Variant report

Variant	rs11549691
Chromosome Location	chr11:63993287-63993288
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	FOXM1	chr11:63993010-63994348	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:63993063-63994621	GM10847	blood:	n/a	n/a
3	STAT5A	chr11:63993170-63994019	GM12878	blood:	n/a	chr11:63993231-63993243 chr11:63993237-63993249
4	ELF1	chr11:63993119-63994612	K562	blood:	n/a	chr11:63993633-63993642 chr11:63993724-63993733
5	RAD21	chr11:63993269-63993413	K562	blood:	n/a	n/a
6	HMGN3	chr11:63993156-63994587	K562	blood:	n/a	n/a
7	POLR2A	chr11:63992736-63995293	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr11:63993136-63993599	K562	blood:	n/a	chr11:63993338-63993356
9	POLR2A	chr11:63989232-63995299	K562	blood:	n/a	n/a
10	CTCF	chr11:63993220-63993370	Hela-S3	cervix:	n/a	chr11:63993338-63993356
11	CTCF	chr11:63993280-63993430	GM12873	blood:	n/a	chr11:63993338-63993356
12	RAD21	chr11:63993117-63993785	H1-hESC	embryonic stem cell:	n/a	n/a
13	HCFC1	chr11:63992684-63994367	Hela-S3	cervix:	n/a	n/a
14	SP1	chr11:63993205-63993989	A549	lung:	n/a	chr11:63993739-63993751 chr11:63993741-63993750 chr11:63993713-63993725 chr11:63993736-63993750 chr11:63993739-63993751 chr11:63993338-63993351 chr11:63993235-63993244 chr11:63993231-63993245 chr11:63993234-63993246 chr11:63993714-63993723 chr11:63993688-63993709
15	CTCF	chr11:63993260-63993410	NHDF-neo	bronchial:	n/a	chr11:63993338-63993356
16	POLR2A	chr11:63989880-63995323	GM12891	blood:	n/a	n/a
17	POLR2A	chr11:63991338-63994677	GM12891	blood:	n/a	n/a
18	CTCF	chr11:63993207-63994348	K562	blood:	n/a	chr11:63993772-63993790 chr11:63993338-63993356 chr11:63993774-63993787 chr11:63993781-63993794
19	CTCF	chr11:63993276-63993439	K562	blood:	n/a	chr11:63993338-63993356
20	CTCF	chr11:63993200-63993350	HUVEC	blood vessel:	n/a	n/a
21	POLR2A	chr11:63991343-63995010	U87	brain:	n/a	n/a
22	MTA3	chr11:63991287-63995175	GM12878	blood:	n/a	n/a
23	SIN3AK20	chr11:63993120-63994011	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr11:63993287-63993399	GM19239	blood:	n/a	chr11:63993338-63993356
25	CTCF	chr11:63993230-63993465	GM12892	blood:	n/a	chr11:63993338-63993356
26	POLR2A	chr11:63991349-63994680	GM12891	blood:	n/a	n/a
27	CTCF	chr11:63993260-63993410	GM12875	blood:	n/a	chr11:63993338-63993356
28	POLR2A	chr11:63991516-63995277	Raji	blood:	n/a	n/a
29	POLR2A	chr11:63991337-63995010	U87	brain:	n/a	n/a
30	POLR2A	chr11:63993284-63993935	HepG2	liver:	n/a	n/a
31	BACH1	chr11:63993173-63993838	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr11:63993277-63993453	H1-hESC	embryonic stem cell:	n/a	chr11:63993338-63993356
33	NR2F2	chr11:63993181-63994570	K562	blood:	n/a	n/a
34	POLR2A	chr11:63991399-63994678	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:63990418-63994603	GM12878	blood:	n/a	n/a
36	MAX	chr11:63993278-63994277	ECC-1	luminal epithelium:	n/a	n/a
37	POLR2A	chr11:63989946-63994682	HL-60	blood:	n/a	n/a
38	MAX	chr11:63992564-63994729	HepG2	liver:	n/a	chr11:63993229-63993239 chr11:63993079-63993088
39	GABPA	chr11:63993192-63994679	SK-N-SH	brain:	n/a	chr11:63993726-63993733 chr11:63993816-63993825
40	MAZ	chr11:63992605-63994798	IMR90	lung:	n/a	chr11:63993229-63993239 chr11:63993079-63993088
41	REST	chr11:63993287-63994024	A549	lung:	n/a	n/a
42	POLR2A	chr11:63990068-63995245	GM18505	blood:	n/a	n/a
43	YY1	chr11:63993266-63993844	GM12892	blood:	n/a	chr11:63993647-63993656 chr11:63993645-63993656
44	MTA3	chr11:63992903-63993720	GM12878	blood:	n/a	n/a
45	POLR2A	chr11:63993284-63994167	GM12878	blood:	n/a	n/a
46	MAZ	chr11:63993066-63993851	HepG2	liver:	n/a	chr11:63993229-63993239 chr11:63993079-63993088
47	POLR2A	chr11:63989981-63995376	GM12892	blood:	n/a	n/a
48	MAX	chr11:63992728-63994709	K562	blood:	n/a	chr11:63993229-63993239 chr11:63993079-63993088
49	POLR2A	chr11:63993075-63994221	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr11:63993240-63993390	NHDF-neo	bronchial:	n/a	chr11:63993338-63993356

No.	Distal block	Cell Line	Cell type
1	chr11:63993069..63993712-chr9:130921932..130922829,2	Hela-S3	cervix:
2	chr11:63991030..63993449-chr16:4673277..4676059,2	K562	blood:
3	chr11:63993205..63994873-chr11:64060700..64063524,2	MCF-7	breast:
4	chr11:63992038..63994216-chr11:64062874..64065506,2	MCF-7	breast:
5	chr11:63990938..63995618-chr11:64068467..64075569,11	MCF-7	breast:
6	chr1:113932898..113933685-chr11:63992576..63993445,2	Hela-S3	cervix:
7	chr11:63962580..63965391-chr11:63991959..63994483,2	MCF-7	breast:
8	chr11:63991810..63993878-chr11:64081220..64083594,2	K562	blood:
9	chr11:63992108..63994970-chr11:64050201..64053443,5	MCF-7	breast:
10	chr11:63993196..63993978-chr19:49117482..49118182,2	NB4	blood:
11	chr11:63951654..63956341-chr11:63991514..63996131,9	MCF-7	breast:

Variant related genes	Relation type
NUDT22	TF binding region
TRPT1	TF binding region
DNAJC4	TF binding region
ENSG00000168439	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000207024	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000105523	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000102858	Chromatin interaction
ENSG00000171159	Chromatin interaction
ENSG00000081026	Chromatin interaction
ENSG00000182450	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1544538	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17851033	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1938817	0.81[EUR][1000 genomes]
rs2070232	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2154984	0.85[EUR][1000 genomes]
rs2186571	0.85[EUR][1000 genomes]
rs2245837	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2622420	0.81[EUR][1000 genomes]
rs2622422	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2622424	0.81[EUR][1000 genomes]
rs2622428	0.81[EUR][1000 genomes]
rs2622430	0.81[EUR][1000 genomes]
rs2701530	0.85[EUR][1000 genomes]
rs2701536	0.81[EUR][1000 genomes]
rs2701537	0.81[EUR][1000 genomes]
rs2701539	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28395878	0.86[AMR][1000 genomes]
rs28395880	0.84[AMR][1000 genomes]
rs4980506	0.81[EUR][1000 genomes]
rs583799	0.81[EUR][1000 genomes]
rs59250939	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs599549	0.81[EUR][1000 genomes]
rs615924	0.81[EUR][1000 genomes]
rs616652	0.81[EUR][1000 genomes]
rs639406	0.81[EUR][1000 genomes]
rs688241	0.81[EUR][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	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription 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	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
11	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
12	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS 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 lncRNA	155 gene(s)	inside rSNPs	diseases
13	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
14	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh 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	227 gene(s)	inside rSNPs	diseases
15	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription 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	212 gene(s)	inside rSNPs	diseases
16	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer 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 target site	212 gene(s)	inside rSNPs	diseases
17	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
18	nsv468595	chr11:63953121-64027888	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription 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	146 gene(s)	inside rSNPs	diseases
19	nsv555187	chr11:63953121-64027888	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
20	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
21	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
22	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS 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	164 gene(s)	inside rSNPs	diseases
23	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic 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 target site	164 gene(s)	inside rSNPs	diseases
24	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer 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	179 gene(s)	inside rSNPs	diseases
25	nsv541061	chr11:63970174-64010995	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
26	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
27	nsv897672	chr11:63979643-64082807	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
28	esv1802320	chr11:63987425-64154633	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Strong transcription 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	178 gene(s)	inside rSNPs	diseases
29	nsv897673	chr11:63991581-64018687	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
30	esv992196	chr11:63992534-64002355	Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11549691	HSPC152	Cis_1M	lymphoblastoid	RTeQTL
rs11549691	PRDX5	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63992400-63993400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:63992400-63993400	Flanking Active TSS	Duodenum Mucosa	Duodenum
3	chr11:63992400-63993400	Flanking Active TSS	Dnd41	blood
4	chr11:63992400-63995200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr11:63992600-63993400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:63992600-63993400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:63992600-63993400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:63992600-63993400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:63992600-63993400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:63992600-63993400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:63992600-63993400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:63992600-63993400	Flanking Active TSS	Brain Cingulate Gyrus	brain
13	chr11:63992600-63993400	Flanking Active TSS	Brain Germinal Matrix	brain
14	chr11:63992600-63993400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
15	chr11:63992600-63993400	Flanking Active TSS	Colon Smooth Muscle	Colon
16	chr11:63992600-63993400	Flanking Active TSS	Fetal Brain Female	brain
17	chr11:63992600-63993400	Flanking Active TSS	Fetal Muscle Trunk	muscle
18	chr11:63992600-63993400	Flanking Active TSS	Gastric	stomach
19	chr11:63992600-63993400	Flanking Active TSS	Osteobl	bone
20	chr11:63992600-63993600	Flanking Active TSS	Liver	Liver
21	chr11:63992600-63993600	Flanking Active TSS	Colonic Mucosa	Colon
22	chr11:63992600-63993600	Flanking Active TSS	Fetal Muscle Leg	muscle
23	chr11:63992600-63993600	Flanking Active TSS	Stomach Smooth Muscle	stomach
24	chr11:63992600-63994000	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr11:63992600-63994000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr11:63992600-63994400	Active TSS	Thymus	Thymus
27	chr11:63992600-63995200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr11:63992600-63995200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr11:63992600-63995400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr11:63992800-63993400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:63992800-63993400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr11:63992800-63993400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
33	chr11:63992800-63993400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:63992800-63993400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr11:63992800-63993400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr11:63992800-63993400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
37	chr11:63992800-63993400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr11:63992800-63993400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
39	chr11:63992800-63993400	Flanking Active TSS	Brain Angular Gyrus	brain
40	chr11:63992800-63993400	Flanking Active TSS	Brain Anterior Caudate	brain
41	chr11:63992800-63993400	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr11:63992800-63993400	Flanking Active TSS	Brain Substantia Nigra	brain
43	chr11:63992800-63993400	Flanking Active TSS	Fetal Intestine Small	intestine
44	chr11:63992800-63993400	Flanking Active TSS	Fetal Lung	lung
45	chr11:63992800-63993400	Flanking Active TSS	Fetal Thymus	thymus
46	chr11:63992800-63993400	Flanking Active TSS	Hela-S3	cervix
47	chr11:63992800-63993400	Flanking Active TSS	HUVEC	blood vessel
48	chr11:63992800-63993400	Flanking Active TSS	NH-A	brain
49	chr11:63992800-63993600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:63992800-63993600	Flanking Active TSS	HMEC	breast

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