Variant report

Variant	rs1194104
Chromosome Location	chr11:65339346-65339347
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	SMC3	chr11:65339335-65339732	K562	blood:	n/a	chr11:65339529-65339543
2	SIX5	chr11:65338948-65339953	A549	lung:	n/a	n/a
3	CTCF	chr11:65339306-65339705	K562	blood:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
4	RAD21	chr11:65339269-65339766	H1-hESC	embryonic stem cell:	n/a	chr11:65339525-65339544
5	RAD21	chr11:65339187-65339859	A549	lung:	n/a	chr11:65339525-65339544
6	CTCF	chr11:65339138-65340071	A549	lung:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
7	RAD21	chr11:65339278-65339880	MCF-7	breast:	n/a	chr11:65339525-65339544
8	RAD21	chr11:65339343-65339704	GM12878	blood:	n/a	chr11:65339525-65339544
9	RAD21	chr11:65339346-65339695	H1-hESC	embryonic stem cell:	n/a	chr11:65339525-65339544
10	POLR2A	chr11:65339319-65339769	HCT-116	colon:	n/a	n/a
11	MXI1	chr11:65338853-65345385	IMR90	lung:	n/a	chr11:65342308-65342323 chr11:65339691-65339700
12	RAD21	chr11:65339253-65339823	MCF-7	breast:	n/a	chr11:65339525-65339544
13	CHD1	chr11:65339226-65340987	IMR90	lung:	n/a	n/a
14	RAD21	chr11:65339104-65340240	HCT-116	colon:	n/a	chr11:65339525-65339544
15	CTCF	chr11:65339320-65339470	NHDF-neo	bronchial:	n/a	n/a
16	ELF1	chr11:65339296-65339769	K562	blood:	n/a	chr11:65339523-65339536
17	CTCF	chr11:65339292-65339650	H1-hESC	embryonic stem cell:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
18	SIN3AK20	chr11:65339278-65339602	A549	lung:	n/a	n/a
19	CTCF	chr11:65339315-65339670	K562	blood:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
20	CTCF	chr11:65339229-65339764	MCF-7	breast:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
21	CTCF	chr11:65339319-65339670	A549	lung:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
22	CTCF	chr11:65339292-65339704	A549	lung:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
23	RAD21	chr11:65339117-65340245	HCT-116	colon:	n/a	chr11:65339525-65339544
24	MAX	chr11:65339266-65340752	A549	lung:	n/a	chr11:65340456-65340466
25	SIN3AK20	chr11:65339329-65340949	PANC-1	pancreas:	n/a	n/a
26	CBX3	chr11:65339246-65340055	K562	blood:	n/a	n/a
27	RAD21	chr11:65339070-65340259	SK-N-SH	brain:	n/a	chr11:65339525-65339544
28	MAX	chr11:65339292-65339752	K562	blood:	n/a	n/a
29	RAD21	chr11:65339342-65339684	HepG2	liver:	n/a	chr11:65339525-65339544
30	MXI1	chr11:65339046-65341120	SK-N-SH	brain:	n/a	chr11:65339691-65339700
31	REST	chr11:65339079-65340865	H1-neurons	neurons:	n/a	chr11:65340460-65340470 chr11:65340455-65340468
32	CTCF	chr11:65339329-65339727	H1-hESC	embryonic stem cell:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
33	CTCF	chr11:65339173-65340168	SK-N-SH	brain:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
34	RAD21	chr11:65339235-65339728	A549	lung:	n/a	chr11:65339525-65339544
35	CTCF	chr11:65339117-65339948	HCT-116	colon:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
36	RAD21	chr11:65339257-65339838	ECC-1	luminal epithelium:	n/a	chr11:65339525-65339544
37	RAD21	chr11:65339314-65339640	HepG2	liver:	n/a	chr11:65339525-65339544
38	CTCF	chr11:65339279-65339740	K562	blood:	n/a	chr11:65339530-65339540 chr11:65339527-65339545 chr11:65339528-65339544 chr11:65339522-65339543
39	RAD21	chr11:65339339-65339720	H1-hESC	embryonic stem cell:	n/a	chr11:65339525-65339544
40	MAX	chr11:65339317-65340604	MCF-7	breast:	n/a	chr11:65340456-65340466
41	RAD21	chr11:65339342-65339723	Hela-S3	cervix:	n/a	chr11:65339525-65339544
42	SP1	chr11:65339302-65340065	A549	lung:	n/a	chr11:65339972-65339984 chr11:65339983-65339994 chr11:65339433-65339440 chr11:65339972-65339983 chr11:65339973-65339983 chr11:65339973-65339982 chr11:65339974-65339983 chr11:65339969-65339983 chr11:65339973-65339983
43	TCF12	chr11:65339250-65340174	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65185945..65193560-chr11:65336627..65344485,19	K562	blood:
2	chr11:65153863..65156638-chr11:65338515..65340857,2	MCF-7	breast:
3	chr11:65182317..65198249-chr11:65333937..65346467,45	MCF-7	breast:
4	chr11:65335401..65344755-chr11:65379602..65385163,20	K562	blood:
5	chr11:65188021..65191759-chr11:65338955..65343877,5	MCF-7	breast:
6	chr11:65262109..65269742-chr11:65336183..65344125,16	MCF-7	breast:
7	chr11:65263786..65274103-chr11:65335962..65346813,28	MCF-7	breast:
8	chr11:65307733..65308892-chr11:65339050..65340029,8	K562	blood:
9	chr11:65109918..65112567-chr11:65337864..65339971,2	K562	blood:
10	chr11:65263724..65269268-chr11:65338505..65344270,10	K562	blood:
11	chr11:65336061..65346997-chr11:65371025..65390625,42	MCF-7	breast:
12	chr11:65307690..65308243-chr11:65339096..65339797,3	MCF-7	breast:
13	chr11:65307312..65308926-chr11:65339023..65340083,15	MCF-7	breast:
14	chr1:43888036..43888922-chr11:65339030..65339732,2	MCF-7	breast:

Variant related genes	Relation type
SSSCA1-AS1	TF binding region
EHBP1L1	TF binding region
FAM89B	TF binding region
ENSG00000270117	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000126391	Chromatin interaction
ENSG00000198198	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000133884	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000197136	Chromatin interaction

Extended variants
information (count: 40 )
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	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1194076	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1194077	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12270054	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2510078	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67924081	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 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
33	esv3371265	chr11:65339201-65341749	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1194104	NEAT1	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65336600-65339800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
2	chr11:65336600-65340800	Active TSS	H9 Cell Line	embryonic stem cell
3	chr11:65337000-65340400	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr11:65337800-65340000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:65338000-65339800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:65338000-65339800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:65338000-65339800	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr11:65338000-65339800	Flanking Active TSS	Colonic Mucosa	Colon
9	chr11:65338000-65339800	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr11:65338000-65340000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
11	chr11:65338000-65340000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr11:65338000-65340000	Flanking Active TSS	Primary B cells from cord blood	blood
13	chr11:65338000-65340000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
14	chr11:65338000-65340000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
15	chr11:65338000-65341600	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:65338000-65345600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:65338200-65339600	Flanking Active TSS	Brain Germinal Matrix	brain
18	chr11:65338200-65339800	Flanking Active TSS	Primary T cells from cord blood	blood
19	chr11:65338200-65339800	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr11:65338200-65339800	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
21	chr11:65338200-65339800	Flanking Active TSS	Brain Angular Gyrus	brain
22	chr11:65338200-65339800	Flanking Active TSS	Brain Cingulate Gyrus	brain
23	chr11:65338200-65339800	Flanking Active TSS	Brain Hippocampus Middle	brain
24	chr11:65338200-65339800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr11:65338200-65339800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr11:65338200-65339800	Flanking Active TSS	Fetal Muscle Trunk	muscle
27	chr11:65338200-65339800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
28	chr11:65338200-65340000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr11:65338200-65340000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr11:65338200-65340000	Flanking Active TSS	Liver	Liver
31	chr11:65338200-65340000	Flanking Active TSS	Fetal Thymus	thymus
32	chr11:65338200-65340000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr11:65338400-65339600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr11:65338400-65339600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
35	chr11:65338400-65339600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr11:65338400-65339600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr11:65338400-65339600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
38	chr11:65338400-65339600	Flanking Active TSS	Fetal Brain Female	brain
39	chr11:65338400-65339600	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr11:65338400-65339800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:65338400-65339800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr11:65338400-65339800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr11:65338400-65339800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr11:65338400-65339800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr11:65338400-65339800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr11:65338400-65339800	Flanking Active TSS	Brain Anterior Caudate	brain
47	chr11:65338400-65339800	Flanking Active TSS	Brain Substantia Nigra	brain
48	chr11:65338400-65339800	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr11:65338400-65339800	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr11:65338400-65339800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum

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