Variant report

Variant	rs11039225
Chromosome Location	chr11:47430599-47430600
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	MAX	chr11:47430563-47430987	Hela-S3	cervix:	n/a	n/a
2	MAZ	chr11:47428435-47431694	IMR90	lung:	n/a	chr11:47430013-47430023 chr11:47428706-47428716
3	TAF1	chr11:47430407-47430932	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr11:47430517-47430880	U87	brain:	n/a	n/a
5	POLR2A	chr11:47429424-47431688	IMR90	lung:	n/a	n/a
6	MAZ	chr11:47428995-47431051	Hela-S3	cervix:	n/a	chr11:47430013-47430023
7	HCFC1	chr11:47428525-47432352	Hela-S3	cervix:	n/a	n/a
8	EP300	chr11:47429381-47431040	SK-N-SH	brain:	n/a	chr11:47430234-47430243 chr11:47430826-47430842 chr11:47430309-47430325 chr11:47430623-47430639 chr11:47430200-47430209 chr11:47429639-47429655 chr11:47429853-47429869 chr11:47430197-47430206 chr11:47430194-47430203
9	FOS	chr11:47430599-47430943	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr11:47429454-47431598	ProgFib	skin:	n/a	n/a
11	POLR2A	chr11:47429033-47431014	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr11:47429062-47431721	SK-N-SH	brain:	n/a	chr11:47430629-47430642 chr11:47431524-47431537 chr11:47429638-47429651
13	POLR2A	chr11:47429342-47431128	HUVEC	blood vessel:	n/a	n/a
14	POLR2A	chr11:47428894-47431242	HepG2	liver:	n/a	n/a
15	MYC	chr11:47430560-47430961	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr11:47429370-47430843	Hela-S3	cervix:	n/a	n/a
17	MYC	chr11:47430598-47430958	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr11:47429344-47431080	PFSK-1	brain:	n/a	n/a
19	TFAP2A	chr11:47429542-47431562	Hela-S3	cervix:	n/a	chr11:47430241-47430253 chr11:47430244-47430252 chr11:47431384-47431398 chr11:47431386-47431396 chr11:47430244-47430252 chr11:47431386-47431396 chr11:47431384-47431398 chr11:47431386-47431396 chr11:47431386-47431401 chr11:47431384-47431398 chr11:47431386-47431396 chr11:47430838-47430848 chr11:47430244-47430252
20	MXI1	chr11:47429542-47431013	HepG2	liver:	n/a	n/a
21	SMARCB1	chr11:47428926-47430979	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr11:47429230-47431154	U87	brain:	n/a	n/a
23	HMGN3	chr11:47429481-47430618	K562	blood:	n/a	chr11:47429694-47429703
24	POLR2A	chr11:47428847-47431024	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr11:47430512-47431017	HUVEC	blood vessel:	n/a	n/a
26	UBTF	chr11:47430592-47430648	K562	blood:	n/a	n/a
27	TAF1	chr11:47430522-47430915	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr11:47428805-47431204	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr11:47429357-47431205	HUVEC	blood vessel:	n/a	n/a
30	MXI1	chr11:47429253-47431626	IMR90	lung:	n/a	n/a
31	MAX	chr11:47429115-47431016	HCT-116	colon:	n/a	chr11:47430013-47430023
32	POLR2A	chr11:47430583-47430876	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr11:47429543-47430919	Gliobla	brain:	n/a	n/a
34	SIN3AK20	chr11:47430458-47430941	SK-N-SH	brain:	n/a	n/a
35	JUN	chr11:47428356-47430878	K562	blood:	n/a	chr11:47429695-47429705 chr11:47429695-47429705 chr11:47429695-47429705 chr11:47429695-47429705
36	CTCF	chr11:47429252-47430641	A549	lung:	n/a	chr11:47429638-47429651
37	POLR2A	chr11:47430530-47430979	Hela-S3	cervix:	n/a	n/a
38	MAX	chr11:47429228-47430989	HepG2	liver:	n/a	chr11:47430013-47430023
39	SIN3AK20	chr11:47429186-47431042	MCF-7	breast:	n/a	n/a
40	MAX	chr11:47429408-47431047	SK-N-SH	brain:	n/a	chr11:47430013-47430023
41	TFAP2C	chr11:47429386-47431572	Hela-S3	cervix:	n/a	chr11:47430834-47430849 chr11:47431382-47431397
42	BHLHE40	chr11:47430532-47430750	K562	blood:	n/a	n/a
43	RCOR1	chr11:47428771-47430664	K562	blood:	n/a	n/a
44	CTCF	chr11:47430591-47430602	GM12878	blood:	n/a	n/a
45	POLR2A	chr11:47430558-47430983	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr11:47429362-47431523	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr11:47428926-47430894	Hela-S3	cervix:	n/a	n/a
48	RAD21	chr11:47429057-47431606	SK-N-SH	brain:	n/a	chr11:47430513-47430527 chr11:47431326-47431340 chr11:47430618-47430637
49	CHD1	chr11:47428857-47432915	IMR90	lung:	n/a	n/a
50	RCOR1	chr11:47430364-47430927	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:47411629..47418031-chr11:47425327..47431880,15	K562	blood:
2	chr11:47429691..47431699-chr11:47584830..47587245,2	MCF-7	breast:
3	chr11:47290389..47294105-chr11:47428413..47432863,5	MCF-7	breast:
4	chr11:47428130..47431471-chr11:47462803..47464877,5	MCF-7	breast:
5	chr11:47205613..47207687-chr11:47429461..47432184,2	K562	blood:
6	chr11:47394067..47402014-chr11:47426765..47432976,19	K562	blood:
7	chr11:47289845..47291400-chr11:47428671..47431411,2	K562	blood:
8	chr11:47429268..47431582-chr20:56284094..56286955,2	MCF-7	breast:
9	chr11:47419914..47422605-chr11:47427478..47432259,7	K562	blood:
10	chr11:47430300..47430981-chr3:160283048..160283883,2	Hela-S3	cervix:
11	chr11:47197465..47200418-chr11:47428077..47430700,3	K562	blood:
12	chr11:47269451..47271860-chr11:47428590..47432270,5	K562	blood:
13	chr11:47391440..47404809-chr11:47427075..47436409,23	K562	blood:
14	chr11:47430075..47430624-chrX:153626608..153627108,2	Hela-S3	cervix:
15	chr11:47429560..47431457-chr11:47788267..47789854,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPI1-1	chr11:47430503-47430741	ENSG00000255197.1
2	lnc-SPI1-1	chr11:47430503-47430643	ENSG00000255197.1

Variant related genes	Relation type
SLC39A13	TF binding region
ENSG00000147403	Chromatin interaction
ENSG00000149187	Chromatin interaction
ENSG00000109920	Chromatin interaction
ENSG00000165917	Chromatin interaction
ENSG00000110514	Chromatin interaction
ENSG00000025434	Chromatin interaction
ENSG00000165912	Chromatin interaction
ENSG00000264583	Chromatin interaction
ENSG00000134575	Chromatin interaction
ENSG00000229320	Chromatin interaction
ENSG00000256746	Chromatin interaction
ENSG00000255197	Chromatin interaction
ENSG00000124225	Chromatin interaction
ENSG00000066336	Chromatin interaction
ENSG00000149182	Chromatin interaction
ENSG00000186432	Chromatin interaction
ENSG00000110536	Chromatin interaction
ENSG00000213619	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10437655	0.92[EUR][1000 genomes]
rs10742802	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10742814	0.84[GIH][hapmap];0.95[JPT][hapmap]
rs10769263	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10769264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10838702	1.00[CEU][hapmap];0.88[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10838705	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10838709	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10838726	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs10838732	0.95[JPT][hapmap]
rs11039221	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11039244	0.84[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs11039280	1.00[JPT][hapmap]
rs11606287	0.92[CEU][hapmap];0.95[TSI][hapmap];0.86[EUR][1000 genomes]
rs12292911	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12361415	0.82[CHB][hapmap]
rs12577643	0.89[ASN][1000 genomes]
rs1377416	0.84[ASW][hapmap];1.00[CEU][hapmap];0.88[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1534576	0.84[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2203712	0.95[JPT][hapmap]
rs2242081	0.84[GIH][hapmap];0.95[JPT][hapmap]
rs2278890	0.92[CEU][hapmap];0.83[EUR][1000 genomes]
rs2293576	0.84[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.98[ASN][1000 genomes]
rs2293579	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35032070	0.86[EUR][1000 genomes]
rs3740689	0.83[CHB][hapmap]
rs3740699	0.84[GIH][hapmap];0.84[JPT][hapmap]
rs3758675	0.83[EUR][1000 genomes]
rs3824869	0.88[CEU][hapmap]
rs4434960	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61897431	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6485758	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6485763	0.84[GIH][hapmap];0.95[JPT][hapmap]
rs7103648	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7104036	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7933019	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs7947450	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7950696	0.95[JPT][hapmap]
rs874896	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs896817	0.92[ASW][hapmap];1.00[CEU][hapmap];0.88[CHB][hapmap];0.95[GIH][hapmap];0.87[LWK][hapmap];0.95[MEX][hapmap];0.86[MKK][hapmap];0.98[TSI][hapmap];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897323	chr11:47182926-47460306	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer 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	96 gene(s)	inside rSNPs	diseases
2	nsv917316	chr11:47232210-47448882	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
3	esv3330173	chr11:47289256-47450681	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
4	esv3416377	chr11:47289276-47450651	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
5	nsv832141	chr11:47333180-47520993	Flanking Active TSS Genic enhancers Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
6	nsv825871	chr11:47376020-47457537	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv554210	chr11:47380593-47449544	Flanking Active TSS Enhancers Weak transcription Active TSS 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	38 gene(s)	inside rSNPs	diseases
8	nsv541034	chr11:47404083-47440081	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
9	nsv897325	chr11:47411736-47600438	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers 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	55 gene(s)	inside rSNPs	diseases
10	nsv1036011	chr11:47413060-47582279	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
11	esv3328586	chr11:47428801-47431349	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
12	esv3353375	chr11:47429076-47431224	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs11039225	MTCH2	cis	cerebellum	SCAN
rs11039225	C1QTNF4	cis	lymphoblastoid	seeQTL
rs11039225	MADD	cis	parietal	SCAN
rs11039225	FNBP4	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47428600-47431200	Active TSS	H9 Cell Line	embryonic stem cell
2	chr11:47429000-47430600	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr11:47429200-47430600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr11:47429200-47430600	Active TSS	Gastric	stomach
5	chr11:47429200-47430600	Active TSS	Placenta Amnion	Placenta Amnion
6	chr11:47429200-47430800	Active TSS	Lung	lung
7	chr11:47429200-47430800	Active TSS	Ovary	ovary
8	chr11:47429200-47431000	Active TSS	Psoas Muscle	Psoas
9	chr11:47429200-47431400	Active TSS	Aorta	Aorta
10	chr11:47429400-47430600	Active TSS	H1 Cell Line	embryonic stem cell
11	chr11:47429400-47430600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:47429400-47430600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:47429400-47430600	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr11:47429400-47430600	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr11:47429400-47430600	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr11:47429400-47430600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:47429400-47430600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:47429400-47430600	Active TSS	Brain Angular Gyrus	brain
19	chr11:47429400-47430600	Active TSS	Fetal Intestine Large	intestine
20	chr11:47429400-47430600	Active TSS	Pancreas	Pancrea
21	chr11:47429400-47430600	Active TSS	Rectal Smooth Muscle	rectum
22	chr11:47429400-47430600	Active TSS	Sigmoid Colon	Sigmoid Colon
23	chr11:47429400-47430600	Active TSS	A549	lung
24	chr11:47429400-47430600	Active TSS	NHDF-Ad	bronchial
25	chr11:47429400-47430800	Active TSS	Left Ventricle	heart
26	chr11:47429400-47430800	Active TSS	Right Ventricle	heart
27	chr11:47429400-47431000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr11:47429400-47431000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr11:47429400-47431000	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr11:47429400-47431000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:47429400-47431000	Active TSS	Esophagus	oesophagus
32	chr11:47429400-47431200	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr11:47429400-47431400	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr11:47429400-47431400	Active TSS	HSMM	muscle
35	chr11:47429400-47431600	Active TSS	Fetal Kidney	kidney
36	chr11:47429600-47430600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr11:47429600-47430600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:47429600-47430600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr11:47429600-47430600	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr11:47429600-47430600	Active TSS	Brain Substantia Nigra	brain
41	chr11:47429600-47430600	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr11:47429600-47430600	Active TSS	Fetal Muscle Leg	muscle
43	chr11:47429600-47430600	Active TSS	Fetal Stomach	stomach
44	chr11:47429600-47430600	Active TSS	Small Intestine	intestine
45	chr11:47429600-47430600	Active TSS	Thymus	Thymus
46	chr11:47429600-47430600	Active TSS	HMEC	breast
47	chr11:47429600-47430600	Active TSS	HSMMtube	muscle
48	chr11:47429600-47430600	Active TSS	NH-A	brain
49	chr11:47429600-47430600	Active TSS	Osteobl	bone
50	chr11:47429600-47430800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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