Variant report

Variant	rs1346
Chromosome Location	chr11:65337251-65337252
allele	A/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	TAF1	chr11:65337204-65338125	H1-hESC	embryonic stem cell:	n/a	n/a
2	MAX	chr11:65336846-65338262	SK-N-SH	brain:	n/a	n/a
3	SP1	chr11:65337162-65338278	A549	lung:	n/a	chr11:65337814-65337823
4	MAZ	chr11:65337073-65338080	GM12878	blood:	n/a	n/a
5	GABPA	chr11:65337128-65338782	MCF-7	breast:	n/a	chr11:65337501-65337515 chr11:65337498-65337512 chr11:65337259-65337273 chr11:65337501-65337512 chr11:65337566-65337575 chr11:65337503-65337512
6	THAP1	chr11:65337168-65338098	K562	blood:	n/a	n/a
7	HEY1	chr11:65336987-65338125	HepG2	liver:	n/a	chr11:65337923-65337932 chr11:65337896-65337911
8	POLR2A	chr11:65337201-65338153	GM19193	blood:	n/a	n/a
9	POLR2A	chr11:65337234-65338158	K562	blood:	n/a	n/a
10	MAX	chr11:65337170-65338237	K562	blood:	n/a	n/a
11	WRNIP1	chr11:65337159-65338125	GM12878	blood:	n/a	n/a
12	MAX	chr11:65336628-65338443	A549	lung:	n/a	n/a
13	ELF1	chr11:65336941-65338228	MCF-7	breast:	n/a	chr11:65337820-65337832
14	UBTF	chr11:65337214-65337956	K562	blood:	n/a	n/a
15	CTCF	chr11:65337140-65337290	HCPEpiC	choroid plexus:	n/a	n/a
16	POLR2A	chr11:65337014-65338325	U87	brain:	n/a	n/a
17	SMARCC1	chr11:65336850-65337821	Hela-S3	cervix:	n/a	n/a
18	HMGN3	chr11:65337174-65338273	K562	blood:	n/a	n/a
19	MAX	chr11:65337030-65338270	ECC-1	luminal epithelium:	n/a	n/a
20	GTF2F1	chr11:65337230-65338093	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:65337082-65338237	Hela-S3	cervix:	n/a	n/a
22	RAD21	chr11:65337125-65338026	A549	lung:	n/a	chr11:65337751-65337761
23	POLR2A	chr11:65336533-65338314	GM12892	blood:	n/a	n/a
24	MAX	chr11:65337021-65338288	ECC-1	luminal epithelium:	n/a	n/a
25	SIN3AK20	chr11:65336852-65338397	MCF-7	breast:	n/a	n/a
26	POLR2A	chr11:65337009-65338227	GM12891	blood:	n/a	n/a
27	JUND	chr11:65337225-65338185	A549	lung:	n/a	n/a
28	POLR2A	chr11:65337159-65338149	HepG2	liver:	n/a	n/a
29	YY1	chr11:65337162-65338227	A549	lung:	n/a	chr11:65337561-65337575 chr11:65337567-65337578 chr11:65337899-65337910 chr11:65337558-65337569
30	NRF1	chr11:65337215-65337713	K562	blood:	n/a	chr11:65337501-65337512 chr11:65337501-65337515 chr11:65337498-65337512 chr11:65337259-65337273 chr11:65337501-65337512 chr11:65337566-65337575 chr11:65337503-65337512
31	POLR2A	chr11:65337144-65338204	GM12891	blood:	n/a	n/a
32	PBX3	chr11:65337219-65338160	SK-N-SH	brain:	n/a	n/a
33	SP1	chr11:65337197-65338365	A549	lung:	n/a	chr11:65337814-65337823
34	POLR2A	chr11:65336528-65338307	SK-N-MC	brain:	n/a	n/a
35	POLR2A	chr11:65337085-65338280	K562	blood:	n/a	n/a
36	POLR2A	chr11:65337238-65338266	PFSK-1	brain:	n/a	n/a
37	MAX	chr11:65336701-65338565	K562	blood:	n/a	n/a
38	EP300	chr11:65336970-65338231	A549	lung:	n/a	chr11:65337899-65337915
39	POLR2A	chr11:65337221-65338278	MCF-7	breast:	n/a	n/a
40	POLR2A	chr11:65337183-65338319	MCF-7	breast:	n/a	n/a
41	POLR2A	chr11:65337222-65338194	HepG2	liver:	n/a	n/a
42	TAF1	chr11:65337134-65338078	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr11:65337220-65337370	HEEpiC	esophagus:	n/a	n/a
44	POLR2A	chr11:65336527-65338249	GM12878	blood:	n/a	n/a
45	MAX	chr11:65337071-65338189	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr11:65337088-65338211	HUVEC	blood vessel:	n/a	n/a
47	TAF1	chr11:65337076-65338337	ECC-1	luminal epithelium:	n/a	n/a
48	TEAD4	chr11:65337228-65338068	HepG2	liver:	n/a	n/a
49	POLR2A	chr11:65337123-65338333	GM12878	blood:	n/a	n/a
50	NRF1	chr11:65337116-65337717	Hela-S3	cervix:	n/a	chr11:65337501-65337512 chr11:65337501-65337515 chr11:65337498-65337512 chr11:65337259-65337273 chr11:65337501-65337512 chr11:65337566-65337575 chr11:65337503-65337512

No.	Distal block	Cell Line	Cell type
1	chr11:65336983..65338518-chr11:65624191..65626684,2	MCF-7	breast:
2	chr11:65336849..65339116-chr11:65404161..65406035,2	K562	blood:
3	chr11:65185945..65193560-chr11:65336627..65344485,19	K562	blood:
4	chr11:65337154..65337825-chr3:67704640..67705581,2	Hela-S3	cervix:
5	chr11:65336349..65338989-chr11:65428353..65432348,4	MCF-7	breast:
6	chr11:65182317..65198249-chr11:65333937..65346467,45	MCF-7	breast:
7	chr11:65335401..65344755-chr11:65379602..65385163,20	K562	blood:
8	chr11:65262109..65269742-chr11:65336183..65344125,16	MCF-7	breast:
9	chr11:65263786..65274103-chr11:65335962..65346813,28	MCF-7	breast:
10	chr11:65337061..65337684-chr12:7053126..7054123,2	NB4	blood:
11	chr11:65307609..65308998-chr11:65336892..65338725,9	K562	blood:
12	chr11:65337115..65337980-chr3:183735318..183736262,2	Hela-S3	cervix:
13	chr11:65308066..65308605-chr11:65337068..65337929,2	Hela-S3	cervix:
14	chr11:65336222..65339291-chr11:65623626..65626992,4	K562	blood:
15	chr11:65307403..65309183-chr11:65336934..65338289,13	MCF-7	breast:
16	chr11:65337074..65337796-chr17:66031903..66032699,2	HCT-116	colon:
17	chr11:65337081..65338062-chrX:15693306..15694079,2	Hela-S3	cervix:
18	chr11:65336061..65346997-chr11:65371025..65390625,42	MCF-7	breast:
19	chr11:65336026..65338505-chr11:65655594..65658699,3	MCF-7	breast:
20	chr11:65149449..65149970-chr11:65336591..65337539,2	K562	blood:
21	chr11:65264659..65267625-chr11:65336211..65338117,2	K562	blood:
22	chr11:65160499..65162253-chr11:65337171..65339326,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LTBP3-1	chr11:65337131-65337744	ENSG00000260233.1
2	lnc-LTBP3-1	chr11:65335953-65337894	ENSG00000260233.1
3	lnc-LTBP3-1	chr11:65333533-65337942	NONHSAT022168
4	lnc-LTBP3-1	chr11:65336691-65337884	NONHSAT022169

Variant related genes	Relation type
FAM89B	TF binding region
SSSCA1	TF binding region
ENSG00000245532	Chromatin interaction
ENSG00000182481	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000114770	Chromatin interaction
ENSG00000162241	Chromatin interaction
ENSG00000111678	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000172340	Chromatin interaction
ENSG00000173039	Chromatin interaction
ENSG00000126391	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000241316	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000172500	Chromatin interaction
ENSG00000186312	Chromatin interaction
ENSG00000213445	Chromatin interaction
ENSG00000175602	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000272173	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10896009	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs10896012	0.84[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap];0.80[YRI][hapmap]
rs10896015	0.89[CEU][hapmap];0.89[JPT][hapmap]
rs11227199	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1144928	0.81[AFR][1000 genomes]
rs1194076	0.89[CEU][hapmap];0.89[JPT][hapmap]
rs1194077	0.81[ASN][1000 genomes]
rs12270054	0.89[CEU][hapmap];0.89[JPT][hapmap]
rs12360896	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs12789028	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17146964	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1783541	0.89[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs1787663	0.89[JPT][hapmap]
rs2846139	0.85[AFR][1000 genomes]
rs3200401	0.84[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap]
rs947791	0.89[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:23 , 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

Variant related diseases (count:1)

Disease	PMID	Source
Vertical cup-disc ratio	25241763	GWAS catalog

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65336200-65337400	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr11:65336200-65337400	Flanking Active TSS	Brain Germinal Matrix	brain
3	chr11:65336200-65337400	Flanking Active TSS	Fetal Brain Male	brain
4	chr11:65336200-65337400	Flanking Active TSS	Rectal Smooth Muscle	rectum
5	chr11:65336200-65337400	Flanking Active TSS	HMEC	breast
6	chr11:65336200-65337400	Flanking Active TSS	K562	blood
7	chr11:65336200-65337600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
8	chr11:65336200-65337600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:65336200-65337600	Flanking Active TSS	Adipose Nuclei	Adipose
10	chr11:65336200-65337600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr11:65336400-65337400	Flanking Active TSS	Primary hematopoietic stem cells	blood
12	chr11:65336400-65337400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
13	chr11:65336400-65337400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr11:65336400-65337400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
15	chr11:65336400-65337400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
16	chr11:65336400-65337400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:65336400-65337400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr11:65336400-65337400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:65336400-65337400	Flanking Active TSS	Liver	Liver
20	chr11:65336400-65337400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
21	chr11:65336400-65337400	Flanking Active TSS	Stomach Smooth Muscle	stomach
22	chr11:65336400-65337400	Flanking Active TSS	Osteobl	bone
23	chr11:65336400-65337600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:65336400-65337600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:65336400-65337600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr11:65336400-65337600	Flanking Active TSS	Fetal Brain Female	brain
27	chr11:65336400-65337800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
28	chr11:65336600-65337400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:65336600-65337400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
30	chr11:65336600-65337400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr11:65336600-65337400	Flanking Active TSS	Primary B cells from peripheral blood	blood
32	chr11:65336600-65337400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
33	chr11:65336600-65337400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr11:65336600-65337400	Flanking Active TSS	Fetal Thymus	thymus
35	chr11:65336600-65337400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr11:65336600-65337400	Flanking Active TSS	Dnd41	blood
37	chr11:65336600-65337600	Flanking Active TSS	Placenta	Placenta
38	chr11:65336600-65337600	Flanking Active TSS	NH-A	brain
39	chr11:65336600-65338600	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr11:65336600-65339800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr11:65336600-65340800	Active TSS	H9 Cell Line	embryonic stem cell
42	chr11:65336800-65337400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:65336800-65337400	Flanking Active TSS	Fetal Muscle Trunk	muscle
44	chr11:65336800-65337400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr11:65336800-65337400	Flanking Active TSS	HUVEC	blood vessel
46	chr11:65336800-65337600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
47	chr11:65336800-65338600	Active TSS	Aorta	Aorta
48	chr11:65336800-65338600	Active TSS	Fetal Kidney	kidney
49	chr11:65336800-65338600	Active TSS	Ovary	ovary
50	chr11:65336800-65338600	Active TSS	Small Intestine	intestine

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