Variant report

Variant	rs1317494
Chromosome Location	chr11:64036688-64036689
allele	C/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	MYC	chr11:64036584-64036737	HUVEC	blood vessel:	n/a	n/a
2	FOSL2	chr11:64036674-64039117	A549	lung:	n/a	chr11:64037049-64037058 chr11:64039034-64039043 chr11:64036952-64036961
3	JUND	chr11:64036449-64037983	MCF-7	breast:	n/a	chr11:64037049-64037058 chr11:64036952-64036961
4	POLR2A	chr11:64036361-64038467	GM18951	blood:	n/a	n/a
5	POLR2A	chr11:64035787-64038520	HCT-116	colon:	n/a	n/a
6	GABPA	chr11:64036446-64036981	A549	lung:	n/a	n/a
7	POLR2A	chr11:64035320-64039757	HUVEC	blood vessel:	n/a	n/a
8	POLR2A	chr11:64035829-64038226	A549	lung:	n/a	n/a
9	PML	chr11:64036205-64038163	K562	blood:	n/a	n/a
10	MAX	chr11:64036372-64038154	NB4	blood:	n/a	n/a
11	ZNF143	chr11:64035912-64039144	Hela-S3	cervix:	n/a	chr11:64037921-64037939 chr11:64039062-64039080 chr11:64038988-64039006 chr11:64038925-64038934 chr11:64038923-64038932 chr11:64038923-64038941 chr11:64038930-64038945
12	BCL3	chr11:64036234-64038431	A549	lung:	n/a	n/a
13	CEBPB	chr11:64036605-64036940	K562	blood:	n/a	chr11:64036790-64036801
14	TBL1XR1	chr11:64036527-64036839	GM12878	blood:	n/a	n/a
15	MYBL2	chr11:64036660-64039291	HepG2	liver:	n/a	n/a
16	BHLHE40	chr11:64036290-64038019	K562	blood:	n/a	chr11:64037083-64037099
17	ZNF263	chr11:64035790-64038233	HEK293-T-REx	kidney:	n/a	chr11:64036721-64036730 chr11:64036384-64036393
18	POLR2A	chr11:64035257-64039912	HepG2	liver:	n/a	n/a
19	GATA1	chr11:64035230-64038709	K562	blood:	n/a	chr11:64036270-64036277 chr11:64036270-64036277 chr11:64036445-64036454 chr11:64036270-64036277 chr11:64036280-64036289 chr11:64036277-64036287
20	ELF1	chr11:64035939-64038377	MCF-7	breast:	n/a	chr11:64037607-64037620 chr11:64037089-64037098
21	POLR2A	chr11:64036579-64036801	HepG2	liver:	n/a	n/a
22	POLR2A	chr11:64035446-64039453	GM12878	blood:	n/a	n/a
23	POLR2A	chr11:64035639-64039628	Hela-S3	cervix:	n/a	n/a
24	REST	chr11:64036286-64038449	H1-neurons	neurons:	n/a	chr11:64036933-64036946
25	POLR2A	chr11:64035524-64039616	PANC-1	pancreas:	n/a	n/a
26	POLR2A	chr11:64035134-64040308	SK-N-MC	brain:	n/a	n/a
27	POLR2A	chr11:64036186-64038025	GM12892	blood:	n/a	n/a
28	MXI1	chr11:64036039-64038149	Hela-S3	cervix:	n/a	n/a
29	BCLAF1	chr11:64036409-64037976	GM12878	blood:	n/a	n/a
30	POLR2A	chr11:64036559-64036808	A549	lung:	n/a	n/a
31	NFATC1	chr11:64036364-64038106	GM12878	blood:	n/a	n/a
32	BCLAF1	chr11:64036416-64038121	GM12878	blood:	n/a	n/a
33	RFX5	chr11:64036023-64036804	Hela-S3	cervix:	n/a	n/a
34	TBL1XR1	chr11:64036440-64036754	K562	blood:	n/a	n/a
35	CEBPD	chr11:64036286-64036826	HepG2	liver:	n/a	n/a
36	TFAP2A	chr11:64035924-64037886	Hela-S3	cervix:	n/a	chr11:64036325-64036339 chr11:64036327-64036337 chr11:64036327-64036337 chr11:64036327-64036337 chr11:64036327-64036337 chr11:64037342-64037357
37	POLR2A	chr11:64036301-64038873	H1-hESC	embryonic stem cell:	n/a	n/a
38	FOXM1	chr11:64036379-64036879	GM12878	blood:	n/a	n/a
39	POLR2A	chr11:64036232-64039547	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr11:64035977-64038360	MCF-7	breast:	n/a	n/a
41	SIN3AK20	chr11:64036338-64038013	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr11:64035924-64038411	A549	lung:	n/a	chr11:64036270-64036277 chr11:64036270-64036277 chr11:64036445-64036454 chr11:64036270-64036277 chr11:64036280-64036289 chr11:64036277-64036287 chr11:64036269-64036277
43	MAZ	chr11:64035990-64038078	Hela-S3	cervix:	n/a	n/a
44	MYC	chr11:64036173-64039279	K562	blood:	n/a	chr11:64038901-64038911
45	POLR2A	chr11:64035350-64039613	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr11:64036033-64038625	GM12891	blood:	n/a	n/a
47	ELF1	chr11:64036482-64038173	K562	blood:	n/a	chr11:64037607-64037620 chr11:64037089-64037098
48	POLR2A	chr11:64035283-64039810	GM12892	blood:	n/a	n/a
49	ETS1	chr11:64036466-64036810	K562	blood:	n/a	n/a
50	CUX1	chr11:64036273-64036701	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64036655..64037510-chr3:105587754..105588423,2	NB4	blood:
2	chr11:62656333..62659258-chr11:64035179..64037351,2	K562	blood:
3	chr11:64034991..64040375-chr11:64070988..64074526,14	MCF-7	breast:
4	chr11:64028329..64041732-chr11:64049023..64058851,39	MCF-7	breast:
5	chr11:64035813..64037361-chr11:64122945..64124562,2	K562	blood:
6	chr11:64032072..64048684-chr11:64048768..64055711,68	MCF-7	breast:
7	chr11:64034814..64037171-chr11:64862133..64864994,2	MCF-7	breast:
8	chr11:64033536..64040775-chr11:64080684..64088458,16	K562	blood:
9	chr11:63932093..63937108-chr11:64035404..64039498,5	MCF-7	breast:
10	chr11:64036345..64039258-chr11:64083551..64087371,5	MCF-7	breast:
11	chr11:64036497..64040979-chr11:64067017..64069343,5	MCF-7	breast:
12	chr11:64033188..64045448-chr11:64059274..64075790,38	MCF-7	breast:
13	chr11:64036573..64037332-chr16:89989081..89989916,2	HCT-116	colon:
14	chr11:63741777..63744026-chr11:64034710..64037556,2	MCF-7	breast:
15	chr11:64036126..64037036-chr8:67578914..67579792,2	NB4	blood:
16	chr11:64035871..64037932-chr11:64108620..64111379,2	K562	blood:
17	chr11:64035104..64037329-chr11:64125264..64127439,2	MCF-7	breast:
18	chr11:64035844..64038435-chr11:64083306..64087822,4	MCF-7	breast:
19	chr11:64035819..64037712-chr11:64056886..64059211,2	MCF-7	breast:
20	chr11:64036423..64038929-chr11:64108620..64112959,5	K562	blood:

Variant related genes	Relation type
GPR137	TF binding region
ENSG00000126432	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000258947	Chromatin interaction
ENSG00000175073	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000257069	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000114423	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000149823	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000207024	Chromatin interaction
ENSG00000173153	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11231741	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[JPT][hapmap];0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11231746	0.82[AMR][1000 genomes]
rs11231749	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs1123251	1.00[JPT][hapmap]
rs12366035	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs15706	1.00[YRI][hapmap]
rs2186643	0.91[JPT][hapmap]
rs28395882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3815362	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4930152	0.96[CEU][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4980525	1.00[JPT][hapmap]
rs56057146	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs627055	1.00[JPT][hapmap]
rs7125217	0.84[AMR][1000 genomes]
rs72922019	0.84[AMR][1000 genomes]
rs72922077	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72924108	0.82[AMR][1000 genomes]
rs731703	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[AMR][1000 genomes]
rs7943988	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9787810	1.00[CEU][hapmap];0.83[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:26 , 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	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	nsv897679	chr11:63994692-64150370	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
25	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' 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	164 gene(s)	inside rSNPs	diseases
26	nsv1043277	chr11:64002997-64132030	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64029400-64037600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:64034800-64036800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:64035200-64036800	Flanking Active TSS	Hela-S3	cervix
4	chr11:64035200-64036800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr11:64035200-64037000	Flanking Active TSS	Stomach Smooth Muscle	stomach
6	chr11:64035400-64036800	Transcr. at gene 5' and 3'	NHEK	skin
7	chr11:64035400-64037000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:64035400-64037000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:64035400-64037000	Flanking Active TSS	Adipose Nuclei	Adipose
10	chr11:64035600-64036800	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:64035600-64036800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
12	chr11:64035600-64036800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
13	chr11:64035600-64037000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr11:64035600-64037000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr11:64035600-64037000	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr11:64035600-64038400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
17	chr11:64035800-64036800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
18	chr11:64035800-64036800	Flanking Active TSS	Brain Germinal Matrix	brain
19	chr11:64035800-64036800	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr11:64035800-64036800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
21	chr11:64035800-64036800	Flanking Active TSS	Rectal Smooth Muscle	rectum
22	chr11:64035800-64036800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr11:64035800-64036800	Flanking Active TSS	A549	lung
24	chr11:64035800-64036800	Flanking Active TSS	Dnd41	blood
25	chr11:64035800-64037000	Flanking Active TSS	Colonic Mucosa	Colon
26	chr11:64036000-64036800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:64036000-64036800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:64036000-64036800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr11:64036000-64036800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
30	chr11:64036000-64036800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
31	chr11:64036000-64036800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:64036000-64036800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr11:64036000-64036800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
34	chr11:64036000-64036800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:64036000-64036800	Flanking Active TSS	Brain Substantia Nigra	brain
36	chr11:64036000-64036800	Flanking Active TSS	Fetal Brain Female	brain
37	chr11:64036000-64036800	Flanking Active TSS	Thymus	Thymus
38	chr11:64036000-64037000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
39	chr11:64036000-64037000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
40	chr11:64036000-64037000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr11:64036000-64037000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr11:64036000-64037200	Flanking Active TSS	Primary B cells from cord blood	blood
43	chr11:64036000-64037200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
44	chr11:64036000-64037400	Flanking Active TSS	HMEC	breast
45	chr11:64036000-64037400	Flanking Active TSS	Osteobl	bone
46	chr11:64036000-64038400	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr11:64036000-64039600	Active TSS	H9 Cell Line	embryonic stem cell
48	chr11:64036000-64039800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:64036200-64036800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
50	chr11:64036200-64036800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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