Variant report

Variant	rs1151496
Chromosome Location	chr11:65338034-65338035
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	TAF1	chr11:65337204-65338125	H1-hESC	embryonic stem cell:	n/a	n/a
2	MYC	chr11:65337427-65338197	MCF-7	breast:	n/a	n/a
3	ELF1	chr11:65337409-65338151	HepG2	liver:	n/a	chr11:65337820-65337832
4	HEY1	chr11:65337740-65338186	K562	blood:	n/a	chr11:65337923-65337932 chr11:65337896-65337911
5	MAX	chr11:65336846-65338262	SK-N-SH	brain:	n/a	n/a
6	SIN3AK20	chr11:65337622-65338149	PFSK-1	brain:	n/a	n/a
7	SP1	chr11:65337162-65338278	A549	lung:	n/a	chr11:65337814-65337823
8	TAF1	chr11:65337791-65338103	GM12892	blood:	n/a	n/a
9	ATF3	chr11:65337435-65338079	GM12878	blood:	n/a	chr11:65337920-65337930 chr11:65337923-65337931 chr11:65337920-65337931 chr11:65337923-65337930 chr11:65337911-65337931
10	NFIC	chr11:65337381-65338188	HepG2	liver:	n/a	n/a
11	GABPA	chr11:65337439-65338236	HepG2	liver:	n/a	chr11:65337501-65337515 chr11:65337498-65337512 chr11:65337501-65337512 chr11:65337566-65337575 chr11:65337503-65337512
12	PBX3	chr11:65337409-65338167	A549	lung:	n/a	n/a
13	TBL1XR1	chr11:65337256-65338100	K562	blood:	n/a	n/a
14	FOXA1	chr11:65337336-65338108	HepG2	liver:	n/a	n/a
15	MAZ	chr11:65337073-65338080	GM12878	blood:	n/a	n/a
16	TRIM28	chr11:65337356-65338133	K562	blood:	n/a	n/a
17	YY1	chr11:65337580-65338134	GM12891	blood:	n/a	chr11:65337899-65337910
18	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
19	THAP1	chr11:65337168-65338098	K562	blood:	n/a	n/a
20	ATF2	chr11:65337392-65338049	H1-hESC	embryonic stem cell:	n/a	n/a
21	SP4	chr11:65337417-65338111	H1-hESC	embryonic stem cell:	n/a	n/a
22	EP300	chr11:65337437-65338185	A549	lung:	n/a	chr11:65337899-65337915
23	ATF1	chr11:65337348-65338118	K562	blood:	n/a	n/a
24	GABPA	chr11:65337453-65338191	K562	blood:	n/a	chr11:65337501-65337515 chr11:65337498-65337512 chr11:65337501-65337512 chr11:65337566-65337575 chr11:65337503-65337512
25	HEY1	chr11:65336987-65338125	HepG2	liver:	n/a	chr11:65337923-65337932 chr11:65337896-65337911
26	ELK4	chr11:65337519-65338149	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr11:65337201-65338153	GM19193	blood:	n/a	n/a
28	POLR2A	chr11:65337234-65338158	K562	blood:	n/a	n/a
29	MAX	chr11:65337170-65338237	K562	blood:	n/a	n/a
30	WRNIP1	chr11:65337159-65338125	GM12878	blood:	n/a	n/a
31	MAX	chr11:65336628-65338443	A549	lung:	n/a	n/a
32	SP1	chr11:65337575-65338126	H1-hESC	embryonic stem cell:	n/a	chr11:65337814-65337823
33	GABPA	chr11:65337324-65338341	SK-N-SH	brain:	n/a	chr11:65337501-65337515 chr11:65337498-65337512 chr11:65337501-65337512 chr11:65337566-65337575 chr11:65337503-65337512
34	MYC	chr11:65337349-65338154	K562	blood:	n/a	n/a
35	SP1	chr11:65337325-65338067	HepG2	liver:	n/a	chr11:65337814-65337823
36	CHD2	chr11:65337277-65338091	Hela-S3	cervix:	n/a	n/a
37	ELF1	chr11:65336941-65338228	MCF-7	breast:	n/a	chr11:65337820-65337832
38	POLR2A	chr11:65337286-65338208	K562	blood:	n/a	n/a
39	FOXP2	chr11:65337315-65338129	SK-N-MC	brain:	n/a	n/a
40	POLR2A	chr11:65337014-65338325	U87	brain:	n/a	n/a
41	ELK1	chr11:65337586-65338081	K562	blood:	n/a	n/a
42	HMGN3	chr11:65337174-65338273	K562	blood:	n/a	n/a
43	EP300	chr11:65337485-65338180	T-47D	breast:	n/a	chr11:65337899-65337915
44	MAX	chr11:65337030-65338270	ECC-1	luminal epithelium:	n/a	n/a
45	GTF2F1	chr11:65337230-65338093	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr11:65337082-65338237	Hela-S3	cervix:	n/a	n/a
47	STAT5A	chr11:65337287-65338140	GM12878	blood:	n/a	chr11:65337579-65337590
48	POLR2A	chr11:65336533-65338314	GM12892	blood:	n/a	n/a
49	JUND	chr11:65337350-65338039	A549	lung:	n/a	n/a
50	MAX	chr11:65337021-65338288	ECC-1	luminal epithelium:	n/a	n/a

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	chr11:65336349..65338989-chr11:65428353..65432348,4	MCF-7	breast:
5	chr11:65182317..65198249-chr11:65333937..65346467,45	MCF-7	breast:
6	chr11:65335401..65344755-chr11:65379602..65385163,20	K562	blood:
7	chr11:65262109..65269742-chr11:65336183..65344125,16	MCF-7	breast:
8	chr11:65263786..65274103-chr11:65335962..65346813,28	MCF-7	breast:
9	chr11:65109918..65112567-chr11:65337864..65339971,2	K562	blood:
10	chr11:65307609..65308998-chr11:65336892..65338725,9	K562	blood:
11	chr11:65336222..65339291-chr11:65623626..65626992,4	K562	blood:
12	chr11:65307403..65309183-chr11:65336934..65338289,13	MCF-7	breast:
13	chr11:65337081..65338062-chrX:15693306..15694079,2	Hela-S3	cervix:
14	chr11:65336061..65346997-chr11:65371025..65390625,42	MCF-7	breast:
15	chr11:65336026..65338505-chr11:65655594..65658699,3	MCF-7	breast:
16	chr11:65264659..65267625-chr11:65336211..65338117,2	K562	blood:
17	chr11:65337533..65338174-chr11:65381408..65382244,2	MCF-7	breast:
18	chr11:65160499..65162253-chr11:65337171..65339326,2	K562	blood:

Variant related genes	Relation type
SSSCA1	TF binding region
FAM89B	TF binding region
SSSCA1-AS1	TF binding region
ENSG00000213445	Chromatin interaction
ENSG00000133884	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000126391	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000173039	Chromatin interaction
ENSG00000186312	Chromatin interaction
ENSG00000172500	Chromatin interaction
ENSG00000175602	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000270117	Chromatin interaction

Extended variants
information (count: 33 )
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]
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]
rs1194104	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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:26 , 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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1151496	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	chr11:65336600-65338600	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr11:65336600-65339800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
3	chr11:65336600-65340800	Active TSS	H9 Cell Line	embryonic stem cell
4	chr11:65336800-65338600	Active TSS	Aorta	Aorta
5	chr11:65336800-65338600	Active TSS	Fetal Kidney	kidney
6	chr11:65336800-65338600	Active TSS	Ovary	ovary
7	chr11:65336800-65338600	Active TSS	Small Intestine	intestine
8	chr11:65336800-65338600	Active TSS	A549	lung
9	chr11:65336800-65338600	Active TSS	GM12878-XiMat	blood
10	chr11:65337000-65338200	Active TSS	Brain Angular Gyrus	brain
11	chr11:65337000-65338200	Active TSS	Brain Cingulate Gyrus	brain
12	chr11:65337000-65338200	Active TSS	Duodenum Smooth Muscle	Duodenum
13	chr11:65337000-65338400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr11:65337000-65338400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:65337000-65338400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr11:65337000-65338400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:65337000-65338400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:65337000-65338400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
19	chr11:65337000-65338400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:65337000-65338400	Active TSS	Colon Smooth Muscle	Colon
21	chr11:65337000-65338400	Active TSS	Fetal Intestine Large	intestine
22	chr11:65337000-65338400	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr11:65337000-65338400	Active TSS	Sigmoid Colon	Sigmoid Colon
24	chr11:65337000-65338400	Active TSS	Thymus	Thymus
25	chr11:65337000-65338400	Bivalent/Poised TSS	HepG2	liver
26	chr11:65337000-65338600	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr11:65337000-65338600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:65337000-65338600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:65337000-65338600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr11:65337000-65338600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr11:65337000-65338600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr11:65337000-65338600	Active TSS	Gastric	stomach
33	chr11:65337000-65338600	Active TSS	Left Ventricle	heart
34	chr11:65337000-65338600	Active TSS	Lung	lung
35	chr11:65337000-65338600	Active TSS	Psoas Muscle	Psoas
36	chr11:65337000-65338600	Active TSS	Right Ventricle	heart
37	chr11:65337000-65338600	Active TSS	HSMM	muscle
38	chr11:65337000-65338600	Active TSS	HSMMtube	muscle
39	chr11:65337000-65338600	Active TSS	NHDF-Ad	bronchial
40	chr11:65337000-65338800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:65337000-65339000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:65337000-65339000	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr11:65337000-65339000	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr11:65337000-65340400	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr11:65337200-65338200	Active TSS	Primary T cells from cord blood	blood
46	chr11:65337200-65338200	Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr11:65337200-65338200	Active TSS	Brain Hippocampus Middle	brain
48	chr11:65337200-65338200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr11:65337200-65338200	Active TSS	Fetal Lung	lung
50	chr11:65337200-65338200	Active TSS	Fetal Muscle Leg	muscle

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