414798 chr11:65414600-65414612
32	TCF12	chr11:65414515-65415361	A549	lung:	n/a	n/a
33	MAX	chr11:65414585-65415094	A549	lung:	n/a	chr11:65414824-65414834
34	MAX	chr11:65414400-65415213	MCF-7	breast:	n/a	chr11:65414824-65414834
35	MAX	chr11:65414354-65415218	A549	lung:	n/a	chr11:65414824-65414834
36	POLR2A	chr11:65414602-65415204	A549	lung:	n/a	n/a
37	MXI1	chr11:65414389-65415306	SK-N-SH	brain:	n/a	n/a
38	SP1	chr11:65414365-65415083	A549	lung:	n/a	chr11:65414824-65414833 chr11:65414594-65414608 chr11:65414788-65414800 chr11:65414824-65414834 chr11:65414573-65414585 chr11:65414788-65414800 chr11:65414836-65414848 chr11:65414573-65414585 chr11:65414824-65414834 chr11:65414825-65414834 chr11:65414593-65414605 chr11:65414837-65414846 chr11:65414575-65414584 chr11:65414836-65414848 chr11:65414789-65414798 chr11:65414808-65414822 chr11:65414823-65414835 chr11:65414823-65414835
39	E2F6	chr11:65414529-65415189	A549	lung:	n/a	chr11:65414789-65414798 chr11:65414600-65414612
40	POLR2A	chr11:65414564-65415173	MCF-7	breast:	n/a	n/a
41	TAF1	chr11:65414478-65414770	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr11:65414674-65415024	K562	blood:	n/a	n/a
43	POLR2A	chr11:65414543-65414767	K562	blood:	n/a	n/a
44	CTBP2	chr11:65413944-65415167	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr11:65414628-65415185	SK-N-SH	brain:	n/a	chr11:65414824-65414834
46	SIN3A	chr11:65414333-65415218	H1-hESC	embryonic stem cell:	n/a	chr11:65414570-65414581 chr11:65414793-65414802
47	POLR2A	chr11:65414346-65415328	H1-hESC	embryonic stem cell:	n/a	n/a
48	MYC	chr11:65414703-65415024	MCF-7	breast:	n/a	chr11:65414824-65414834
49	POLR2A	chr11:65414618-65415150	MCF-7	breast:	n/a	n/a
50	POLR2A	chr11:65414551-65415176	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65413332..65415260-chr11:65625154..65627683,2	K562	blood:
2	chr11:65412642..65414860-chr11:65428206..65431618,3	MCF-7	breast:
3	chr11:65394604..65399186-chr11:65411487..65416339,5	MCF-7	breast:

Variant related genes	Relation type
MIR4489	TF binding region
SIPA1	TF binding region
ENSG00000172732	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000173039	Chromatin interaction
ENSG00000197136	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11227247	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12417989	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12418567	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12418630	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12418683	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12419110	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12420405	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12420618	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12421691	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1962691	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1963977	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2127510	0.86[AMR][1000 genomes]
rs2306365	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35927673	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36028748	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs36091060	0.88[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs36113281	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3741378	0.95[EUR][1000 genomes]
rs3782086	0.80[EUR][1000 genomes]
rs4578394	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4645916	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4930158	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4930299	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55758897	0.84[ASN][1000 genomes]
rs56115979	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7101916	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7107503	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7119750	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7122081	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7122098	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 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	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
4	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
5	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
6	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
7	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
8	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
9	nsv468599	chr11:65335705-65427346	ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
10	nsv555213	chr11:65335705-65427346	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Enhancers 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	78 gene(s)	inside rSNPs	diseases
11	nsv897732	chr11:65335705-65427346	Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Active 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	78 gene(s)	inside rSNPs	diseases
12	nsv468600	chr11:65335705-65431360	Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
13	nsv555214	chr11:65335705-65431360	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers 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	92 gene(s)	inside rSNPs	diseases
14	nsv897733	chr11:65335705-65431360	Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers 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	92 gene(s)	inside rSNPs	diseases
15	nsv897734	chr11:65335705-65436888	Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
16	nsv897735	chr11:65335705-65481166	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
17	nsv897736	chr11:65335705-65676516	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' 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	227 gene(s)	inside rSNPs	diseases
18	nsv897746	chr11:65349756-65427346	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription 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 miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
19	nsv897747	chr11:65353906-65481166	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active 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 miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
20	esv1831135	chr11:65387352-65420872	Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	43 gene(s)	inside rSNPs	diseases
21	nsv897748	chr11:65392695-65466911	Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
22	nsv897749	chr11:65401748-65420760	Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	39 gene(s)	inside rSNPs	diseases
23	nsv897750	chr11:65401748-65421476	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
24	nsv897751	chr11:65401748-65425167	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
25	nsv897752	chr11:65405300-65421476	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
26	nsv897753	chr11:65405300-65422693	Genic enhancers Active TSS Flanking Active TSS Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
27	nsv897754	chr11:65405300-65436888	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers 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	59 gene(s)	inside rSNPs	diseases
28	nsv897755	chr11:65405300-65481166	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
29	nsv897756	chr11:65406393-65425167	Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
30	nsv897757	chr11:65406393-65427568	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2075660	MALAT1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65406400-65416800	Weak transcription	Aorta	Aorta
2	chr11:65406600-65419200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:65407000-65415000	Genic enhancers	Fetal Muscle Trunk	muscle
4	chr11:65408800-65414800	Genic enhancers	Spleen	Spleen
5	chr11:65409200-65416200	Weak transcription	Fetal Lung	lung
6	chr11:65409200-65419000	Weak transcription	Right Atrium	heart
7	chr11:65409400-65415000	Weak transcription	Brain Angular Gyrus	brain
8	chr11:65409600-65415200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:65409600-65416000	Strong transcription	Thymus	Thymus
10	chr11:65410000-65416400	Strong transcription	Adipose Nuclei	Adipose
11	chr11:65410000-65417000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:65410800-65415200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:65410800-65418200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr11:65411200-65415800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:65411200-65419000	Weak transcription	HSMM	muscle
16	chr11:65411400-65418800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr11:65411600-65415600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr11:65411600-65417200	Strong transcription	Fetal Thymus	thymus
19	chr11:65411600-65417400	Strong transcription	Primary neutrophils fromperipheralblood	blood
20	chr11:65411600-65418600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr11:65411600-65418800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr11:65411600-65419000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr11:65411800-65417000	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr11:65411800-65419200	Strong transcription	Primary T cells from cord blood	blood
25	chr11:65412000-65417000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:65412000-65417600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:65412000-65418800	Weak transcription	Hela-S3	cervix
28	chr11:65412000-65419000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:65412200-65415200	Strong transcription	Left Ventricle	heart
30	chr11:65412200-65418400	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr11:65412200-65418800	Weak transcription	HepG2	liver
32	chr11:65412400-65416600	Strong transcription	Primary B cells from peripheral blood	blood
33	chr11:65412400-65417600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:65412400-65418400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr11:65412600-65416600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:65412600-65419600	Genic enhancers	Fetal Muscle Leg	muscle
37	chr11:65413000-65414800	Genic enhancers	Lung	lung
38	chr11:65413000-65417000	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr11:65413200-65415400	Genic enhancers	Placenta	Placenta
40	chr11:65413200-65416400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr11:65413200-65418000	Weak transcription	Colon Smooth Muscle	Colon
42	chr11:65413200-65418800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr11:65413400-65415200	Strong transcription	NHLF	lung
44	chr11:65413400-65418200	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr11:65413400-65419000	Weak transcription	NHDF-Ad	bronchial
46	chr11:65413600-65418600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr11:65413600-65419000	Weak transcription	HSMMtube	muscle
48	chr11:65413800-65415200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr11:65413800-65415400	Weak transcription	Primary hematopoietic stem cells	blood
50	chr11:65413800-65415600	Active TSS	HUES6 Cell Line	embryonic stem cell

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