Variant report

Variant	rs67924081
Chromosome Location	chr11:65342981-65342982
allele	A/G
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	POU2F2	chr11:65342945-65343325	GM12878	blood:	n/a	n/a
2	MYC	chr11:65342403-65343733	K562	blood:	n/a	n/a
3	POLR2A	chr11:65342306-65343339	PBDE	blood:	n/a	n/a
4	POLR2A	chr11:65342333-65343432	U87	brain:	n/a	n/a
5	EBF1	chr11:65342788-65343521	GM12878	blood:	n/a	n/a
6	SIN3AK20	chr11:65342967-65343289	A549	lung:	n/a	n/a
7	TBP	chr11:65342750-65343032	K562	blood:	n/a	n/a
8	POLR2A	chr11:65342299-65343347	GM12891	blood:	n/a	n/a
9	POLR2A	chr11:65341766-65343752	GM18505	blood:	n/a	n/a
10	POLR2A	chr11:65342974-65343778	GM12892	blood:	n/a	n/a
11	EGR1	chr11:65342908-65343639	MCF-7	breast:	n/a	chr11:65343492-65343502
12	SIN3AK20	chr11:65342492-65343319	PANC-1	pancreas:	n/a	n/a
13	POLR2A	chr11:65342911-65343336	MCF10A-Er-Src	breast:	n/a	n/a
14	BHLHE40	chr11:65342912-65343345	GM12878	blood:	n/a	n/a
15	MTA3	chr11:65340869-65345892	GM12878	blood:	n/a	n/a
16	POLR2A	chr11:65342740-65343749	HUVEC	blood vessel:	n/a	n/a
17	SPI1	chr11:65342752-65343402	GM12878	blood:	n/a	n/a
18	ETS1	chr11:65342954-65343426	A549	lung:	n/a	n/a
19	NFIC	chr11:65342923-65343427	ECC-1	luminal epithelium:	n/a	n/a
20	JUND	chr11:65342399-65343260	K562	blood:	n/a	n/a
21	ZNF274	chr11:65342520-65343068	K562	blood:	n/a	n/a
22	ATF2	chr11:65342530-65343426	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:65342416-65343742	Raji	blood:	n/a	n/a
24	STAT5A	chr11:65342326-65343218	K562	blood:	n/a	n/a
25	MYC	chr11:65342561-65343063	K562	blood:	n/a	n/a
26	POLR2A	chr11:65341578-65343572	U87	brain:	n/a	n/a
27	PML	chr11:65341446-65344423	GM12878	blood:	n/a	n/a
28	ELF1	chr11:65342913-65344310	GM12878	blood:	n/a	chr11:65343714-65343726 chr11:65343615-65343624
29	TCF3	chr11:65342962-65343408	GM12878	blood:	n/a	n/a
30	POLR2A	chr11:65341282-65343412	HUVEC	blood vessel:	n/a	n/a
31	HA-E2F1	chr11:65342425-65343295	MCF-7	breast:	n/a	n/a
32	EGR1	chr11:65342976-65343532	GM12878	blood:	n/a	chr11:65343492-65343502
33	PAX5	chr11:65342793-65343347	GM12878	blood:	n/a	n/a
34	MEF2A	chr11:65342746-65343412	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:65341540-65343353	Hela-S3	cervix:	n/a	n/a
36	GATA2	chr11:65342487-65342993	K562	blood:	n/a	n/a
37	EGR1	chr11:65342503-65344209	K562	blood:	n/a	chr11:65343889-65343899 chr11:65343761-65343771 chr11:65343492-65343502 chr11:65343892-65343902 chr11:65344067-65344080
38	PBX3	chr11:65342506-65344038	SK-N-SH	brain:	n/a	n/a
39	POLR2A	chr11:65341633-65343947	HL-60	blood:	n/a	n/a
40	POLR2A	chr11:65341720-65343430	SK-N-SH	brain:	n/a	n/a
41	ZC3H11A	chr11:65342702-65343079	K562	blood:	n/a	n/a
42	SIN3AK20	chr11:65341304-65343937	MCF-7	breast:	n/a	n/a
43	POLR2A	chr11:65342125-65343365	GM12891	blood:	n/a	n/a
44	POLR2A	chr11:65341563-65343980	HUVEC	blood vessel:	n/a	n/a
45	MXI1	chr11:65338853-65345385	IMR90	lung:	n/a	chr11:65342308-65342323 chr11:65339691-65339700
46	RCOR1	chr11:65342830-65343259	HepG2	liver:	n/a	n/a
47	EGR1	chr11:65342948-65343609	GM12878	blood:	n/a	chr11:65343492-65343502
48	SP1	chr11:65341363-65343811	HCT-116	colon:	n/a	chr11:65341901-65341915 chr11:65341763-65341777 chr11:65341755-65341764 chr11:65342003-65342012 chr11:65341762-65341774 chr11:65343490-65343502 chr11:65341802-65341811 chr11:65341753-65341765 chr11:65341764-65341773 chr11:65342002-65342011 chr11:65341754-65341768 chr11:65341801-65341810 chr11:65341762-65341774 chr11:65341802-65341811 chr11:65343490-65343502 chr11:65342002-65342012 chr11:65342117-65342131 chr11:65342001-65342013 chr11:65343491-65343500 chr11:65342001-65342013 chr11:65341763-65341772 chr11:65341800-65341812 chr11:65341753-65341765 chr11:65341800-65341812 chr11:65342003-65342012
49	POLR2A	chr11:65342874-65343425	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr11:65342776-65343934	PFSK-1	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65342372..65345081-chr11:65416714..65420575,4	MCF-7	breast:
2	chr11:65341415..65343423-chr11:65622094..65625636,3	K562	blood:
3	chr11:65105589..65107850-chr11:65341352..65343496,2	K562	blood:
4	chr11:65185945..65193560-chr11:65336627..65344485,19	K562	blood:
5	chr11:65341043..65343475-chr11:65375673..65377829,2	K562	blood:
6	chr11:65182317..65198249-chr11:65333937..65346467,45	MCF-7	breast:
7	chr11:65335401..65344755-chr11:65379602..65385163,20	K562	blood:
8	chr11:65188021..65191759-chr11:65338955..65343877,5	MCF-7	breast:
9	chr11:65340278..65343049-chr11:65386590..65388396,2	K562	blood:
10	chr11:65262109..65269742-chr11:65336183..65344125,16	MCF-7	breast:
11	chr11:65263786..65274103-chr11:65335962..65346813,28	MCF-7	breast:
12	chr11:65342886..65345023-chr11:65685103..65687892,2	MCF-7	breast:
13	chr11:65342220..65344396-chr11:65728106..65729941,2	MCF-7	breast:
14	chr11:65263724..65269268-chr11:65338505..65344270,10	K562	blood:
15	chr11:65341380..65343609-chr11:65408104..65410405,2	MCF-7	breast:
16	chr11:65342484..65343193-chr19:10613569..10614276,2	HCT-116	colon:
17	chr11:65336061..65346997-chr11:65371025..65390625,42	MCF-7	breast:
18	chr11:65342220..65345077-chr11:65403229..65406787,3	K562	blood:
19	chr11:64877474..64879697-chr11:65341982..65344398,2	MCF-7	breast:
20	chr11:65342281..65343040-chr5:37248938..37249873,2	Hela-S3	cervix:
21	chr11:65339484..65343401-chr11:65428921..65432383,5	MCF-7	breast:
22	chr11:65340642..65343423-chr11:65617979..65623594,4	K562	blood:
23	chr11:65342557..65345868-chr11:65665917..65668139,3	K562	blood:
24	chr11:65341604..65343487-chr11:65676828..65679293,2	MCF-7	breast:
25	chr11:64880625..64882228-chr11:65341727..65343311,2	MCF-7	breast:
26	chr11:65180960..65183956-chr11:65341785..65343462,2	MCF-7	breast:
27	chr11:65148557..65151141-chr11:65342655..65344676,2	MCF-7	breast:
28	chr11:65341009..65346216-chr11:65370852..65374605,4	K562	blood:
29	chr11:65184392..65191686-chr11:65339528..65345365,10	K562	blood:

Variant related genes	Relation type
EHBP1L1	TF binding region
ENSG00000172757	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000254501	Chromatin interaction
ENSG00000197603	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000175592	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000175573	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000079999	Chromatin interaction
ENSG00000149823	Chromatin interaction
ENSG00000149809	Chromatin interaction
ENSG00000175467	Chromatin interaction
ENSG00000213445	Chromatin interaction
ENSG00000162241	Chromatin interaction
ENSG00000175550	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000266041	Chromatin interaction
ENSG00000173039	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10896015	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1151496	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1194076	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1194077	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1194104	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12270054	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2510078	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	nsv897737	chr11:65337714-65361765	Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
25	nsv897738	chr11:65337714-65380248	Genic enhancers Active TSS Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
26	nsv897739	chr11:65337714-65388300	Genic enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
27	nsv897740	chr11:65338589-65371604	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
28	nsv897741	chr11:65338589-65376484	Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
29	nsv897742	chr11:65338589-65380248	Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
30	nsv897743	chr11:65338589-65382564	Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
31	nsv897744	chr11:65339099-65359435	Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Enhancers 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	37 gene(s)	inside rSNPs	diseases
32	nsv897745	chr11:65339099-65367253	Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs67924081	NEAT1	cis	Nerve Tibial	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65338000-65345600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr11:65338800-65344200	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr11:65340200-65343400	Flanking Active TSS	Primary hematopoietic stem cells	blood
4	chr11:65340400-65343400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
5	chr11:65340400-65345200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chr11:65340600-65343200	Transcr. at gene 5' and 3'	Brain Germinal Matrix	brain
7	chr11:65340800-65343000	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
8	chr11:65341000-65343000	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
9	chr11:65341400-65343200	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr11:65341400-65344800	Active TSS	Small Intestine	intestine
11	chr11:65341600-65343800	Active TSS	Lung	lung
12	chr11:65341600-65344200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr11:65341800-65343400	Flanking Active TSS	HMEC	breast
14	chr11:65341800-65344200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
15	chr11:65341800-65344200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
16	chr11:65342000-65343000	Flanking Active TSS	Primary B cells from cord blood	blood
17	chr11:65342200-65343000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
18	chr11:65342200-65343000	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:65342200-65343000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:65342200-65343000	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
21	chr11:65342200-65343000	Transcr. at gene 5' and 3'	NHLF	lung
22	chr11:65342200-65343200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
23	chr11:65342200-65343200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:65342200-65343200	Flanking Active TSS	Primary B cells from peripheral blood	blood
25	chr11:65342200-65343200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
26	chr11:65342200-65343200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
27	chr11:65342200-65343200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
28	chr11:65342200-65343200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr11:65342200-65343200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
30	chr11:65342200-65343200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr11:65342200-65343200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:65342200-65343200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:65342200-65343200	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr11:65342200-65343200	Flanking Active TSS	Colonic Mucosa	Colon
35	chr11:65342200-65343200	Flanking Active TSS	Esophagus	oesophagus
36	chr11:65342200-65343200	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
37	chr11:65342200-65343200	Weak transcription	Ovary	ovary
38	chr11:65342200-65343200	Flanking Active TSS	Hela-S3	cervix
39	chr11:65342200-65343200	Flanking Active TSS	NHEK	skin
40	chr11:65342200-65343400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr11:65342200-65343400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
42	chr11:65342200-65343400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr11:65342200-65343400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr11:65342200-65343400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr11:65342200-65343400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr11:65342200-65343400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
47	chr11:65342200-65343400	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr11:65342200-65343400	Flanking Active TSS	Liver	Liver
49	chr11:65342200-65343400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr11:65342200-65343400	Flanking Active TSS	Fetal Intestine Large	intestine

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