Variant report

Variant	rs876064
Chromosome Location	chr11:64037033-64037034
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	FOSL2	chr11:64036674-64039117	A549	lung:	n/a	chr11:64037049-64037058 chr11:64039034-64039043 chr11:64036952-64036961
2	JUND	chr11:64036449-64037983	MCF-7	breast:	n/a	chr11:64037049-64037058 chr11:64036952-64036961
3	POLR2A	chr11:64036361-64038467	GM18951	blood:	n/a	n/a
4	TAF1	chr11:64036873-64037828	H1-neurons	neurons:	n/a	n/a
5	ELF1	chr11:64036996-64038180	K562	blood:	n/a	chr11:64037607-64037620 chr11:64037089-64037098
6	REST	chr11:64036854-64038122	A549	lung:	n/a	chr11:64036933-64036946
7	SIN3AK20	chr11:64037000-64038123	K562	blood:	n/a	n/a
8	E2F6	chr11:64036760-64037824	H1-hESC	embryonic stem cell:	n/a	chr11:64036948-64036960
9	POLR2A	chr11:64035787-64038520	HCT-116	colon:	n/a	n/a
10	POLR2A	chr11:64035320-64039757	HUVEC	blood vessel:	n/a	n/a
11	POLR2A	chr11:64035829-64038226	A549	lung:	n/a	n/a
12	PML	chr11:64036205-64038163	K562	blood:	n/a	n/a
13	MAX	chr11:64036372-64038154	NB4	blood:	n/a	n/a
14	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
15	BCL3	chr11:64036234-64038431	A549	lung:	n/a	n/a
16	CTCF	chr11:64037020-64037170	GM12867	blood:	n/a	n/a
17	YY1	chr11:64036987-64038369	K562	blood:	n/a	chr11:64037623-64037635 chr11:64037619-64037636
18	RAD21	chr11:64036887-64037808	H1-hESC	embryonic stem cell:	n/a	n/a
19	RAD21	chr11:64037027-64037307	HepG2	liver:	n/a	n/a
20	RAD21	chr11:64036985-64037436	K562	blood:	n/a	n/a
21	MYBL2	chr11:64036660-64039291	HepG2	liver:	n/a	n/a
22	E2F6	chr11:64036872-64037629	K562	blood:	n/a	chr11:64036948-64036960
23	MAX	chr11:64036911-64038402	SK-N-SH	brain:	n/a	n/a
24	BHLHE40	chr11:64036290-64038019	K562	blood:	n/a	chr11:64037083-64037099
25	ZNF263	chr11:64035790-64038233	HEK293-T-REx	kidney:	n/a	chr11:64036721-64036730 chr11:64036384-64036393
26	POLR2A	chr11:64035257-64039912	HepG2	liver:	n/a	n/a
27	FOXP2	chr11:64036867-64037852	PFSK-1	brain:	n/a	n/a
28	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
29	ELF1	chr11:64035939-64038377	MCF-7	breast:	n/a	chr11:64037607-64037620 chr11:64037089-64037098
30	JUND	chr11:64036915-64037046	H1-hESC	embryonic stem cell:	n/a	chr11:64036952-64036961
31	MAX	chr11:64036956-64038297	H1-hESC	embryonic stem cell:	n/a	n/a
32	NANOG	chr11:64036808-64037158	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr11:64035446-64039453	GM12878	blood:	n/a	n/a
34	YY1	chr11:64037028-64038417	K562	blood:	n/a	chr11:64037623-64037635 chr11:64037619-64037636
35	POLR2A	chr11:64035639-64039628	Hela-S3	cervix:	n/a	n/a
36	REST	chr11:64036286-64038449	H1-neurons	neurons:	n/a	chr11:64036933-64036946
37	POLR2A	chr11:64035524-64039616	PANC-1	pancreas:	n/a	n/a
38	POLR2A	chr11:64035134-64040308	SK-N-MC	brain:	n/a	n/a
39	POLR2A	chr11:64036186-64038025	GM12892	blood:	n/a	n/a
40	MXI1	chr11:64036039-64038149	Hela-S3	cervix:	n/a	n/a
41	BCLAF1	chr11:64036409-64037976	GM12878	blood:	n/a	n/a
42	CHD1	chr11:64036781-64037266	H1-hESC	embryonic stem cell:	n/a	n/a
43	NFATC1	chr11:64036364-64038106	GM12878	blood:	n/a	n/a
44	BCLAF1	chr11:64036416-64038121	GM12878	blood:	n/a	n/a
45	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
46	GABPA	chr11:64036971-64038549	SK-N-SH	brain:	n/a	n/a
47	POLR2A	chr11:64036301-64038873	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr11:64036232-64039547	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr11:64035977-64038360	MCF-7	breast:	n/a	n/a
50	SIN3AK20	chr11:64036338-64038013	SK-N-SH	brain:	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	chr11:64037018..64037949-chr15:81282063..81282760,2	HCT-116	colon:
19	chr11:64035844..64038435-chr11:64083306..64087822,4	MCF-7	breast:
20	chr11:64035819..64037712-chr11:64056886..64059211,2	MCF-7	breast:
21	chr11:64036423..64038929-chr11:64108620..64112959,5	K562	blood:

Variant related genes	Relation type
GPR137	TF binding region
ENSG00000258947	Chromatin interaction
ENSG00000133315	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000207024	Chromatin interaction
ENSG00000114423	Chromatin interaction
ENSG00000257069	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000117899	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000175073	Chromatin interaction
ENSG00000002330	Chromatin interaction
ENSG00000149823	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10792430	0.88[YRI][hapmap]
rs10897488	0.88[YRI][hapmap]
rs11231713	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[JPT][hapmap]
rs11606081	0.88[YRI][hapmap]
rs1199046	0.88[YRI][hapmap]
rs12146487	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12421615	0.95[ASN][1000 genomes]
rs2096706	1.00[ASW][hapmap];0.89[JPT][hapmap]
rs2186572	0.81[CEU][hapmap];0.89[JPT][hapmap]
rs2286615	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs508168	0.88[YRI][hapmap]
rs516124	0.88[YRI][hapmap]
rs538147	0.88[YRI][hapmap]
rs57831436	0.88[EUR][1000 genomes]
rs58779949	0.88[EUR][1000 genomes]
rs602534	0.82[ASN][1000 genomes]
rs618160	0.82[ASN][1000 genomes]
rs645078	0.88[YRI][hapmap]
rs646384	1.00[ASW][hapmap]
rs660070	1.00[ASW][hapmap]
rs7123026	0.89[JPT][hapmap]
rs915987	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.89[MEX][hapmap];0.96[TSI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs947939	1.00[ASW][hapmap];0.81[CEU][hapmap];1.00[JPT][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

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs876064	TMEM138	cis	parietal	SCAN
rs876064	CCDC88B	cis	lymphoblastoid	seeQTL
rs876064	RBM14	cis	cerebellum	SCAN
rs876064	ESRRA	cis	cerebellum	SCAN
rs876064	MALAT1	cis	cerebellum	SCAN
rs876064	FKBP2	cis	cerebellum	SCAN
rs876064	CCDC88B	cis	cerebellum	SCAN
rs876064	RCE1	cis	cerebellum	SCAN
rs876064	FKBP2	cis	parietal	SCAN
rs876064	CCDC88	cis	multi-tissue	Pritchard
rs876064	CCS	cis	cerebellum	SCAN

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	chr11:64035600-64038400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
3	chr11:64036000-64037200	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr11:64036000-64037200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:64036000-64037400	Flanking Active TSS	HMEC	breast
6	chr11:64036000-64037400	Flanking Active TSS	Osteobl	bone
7	chr11:64036000-64038400	Flanking Active TSS	Primary hematopoietic stem cells	blood
8	chr11:64036000-64039600	Active TSS	H9 Cell Line	embryonic stem cell
9	chr11:64036000-64039800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:64036200-64037400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:64036200-64038200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr11:64036200-64039400	Active TSS	Ovary	ovary
13	chr11:64036200-64039600	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr11:64036200-64039600	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr11:64036200-64039600	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr11:64036200-64039600	Active TSS	Psoas Muscle	Psoas
17	chr11:64036400-64037200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:64036400-64037200	Flanking Active TSS	NH-A	brain
19	chr11:64036400-64037400	Flanking Active TSS	HUVEC	blood vessel
20	chr11:64036400-64039400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr11:64036400-64039400	Active TSS	Lung	lung
22	chr11:64036400-64039600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr11:64036400-64039600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:64036400-64039600	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr11:64036600-64037200	Flanking Active TSS	NHLF	lung
26	chr11:64036600-64037800	Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr11:64036600-64037800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
28	chr11:64036600-64037800	Transcr. at gene 5' and 3'	Right Atrium	heart
29	chr11:64036600-64037800	Active TSS	HepG2	liver
30	chr11:64036600-64039200	Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr11:64036600-64039200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:64036600-64039200	Active TSS	Left Ventricle	heart
33	chr11:64036600-64039200	Active TSS	K562	blood
34	chr11:64036600-64039400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:64036600-64039400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr11:64036600-64039400	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr11:64036600-64039400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr11:64036600-64039400	Active TSS	Aorta	Aorta
39	chr11:64036600-64039400	Active TSS	Colon Smooth Muscle	Colon
40	chr11:64036600-64039400	Active TSS	Gastric	stomach
41	chr11:64036600-64039400	Active TSS	Small Intestine	intestine
42	chr11:64036600-64039400	Active TSS	Spleen	Spleen
43	chr11:64036600-64039600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr11:64036600-64039600	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr11:64036600-64039600	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr11:64036600-64039600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:64036600-64039600	Active TSS	Fetal Kidney	kidney
48	chr11:64036600-64039600	Active TSS	Right Ventricle	heart
49	chr11:64036600-64039800	Active TSS	GM12878-XiMat	blood
50	chr11:64036800-64037400	Flanking Active TSS	NHEK	skin

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