Variant report

Variant	rs7125986
Chromosome Location	chr11:65624934-65624935
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	chr11:65624256-65626280	HepG2	liver:	n/a	chr11:65624498-65624507 chr11:65624497-65624508 chr11:65624496-65624509 chr11:65624435-65624445 chr11:65624498-65624507
2	POLR2A	chr11:65623326-65628516	K562	blood:	n/a	n/a
3	POLR2A	chr11:65624629-65625041	MCF10A-Er-Src	breast:	n/a	n/a
4	CTCF	chr11:65624840-65624990	GM06990	blood:	n/a	n/a
5	POLR2A	chr11:65624266-65626013	MCF-7	breast:	n/a	n/a
6	TAF1	chr11:65624783-65624977	SK-N-SH	brain:	n/a	n/a
7	REST	chr11:65624481-65625050	A549	lung:	n/a	n/a
8	HEY1	chr11:65624342-65625036	HepG2	liver:	n/a	chr11:65624828-65624843
9	EP300	chr11:65624932-65625992	SK-N-SH_RA	brain:	n/a	chr11:65625187-65625203 chr11:65625628-65625644 chr11:65625187-65625196 chr11:65625057-65625073 chr11:65625056-65625072 chr11:65625035-65625051 chr11:65625861-65625877
10	ELF1	chr11:65624047-65625007	K562	blood:	n/a	n/a
11	IRF1	chr11:65624180-65624946	K562	blood:	n/a	chr11:65624721-65624735 chr11:65624522-65624536 chr11:65624688-65624700
12	HA-E2F1	chr11:65624516-65626263	MCF-7	breast:	n/a	chr11:65625791-65625803 chr11:65624854-65624863 chr11:65625409-65625418 chr11:65625248-65625255 chr11:65624722-65624731 chr11:65625504-65625516
13	POLR2A	chr11:65624504-65626425	NB4	blood:	n/a	n/a
14	JUND	chr11:65624646-65626103	MCF-7	breast:	n/a	n/a
15	GABPA	chr11:65624271-65624997	Hela-S3	cervix:	n/a	chr11:65624853-65624864 chr11:65624523-65624532 chr11:65624853-65624862 chr11:65624722-65624731 chr11:65624850-65624864
16	USF1	chr11:65624038-65625135	HCT-116	colon:	n/a	chr11:65624497-65624508 chr11:65625104-65625120 chr11:65625048-65625064 chr11:65624826-65624842 chr11:65625040-65625056
17	POLR2A	chr11:65617944-65626197	K562	blood:	n/a	n/a
18	HEY1	chr11:65624312-65626436	K562	blood:	n/a	chr11:65625188-65625203 chr11:65625757-65625772 chr11:65624828-65624843
19	GABPA	chr11:65624286-65626000	K562	blood:	n/a	chr11:65624853-65624864 chr11:65624523-65624532 chr11:65625323-65625337 chr11:65625408-65625419 chr11:65625512-65625521 chr11:65624853-65624862 chr11:65625408-65625417 chr11:65625405-65625419 chr11:65625408-65625422 chr11:65624722-65624731 chr11:65625320-65625334 chr11:65624850-65624864
20	HCFC1	chr11:65623229-65629451	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:65617092-65633870	K562	blood:	n/a	n/a
22	POLR2A	chr11:65623808-65626436	PFSK-1	brain:	n/a	n/a
23	NFATC1	chr11:65623447-65625282	GM12878	blood:	n/a	n/a
24	MAX	chr11:65624318-65626312	Hela-S3	cervix:	n/a	chr11:65624498-65624507 chr11:65624497-65624508 chr11:65624496-65624509 chr11:65624435-65624445 chr11:65624498-65624507
25	POLR2A	chr11:65624567-65625101	PBDE	blood:	n/a	n/a
26	ZNF143	chr11:65624824-65628112	K562	blood:	n/a	chr11:65625465-65625483 chr11:65625821-65625839 chr11:65625425-65625435 chr11:65625773-65625791 chr11:65625757-65625767 chr11:65625463-65625473 chr11:65625828-65625837 chr11:65626696-65626714 chr11:65627928-65627938 chr11:65627521-65627540 chr11:65625063-65625073
27	CTCF	chr11:65624820-65624970	Hela-S3	cervix:	n/a	n/a
28	TAF1	chr11:65624375-65626143	ECC-1	luminal epithelium:	n/a	n/a
29	MXI1	chr11:65624350-65625197	HepG2	liver:	n/a	chr11:65624499-65624508
30	CHD2	chr11:65624457-65625106	H1-hESC	embryonic stem cell:	n/a	chr11:65624723-65624733
31	SP1	chr11:65624314-65624956	GM12878	blood:	n/a	chr11:65624522-65624534 chr11:65624722-65624732 chr11:65624722-65624731 chr11:65624722-65624732 chr11:65624723-65624732 chr11:65624523-65624532 chr11:65624723-65624732 chr11:65624548-65624560 chr11:65624721-65624733 chr11:65624548-65624560 chr11:65624431-65624445 chr11:65624434-65624446 chr11:65624721-65624733
32	SIN3AK20	chr11:65623944-65626089	MCF-7	breast:	n/a	n/a
33	SIN3AK20	chr11:65624289-65624946	PFSK-1	brain:	n/a	n/a
34	POLR2A	chr11:65623812-65628919	HUVEC	blood vessel:	n/a	n/a
35	MXI1	chr11:65624270-65626274	GM12878	blood:	n/a	chr11:65624499-65624508
36	MYC	chr11:65624329-65626294	K562	blood:	n/a	chr11:65624498-65624507 chr11:65624497-65624508 chr11:65624496-65624509 chr11:65624435-65624445 chr11:65624498-65624507
37	USF2	chr11:65624308-65624958	GM12878	blood:	n/a	chr11:65624826-65624842 chr11:65624497-65624508
38	EP300	chr11:65624831-65625383	ECC-1	luminal epithelium:	n/a	chr11:65625187-65625203 chr11:65625187-65625196 chr11:65625057-65625073 chr11:65625056-65625072 chr11:65625035-65625051
39	SP4	chr11:65624175-65624987	H1-hESC	embryonic stem cell:	n/a	chr11:65624520-65624536 chr11:65624717-65624733 chr11:65624518-65624534
40	ELK4	chr11:65623491-65625123	Hela-S3	cervix:	n/a	n/a
41	TCF12	chr11:65624458-65626077	ECC-1	luminal epithelium:	n/a	chr11:65625082-65625092
42	ELF1	chr11:65624049-65626168	MCF-7	breast:	n/a	chr11:65625761-65625770 chr11:65625630-65625639
43	MAX	chr11:65624166-65625368	ECC-1	luminal epithelium:	n/a	chr11:65624498-65624507 chr11:65624497-65624508 chr11:65624496-65624509 chr11:65624435-65624445 chr11:65624498-65624507
44	TAF1	chr11:65624694-65626021	ECC-1	luminal epithelium:	n/a	n/a
45	MYC	chr11:65624325-65626324	MCF10A-Er-Src	breast:	n/a	chr11:65624498-65624507 chr11:65624497-65624508 chr11:65624496-65624509 chr11:65624435-65624445 chr11:65624498-65624507
46	TAL1	chr11:65624321-65625804	K562	blood:	n/a	n/a
47	POLR2A	chr11:65624455-65628614	Raji	blood:	n/a	n/a
48	BCLAF1	chr11:65624335-65625273	GM12878	blood:	n/a	chr11:65625098-65625111 chr11:65624826-65624839 chr11:65625187-65625200
49	MAX	chr11:65624339-65626311	A549	lung:	n/a	chr11:65624498-65624507 chr11:65624497-65624508 chr11:65624496-65624509 chr11:65624435-65624445 chr11:65624498-65624507
50	FOXM1	chr11:65624103-65628727	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65624916..65625735-chr14:92302236..92302911,2	Hela-S3	cervix:
2	chr11:65381104..65384699-chr11:65624758..65628552,6	MCF-7	breast:
3	chr11:65601147..65603673-chr11:65623876..65625928,3	MCF-7	breast:
4	chr11:65472429..65485450-chr11:65615794..65629774,38	K562	blood:
5	chr11:65624298..65626384-chr11:66036037..66037653,2	MCF-7	breast:
6	chr11:65624293..65627593-chr11:65778197..65781174,3	MCF-7	breast:
7	chr11:65461869..65464366-chr11:65623666..65626207,3	MCF-7	breast:
8	chr11:65624058..65625682-chr6:32937606..32939507,2	K562	blood:
9	chr11:64544371..64546795-chr11:65624012..65625591,2	K562	blood:
10	chr11:65428959..65430837-chr11:65624739..65627866,4	K562	blood:
11	chr11:65624744..65625733-chr11:65729067..65729662,2	MCF-7	breast:
12	chr11:65263752..65266788-chr11:65624237..65626722,4	K562	blood:
13	chr11:65428923..65432488-chr11:65624731..65627563,6	MCF-7	breast:
14	chr11:65623212..65627104-chr11:65728021..65730947,7	MCF-7	breast:
15	chr11:65429132..65432605-chr11:65622916..65626202,6	MCF-7	breast:
16	chr11:502665..504183-chr11:65623020..65625621,2	K562	blood:
17	chr11:65545624..65552162-chr11:65622017..65629334,15	K562	blood:
18	chr11:65336983..65338518-chr11:65624191..65626684,2	MCF-7	breast:
19	chr11:65624341..65625267-chr6:34664302..34664857,2	Hela-S3	cervix:
20	chr11:65343451..65346634-chr11:65622563..65625144,3	K562	blood:
21	chr11:65624135..65626330-chr16:2009225..2011053,2	K562	blood:
22	chr11:65401684..65404221-chr11:65623185..65625956,3	K562	blood:
23	chr11:65622510..65630779-chr11:65675126..65689187,23	MCF-7	breast:
24	chr11:65482499..65489390-chr11:65622947..65628870,15	MCF-7	breast:
25	chr11:65423887..65432217-chr11:65622069..65628988,12	K562	blood:
26	chr11:65405500..65407998-chr11:65624581..65626384,2	K562	blood:
27	chr11:65485004..65489716-chr11:65621545..65626984,9	K562	blood:
28	chr11:65336222..65339291-chr11:65623626..65626992,4	K562	blood:
29	chr11:65408028..65411075-chr11:65624392..65627555,3	K562	blood:
30	chr11:65624197..65625879-chr11:65767979..65770257,2	MCF-7	breast:
31	chr11:65624805..65625720-chr12:125398909..125399816,2	Hela-S3	cervix:
32	chr11:65263752..65266249-chr11:65624237..65626407,2	K562	blood:
33	chr11:65623413..65628719-chr11:65768360..65773657,11	MCF-7	breast:
34	chr11:65624857..65625763-chr6:116891788..116892734,2	Hela-S3	cervix:
35	chr11:65624882..65627968-chr11:66034504..66038316,6	K562	blood:
36	chr11:65556531..65558931-chr11:65624353..65626096,2	K562	blood:
37	chr11:65377447..65384699-chr11:65622853..65629192,15	MCF-7	breast:
38	chr11:65485735..65490975-chr11:65621882..65626984,8	K562	blood:
39	chr11:65624126..65626253-chr11:66048758..66051466,2	K562	blood:
40	chr11:65545480..65548295-chr11:65624014..65629369,5	MCF-7	breast:
41	chr11:65545624..65551607-chr11:65624049..65629334,14	K562	blood:
42	chr11:65189338..65192942-chr11:65624454..65628332,4	K562	blood:
43	chr11:65623999..65626428-chr11:65787537..65789052,2	MCF-7	breast:
44	chr11:65622512..65626950-chr11:65664131..65668520,8	MCF-7	breast:
45	chr11:65381645..65384488-chr11:65623214..65626222,3	K562	blood:
46	chr11:65623430..65625691-chr11:65837839..65839866,2	K562	blood:
47	chr11:65311405..65314216-chr11:65624257..65626834,2	MCF-7	breast:
48	chr11:65624192..65626245-chr11:65751532..65753123,2	MCF-7	breast:
49	chr11:65401684..65407000-chr11:65623220..65627704,6	K562	blood:
50	chr11:65544951..65562337-chr11:65623093..65630859,34	MCF-7	breast:

Variant related genes	Relation type
MUS81	TF binding region
CFL1	TF binding region
ENSG00000175827	Chromatin interaction
ENSG00000175334	Chromatin interaction
ENSG00000173465	Chromatin interaction
ENSG00000254762	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000260233	Chromatin interaction
ENSG00000174871	Chromatin interaction
ENSG00000272288	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000172818	Chromatin interaction
ENSG00000175376	Chromatin interaction
ENSG00000196821	Chromatin interaction
ENSG00000168066	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000255120	Chromatin interaction
ENSG00000175592	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000266041	Chromatin interaction
ENSG00000269038	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000213445	Chromatin interaction
ENSG00000238752	Chromatin interaction
ENSG00000165929	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000175294	Chromatin interaction
ENSG00000254867	Chromatin interaction
ENSG00000023191	Chromatin interaction
ENSG00000172977	Chromatin interaction
ENSG00000173039	Chromatin interaction
ENSG00000172922	Chromatin interaction
ENSG00000172803	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000239356	Chromatin interaction
ENSG00000175573	Chromatin interaction
ENSG00000223837	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000175550	Chromatin interaction
ENSG00000140990	Chromatin interaction
ENSG00000087365	Chromatin interaction
ENSG00000174903	Chromatin interaction
ENSG00000175467	Chromatin interaction
ENSG00000111832	Chromatin interaction
ENSG00000175315	Chromatin interaction
ENSG00000150991	Chromatin interaction
ENSG00000175115	Chromatin interaction
ENSG00000254470	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10791828	0.83[AMR][1000 genomes]
rs13817	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1939212	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4621	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs508548	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs538394	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs545500	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs558114	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs630303	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs630755	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs633877	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs635375	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs648732	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs652021	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs656040	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs665306	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs667555	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs668356	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs679147	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7947741	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7947929	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
3	esv2758274	chr11:65559893-65722363	Genic enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
4	esv2759834	chr11:65559893-65722363	Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers 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	178 gene(s)	inside rSNPs	diseases
5	nsv427890	chr11:65559893-65722363	Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Genic enhancers 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 target site	178 gene(s)	inside rSNPs	diseases
6	nsv897761	chr11:65580638-65738566	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	186 gene(s)	inside rSNPs	diseases
7	nsv555215	chr11:65581579-65676516	Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers 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	165 gene(s)	inside rSNPs	diseases
8	nsv897762	chr11:65613218-65758854	Active TSS Flanking Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	185 gene(s)	inside rSNPs	diseases
9	nsv897763	chr11:65613348-65644027	Weak transcription Genic enhancers Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	121 gene(s)	inside rSNPs	diseases
10	nsv897764	chr11:65613348-65695222	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
11	nsv897765	chr11:65623708-65758854	Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
12	nsv897766	chr11:65624025-65644027	Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7125986	RBM4,RBM14	cis	brain	BrainEAC
rs7125986	SNX32	cis	Esophagus Muscularis	GTEx
rs7125986	SNX32	cis	Thyroid	GTEx
rs7125986	SNX32	cis	Whole Blood	GTEx
rs7125986	FIBP	Cis_1M	lymphoblastoid	RTeQTL
rs7125986	SNX32	cis	Artery Tibial	GTEx

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65616800-65625000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:65623000-65625000	Transcr. at gene 5' and 3'	A549	lung
3	chr11:65623200-65625000	Transcr. at gene 5' and 3'	NHLF	lung
4	chr11:65623400-65625000	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:65623400-65625000	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
6	chr11:65623400-65625000	Transcr. at gene 5' and 3'	NHEK	skin
7	chr11:65623400-65625200	Transcr. at gene 5' and 3'	Dnd41	blood
8	chr11:65623600-65626000	Active TSS	HSMMtube	muscle
9	chr11:65623800-65625200	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr11:65623800-65625200	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
11	chr11:65623800-65625200	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
12	chr11:65623800-65625600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
13	chr11:65623800-65628800	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr11:65623800-65629200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:65624000-65625000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr11:65624000-65625000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:65624000-65625200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
18	chr11:65624000-65626000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:65624000-65627200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:65624000-65628600	Active TSS	H1 Cell Line	embryonic stem cell
21	chr11:65624000-65628600	Active TSS	Lung	lung
22	chr11:65624000-65628800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr11:65624000-65628800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:65624000-65629000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr11:65624000-65629000	Active TSS	H9 Cell Line	embryonic stem cell
26	chr11:65624200-65626000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:65624200-65626000	Active TSS	Fetal Intestine Large	intestine
28	chr11:65624200-65626000	Active TSS	Fetal Kidney	kidney
29	chr11:65624200-65627000	Active TSS	Spleen	Spleen
30	chr11:65624200-65627200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:65624200-65628600	Active TSS	Right Ventricle	heart
32	chr11:65624200-65628600	Active TSS	Sigmoid Colon	Sigmoid Colon
33	chr11:65624200-65628800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:65624200-65628800	Active TSS	Gastric	stomach
35	chr11:65624200-65629000	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr11:65624200-65629000	Active TSS	Aorta	Aorta
37	chr11:65624200-65629000	Active TSS	Ovary	ovary
38	chr11:65624200-65629200	Active TSS	Small Intestine	intestine
39	chr11:65624400-65625000	Active TSS	Fetal Heart	heart
40	chr11:65624400-65625200	Active TSS	Stomach Mucosa	stomach
41	chr11:65624400-65625800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
42	chr11:65624400-65626000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:65624400-65626000	Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr11:65624400-65626000	Active TSS	Primary monocytes fromperipheralblood	blood
45	chr11:65624400-65626000	Active TSS	Primary B cells from peripheral blood	blood
46	chr11:65624400-65626000	Active TSS	Primary T cells from cord blood	blood
47	chr11:65624400-65626000	Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr11:65624400-65626000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr11:65624400-65626000	Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr11:65624400-65626000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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