Variant report

Variant	rs7101916
Chromosome Location	chr11:65431360-65431361
allele	C/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	PML	chr11:65429838-65431778	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:65430009-65431444	MCF-7	breast:	n/a	n/a
3	USF2	chr11:65430967-65431438	GM12878	blood:	n/a	chr11:65431261-65431272
4	RUNX3	chr11:65430404-65431671	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:65430164-65431525	U87	brain:	n/a	n/a
6	POLR2A	chr11:65430160-65431538	SK-N-SH	brain:	n/a	n/a
7	POLR2A	chr11:65428366-65431647	GM12878	blood:	n/a	n/a
8	YY1	chr11:65431088-65431544	H1-hESC	embryonic stem cell:	n/a	chr11:65431203-65431214
9	USF1	chr11:65431050-65431501	ECC-1	luminal epithelium:	n/a	chr11:65431261-65431272
10	MAZ	chr11:65429997-65431411	Hela-S3	cervix:	n/a	chr11:65431210-65431220 chr11:65431262-65431271
11	ZBTB7A	chr11:65430887-65431397	K562	blood:	n/a	chr11:65431192-65431203
12	SPI1	chr11:65431336-65431619	GM12878	blood:	n/a	chr11:65431507-65431520
13	TCF12	chr11:65430195-65431360	ECC-1	luminal epithelium:	n/a	chr11:65431153-65431160
14	CTCF	chr11:65431360-65431510	NHDF-neo	bronchial:	n/a	chr11:65431379-65431392
15	MAX	chr11:65430247-65431409	GM12878	blood:	n/a	chr11:65431210-65431220 chr11:65431262-65431271
16	POLR2A	chr11:65430067-65431659	GM12878	blood:	n/a	n/a
17	USF1	chr11:65430907-65431625	K562	blood:	n/a	chr11:65431261-65431272
18	HCFC1	chr11:65428690-65431781	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr11:65431149-65431391	SK-N-SH	brain:	n/a	n/a
20	TEAD4	chr11:65431198-65431812	K562	blood:	n/a	n/a
21	MXI1	chr11:65430164-65431708	GM12878	blood:	n/a	n/a
22	USF2	chr11:65431126-65431377	H1-hESC	embryonic stem cell:	n/a	chr11:65431261-65431272
23	POLR2A	chr11:65430115-65431562	GM12891	blood:	n/a	n/a
24	USF1	chr11:65431145-65431390	GM12878	blood:	n/a	chr11:65431261-65431272
25	POLR2A	chr11:65430229-65431509	GM12892	blood:	n/a	n/a
26	EBF1	chr11:65431191-65431537	GM12878	blood:	n/a	n/a
27	MAX	chr11:65431152-65431369	K562	blood:	n/a	chr11:65431210-65431220 chr11:65431262-65431271
28	MTA3	chr11:65430370-65431685	GM12878	blood:	n/a	n/a
29	EGR1	chr11:65431164-65431704	K562	blood:	n/a	chr11:65431609-65431622 chr11:65431544-65431557 chr11:65431545-65431555 chr11:65431608-65431618 chr11:65431545-65431556 chr11:65431544-65431557 chr11:65431541-65431555 chr11:65431337-65431350 chr11:65431544-65431557 chr11:65431207-65431220 chr11:65431543-65431558 chr11:65431543-65431557
30	POLR2A	chr11:65430164-65431510	U87	brain:	n/a	n/a
31	POLR2A	chr11:65430153-65431366	GM19193	blood:	n/a	n/a
32	POLR2A	chr11:65430078-65431510	GM12891	blood:	n/a	n/a
33	EGR1	chr11:65431301-65431697	MCF-7	breast:	n/a	chr11:65431609-65431622 chr11:65431544-65431557 chr11:65431545-65431555 chr11:65431608-65431618 chr11:65431545-65431556 chr11:65431544-65431557 chr11:65431541-65431555 chr11:65431337-65431350 chr11:65431544-65431557 chr11:65431543-65431558 chr11:65431543-65431557
34	POLR2A	chr11:65430088-65431474	K562	blood:	n/a	n/a
35	SPI1	chr11:65431322-65431641	GM12891	blood:	n/a	chr11:65431507-65431520
36	POLR2A	chr11:65429988-65431426	H1-neurons	neurons:	n/a	n/a
37	RCOR1	chr11:65430364-65431685	GM12878	blood:	n/a	n/a
38	POLR2A	chr11:65429366-65431700	K562	blood:	n/a	n/a
39	MAX	chr11:65429928-65431636	A549	lung:	n/a	chr11:65431210-65431220 chr11:65431262-65431271
40	RELA	chr11:65430391-65431599	GM19193	blood:	n/a	n/a
41	CHD2	chr11:65430342-65431547	GM12878	blood:	n/a	n/a
42	POLR2A	chr11:65430684-65431603	GM12891	blood:	n/a	n/a
43	MYC	chr11:65431240-65431372	MCF-7	breast:	n/a	chr11:65431262-65431271
44	POLR2A	chr11:65428919-65431637	GM12892	blood:	n/a	n/a
45	HEY1	chr11:65430133-65431400	K562	blood:	n/a	chr11:65430246-65430261 chr11:65430784-65430799 chr11:65430390-65430405 chr11:65430741-65430756 chr11:65430223-65430238 chr11:65430388-65430403
46	HEY1	chr11:65430178-65431521	HepG2	liver:	n/a	chr11:65430246-65430261 chr11:65430784-65430799 chr11:65430390-65430405 chr11:65430741-65430756 chr11:65430223-65430238 chr11:65430388-65430403
47	TAF1	chr11:65430202-65431364	ECC-1	luminal epithelium:	n/a	n/a
48	CHD2	chr11:65431205-65431382	Hela-S3	cervix:	n/a	n/a
49	FOXA2	chr11:65431094-65431764	A549	lung:	n/a	n/a
50	UBTF	chr11:65430342-65431388	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65412642..65414860-chr11:65428206..65431618,3	MCF-7	breast:
2	chr11:65307679..65310014-chr11:65429997..65432824,2	MCF-7	breast:
3	chr11:65380932..65386957-chr11:65428679..65431812,7	MCF-7	breast:
4	chr11:65400163..65404871-chr11:65428865..65432129,6	MCF-7	breast:
5	chr11:65428955..65432251-chr11:65654758..65658672,5	K562	blood:
6	chr11:65339484..65343401-chr11:65428921..65432383,5	MCF-7	breast:
7	chr1:153506112..153506833-chr11:65430861..65431455,2	Hela-S3	cervix:
8	chr11:65428607..65431563-chr11:65477387..65481608,5	MCF-7	breast:
9	chr11:65429991..65432005-chr11:65562169..65564755,2	K562	blood:
10	chr11:65430177..65431911-chr11:65686267..65688055,2	K562	blood:
11	chr11:65423887..65432217-chr11:65622069..65628988,12	K562	blood:
12	chr11:65429766..65432533-chr11:65462094..65464981,2	MCF-7	breast:
13	chr11:65429376..65431458-chr8:146016410..146018952,2	MCF-7	breast:
14	chr11:65188743..65190282-chr11:65428876..65431588,2	MCF-7	breast:
15	chr11:65429132..65432605-chr11:65622916..65626202,6	MCF-7	breast:
16	chr11:65429132..65431872-chr11:65817636..65822281,4	MCF-7	breast:
17	chr11:65429800..65432139-chr11:65653071..65655699,2	MCF-7	breast:
18	chr11:65265117..65266625-chr11:65429410..65431565,2	K562	blood:
19	chr11:65430022..65431720-chr11:65728429..65730460,2	MCF-7	breast:
20	chr11:65336349..65338989-chr11:65428353..65432348,4	MCF-7	breast:
21	chr11:65381571..65386287-chr11:65427993..65433260,8	MCF-7	breast:
22	chr11:65428923..65432488-chr11:65624731..65627563,6	MCF-7	breast:
23	chr11:65430466..65432280-chr11:65478658..65481830,3	K562	blood:
24	chr11:65430893..65432531-chr11:65618937..65620451,2	K562	blood:
25	chr11:65430719..65431589-chr11:65756537..65757127,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SIPA1-2	chr11:65430445-65432196	NONHSAT022201

Variant related genes	Relation type
RELA	TF binding region
ENSG00000266041	Chromatin interaction
ENSG00000175467	Chromatin interaction
ENSG00000175602	Chromatin interaction
ENSG00000245532	Chromatin interaction
ENSG00000172757	Chromatin interaction
ENSG00000213445	Chromatin interaction
ENSG00000175550	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000255404	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000175573	Chromatin interaction
ENSG00000172500	Chromatin interaction
ENSG00000172732	Chromatin interaction
ENSG00000260233	Chromatin interaction
ENSG00000173465	Chromatin interaction
ENSG00000176973	Chromatin interaction
ENSG00000239356	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000161016	Chromatin interaction
ENSG00000087365	Chromatin interaction
ENSG00000172977	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000238752	Chromatin interaction
ENSG00000173327	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11227247	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12417989	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12418567	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12418630	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12418683	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12419110	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12420405	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12420618	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12421691	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1962691	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1963977	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2075660	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2127510	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2236683	0.89[EUR][1000 genomes]
rs2306365	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35927673	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36028748	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs36091060	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs36113281	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3741378	0.93[ASW][hapmap];0.81[CEU][hapmap];0.81[CHB][hapmap];1.00[GIH][hapmap];0.82[JPT][hapmap];0.92[TSI][hapmap];0.89[EUR][1000 genomes]
rs4578394	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4645916	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4645917	0.82[EUR][1000 genomes]
rs4930158	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4930299	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55758897	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56115979	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7107503	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7119750	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7122081	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7122098	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	nsv897747	chr11:65353906-65481166	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
13	nsv897748	chr11:65392695-65466911	Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
14	nsv897754	chr11:65405300-65436888	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers 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	59 gene(s)	inside rSNPs	diseases
15	nsv897755	chr11:65405300-65481166	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
16	nsv430401	chr11:65419324-65788024	Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
17	esv3415004	chr11:65429526-65431424	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7101916	MALAT1	cis	parietal	SCAN
rs7101916	GPHA2	cis	parietal	SCAN
rs7101916	FAM89B	cis	parietal	SCAN
rs7101916	PLA2G16	cis	parietal	SCAN
rs7101916	PRDX5	cis	parietal	SCAN
rs7101916	SF3B2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65429000-65431400	Active TSS	iPS-18 Cell Line	embryonic stem cell
2	chr11:65429000-65431600	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr11:65429200-65431400	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr11:65429200-65431600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:65429200-65431800	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr11:65429400-65431400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:65429400-65431400	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr11:65429400-65431600	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr11:65429400-65431600	Active TSS	H9 Cell Line	embryonic stem cell
10	chr11:65429400-65431600	Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr11:65429400-65431600	Active TSS	Small Intestine	intestine
12	chr11:65429600-65431400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:65429600-65431400	Active TSS	Gastric	stomach
14	chr11:65429600-65431400	Active TSS	NHEK	skin
15	chr11:65429600-65431600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr11:65429600-65431600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:65429600-65431600	Active TSS	Aorta	Aorta
18	chr11:65429600-65431600	Active TSS	Brain Angular Gyrus	brain
19	chr11:65429600-65431600	Active TSS	Fetal Kidney	kidney
20	chr11:65429600-65431600	Active TSS	Ovary	ovary
21	chr11:65429600-65431600	Active TSS	Psoas Muscle	Psoas
22	chr11:65429600-65431600	Active TSS	HSMM	muscle
23	chr11:65429600-65431600	Active TSS	HSMMtube	muscle
24	chr11:65429600-65431800	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr11:65429600-65431800	Active TSS	Breast Myoepithelial Primary Cells	Breast
26	chr11:65429600-65432000	Active TSS	GM12878-XiMat	blood
27	chr11:65429800-65431400	Active TSS	Primary T helper cells PMA-I stimulated	--
28	chr11:65429800-65431400	Active TSS	Primary T killer naive cells fromperipheralblood	blood
29	chr11:65429800-65431400	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr11:65429800-65431400	Active TSS	Left Ventricle	heart
31	chr11:65429800-65431400	Active TSS	Spleen	Spleen
32	chr11:65429800-65431600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
33	chr11:65429800-65431600	Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr11:65429800-65431600	Active TSS	Brain Substantia Nigra	brain
35	chr11:65429800-65431600	Active TSS	Colon Smooth Muscle	Colon
36	chr11:65429800-65431600	Active TSS	Fetal Intestine Large	intestine
37	chr11:65429800-65431600	Active TSS	Pancreas	Pancrea
38	chr11:65429800-65431600	Active TSS	Right Atrium	heart
39	chr11:65429800-65431600	Active TSS	Right Ventricle	heart
40	chr11:65429800-65431600	Active TSS	Sigmoid Colon	Sigmoid Colon
41	chr11:65429800-65431600	Active TSS	NHDF-Ad	bronchial
42	chr11:65429800-65431800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr11:65429800-65431800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:65429800-65431800	Active TSS	K562	blood
45	chr11:65429800-65431800	Active TSS	NHLF	lung
46	chr11:65429800-65432000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr11:65430000-65431400	Active TSS	H1 Cell Line	embryonic stem cell
48	chr11:65430000-65431400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:65430000-65431400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:65430000-65431400	Active TSS	Primary T cells from cord blood	blood

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